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Sortase A-Inhibitory Metabolites from a Marine-Derived Fungus Aspergillus sp.

Seven alkaloidal compounds (2–8) and one polyketide (1) were isolated from a semisolid rice culture of the marine-derived fungus Aspergillus sp. F452. Structures of the isolated compounds were elucidated based on spectroscopic data and comparisons with previously reported data. The alkaloidal compou...

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Autores principales: Park, Sung Chul, Chung, Beomkoo, Lee, Jayho, Cho, Eunji, Hwang, Ji-Yeon, Oh, Dong-Chan, Shin, Jongheon, Oh, Ki-Bong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7401278/
https://www.ncbi.nlm.nih.gov/pubmed/32668629
http://dx.doi.org/10.3390/md18070359
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author Park, Sung Chul
Chung, Beomkoo
Lee, Jayho
Cho, Eunji
Hwang, Ji-Yeon
Oh, Dong-Chan
Shin, Jongheon
Oh, Ki-Bong
author_facet Park, Sung Chul
Chung, Beomkoo
Lee, Jayho
Cho, Eunji
Hwang, Ji-Yeon
Oh, Dong-Chan
Shin, Jongheon
Oh, Ki-Bong
author_sort Park, Sung Chul
collection PubMed
description Seven alkaloidal compounds (2–8) and one polyketide (1) were isolated from a semisolid rice culture of the marine-derived fungus Aspergillus sp. F452. Structures of the isolated compounds were elucidated based on spectroscopic data and comparisons with previously reported data. The alkaloidal compounds (2–8) displayed weak to moderate inhibitory activities against Staphylococcus aureus-derived sortase A (SrtA) without affecting cell viability. Aspermytin A (1) strongly inhibited SrtA activity, with an IC(50) value of 146.0 μM, and significantly reduced bacterial adherence to fibronectin-coated surfaces. The present results indicate that the underlying mechanism of action of compound 1 is associated with the inhibition of SrtA-mediated S. aureus adhesion to fibronectin, thus potentially serving as an SrtA inhibitor.
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spelling pubmed-74012782020-08-18 Sortase A-Inhibitory Metabolites from a Marine-Derived Fungus Aspergillus sp. Park, Sung Chul Chung, Beomkoo Lee, Jayho Cho, Eunji Hwang, Ji-Yeon Oh, Dong-Chan Shin, Jongheon Oh, Ki-Bong Mar Drugs Article Seven alkaloidal compounds (2–8) and one polyketide (1) were isolated from a semisolid rice culture of the marine-derived fungus Aspergillus sp. F452. Structures of the isolated compounds were elucidated based on spectroscopic data and comparisons with previously reported data. The alkaloidal compounds (2–8) displayed weak to moderate inhibitory activities against Staphylococcus aureus-derived sortase A (SrtA) without affecting cell viability. Aspermytin A (1) strongly inhibited SrtA activity, with an IC(50) value of 146.0 μM, and significantly reduced bacterial adherence to fibronectin-coated surfaces. The present results indicate that the underlying mechanism of action of compound 1 is associated with the inhibition of SrtA-mediated S. aureus adhesion to fibronectin, thus potentially serving as an SrtA inhibitor. MDPI 2020-07-13 /pmc/articles/PMC7401278/ /pubmed/32668629 http://dx.doi.org/10.3390/md18070359 Text en © 2020 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
Park, Sung Chul
Chung, Beomkoo
Lee, Jayho
Cho, Eunji
Hwang, Ji-Yeon
Oh, Dong-Chan
Shin, Jongheon
Oh, Ki-Bong
Sortase A-Inhibitory Metabolites from a Marine-Derived Fungus Aspergillus sp.
title Sortase A-Inhibitory Metabolites from a Marine-Derived Fungus Aspergillus sp.
title_full Sortase A-Inhibitory Metabolites from a Marine-Derived Fungus Aspergillus sp.
title_fullStr Sortase A-Inhibitory Metabolites from a Marine-Derived Fungus Aspergillus sp.
title_full_unstemmed Sortase A-Inhibitory Metabolites from a Marine-Derived Fungus Aspergillus sp.
title_short Sortase A-Inhibitory Metabolites from a Marine-Derived Fungus Aspergillus sp.
title_sort sortase a-inhibitory metabolites from a marine-derived fungus aspergillus sp.
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7401278/
https://www.ncbi.nlm.nih.gov/pubmed/32668629
http://dx.doi.org/10.3390/md18070359
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