US20090042266A1 - Treatment of cellulosic material and enzymes useful thererin - Google Patents

Treatment of cellulosic material and enzymes useful thererin Download PDF

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US20090042266A1
US20090042266A1 US12/141,976 US14197608A US2009042266A1 US 20090042266 A1 US20090042266 A1 US 20090042266A1 US 14197608 A US14197608 A US 14197608A US 2009042266 A1 US2009042266 A1 US 2009042266A1
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identity
dsm
cel7a
fragment
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Jari Vehmaanpera
Marika Alapuranen
Terhi Puranen
Matti Siika-aho
Jarno Kallio
Satu Hooman
Sanni Voutilainen
Teemu Halonen
Liisa Viikari
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Roal Oy
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Roal Oy
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Priority to US12/141,976 priority Critical patent/US20090042266A1/en
Assigned to ROAL OY reassignment ROAL OY ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: ALAPURANEN, MARIKA, HALONEN, TEEMU, HOOMAN, SATU, KALLIO, JARNO, PURANEN, TERHI, SIIKA-AHO, MATTI, VEHMAANPERA, JARI, VIIKARI, LIISA, VOUTILAINEN, SANNI
Publication of US20090042266A1 publication Critical patent/US20090042266A1/en
Priority to US12/917,603 priority patent/US8409836B2/en
Priority to US13/774,465 priority patent/US9758777B2/en
Priority to US14/045,236 priority patent/US9593324B2/en
Priority to US15/690,513 priority patent/US20180044656A1/en
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    • C—CHEMISTRY; METALLURGY
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    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/14—Hydrolases (3)
    • C12N9/24—Hydrolases (3) acting on glycosyl compounds (3.2)
    • C12N9/2402—Hydrolases (3) acting on glycosyl compounds (3.2) hydrolysing O- and S- glycosyl compounds (3.2.1)
    • C12N9/2405—Glucanases
    • C12N9/2434—Glucanases acting on beta-1,4-glucosidic bonds
    • C12N9/2437—Cellulases (3.2.1.4; 3.2.1.74; 3.2.1.91; 3.2.1.150)
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    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
    • C12N15/52—Genes encoding for enzymes or proenzymes
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    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
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    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/14—Hydrolases (3)
    • C12N9/24—Hydrolases (3) acting on glycosyl compounds (3.2)
    • C12N9/2402—Hydrolases (3) acting on glycosyl compounds (3.2) hydrolysing O- and S- glycosyl compounds (3.2.1)
    • C12N9/2405—Glucanases
    • C12N9/2434—Glucanases acting on beta-1,4-glucosidic bonds
    • C12N9/2445—Beta-glucosidase (3.2.1.21)
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/96—Stabilising an enzyme by forming an adduct or a composition; Forming enzyme conjugates
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P19/00—Preparation of compounds containing saccharide radicals
    • C12P19/02—Monosaccharides
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    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P7/00—Preparation of oxygen-containing organic compounds
    • C12P7/02—Preparation of oxygen-containing organic compounds containing a hydroxy group
    • C12P7/04—Preparation of oxygen-containing organic compounds containing a hydroxy group acyclic
    • C12P7/06—Ethanol, i.e. non-beverage
    • C12P7/08—Ethanol, i.e. non-beverage produced as by-product or from waste or cellulosic material substrate
    • C12P7/10—Ethanol, i.e. non-beverage produced as by-product or from waste or cellulosic material substrate substrate containing cellulosic material
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    • C12Y—ENZYMES
    • C12Y302/00—Hydrolases acting on glycosyl compounds, i.e. glycosylases (3.2)
    • C12Y302/01—Glycosidases, i.e. enzymes hydrolysing O- and S-glycosyl compounds (3.2.1)
    • C12Y302/01004—Cellulase (3.2.1.4), i.e. endo-1,4-beta-glucanase
    • C—CHEMISTRY; METALLURGY
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    • C12Y—ENZYMES
    • C12Y302/00—Hydrolases acting on glycosyl compounds, i.e. glycosylases (3.2)
    • C12Y302/01—Glycosidases, i.e. enzymes hydrolysing O- and S-glycosyl compounds (3.2.1)
    • C12Y302/01021—Beta-glucosidase (3.2.1.21)
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Y—ENZYMES
    • C12Y302/00—Hydrolases acting on glycosyl compounds, i.e. glycosylases (3.2)
    • C12Y302/01—Glycosidases, i.e. enzymes hydrolysing O- and S-glycosyl compounds (3.2.1)
    • C12Y302/01091—Cellulose 1,4-beta-cellobiosidase (3.2.1.91)
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E50/00—Technologies for the production of fuel of non-fossil origin
    • Y02E50/10—Biofuels, e.g. bio-diesel
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/50—Improvements relating to the production of bulk chemicals
    • Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts

Definitions

  • the present invention relates to the production of sugar hydrolysates from cellulosic material. More precisely the invention relates to production of fermentable sugars from lignocellulosic material by enzymatic conversion.
  • the fermentable sugars are useful e.g. in the production of bioethanol, or for other purposes.
  • the invention is directed to a method for treating cellulosic material with cellobiohydrolase, endoglucanase, beta-glucosidase, and optionally xylanase, and to enzyme preparations and the uses thereof.
  • the invention is further directed to novel cellulolytic polypeptides, polynucleotides encoding them, and to vectors and host cells containing the polynucleotides. Still further the invention is directed to uses of the polypeptides and to a method of preparing them.
  • Sugar hydrolysates can be used for microbial production of a variety of fine chemicals or biopolymers, such as organic acids e.g. lactic acid, or ethanol or other alcohols e.g. n-butanol, 1,3-propanediol, or polyhydroxyalkanoates (PHAs).
  • the sugar hydrolysates may also serve as raw material for other non-microbial processes, e.g., for enrichment, isolation and purification of high value sugars or various polymerization processes.
  • One of the major uses of the sugar hydrolysates is in the production of biofuels. The production of bioethanol and/or other chemicals may take place in an integrated process in a biorefinery (Wyman 2001).
  • lignocellulose which essentially consists of cellulose, hemicellulose, pectin and lignin.
  • lignocellulose-to-ethanol process the lignocellulosic material is first pretreated either chemically or physically to make the cellulose fraction more accessible to hydrolysis. The cellulose fraction is then hydrolysed to obtain sugars that can be fermented by yeast into ethanol. Lignin is obtained as a main co-product that may be used as a solid fuel.
  • Enzymatic hydrolysis is considered the most promising technology for converting cellulosic biomass into fermentable sugars.
  • enzymatic hydrolysis is used only to a limited amount at industrial scale, and especially when using strongly lignified material such as wood or agricultural waste the technology is not satisfactory.
  • the cost of the enzymatic step is one of the major economical factors of the process. Efforts have been made to improve the efficiency of the enzymatic hydrolysis of the cellulosic material (Badger 2002).
  • US 2002/0192774 A1 describes a continuous process for converting solid lignocellulosic biomass into combustible fuel products. After pretreatment by wet oxidation or steam explosion the biomass is partially separated into cellulose, hemicellulose and lignin, and is then subjected to partial hydrolysis using one or more carbohydrase enzymes (EC 3.2). CelluclastTM, a commercial product by Novo Nordisk A/S containing cellulase and xylanase activities is given as an example.
  • US 2004/000 5674 A1 describes novel enzyme mixtures that can be used directly on lignocellulose substrate, whereby toxic waste products formed during pretreatment processes may be avoided, and energy may be saved.
  • the synergistic enzyme mixture contains a cellulase and an auxiliary enzyme such as cellulase, xylanase, ligninase, amylase, protease, lipidase or glucuronidase, or any combination thereof.
  • Cellulase in considered to include endoglucanase (EG), beta-glucosidase (BG) and cellobiohydrolase (CBH).
  • EG endoglucanase
  • BG beta-glucosidase
  • CBH cellobiohydrolase
  • Kurabi et al. (2005) have investigated enzymatic hydrolysis of steam-exploded and ethanol organosolv-pretreated Douglas-fir by novel and commercial fungal cellulases. They tested two commercial Trichoderma reesei cellulase preparations, and two novel preparations produced by mutant strains of Trichoderma sp. and Penicillium sp. The Trichoderma sp. preparation showed significantly better performance than the other preparations. The better performance was believed to be at least partly due to a significantly higher beta-glucosidase activity, which relieves product inhibition of cellobiohydrolase and endoglucanase.
  • US 2004/005 3373 A1 pertains a method of converting cellulose to glucose by treating a pretreated lignocellulosic substrate with an enzyme mixture comprising cellulase and a modified cellobiohydrolase I (CBHI).
  • the CBHI has been modified by inactivating its cellulose binding domain (CBD). Advantages of CBHI modification are e.g. better recovery and higher hydrolysis rate with high substrate concentration.
  • the cellulase is selected from the group consisting of EG, CBH and BG.
  • the CBHI is preferably obtained from Trichoderma.
  • US 2005/016 4355 A1 describes a method for degrading lignocellulosic material with one or more cellulolytic enzymes in the presence of at least one surfactant. Additional enzymes such as hemicellulases, esterase, peroxidase, protease, laccase or mixture thereof may also be used. The presence of surfactant increases the degradation of lignocellulosic material compared to the absence of surfactant.
  • the cellulolytic enzymes may be any enzyme involved in the degradation of lignocellulose including CBH, EG, and BG.
  • CBHs Cellobiohydrolases
  • WO 03/000 941 which relates to CBHI enzymes obtained from various fungi. No physiological properties of the enzymes are provided, nor any examples of their uses.
  • Hong et al. (2003b) characterizes CBHI of Thermoascus aurantiacus produced in yeast. Applications of the enzyme are not described.
  • Tuohy et al. (2002) describe three forms of cellobiohydrolases from Talaromyces emersonii.
  • Endoglucanases of the cel5 family are described e.g. in WO 03/062 409, which relates to compositions comprising at least two thermostable enzymes for use in feed applications.
  • Hong et al. (2003a) describe production of thermostable endo- ⁇ -1,4-glucanase from T. aurantiacus in yeast. No applications are explained.
  • WO 01/70998 relates to ⁇ -glucanases from Talaromyces . They also describe ⁇ -glucanases from Talaromyces emersonii . Food, feed, beverage, brewing, and detergent applications are discussed. Lignocellulose hydrolysis is not mentioned.
  • WO 98/06 858 describes beta-1,4-endoglucanase from Aspergillus niger and discusses feed and food applications of the enzyme.
  • WO 97/13853 describes methods for screening DNA fragments encoding enzymes in cDNA libraries.
  • the cDNA library is of yeast or fungal origin, preferably from Aspergillus .
  • the enzyme is preferably a cellulase.
  • Van Petegem et al. describe the 3D-structure of an endoglucanase of the cel5 family from Thermoascus aurantiacus .
  • Parry et al. describe the mode of action of an endoglucanase of the cel5 family from Thermoascus aurantiacus.
  • Endoglucanases of the cel7 family are disclosed e.g. in U.S. Pat. No. 5,912,157, which pertains Myceliphthora endoglucanase and its homologues and applications thereof in detergent, textile, and pulp.
  • U.S. Pat. No. 6,071,735 describes cellulases exhibiting high endoglucanase activity in alkaline conditions. Uses as detergent, in pulp and paper, and textile applications are discussed. Bioethanol is not mentioned.
  • U.S. Pat. No. 5,763,254 discloses enzymes degrading cellulose/hemicellulose and having conserved amino acid residues in CBD.
  • Endoglucanases of the cel45 family are described e.g. in U.S. Pat. No. 6,001,639, which relates to enzymes having endoglucanase activity and having two conserved amino acid sequences. Uses in textile, detergent, and pulp and paper applications are generally discussed and treating of lignocellulosic material is mentioned but no examples are given.
  • WO 2004/053039 is directed to detergent applications of endoglucanases.
  • U.S. Pat. No. 5,958,082 discloses the use of endoglucanase, especially from Thielavia terrestris in textile application.
  • EP 0495258 relates to detergent compositions containing Humicola cellulase.
  • U.S. Pat. No. 5,948,672 describes a cellulase preparation containing endoglucanase, especially from Humicola and its use in textile and pulp applications. Lignocellulose hydrolysis is not mentioned.
  • Beta-glucosidase enhances hydrolysis of biomass to glucose by hydrolyzing cellobiose produced by cellobiohydrolases. Cellobiose conversion to glucose is usually the major rate-limiting step.
  • Beta-glucosidases are disclosed e.g. in US 2005/021 4920, which relates to BG from Aspergillus fumigatus . The enzyme has been produced in Aspergillus oryzae and Trichoderma reesei . Use of the enzyme in degradation of biomass or detergent applications is generally discussed but not exemplified.
  • WO02/095 014 describes an Aspergillus oryzae enzyme having cellobiase activity.
  • WO2005/074656 discloses polypeptides having cellulolytic enhancing activity derived e.g. from T. aurantiacus; A. fumigatus; T. terrestris and T. aurantiacus .
  • WO02/26979 discloses enzymatic processing of plant material.
  • U.S. Pat. No. 6,022,725 describes cloning and amplification of the beta-gluco-sidase gene of Trichoderma reesei
  • U.S. Pat. No. 6,103,464 describes a method for detecting DNA encoding a beta-glucosidase from a filamentous fungus. No application examples are given.
  • Xylanases are described e.g. in FR2786784, which relates to a heat-stable xylanase, useful e.g. in treating animal feed and in bread making.
  • the enzyme is derived from a thermophilic fungus, particularly of the genus Thermoascus.
  • U.S. Pat. No. 6,197,564 describes enzymes having xylanase activity, and obtained from Aspergillus aculeatus . Their application in baking is exemplified.
  • WO 02/24926 relates to Talaromyces xylanases . Feed and baking examples are given.
  • WO01/42433 discloses thermostable xylanase from Talaromyces emersonii for use in food and feed applications.
  • Trichoderma reesei the anamorph of Hypocrea jecorina . Consequently also most of the commercially available fungal cellulases are derived from Trichoderma reesei .
  • the majority of cellulases from less known fungi have not been applied in processes of practical importance such as in degrading cellulosic material, including lignocellulose.
  • cellulolytic enzymes and especially cellobiohydrolases obtainable from Thermoascus aurantiacus, Acremonium thermophilum , or Chaetomium thermophilum are particularly useful in hydrolyzing cellulosic material.
  • these fungi also have endoglucanases, beta-glucosidases and xylanases that are very suitable for degrading cellulosic material.
  • the enzymes are kinetically very effective over a broad range of temperatures, and although they have high activity at high temperatures, they are also very efficient at standard hydrolysis temperatures. This makes them extremely well suited for varying cellulosic substrate hydrolysis processes carried out both at conventional temperatures and at elevated temperatures.
  • the present invention provides a method for treating cellulosic material with cellobiohydrolase, endoglucanase and beta-glucosidase, whereby said cellobiohydrolase comprises an amino acid sequence having at least 80% identity to SEQ ID NO: 2, 4, 6 or 8, or to an enzymatically active fragment thereof.
  • the invention further provides an enzyme preparation comprising cellobiohydrolase, endoglucanase and beta-glucosidase, wherein said cellobiohydrolase comprises an amino acid sequence having at least 80% identity to SEQ ID NO: 2, 4, 6 or 8, or to an enzymatically active fragment thereof.
  • the invention is also directed to a polypeptide comprising a fragment having cellulolytic activity and being selected from the group consisting of:
  • a polypeptide comprising an amino acid sequence having at least 66% identity to SEQ ID NO:4, 79% identity to SEQ ID NO:6, 78% identity to SEQ ID NO:12, 68% identity to SEQ ID NO:14, 72% identity to SEQ ID NO:16, 68% identity to SEQ ID NO:20, 74% identity to SEQ ID NO:22 or 24, or 78% identity to SEQ ID NO:26;
  • One further object of the invention is an isolated polynucleotide selected from the group consisting of:
  • the invention still further provides a vector, which comprises said polynucleotide as a heterologous sequence, and a host cell comprising said vector.
  • Escherichia coli strains having accession number DSM 16728, DSM 16729, DSM 17324, DSM 17323, DSM 17729, DSM 16726, DSM 16725, DSM 17325 or DSM 17667 are also included in the invention.
  • enzyme preparations comprising at least one of the novel polypeptides, and the use of said polypeptide or enzyme preparation in fuel, textile, detergent, pulp and paper, food, feed or beverage industry.
