| Literature DB >> 27305319 |
Zhongying Xiao1, Yuxi Guo1, Yunpeng Liu1, Lei Li1, Qing Zhang1, Liuqing Wen1, Xuan Wang1, Shukkoor Muhammed Kondengaden1, Zhigang Wu1, Jun Zhou1, Xuefeng Cao1, Xu Li1, Cheng Ma1, Peng George Wang1.
Abstract
Human milk oligosaccharides (HMOs) are a family of diverse unconjugated glycans that exist in human milk as one of the major components. Characterization, quantification, and biofunctional studies of HMOs remain a great challenge due to their diversity and complexity. The accessibility of a homogeneous HMO library is essential to solve these issues which have beset academia for several decades. In this study, an efficient chemoenzymatic strategy, namely core synthesis/enzymatic extension (CSEE), for rapid production of diverse HMOs was reported. On the basis of 3 versatile building blocks, 3 core structures were chemically synthesized via consistent use of oligosaccharyl thioether and oligosaccharyl bromide as glycosylation donors in a convergent fragment coupling strategy. Each of these core structures was then extended to up to 11 HMOs by 4 robust glycosyltransferases. A library of 31 HMOs were chemoenzymatically synthesized and characterized by MS and NMR. CSEE indeed provides a practical approach to harvest structurally defined HMOs for various applications.Entities:
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Year: 2016 PMID: 27305319 PMCID: PMC5953189 DOI: 10.1021/acs.joc.6b00478
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354