人参皂甙
枯草芽孢杆菌
化学
糖基转移酶
人参
生物化学
ATP合酶
蔗糖
酶
生物
细菌
遗传学
医学
病理
替代医学
作者
Longhai Dai,Can Liu,Jiao Li,Caixia Dong,Jiangang Yang,Zhubo Dai,Xueli Zhang,Yuanxia Sun
标识
DOI:10.1021/acs.jafc.8b00597
摘要
Ginsenosides, the major effective ingredients of Panax ginseng, exhibit various biological properties. UDP-glycosyltransferase (UGT)-mediated glycosylation is the last biosynthetic step of ginsenosides and contributes to their immense structural and functional diversity. In this study, UGT Bs-YjiC from Bacillus subtilis 168 was demonstrated to transfer a glucosyl moiety to the free C3-OH and C12-OH of protopanaxadiol (PPD) and PPD-type ginsenosides to synthesize natural and unnatural ginsenosides. In vitro assays showed that unnatural ginsenoside F12 (3- O -β- d -glucopyranosyl-12- O -β- d -glucopyranosyl-20( S )-protopanaxadiol) exhibited remarkable activity against diverse human cancer cell lines. A one-pot reaction by coupling Bs-YjiC to sucrose synthase (SuSy) was performed to regenerate UDP-glucose from sucrose and UDP. With PPD as the aglycon, an unprecedented high yield of ginsenosides F12 (3.98 g L –1 ) and Rh2 (0.20 g L –1 ) was obtained by optimizing the conversion conditions. This study provides an efficient approach for the biosynthesis of ginsenosides using a UGT-SuSy cascade reaction.
科研通智能强力驱动
Strongly Powered by AbleSci AI