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Fusarisolins A–E, Polyketides from the Marine-Derived Fungus Fusarium solani H918

Five new (fusarisolins A–E, 1 to 5) and three known (6 to 8) polyketides were isolated from the marine-derived fungus Fusarium solani H918, along with six known phenolics (9 to 14). Their structures were established by comprehensive spectroscopic data analyses, methoxyphenylacetic acid (MPA) method,...

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Autores principales: Niu, Siwen, Tang, Xi-Xiang, Fan, Zuowang, Xia, Jin-Mei, Xie, Chun-Lan, Yang, Xian-Wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6410219/
https://www.ncbi.nlm.nih.gov/pubmed/30791608
http://dx.doi.org/10.3390/md17020125
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author Niu, Siwen
Tang, Xi-Xiang
Fan, Zuowang
Xia, Jin-Mei
Xie, Chun-Lan
Yang, Xian-Wen
author_facet Niu, Siwen
Tang, Xi-Xiang
Fan, Zuowang
Xia, Jin-Mei
Xie, Chun-Lan
Yang, Xian-Wen
author_sort Niu, Siwen
collection PubMed
description Five new (fusarisolins A–E, 1 to 5) and three known (6 to 8) polyketides were isolated from the marine-derived fungus Fusarium solani H918, along with six known phenolics (9 to 14). Their structures were established by comprehensive spectroscopic data analyses, methoxyphenylacetic acid (MPA) method, chemical conversion, and by comparison with data reported in the literature. Compounds 1 and 2 are the first two naturally occurring 21 carbons polyketides featuring a rare β- and γ-lactone unit, respectively. All isolates (1 to 14) were evaluated for their inhibitory effects against tea pathogenic fungus Pestalotiopsis theae and 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) synthase gene expression. Compound 8 showed potent antifungal activity with an ED(50) value of 55 μM, while 1, 8, 13, and 14 significantly inhibited HMG-CoA synthase gene expression.
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spelling pubmed-64102192019-03-29 Fusarisolins A–E, Polyketides from the Marine-Derived Fungus Fusarium solani H918 Niu, Siwen Tang, Xi-Xiang Fan, Zuowang Xia, Jin-Mei Xie, Chun-Lan Yang, Xian-Wen Mar Drugs Article Five new (fusarisolins A–E, 1 to 5) and three known (6 to 8) polyketides were isolated from the marine-derived fungus Fusarium solani H918, along with six known phenolics (9 to 14). Their structures were established by comprehensive spectroscopic data analyses, methoxyphenylacetic acid (MPA) method, chemical conversion, and by comparison with data reported in the literature. Compounds 1 and 2 are the first two naturally occurring 21 carbons polyketides featuring a rare β- and γ-lactone unit, respectively. All isolates (1 to 14) were evaluated for their inhibitory effects against tea pathogenic fungus Pestalotiopsis theae and 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) synthase gene expression. Compound 8 showed potent antifungal activity with an ED(50) value of 55 μM, while 1, 8, 13, and 14 significantly inhibited HMG-CoA synthase gene expression. MDPI 2019-02-20 /pmc/articles/PMC6410219/ /pubmed/30791608 http://dx.doi.org/10.3390/md17020125 Text en © 2019 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 (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Niu, Siwen
Tang, Xi-Xiang
Fan, Zuowang
Xia, Jin-Mei
Xie, Chun-Lan
Yang, Xian-Wen
Fusarisolins A–E, Polyketides from the Marine-Derived Fungus Fusarium solani H918
title Fusarisolins A–E, Polyketides from the Marine-Derived Fungus Fusarium solani H918
title_full Fusarisolins A–E, Polyketides from the Marine-Derived Fungus Fusarium solani H918
title_fullStr Fusarisolins A–E, Polyketides from the Marine-Derived Fungus Fusarium solani H918
title_full_unstemmed Fusarisolins A–E, Polyketides from the Marine-Derived Fungus Fusarium solani H918
title_short Fusarisolins A–E, Polyketides from the Marine-Derived Fungus Fusarium solani H918
title_sort fusarisolins a–e, polyketides from the marine-derived fungus fusarium solani h918
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6410219/
https://www.ncbi.nlm.nih.gov/pubmed/30791608
http://dx.doi.org/10.3390/md17020125
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