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利用酰胺键形成连接酶合成酰胺。

Harnessing and engineering amide bond forming ligases for the synthesis of amides.

机构信息

School of Chemistry and Manchester Institute of Biotechnology (MIB), The University of Manchester, 131 Princess Street, Manchester M1 7DN, UK.

School of Chemistry, University of Edinburgh, David Brewster Road, King's Buildings, Edinburgh, EH9 3FJ, UK.

出版信息

Curr Opin Chem Biol. 2020 Apr;55:77-85. doi: 10.1016/j.cbpa.2019.12.004. Epub 2020 Feb 12.

Abstract

The amide functional group is ubiquitous in nature and one of the most important motifs in pharmaceuticals, agrochemicals, and other valuable products. While coupling amides and carboxylic acids is a trivial synthetic transformation, it often requires protective group manipulation, along with stoichiometric quantities of expensive and deleterious coupling reagents. Nature has evolved a range of enzymes to construct amide bonds, the vast majority of which utilize adenosine triphosphate to activate the carboxylic acid substrate for amine coupling. Despite the fact that these enzymes operate under mild conditions, as well as possessing chemoselectivity and regioselectivity that obviates the need for protecting groups, their synthetic potential has been largely unexplored. In this review, we discuss recent research into the discovery, characterization, and development of amide bond forming enzymes, with an emphasis on stand-alone ligase enzymes that can generate amides directly from simple carboxylic acid and amine substrates.

摘要

酰胺官能团在自然界中无处不在,是制药、农用化学品和其他有价值产品中最重要的基序之一。虽然酰胺和羧酸的偶联是一种简单的合成转化,但它通常需要保护基团的操作,以及大量昂贵和有害的偶联试剂。自然界已经进化出一系列的酶来构建酰胺键,其中绝大多数利用三磷酸腺苷来激活羧酸底物进行胺偶联。尽管这些酶在温和的条件下运行,并且具有化学选择性和区域选择性,不需要保护基团,但它们的合成潜力在很大程度上尚未得到探索。在这篇综述中,我们讨论了酰胺键形成酶的发现、表征和开发的最新研究进展,重点介绍了可以直接从简单的羧酸和胺底物生成酰胺的独立连接酶。

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