  • a polypeptide comprising an amino acid sequence having at least 66% identity to SEQ ID NO:4, 79% identity to SEQ ID NO:6, 78% identity to SEQ ID NO:12, 68% identity to SEQ ID NO:14, 72% identity to SEQ ID NO:16, 68% identity to SEQ ID NO:20, 74% identity to SEQ ID NO:22 or 24, or 78% identity to SEQ ID NO:26;
  • said method comprising transforming a host cell with a vector encoding said polypeptide, and culturing said host cell under conditions enabling expression of said polypeptide, and optionally recovering and purifying the polypeptide produced.
  • FIG. 1 Temperature dependencies of the cellulase and beta-glucosidase activities in the supernatants of the tested six fungal strains.
  • the incubation time in the assay was 60 min at the given temperature, the assay pH was 5.0 (MUL-activity) or 4.8 (CMCase or BGU).
  • Activity obtained at 60° C. is set as the relative activity of 100%.
  • FIG. 2 Schematic picture of the expression cassettes used in the transformation of Trichoderma reesei protoplasts for producing the recombinant fungal proteins.
  • the recombinant genes were under the control of T. reesei cbh1 (cel7A) promoter (cbh1 prom) and the termination of the transcription was ensured by using T. reesei cbh1 terminator sequence (cbh1 term).
  • the amdS gene was included as a transformation marker.
  • FIG. 3 A) pH optima of the recombinant CBH/Cel7 protein preparations from Thermoascus aurantiacus ALKO4242, Chaetomium thermophilum ALKO4265 and Acremonium thermophilum ALKO4245 determined on 4-meth-ylumbelliferyl- ⁇ -D-lactoside (MUL) at 50° C., 10 min. The results are given as mean ( ⁇ SD) of three separate measurements.
  • MUL 4-meth-ylumbelliferyl- ⁇ -D-lactoside
  • FIG. 4 Crystalline cellulose (Avicel) hydrolysis by the purified recombinant cellobiohydrolases at 45° C. Substrate concentration 1% (w/v), pH 5.0, enzyme concentration 1.4 ⁇ M. A) Cellobiohydrolases harboring a CBD, B) cellobiohydrolases (core) without a CBD.
  • FIG. 5 Crystalline cellulose (Avicel) hydrolysis by the purified recombinant cellobiohydrolases at 70° C. Substrate concentration 1% (w/v), pH 5.0, enzyme concentration 1.4 ⁇ M. A) Cellobiohydrolases harboring a CBD, B) cellobiohydrolases (core) without a CBD.
  • FIG. 6 A) The pH dependency of the heterologously produced Acremonium EG — 40/Cel45A, EG — 40_like/Cel45B and Thermoascus EG — 28/Cel5A activity was determined with CMC substrate in a 10 min reaction at 50° C. B) Temperature optimum of the Acremonium EG — 40/Cel45A, EG — 40_like/Cel45B and Thermoascus EG — 28/Cel5A was determined at pH 5.5, 4.8, and 6.0, respectively. The reaction containing CMC as substrate was performed for 60 min, except for EG — 28/Cel5A for 10 min. BSA (100 ⁇ g/ml) was added as a stabilizer.
  • FIG. 7 A) The pH dependency of the heterologously produced Acremonium BG — 101/Cel3A, Chaetomium BG — 76/Cel3A, and Thermoascus BG — 81/Cel3A activity was determined with 4-nitrophenyl- ⁇ -D-glucopyranoside substrate in a 10 min reaction at 50° C.
  • FIG. 8 A) The pH dependency of the heterologously produced Thermoascus XYN — 30/Xyn10A xylanase activity was determined with birch xylan substrate in a 10 min reaction at 50° C. B) Temperature optimum of XYN — 30/Xyn10A was determined at pH 5.3 in a 60 min reaction, BSA (100 ⁇ g/ml) was added as a stabilizer.
  • FIG. 9 Hydrolysis of washed steam exploded spruce fibre (10 mg/ml) with a mixture of thermophilic enzymes (MIXTURE 1) and T. reesei enzymes at 55 and 60° C. Enzyme dosage is given by FPU/g dry matter of substrate, FPU assayed at 50° C., pH 5. Hydrolysis was carried out for 72 h at pH 5, with mixing. The results are given as mean ( ⁇ SD) of three separate measurements.
  • FIG. 10 Hydrolysis of steam exploded corn stover (10 mg/ml) with a mixture of thermophilic enzymes (MIXTURE 2) and T. reesei enzymes at 45, 55 and 57.5° C. Enzyme dosage was for “MIXTURE 2” 5 FPU/g dry matter of substrate and for T. reesei enzymes 5 FPU/g dry matter Celluclast supplemented with 100 nkat/g dry matter Novozym 188 (filter paper activity was assayed at 50° C., pH 5). Hydrolysis was carried out for 72 h at pH 5, with mixing. The results are given as mean ( ⁇ SD) of three separate measurements. The substrate contained soluble reducing sugars (ca 0.7 mg/ml). This background sugar content was subtracted from the reducing sugars formed during the hydrolysis.
  • MIXTURE 2 thermophilic enzymes
  • T. reesei enzymes 5 FPU/g dry matter Celluclast supplemented with 100 nkat/g dry matter Novozym 188 (filter paper
  • FIG. 11 Hydrolysis of steam exploded corn stover (10 mg/ml) with a mixture of thermophilic enzymes containing a new thermophilic xylanase from Thermoascus aurantiacus (MIXTURE 3) and T. reesei enzymes at 45, 55 and 60° C.
  • Enzyme dosage was for “MIXTURE 3” 5 FPU/g dry matter of substrate and for T. reesei enzymes 5 FPU/g dry matter Celluclast supplemented with 100 nkat/g dry matter Novozym 188 (filter paper activity was assayed at 50° C., pH 5). Hydrolysis was carried out for 72 h at pH 5, with mixing. The results are given as mean ( ⁇ SD) of three separate measurements.
  • the substrate contained soluble reducing sugars (ca 0.7 mg/ml). This background sugar content was subtracted from the reducing sugars formed during the hydrolysis.
  • FIG. 12 Hydrolysis of steam exploded spruce fibre (10 mg/ml) with a mixture of thermophilic enzymes containing a new thermophilic xylanase XYN — 30/Xyn10A from Thermoascus aurantiacus (MIXTURE 3) and T. reesei enzymes at 45, 55 and 60° C.
  • Enzyme dosage for “MIXTURE 3” was 5 FPU/g dry matter of substrate and for T. reesei enzymes 5 FPU/g dry matter Celluclast supplemented with 100 nkat/g dry matter Novozym 188 (filter paper activity was assayed at 50° C., pH 5). Hydrolysis was carried out for 72 h at pH 5, with mixing. The results are given as mean ( ⁇ SD) of three separate measurements.
  • FIG. 13 The effect of glucose on activity of different ⁇ -glucosidase preparations.
  • the standard assay using p-nitrophenyl- ⁇ -D-glucopyranoside as substrate was carried out in the presence of glucose in the assay mixture.
  • the activity is presented as percentage of the activity obtained without glucose.
  • FIG. 14 FPU activities of the enzyme mixtures at temperatures from 50° C. to 70° C., presented as a percentage of the activity under the standard conditions (50° C., 1 h).
  • FIG. 15 The relative cellulase activity of two different T. reesei strains grown in media containing untreated Nutriose (NO) or BG — 81/Cel3A pretreated Nutriose (NBG81) as a carbon source.
  • Cellulose is the major structural component of higher plants. It provides plant cells with high tensile strength helping them to resist mechanical stress and osmotic pressure.
  • Cellulose is a ⁇ -1,4-glucan composed of linear chains of glucose residues joined by ⁇ -1,4-glycosidic linkages.
  • Cellobiose is the smallest repeating unit of cellulose. In cell walls cellulose is packed in variously oriented sheets, which are embedded in a matrix of hemicellulose and lignin.
  • Hemicellulose is a heterogeneous group of carbohydrate polymers containing mainly different glucans, xylans and mannans.
  • Hemicellulose consists of a linear backbone with ⁇ -1,4-linked residues substituted with short side chains usually containing acetyl, glucuronyl, arabinosyl and galactosyl. Hemicellulose can be chemically cross-linked to lignin. Lignin is a complex cross-linked polymer of variously substituted p-hydroxyphenylpropane units that provides strength to the cell wall to withstand mechanical stress, and it also protects cellulose from enzymatic hydrolysis.
  • Lignocellulose is a combination of cellulose and hemicellulose and polymers of phenol propanol units and lignin. It is physically hard, dense, and inaccessible and the most abundant biochemical material in the biosphere.
  • Lignocellulose containing materials are for example: hardwood and softwood chips, wood pulp, sawdust and forestry and wood industrial waste; agricultural biomass as cereal straws, sugar beet pulp, corn stover and cobs, sugar cane bagasse, stems, leaves, hulls, husks, and the like; waste products as municipal solid waste, newspaper and waste office paper, milling waste of e.g. grains; dedicated energy crops (e.g., willow, poplar, switchgrass or reed canarygrass, and the like).
  • Preferred examples are corn stover, switchgrass, cereal straw, sugarcane bagasse and wood derived materials.
  • Cellulosic material as used herein, relates to any material comprising cellulose, hemicellulose and/or lignocellulose as a significant component.
  • “Lignocellulosic material” means any material comprising lignocellulose. Such materials are e.g. plant materials such as wood including softwood and hardwood, herbaceous crops, agricultural residues, pulp and paper residues, waste paper, wastes of food and feed industry etc. Textile fibres such as cotton, fibres derived from cotton, linen, hemp, jute and man made cellulosic fibres as modal, viscose, lyocel are specific examples of cellulosic materials.
  • Cellulosic material is degraded in nature by a number of various organisms including bacteria and fungi.
  • Cellulose is typically degraded by different cellulases acting sequentially or simultaneously.
  • the biological conversion of cellulose to glucose generally requires three types of hydrolytic enzymes: (1) Endoglucanases which cut internal beta-1,4-glucosidic bonds; (2) Exocellobiohydrolases that cut the dissaccharide cellobiose from the end of the cellulose polymer chain; (3) Beta-1,4-glucosidases which hydrolyze the cellobiose and other short cello-oligosaccharides to glucose.
  • the three major groups of cellulases are cellobiohydrolases (CBH), endoglucanases (EG) and beta-glucosidases (BG).
  • lignocellulose is degraded by hemicellulases, like xylanases and mannanases.
  • Hemicellulase is an enzyme hydrolysing hemicellulose.
  • Cellulolytic enzymes are enzymes having “cellulolytic activity,” which means that they are capable of hydrolysing cellulosic substrates or derivatives thereof into smaller saccharides. Cellulolytic enzymes thus include both cellulases and hemicellulases. Cellulases as used herein include cellobiohydrolase, endoglucanase and beta-glucosidase.
  • T. reesei has a well known and effective cellulase system containing two CBHs, two major and several minor EGs and BGs.
  • T. reesei CBHI (Cel7A) cuts sugar from the reducing end of the cellulose chain, has a C-terminal cellulose binding domain (CBD) and may constitute up to 60% of the total secreted protein.
  • T. reesei CBHII (Cel6A) cuts sugar from the non-reducing end of the cellulose chain, has an N-terminal cellulose binding domain and may constitute up to 20% of the total secreted protein.
  • Endoglucanases EGI (Cel7B), and EGV (Cel45A) have a CBD in their C-terminus
  • EGII (Cel5A) has an N-terminal CBD
  • EGIII (Cel12A) does not have a cellulose binding domain at all.
  • CBHI, CBHII, EGI and EGII are so called “major cellulases” of Trichoderma comprising together 80-90% of total secreted proteins. It is known to a man skilled in the art that an enzyme may be active on several substrates and enzymatic activities can be measured using different substrates, methods and conditions. Identifying different cellulolytic activities is discussed for example in van Tilbeurgh et al. 1988.
  • cellulolytic enzymes may comprise one or more cellulose binding domains (CBDs), also named as carbohydrate binding domains/modules (CBD/CBM), which can be located either at the N- or C-terminus of the catalytic domain.
  • CBDs have carbohydrate-binding activity and they mediate the binding of the cellulase to crystalline cellulose but have little or no effect on cellulase hydrolytic activity of the enzyme on soluble substrates. These two domains are typically connected via a flexible and highly glycosylated linker region.
  • CBH Cerellobiohydrolase
  • Endoglucanase or “EG” refers to enzymes that cut internal glycosidic bonds of the cellulose chain. They are classified as EC 3.2.1.4. They are 1,4-beta-D-glucan 4-glucanohydrolases and catalyze endohydrolysis of 1,4-beta-D-glycosidic linkages in polymers of glucose such as cellulose and derivatives thereof. Some naturally occurring endoglucanases have a cellulose binding domain, while others do not. Some endoglucanases have also xylanase activity (Bailey et al., 1993).
  • Beta-glucosidase or “BG” or “G” refers to enzymes that degrade small soluble oligosaccharides including cellobiose to glucose. They are classified as EC 3.2.1.21. They are beta-D-glucoside glucohydrolases, which typically catalyze the hydrolysis of terminal non-reducing beta-D-glucose residues. These enzymes recognize oligosaccharides of glucose. Typical substrates are cellobiose and cellotriose. Cellobiose is an inhibitor of cellobiohydrolases, wherefore the degradation of cellobiose is important to overcome end-product inhibition of cellobiohydrolases.
  • Xylanases are enzymes that are capable of recognizing and hydrolyzing hemicellulose. They include both exohydrolytic and endohydrolytic enzymes. Typically they have endo-1,4-beta-xylanase (EC 3.2.1.8) or beta-D-xylosidase (EC 3.2.1.37) activity that breaks down hemicellulose to xylose.
  • endo-1,4-beta-xylanase EC 3.2.1.8
  • beta-D-xylosidase EC 3.2.1.37 activity that breaks down hemicellulose to xylose.
  • “Xylanase” or “Xyn” in connection with the present invention refers especially to an enzyme classified as EC 3.2.1.8 hydrolyzing xylose polymers of lignocellulosic substrate or purified xylan.
  • glycosyl hydrolase families In addition to this cellulases can be classified to various glycosyl hydrolase families according their primary sequence, supported by analysis of the three dimensional structure of some members of the family (Henrissat 1991, Henrissat and Bairoch 1993, 1996). Some glycosyl hydrolases are multifunctional enzymes that contain catalytic domains that belong to different glycosylhydrolase families.
  • Family 3 consists of beta-glucosidases (EC 3.2.1.21) such as Ta BG — 81, At BG — 101 and Ct BG — 76 described herein.
  • Family 5 (formerly known as celA) consists mainly of endoglucanases (EC 3.2.1.4) such as Ta EG — 28 described herein.
  • Family 7 (formerly cellulase family ceIC) contains endoglucanases (EC 3.2.1.4) and cellobiohydrolases (EC 3.2.1.91) such as Ct EG — 54, Ta CBH, At CBH_A, At CBH_C and Ct CBH described herein.
  • Family 10 (formerly ceIF) consists mainly of xylanases (EC 3.2.1.8) such as Ta XYN — 30 and At XYN — 60 described herein.
  • Family 45 (formerly celK) contains endoglucanases (EC 3.2.1.4) such as At EG — 40 and At EG — 40_like described herein.
  • Cellulolytic enzymes useful for hydrolyzing cellulosic material are obtainable from Thermoascus aurantiacus, Acremonium thermophilum , or Chaetomium thermophilum . “Obtainable from” means that they can be obtained from said species, but it does not exclude the possibility of obtaining them from other sources. In other words they may originate from any organism including plants. Preferably they originate from microorganisms e.g. bacteria or fungi. The bacteria may be for example from a genus selected from Bacillus, Azospirillum and Streptomyces .
  • the enzyme originates from fungi (including filamentous fungi and yeasts), for example from a genus selected from the group consisting of Thermoascus, Acremonium, Chaetomium, Achaetomium, Thielavia, Aspergillus, Botrytis, Chrysosporium, Collybia, Fomes, Fusarium, Humicola, Hypocrea, Lentinus, Melanocarpus, Myceliophthora, Myriococcum, Neurospora, Penicillium, Phanerochaete, Phlebia, Pleurotus, Podospora, Polyporus, Rhizoctonia, Scytalidium, Pycnoporus, Trametes and Trichoderma.
