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重新审视模块化聚酮合酶的模块性

Revisiting the modularity of modular polyketide synthases.

作者信息

Khosla Chaitan, Kapur Shiven, Cane David E

机构信息

Department of Chemistry, Stanford University, Stanford, CA 94305-5080, USA.

出版信息

Curr Opin Chem Biol. 2009 Apr;13(2):135-43. doi: 10.1016/j.cbpa.2008.12.018. Epub 2009 Feb 11.

Abstract

Modularity is a highly sought after feature in engineering design. A modular catalyst is a multi-component system whose parts can be predictably interchanged for functional flexibility and variety. Nearly two decades after the discovery of the first modular polyketide synthase (PKS), we critically assess PKS modularity in the face of a growing body of atomic structural and in vitro biochemical investigations. Both the architectural modularity and the functional modularity of this family of enzymatic assembly lines are reviewed, and the fundamental challenges that lie ahead for the rational exploitation of their full biosynthetic potential are discussed.

摘要

模块化是工程设计中备受追捧的一个特性。模块化催化剂是一种多组分系统,其各个部分可以通过可预测的方式进行互换,以实现功能的灵活性和多样性。在首个模块化聚酮合酶(PKS)被发现近二十年后,面对越来越多的原子结构和体外生化研究,我们对PKS模块化进行了批判性评估。本文综述了这类酶促装配线家族的结构模块化和功能模块化,并讨论了合理开发其全部生物合成潜力所面临的基本挑战。

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