Pectate lyases
AssigneeNovozymes A/S
InventorsLene Nonboe Andersen, Martin Schülein, Niels Erik Krebs Lange
Life of this patent
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Abstract
The present invention relates to microbial pectate lyases, more specifically to microbial enzymes exhibiting pectate lyase activity as their major enzymatic activity in the neutral and alkaline pH ranges, to a method of producing such an enzyme, and to methods for using such enzymes in the textile, detergent and cellulose fiber processing industries.
Claims5
A method for improving the properties of cellulosic material, said method comprising treating said material with an effective amount of a polypeptide having pectate lyase activity, wherein said polypeptide is selected from the group consisting of:
- a) a polypeptide comprising an amino acid sequence as shown in SEQ ID NO:
- 2 from residue 1 to residue 341;
- b) a polypeptide having at least 95% identity to the sequence of SEQ ID NO:
- 2 from amino acid residue 1 to amino acid residue 341, wherein said identity is determined by the GAP program, using a GAP creation penalty of 3.0 and a GAP extension penalty of 0.1;
- and
- c) a polypeptide encoded by a DNA sequence that hybridizes to the DNA sequence of SEQ ID NO:1 under high stringency conditions, wherein said high stringency conditions comprise hybridization in 5×SSC at 45° C. and washing in 2×SSC at 70° C.
A method for degradation or modification of plant material said method comprising treating the plant material with an effective amount of a polypeptide having pectate lyase activity, wherein said polypeptide is selected from the group consisting of:
- a) a polypeptide comprising an amino acid sequence as shown in SEQ ID NO:
- 2 from residue 1 to residue 341;
- b) a polypeptide having at least 95% identity to the sequence of SEQ ID NO:
- 2 from amino acid residue 1 to amino acid residue 341, wherein said identity is determined by the GAP program, using a GAP creation penalty of 3.0 and a GAP extension penalty of 0.1;
- and
- c) a polypeptide encoded by a DNA sequence that hybridizes to the DNA sequence of SEQ ID NO:1 under high stringency conditions, wherein said high stringency conditions comprise hybridization in 5×SSC at 45° C. and washing in 2×SSC at 70° C.
Dependencies are inferred from the claim text.