IP Library Granted Patent US 9,376,670
Granted Patent B2
US 9,376,670 · App. 14/277,231 · Granted Jun 28, 2016

Polypeptides having cellobiohydrolase activity and polynucleotides encoding same

Inventor: Nikolaj Spodsberg (Bagsvaerd, DK)
Assignee: Novozymes Inc.
C12N9/2437C12P7/14C12P19/02C12P19/14C12Y302/01091C12P2203/00Y02P20/52
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,376,670
App. No.
14/277,231
Granted
Jun 28, 2016
Kind
B2
Abstract

The present invention relates to isolated polypeptides having cellobiohydrolase activity and polynucleotides encoding the polypeptides. The invention also relates to nucleic acid constructs, vectors, and host cells comprising the polynucleotides as well as methods of producing and using the polypeptides.

Claims (64)

1. A nucleic acid construct comprising a polynucleotide encoding a polypeptide having cellobiohydrolase activity, wherein the polynucleotide is operably linked to one or more heteroloqous control sequences that direct production of the polypeptide in an expression host, and wherein the polypeptide is selected from:

(a) a polypeptide having at least 90% sequence identity to the sequence of amino acids 26 to 532 of SEQ ID NO: 2;

(b) a polypeptide encoded by a polynucleotide that hybridizes under high stringency conditions with the full-length complement of the sequence of nucleotides 76 to 1596 of SEQ ID NO: 1 or the cDNA sequence thereof, wherein the high stringency conditions are defined as prehybridization and hybridization at 42° C. in 5X SSPE, 0.3% SDS, 200 micrograms/ml sheared and denatured salmon sperm DNA, and 50% formamide, following standard Southern blotting procedures for 12 to 24 hours, followed by washing three times each for 15 minutes using 2×SSC, 0.2% SDS at 65° C.; and

(c) a fragment of the sequence of amino acids 26 to 532 of SEQ ID NO: 2 that has cellobiohydrolase activity.

2. The nucleic acid construct of claim 1 , wherein the polypeptide having cellobiohydrolase activity has at least 95% sequence identity to the sequence of amino acids 26 to 532 of SEQ ID NO: 2.

3. The nucleic acid construct of claim 1 , wherein the polypeptide having cellobiohydrolase activity has at least 97% sequence identity to the sequence of amino acids 26 to 532 of SEQ ID NO: 2.

4. The nucleic acid construct of claim 1 , wherein the polypeptide having cellobiohydrolase activity is encoded by a polynucleotide having at least 95% sequence identity to nucleotides 76 to 1596 of SEQ ID NO: 1.

5. The nucleic acid construct of claim 1 , wherein the polypeptide having cellobiohydrolase activity is a variant having at least 98% sequence identity to the sequence of amino acids 26 to 532 of SEQ ID NO: 2 comprising a substitution, deletion, and/or insertion at one or more positions.

6. The nucleic acid construct of claim 1 , wherein the polypeptide having cellobiohydrolase activity comprises the sequence of amino acids 26 to 532 of SEQ ID NO: 2.

7. The nucleic acid construct of claim 1 , wherein the polypeptide having cellobiohydrolase activity is a fragment of the sequence of amino acids 26 to 532 of SEQ ID NO: 2, wherein the fragment has cellobiohydrolase activity.

8. A recombinant host cell transformed with the nucleic acid construct of claim 1 .

9. A method of producing a polypeptide having cellobiohydrolase activity, comprising:

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

(b) recovering the polypeptide.

10. A nucleic acid construct comprising a polynucleotide encoding a polypeptide having cellobiohydrolase activity and a catalytic domain, wherein the polynucleotide is operably linked to one or more heterologous control sequences that direct production of the polypeptide in an expression host, and wherein the catalytic domain is selected from:

(a) a catalytic domain having at least 90% sequence identity to the sequence of amino acids 26 to 460 of SEQ ID NO: 2; and

(b) a fragment of the sequence of amino acids 26 to 460 of SEQ ID NO: 2, which has cellobiohydrolase activity.

11. The nucleic acid construct of claim 10 , wherein the polypeptide further comprises a cellulose binding domain.

12. The nucleic acid construct of claim 10 , wherein the catalytic domain has at least 95% sequence identity to the sequence of amino acids 26 to 460 of SEQ ID NO: 2.

13. The nucleic acid construct of claim 10 , wherein the catalytic domain has at least 97% sequence identity to the sequence of amino acids 26 to 460 of SEQ ID NO: 2.

14. The nucleic acid construct of claim 10 , wherein the catalytic domain comprises the sequence of amino acids 26 to 460 of SEQ ID NO: 2.

