Thermophilic and thermoacidophilic biopolymer-degrading genes and enzymes from
Isolated and/or purified polypeptides and nucleic acid sequences encoding polypeptides from Alicyclobacillus acidocaldarius are provided. Further provided are methods of at least partially degrading, cleaving, or removing polysaccharides, lignocellulose, cellulose, hemicellulose, lignin, starch, chitin, polyhydroxybutyrate, heteroxylans, glycosides, xylan-, glucan-, galactan-, or mannan-decorating groups using isolated and/or purified polypeptides and nucleic acid sequences encoding polypeptides from Alicyclobacillus acidocaldarius.
1. A method of at least partially degrading, cleaving, or removing polysaccharides, lignocellulose, cellulose, hemicellulose, lignin, starch, chitin, polyhydroxybutyrate, heteroxylans, glycosides, xylan-, glucan-, galactan, or mannan-decorating groups, the method comprising:
placing a polypeptide at least 93% sequence identity to SEQ ID No. 462 in fluid contact with a polysaccharide, lignocellulose, cellulose, hemicellulose, lignin, starch, chitin, polyhydroxybutyrate, heteroxylans, glycoside, xylan-, glucan-, galactan, or mannan-decorating group;
wherein the polypeptide has an enzymatic activity as an Endo-beta-1,4-mannanase.
2. The method according to claim 1 , wherein placing a polypeptide at least 93% sequence identity to SEQ ID No. 462 in fluid contact with a polysaccharide, lignocellulose, cellulose, hemicellulose, lignin, starch, chitin, polyhydroxybutyrate, heteroxylans, glycoside, xylan-, glucan-, galactan, or mannan-decorating group occurs at or below about pH 4.
3. The method according to claim 1 , wherein placing a polypeptide having at least 93% sequence identity to SEQ ID No. 462 in fluid contact with a polysaccharide, lignocellulose, cellulose, hemicellulose, lignin, starch, chitin, polyhydroxybutyrate, heteroxylans, glycoside, xylan-, glucan-, galactan, or mannan-decorating group occurs at a temperature at or above 50 degrees Celsius.
4. The method according to claim 1 , wherein the polypeptide is glycosylated, pegylated, or otherwise posttranslationally modified.
5. The method according to claim 1 , wherein the polypeptide is encoded by a nucleic acid having at least 90% identity to SEQ ID NO:461.
6. The method according to claim 1 , wherein placing a polypeptide having at least 93% sequence identity to SEQ ID NO:462 in fluid contact with a polysaccharide, lignocellulose, cellulose, hemicellulose, lignin, starch, chitin, polyhydroxybutyrate, heteroxylans, glycoside, xylan-, glucan-, galactan, or mannan-decorating group comprises translating a nucleic acid having at least 90% identity to SEQ ID NO:461 in fluid contact with the polysaccharide, lignocellulose, cellulose, hemicellulose, lignin, starch, chitin, polyhydroxybutyrate, heteroxylans, glycoside, xylan-, glucan-, galactan, or mannan-decorating group.