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Cyclodepsipeptides and Other O-Containing Heterocyclic Metabolites from Beauveria felina EN-135, a Marine-Derived Entomopathogenic Fungus

Bioassay-guided fractionation of a culture extract of Beauveria felina EN-135, an entomopathogenic fungus isolated from a marine bryozoan, led to the isolation of a new cyclodepsipeptide, iso-isariin D (1); two new O-containing heterocyclic compounds that we have named felinones A and B (2 and 3); a...

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Autores principales: Du, Feng-Yu, Li, Xiao-Ming, Zhang, Peng, Li, Chun-Shun, Wang, Bin-Gui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4052318/
https://www.ncbi.nlm.nih.gov/pubmed/24828289
http://dx.doi.org/10.3390/md12052816
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author Du, Feng-Yu
Li, Xiao-Ming
Zhang, Peng
Li, Chun-Shun
Wang, Bin-Gui
author_facet Du, Feng-Yu
Li, Xiao-Ming
Zhang, Peng
Li, Chun-Shun
Wang, Bin-Gui
author_sort Du, Feng-Yu
collection PubMed
description Bioassay-guided fractionation of a culture extract of Beauveria felina EN-135, an entomopathogenic fungus isolated from a marine bryozoan, led to the isolation of a new cyclodepsipeptide, iso-isariin D (1); two new O-containing heterocyclic compounds that we have named felinones A and B (2 and 3); and four known cyclodepsipeptides (4–7). The structures were elucidated via spectroscopic analysis, and the absolute configurations of 1 and 2 were determined using single-crystal X-ray diffraction and CD, respectively. All isolated compounds were evaluated for antimicrobial activity and brine-shrimp (Artemia salina) lethality.
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spelling pubmed-40523182014-06-11 Cyclodepsipeptides and Other O-Containing Heterocyclic Metabolites from Beauveria felina EN-135, a Marine-Derived Entomopathogenic Fungus Du, Feng-Yu Li, Xiao-Ming Zhang, Peng Li, Chun-Shun Wang, Bin-Gui Mar Drugs Article Bioassay-guided fractionation of a culture extract of Beauveria felina EN-135, an entomopathogenic fungus isolated from a marine bryozoan, led to the isolation of a new cyclodepsipeptide, iso-isariin D (1); two new O-containing heterocyclic compounds that we have named felinones A and B (2 and 3); and four known cyclodepsipeptides (4–7). The structures were elucidated via spectroscopic analysis, and the absolute configurations of 1 and 2 were determined using single-crystal X-ray diffraction and CD, respectively. All isolated compounds were evaluated for antimicrobial activity and brine-shrimp (Artemia salina) lethality. MDPI 2014-05-13 /pmc/articles/PMC4052318/ /pubmed/24828289 http://dx.doi.org/10.3390/md12052816 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Du, Feng-Yu
Li, Xiao-Ming
Zhang, Peng
Li, Chun-Shun
Wang, Bin-Gui
Cyclodepsipeptides and Other O-Containing Heterocyclic Metabolites from Beauveria felina EN-135, a Marine-Derived Entomopathogenic Fungus
title Cyclodepsipeptides and Other O-Containing Heterocyclic Metabolites from Beauveria felina EN-135, a Marine-Derived Entomopathogenic Fungus
title_full Cyclodepsipeptides and Other O-Containing Heterocyclic Metabolites from Beauveria felina EN-135, a Marine-Derived Entomopathogenic Fungus
title_fullStr Cyclodepsipeptides and Other O-Containing Heterocyclic Metabolites from Beauveria felina EN-135, a Marine-Derived Entomopathogenic Fungus
title_full_unstemmed Cyclodepsipeptides and Other O-Containing Heterocyclic Metabolites from Beauveria felina EN-135, a Marine-Derived Entomopathogenic Fungus
title_short Cyclodepsipeptides and Other O-Containing Heterocyclic Metabolites from Beauveria felina EN-135, a Marine-Derived Entomopathogenic Fungus
title_sort cyclodepsipeptides and other o-containing heterocyclic metabolites from beauveria felina en-135, a marine-derived entomopathogenic fungus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4052318/
https://www.ncbi.nlm.nih.gov/pubmed/24828289
http://dx.doi.org/10.3390/md12052816
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