  • fungi including filamentous fungi and yeasts
  • a genus selected from the group consisting of Thermoascus, Acremonium, Chaetomium, Achaetomium, Thielavi
  • the enzymes are obtainable from Thermoascus aurantiacus strain ALKO4242 deposited as CBS 116239, strain ALKO4245 deposited as CBS 116240 presently classified as Acremonium thermophilium , or Chaetomium thermophilum strain ALKO4265 deposited as CBS 730.95.
  • the cellobiohydrolase preferably comprises an amino acid sequence having at least 80% identity to SEQ ID NO: 2, 4, 6 or 8, or an enzymatically active fragment thereof.
  • CBHs have an advantageous cellulose inhibition constant compared to that of Trichoderma reesei CBH, and they show improved hydrolysis results when testing various cellulosic substrates.
  • SEQ ID NO: 2 and 4 do not comprise a CBD.
  • Particularly enhanced hydrolysis results may be obtained when a cellulose binding domain (CBD) is attached to a CBH that has no CBD of its own.
  • the CBD may be obtained e.g. from a Trichoderma or Chaetomium species, and it is preferably attached to the CBH via a linker.
  • the resulting fusion protein containing a CBH core region attached to a CBD via a linker may comprise an amino acid sequence having at least 80% identity to SEQ ID NO: 28 or 30.
  • Polynucleotides comprising a sequence of SEQ ID NO: 27 or 29 encode such fusion proteins.
  • the endoglucanase may comprise an amino acid sequence having at least 80% identity to SEQ ID NO: 10, 12, 14 or 16, or an enzymatically active fragment thereof. These endoglucanases have good thermostability.
  • the beta-glucosidase may comprise an amino acid sequence having at least 80% identity to SEQ ID NO: 22, 24 or 26, or an enzymatically active fragment thereof. These beta-glucosidases have good resistance to glucose inhibition, which is advantageous to avoid end product inhibition during enzymatic hydrolysis of cellulosic material.
  • the beta-glucosidases may also be used in preparing sophorose, a cellulase inducer used in cultivation of T. reesei .
  • Beta- Obtainable nucleic acid amino acid glucosidase Gene from SEQ ID NO: SEQ ID NO: Ta BG_81 Ta cel3A T. aurantiacus 21 22 At BG_101 At cel3A A. thermophilum 23 24 Ct BG_76 Ct cel3A C. thermophilum 25 26
  • the xylanase may comprise an amino acid sequence having at least 80% identity to SEQ ID NO: 18 or 20, or an enzymatically active fragment thereof.
  • identity is here meant the global identity between two amino acid sequences compared to each other from the first amino acid encoded by the corresponding gene to the last amino acid.
  • the identity of the full-length sequences is measured by using Needleman-Wunsch global alignment program at EMBOSS (European Molecular Biology Open Software Suite; Rice et al., 2000) program package, version 3.0.0, with the following parameters: EMBLOSUM62, Gap penalty 10.0, Extend penalty 0.5.
  • the algorithm is described in Needleman and Wunsch (1970). The man skilled in the art is aware of the fact that results using Needleman-Wunsch algorithm are comparable only when aligning corresponding domains of the sequence. Consequently comparison of e.g. cellulase sequences including CBD or signal sequences with sequences lacking those elements cannot be done.
  • a cellulolytic polypeptide is used that has at least 80, 85, 90, 95 or 99% identity to SEQ ID NO: 2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24 or 26 or at least to its enzymatically active fragment.
  • an enzymatically active fragment is meant any fragment of a defined sequence that has cellulolytic activity.
  • an enzymatically active fragment may be the mature protein part of the defined sequence, or it may be only an fragment of the mature protein part, provided that it still has cellobiohydrolase, endoglucanase, beta-glucosidase or xylanase activity.
  • the cellulolytic enzymes are preferably recombinant enzymes, which may be produced in a generally known manner.
  • a polynucleotide fragment comprising the enzyme gene is isolated, the gene is inserted under a strong promoter in an expression vector, the vector is transferred into suitable host cells and the host cells are cultivated under conditions provoking production of the enzyme.
  • Methods for protein production by recombinant technology in different host systems are well known in the art (Sambrook et al., 1989; Coen, 2001; Gellissen, 2005).
  • the enzymes are produced as extracellular enzymes that are secreted into the culture medium, from which they can easily be recovered and isolated.
  • the spent culture medium of the production host can be used as such, or the host cells may be removed therefrom, and/or it may be concentrated, filtrated or fractionated. It may also be dried.
  • Isolated polypeptide in the present context may simply mean that the cells and cell debris have been removed from the culture medium containing the polypeptide.
  • the polypeptides are isolated e.g. by adding anionic and/or cationic polymers to the spent culture medium to enhance precipitation of cells, cell debris and some enzymes that have unwanted side activities.
  • the medium is then filtrated using an inorganic filtering agent and a filter to remove the precipitants formed. After this the filtrate is further processed using a semi-permeable membrane to remove excess of salts, sugars and metabolic products.
  • the heterologous polynucleotide comprises a gene similar to that included in a microorganism having accession number DSM 16723, DSM 16728, DSM 16729, DSM 16727, DSM 17326, DSM 17324, DSM 17323, DSM 17729, DSM 16724, DSM 16726, DSM 16725, DSM 17325 or DSM 17667.
  • the production host can be any organism capable of expressing the cellulolytic enzyme.
  • the host is a microbial cell, more preferably a fungus. Most preferably the host is a filamentous fungus.
  • the recombinant host is modified to express and secrete cellulolytic enzymes as its main activity or one of its main activities. This can be done by deleting major homologous secreted genes e.g. the four major cellulases of Trichoderma and by targeting heterologous genes to a locus that has been modified to ensure high expression and production levels.
  • Preferred hosts for producing the cellulolytic enzymes are in particular strains from the genus Trichoderma or Aspergillus.
  • the enzymes needed for the hydrolysis of the cellulosic material according to the invention may be added in an enzymatically effective amount either simultaneously e.g. in the form of an enzyme mixture, or sequentially, or as a part of the simultaneous saccharification and fermentation (SSF).
  • Any combination of the cellobiohydrolases comprising an amino acid sequence having at least 80% identity to SEQ ID NO: 2, 4, 6 or 8 or to an enzymatically active fragment thereof may be used together with any combination of endoglucanases and beta-glucosidases.
  • the cellulosic material comprises hemicellulose, hemicellulases, preferably xylanases are additionally used for the degradation.
  • endoglucanases, beta-glucosidases and xylanases may be selected from those described herein, but are not limited to them. They can for example also be commercially available enzyme preparations.
  • one or more other enzymes may be used, for example proteases, amylases, laccases, lipases, pectinases, esterases and/or peroxidases. Another enzyme treatment may be carried out before, during or after the cellulase treatment.
  • the term “enzyme preparation” denotes to a composition comprising at least one of the desired enzymes.
  • the preparation may contain the enzymes in at least partially purified and isolated form. It may even essentially consist of the desired enzyme or enzymes.
  • the preparation may be a spent culture medium or filtrate containing one or more cellulolytic enzymes.
  • the preparation may contain additives, such as mediators, stabilizers, buffers, preservatives, surfactants and/or culture medium components. Preferred additives are such, which are commonly used in enzyme preparations intended for a particular application.
  • the enzyme preparation may be in the form of liquid, powder or granulate.
  • the enzyme preparation is spent culture medium.
  • Spent culture medium refers to the culture medium of the host comprising the produced enzymes.
  • the host cells are separated from the said medium after the production.
  • the enzyme preparation comprises a mixture of CBH, EG and BG, optionally together with xylanase and/or other enzymes.
  • the CBH comprises an amino acid sequence having at least 80% identity to SEQ ID NO: 2, 4, 6 or 8 or to an enzymatically active fragment thereof, and it may be obtained from Thermoascus aurantiacus, Acremonium thermophilum , or Chaetomium thermophilum
  • EG, BG and xylanase may be of any origin including from said organisms.
  • Other enzymes that might be present in the preparation are e.g. proteases, amylases, laccases, lipases, pectinases, esterases and/or peroxidases.
  • thermostable enzymes are chosen.
  • a combination of a CBH of family 7 with an endoglucanase of family 45, optionally in combination with a BG of family 3 and/or a xylanase of family 10 had excellent hydrolysis performance both at 45° C., and at elevated temperatures.
  • Cellulolytic enzymes of Trichoderma reesei are conventionally used at temperatures in the range of about 40-50° C. in the hydrolysis, and at 30-40° C. in SSF.
  • CBH, EG, BG and Xyn obtainable from Thermoascus aurantiacus, Acremonium thermophilum , or Chaetomium thermophilum are efficient at these temperatures too, but in addition most of them also function extremely well at temperatures between 50° C. and 75° C., or even up to 80° C. and 85° C., such as between 55° C. and 70° C., e.g. between 60° C. and 65° C. For short incubation times enzyme mixtures are functional up to even 85° C., for complete hydrolysis lower temperatures are normally used.
  • the method for treating cellulosic material with CBH, EG, BG and Xyn is especially suitable for producing fermentable sugars from lignocellulosic material.
  • the fermentable sugars may then be fermented by yeast into ethanol, and used as fuel. They can also be used as intermediates or raw materials for the production of various chemicals or building blocks for the processes of chemical industry, e.g. in so called biorefinery.
  • the lignocellulosic material may be pretreated before the enzymatic hydrolysis to disrupt the fiber structure of cellulosic substrates and make the cellulose fraction more accessible to the cellulolytic enzymes. Current pretreatments include mechanical, chemical or thermal processes and combinations thereof.
  • the material may for example be pretreated by steam explosion or acid hydrolysis.
  • novel cellulolytic polypeptides were found in Thermoascus aurantiacus, Acremonium thermophilum , and Chaetomium thermophilum .
  • the novel polypeptides may comprise a fragment having cellulolytic activity and be selected from the group consisting of a polypeptide comprising an amino acid sequence having at least 66%, preferably 70% or 75%, identity to SEQ ID NO: 4, 79% identity to SEQ ID NO: 6, 78% identity to SEQ ID NO: 12, 68%, preferably 70% or 75%, identity to SEQ ID NO: 14, 72%, preferably 75%, identity to SEQ ID NO: 16, 68%, preferably 70% or 75%, identity to SEQ ID NO: 20, 74% identity to SEQ ID NO: 22 or 24, or 78% identity to SEQ ID NO: 26.
  • novel polypeptides may also be variants of said polypeptides.
  • a “variant” may be a polypeptide that occurs naturally e.g. as an allelic variant within the same strain, species or genus, or it may have been generated by mutagenesis. It may comprise amino acid substitutions, deletions or insertions, but it still functions in a substantially similar manner to the enzymes defined above i.e. it comprises a fragment having cellulolytic activity.
  • the cellulolytic polypeptides are usually produced in the cell as immature polypeptides comprising a signal sequence that is cleaved off during secretion of the protein. They may also be further processed during secretion both at the N-terminal and/or C-terminal end to give a mature, enzymatically active protein.
  • a polypeptide “comprising a fragment having cellulolytic activity” thus means that the polypeptide may be either in immature or mature form, preferably it is in mature form, i.e. the processing has taken place.
  • the novel polypeptides may further be a “fragment of the polypeptides or variants” mentioned above.
  • the fragment may be the mature form of the proteins mentioned above, or it may be only an enzymatically active part of the mature protein.
  • the polypeptide has an amino acid sequence having at least 80, 85, 90, 95, or 99% identity to SEQ ID NO: 4, 6, 12, 14, 16, 20, 22, 24 or 26, or to a cellulolytically active fragment thereof. It may also be a variant thereof, or a fragment thereof having cellobiohydrolase, endoglucanase, xylanase, or beta-glucosidase activity.
  • the polypeptide consists essentially of a cellulolytically active fragment of a sequence of SEQ ID NO: 4, 6, 12, 14, 16, 20, 22, 24 or 26.
  • the novel polynucleotides may comprise a nucleotide sequence of SEQ ID NO: 3, 5, 11, 13, 15, 19, 21, 23 or 25, or a sequence encoding a novel polypeptide as defined above, including complementary strands thereof.
  • Polynucleotide as used herein refers to both RNA and DNA, and it may be single stranded or double stranded.
  • the polynucleotide may also be a fragment of said polynucleotides comprising at least 20 nucleotides, e.g. at least 25, 30 or 40 nucleotides. According to one embodiment of the invention it is at least 100, 200 or 300 nucleotides in length. Further the polynucleotide may be degenerate as a result of the genetic code to any one of the sequences as defined above. This means that different codons may code for the same amino acid.
  • the polynucleotide is “comprised in” SEQ ID NO: 3, 5, 11, 13, 15, 19, 21, 23 or 25, which means that the sequence has at least part of the sequence mentioned.
  • the polynucleotide comprises a gene similar to that included in a microorganism having accession number DSM 16728, DSM 16729, DSM 17324, DSM 17323, DSM 17729, DSM 16726, DSM 16725, DSM 17325 or DSM 17667.
  • novel proteins/polypeptides may be prepared as described above.
  • the novel polynucleotides may be inserted into a vector, which is capable of expressing the polypeptide encoded by the heterologous sequence, and the vector may be inserted into a host cell capable of expressing said polypeptide.
  • the host cell is preferably of the genus Trichoderma or Aspergillus.
  • a heterologous gene encoding the novel polypeptides has been introduced on a plasmid into an Escherichia coli strain having accession number DSM 16728, DSM 16729, DSM 17324, DSM 17323, DSM 17729, DSM 16726, DSM 16725, DSM 17325 or DSM 17667.
  • the novel enzymes may be components of an enzyme preparation.
  • the enzyme preparation may comprise one or more of the novel polypeptides, and it may be e.g. in the form of spent culture medium, powder, granules or liquid. According to one embodiment of the invention it comprises cellobiohydrolase, endoglucanase, beta-glucosidase, and optionally xylanase activity and/or other enzyme activities. It may further comprise any conventional additives.
  • novel enzymes may be applied in any process involving cellulolytic enzymes, such as in fuel, textile, detergent, pulp and paper, food, feed or beverage industry, and especially in hydrolysing cellulosic material for the production of biofuel comprising ethanol.
  • cellulolytic enzymes such as in fuel, textile, detergent, pulp and paper, food, feed or beverage industry, and especially in hydrolysing cellulosic material for the production of biofuel comprising ethanol.
  • pulp and paper industry they may be used to modify cellulosic fibre for example in treating kraft pulp, mechanical pulp, or recycled paper.
  • the strains ALKO4239, ALKO4242 and ALKO4246 were cultivated in shake flasks at 42° C. for 7 d in the medium 3 ⁇ B, which contains g/litre: Solka Floc cellulose 18, distiller's spent grain 18, oats spelt xylan 9, CaCO 3 2, soybean meal 4.5, (NH 4 )HPO 4 4.5, wheat bran 3.0, KH 2 PO 4 1.5, MgSO 4 .H 2 O 1.5, NaCl 0.5, KNO 3 0.9, locust bean gum 9.0, trace element solution #1 0.5, trace element solution #2 0.5 and Struktol (Stow, Ohio, USA) antifoam 0.5 ml; the pH was adjusted to 6.5.
  • Trace element solution #1 has g/litre: MnSO 4 1.6, ZnSO 4 .7H 2 O 3.45 and CoCl 2 .6H 2 O 2.0; trace element solution #2 has g/litre: FeSO 4 .7H 2 O 5.0 with two drops of concentrated H 2 SO 4 .
  • the strain ALKO4261 was cultivated in shake flasks in the medium 1 ⁇ B, which has one third of each of the constituents of the 3 ⁇ B medium (above) except it has same concentrations for CaCO 3 , NaCl and the trace elements.
  • the strain was cultivated at 45° C. for 7 d.
  • the strain ALKO4265 was cultivated in shake flasks in the following medium, g/l: Solka Floc cellulose 40, PharmamediaTM (Traders Protein, Memphis, Tenn., USA) 10, corn steep powder 5, (NH 4 ) 2 SO 4 5 and KH 2 PO 4 15; the pH was adjusted to 6.5. The strain was cultivated at 45° C. for 7 d.
  • thermoactivity assays were performed of the shake flask cultivation preparations at 50° C., 60° C., 65° C., 70° C. and 75° C. for 1 h, in the presence of 100 ⁇ g bovine serum albumin (BSA)/ml as a stabilizer.
  • BSA bovine serum albumin
  • Preliminary assays were performed at 50° C. and 65° C. at two different pH values (4.8/5.0 or 6.0) in order to clarify, which pH was more appropriate for the thermoactivity assay.
