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Iterative Methylations Resulting in the Biosynthesis of the t-Butyl Group Catalyzed by a B12-Dependent Radical SAM Enzyme in Cystobactamid Biosynthesis.
Wang, Yuanyou; Schnell, Bastien; Müller, Rolf; Begley, Tadhg P.
Afiliação
  • Wang Y; Department of Chemistry, Texas A&M University, College Station, TX, United States.
  • Schnell B; Department of Microbial Natural Products, Helmholtz Institute for Pharmaceutical Research Saarland, Helmholtz Center for Infection Research, Saarland University, Saarbrücken, Germany.
  • Müller R; Department of Microbial Natural Products, Helmholtz Institute for Pharmaceutical Research Saarland, Helmholtz Center for Infection Research, Saarland University, Saarbrücken, Germany.
  • Begley TP; Department of Chemistry, Texas A&M University, College Station, TX, United States. Electronic address: begley@tamu.edu.
Methods Enzymol ; 606: 199-216, 2018.
Article em En | MEDLINE | ID: mdl-30097093
ABSTRACT
B12-dependent radical SAM enzymes that can perform methylations on sp3 carbon centers are important for functional diversity and regulation of biological activity in several nonribosomal peptides. Detailed studies on these enzymes are hindered by the complexity of the substrates and low levels of expression of active enzymes. CysS can catalyze iterative methylations of a methoxybenzene moiety during the biosynthesis of the cystobactamids. Here, we describe the overexpression, purification, substrate identification, and mechanism of this enzyme.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas de Bactérias / Ensaios Enzimáticos / Metiltransferases / Nitrocompostos Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas de Bactérias / Ensaios Enzimáticos / Metiltransferases / Nitrocompostos Idioma: En Ano de publicação: 2018 Tipo de documento: Article