Polypeptides having cellulolytic enhancing activity and polynucleotides encoding same

1. A DNA construct or recombinant expression vector comprising an isolated polynucleotide comprising a nucleotide sequence that encodes a GH61 polypeptide having cellulolytic enhancing activity, wherein the isolated polynucleotide is operably linked to one or more heterologous control sequences that direct the production of the polypeptide in an expression host, wherein the GH61 polypeptide having cellulolytic enhancing activity is selected from the group consisting of:

(a) a GH61 polypeptide having at least 95% sequence identity to amino acids 20 to 334 of SEQ ID NO: 4;

(b) a GH61 polypeptide encoded by a polynucleotide that hybridizes under very high stringency conditions with (i) nucleotides 58 to 1250 of SEQ ID NO: 3, (ii) the cDNA sequence of nucleotides 58 to 1250 of SEQ ID NO: 3, or (iii) the full-length complement of (i) or (ii), wherein very high stringency conditions are defined as prehybridization and hybridization at 42° in 5×SSPE, 0.3% SDS, 200 micrograms/ml sheared and denatured salmon sperm DNA, and 50% formamide and washing three times each for 15 minutes using 2×SSC, 0.2% SDS at 70° C.; the cDNA sequence of nucleotides 58 to 1250 of SEQ ID NO: 3;

(c) a GH61 polypeptide encoded by a polynucleotide having at least 99% sequence identity to nucleotides 58 to 1250 of SEQ ID NO: 3, or a GH61 polypeptide encoded by the cDNA of nucleotides 58 to 1250 of SEQ ID NO: 3; and

(d) an isolated fragment of a GH61 polypeptide of (a), (b), or (c) that has cellulolytic enhancing activity.

2. A recombinant host cell comprising the DNA construct or recombinant expression vector of claim 1 .

3. A method of producing a GH61 polypeptide having cellulolytic enhancing activity, said method comprising:

(a) cultivating the recombinant host cell of claim 2 under conditions conducive for production of the polypeptide; and

(b) recovering the polypeptide.

4. A DNA construct comprising a nucleic acid encoding a signal peptide comprising amino acids 1 to 19 of SEQ ID NO: 4, wherein the nucleic acid is operably linked to a heterologous nucleic acid encoding a protein.

5. A recombinant host cell comprising a nucleic acid encoding a protein, wherein the nucleic acid is operably linked to an isolated polynucleotide encoding a signal peptide comprising amino acids 1 to 19 of SEQ ID NO: 4, wherein the nucleic acid is foreign to the polynucleotide encoding the signal peptide.

6. A method of producing a protein, said method comprising:

(a) cultivating the recombinant host cell of claim 5 under conditions conducive for production of the protein; and

(b) recovering the protein.

7. The method of claim 6 , wherein the nucleic acid is operably linked to an isolated polynucleotide encoding a signal peptide consisting of amino acids 1 to 19 of SEQ ID NO: 4, wherein the nucleic acid is foreign to the polynucleotide encoding the signal peptide.

8. A method of producing a GH61 polypeptide having cellulolytic enhancing activity, said method comprising:

(i) cultivating an isolated Thielavia terrestris cell under conditions conducive for production of the polypeptide; and

(ii) recovering the polypeptide,

wherein the GH61 polypeptide having cellulolytic enhancing activity is selected from the group consisting of:

(a) a GH61 polypeptide having at least 95% sequence identity to amino acids 20 to 334 of SEQ ID NO: 4;

(b) a GH61 polypeptide encoded by a polynucleotide that hybridizes under very high stringency conditions with (i) nucleotides 58 to 1250 of SEQ ID NO: 3, (ii) the cDNA sequence of nucleotides 58 to 1250 of SEQ ID NO: 3, or (iii) the full-length complement of (i) or (ii), wherein very high stringency conditions are defined as prehybridization and hybridization at 42° in 5×SSPE, 0.3% SDS, 200 micrograms/ml sheared and denatured salmon sperm DNA, and 50% formamide and washing three times each for 15 minutes using 2×SSC, 0.2% SDS at 70° C.; the cDNA sequence of nucleotides 58 to 1250 of SEQ ID NO: 3;

(c) a GH61 polypeptide encoded by a polynucleotide having at least 99% sequence identity to nucleotides 58 to 1250 of SEQ ID NO: 3, or a GH61 polypeptide encoded by the cDNA of nucleotides 58 to 1250 of SEQ ID NO: 3; and

(d) an isolated fragment of a GH61 polypeptide of (a), (b), or (c) that has cellulolytic enhancing activity.

9. A transgenic plant, plant part or plant cell transformed with a polynucleotide encoding a GH61 polypeptide having cellulolytic enhancing activity, wherein the polypeptide comprises a signal peptide directing the polypeptide into the secretory pathway, and wherein the GH61 polypeptide having cellulolytic enhancing activity is selected from the group consisting of:

(a) a GH61 polypeptide having at least 95% sequence identity to amino acids 20 to 334 of SEQ ID NO: 4;

(b) a GH61 polypeptide encoded by a polynucleotide that hybridizes under very high stringency conditions with (i) nucleotides 58 to 1250 of SEQ ID NO: 3, (ii) the cDNA sequence of nucleotides 58 to 1250 of SEQ ID NO: 3, or (iii) the full-length complement of (i) or (ii), wherein very high stringency conditions are defined as prehybridization and hybridization at 42° in 5×SSPE, 0.3% SDS, 200 micrograms/ml sheared and denatured salmon sperm DNA, and 50% formamide and washing three times each for 15 minutes using 2×SSC, 0.2% SDS at 70° C.; the cDNA sequence of nucleotides 58 to 1250 of SEQ ID NO: 3;

(c) a GH61 polypeptide encoded by a polynucleotide having at least 99% sequence identity to nucleotides 58 to 1250 of SEQ ID NO: 3, or a GH61 polypeptide encoded by the cDNA of nucleotides 58 to 1250 of SEQ ID NO: 3; and

(d) an isolated fragment of a GH61 polypeptide of (a), (b), or (c) that has cellulolytic enhancing activity.

