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Calcarides A–E, Antibacterial Macrocyclic and Linear Polyesters from a Calcarisporium Strain

Bioactive compounds were detected in crude extracts of the fungus, Calcarisporium sp. KF525, which was isolated from German Wadden Sea water samples. Purification of the metabolites from the extracts yielded the five known polyesters, 15G256α, α-2, β, β-2 and π (1–5), and five new derivatives thereo...

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Autores principales: Silber, Johanna, Ohlendorf, Birgit, Labes, Antje, Erhard, Arlette, Imhoff, Johannes F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3801122/
https://www.ncbi.nlm.nih.gov/pubmed/23994907
http://dx.doi.org/10.3390/md11093309
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author Silber, Johanna
Ohlendorf, Birgit
Labes, Antje
Erhard, Arlette
Imhoff, Johannes F.
author_facet Silber, Johanna
Ohlendorf, Birgit
Labes, Antje
Erhard, Arlette
Imhoff, Johannes F.
author_sort Silber, Johanna
collection PubMed
description Bioactive compounds were detected in crude extracts of the fungus, Calcarisporium sp. KF525, which was isolated from German Wadden Sea water samples. Purification of the metabolites from the extracts yielded the five known polyesters, 15G256α, α-2, β, β-2 and π (1–5), and five new derivatives thereof, named calcarides A–E (6–10). The chemical structures of the isolated compounds were elucidated on the basis of one- and two-dimensional NMR spectroscopy supported by UV and HRESIMS data. The compounds exhibited inhibitory activities against Staphylococcus epidermidis, Xanthomonas campestris and Propionibacterium acnes. As the antibacterial activities were highly specific with regard to compound and test strain, a tight structure-activity relationship is assumed.
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spelling pubmed-38011222013-10-22 Calcarides A–E, Antibacterial Macrocyclic and Linear Polyesters from a Calcarisporium Strain Silber, Johanna Ohlendorf, Birgit Labes, Antje Erhard, Arlette Imhoff, Johannes F. Mar Drugs Article Bioactive compounds were detected in crude extracts of the fungus, Calcarisporium sp. KF525, which was isolated from German Wadden Sea water samples. Purification of the metabolites from the extracts yielded the five known polyesters, 15G256α, α-2, β, β-2 and π (1–5), and five new derivatives thereof, named calcarides A–E (6–10). The chemical structures of the isolated compounds were elucidated on the basis of one- and two-dimensional NMR spectroscopy supported by UV and HRESIMS data. The compounds exhibited inhibitory activities against Staphylococcus epidermidis, Xanthomonas campestris and Propionibacterium acnes. As the antibacterial activities were highly specific with regard to compound and test strain, a tight structure-activity relationship is assumed. MDPI 2013-08-29 /pmc/articles/PMC3801122/ /pubmed/23994907 http://dx.doi.org/10.3390/md11093309 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ 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
Silber, Johanna
Ohlendorf, Birgit
Labes, Antje
Erhard, Arlette
Imhoff, Johannes F.
Calcarides A–E, Antibacterial Macrocyclic and Linear Polyesters from a Calcarisporium Strain
title Calcarides A–E, Antibacterial Macrocyclic and Linear Polyesters from a Calcarisporium Strain
title_full Calcarides A–E, Antibacterial Macrocyclic and Linear Polyesters from a Calcarisporium Strain
title_fullStr Calcarides A–E, Antibacterial Macrocyclic and Linear Polyesters from a Calcarisporium Strain
title_full_unstemmed Calcarides A–E, Antibacterial Macrocyclic and Linear Polyesters from a Calcarisporium Strain
title_short Calcarides A–E, Antibacterial Macrocyclic and Linear Polyesters from a Calcarisporium Strain
title_sort calcarides a–e, antibacterial macrocyclic and linear polyesters from a calcarisporium strain
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3801122/
https://www.ncbi.nlm.nih.gov/pubmed/23994907
http://dx.doi.org/10.3390/md11093309
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