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Antibacterial Polyketides Isolated from the Marine-Derived Fungus Fusarium solani 8388
Seven new polyketides named fusarisolins F-K (1–6) and fusarin I (7) were isolated from the marine-derived fungus Fusarium solani 8388, together with the known anhydrojavanicin (8), 5-deoxybostry coidin (9), and scytalol A (10). Their structures were established by comprehensive spectroscopic data a...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10532693/ https://www.ncbi.nlm.nih.gov/pubmed/37754983 http://dx.doi.org/10.3390/jof9090875 |
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author | Lin, Cankai Huang, Rongchun Liu, Juntao Li, Hong Zhu, Liping Huang, Xin Ding, Bo Liu, Lan Huang, Hongbo Tao, Yiwen |
author_facet | Lin, Cankai Huang, Rongchun Liu, Juntao Li, Hong Zhu, Liping Huang, Xin Ding, Bo Liu, Lan Huang, Hongbo Tao, Yiwen |
author_sort | Lin, Cankai |
collection | PubMed |
description | Seven new polyketides named fusarisolins F-K (1–6) and fusarin I (7) were isolated from the marine-derived fungus Fusarium solani 8388, together with the known anhydrojavanicin (8), 5-deoxybostry coidin (9), and scytalol A (10). Their structures were established by comprehensive spectroscopic data analyses, and by comparison of the (1)H and (13)C NMR data with those reported in literature. Fusarisolin F (1) contained both a dichlorobenzene group and an ethylene oxide unit, which was rare in nature. In the bioassays, fusarisolin I (4), fusarisolin J (5), and 5-deoxybostry coidin (9) exhibited obvious antibacterial activities against methicillin-resistant Staphylococcus aureus n315 with MIC values of 3, 3, and 6 μg/mL, respectively. Fusarisolin H (3) and fusarisolin J (5) showed inhibitory effects against methicillin-resistant Staphylococcus aureus NCTC 10442 with the same MIC value of 6 μg/mL. With the exception of 5, all other compounds did not show or showed weak cytotoxicities against HeLa, A549, and KB cells; while fusarisolin J (5) demonstrated moderate cytotoxicities against the three human cancer cell lines with CC(50) values between 9.21 and 14.02 μM. |
format | Online Article Text |
id | pubmed-10532693 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-105326932023-09-28 Antibacterial Polyketides Isolated from the Marine-Derived Fungus Fusarium solani 8388 Lin, Cankai Huang, Rongchun Liu, Juntao Li, Hong Zhu, Liping Huang, Xin Ding, Bo Liu, Lan Huang, Hongbo Tao, Yiwen J Fungi (Basel) Article Seven new polyketides named fusarisolins F-K (1–6) and fusarin I (7) were isolated from the marine-derived fungus Fusarium solani 8388, together with the known anhydrojavanicin (8), 5-deoxybostry coidin (9), and scytalol A (10). Their structures were established by comprehensive spectroscopic data analyses, and by comparison of the (1)H and (13)C NMR data with those reported in literature. Fusarisolin F (1) contained both a dichlorobenzene group and an ethylene oxide unit, which was rare in nature. In the bioassays, fusarisolin I (4), fusarisolin J (5), and 5-deoxybostry coidin (9) exhibited obvious antibacterial activities against methicillin-resistant Staphylococcus aureus n315 with MIC values of 3, 3, and 6 μg/mL, respectively. Fusarisolin H (3) and fusarisolin J (5) showed inhibitory effects against methicillin-resistant Staphylococcus aureus NCTC 10442 with the same MIC value of 6 μg/mL. With the exception of 5, all other compounds did not show or showed weak cytotoxicities against HeLa, A549, and KB cells; while fusarisolin J (5) demonstrated moderate cytotoxicities against the three human cancer cell lines with CC(50) values between 9.21 and 14.02 μM. MDPI 2023-08-24 /pmc/articles/PMC10532693/ /pubmed/37754983 http://dx.doi.org/10.3390/jof9090875 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Lin, Cankai Huang, Rongchun Liu, Juntao Li, Hong Zhu, Liping Huang, Xin Ding, Bo Liu, Lan Huang, Hongbo Tao, Yiwen Antibacterial Polyketides Isolated from the Marine-Derived Fungus Fusarium solani 8388 |
title | Antibacterial Polyketides Isolated from the Marine-Derived Fungus Fusarium solani 8388 |
title_full | Antibacterial Polyketides Isolated from the Marine-Derived Fungus Fusarium solani 8388 |
title_fullStr | Antibacterial Polyketides Isolated from the Marine-Derived Fungus Fusarium solani 8388 |
title_full_unstemmed | Antibacterial Polyketides Isolated from the Marine-Derived Fungus Fusarium solani 8388 |
title_short | Antibacterial Polyketides Isolated from the Marine-Derived Fungus Fusarium solani 8388 |
title_sort | antibacterial polyketides isolated from the marine-derived fungus fusarium solani 8388 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10532693/ https://www.ncbi.nlm.nih.gov/pubmed/37754983 http://dx.doi.org/10.3390/jof9090875 |
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