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理性聚酮合酶设计的工程策略。

Engineering strategies for rational polyketide synthase design.

机构信息

Institute of Organic Chemistry and Chemical Biology, Buchmann Institute for Molecular Life Sciences, Cluster of Excellence for Macromolecular Complexes, Goethe University Frankfurt, Max-von-Laue-Str. 15, 60438 Frankfurt am Main, Germany.

出版信息

Nat Prod Rep. 2018 Oct 17;35(10):1070-1081. doi: 10.1039/c8np00030a.

Abstract

Covering: mid 1990s to 2018 Over the last two decades, diverse approaches have been explored to generate new polyketides by engineering polyketide synthases (PKSs). Although it has been proven possible to produce new compounds by designed PKSs, engineering strategies failed to make polyketides available via widely applicable rules and protocols. Still, organic synthetic routes have to be employed whenever new polyketides are needed for applications in medicine, agriculture, and industry. In light of the rising demand for commodity products from feedstock and for fast and cheap access to pharmaceutical compounds, the need for harnessing PKSs to produce such molecules is more urgent than ever before. In this review, we focus on a multitude of approaches to engineer modular PKSs by swapping and replacing PKS modules and domains, which we analyze in the light of recent structural and biochemical data. We conclude with an outlook on possible strategies on how to increase success rates of PKS engineering in future.

摘要

涵盖年代

20 世纪 90 年代中期至 2018 年 在过去的二十年中,人们探索了多种方法来通过工程化聚酮合酶(PKSs)来产生新的聚酮化合物。虽然已经证明可以通过设计的 PKS 产生新的化合物,但工程化策略未能通过广泛适用的规则和协议来使聚酮化合物可用。不过,每当需要新的聚酮化合物用于医学、农业和工业等领域的应用时,仍需要采用有机合成路线。鉴于对来自原料的商品产品的需求不断增长,以及对快速廉价获得药物化合物的需求,利用 PKS 来生产此类分子的需求比以往任何时候都更加迫切。在这篇综述中,我们专注于通过交换和替换 PKS 模块和结构域来工程化模块化 PKS 的多种方法,并根据最近的结构和生化数据对其进行分析。我们最后展望了未来如何提高 PKS 工程化成功率的可能策略。

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