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对细菌6-甲基水杨酸合酶的见解及其改造为用于生成多杀霉素的苔色酸合酶的研究。

Insights into bacterial 6-methylsalicylic acid synthase and its engineering to orsellinic acid synthase for spirotetronate generation.

作者信息

Ding Wei, Lei Chun, He Qingli, Zhang Qinglin, Bi Yurong, Liu Wen

机构信息

State Key Laboratory of Bioorganic and Natural Products Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China.

出版信息

Chem Biol. 2010 May 28;17(5):495-503. doi: 10.1016/j.chembiol.2010.04.009.

Abstract

The enzymes 6-methylsalicylic acid (6-MSA) synthases (6-MSASs) are involved in the building of an aryl moiety in many bioactive secondary metabolites produced by fungi and bacteria. Using the bacterial 6-MSAS ChlB1 in the biosynthesis of spirotetronate antibiotic chlorothricin (CHL) as a model, functional analysis of its dehydratase (DH) and ketoreductase (KR) domains by site-specific mutagenesis revealed that selective ketoreduction is not essential for polyketide chain extension. Promiscuity of the ketoacylsynthase domain in beta functionality recognition allows for engineering ChlB1 to an orsellinic acid (OSA) synthase (OSAS) by inactivating KR at the active site. The engineered ChlB1 is compatible with the enzymes for late-stage tailoring in CHL biosynthesis, featuring specific protein recognitions that facilitate variable aryl group incorporation. The resulting spirotetronates, which bear an OSA-derived aryl group, exhibited antibacterial activities comparable to those of the parent products.

摘要

6-甲基水杨酸(6-MSA)合酶(6-MSASs)参与真菌和细菌产生的许多生物活性次级代谢产物中芳基部分的构建。以细菌6-MSAS ChlB1在螺环四醇类抗生素绿硫菌素(CHL)生物合成中的应用为模型,通过定点诱变对其脱水酶(DH)和酮还原酶(KR)结构域进行功能分析,结果表明选择性酮还原对于聚酮链延伸并非必不可少。酮酰基合酶结构域在β-功能识别中的混杂性使得通过在活性位点使KR失活,可将ChlB1工程改造为苔色酸(OSA)合酶(OSAS)。工程改造后的ChlB1与CHL生物合成后期修饰所需的酶兼容,具有促进可变芳基掺入的特异性蛋白质识别功能。所得带有OSA衍生芳基的螺环四醇类化合物表现出与母体产物相当的抗菌活性。

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