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Paecilosetin Derivatives as Potent Antimicrobial Agents from Isaria farinosa
Author(s) -
Orianne Brel,
Seindé Touré,
Marceau Levasseur,
Christian Lechat,
Léonie Pellissier,
JeanLuc Wolfender,
Elsa Van Elslande,
Marc Litaudon,
Isabelle Dusfour,
Didier Stien,
Véronique Éparvier
Publication year - 2020
Publication title -
journal of natural products
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.976
H-Index - 139
eISSN - 1520-6025
pISSN - 0163-3864
DOI - 10.1021/acs.jnatprod.0c00444
Subject(s) - antimicrobial , biology , botany , stereochemistry , microbiology and biotechnology , chemistry
Fifty-seven entomopathogenic microorganisms were screened against human pathogens and subjected to mass spectrometry molecular networking based dereplication. Isaria farinosa BSNB-1250, shown to produce potentially novel biologically active metabolites, was grown on a large scale on potato dextrose agar, and paecilosetin ( 1 ) and five new analogues ( 2 - 6 ) were subsequently isolated. The structures of the new compounds were elucidated using 1D and 2D NMR. The absolute configurations of compounds 1 - 6 were determined using Mosher ester derivatives ( 1 , 3 , 4 ), comparison of experimental and calculated ECD spectra ( 2 - 4 and 6 ), and single-crystal X-ray diffraction analysis ( 5 ). Compounds 1 and 5 exhibited strong antibacterial activity against MSSA and MRSA with MIC values of 1-2 μg/mL.

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