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糖苷酶和糖基合成酶体外合成人工多糖

In vitro synthesis of artificial polysaccharides by glycosidases and glycosynthases.

作者信息

Faijes Magda, Planas Antoni

机构信息

Laboratory of Biochemistry, Institut Químic de Sarrià, Universitat Ramon Llull, Via Augusta 390, 08017 Barcelona, Spain.

出版信息

Carbohydr Res. 2007 Sep 3;342(12-13):1581-94. doi: 10.1016/j.carres.2007.06.015. Epub 2007 Jun 16.

Abstract

Artificial polysaccharides produced by in vitro enzymatic synthesis are new biomaterials with defined structures that either mimic natural polysaccharides or have unnatural structures and functionalities. This review summarizes recent developments in the in vitro polysaccharide synthesis by endo-glycosidases, grouped in two major strategies: (a) native retaining endo-glycosidases under kinetically controlled conditions (transglycosylation with activated glycosyl donors), and (b) glycosynthases, engineered glycosidases devoid of hydrolase activity but with high transglycosylation activity. Polysaccharides are obtained by enzymatic polymerization of simple glycosyl donors by repetitive condensation. This approach not only provides a powerful methodology to produce polysaccharides with defined structures and morphologies as novel biomaterials, but is also a valuable tool to analyze the mechanisms of polymerization and packing to acquire high-order molecular assemblies.

摘要

通过体外酶促合成产生的人工多糖是具有明确结构的新型生物材料,这些结构要么模仿天然多糖,要么具有非天然的结构和功能。本综述总结了内切糖苷酶体外合成多糖的最新进展,分为两种主要策略:(a) 在动力学控制条件下的天然保留内切糖苷酶(与活化糖基供体进行转糖基化反应),以及 (b) 糖合成酶,即经过改造的缺乏水解酶活性但具有高转糖基化活性的糖苷酶。多糖是通过简单糖基供体的酶促聚合,经重复缩合反应获得的。这种方法不仅为生产具有明确结构和形态的多糖作为新型生物材料提供了一种强大的方法,也是分析聚合和堆积机制以获得高阶分子组装体的有价值工具。

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