| Literature DB >> 25124522 |
Bingyang Sun1, Wenzheng Bao2, Xiaobo Tian3, Mingjing Li2, Hong Liu3, Jinhua Dong4, Wei Huang5.
Abstract
Heterogeneity of glycan structures in native glycoconjugates always hampers precise studies on carbohydrate-involved biological functions. To construct homogeneous glycoconjugates from natural resource of homogeneous glycans is therefore a practical approach to solve this problem. We report here an optimized procedure for gram-scale production of sialylglycopeptide (SGP) containing a disialyl biantennary complex-type N-glycan from egg yolks. Our new procedure simplified the extraction process by treating the egg yolk powder with 40% acetone, avoiding massive emulsification, high-speed centrifugation, and sophisticated chromatography in reported methods. Subsequent semi-synthesis of the N-glycan core Man3GlcNAc oxazoline from SGP was accomplished for the first-time via glyco-trimming and successive oxazoline formation. This efficient semi-synthesis provides an alternative to the pure chemical approach that involves multi-step total synthesis and facilitates the application of endo-glycosidase-enabled chemoenzymatic synthesis of various homogeneous glycoconjugates.Entities:
Keywords: Chemoenzymatic transglycosylation; Egg yolk; Man3GlcNAc oxazoline; Sialylglycopeptide
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Year: 2014 PMID: 25124522 DOI: 10.1016/j.carres.2014.07.013
Source DB: PubMed Journal: Carbohydr Res ISSN: 0008-6215 Impact factor: 2.104