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β-内酰胺蛋白酶体抑制剂贝拉美素和胱天蛋白酶的生物合成。

Biosynthesis of the β-Lactone Proteasome Inhibitors Belactosin and Cystargolide.

机构信息

Department of Pharmaceutical Biology, Pharmaceutical Institute, University of Tuebingen, 72076, Tuebingen, Germany.

German Centre for Infection Research (DZIF), partner site Tuebingen, 72076, Tuebingen, Germany.

出版信息

Angew Chem Int Ed Engl. 2017 Jun 1;56(23):6665-6668. doi: 10.1002/anie.201612076. Epub 2017 Apr 28.

Abstract

Belactosins and cystargolides are natural product proteasome inhibitors from Actinobacteria. Both feature dipeptidic backbones and a unique β-lactone building block. Herein, we present a detailed investigation of their biosynthesis. Identification and analysis of the corresponding gene clusters indicated that both compounds are assembled by rare single-enzyme amino acid ligases. Feeding experiments with isotope-labeled precursors and in vitro biochemistry showed that the formation of the β-lactone warhead is unprecedented and reminiscent of leucine biosynthesis, and that it involves the action of isopropylmalate synthase homologues.

摘要

贝拉唑素和胱硫醚内酯是放线菌来源的天然产物蛋白酶体抑制剂。两者均具有二肽骨架和独特的β-内酰胺结构单元。本文详细研究了它们的生物合成。通过对相应基因簇的鉴定和分析,表明这两种化合物都是由罕见的单酶氨基酸连接酶组装而成。利用同位素标记前体的饲喂实验和体外生物化学实验表明,β-内酰胺弹头的形成是前所未有的,类似于亮氨酸生物合成,并且涉及异丙基苹果酸合酶同系物的作用。

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