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Accessing and exploring the unusual chemistry by radical SAM-RiPP enzymes.
Guo, Qianqian; Morinaka, Brandon I.
Afiliación
  • Guo Q; Department of Pharmacy and Pharmaceutical Sciences, Faculty of Science, National University of Singapore, Singapore.
  • Morinaka BI; Department of Pharmacy and Pharmaceutical Sciences, Faculty of Science, National University of Singapore, Singapore. Electronic address: phambi@nus.edu.sg.
Curr Opin Chem Biol ; 81: 102483, 2024 Aug.
Article en En | MEDLINE | ID: mdl-38917731
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.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: S-Adenosilmetionina Idioma: En Revista: Curr Opin Chem Biol Asunto de la revista: BIOQUIMICA Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: S-Adenosilmetionina Idioma: En Revista: Curr Opin Chem Biol Asunto de la revista: BIOQUIMICA Año: 2024 Tipo del documento: Article