Mutant xylanase, manufacturing method and use therefor, and method for manufacturing saccharified lignocellulose

Patent metadata

Field	Value
Publication number	US-9567617-B2
Application number	US-201615042395-A
Country	US
Kind code	B2
Filing date	Feb 12, 2016
Priority date	Nov 25, 2011
Publication date	Feb 14, 2017
Grant date	Feb 14, 2017

Abstract

What is aimed at is provision of an inexpensive and efficient saccharification method for lignocellulose using a thermostable xylanase and provision of a mutant xylanase that has a substitute amino acid residue, and that exhibits stable activity even under severe conditions in which enzymes easily inactivate, and that provides an initial rate of reaction not significantly reduced as compared to a wild-type xylanase corresponding to the mutant xylanase. Provided is a method of producing a saccharified product of lignocellulose, including contacting a lignocellulosic raw material with a thermostable xylanase, and a mutant xylanase that provides an initial rate of reaction that is at least 70% of that provided by a wild-type xylanase corresponding thereto, that has a xylanase activity after heat treatment at 50° C. for 24 hours that is at least 50% of its xylanase activity before the heat treatment, and that has a substitute amino acid residue.

First claim

The invention claimed is:

1. A nucleic acid encoding a mutant xylanase, the mutant xylanase comprising the following amino acid residues substitutions in the amino acid sequence of SEQ ID NO: 1:
a leucine residue substituted for an asparagine residue at position 29;
an arginine residue substituted for a lysine residue at position 58;
an amino acid residue, other than a tyrosine residue, substituted for a tyrosine residue at position 27; and
an amino acid residue, other than an asparagine residue, substituted for an asparagine residue at position 44, or
the mutant xylanase comprising 1 to 10 amino acid residues substitution in the amino acid sequence of SEQ ID NO: 1 in addition of the following amino acid residues substitutions:
a leucine residue substituted for an asparagine residue at position 29,
an arginine residue substituted for a lysine residue at position 58,
a phenylalanine residue substituted for a tyrosine residue at position 27, and
a serine residue substituted for an asparagine residue at position 44.

2. The nucleic acid according to claim 1 , wherein the amino acid residue, other than a tyrosine residue, substituted for the tyrosine residue at position 27 in the amino acid sequence of SEQ ID NO: 1 is a phenylalanine residue, and the amino acid residue, other than an asparagine residue, substituted for an asparagine residue at position 44 in the amino acid sequence of SEQ ID NO: 1 is a serine residue.

3. An expression vector comprising the nucleic acid according to claim 1 .

4. A transformant comprising the expression vector according to claim 3 .

5. The transformant according to claim 4 , wherein a host cell of the transformant is a cell obtained from Escherichia coli, Bacillus subtilis , yeast, an actinomycete, or a filamentous fungus.

6. The transformant according to claim 5 , wherein the filamentous fungus belongs to the genus Trichoderma , the genus Acremonium , the genus Humicola , or the genus Aspergillus.

7. The transformant according to claim 5 , wherein the filamentous fungus is Trichoderma viride, Acremonium cellulolyticus, Humicola insolens , or Aspergillus niger.

8. A method of producing a mutant xylanase, the method comprising culturing the transformant according to claim 4 and recovering the mutant xylanase from at least one of the cultured transformant or a culture product of the transformant.

Assignees

• Mitsui Chemicals Inc
• Meiji Seika Pharma Co Ltd

Inventors

• Yanai Hisaaki
• Tamai Hiroki
• Osabe Masami
• Yokoyama Fumikazu
• Okakura Kaoru
• Inoue Atsushi

Classifications

• Y02E50/10

  Biofuels, e.g. bio-diesel · CPC title

• C11D3/38636

  containing enzymes other than protease, amylase, lipase, cellulase, oxidase or reductase · CPC title

• C12Y302/01004

  Cellulase (3.2.1.4), i.e. endo-1,4-beta-glucanase · CPC title

• C12P19/02 Primary

  Monosaccharides (2-ketogulonic acid C12P7/60) · CPC title

• C12P19/14 Primary

  produced by the action of a carbohydrase {(EC 3.2.x)}, e.g. by alpha-amylase {, e.g. by cellulase, hemicellulase} · CPC title