Accessing and exploring the unusual chemistry by radical SAM-RiPP enzymes

IF 6.9 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Qianqian Guo, Brandon I. Morinaka
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引用次数: 0

Abstract

Radical SAM enzymes involved in the biosynthesis of ribosomally synthesized and post-translationally modified peptides catalyze unusual transformations that lead to unique peptide scaffolds and building blocks. Several natural products from these pathways show encouraging antimicrobial activities and represent next-generation therapeutics for infectious diseases. These systems are uniquely configured to benefit from genome-mining approaches because minimal substrate and cognate modifying enzyme expression can reveal unique, chemically complex transformations that outperform late-stage chemical reactions. This report highlights the main strategies used to reveal these enzymatic transformations, which have relied mainly on genome mining using enzyme-first approaches. We describe the general biosynthetic components for rSAM enzymes and highlight emerging approaches that may broaden the discovery and study of rSAM-RiPP enzymes. The large number of uncharacterized rSAM proteins, coupled with their unpredictable transformations, will continue to be an essential and exciting resource for enzyme discovery.

通过自由基 SAM-RiPP 酶获取和探索不寻常的化学性质。
参与核糖体合成和翻译后修饰肽生物合成的激肽 SAM 酶会催化不寻常的转化,从而产生独特的肽支架和构件。来自这些途径的一些天然产物显示出令人鼓舞的抗菌活性,是治疗传染性疾病的新一代疗法。这些系统配置独特,可以从基因组挖掘方法中获益,因为最低限度的底物和同源修饰酶表达可以揭示独特的、化学上复杂的转化过程,其效果优于后期的化学反应。本报告重点介绍了用于揭示这些酶转化的主要策略,这些策略主要依赖于使用酶优先方法进行基因组挖掘。我们描述了 rSAM 酶的一般生物合成成分,并重点介绍了可扩大 rSAM-RiPP 酶发现和研究范围的新兴方法。大量未表征的 rSAM 蛋白,加上它们不可预测的转化,将继续成为发现酶的重要和令人兴奋的资源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Current Opinion in Chemical Biology
Current Opinion in Chemical Biology 生物-生化与分子生物学
CiteScore
13.30
自引率
1.30%
发文量
113
审稿时长
74 days
期刊介绍: COCHBI (Current Opinion in Chemical Biology) is a systematic review journal designed to offer specialists a unique and educational platform. Its goal is to help professionals stay informed about the growing volume of information in the field of Chemical Biology through systematic reviews.
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