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Title: Transglucosylation of tertiary alcohols using cassava beta-glucosidase. Author: Svasti J, Phongsak T, Sarnthima R. Journal: Biochem Biophys Res Commun; 2003 Jun 06; 305(3):470-5. PubMed ID: 12763016. Abstract: We have compared the ability of beta-glucosidases from cassava, Thai rosewood, and almond to synthesize alkyl glucosides by transglucosylating alkyl alcohols of chain length C(1)-C(8). Cassava linamarase shows greater ability to transfer glucose from p-nitrophenyl-beta-glucoside to secondary alcohol acceptors than other beta-glucosidases, and is unique in being able to synthesize C(4), C(5), and C(6) tertiary alkyl beta-glucosides with high yields of 94%, 82%, and 56%, respectively. Yields of alkyl glucosides could be optimized by selecting appropriate enzyme concentrations and incubation times. Cassava linamarase required pNP-glycosides as donors and could not use mono- or di-saccharides as sugar donors in alkyl glucoside synthesis.[Abstract] [Full Text] [Related] [New Search]