IP Library Granted Patent US 8,202,704
Granted Patent B2
US 8,202,704 · App. 13/029,919 · Granted Jun 19, 2012

Trichoderma genes

Assignee: Danisco US Inc.
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 8,202,704
App. No.
13/029,919
Granted
Jun 19, 2012
Kind
B2
Abstract

Described herein are novel gene sequences isolated from Trichoderma reesei . Two genes encoding proteins comprising a cellulose binding domain, one encoding an arabionfuranosidase and one encoding an acetylxylanesterase are described. The sequences, CIP1 and CIP2, contain a cellulose binding domain. These proteins are especially useful in the textile and detergent industry and in pulp and paper industry.

Claims (26)

1. An isolated polynucleotide encoding a protein having cellulose binding activity which is:

(a) a nucleic acid sequence which encodes or is complementary to a sequence which encodes a CIP1 polypeptide having at least 90% sequence identity to the amino acid sequence presented as SEQ ID NO:5;

(b) a nucleic acid sequence which encodes or is complementary to a sequence which encodes a CIP1 polypeptide having at least 95% sequence identity to the amino acid sequence presented as SEQ ID NO:5;

(c) a nucleic acid sequence which encodes or is complementary to a sequence which encodes a CIP1 polypeptide having at least 98% sequence identity to the amino acid sequence presented as SEQ ID NO:5;

(d) a nucleic acid sequence which encodes or is complementary to a sequence which encodes a CIP1 polypeptide having the amino acid sequence presented as SEQ ID NO:5;

(e) a nucleic acid sequence which encodes or is complementary to a sequence which encodes a CIP1 polypeptide having at least 95% sequence identity to the amino acid sequence presented as SEQ ID NO:3;

(f) a nucleic acid sequence which encodes or is complementary to a sequence which encodes a CIP1 polypeptide having at least 98% sequence identity to the amino acid sequence presented as SEQ ID NO:3;

(g) a nucleic acid sequence which encodes or is complementary to a sequence which encodes a CIP1 polypeptide having the amino acid sequence presented as SEQ ID NO:3;

(h) a nucleic acid sequence presented as SEQ ID NO:2, or the complement thereof, wherein % identity is calculated using the CLUSTAL-W program in MacVector version 6.5, operated with default parameters, including an open gap penalty of 10.0, an extended gap penalty of 0.1, and a BLOSUM 30 similarity matrix; or

(i) a nucleic acid sequence that hybridizes, under high stringency conditions to the sequence presented as SEQ ID NO:2, or the complement or a fragment thereof, wherein hybridization is conducted at 42° C. in 50% formamide, 6×SSC, 5×Denhardt's solution, 0.5% SDS and 100 μg/ml denatured carrier DNA followed by washing two times in 2×SSPE and 0.5% SDS at room temperature and two additional times in 0.1 SSPE and 0.5% SDS at 42° C.

2. The isolated polynucleotide of claim 1 , wherein the enzyme is derived from a Trichoderma source.

3. The isolated polynucleotide of claim 2 , wherein the enzyme is derived from Trichoderma reesei.

4. An expression construct comprising the isolated polynucleotide of claim 1 .

5. A vector comprising the expression construct of claim 4 .

6. A vector comprising the isolated polynucleotide of claim 1 , operably linked to control sequences recognized by a host cell transformed with the vector.

7. A host cell transformed with the vector of claim 5 .

8. A host cell transformed with the vector of claim 6 .

9. The host cell of claim 7 , which is a prokaryotic cell.

10. The host cell of claim 8 , which is a eukaryotic cell.

11. A recombinant host cell comprising the isolated polynucleotide of claim 1 .

12. The recombinant host cell of claim 11 , which is a prokaryotic cell.

13. The isolated polynucleotide of claim 1 , wherein said polynucleotide is an RNA.

14. A method of producing an enzyme having cellulose binding activity comprising cultivating the host cell of claim 7 under condition suitable for the host cell to produce the enzyme, and recovering the enzyme.

15. A method of producing an enzyme having cellulose binding activity comprising cultivating the host cell of claim 8 under condition suitable for the host cell to produce the enzyme, and recovering the enzyme.

16. The method of claim 14 , wherein the host cell is a filamentous fungi or yeast cell.

17. The method of claim 15 , wherein the host cell is a filamentous fungi or yeast cell.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 6, 2011
From: FOREMAN, PAMELA; GOEDEGEBUUR, FRITS; VAN SOLINGEN, PIETER; WARD, MICHAEL
To: GENENCOR INTERNATIONAL, INC.
Reel/Frame 026237/0399 →
CHANGE OF NAME Recorded May 6, 2011
From: GENENCOR INTERNATIONAL, INC.
To: DANISCO US INC.
Reel/Frame 026240/0660 →
Continuity (5)
Division 12683108 · Jan 6, 2010
Division 10555358
Provisional Application 60474411 · May 29, 2003
Provisional Application 60475826 · Jun 3, 2003
Related Publication 20110287511A1 · Nov 24, 2011