10. A method of producing a GH61 polypeptide having cellulolytic enhancing activity, said method comprising:

(a) cultivating the transgenic plant or plant cell of claim 8 under conditions conducive for production of the polypeptide; and

(b) recovering the polypeptide.

11. A method for degrading a cellulosic material comprising treating the cellulosic material with an enzyme composition in the presence of a GH61 polypeptide having cellulolytic enhancing activity, and recovering the degraded cellulosic material, wherein the GH61 polypeptide having cellulolytic enhancing activity is selected from the group consisting of:

(a) a GH61 polypeptide having at least 95% sequence identity to amino acids 20 to 334 of SEQ ID NO: 4;

(b) a GH61 polypeptide encoded by a polynucleotide that hybridizes under very high stringency conditions with (i) nucleotides 58 to 1250 of SEQ ID NO: 3, (ii) the cDNA sequence of nucleotides 58 to 1250 of SEQ ID NO: 3, or (iii) the full-length complement of (i) or (ii), wherein very high stringency conditions are defined as prehybridization and hybridization at 42° in 5×SSPE, 0.3% SDS, 200 micrograms/ml sheared and denatured salmon sperm DNA, and 50% formamide and washing three times each for 15 minutes using 2×SSC, 0.2% SDS at 70° C.; the cDNA sequence of nucleotides 58 to 1250 of SEQ ID NO: 3;

(c) a GH61 polypeptide encoded by a polynucleotide having at least 99% sequence identity to nucleotides 58 to 1250 of SEQ ID NO: 3, or a GH61 polypeptide encoded by the cDNA of nucleotides 58 to 1250 of SEQ ID NO: 3; and

(d) an isolated fragment of a GH61 polypeptide of (a), (b), or (c) that has cellulolytic enhancing activity.

12. A method for producing a fermentation product, said method comprising:

(i) saccharifying a cellulosic material with an enzyme composition in the presence of a GH61 polypeptide having cellulolytic enhancing activity;

(ii) fermenting the saccharified cellulosic material with one or more fermenting microorganisms to produce the fermentation product; and

(iii) recovering the fermentation product from the fermentation;

wherein the GH61 polypeptide having cellulolytic enhancing activity is selected from the group consisting of:

(a) a GH61 polypeptide having at least 95% sequence identity to amino acids 20 to 334 of SEQ ID NO: 4;

(b) a GH61 polypeptide encoded by a polynucleotide that hybridizes under very high stringency conditions with (i) nucleotides 58 to 1250 of SEQ ID NO: 3, (ii) the cDNA sequence of nucleotides 58 to 1250 of SEQ ID NO: 3, or (iii) the full-length complement of (i) or (ii), wherein very high stringency conditions are defined as prehybridization and hybridization at 42° in 5×SSPE, 0.3% SDS, 200 micrograms/ml sheared and denatured salmon sperm DNA, and 50% formamide and washing three times each for 15 minutes using 2×SSC, 0.2% SDS at 70° C.; the cDNA sequence of nucleotides 58 to 1250 of SEQ ID NO: 3;

(c) a GH61 polypeptide encoded by a polynucleotide having at least 99% sequence identity to nucleotides 58 to 1250 of SEQ ID NO: 3, or a GH61 polypeptide encoded by the cDNA of nucleotides 58 to 1250 of SEQ ID NO: 3; and

(d) an isolated fragment of a GH61 polypeptide of (a), (b), or (c) that has cellulolytic enhancing activity.

13. The method of claim 12 , wherein steps (i) and (ii) are performed simultaneously.

14. A method of fermenting a cellulosic material, said process comprising:

(i) fermenting the cellulosic material with one or more fermenting microorganisms, wherein the cellulosic material is saccharified with an enzyme composition in the presence of a polypeptide having cellulolytic enhancing activity, wherein the fermenting of the cellulosic material produces a fermentation product; and

(ii) recovering the fermentation product from the fermentation;

wherein the GH61 polypeptide having cellulolytic enhancing activity is selected from the group consisting of:

(a) a GH61 polypeptide having at least 95% sequence identity to amino acids 20 to 334 of SEQ ID NO: 4;

(b) a GH61 polypeptide encoded by a polynucleotide that hybridizes under very high stringency conditions with (i) nucleotides 58 to 1250 of SEQ ID NO: 3, (ii) the cDNA sequence of nucleotides 58 to 1250 of SEQ ID NO: 3, or (iii) the full-length complement of (i) or (ii), wherein very high stringency conditions are defined as prehybridization and hybridization at 42° in 5×SSPE, 0.3% SDS, 200 micrograms/ml sheared and denatured salmon sperm DNA, and 50% formamide and washing three times each for 15 minutes using 2×SSC, 0.2% SDS at 70° C.; the cDNA sequence of nucleotides 58 to 1250 of SEQ ID NO: 3;

(c) a GH61 polypeptide encoded by a polynucleotide having at least 99% sequence identity to nucleotides 58 to 1250 of SEQ ID NO: 3, or a GH61 polypeptide encoded by the cDNA of nucleotides 58 to 1250 of SEQ ID NO: 3; and

(d) an isolated fragment of a GH61 polypeptide of (a), (b), or (c) that has cellulolytic enhancing activity.