{"title":"One-Pot Chemoenzymatic Synthesis of Arsinothricin and the Mechanistic Insights into the Noncanonical Radical SAM Enzyme ArsL","authors":"He Li, Fener Chen, Wei Ding, Qi Zhang","doi":"10.1021/acscatal.4c04938","DOIUrl":null,"url":null,"abstract":"Arsinothricin (AST) is a broad-spectrum arsenic-containing antibiotic with promising pharmaceutical properties. In this study, we report the one-pot chemoenzymatic synthesis of AST starting from methylarsenate, a commonly used agricultural herbicide. Although a single point mutation in the C-terminal region of ArsL completely abolished its activity toward the natural substrate inorganic arsenite, this mutation unexpectedly enhanced its activity toward methylarsenate by over 50-fold, enabling subgram scale production of AST in a cell-free system. These findings offer valuable mechanistic insights into ArsL and highlight the significant potential of manipulating the radical SAM superfamily enzymes in synthetic applications.","PeriodicalId":9,"journal":{"name":"ACS Catalysis ","volume":"261 1","pages":""},"PeriodicalIF":11.3000,"publicationDate":"2024-12-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Catalysis ","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acscatal.4c04938","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Arsinothricin (AST) is a broad-spectrum arsenic-containing antibiotic with promising pharmaceutical properties. In this study, we report the one-pot chemoenzymatic synthesis of AST starting from methylarsenate, a commonly used agricultural herbicide. Although a single point mutation in the C-terminal region of ArsL completely abolished its activity toward the natural substrate inorganic arsenite, this mutation unexpectedly enhanced its activity toward methylarsenate by over 50-fold, enabling subgram scale production of AST in a cell-free system. These findings offer valuable mechanistic insights into ArsL and highlight the significant potential of manipulating the radical SAM superfamily enzymes in synthetic applications.
期刊介绍:
ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels.
The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.