  • CMCase The endoglucanase (CMCase) activity:
  • CMC carboxymethylcellulose
  • Beta-glucosidase (BGU) activity is:
  • the relative activities of the enzymes are presented in FIG. 1 .
  • the relative activities were presented by setting the activity at 60° C. as 100% ( FIG. 1 ). All strains produced enzymes, which had high activity at high temperatures (65° C.-75° C.).
  • ALKO4242 was also grown in a 2 litre bioreactor (Braun Biostat® B, Braun, Melsungen, Germany) in the following medium, g/litre: Solka Floc cellulose 40, soybean meal 10, NH 4 NO 3 5, KH 2 PO 4 5, MgSO 4 .7H 2 O 0.5, CaCl 2 .2H 2 O 0.05, trace element solution #1 0.5, trace element solution #2 0.5.
  • the aeration was 1 vvm, antifoam control with Struktol, stirring 200-800 rpm and temperature at 47° C. Two batches were run, one at pH 4.7 ⁇ 0.2 (NH 3 /H 2 SO 4 ) and the other with initial pH of pH 4.5.
  • the cultivation time was 7 d. After the cultivation the cells and other solids were removed by centrifugation.
  • the strain ALKO4245 was grown in 2 litre bioreactor (Braun Biostat® B, Braun, Melsungen, Germany) in the following medium, g/litre: Solka Floc cellulose 40, corn steep powder 15, distiller's spent grain 5, oats spelt xylan 3, locust bean gum 3, (NH 4 ) 2 SO 4 5 and KH 2 PO 4 5.
  • the pH range was 5.2 ⁇ 0.2 (NH 3 /H 2 SO 4 ), aeration 1 vvm, stirring 300-600 rpm, antifoam control with Struktol and the temperature 42° C.
  • the cultivation time was 4 d. After the cultivation the cells and other solids were removed by centrifugation.
  • ALKO4261 was grown in a 10 litre bioreactor (Braun Biostat® ED, Braun, Melsungen, Germany) in the following medium, g/litre: Solka Floc cellulose 30, distiller's spent grain 10, oats spelt xylan 5, CaCO 3 2, soybean meal 10, wheat bran 3.0, (NH 4 ) 2 SO 4 5, KH 2 PO 4 5, MgSO 4 .7H 2 O 0.5, NaCl 0.5, KNO 3 0.3, trace element solution #1 0.5 and trace element solution #2 0.5.
  • the pH range was 5.2 ⁇ 0.2 (NH 3 /H 2 SO 4 ), aeration 1 vvm, stirring 200-600 rpm, antifoam control with Struktol and the temperature 42° C.
  • the cultivation time was 5 d.
  • a second batch was grown under similar conditions except that Solka Floc was added to 40 g/l and spent grain to 15 g/l.
  • the supernatants were recovered by centrifugation and filtering through Seitz-K 150 and EK filters (Pall SeitzSchenk Filtersystems GmbH, Bad Kreuznach, Germany). The latter supernatant was concentrated about ten fold using the Pellicon mini ultrafiltration system (filter NMWL 10 kDa; Millipore, Billerica, Mass., USA).
  • ALKO4265 was also grown in a 10 litre bioreactor (Braun Biostat® ED, Braun, Melsungen, Germany) in the same medium as above, except KH 2 PO 4 was added to 2.5 g/l.
  • the pH range was 5.3 ⁇ 0.3 (NH 3 /H 3 PO 4 ), aeration 0.6 vvm, stirring 500 rpm, antifoam control with Struktol and the temperature 43° C.
  • the cultivation time was 7 d.
  • the supernatants were recovered by centrifugation and filtering through Seitz-K 150 and EK filters (Pall SeitzSchenk Filtersystems GmbH, Bad Kreuznach, Germany). The latter supernatant was concentrated about 20 fold using the Pellicon mini ultrafiltration system (filter NMWL 10 kDa; Millipore, Billerica, Mass., USA).
  • thermophilum ALKO4245 and Chaetomium thermophilum ALKO4265 were grown as described in Example 1.
  • the main cellobiohydrolases were purified using p-aminobenzyl 1-thio- ⁇ -cellobioside-based affinity column, prepared as described by Tomme et al., 1988.
  • the culture supernatants were first buffered into 50 mM sodium acetate buffer pH 5.0, containing 1 mM ⁇ -gluconolactone and 0.1 M glucose in order to retard ligand hydrolysis in the presence of ⁇ -glucosidases.
  • Cellobiohydrolases were eluted with 0.1 M lactose and finally purified by gel filtration chromatography using Superdex 200 HR 10/30 columns in the ⁇ KTA system (Amersham Pharmacia Biotech).
  • the buffer used in gel filtration was 50 mM sodium phosphate pH 7.0, containing 0.15 M sodium chloride.
  • Purified cellobiohydrolases were analysed by SDS-polyacrylamide gel electrophoresis and the molecular mass of both proteins was determined to be approximately 70 kDa evaluated on the basis of the molecular mass standards (Low molecular weight calibration kit, Amersham Biosciences).
  • Purified Acremonium and Chaetomium cellobiohydrolases were designated as At Cel7A and Ct Cel7A, respectively, following the scheme in Henrissat et al. (1998) (Henrissat, 1991; Henrissat and Bairoch, 1993).
  • the specific activity of the preparations was determined using 4-methylumbelliferyl- ⁇ -D-lactoside (MUL), 4-methylumbelliferyl- ⁇ -D-cellobioside (MUG2) or 4-methylumbelliferyl- ⁇ -D-cellotrioside (MUG3) as substrate (van Tilbeurgh et al., 1988) in 0.05 M sodium citrate buffer pH 5 at 50° C. for 10 min.
  • Endoglucanase and xylanase activities were determined by standard procedures (according to IUPAC, 1987) using carboxymethyl cellulose (CMC) and birch glucuronoxylan (Bailey et al., 1992) as substrates.
  • the specific activities of the purified enzymes and that of T. reesei CBHI/Cel7A are presented in Table 1.
  • the purified At Cel7A and Ct Cel7A cellobiohydrolases possess higher specific activities against small synthetic substrates as compared to T. reesei CBHI/Cel7A.
  • the specific activity against Avicel was clearly higher with the herein disclosed enzymes.
  • Low activities of the purified enzyme preparations against xylan and CMC may either be due to the properties of the proteins themselves, or at least partially to the remaining minor amounts of contaminating enzymes.
  • the major end product of cellulose hydrolysis by all purified enzymes was cellobiose which is typical to cellobiohydrolases.
  • thermophilum ALKO4265 CBH/Cel7A and A. thermophilum ALKO4245 CBH/Cel7A were stable up to 65° and 60° C., respectively.
  • the T. reesei reference enzyme (CBHI/Cel7A) retained 100% of activity up to 55° C.
  • Acremonium thermophilum ALKO4245 was grown as described in Example 1. The culture supernatant was incubated at 70° C. for 24 hours after which it was concentrated by ultrafiltration. The pure endoglucanase was obtained by sequential purification with hydrophobic interaction and cation exchange chromatography followed by gel filtration. The endoglucanase activity of the fractions collected during purification was determined using carboxymethyl cellulose (CMC) as substrate (procedure of IUPAC 1987). Protein content was measured by BioRad Assay Kit (Bio-Rad Laboratories) using bovine serum albumine as standard.
  • CMC carboxymethyl cellulose
  • the concentrated culture supernatant was applied to a HiPrep 16/10 Butyl FF hydrophobic interaction column equilibrated with 20 mM potassium phosphate buffer pH 6.0, containing 1 M (NH 4 ) 2 SO 4 . Bound proteins were eluted with the linear gradient from the above buffer to 5 mM potassium phosphate, pH 6.0. Fractions were collected and the endoglucanase activity was determined as described above. The endoglucanase activity was eluted in a broad conductivity area of 120 to 15 mS/cm.
  • the dissolved sample was loaded onto a Superdex 75 HR10/30 gel filtration column equilibrated with 20 mM sodium phosphate buffer pH 7.0, containing 0.15 M NaCl.
  • the main protein fraction was eluted from the column with the retention volume of 13.3 ml.
  • the protein eluate was judged to be pure by SDS-polyacryl amide gel electrophoresis and the molecular weight was evaluated to be 40 kDa.
  • the specific activity of the purified protein, designated as At EG-40, at 50° C. was determined to be 450 nkat/mg (procedure of IUPAC 1987, using CMC as substrate).
  • Thermal stability of the purified endoglucanase was determined at different temperatures. The reaction was performed in the presence of 0.1 mg/ml BSA at pH 5.0 for 60 min using carboxymethyl cellulose as substrate. A. thermophilum EG — 40/Cel45A was stable up to 80° C. The T. reesei reference enzymes EGI (Cel7B) and EGII (Cel5A) retained 100% of activity up to 60° C. and 65° C., respectively.
  • Chaetomium thermophilum ALKO4261 was grown as described in Example 1.
  • the pure endoglucanase was obtained by sequential purification with hydrophobic interaction and cation exchange chromatography followed by gel filtration.
  • the endoglucanase activity of the fractions collected during purification was determined using carboxymethyl cellulose (CMC) as substrate (procedure of IUPAC 1987).
  • Ammonium sulfate was added to the culture supernatant to reach the same conductivity as 20 mM potassium phosphate pH 6.0, containing 1 M (NH 4 ) 2 SO 4 .
  • the sample was applied to a HiPrep 16/10 Phenyl FF hydrophobic interaction column equilibrated with 20 mM potassium phosphate pH 6.0, containing 1 M (NH 4 ) 2 SO 4 . Elution was carried out with a linear gradient of 20 to 0 mM potassium phosphate, pH 6.0, followed by 5 mM potassium phosphate, pH 6.0 and water. Bound proteins were eluted with a linear gradient of 0 to 6 M Urea. Fractions were collected and the endoglucanase activity was analysed as described above. The protein containing endoglucanase activity was eluted in the beginning of the urea gradient.
  • the sample was equilibrated to 15 mM sodium acetate, pH 4.5 by 10DG column (Bio-Rad) and applied to a HiTrap SP XL cation exchange column equilibrated with 20 mM sodium acetate pH 4.5. Proteins were eluted with a linear gradient from 0 to 0.4 M sodium acetate, pH 4.5. Endoglucanase activity was eluted in the range of 1-10 mS/cm. The collected sample was lyophilized.
  • the sample was dissolved in water and applied to a Superdex 75 HR 10/30 gel filtration column equilibrated with 20 mM sodium phosphate pH 6.0, containing 0.15 M NaCl. Fractions were collected and those containing endoglucanase activity were combined.
  • the protein eluate was judged to be pure by SDS-polyacrylamide gel electrophoresis and the molecular mass was evaluated on the basis of molecular mass standards (prestained SDS-PAGE standards, Broad Range, Bio-Rad) to be 54 kDa.
  • the pl of the purified protein, designated as Ct EG — 54 was determined with PhastSystem (Pharmacia) to be ca 5.5.
  • Thermoascus aurantiacus ALKO4242 was grown as described in Example 1.
  • the pure endoglucanase was obtained by sequential purification with hydrophobic interaction and anion exchange chromatography followed by gel filtration.
  • the endoglucanase activity of the fractions collected during purification was determined using carboxymethyl cellulose (CMC) as substrate (procedure of IUPAC 1987). Protein content was measured by BioRad Assay Kit (Bio-Rad Laboratories) using bovine serum albumine as standard.
  • the sample was desalted in 10DG columns (Bio-Rad) and applied to a HiTrap DEAE FF anion exchange column equilibrated with 15 mM Tris-HCL, pH 7.0. Bound proteins were eluted with a linear gradient from 0 to 0.4 M NaCl in the equilibration buffer. The protein containing endoglucanase activity was eluted at the conductivity area of 15-21 mS/cm. Collected fractions were combined and concentrated as above.
  • the sample was applied to a Sephacryl S-100 HR 26/60 gel filtration column equilibrated with 50 mM sodium acetate buffer pH 5.0, containing 0.05 M NaCl.
  • the protein fraction containing endoglucanase activity was eluted from the column with a retention volume corresponding to a molecular weight of 16 kDa. Collected fractions were combined, concentrated and gel filtration was repeated.
  • the protein eluate was judged to be pure by SDS-polyacryl amide gel electrophoresis and the molecular weight was evaluated to be 28 kDa.
  • the pI of the purified protein, designated as Ta EG — 28, was determined in an IEF gel (PhastSystem, Pharmacia) to be about 3.5.
  • the specific activity of Ta EG — 28 at 50° C. was determined to be 4290 nkat/mg (procedure of IUPAC 1987, using CMC as substrate).
  • the culture supernatant was applied to a HiPrep 16/10 Phenyl Sepharose FF hydrophobic interaction column equilibrated with 20 mM potassium phosphate pH 6.0, containing 1 M (NH 4 ) 2 SO 4 .
  • Bound proteins were eluted with a linear gradient from the equilibration buffer to 5 mM potassium phosphate in the conductivity area 137-16 mS/cm. Collected fractions were combined and concentrated by ultrafiltration.
  • the sample was desalted in 10DG columns (Bio-Rad) and applied to a HiTrap DEAE FF anion exchange column equilibrated with 10 mM potassium phosphate pH 7.0. Bound proteins were eluted with a linear gradient from the equilibration buffer to the same buffer containing 0.25 M NaCl in the conductivity area 1.5-12 mS/cm. Anion exchange chromatography was repeated as above, except that 4 mM potassium phosphate buffer pH 7.2 was used. Proteins were eluted at the conductivity area of 6-9 mS/cm. Fractions containing ⁇ -glucosidase activity were collected, combined, and concentrated.
  • the active material from the anion exchange chromatography was applied to a Sephacryl S-300 HR 26/60 column equilibrated with 20 mM sodium phosphate pH 6.5, containing 0.15 M NaCl.
  • the protein with ⁇ -glucosidase activity was eluted with a retention volume corresponding to a molecular weight of 243 kDa.
  • the protein was judged to be pure by SDS-polyacrylamide gel electrophoresis and the molecular weight was evaluated to be 101 kDa.
  • the pI of the purified protein, designated as At ⁇ G — 101 was determined in an IEF gel (PhastSystem, Pharmacia) to be in the area of 5.6-4.9.
  • the specific activity of At ⁇ G — 101 at 50° C. was determined to be 1100 nkat/mg (using 4-nitrophenyl- ⁇ -D-glucopyranoside as substrate, Bailey and Linko, 1990).
  • thermophilum ⁇ G — 101 was stable up to 70° C.
  • the Aspergillus reference enzyme (Novozym 188) retained 100% of activity up to 600.
  • Chaetomium thermophilum ALKO4261 was grown as described in Example 1.
  • the pure ⁇ -glucosidase was obtained by sequential purification with hydrophobic interaction, anion and cation exchange chromatography followed by gel filtration.
  • the ⁇ -glucosidase activity of the fractions collected during purification was determined using 4-nitrophenyl- ⁇ -D-glucopyranoside as substrate (Bailey and Linko, 1990).
  • the culture supernatant was applied to a HiPrep 16/10 Phenyl Sepharose FF hydrophobic interaction column equilibrated with 20 mM potassium phosphate pH 6.0, containing 0.8 M (NH 4 ) 2 SO 4 .
  • the elution was carried out with a linear gradient from the equilibration buffer to 3 mM potassium phosphate, pH 6.0, followed by elution with water and 6 M urea.
  • the first fractions with ⁇ -glucosidase activity were eluted in the conductivity area of 80-30 mS/cm.
  • the second ⁇ -glucosidase activity was eluted with 6 M urea.
  • the active fractions eluted by urea were pooled and desalted in 10DG columns (Bio-Rad) equilibrated with 10 mM Tris-HCl pH 7.0.
  • the sample from the anion exchange chromatography was applied to a HiTrap SP FF cation exchange column equilibrated with 10 mM sodium acetate pH 4.5. Bound proteins were eluted with a linear gradient from 10 mM to 400 mM sodium acetate, pH 4.5. The fractions with ⁇ -glucosidase activity eluting in conductivity area of 6.5-12 mS/cm were collected, desalted in 10DG columns (Bio-Rad) equilibrated with 7 mM sodium acetate, pH 4.5 and lyophilized.
  • the lyophilized sample was diluted to 100 ⁇ l of water and applied to a Superdex 75 HF10/30 gel filtration column equilibrated with 20 mM sodium phosphate pH 4.5, containing 0.15 M NaCl.
