| Literature DB >> 32058241 |
Michael Winn1, Shona M Richardson2, Dominic J Campopiano3, Jason Micklefield4.
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.Entities:
Keywords: ANL superfamily; ATP grasp; amide bond synthetases; amide ligase; amide synthesis; biocatalysis; ligase engineering
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Year: 2020 PMID: 32058241 DOI: 10.1016/j.cbpa.2019.12.004
Source DB: PubMed Journal: Curr Opin Chem Biol ISSN: 1367-5931 Impact factor: 8.822