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模块化聚酮合酶进行流水线式合成的酶学

Enzymology of assembly line synthesis by modular polyketide synthases.

作者信息

Grininger Martin

机构信息

Institute of Organic Chemistry and Chemical Biology, Buchmann Institute for Molecular Life Sciences, Goethe University Frankfurt, Frankfurt am Main, Germany.

出版信息

Nat Chem Biol. 2023 Apr;19(4):401-415. doi: 10.1038/s41589-023-01277-7. Epub 2023 Mar 13.

Abstract

Modular polyketide synthases (PKSs) run catalytic reactions over dozens of steps in a highly orchestrated manner. To accomplish this synthetic feat, they form megadalton multienzyme complexes that are among the most intricate proteins on earth. Polyketide products are of elaborate chemistry with molecular weights of usually several hundred daltons and include clinically important drugs such as erythromycin (antibiotic), rapamycin (immunosuppressant) and epothilone (anticancer drug). The term 'modular' refers to a hierarchical structuring of modules and domains within an overall assembly line arrangement, in which PKS organization is colinearly translated into the polyketide structure. New structural information obtained during the past few years provides substantial direct insight into the orchestration of catalytic events within a PKS module and leads to plausible models for synthetic progress along assembly lines. In light of these structural insights, the PKS engineering field is poised to enter a new era of engineering.

摘要

模块化聚酮合酶(PKSs)以高度协调的方式进行数十步催化反应。为了实现这一合成壮举,它们形成了兆道尔顿多酶复合物,这些复合物是地球上最复杂的蛋白质之一。聚酮化合物产物具有复杂的化学结构,分子量通常为几百道尔顿,包括临床上重要的药物,如红霉素(抗生素)、雷帕霉素(免疫抑制剂)和埃博霉素(抗癌药物)。“模块化”一词指的是在整体装配线排列中模块和结构域的层次结构,其中PKS组织按线性方式转化为聚酮化合物结构。在过去几年中获得的新结构信息为深入了解PKS模块内催化事件的协调提供了大量直接见解,并为沿着装配线的合成过程提供了合理的模型。鉴于这些结构见解,PKS工程领域即将进入一个新的工程时代。

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