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基于细胞的糖胺聚糖合成酶高通量筛选方法:开发与应用。

Cell-Based Assay Approaches for Glycosaminoglycan Synthase High-Throughput Screening: Development and Applications.

机构信息

Key Laboratory of Chemical Biology (Ministry of Education), School of Pharmaceutical Sciences, Cheeloo College of Medicine, Shandong University, Jinan 250012, Shandong, China.

NMPA Key Laboratory for Quality Research and Evaluation of Carbohydrate-Based Medicine, National Glycoengineering Research Center, Shandong University, Jinan 250012, Shandong, China.

出版信息

ACS Chem Biol. 2023 Jul 21;18(7):1632-1641. doi: 10.1021/acschembio.3c00244. Epub 2023 Jul 10.

Abstract

Glycosaminoglycan synthases have immense potential in applications involving synthesis of oligosaccharides, using enzymatic approaches and construction of cell factories that produce polysaccharides as critical metabolic components. However, the use of high-throughput activity assays to screen for the evolution of these enzymes can be challenging because there are no significant changes in fluorescence or absorbance associated with glycosidic bond formation. Here, using incorporation of azido-labeled -acetylhexosamine analogs into bacterial capsule polysaccharides via bacterial metabolism and bioorthogonal chemistry, fluorophores were specifically introduced onto cell surfaces. Furthermore, correlations between detectable fluorescence signals and the polysaccharide-synthesizing capacity of individual bacteria were established. Among 10 candidate genes, 6 members of the chondroitin synthase family were quickly identified in a recombinant host strain. Additionally, directed evolution of heparosan synthase was successfully performed using fluorescence-activated cell sorting of recombinant O10:K5(L):H4, yielding several mutants with increased activity. Cell-based approaches that selectively detect the presence or absence of synthases within an individual colony of bacterial cells, as well as their level of activity, have broad potential in the exploration and engineering of glycosaminoglycan synthases. These approaches also support the creation of novel strategies for high-throughput screening of enzyme activity based on cell systems.

摘要

糖胺聚糖合成酶在涉及使用酶法合成寡糖和构建产生多糖作为关键代谢成分的细胞工厂的应用中具有巨大的潜力。然而,由于糖苷键形成与荧光或吸光度没有显著变化,因此使用高通量活性测定来筛选这些酶的进化可能具有挑战性。在这里,通过细菌代谢和生物正交化学,将叠氮标记的乙酰己糖胺类似物掺入细菌荚膜多糖中,从而在细胞表面特异性引入荧光团。此外,建立了可检测荧光信号与单个细菌合成多糖能力之间的相关性。在 10 个候选基因中,6 种软骨素合成酶家族成员在重组 宿主菌株中迅速被鉴定出来。此外,使用荧光激活细胞分选对肝素聚糖合成酶进行了定向进化,得到了几个活性增加的突变体。基于细胞的方法可以选择性地检测单个细菌细胞菌落中合成酶的存在与否及其活性水平,在探索和工程糖胺聚糖合成酶方面具有广泛的潜力。这些方法还支持基于细胞系统的酶活性高通量筛选的新策略的创建。

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