  • the ⁇ -glucosidase activity was eluted at a retention volume of 13.64 ml. Collected fractions were combined, lyophilized and dissolved in water.
  • the protein was judged to be pure by SDS-polyacryl amide gel electrophoresis and the molecular weight was evaluated to be 76 kDa.
  • the protein was designated as Ct ⁇ G — 76.
  • Thermoascus aurantiacus ALKO4242 was grown as described in Example 1.
  • the pure ⁇ -glucosidase was obtained by sequential purification with hydrophobic interaction, anion and cation exchange chromatography followed by gel filtration.
  • the ⁇ -glucosidase activity of the fractions collected during purification was determined using 4-nitrophenyl- ⁇ -D-glucopyranoside as substrate (Bailey and Linko, 1990). Protein content was measured by BioRad Assay Kit (Bio-Rad Laboratories) using bovine serum albumine as standard.
  • the culture supernatant was applied to a HiPrep 16/10 Phenyl Sepharose FF hydrophobic interaction column equilibrated with 20 mM potassium phosphate pH 6.0, containing 0.7 M (NH 4 ) 2 SO 4 . Bound proteins were eluted with a linear gradient from 0.2 M (NH 4 ) 2 SO 4 to 5 mM potassium phosphate, pH 6.0. The ⁇ -glucosidase activity was eluted during the gradient in the conductivity area of 28.0-1.1 mS/cm. Fractions were combined and concentrated by ultrafiltration.
  • the sample was desalted in 10DG columns (Bio-Rad) and applied to a HiTrap DEAE FF anion exchange column equilibrated with 20 mM Tris-HCl pH 7.0.
  • the enzyme was eluted with a linear gradient from 0 to 0.2 M NaCl in the equilibration buffer and with delayed elution by 20 mM Tris-HCl, containing 0.4 M NaCl.
  • the sample eluting in the conductivity area of ca. 10-30 mS/cm was concentrated by ultrafiltration and desalted by 10DG column (Bio-Rad).
  • the sample was applied to a HiTrap SP XL cation exchange column equilibrated with 9 mM sodium acetate pH 4.5.
  • the enzyme was eluted with a linear gradient from 10 mM to 400 mM NaAc and by delayed elution using 400 mM NaAc pH 4.5 Proteins with ⁇ -glucosidase activity were eluted broadly during the linear gradient in the conductivity area of 5.0-11.3 mS/cm.
  • the active material from the cation exchange chromatography was applied to a Sephacryl S-300 HR 26/60 column equilibrated with 20 mM sodium phosphate pH 7.0, containing 0.15 M NaCl.
  • the protein with ⁇ -glucosidase activity was eluted with a retention volume corresponding to a molecular weight of 294 kDa. Collected fractions were combined, lyophilized and dissolved in water.
  • the protein was judged to be pure by SDS-polyacrylamide gel electrophoresis and the molecular weight was evaluated to be 81 kDa, representing most likely the monomeric form of the protein.
  • Isoelectric focusing (IEF) was carried out using a 3-9 ⁇ l gel.
  • the specific activity of the purified protein, designated as Ta ⁇ G — 81, at 50° C. was determined to be 600 nkat/mg using 4-nitrophenyl- ⁇ -D-glucopyranoside as substrate (Bailey and Linko, 1990).
  • Thermal stability of the purified ⁇ -glucosidase was determined at different temperatures. The reaction was performed in the presence of 0.1 mg/ml BSA at pH 5.0 for 60 min using 4-nitrophenyl- ⁇ -D-glucopyranoside as substrate. T. aurantiacus ⁇ G — 81 was stable up to 75° C. The Aspergillus reference enzyme (Novozym 188) retained 100% of activity up to 60° C.
  • Acremonium thermophilum ALKO4245 was grown as described in Example 1. The culture supernatant was incubated at 70° C. for 24 hours after which, it was concentrated by ultrafiltration. The pure xylanase was obtained by sequential purification with hydrophobic interaction and cation exchange chromatography followed by gel filtration. The xylanase activity was determined using birch xylan as substrate (procedure of IUPAC 1987). Protein was assayed by BioRad Protein Assay Kit (Bio-Rad Laboratories) using bovine serum albumin as standard.
  • the concentrated culture supernatant was applied to a HiPrep 16/10 Butyl FF hydrophobic interaction column equilibrated with 20 mM potassium phosphate buffer pH 6.0, containing 1 M (NH 4 ) 2 SO 4 . Bound proteins were eluted with the linear gradient from the above buffer to 5 mM potassium phosphate, pH 6.0. The protein fraction was eluted in a broad conductivity area of 120 to 15 mS/cm.
  • the sample from the hydrophobic interaction column was applied to a HiTrap SP XL cation exchange column equilibrated with 8 mM sodium acetate, pH 4.5.
  • the protein did not bind to this column but was eluted in the flow-through during sample feed. This eluate was concentrated by ultrafiltration.
  • the hydrophobic chromatography was repeated as described above. The unbound proteins were collected and freeze dried.
  • the dissolved sample was loaded onto the Superdex 75 HR10/30 gel filtration column equilibrated with 20 mM sodium phosphate buffer pH 7.0, containing 0.15 M NaCl.
  • the protein eluted from the column with the retention volume of 11.2 ml was judged to be pure by SDS-polyacryl amide gel electrophoresis.
  • the molecular mass of the purified protein was evaluated on the basis of molecular mass standards (prestained SDS-PAGE standards, Broad Range, Bio-Rad) to be 60 kDa.
  • the specific activity of the protein designated as At XYN — 60, at 50° C.
  • Thermoascus aurantiacus ALKO4242 was grown as described in Example 1.
  • the pure xylanase was obtained by sequential purification with hydrophobic interaction, anion, and cation exchange chromatography followed by gel filtration.
  • the xylanase activity was determined using birch xylan as substrate (procedure of IUPAC 1987). Protein was assayed by BioRad Protein Assay Kit (Bio-Rad Laboratories) using bovine serum albumin as standard.
  • the culture supernatant was applied to a HiPrep 16/10 Phenyl Sepharose FF hydrophobic interaction column equilibrated with 20 mM potassium phosphate buffer pH 6.0, containing 0.7 M (NH 4 ) 2 SO 4 .
  • Bound proteins were eluted with a two-step elution protocol. The elution was carried out by dropping the salt concentration first to 0.2 M (NH 4 ) 2 SO 4 and after that a linear gradient from 20 mM potassium phosphate pH 6.0, containing 0.2 M (NH 4 ) 2 SO 4 to 5 mM potassium phosphate pH 6.0 was applied.
  • the sample was desalted in 10DG columns (Bio-Rad) and applied to a HiTrap DEAE FF anion exchange column equilibrated with 15 mM Tris-HCL, pH 7.0.
  • the protein did not bind to the anion exchange column but was eluted in the flow-through.
  • the conductivity of the sample was adjusted to correspond that of 20 mM sodium acetate, pH 4.5 by adding water and pH was adjusted to 4.5 during concentration by ultrafiltration.
  • the sample was applied to a HiTrap SP XL cation exchange column equilibrated with 20 mM sodium acetate, pH 4.5. Bound proteins were eluted with a linear gradient from the equilibration buffer to the same buffer containing 1 M NaCl. The enzyme was eluted at the conductivity area of 1-7 mS/cm. The sample was lyophilized and thereafter dissolved in water.
  • the lyophilised sample was dissolved in water and applied to a Superdex 75 HR 10/30 gel filtration column equilibrated with 20 mM sodium phosphate pH 7.0, containing 0.15 M NaCl.
  • the protein was eluted from the column with a retention volume corresponding to a molecular weight of 26 kDa.
  • the protein was judged to be pure by SDS-polyacrylamide gel electrophoresis.
  • the molecular mass of the pure protein was 30 kDa as evaluated on the basis of molecular mass standards (prestained SDS-PAGE standards, Broad Range, Bio-Rad).
  • the pI of the purified protein, designated as Ta XYN — 30 was determined with PhastSystem (Pharmacia) to be ca. 6.8.
  • the specific activity of Ta XYN — 30 at 50° C. was determined to be 4800 nkat/mg (procedure of IUPAC 1987, using birch xylan as
  • the internal peptides were sequenced by electrospray ionization combined to tandem mass spectrometry (ESI-MS/MS) using the Q-TOF1 (Micromass) instrument.
  • the protein was first alkylated and digested into tryptic peptides. Generated peptides were desalted and partially separated by nano liquid chromatography (reverse-phase) before applying to the Q-TOF1 instrument.
  • the internal peptide sequences for Chaetomium thermophilum and Acremonium thermophilum cellobiohydrolases are shown in Table 2.
  • the peptides from Chaetomium CBH were obtained after the corresponding cbh gene had been cloned.
  • the peptides determined from Acremonium CBH were not utilized in the cloning of the corresponding gene.
  • the internal peptide sequences of purified endoglucanases, ⁇ -glucosidases, and xylanases of Acremonium thermophilum ALKO4245, Chaetomium thermophilum ALKO4261 and Thermoascus aurantiacus ALKO4242 are listed in Table 3, Table 4 and Table 5.
  • the genomic library of Chaetomium thermophilum ALKO4265 and Acremonium thermophilum ALKO4245 were made to Lambda DASH®II vector (Stratagene, USA) according to the instructions from the supplier.
  • the chromosomal DNAs, isolated by the method of Raeder and Broda (1985), were partially digested with Sau3A.
  • the digested DNAs were size-fractionated and the fragments of the chosen size ( ⁇ 5-23 kb) were dephosphorylated and ligated to the BamHI digested lambda vector arms.
  • the ligation mixtures were packaged using Gigapack III Gold packaging extracts according to the manufacturer's instructions (Stratagene, USA).
  • the titers of the Chaetomium thermophilum and Acremonium thermophilum genomic libraries were 3.6 ⁇ 10 6 pfu/ml and 3.7 ⁇ 10 5 pfu/ml and those of the amplified libraries were 6.5 ⁇ 10 10 pfu/ml and 4.2 ⁇ 10 8 pfu/ml, respectively.
  • Lambda FIX® II/Xho I Partial Fill-In Vector Kit (Stratagene, USA) was used in the construction of the genomic libraries for Thermoascus aurantiacus ALKO4242 and Chaetomium thermophilum ALKO4261 according to the instructions from the supplier.
  • the chromosomal DNAs isolated by the method of Raeder and Broda (1985), were partially digested with Sau3A. The digested DNAs were size-fractionated and the fragments of the chosen size (6-23 kb) were filled-in and ligated to the XhoI digested Lambda FIX II vector arms.
  • the ligation mixtures were packaged using Gigapack III Gold packaging extracts according to the manufacturer's instructions (Stratagene, USA).
  • the titers of the Thermoascus aurantiacus ALKO4242 and Chaetomium thermophilum ALKO4261 genomic libraries were 0.2 ⁇ 10 6 and 0.3 ⁇ 10 6 pfu/ml and those of the amplified libraries were 1.8 ⁇ 10 9 and 3.8 ⁇ 10 9 pfu/ml, respectively.
  • Standard molecular biology methods were used in the isolation and enzyme treatments of DNA (plasmids, DNA fragments), in E. coli transformations, etc.
  • the basic methods used are described in the standard molecular biology handbooks, e.g., Sambrook et al. (1989) and Sambrook and Russell (2001).
  • the probes for screening the genomic libraries which were constructed as described in Example 12 were amplified by PCR using the Thermoascus aurantiacus ALKO4242, Chaetomium thermophilum ALKO4265 and Acremonium thermophilum ALKO4245 genomic DNAs as templates in the reactions.
  • Several primers tested in PCR reactions were designed according to the published nucleotide sequence (WO 03/000941, Hong et al., 2003b).
  • the PCR reaction mixtures contained 50 mM Tris-HCl, pH 9.0, 15 mM (NH 4 ) 2 SO 4 , 0.1% Triton X-100, 1.5 mM MgCl 2 , 0.2 mM dNTPs, 5 ⁇ M each primer and 1 units of Dynazyme EXT DNA polymerase (Finnzymes, Finland) and 0.5-1 ⁇ g of the genomic DNA.
  • the conditions for the PCR reactions were the following: 5 min initial denaturation at 95° C., followed by 30 cycles of 1 min at 95° C., either 1 min annealing at 62° C. ( ⁇ 8° C.
  • Thermoascus ALKO4242 and Chaetomium ALKO4265 templates or 1 min annealing at 58° C. ( ⁇ 6° C. gradient) for Acremonium ALKO4245 template, 2 min extension at 72° C. and a final extension at 72° C. for 10 min.
  • DNA products of the expected sizes were obtained from all genomic templates used.
  • the DNA fragments of the expected sizes were isolated from the most specific PCR reactions and they were cloned to pCR® Blunt-TOPO® vector (Invitrogen, USA).
  • the inserts were characterized by sequencing and by performing Southern blot hybridizations to the genomic DNAs digested with several restriction enzymes.
  • the PCR fragments which were chosen to be used as probes for screening of the Thermoascus aurantiacus, Chaetomium thermophilum and Acremonium thermophilum genomic libraries are presented in Table 6.
  • the inserts from the plasmids listed in Table 6 were labeled with digoxigenin according to the supplier's instructions (Roche, Germany), and the amplified genomic libraries (2 ⁇ 10 5 -3 ⁇ 10 5 plaques) were screened with the labeled probe fragments.
  • the hybridization temperature for the filters was 68° C. and the filters were washed 2 ⁇ 5 min at RT using 2 ⁇ SSC-0.1% SDS followed by 2 ⁇ 15 min at 68° C. using 0.1 ⁇ SSC-0.1% SDS with the homologous probes used.
  • Several positive plaques were obtained from each of the hybridizations.
  • Predicted Predicted No Length of MW pl Putative SEQ CBH of ss C-terminal (Da, ss (ss not N-glycosylation ID protein aas NN/HMM (a CBD (b not incl) (c incl) sites (d NO: Ta Cel7A 457 17/17 NO 46 873 4.44 2 2 Ct Cel7A 532 18/18 YES, 54 564 5.05 3 8 T497 to L532 At Cel7B 459 21/21 NO 47 073 4.83 2 4 At Cel7A 523 17/17 YES, 53 696 4.67 4 6 Q488 to L523 ss, signal sequence.
  • the deduced amino acid sequences of Thermoascus aurantiacus Cel7A and Acremonium thermophilum Cel7A were most homologous to each other (analyzed by Needleman-Wunsch global alignment, EMBOSS 3.0.0 Needle, with Matrix EBLOSUM62, Gap Penalty 10.0 and Extend Penalty 0.5; Needleman and Wunsch, 1970).
  • the deduced Acremonium thermophilum Cel7A had a lower identity to the deduced Chaetomium thermophilum Cel7A.
  • the Acremonium thermophilum Cel7B was most distinct from the CBH/Cel7 sequences of the invention.
  • the deduced Chaetomium Cel7A sequence possessed the highest identities (analyzed by Needleman-Wunsch global alignment, EMBOSS Needle, see above) to polypeptides of Chaetomium thermophilum, Scytalidium thermophilum and Thielavia australiensis CBHI described in WO 03/000941.
  • the deduced Thermoascus aurantiacus Cel7A sequence was highly identical to the published CBHI of the Thermoascus aurantiacus (WO 03/000941, Hong et al., 2003b).
  • Acremonium thermophilum Cel7B had significantly lower identities to the previously published sequences, being more closely related to the CBHI polypeptide from Oryza sativa .
  • the highest homologies of the deduced Acremonium thermophilum Cel7A sequence were to Exidia gladulosa and Acremonium thermophilum CBHI polynucleotides (WO 03/000941).
  • the alignment indicates that the cloned Thermoascus aurantiacus ALKO4242, Chaetomium thermophilum ALKO4265 and Acremonium thermophilum ALKO4245 sequences encode the CBH proteins having high homology to the polypeptides of the glycoside hydrolase family 7, therefore these were designated as Cel7A or Cel7B (Henrissat et al. 1998).