15. A recombinant host cell transformed with the nucleic acid construct of claim 10 .

16. A recombinant host cell transformed with a nucleic acid construct or expression vector comprising a polynucleotide encoding a polypeptide having cellobiohydrolase activity, wherein the polypeptide having cellobiohydrolase activity has a catalytic domain selected from:

(a) a catalytic domain having at least 90% sequence identity to the sequence of amino acids 26 to 460 of SEQ ID NO: 2; and

(b) a fragment of the sequence of amino acids 26 to 460 of SEQ ID NO: 2, which has cellobiohydrolase activity.

17. The recombinant host cell of claim 16 , wherein the catalytic domain has at least 95% sequence identity to the sequence of amino acids 26 to 460 of SEQ ID NO: 2.

18. The recombinant host cell of claim 16 , wherein the catalytic domain comprises the sequence of amino acids 26 to 460 of SEQ ID NO: 2.

19. A recombinant host cell transformed with a nucleic acid construct or expression vector comprising a polynucleotide encoding a polypeptide having cellobiohydrolase activity, wherein the polypeptide having cellobiohydrolase activity is selected from:

(a) a polypeptide having at least 90% sequence identity to the sequence of amino acids 26 to 532 of SEQ ID NO: 2;

(b) a polypeptide encoded by a polynucleotide that hybridizes under high stringency conditions with the full-length complement of the sequence of nucleotides 76 to 1596 of SEQ ID NO: 1 wherein the high stringency conditions are defined as prehybridization and hybridization at 42° C. in 5X SSPE, 0.3% SDS, 200 micrograms/ml sheared and denatured salmon sperm DNA, and 50% formamide, following standard Southern blotting procedures for 12 to 24 hours, followed by washing three times each for 15 minutes using 2X SSC, 0.2% SDS at 65° C.; and

(c) a fragment of the sequence of amino acids 26 to 532 of SEQ ID NO: 2 that has cellobiohydrolase activity.

20. The recombinant host cell of claim 19 , wherein the polypeptide having cellobiohydrolase activity has at least 95% sequence identity to the sequence of amino acids 26 to 532 of SEQ ID NO: 2.

21. The recombinant host cell of claim 19 , wherein the polypeptide having cellobiohydrolase activity comprises the sequence of amino acids 26 to 532 of SEQ ID NO: 2.

22. A recombinant host cell transformed with the nucleic acid construct of claim 2 .

23. A recombinant host cell transformed with the nucleic acid construct of claim 3 .

24. A recombinant host cell transformed with the nucleic acid construct of claim 12 .

25. A recombinant host cell transformed with the nucleic acid construct of claim 13 .

26. A method of producing a polypeptide having cellobiohydrolase activity, comprising:

(a) cultivating the host cell of claim 15 under conditions conducive for production of the polypeptide; and

(b) recovering the polypeptide.

27. A method of producing a polypeptide having cellobiohydrolase activity, comprising:

(a) cultivating the host cell of claim 16 under conditions conducive for production of the polypeptide; and

(b) recovering the polypeptide.

28. A method of producing a polypeptide having cellobiohydrolase activity, comprising:

(a) cultivating the host cell of claim 17 under conditions conducive for production of the polypeptide; and

(b) recovering the polypeptide.

29. A method of producing a polypeptide having cellobiohydrolase activity, comprising:

(a) cultivating the host cell of claim 19 under conditions conducive for production of the polypeptide; and

(b) recovering the polypeptide.

30. A method of producing a polypeptide having cellobiohydrolase activity, comprising:

(a) cultivating the host cell of claim 20 under conditions conducive for production of the polypeptide; and

(b) recovering the polypeptide.

31. A method of producing a polypeptide having cellobiohydrolase activity, comprising:

(a) cultivating the host cell of claim 22 under conditions conducive for production of the polypeptide; and

(b) recovering the polypeptide.

32. A method of producing a polypeptide having cellobiohydrolase activity, comprising:

(a) cultivating the host cell of claim 23 under conditions conducive for production of the polypeptide; and

(b) recovering the polypeptide.

33. A method of producing a polypeptide having cellobiohydrolase activity, comprising:

(a) cultivating the host cell of claim 24 under conditions conducive for production of the polypeptide; and

(b) recovering the polypeptide.

34. A method of producing a polypeptide having cellobiohydrolase activity, comprising:

(a) cultivating the host cell of claim 25 under conditions conducive for production of the polypeptide; and

(b) recovering the polypeptide.

Assignments (1)
CONFIRMATORY LICENSE Recorded Aug 29, 2019
From: NOVOZYMES, INC.
To: UNITED STATES DEPARTMENT OF ENERGY
Reel/Frame 050207/0905 →
Priority Claims (2)
EP 11152252 · Jan 26, 2011 · regional
EP 11250695 · Aug 4, 2011 · regional
Continuity (3)
Division 13996027
Provisional Application 61531394 · Sep 6, 2011
Related Publication 20140342410A1 · Nov 20, 2014