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Chemical Exchanges between Multilateral Symbionts.
Bae, Munhyung; Mevers, Emily; Pishchany, Gleb; Whaley, Sarah G; Rock, Charles O; Andes, David R; Currie, Cameron R; Pupo, Monica T; Clardy, Jon.
Afiliação
  • Bae M; Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts 02115, United States.
  • Mevers E; Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts 02115, United States.
  • Pishchany G; Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts 02115, United States.
  • Whaley SG; Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, Tennessee 38105, United States.
  • Rock CO; Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, Tennessee 38105, United States.
  • Andes DR; Department of Medicine, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin 53705, United States.
  • Currie CR; Department of Bacteriology, University of Wisconsin-Madison, Madison, Wisconsin 53706, United States.
  • Pupo MT; School of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, Ribeirão Preto, SP 14040-903, Brazil.
  • Clardy J; Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts 02115, United States.
Org Lett ; 23(5): 1648-1652, 2021 03 05.
Article em En | MEDLINE | ID: mdl-33591189
ABSTRACT
Herein is a report on the molecular exchange occurring between multilateral symbiosis partners-a tit-for-tat exchange that led to the characterization of two new metabolites, conocandin B (fungal-derived) and dentigerumycin F (bacterial-derived). The structures were determined by NMR, mass spectrometry, genomic analysis, and chemical derivatizations. Conocandin B exhibits antimicrobial activity against both the bacterial symbionts of fungus-growing ant and human pathogenic strains by selectively inhibiting FabH, thus disrupting fatty acid biosynthesis.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Simbiose / Bactérias / Fungos Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Simbiose / Bactérias / Fungos Idioma: En Ano de publicação: 2021 Tipo de documento: Article