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Argicyclamides A-C Unveil Enzymatic Basis for Guanidine Bis-prenylation.
Phan, Chin-Soon; Matsuda, Kenichi; Balloo, Nandani; Fujita, Kei; Wakimoto, Toshiyuki; Okino, Tatsufumi.
Afiliação
  • Matsuda K; Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo 060-0812, Japan.
  • Balloo N; Global Station for Biosurfaces and Drug Discovery, Hokkaido University, Kita 12, Nishi 6, Sapporo 060-0812, Japan.
  • Wakimoto T; Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo 060-0812, Japan.
  • Okino T; Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo 060-0812, Japan.
J Am Chem Soc ; 143(27): 10083-10087, 2021 07 14.
Article em En | MEDLINE | ID: mdl-34181406
ABSTRACT
Guanidine prenylation is an outstanding modification in alkaloid and peptide biosynthesis, but its enzymatic basis has remained elusive. We report the isolation of argicyclamides, a new class of cyanobactins with unique mono- and bis-prenylations on guanidine moieties, from Microcystis aeruginosa NIES-88. The genetic basis of argicyclamide biosynthesis was established by the heterologous expression and in vitro characterization of biosynthetic enzymes including AgcF, a new guanidine prenyltransferase. This study provides important insight into the biosynthesis of prenylated guanidines and offers a new toolkit for peptide modification.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Peptídeos Cíclicos / Guanidina / Microcystis Idioma: En Revista: J Am Chem Soc Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Peptídeos Cíclicos / Guanidina / Microcystis Idioma: En Revista: J Am Chem Soc Ano de publicação: 2021 Tipo de documento: Article