Publication:
Transglucosylation of tertiary alcohols using cassava β-glucosidase

dc.contributor.authorJisnuson Svastien_US
dc.contributor.authorThanawat Phongsaken_US
dc.contributor.authorRakrudee Sarnthimaen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-07-24T03:19:42Z
dc.date.available2018-07-24T03:19:42Z
dc.date.issued2003-06-06en_US
dc.description.abstractWe have compared the ability of β-glucosidases from cassava, Thai rosewood, and almond to synthesize alkyl glucosides by transglucosylating alkyl alcohols of chain length C1-C8. Cassava linamarase shows greater ability to transfer glucose from p-nitrophenyl-β-glucoside to secondary alcohol acceptors than other β-glucosidases, and is unique in being able to synthesize C4, C5, and C6tertiary alkyl β-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. © 2003 Elsevier Science (USA). All rights reserved.en_US
dc.identifier.citationBiochemical and Biophysical Research Communications. Vol.305, No.3 (2003), 470-475en_US
dc.identifier.doi10.1016/S0006-291X(03)00793-9en_US
dc.identifier.issn0006291Xen_US
dc.identifier.other2-s2.0-0037902560en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/20719
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0037902560&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.titleTransglucosylation of tertiary alcohols using cassava β-glucosidaseen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0037902560&origin=inwarden_US

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