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Ansalactams B-D Illustrate Further Biosynthetic Plasticity within the Ansamycin Pathway.
Le, Tu Cam; Yang, Inho; Yoon, Yeo Joon; Nam, Sang-Jip; Fenical, William.
Afiliação
  • Le TC; Department of Chemistry and Nano Science, Global Top 5 program, Ewha Womans University , Seoul 03760, Korea.
  • Yang I; Department of Chemistry and Nano Science, Global Top 5 program, Ewha Womans University , Seoul 03760, Korea.
  • Yoon YJ; Department of Chemistry and Nano Science, Global Top 5 program, Ewha Womans University , Seoul 03760, Korea.
  • Nam SJ; Department of Chemistry and Nano Science, Global Top 5 program, Ewha Womans University , Seoul 03760, Korea.
  • Fenical W; Center for Marine Biotechnology and Biomedicine, Scripps Institution of Oceanography, University of California San Diego , La Jolla, California 92093-0204, United States.
Org Lett ; 18(9): 2256-9, 2016 05 06.
Article em En | MEDLINE | ID: mdl-27120128
ABSTRACT
Further chemical investigation of a marine-derived bacterium of the genus Streptomyces has led to the isolation of ansalactams B-D (1-3) along with the previously reported metabolite ansalactam A (4). Ansalactams B-D are significantly modified ansamycins, representing three new carbon skeletons and further illustrating the biosynthetic plasticity of the ansalactam class. Unlike ansalactam A, ansalactams B and D are penta- and hexacyclic metabolites, while ansalactam C illustrates an open polyene chain with a terminal carboxylic acid.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Streptomyces / Rifabutina / Staphylococcus aureus Resistente à Meticilina / Policetídeos Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Streptomyces / Rifabutina / Staphylococcus aureus Resistente à Meticilina / Policetídeos Idioma: En Ano de publicação: 2016 Tipo de documento: Article