  • Organism, enzyme and accession number Identity (%) * Thermoascus aurantiacus Cel7A 100.0 Thermoascus aurantiacus , AY840982 99.6 Thermoascus aurantiacus , AX657575 99.1 Thermoascus aurantiacus , AF421954 97.8 Talaromyces emersonii , AY081766 79.5 Chaetomidium pingtungium , AX657623 76.4 Trichophaea saccata , AX657607 73.4 * Acremonium thermophilum Cel7A (core) 70.6 Emericella nidulans , AF420020 (core) 70.4 * Chaetomium thermophilum Cel7A (core) 66.4 * Chaetomium thermophilum Cel7A 100.0 Chaetomium thermophilum , AY861347 91.9 Chaetomium thermophilum ,
  • Expression plasmids were constructed for production of the recombinant CBH/Cel7 proteins from Thermoascus aurantiacus (Ta Cel7A), Chaetomium thermophilum (Ct Cel7A) and Acremonium thermophilum (At Cel7A, At Cel7B; at early phase of the work these proteins had the temporary codes At CBH_C and At CBH_A, respectively).
  • the expression plasmids constructed are listed in Table 11.
  • the recombinant cbh/cel7 genes, including their own signal sequences, were exactly fused to the T. reesei cbh1 (cel7A) promoter by PCR. The transcription termination was ensured by the T.
  • CBH/Cel7 plasmid cassette (a cel7A terminator (b Ta Cel7A pALK1851 9.0 kb 245 bp (XbaI) Ct Cel7A pALK1857 9.2 kb 240 bp (HindIII) At Cel7B pALK1860 9.4 kb 361 bp (EcoRI) At Cel7A pALK1865 9.5 kb 427 bp (EcoRV) (a The expression cassette for T. reesei transformation was isolated from the vector backbone by using EcoRI digestion. (b The number of the nucleotides from the genomic cbh1/cel7A terminator region after the STOP codon. The restriction site at the 3'-end, used in excising the genomic gene fragment, is included in the parenthesis.
  • the CBH/Cel7 production of the transformants was analysed from the culture supernatants of the shake flask cultivations (50 ml).
  • the transformants were grown for 7 days at 28° C. in a complex lactose-based cellulase-inducing medium (Joutsjoki et al. 1993) buffered with 5% KH 2 PO 4 .
  • the cellobiohydrolase activity was assayed using 4-methylumbelliferyl- ⁇ -D-lactoside (MUL) substrate according to van Tilbeurgh et al., 1988.
  • MUL 4-methylumbelliferyl- ⁇ -D-lactoside
  • the recombinant CBH/Cel7 enzyme preparations were characterized in terms of pH optimum and thermal stability.
  • the pH optimum of the recombinant CBH/Cel7 proteins from Thermoascus aurantiacus, Chaetomium thermophilum , and Acremonium thermophilum were determined in the universal McIlvaine buffer within a pH range of 3.0-8.0 using 4-methylumbelliferyl- ⁇ -D-lactoside (MUL) as a substrate ( FIG. 3 A).
  • MUL 4-methylumbelliferyl- ⁇ -D-lactoside
  • the pH optimum for Ct Cel7A and At Cel7A enzymes is at 5.5, above which the activity starts to gradually drop.
  • the pH optimum of the recombinant crude Ta Cel7A is at 5.0 ( FIG. 3 A).
  • the chosen CBH/Cel7 transformants were cultivated in lab bioreactors at 28° C. in the medium indicated above for 3-4 days with pH control 4.4 ⁇ 0.2 (NH 3 /H 3 PO 4 ) to obtain material for the application tests.
  • the supernatants were recovered by centrifugation and filtering through Seitz-K 150 and EK filters (Pall SeitzSchenk Filtersystems GmbH, Bad Kreuznach, Germany).
  • Thermoascus aurantiacus Cel7A was fused to linker and CBD of Chaetomium thermophilum Cel7A (SEQ ID. NO: 7) (Ct CBD).
  • CBD Chaetomium thermophilum Cel7A
  • the coding sequence of the linker and the CBD of Chaetomium thermophilum Cel7A were synthesized by PCR using following primers:
  • the PCR reaction mixture contained 1 ⁇ DyNAzymeTM EXT reaction buffer (Finnzymes, Finland), 15 mM Mg 2+ , 0.2 mM dNTPs, 2 ⁇ M of each primer, 0.6 units of DyNAzymeTM EXT DNA polymerase (Finnzymes, Finland), and approximately 75 ng/30 ⁇ l of template DNA, containing full-length cel7A gene from the Chaetomium thermophilum.
  • the conditions for the PCR reaction were the following: 2 min initial denaturation at 98° C., followed by 30 cycles of 30 sec at 98° C., 30 sec annealing at 68° C. (+4° C. gradient), 30 sec extension at 72° C. and a final extension at 72° C.
  • the specific DNA fragment in PCR reaction was obtained at annealing temperature range from 64° C. to 68.5° C.
  • the synthesized CBD fragment of the Chaetomium thermophilum was ligated after Thermoascus aurantiacus cel7A gene resulting in a junction point of GPIGST between the domains.
  • the PCR amplified fragment in the plasmid was confirmed by sequencing (SEQ ID. NO: 29).
  • the constructed fusion cel7A gene was exactly fused to the T. reesei cbh1 (cel7A) promoter.
  • the transcription termination was ensured by the T. reesei ceI7A terminator and the A. nidulans amdS marker gene was used for selection of the transformants as described in Paloheimo et al. (2003).
  • the linear expression cassette was isolated from the vector backbone after NotI digestion and was transformed to T. reesei A96 protoplasts.
  • the transformations were performed as in Penttila et al. (1987) with the modifications described in Karhunen et al. (1993), selecting with acetamide as a sole nitrogen source.
  • the transformants were purified on selection plates through single conidia prior to sporulating them on PD.
  • Thermoascus aurantiacus Cel7A+CBD (SEQ ID. NO: 28 and 30) production of the transformants was analyzed from the culture supernatants of the shake flask cultivations (50 ml). The transformants were grown for 7 days in a complex cellulase-inducing medium (Joutsjoki et al. 1993) buffered with 5% KH 2 PO 4 at pH 5.5. The cellobiohydrolase activity was assayed using 4-methylumbelliferyl- ⁇ -D-lactoside (MUL) substrate according to van Tilbeurgh et al., 1988.
  • MUL 4-methylumbelliferyl- ⁇ -D-lactoside
  • the genotypes of the chosen transformants were confirmed by using Southern blots in which several genomic digests were included and the expression cassette was used as a probe.
  • the SDS-PAGE analyses showed that the recombinant Thermoascus aurantiacus Cel7A+CBD enzymes were produced as stable fusion proteins in T. reesei.
  • the chosen transformant producing the Ta Cel7A+Tr CBD fusion protein (SEQ ID. NO: 28) was also cultivated in 2 litre bioreactor at 28° C. in the medium indicated above for 3-4 days with pH control 4.4 ⁇ 0.2 (NH 3 /H 3 PO 4 ) to obtain material for the application tests.
  • the supernatants were recovered by centrifugation and filtering through Seitz-K 150 and EK filters (Pall SeitzSchenk Filtersystems GmbH, Bad Kreuznach, Germany).
  • the Michaelis-Menten and cellobiose inhibition constants were determined from the cellobiohydrolases produced heterologously in T. reesei (Examples 14 and 15).
  • the enzymes were purified as described in Example 2. Protein concentrations of purified enzymes were measured by their absorption at 280 nm using a theoretical molar extinction co-efficient, which were calculated from the amino acid sequences (Gill and von Hippel, 1989).
  • Km and kcat values Kinetic constants (Km and kcat values) and cellobiose inhibition constant (Ki) for Tr CBHI/Cel7A, Ta CBH/Cel7A, At CBH/Cel7A and Ct CBH/Cel7A, were measured using CNPLac (2-Chloro-4-nitrophenyl- ⁇ -D-lactoside) as substrate at ambient temperature (22° C.) in 50 mM sodium phosphate buffer, pH 5.7.
  • the inhibition constant (Ki) eight different substrate concentrations (31-4000 ⁇ M) in the presence of a range of five inhibitor concentrations (0-100 ⁇ M or 0-400 ⁇ M), which bracket the K i value, were used.
  • the Km and kcat constants were calculated from the fitting of the Michaelis-Menten equation using the programme of Origin. Lineweaver-Burk plots, replots (LWB slope versus [Glc2; cellobiose]) and Hanes plots were used to distinguish between competitive and mixed type inhibition and to determine the inhibition constants (Ki).
  • the purified recombinant cellobiohydrolases Ct Cel7A, Ta Cel7A, Ta Cel7A+ Tr CBD, Ta Cel7A+ Ct CBD, At Cel7A as well as the core version of Ct Cel7A (see below) were tested in equimolar amounts in crystalline cellulose hydrolysis at two temperatures, 45° C. and 70° C.; the purified T. reesei Tr Cel7A and its core version (see below) were used as comparison.
  • the crystalline cellulose (Ph 101, Avicel; Fluka, Bucsh, Switzerland) hydrolysis assays were performed in 1.5 ml tube scale 50 mM sodium acetate, pH 5.0. Avicel was shaken at 45° C.
  • the core versions of the cellobiohydrolases harboring a CBD in their native form were obtained as follows: Ct Cel7A and Tr Cel7A were exposed to proteolytic digestion to remove the cellulose-binding domain.
  • Papain (Papaya Latex, 14 U/mg, Sigma) digestion of the native cellobiohydrolases was performed at 37° C. for 24 h in a reaction mixture composed of 10 mM L-cystein and 2 mM EDTA in 50 mM sodium acetate buffer (pH 5.0) with addition of papain (two papain concentrations were tested: of one fifth or one tenth amount of papain of the total amount of the Cel7A in the reaction mixture).
  • the resultant core protein was purified with DEAE Sepharose FF (Pharmacia, Uppsala, Sweden) anion exchange column as described above. The product was analysed in SDS-PAGE.
  • thermostable cellobiohydrolases from Thermoascus aurantiacus ALKO4242 and Chaetomium thermophilum ALKO4265 are superior as compared to the T. reesei Cel7A, also in the case where the Thermoascus Cel 7A core is linked to the CBD of T.
  • Example 13 Standard molecular biology methods were used as described in Example 13. The construction of the Acremonium, Chaetomium , and Thermoascus genomic libraries has been described in Example 12.
  • the peptides derived from the purified Acremonium and Chaetomium endoglucanases shared homology with several endoglucanases of glycosyl hydrolase family 45 such as Melanocarpus albomyces Cel45A endoglucanase (AJ515703) and Humicola insolens endoglucanase (A35275), respectively.
  • Peptides derived from the Thermoascus endoglucanase shared almost 100% identity with the published Thermoascus aurantiacus EG1 endoglucanase sequence (AF487830).
  • albomyces Cel45A sequence (AJ515703) homologous to EG_40. (d A Hind III restriction site was added to the 5′ end of the oligonucleotide (e An EcoRI restriction site was added to the 5′ end of the oligonucleotide
  • the Acremonium thermophilum cel45A gene specific probe to screen the genomic library was amplified with the forward (TAYTGGGAYTGYTGYAARCC) and reverse (RTTRTCNGCRTTYTGRAACCA) primers using genomic DNA as a template.
  • the PCR reaction mixtures contained 50 mM Tris-HCl, pH 9.0, 15 mM (NH 4 ) 2 SO 4 , 0.1% Triton X-100, 1.5 mM MgCl 2 , 0.1 mM dNTPs, 0.5 ⁇ g each primer, 1 unit of Dynazyme EXT DNA polymerase (Finnzymes, Finland) and approximately 0.5 ⁇ g of Acremonium genomic DNA.
  • the conditions for PCR reactions were the following: 5 min initial denaturation at 95° C., followed by 30 cycles of 1 min at 95° C., 1 min annealing at 50-60° C., 2 min extension at 72° C. and a final extension at 72° C. for 10 min.
  • a forward primer GGAATTCGAYCARACNGARCARTA
  • a reverse primer GCAAGCTTCGRCARAARTCRTCRTT
  • the PCR reaction mixtures contained 10 mM Tris-HCl, pH 8.8, 50 mM KCl, 0.1% Triton X-100, 1.5 mM MgCl 2 , 0.2 mM dNTPs, 250 ⁇ mol each primer, 2 unit of Dynazyme II DNA polymerase (Finnzymes, Finland) and approximately 2 ⁇ g of Chaetomium genomic DNA.
  • the conditions for PCR reaction were as described above, except that annealing was performed at 45-50° C.
  • Two PCR products were obtained from the Acremonium PCR reaction. DNA fragments of about 0.6 kb and 0.8 kb were isolated from agarose gel and were cloned into the pCR4-TOPO® TA vector (Invitrogen, USA) resulting in plasmids pALK1710 and pALK1711, respectively.
  • the DNA products were characterized by sequencing and by performing Southern blot hybridizations to the genomic Acremonium DNA digested with several restriction enzymes. The hybridization patterns obtained with the two fragments in stringent washing conditions suggest that two putative endoglucanase genes could be screened from the Acremonium genomic library.
  • the deduced amino acid sequences of both PCR products have homology to several published endoglucanase sequences of glycosyl hydrolase family 45 (BLAST program, National Center for Biotechnology Information; Altschul et al., 1990).
  • PCR product of expected size was obtained from the Chaetomium PCR reaction. This DNA fragment of about 0.7 kb was cloned into the pCR4-TOPO® TA vector (Invitrogen, USA) resulting in plasmid pALK2005 and analyzed as described above.
  • the deduced amino acid sequence of the PCR product has homology to several published cellulase sequences of glycosyl hydrolase family 7 (BLAST program, version 2.2.9 at NCBI, National Center for Biotechnology Information; Altschul et al., 1990).
  • the insert from plasmids pALK1710, pALK1711, and pALK2005 was isolated by restriction enzyme digestion and labeled with digoxigenin according to the supplier's instructions (Roche, Germany). About 1-2 ⁇ 10 5 plaques from the amplified Acremonium or Chaetomium genomic library were screened. The temperature for hybridisation was 68° C. and the filters were washed 2 ⁇ 5 min at RT using 2 ⁇ SSC-0.1% SDS followed by 2 ⁇ 15 min at 68° C. using 0.1 ⁇ SSC-0.1% SDS. Several positive plaques were obtained, of which five to six strongly hybridizing plaques were purified from each screening. Phage DNAs were isolated and analysed by Southern blot hybridization.
  • Thermoascus aurantiacus cel5A gene (coding for EG — 28) (SEQ ID NO: 9) was amplified directly from the isolated genomic DNA by PCR reaction.
  • the forward (ATTAACCGCGGACTGCGCATCATGAAGCTCGGCTCTCTCGTGCTC) and reverse (AACTGAGGCATAGAAACTGACGTCATATT) primers that were used for amplification were designed on the basis of the published T. aurantiacus eg1 gene (AF487830).
  • the PCR reaction mixtures contained 1 ⁇ Phusion HF buffer, 0.3 mM dNTPs, 0.5 ⁇ M of each primer, 2 units of PhusionTM DNA polymerase (Finnzymes, Finland) and approximately 0.25 ⁇ g of Thermoascus genomic DNA.
  • the conditions for PCR reactions were the following: 5 min initial denaturation at 95° C., followed by 25 cycles of 30 s at 95° C., 30 s annealing at 57-67° C., 2.5 min extension at 72° C. and a final extension at 72° C. for 5 min.
  • the amplified 1.3 kb product containing the exact gene was cloned as a SacII-PstI fragment into the pBluescript II KS+vector. Two independent clones were sequenced and one clone was selected and designated as pALK1926.
  • the deposit number of the E. coli strain containing pALK1926 in the Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH culture collection is DSM 17326.
  • the deduced protein sequences of Acremonium EG — 40 (At Cel45A) and EG — 40_like (At Cel45B), Chaetomium EG — 54 (Ct Cel7B), and Thermoascus EG — 28 (Ta Cel5A) endoglucanases share homology with cellulases of glycosyl hydrolase family 45 (Acremonium), family 7 ( Chaetomium ), and family 5 ( Thermoascus ), thus identifying the isolated genes as members of these gene families.
  • the closest homologies of the Acremonium endoglucanases EG — 40/Cel45A and EG — 40_like/Cel45B are endoglucanases of Thielavia terrestris (CQ827970, 77.3% identity) and Myceliophthora thermophila (AR094305, 66.9% identity), respectively (Table 18).
  • the two isolated Acremonium family 45 endoglucanases share only an identity of 53.7% with each other. Of these enzymes only EG-40/Cel45A contains a cellulose binding domain (CBD).
  • the protein sequence of the isolated Thermoascus aurantiacus endoglucanase is completely identical with that of the published T. aurantiacus EGI (AF487830, Table 18). The closest homology was found in a ⁇ -glucanase sequence of Talaromyces emersonii (AX254752, 71.1% identity).
