Enzymic production of neoagarobiose
The present invention is directed to methods and systems of producing neoagarobiose, useful in whitening melanoma cells and in cosmetics, using polypeptides having neoagarobiosebiohydralase activity, including Aga86E from Saccharophagus degradans . The reaction can be enhanced by including other agarases, including Aga16B, also from S. degradans.
1. A method of producing neoagarobiose, comprising:
(a) providing a substrate selected from the group consisting of agar, agarose, neoagarotetraose, agarooligosaccharides, and derivatives thereof;
(b) contacting the substrate with a Saccharophagus degradans glycoside hydrolase (GH) polypeptide having at least 80% sequence identity with the amino acid sequence of SEQ ID NO:9, wherein the Saccharophagus degradans glycoside hydrolase (GH) polypeptide has exo-acting β-agarase activity, thereby creating a reaction mix; and
(c) incubating the reaction mix under suitable conditions and sufficient time to produce neoagarobiose from the substrate.
2. The method of claim 1 , wherein the polypeptide comprises the amino acid sequence of SEQ ID NO:9.
3. The method of claim 1 , wherein the polypeptide consists of the amino acid sequence of SEQ ID NO:9.
4. The method of claim 1 , further comprising contacting the substrate with at least one carbohydrate binding module polypeptide having at least 80% sequence identity with an amino acid sequence selected from the group consisting of SEQ ID NOs:5, 6 and 7.
5. The method of claim 4 , wherein the at least one carbohydrate binding module polypeptide has at least 90% sequence identity with the amino acid sequence selected from the group consisting of SEQ ID NOs:5, 6 and 7.
6. The method of claim 4 , wherein the at least one carbohydrate binding module polypeptide is selected from the group consisting of SEQ ID NOs:5, 6 and 7.
7. The method of claim 4 , wherein the substrate is contacted with a carbohydrate binding module of SEQ ID NO:5, a carbohydrate binding module of SEQ ID NO:6, and a carbohydrate binding module of SEQ ID NO:7.
8. The method of claim 1 , further comprising contacting the substrate with a second polypeptide comprising an amino acid sequence having at least 80% sequence identity with an amino acid sequence of SEQ ID NO:12.
9. The method of claim 8 , wherein the second polypeptide comprises an amino acid sequence having at least 90% sequence identity with the amino acid sequence of SEQ ID NO:12.
10. The method of claim 8 , wherein the second polypeptide comprises an amino acid sequence of SEQ ID NO:12.
11. The method of claim 8 , wherein the substrate is first contacted with the second polypeptide.
12. The method of claim 8 , further comprising contacting the substrate with at least one carbohydrate binding module polypeptide having at least 80% sequence identity with an amino acid sequence of SEQ ID NO:10 or 11.
13. The method of claim 8 , further comprising contacting the substrate with at least one carbohydrate binding module polypeptide having at least 90% sequence identity with an amino acid sequence of SEQ ID NO:10 or 11.
14. The method of claim 8 , further comprising contacting the substrate with at least one carbohydrate binding module polypeptide comprising an amino acid sequence of SEQ ID NO:10 or 11.
15. A method of producing neoagarobiose, comprising:
(a) providing a substrate selected from the group consisting of agar, agarose, neoagarotetraose, agarooligosaccharides, and derivatives thereof;
(b) contacting the substrate with a Saccharophagus degradans polypeptide having at least 90% sequence identity with the amino acid sequence of SEQ ID NO:9, wherein the Saccharophagus degradans polypeptide has exo-acting β-agarose activity, thereby creating a reaction mix; and
(c) incubating the reaction mix under suitable conditions and sufficient time to produce neoagarobiose from the substrate.