Design, Synthesis and Bioactivity of Core 1 O-glycan and its Derivative on Human Gut Microbiota

被引:0
|
作者
Qu, Huanhuan [1 ]
Li, Baixue [2 ]
Yang, Jingyi [3 ]
Liang, Huaiwen [3 ]
Li, Meixia [1 ]
Ding, Kan [1 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Mat Med, Glycochem & Glycobiol Lab, Key Lab Receptor Res, 555 Zu Chong Zhi Rd, Shanghai 201203, Peoples R China
[2] Chengdu Univ Tradit Chinese Med, Dept Basic Mediclal Sci, Chengdu 610075, Sichuan, Peoples R China
[3] Shanghai Univ Tradit Chinese Med, Dept Pharm, Shanghai 201203, Peoples R China
基金
上海市科技启明星计划; 中国国家自然科学基金;
关键词
Bioactivity; core; 1; derivative; human gut microbiota; O-glycan; synthesis; CHEMOENZYMATIC SYNTHESIS; SUPPLEMENTATION; DIGESTIBILITY; PERFORMANCE; ANTIGEN;
D O I
10.2174/1570180816666181218143207
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Background: Disaccharide core 1 (Gal beta 1-3GalNAc) is a common O-glycan structure in nature. Biochemical studies have confirmed that the formation of the core 1 structure is an important initial step in O-glycan biosynthesis and it is of great importance for human body. Objective: Our study will provide meaningful and useful sights for O-glycan synthesis and their bioassay. And all the synthetic glycosides would be used as intermediate building blocks in the scheme developed for oligosaccharide construction. Methods: In this article, we firstly used chemical procedures to prepare core 1 and its derivative, and a novel disaccharide was efficiently synthesized. The structures of the synthesized compounds were elucidated and confirmed by H-1 NMR, C-13 NMR and MS. Then we employed three human gut symbionts belonging to Bacteroidetes, a predominantphyla in the distal gut, as models to study the bioactivity of core 1 and its derivative on human gut microbiota. Results: According to our results, both core 1 and derivative could support the growth of B. fragilis, especially the core 1 derivative, while failed to support the growth of B. thetaiotaomicron and B. ovatus. Conclusion: This suggested that the B. fragilis might have the specificity glycohydrolase to cut the glycosidic bond for acquiring monosaccharide.
引用
收藏
页码:1348 / 1353
页数:6
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