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脱水双模块在反式酰基转移酶聚酮化合物生物合成中的机制:以保肝 hangtaimycin 为例的研究

The Mechanism of Dehydrating Bimodules in trans-Acyltransferase Polyketide Biosynthesis: A Showcase Study on Hepatoprotective Hangtaimycin.

机构信息

Key Laboratory of Combinatorial Biosynthesis and Drug Discovery, Ministry of Education, and School of Pharmaceutical Sciences, Wuhan University, No. 185 East Lake Road, Wuhan, 430071, People's Republic of China.

Kekulé-Institute for Organic Chemistry and Biochemistry, University of Bonn, Gerhard-Domagk-Straße 1, 53121, Bonn, Germany.

出版信息

Angew Chem Int Ed Engl. 2021 Aug 23;60(35):19139-19143. doi: 10.1002/anie.202106250. Epub 2021 Jul 28.

Abstract

A bioassay-guided fractionation led to the isolation of hangtaimycin (HTM) from Streptomyces spectabilis CCTCC M2017417 and the discovery of its hepatoprotective properties. Structure elucidation by NMR suggested the need for a structural revision. A putative HTM degradation product was also isolated and its structure was confirmed by total synthesis. The biosynthetic gene cluster was identified and resembles a hybrid trans-AT PKS/NRPS biosynthetic machinery whose first PKS enzyme contains an internal dehydrating bimodule, which is usually found split in other trans-AT PKSs. The mechanisms of such dehydrating bimodules have often been proposed, but have never been deeply investigated. Here we present in vivo mutations and in vitro enzymatic experiments that give first and detailed mechanistic insights into catalysis by dehydrating bimodules.

摘要

生物测定指导的分段分离导致了来自壮观链霉菌 CCTCC M2017417 的杭太米星(HTM)的分离和其保肝特性的发现。通过 NMR 进行的结构阐明表明需要进行结构修订。还分离出了一个假定的 HTM 降解产物,并通过全合成确定了其结构。鉴定了生物合成基因簇,并且类似于混合的跨酰基转移酶/非核糖体肽合酶生物合成机制,其第一个 PKS 酶含有内部脱水双模块,该模块通常在其他跨酰基转移酶中发现分裂。已经提出了这种脱水双模块的机制,但从未进行过深入研究。在这里,我们介绍体内突变和体外酶实验,为脱水双模块的催化作用提供了第一手和详细的机制见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8b0/8456789/3117512a00b8/ANIE-60-19139-g004.jpg

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