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Antibacterial Spirotetronate Polyketides from an Actinomadura sp. Strain A30804
Large scale cultivation and chemical investigation of an extract obtained from Actimonadura sp. resulted in the identification of six previously undescribed spirotetronates (pyrrolosporin B and decatromicins C–G; 7–12), along with six known congeners, namely decatromicins A–B (1–2), BE-45722B–D (3–5...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9737171/ https://www.ncbi.nlm.nih.gov/pubmed/36500287 http://dx.doi.org/10.3390/molecules27238196 |
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author | Ching, Kuan-Chieh Chin, Elaine J. Wibowo, Mario Tan, Zann Y. Yang, Lay-Kien Seow, Deborah C. Leong, Chung-Yan Ng, Veronica W. Ng, Siew-Bee Kanagasundaram, Yoganathan |
author_facet | Ching, Kuan-Chieh Chin, Elaine J. Wibowo, Mario Tan, Zann Y. Yang, Lay-Kien Seow, Deborah C. Leong, Chung-Yan Ng, Veronica W. Ng, Siew-Bee Kanagasundaram, Yoganathan |
author_sort | Ching, Kuan-Chieh |
collection | PubMed |
description | Large scale cultivation and chemical investigation of an extract obtained from Actimonadura sp. resulted in the identification of six previously undescribed spirotetronates (pyrrolosporin B and decatromicins C–G; 7–12), along with six known congeners, namely decatromicins A–B (1–2), BE-45722B–D (3–5), and pyrrolosporin A (6). The chemical structures of compounds 1–12 were characterized via comparison with previously reported data and analysis of 1D/2D NMR and MS data. The structures of all new compounds were highly related to the spirotetronate type compounds, decatromicin and pyrrolosporin, with variations in the substituents on the pyrrole and aglycone moieties. All compounds were evaluated for antibacterial activity against the Gram-negative bacteria, Acinetobacter baumannii and Gram-positive bacteria, Staphylococcus aureus and were investigated for their cytotoxicity against the human cancer cell line A549. Of these, decatromicin B (2), BE-45722B (3), and pyrrolosporin B (7) exhibited potent antibacterial activities against both Gram-positive (MIC(90) between 1–3 μM) and Gram-negative bacteria (MIC(90) values ranging from 12–36 μM) with weak or no cytotoxic activity against A549 cells. |
format | Online Article Text |
id | pubmed-9737171 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-97371712022-12-11 Antibacterial Spirotetronate Polyketides from an Actinomadura sp. Strain A30804 Ching, Kuan-Chieh Chin, Elaine J. Wibowo, Mario Tan, Zann Y. Yang, Lay-Kien Seow, Deborah C. Leong, Chung-Yan Ng, Veronica W. Ng, Siew-Bee Kanagasundaram, Yoganathan Molecules Communication Large scale cultivation and chemical investigation of an extract obtained from Actimonadura sp. resulted in the identification of six previously undescribed spirotetronates (pyrrolosporin B and decatromicins C–G; 7–12), along with six known congeners, namely decatromicins A–B (1–2), BE-45722B–D (3–5), and pyrrolosporin A (6). The chemical structures of compounds 1–12 were characterized via comparison with previously reported data and analysis of 1D/2D NMR and MS data. The structures of all new compounds were highly related to the spirotetronate type compounds, decatromicin and pyrrolosporin, with variations in the substituents on the pyrrole and aglycone moieties. All compounds were evaluated for antibacterial activity against the Gram-negative bacteria, Acinetobacter baumannii and Gram-positive bacteria, Staphylococcus aureus and were investigated for their cytotoxicity against the human cancer cell line A549. Of these, decatromicin B (2), BE-45722B (3), and pyrrolosporin B (7) exhibited potent antibacterial activities against both Gram-positive (MIC(90) between 1–3 μM) and Gram-negative bacteria (MIC(90) values ranging from 12–36 μM) with weak or no cytotoxic activity against A549 cells. MDPI 2022-11-24 /pmc/articles/PMC9737171/ /pubmed/36500287 http://dx.doi.org/10.3390/molecules27238196 Text en © 2022 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 | Communication Ching, Kuan-Chieh Chin, Elaine J. Wibowo, Mario Tan, Zann Y. Yang, Lay-Kien Seow, Deborah C. Leong, Chung-Yan Ng, Veronica W. Ng, Siew-Bee Kanagasundaram, Yoganathan Antibacterial Spirotetronate Polyketides from an Actinomadura sp. Strain A30804 |
title | Antibacterial Spirotetronate Polyketides from an Actinomadura sp. Strain A30804 |
title_full | Antibacterial Spirotetronate Polyketides from an Actinomadura sp. Strain A30804 |
title_fullStr | Antibacterial Spirotetronate Polyketides from an Actinomadura sp. Strain A30804 |
title_full_unstemmed | Antibacterial Spirotetronate Polyketides from an Actinomadura sp. Strain A30804 |
title_short | Antibacterial Spirotetronate Polyketides from an Actinomadura sp. Strain A30804 |
title_sort | antibacterial spirotetronate polyketides from an actinomadura sp. strain a30804 |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9737171/ https://www.ncbi.nlm.nih.gov/pubmed/36500287 http://dx.doi.org/10.3390/molecules27238196 |
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