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本文引用的文献

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One-pot multienzyme (OPME) systems for chemoenzymatic synthesis of carbohydrates.用于碳水化合物化学酶法合成的一锅多酶(OPME)系统。
Org Biomol Chem. 2016 Mar 14;14(10):2809-18. doi: 10.1039/c6ob00058d.
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One-pot multienzyme synthesis of Lewis x and sialyl Lewis x antigens.Lewis x和唾液酸化Lewis x抗原的一锅多酶合成。
Curr Protoc Chem Biol. 2012 Sep 1;4:233-247. doi: 10.1002/9780470559277.ch110277.
3
Stereoselective synthesis of a sulfated tetrasaccharide corresponding to a rare sequence in the galactofucan isolated from Sargassum polycystum.对来源于半叶马尾藻的半乳岩藻聚糖中稀有序列的四糖硫酸盐进行立体选择性合成。
J Org Chem. 2014 May 16;79(10):4718-26. doi: 10.1021/jo500503r. Epub 2014 May 2.
4
A chemoenzymatic total synthesis of the neurogenic starfish ganglioside LLG-3 using an engineered and evolved synthase.采用工程化和进化的合酶对神经源性海星神经节苷脂 LLG-3 进行的化学酶法全合成。
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A sialyltransferase mutant with decreased donor hydrolysis and reduced sialidase activities for directly sialylating LewisX.一种唾液酸转移酶突变体,其供体水解活性降低,唾液酸酶活性降低,可直接唾液酸化 LewisX。
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Efficiently synthesizing lacto-ganglio-series gangliosides by using a glucosyl ceramide cassette approach: the total synthesis of ganglioside X2.通过使用葡萄糖神经酰胺盒式方法高效合成乳酰神经节苷脂系列神经节苷脂:神经节苷脂 X2 的全合成。
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PmST3 from Pasteurella multocida encoded by Pm1174 gene is a monofunctional α2-3-sialyltransferase.多杀巴斯德氏菌的 PmST3 由 Pm1174 基因编码,是一种单功能的α2-3-唾液酸转移酶。
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Glycosphingolipid synthesis employing a combination of recombinant glycosyltransferases and an endoglycoceramidase glycosynthase.利用重组糖苷转移酶和内切糖苷神经酰胺合成酶进行糖脂合成。
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Substrate promiscuity of N-acetylhexosamine 1-kinases.N-乙酰己糖胺 1-激酶的底物混杂性。
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PmST2: a novel Pasteurella multocida glycolipid α2-3-sialyltransferase.PmST2:一种新型多杀巴斯德氏菌糖脂 α2-3-唾液酸转移酶。
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一种用于合成糖鞘脂的通用化学酶促策略。

A General Chemoenzymatic Strategy for the Synthesis of Glycosphingolipids.

作者信息

Liu Yunpeng, Wen Liuqing, Li Lei, Gadi Madhusudhan Reddy, Guan Wanyi, Huang Kenneth, Xiao Zhongying, Wei Mohui, Ma Cheng, Zhang Qing, Yu Hai, Chen Xi, Wang Peng George, Fang Junqiang

机构信息

National Glycoengineering Research Center, Shandong Provincial Key Lab of Carbohydrate Chemistry, and State Key Lab of Microbial Technology, Shandong University, Jinan, Shandong 250100, People's Republic of China.

Department of Chemistry, Georgia State University, Atlanta, Georgia 30303, USA, http://lithium.gsu.edu/faculty/PWang/.

出版信息

European J Org Chem. 2016 Sep;2016(25):4315-4320. doi: 10.1002/ejoc.201600950. Epub 2016 Aug 16.

DOI:10.1002/ejoc.201600950
PMID:28824290
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5560440/
Abstract

A concise, prototypical, and stereoselective strategy for the synthesis of therapeutically and immunologically significant glycosphingolipids has been developed. This strategy provides a universal platform for glycosphingolipid synthesis by block coupling of enzymatically prepared free oligosaccharideglycans to lipids using glycosyl -phenyltrifluoroacetimidates as efficient activated intermediates. As demonstrated here, two different types of glycosphingolipids were obtained in excellent yields using the method.

摘要

已经开发出一种简洁、典型且立体选择性的策略来合成具有治疗和免疫意义的糖鞘脂。该策略通过使用糖基-苯基三氟乙酰亚胺酯作为高效活化中间体,将酶促制备的游离寡糖聚糖与脂质进行片段偶联,为糖鞘脂合成提供了一个通用平台。如此处所示,使用该方法以优异的产率获得了两种不同类型的糖鞘脂。

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