  • Organism, enzyme, and accession number Identity (%) Acremonium thermophilum EG_40 100.0 Thielavia terrestris EG45, CQ827970 77.3 Melanocarpus albomyces Cel45A, AJ515703 75.3 Neurospora crassa , hypothetical XM_324477 68.9 Humicola grisea var thermoidea , EGL3, AB003107 67.5 Humicola insolens EG5, A23635 67.3 Myceliophthora thermophila fam 45, AR094305 57.9 * Acremonium thermophilum EG_40_like 53.7 Acremonium thermophilum EG_40_like 100.0 Myceliophthora thermophila fam 45, AR094305 66.9 Magnaporthe grisea 70-15 hypothetical XM_363402 61.9 Thielavia terrestris EG45, CQ827970 * Acremonium thermophilum EG_40 56.8 Melano
  • Expression plasmids were constructed for production of the recombinant Acremonium EG — 40/Cel45A, EG — 40_like/Cel45B, and Thermoascus EG — 28/Cel5A proteins as described in Example 14.
  • Linear expression cassettes (Table 19) were isolated from the vector backbone by restriction enzyme digestion, transformed into T. reesei A96 and transformants purified as described in Example 14.
  • the endoglucanase production of the transformants was analyzed from the culture supernatants of shake flask cultivations (50 ml). Transformants were grown as in Example 14 and the enzyme activity of the recombinant protein was measured from the culture supernatant as the release of reducing sugars from carboxymethylcellulose (2% (w/v) CMC) at 50° C. in 50 mM citrate buffer pH 4.8 essentially as described by Bailey and Nevalainen 1981; Haakana et al. 2004. Production of the recombinant proteins was also detected from culture supernatants by SDS-polyacrylamide gel electrophoresis. Acremonium EG — 40-specific polyclonal antibodies were produced in rabbits (University of Helsinki, Finland).
  • EG — 40 The expression of EG — 40 was verified by Western blot analysis with anti-EG — 40 antibodies using the ProtoBlot Western blot AP system (Promega). The genotypes of the chosen transformants were analysed by Southern blotting using the expression cassette as a probe.
  • the pH optimum of the heterologously produced endoglucanases was determined in the universal Mcilvaine's buffer within a pH range of 4.0-8.0 using carboxymethylcellulose as substrate. As shown in FIG. 6 A the broadest pH range (4.5-6.0) is that of the Acremonium EG — 40/Cel45A protein, the optimum being at pH 5.5.
  • the pH optima for the other heterologously produced endoglucanases are pH 5.0-5.5 and 6.0 for Acremonium EG — 40_like/Cel45B and Thermoascus EG — 28/Cel5A, respectively.
  • the optimal temperature for enzymatic activity of these endoglucanases was determined at the temperature range of 50-85° C.
  • the highest activity of the enzymes was determined to be at 75° C., 60° C., and 75° C. for the Acremonium EG — 40/Cel45A, EG — 40_like/Cel45B, and Thermoascus EG — 28/Cel5A, respectively ( FIG. 6 B).
  • the chosen transformants were cultivated, as described in Example 14, in a 2 litre bioreactor for four days (28° C., pH 4.2) to obtain material for the application tests.
  • Example 13 Standard molecular biology methods were used as described in Example 13. The construction of the Acremonium, Chaetomium , and Thermoascus genomic libraries has been described in Example 12.
  • the peptides derived from the purified Acremonium, Chaetomium , and Thermoascus ⁇ -glucosidases shared homology with several ⁇ -glucosidases of glycosyl hydrolase family 3 such as Acremonium cellulolyticus (BD168028), Trichoderma viride (AY368687), and Talaromyces emersonil (AY072918) ⁇ -glucosidases, respectively.
  • degenerate primers were designed on the basis of the peptide sequences.
  • Primer Protein Peptide location (a Primer Sequence (b At ⁇ G_101 EKVNLT (c GARAARGTNAAYCTNAC Peptide 4 6-11 YTTRCCRTTRTTSGGRGTR TA Ct ⁇ G_76 Peptide 6 4-9 TNTGYCTNCARGAYGG Peptide 1 3-8 TCRAARTGSCGRTARTCRA TRAASAG Ta ⁇ G_81 Peptide 3 1-5 AARGGYGTSGAYGTSCAR Peptide 1 2-7 YTTRCCCCASGTRAASGG (a Amino acids of the peptide used for designing the primer sequence (b To reduce degeneracy, some codons were chosen according to fungal preference.
  • N A, C, G, or T
  • R A or G
  • S C or G
  • Y C or T
  • the probes for screening genomic libraries constructed were amplified with the listed primer combinations (Table 20) using Acremonium, Chaetomium , or Thermoascus genomic DNA as template.
  • the PCR reaction mixtures contained 50 mM Tris-HCl, pH 9.0, 15 mM (NH 4 ) 2 SO 4 , 0.1% Triton X-100, 1.5 mM MgCl 2 , 0.1-0.2 mM dNTPs, 0.25 ⁇ g each primer, 1 unit of Dynazyme EXT DNA polymerase (Finnzymes, Finland) and approximately 0.5 ⁇ g of genomic DNA.
  • the conditions for PCR reactions were the following: 5 min initial denaturation at 95° C., followed by 30 cycles of 1 min at 95° C., 1 min annealing at 40° C. (Acremonium DNA as a template), at 50° C. (Chaetomium DNA as a template), or at 63° C. (Thermoascus DNA as a template), 2-3 min extension at 72° C. and a final extension at 72° C. for 5-10 min.
  • PCR products of expected size were isolated from the agarose gel.
  • DNA fragments of about 1.8 kb (Acremonium), 1.5 kb ( Chaetomium ), and 1.52 kb ( Thermoascus ) were cloned into the pCR4-TOPO® TA vector (Invitrogen, USA) resulting in plasmids pALK1924, pALK1935, and pALK1713, respectively.
  • the DNA products were characterized by sequencing and by performing Southern blot hybridizations to the genomic DNA digested with several restriction enzymes.
  • the hybridization patterns in stringent washing conditions suggest that one putative ⁇ -glucosidase gene could be isolated from the Acremonium, Chaetomium , and Thermoascus genomic library.
  • the deduced amino acid sequences of all three PCR products have homology to several published ⁇ -glucosidase sequences of glycosyl hydrolase family 3 (BLAST program, National Center for Biotechnology Information; Altschul et al., 1990).
  • the insert from plasmids pALK1713, pALK1924, and pALK1935 was isolated by restriction enzyme digestion and labeled with digoxigenin according to the supplier's instructions (Roche, Germany). About 1-2 ⁇ 10 5 plaques from the amplified Acremonium, Chaetomium , or Thermoascus genomic library were screened as described in Example 18. Several positive plaques were obtained, of which five to six strongly hybridizing plaques were purified from each screening. Phage DNAs were isolated and analysed by Southern blot hybridization. Restriction fragments hybridizing to the probe were subcloned into the pBluescript II KS+vector (Stratagene, USA) and the relevant parts were sequenced.
  • the subcloned phage fragment contains the full-length gene of interest.
  • Table 21 summarises the information of the probes used for screening of the ⁇ -glucosidase genes, phage clones from which the genes were isolated, chosen restriction fragments containing the full-length genes with their promoter and terminator regions, names of plasmids containing the subcloned phage fragment, and the deposit numbers in the Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH culture collection (DSM) for E. coli strains carrying these plasmids.
  • DSM Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH culture collection
  • the deduced protein sequences of Acremonium ⁇ G-101/Cel3A, Chaetomium ⁇ G — 76/Cel3A, and Thermoascus ⁇ G — 81/Cel3A ⁇ -glucosidases share homology with enzymes of glycosyl hydrolase family 3, thus identifying that the isolated genes belong to this gene family.
  • the closest counterparts of the Acremonium, Chaetomium , and Thermoascus ⁇ -glucosidases are those of Magnaporthe grisea ( ⁇ -glucosidase, AY849670), Neurospora crassa (hypothetical, XM — 324308), and Talaromyces emersonii ( ⁇ -glucosidase, AY072918), respectively (Table 24).
  • Organism, enzyme, and accession number Identity (%) * Acremonium thermophilum ⁇ G_101 100.0 Magnaporthe grisea ⁇ -glucosidase, AY849670 73.1 Neurospora crassa hypothetical, XM_330871 71.1 Trichoderma reesei Cel3B, AY281374 65.2 * Thermoascus aurantiacus ⁇ G_81 62.2 Aspergillus aculeatus ⁇ -glucosidase, D64088 59.5 Talaromyces emersonii ⁇ -glucosidase, AY072918 58.9 Aspergillus oryzae , AX616738 58.2 Acremonium cellulolyticus ⁇ -glucosidase, BD168028 57.2 * Chaetomium thermophilum ⁇ G_76 40.9 Chaetomium thermophilum ⁇ G_76 100.0 Neurospora crassa , hypothetical
  • Expression plasmids were constructed for production of the recombinant Acremonium ⁇ G — 101/Cel3A, Chaetomium ⁇ G — 76/Cel3A, and Thermoascus ⁇ G — 81/Cel3A proteins as described in Example 14.
  • Linear expression cassettes (Table 25) were isolated from the vector backbone by restriction enzyme digestion, transformed into T. reesei A96 or A33 (both strains have the genes encoding the four major cellulases CBHI/Cel7A, CBHII/Cel6A, EGI/Cel7B and EGII/Cel5A deleted) and transformants purified as described in Example 14.
  • the beta-glucosidase production of the transformants was analyzed from the culture supernatants of shake flask cultivations (50 ml). Transformants were grown as in Example 14 and the enzyme activity of the recombinant protein was measured from the culture supernatant using 4-nitrophenyl- ⁇ -D-glucopyranoside substrate as described by Bailey and Nevalainen 1981. Production of the recombinant proteins was also detected from culture supernatants by SDS-polyacrylamide gel electrophoresis. In addition, the expression of Thermoascus ⁇ G — 81 was verified by Western blot analysis with anti- ⁇ G — 81 antibodies as described in Example 19. The genotypes of the chosen transformants were analysed by Southern blotting using the expression cassette as a probe.
  • the pH optimum of the heterologously produced ⁇ -glucosidases was determined in the universal Mcilvaine's buffer within a pH range of 3.0-8.0 using 4-nitrophenyl- ⁇ -D-glucopyranoside as substrate.
  • the pH optima for the Acremonium ⁇ G — 101, Chaetomium ⁇ G — 76, and Thermoascus ⁇ G — 81 are pH 4.5, 5.5, and 4.5, respectively ( FIG. 7 A).
  • the optimal temperature for enzymatic activity of these ⁇ -glucosidases was determined at the temperature range of 50-85° C. as described above. The highest activity of the enzymes was determined to be at 70° C., 65° C., and 75° C.
  • the chosen transformants were cultivated, as described in Example 14, in a 2 litre bioreactor for four days (28° C., pH 4.2) to obtain material for the application tests.
  • the peptides derived from the purified Acremonium xylanase shared homology with xylanases of the glycosyl hydrolase family 10 such as Humicola grisea XYNI (AB01030). All peptides derived from the Thermoascus xylanase were completely identical with the published Thermoascus aurantiacus XYNA sequence (AJ132635) thus identifying the purified protein as the same enzyme. Due to this the Thermoascus xylanase gene was amplified by PCR from the genomic DNA.
  • degenerate primers were designed on the basis of the peptide sequences (Example 11, Table 5). The order of the peptides in the protein sequence and the corresponding sense or antisense nature of the primers was deduced from the comparison with the homologous Humicola insolens XYNI sequence (ABOO1030).
  • the sense primer sequence (GAYGGYGAYGCSACYTAYATG) is based on Peptide 3 (amino acids 2-8) and anti-sense primer (YTTYTGRTCRTAYTCSAGRTTRTA) on Peptide 1 (amino acids 4-11).
  • a PCR product of expected size (estimated from the homologous Humicola insolens XYNI sequence ABOO1030) was obtained from the reaction. This DNA fragment of about 0.7 kb was cloned into the pCR4-TOPO® TA vector (Invitrogen, USA) resulting in plasmid pALK1714, and was characterized by sequencing.
  • the deduced amino acid sequence of the PCR product has homology to several published xylanase sequences of glycosyl hydrolase family 10 (BLAST program, National Center for Biotechnology Information; Altschul et al., 1990).
  • the insert from plasmid pALK1714 was isolated by restriction enzyme digestion and labeled with digoxigenin according to the supplier's instructions (Roche, Germany). About 1-2 ⁇ 10 5 plaques from the amplified Acremonium genomic library were screened as described in Example 18. Several positive plaques were obtained, of which five strongly hybridizing plaques were purified. Phage DNAs were isolated and analysed by Southern blot hybridization. A 3.0 kb XbaI restriction fragment hybridizing to the probe was subcloned into the pBluescript II KS+ vector (Stratagene, USA) resulting in plasmid pALK1725.
  • pALK1725 Relevant parts of pALK1725 were sequenced and found to contain the full-length Acremonium thermophilum xyn10A gene (SEQ ID NO: 19).
  • SEQ ID NO: 19 The deposit number of the E. coli strain containing pALK1725 in the Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH culture collection is DSM 16726.
  • Thermoascus aurantiacus xyn10A gene (SEQ ID NO: 17) was amplified directly from the isolated genomic DNA by PCR reaction.
  • the forward (TTATACCGCGGGAAGCCATGGTTCGACCAACGATCCTAC) and reverse (TTATAGGATCCACCGGTCTATACTCACTGCTGCAGGTCCTG) primers that were used in the amplification of the gene were designed on the basis of the published T. aurantiacus xynA gene (AJ132635).
  • the PCR reaction mixtures contained 50 mM Tris-HCl, pH 9.0, 15 mM (NH 4 ) 2 SO 4 , 0.1% Triton X-100, 1.5 mM MgCl2, 0.3 mM dNTPs, 1 ⁇ M each primer, 1 unit of Dynazyme EXT DNA polymerase (Finnzymes, Finland) and approximately 0.5 ⁇ g of Thermoascus genomic DNA.
  • the conditions for PCR reactions were the following: 5 min initial denaturation at 95° C., followed by 30 cycles of 1 min at 95° C., 1 min annealing at 60-66° C., 3 min extension at 72° C. and a final extension at 72° C. for 10 min.
  • the amplified 1.9 kb product containing the exact gene was cloned as a SacII-BamHI fragment into the pBluescript II KS+vector. Three independent clones were sequenced and one clone was selected and designated as pALK1715.
  • the deposit number of the E. coli strain containing pALK1715 in the Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH culture collection is DSM 16724.
  • the deduced protein sequences of Acremonium and Thermoascus xylanases share homology with several enzymes of glycosyl hydrolase family 10, identifying the corresponding genes as members of family 10 xylanases.
  • the closest counterpart for the Acremonium XYN-60/Xyn10A found is the Humicola grisea XYLI (AB001030) showing 67.1% identity with XYN — 60 (Table 28).
  • the predicted protein sequence of the isolated Thermoascus aurantiacus XYN — 30/Xyn10A xylanase is completely identical with that of the published T. aurantiacus XYNA (P23360, Table 28).
  • the closest homology was found in a xylanase sequence of Aspergillus niger (A62445, 69.7% identity).
  • Organism, enzyme, and accession number Identity (%) * Thermoascus aurantiacus XYN_30 100.0 Thermoascus aurantiacus XynA, P23360 100.0 Thermoascus aurantiacus XynA, AF127529 99.4 Aspergillus niger xylanase, A62445 69.7 Aspergillus aculeatus xylanase, AR137844 69.9 Aspergillus terreus fam 10 xyn, DQ087436 65.0 Aspergillus sojae , XynXI AB040414 63.8 Penicillium chrysogenum xylanase, AY583585 62.5 * Acremonium thermophilum XYN_60 100.0 Humicola grisea XYL I, AB001030 67.1 Magnaporthe grisea 70-15, hypothetical
  • Expression plasmids were constructed for production of the recombinant Acremonium XYN-60/Xyn10A and Thermoascus XYN — 30/Xyn10A proteins as described in Example 14.
  • Linear expression cassettes (Table 29) were isolated from the vector backbone by restriction enzyme digestion, transformed into T. reesei A96, and transformants purified as described in Example 14.
