| Literature DB >> 16098548 |
Phimonphan Chuankhayan1, Yanling Hua, Jisnuson Svasti, Santi Sakdarat, Patrick A Sullivan, James R Ketudat Cairns.
Abstract
A beta-glycosidase was purified from the seeds of Dalbergia nigescens Kurz based on its ability to hydrolyse p-nitrophenyl beta-glucoside and beta-fucoside. This enzyme did not hydrolyze various glycosidic substrates efficiently, so it was used to identify its own natural substrates. Two substrates were identified, isolated and their structures determined as: compound 1, dalpatein 7-O-beta-D-apiofuranosyl-(1-->6)-beta-D-glucopyranoside and compound 2, 6,2',4',5'-tetramethoxy-7-hydroxy-7-O-beta-D-apiofuranosyl-(1-->6)-beta-D-glucopyranoside (dalnigrein7-O-beta-D-apiofuranosyl-(1-->6)-beta-D-glucopyranoside). The beta-glycosidase removes the sugar from these glycosides as a disaccharide, despite its initial identification as a beta-glucosidase and beta-fucosidase.Entities:
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Year: 2005 PMID: 16098548 DOI: 10.1016/j.phytochem.2005.06.024
Source DB: PubMed Journal: Phytochemistry ISSN: 0031-9422 Impact factor: 4.072