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迭代型 I 聚酮合酶的结构酶学:催化编程的各种途径。

Structural enzymology of iterative type I polyketide synthases: various routes to catalytic programming.

机构信息

State Key Laboratory of Microbial Metabolism, Joint International Research Laboratory of Metabolic & Developmental Sciences, School of Life Science & Biotechnology, Shanghai Jiao Tong University, Shanghai, China.

出版信息

Nat Prod Rep. 2023 Sep 20;40(9):1498-1520. doi: 10.1039/d3np00015j.

Abstract

Time span of literature covered: up to mid-2023Iterative type I polyketide synthases (iPKSs) are outstanding natural chemists: megaenzymes that repeatedly utilize their catalytic domains to synthesize complex natural products with diverse bioactivities. Perhaps the most fascinating but least understood question about type I iPKSs is how they perform the iterative yet programmed reactions in which the usage of domain combinations varies during the synthetic cycle. The programmed patterns are fulfilled by multiple factors, and strongly influence the complexity of the resulting natural products. This article reviews selected reports on the structural enzymology of iPKSs, focusing on the individual domain structures followed by highlighting the representative programming activities that each domain may contribute.

摘要

涵盖的文献时间跨度

截至 2023 年年中

迭代型 I 聚酮合酶(iPKSs)是杰出的天然化学家:它们是巨型酶,可反复利用其催化结构域合成具有多种生物活性的复杂天然产物。关于 I 型 iPKSs,最令人着迷但也最不为人知的问题或许是它们如何执行迭代但又可编程的反应,在这些反应中,结构域组合的使用在合成周期中会发生变化。编程模式由多种因素决定,并强烈影响最终天然产物的复杂性。本文回顾了关于 iPKS 结构酶学的选定报告,重点介绍了各个结构域的结构,并强调了每个结构域可能做出的代表性编程活动。

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