  • the xylanase production of the transformants was analyzed from the culture supernatants of shake flask cultivations (50 ml). Transformants were grown as in Example 14 and the enzyme activity of the recombinant protein was measured from the culture supernatant as the release of reducing sugars from birch xylan (1% w/v) at 50° C. in 50 mM citrate buffer pH 5.3 as described by Bailey and Poutanen 1989. Production of the recombinant protein was also analyzed from culture supernatant by SDS-polyacrylamide gel electrophoresis.
  • both xylanases was determined by Western blot analysis with anti-XYN — 30 or anti-XYN — 60 antibodies as described in Example 19.
  • the genotypes of the chosen transformants were analysed by Southern blotting using the expression cassette as a probe.
  • Thermoascus XYN-30/Xyn10A was produced in T. reesei and the pH optimum of the heterologously produced protein was determined in the universal Mcilvaine's buffer within a pH range of 3.0-8.0 using birch xylan as substrate (FIG. 8 A). The optimal pH was determined to be 4.5. The temperature optimum for the enzymatic activity of XYN — 30 was determined to be 75° C. ( FIG. 8 B).
  • the chosen transformants were cultivated, as described in Example 14, in a 2 litre bioreactor for four days (28° C., pH 4.2) to obtain material for the application tests.
  • the performance of the purified recombinant cellobiohydrolases was evaluated in the hydrolysis studies with purified T. reesei enzymes. Hydrolysis was carried out with controlled mixtures of purified enzymes on several pre-treated substrates. Culture filtrates of T. reesei , containing different cloned CBH/Cel7 enzymes were obtained as described in Examples 14 and 15, and the CBH enzymes were purified by affinity chromatography as described in Example 2. In addition, pure T. reesei cellulases (purified as described by Suurnakki et al., 2000) were used in the enzyme mixtures. The cellobiohydrolases used in the experiment were:
  • Thermoascus aurantiacus ALKO4242 CBH (Ta Cel7A)
  • Thermoascus aurantiacus ALKO4242 CBH (Ta Cel7A) with genetically attached CBD of Trichoderma reesei (Ta Cel7A+Tr CBD)
  • Thermoascus aurantiacus ALKO4242 CBH (Ta Cel7A) with genetically attached CBD of Chaetomium thermophilum (Ta Cel7A+Ct CBD)
  • Each CBH/Cel7 to be tested (dosage 14.5 mg/g dry matter of substrate) was used either together with EGII/Cel5A of T. reesei (3.6 mg/g) or with a mixture containing T. reesei EGI/Cel7B (1.8 mg/g), EGII/Cel5A (1.8 mg/g), xylanase pl 9 (Tenkanen et al. 1992) (5000 nkat/g) and acetyl xylan esterase (AXE) (Sundberg and Poutanen, 1991) (250 nkat/g).
  • Washed steam pre-treated spruce fibre impregnation with 3% w/w SO 2 for 20 min, followed by steam pre-treatment at 215° C. for 5 min), dry matter 25.9% (SPRUCE).
  • Washed wet oxidized corn stover fibre (WOCS).
  • Washed steam pre-treated willow fibre pre-treatment for 14 min at 210° C.
  • dry matter 23.0% WILLOW
  • CBH cellobiohydrolase
  • EGI endoglucanase I (Cel7B) of T. reesei
  • EGII endoglucanase II (Cel5A) of T. reesei
  • bG ⁇ -glucosidase (from Novozym 188)
  • XYL xylanase pl 9 (XYN II) of T. reesei
  • thermophilum Cel7A produced hydrolysis products on the same level than T. reesei CBHI/Cel7A.
  • the cellulose binding domain of T. reesei seemed to give slightly better efficiency than CBD of C. thermophilum in the hydrolytic performance of T. aurantiacus Cel7A, even though the difference was rather small.
  • the preparations containing the endoglucanases were compared in hydrolysis studies mixed with the purified CBH/Cel7 and CBH/Cel6 enzymes on several pre-treated substrates.
  • Culture filtrates of T. reesei containing different cloned endoglucanase enzymes were obtained as described in Example 19.
  • the enzymes were enriched by removing thermolabile proteins from the mixtures by a heat treatment (60° C., 2 h, pH 5) and the supernatant was used for the hydrolysis studies.
  • pure T. reesei cellulases purified as described by Suurnakki et al., 2000) were used in the enzyme mixtures.
  • the endoglucanases used in the experiment were:
  • Washed steam pre-treated spruce fibre impregnation with 3% SO 2 for 20 min, followed by steam pre-treatment at 215° C. for 5 min), dry matter 25.9% (SPRUCE).
  • the endoglucanases to be studied were used either with cellobiohydrolases of T. reesei (CBHI/Cel7A, 8.1 mg/g d.m. and CBHII/Cel6A, 2.0 mg/g d.m.) or with Thermoascus aurantiacus Cel7A with genetically attached CBD of T. reesei (10.1 mg/g d.m.).
  • EGI Cel7B
  • EGII Cel5A
  • Triplicate tubes were incubated in mixing at 45° C. for 48 h and reference samples with inactivated enzymes and corresponding substrates were prepared. The release of hydrolysis products was measured as reducing sugars with DNS method using glucose as standard (Table 31).
  • CBHI cellobiohydrolase I (Cel7A) of T. reesei ;
  • CBHII cellobiohydrolase II (Cel6A) of T. reesei ;
  • EGI endoglucanase I (Cel7B) of T. reesei ,
  • EGII endoglucanase II (Cel5A) of T. reesei ;
  • thermophilum endoglucanases have similar performance to T. reesei EGI/Cel7B which is a very efficient enzyme on hemicellulose-containing corn stover substrate due to its strong xylanase side activity.
  • T. aurantiacus endoglucanase Cel5A (ALKO4242 EG — 28) showed lower hydrolysis than T. reesei enzymes.
  • Washed steam exploded spruce fibre (impregnation with 3% w/w SO 2 for 20 min, followed by steam pre-treatment at 215° C. for 5 min), with dry matter of 25.9% was suspended in 5 ml of 0.05 M sodium acetate buffer in the consistency of 10 mg/ml.
  • This substrate was hydrolysed using different enzyme mixtures in test tubes with magnetic stirring in the water bath adjusted in different temperatures for 72 h. For each sample point, a triplicate of test tubes was withdrawn from hydrolysis, boiled for 10 min in order to terminate the enzyme hydrolysis, centrifuged, and the supernatant was analysed for reaction products from hydrolysis. The blanks containing the substrate alone (only buffer added instead of enzymes) were also incubated in the corresponding conditions.
  • thermophilic cellulases A mixture of thermophilic cellulases was prepared using the following components:
  • the protein preparation was produced as described in Example 15 and purified according to Example 2 resulting in the purified Ta Cel7A+Tr CBD preparation with protein content of 5.6 mg/ml.
  • the protein was produced in T. reesei as described in Example 19.
  • the spent culture medium was heat treated (60° C. for 2 hours).
  • the preparation obtained contained protein 4.9 mg/ml and endoglucanase activity (according to IUPAC, 1987) 422 nkat/ml.
  • Thermophilic ⁇ -glucosidase preparation prepared as described in Example 21 containing Thermoascus aurantiacus ALKO4242 ⁇ -glucosidase Ta ⁇ G — 81/Cel3A.
  • the fermentor broth was heat treated (65° C. for 2 hours).
  • the preparation obtained contained 4.3 mg/ml protein and ⁇ -glucosidase activity of 6270 nkat/ml (according to Bailey and Linko, 1990).
  • thermophilic enzyme preparations were combined as follows (per 10 ml of mixture): CBH/Cel7-preparation 4.51 ml, endoglucanase preparation 5.19 ml and ⁇ -glucosidase preparation 0.29 ml. This mixture was used as “MIXTURE 1” of the thermophilic enzymes.
  • Enzymes were dosed on the basis of the FPU activity of the mixtures: “MIXTURE 1” using the dosage of 5.5 FPU per 1 gram of dry matter in the spruce substrate, and “ T. Reesei ENZYMES” using 5.8 FPU per 1 gram of dry matter in the spruce substrate.
  • thermophilic cellulases A mixture of herein described thermophilic cellulases was constructed using the following components:
  • the protein content of the preparation was 31 mg/ml.
  • Thermophilic endoglucanase preparation containing Acremonium thermophilum ALKO4245 endoglucanase At EG — 40/Cel45A was obtained as described in Example 19.
  • the concentrated enzyme preparation contained endoglucanase activity (according to IUPAC, 1987) of 2057 nkat/ml.
  • Thermophilic ⁇ -glucosidase preparation containing Thermoascus aurantiacus ALKO 4242 ⁇ -glucosidase Ta ⁇ G — 81/Cel3A was obtained as described in Example 21 containing ⁇ -glucosidase activity (according to Bailey and Linko, 1990) of 11500 nkat/ml.
  • Thermophilic xylanase product containing an AM24 xylanase originating from Nonomuraea flexuosa DSM43186.
  • the product was prepared by using a recombinant Trichoderma reesei strain that had been transformed with the expression cassette pALK1502, as described in WO2005/100557.
  • the solid product was dissolved in water to make a 10% solution and an enzyme preparation with xylanase activity (assayed according to Bailey et al., 1992) of 208000 nkat/ml was obtained.
  • thermophilic enzyme preparations were combined as follows (per 10 ml of mixture): CBH/Cel7 preparation 7.79 ml, endoglucanase preparation 0.96 ml, ⁇ -glucosidase preparation 1.14 ml and xylanase preparation 0.31 ml. This mixture was used as “MIXTURE 2” of the thermophilic enzymes.
  • Trichoderma reesei enzymes As a comparison and reference, a state-of art mixture of commercial Trichoderma reesei enzymes was constructed by combining (per 10 ml) 8.05 ml Celluclast 1.5 L FG (from Novozymes A/S) and 1.95 ml Novozym 188 (from Novozymes A/S). This was designated as “ T. Reesei ENZYMES.”
  • thermophilic enzymes showed more efficient hydrolysis as compared to T. reesei enzymes: The hydrolysis was faster and higher sugar yields were also obtained. On the basis of HPLC analysis the maximum yield of sugars (including free soluble sugars in the unwashed substrate that was used) from the substrate would be 5.73 mg per 10 mg of dry substrate. Thus, the hydrolysis by the MIXTURE 2 enzymes was nearly complete within 48 hours. In 55° C. and 57.5° C. the herein described thermophilic enzymes showed also clearly better performance in the hydrolysis as compared to the state-of art Trichoderma enzymes.
  • Example 27 The procedure explained in Example 27 was repeated except that the xylanase product XT 02026A3 was replaced by thermophilic xylanase preparation containing Thermoascus aurantiacus ALKO4242 xylanase Ta XYN — 30/Xynl OA produced in T. reesei .
  • the fermentor broth, produced as described in Example 23 contained xylanase activity of 132 000 nkat/ml (assayed according to Bailey et al., 1992).
  • thermophilic enzyme preparations were combined as follows (per 10 ml of mixture): CBH/Cel7-preparation 7.64 ml, endoglucanase preparation 0.96 ml, ⁇ -glucosidase preparation 1.15 ml and xylanase preparation 0.25 ml. This mixture was used as “MIXTURE 3” of the thermophilic enzymes.
  • Trichoderma reesei enzymes As a comparison and reference, a state-of-art mixture of commercial Trichoderma reesei enzymes was constructed by combining (per 10 ml) 8.05 ml Celluclast 1.5 L FG (from Novozymes A/S) and 1.95 ml Novozym 188 (from Novozymes A/S). This was designated as “ T. Reesei ENZYMES.”
  • thermophilic enzymes showed more efficient hydrolysis as compared to T. reesei enzymes.
  • thermophilic enzymes showed clearly better performance in the hydrolysis as compared to the state-of art Trichoderma enzymes.
  • the performance of the new enzyme mixture at 60° C. was at the same level than the performance of state-of-art enzymes at 45° C.
  • Example 28 Procedure as described in Example 28 was repeated with washed steam exploded spruce fibre (impregnation with 3% w/w SO 2 for 20 min, followed by steam pre-treatment at 215° C. for 5 min, with dry matter of 25.9%) as substrate using hydrolysis temperatures 45° C., 55° C. and 60° C. Samples were taken from the hydrolysis after 24, 48 and 72 h and treated as described above. The hydrolysis products were quantified using the assay for reducing sugars (Bernfeld, 1955), using glucose as standard. The results from the substrate blanks were subtracted from the samples with enzymes, and the concentration of hydrolysis products as reducing sugars is presented in FIG. 12 .
  • thermophilic enzymes showed more efficient hydrolysis as compared to T. reesei enzymes, evidently due to the better stability in long term hydrolysis.
  • efficiency of the mixture of herein described enzymes was still on the same level than at 45° C., whereas the state-of-art mixture was inefficient with the substrate used in this temperature.
  • the herein described thermophilic enzymes showed decreased hydrolysis although the hydrolysis was nearly at the same level as the performance of the state-of-art enzymes at 45° C.
  • the culture filtrates produced by Acremonium thermophilium ALKO4245, Chaetomium thermophilum ALKO4261 and Thermoascus aurantiacus ALKO4242 strains are described in Example 1.
  • the ⁇ -glucosidase activities (measured according to Bailey and Linko, 1990) of these preparations were 21.4 nkat/ml, 5.6 nkat/ml and 18.6 nkat/ml, respectively.
  • commercial enzymes Celluclast 1.5 L ( ⁇ -glucosidase 534 nkat/ml) and Novozym 188 ( ⁇ -glucosidase 5840 nkat/ml) were also included in the experiment.
  • the standard activity assay procedure was performed in the presence of different concentrations of glucose.
  • the substrate (p-nitrophenyl- ⁇ -D-glucopyranoside) solutions for ⁇ -glucosidase activity assay were supplemented by glucose so that the glucose concentration in the assay mixture was adjusted to the values from 0 to 0.5 M. Except this glucose addition the assay was performed using the standard procedure (Bailey and Linko, 1990). The activities in the presence of varying glucose concentrations as a percentage of the activity without glucose are presented in FIG. 13 .
  • thermophilum showed behaviour comparable to T. reesei enzyme of Celluclast. Especially C. thermophilum enzyme was clearly less affected by high glucose concentration.
  • Filter paper activity of enzyme preparations was measured according to the method of IUPAC (1987) as described in the procedure except enzyme reaction was performed at temperatures from 50° C. to 70° C.
  • the calculated FPU activity is based on the amount of enzyme required to hydrolyse 4% of filter paper substrate in 1 h under the experimental conditions.
  • the FPU activity is considered to represent the total overall cellulase activity of an enzyme preparation.
  • MIXTURE 2 prepared as described in Example 27, MIXTURE 3 prepared as described in Example 28, and MIXTURE 4.
  • MIXTURE 4 was prepared by combining enzyme preparations described in Example 27 as follows (per 10 ml of mixture): CBH/Cel7-preparation 7.84 ml, endoglucanase preparation 0.99 ml and ⁇ -glucosidase preparation 1.17 ml.
  • T. Reesei ENZYMES A prepared as preparation “ T. Reesei ENZYMES” described in Example 26.
  • T. Reesei ENZYMES B was constructed combining (per 10 ml) 8.05 ml Econase CE (a commercial T. reesei cellulase preparation from AB Enzymes Oy, Rajamaki, Finland) and 1.95 ml Novozym 188 (from Novozymes A/S).
  • the FPU activities measured for the enzyme preparations at different temperatures are presented in FIG. 14 as percentages of the activity under standard (IUPAC, 1987) conditions (at 50° C.).
  • a high concentration starch hydrolysate mixture (Nutriose 74/968, Roquette) was treated with Thermoascus aurantiacus ⁇ G — 81/Cel3A enriched enzyme preparation produced as described in Example 21 to produce a sugar mixture containing appreciable amounts of cellulase inducer (sophorose) to overcome the glucose repression.
  • the Ta ⁇ G — 81/Cel3A enriched enzyme preparation was added to a 70% (w/w) Nutriose solution to a final concentration of 1 g total protein/litre.
  • the container of the mixture was incubated in a water bath at 65° C. for 3 days with constant stirring and used as a carbon source in a shake flask medium for two different Trichoderma -strains (A47 and Rut-C30).
  • the effect of the enzyme treatment was measured as an endoglucanase activity formed during a 7 days shake flask cultivation.
  • As a reference cultivations were performed under the same conditions with untreated Nutriose as a carbon source. More than two-fold increase in the activities was obtained in the shake flask cultivations performed on Ta ⁇ G — 81/Cel3A pretreated Nutriose media with the strains tested. Results are shown in FIG. 15 .

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