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使用重组β-甘露糖基转移酶进行N-连接寡糖核心三糖的化学酶法合成。

The chemoenzymatic synthesis of the core trisaccharide of N-linked oligosaccharides using a recombinant beta-mannosyltransferase.

作者信息

Watt G M, Revers L, Webberley M C, Wilson I B, Flitsch S L

机构信息

Edinburgh Centre for Protein Technology, Department of Chemistry, University of Edinburgh, UK.

出版信息

Carbohydr Res. 1997 Dec;305(3-4):533-41. doi: 10.1016/s0008-6215(97)00261-9.

Abstract

The chemical synthesis of the beta-mannosyl linkage of N-glycans has presented a great challenge to synthetic carbohydrate chemists. We have therefore investigated the application of beta-mannosyltransferases to the preparative synthesis N-linked core oligosaccharides. In this paper we report the chemoenzymatic synthesis of beta-D-mannopyranosyl-(1-->4)-2-acetamido-2-deoxy-beta-D-glucopyranosyl- (1-->4)-2-acetamido-2-deoxy-alpha-D-glucopyranose on a preparative scale using a phytanyl-linked acceptor in the presence of a recombinant beta-(1-->4)-mannosyltransferase.

摘要

N-聚糖中β-甘露糖基连接的化学合成对合成碳水化合物化学家来说是一个巨大的挑战。因此,我们研究了β-甘露糖基转移酶在制备合成N-连接核心寡糖中的应用。在本文中,我们报道了在重组β-(1→4)-甘露糖基转移酶存在下,使用植烷基连接的受体在制备规模上化学酶促合成β-D-甘露吡喃糖基-(1→4)-2-乙酰氨基-2-脱氧-β-D-葡萄糖吡喃糖基-(1→4)-2-乙酰氨基-2-脱氧-α-D-葡萄糖吡喃糖。

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