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利用叠氮糖进行糖基合成酶的高通量筛选用于寡糖合成。

High-throughput screening of glycosynthases using azido sugars for oligosaccharides synthesis.

机构信息

Department of Chemical and Biochemical Engineering, Rutgers, The State University of New Jersey, Piscataway, NJ, United States.

Department of Chemical and Biochemical Engineering, Rutgers, The State University of New Jersey, Piscataway, NJ, United States.

出版信息

Methods Enzymol. 2023;682:211-245. doi: 10.1016/bs.mie.2022.12.002. Epub 2023 Jan 20.

DOI:10.1016/bs.mie.2022.12.002
PMID:36948703
Abstract

Glycosynthases are mutant glycosyl hydrolases that can synthesize glycosidic bonds between acceptor glycone/aglycone groups and activated donor sugars with suitable leaving groups (e.g., azido, fluoro). However, it has been challenging to rapidly detect glycosynthase reaction products involving azido sugars as donor sugars. This has limited our ability to apply rational engineering and directed evolution methods to rapidly screen for improved glycosynthases that are capable of synthesizing bespoke glycans. Here, we outline our recently developed screening methodologies for rapidly detecting glycosynthase activity using a model fucosynthase enzyme engineered to be active on fucosyl azide as donor sugar. We created a diverse library of fucosynthase mutants using semi-random and random error prone mutagenesis and then identified improved fucosynthase mutants with desired activity using two distinct screening methods developed by our group to detect glycosynthase activity (i.e., by detecting azide formed upon completion of fucosynthase reaction); (a) pCyn-GFP regulon method, and (b) Click chemistry method. Finally, we provide some proof-of-concept results illustrating the utility of both these screening methods to rapidly detect products of glycosynthase reactions involving azido sugars as donor groups.

摘要

糖基合成酶是突变的糖基水解酶,能够在具有合适离去基团(如叠氮基、氟基)的受体糖/糖苷基团和活化供体糖之间合成糖苷键。然而,快速检测涉及叠氮基糖作为供体糖的糖基合成酶反应产物一直具有挑战性。这限制了我们应用合理的工程和定向进化方法来快速筛选能够合成定制聚糖的改良糖基合成酶的能力。在这里,我们概述了我们最近开发的筛选方法,用于使用经过工程改造以具有活性的岩藻糖基叠氮化物作为供体糖的模型岩藻糖合酶来快速检测糖基合成酶活性。我们使用半随机和随机易错诱变创建了岩藻糖合酶突变体的多样性文库,然后使用我们小组开发的两种不同的筛选方法来鉴定具有所需活性的改良岩藻糖合酶突变体,以检测糖基合成酶活性(即在岩藻糖合酶反应完成后检测形成的叠氮化物):(a)pCyn-GFP 调控子方法,和(b)点击化学方法。最后,我们提供了一些概念验证结果,说明这两种筛选方法在快速检测涉及叠氮基糖作为供体基团的糖基合成酶反应产物方面的实用性。

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