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Tetroazolemycins A and B, Two New Oxazole-Thiazole Siderophores from Deep-Sea Streptomyces olivaceus FXJ8.012
Two new oxazole/thiazole derivatives, named tetroazolemycins A (1) and B (2), have been isolated from the acetone extract of the mycelium of Streptomyces olivaceus FXJ8.012 derived from deep-sea water, together with three known compounds, spoxazomicins A–C (3–5), isolated from the fermentation super...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3707159/ https://www.ncbi.nlm.nih.gov/pubmed/23665958 http://dx.doi.org/10.3390/md11051524 |
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author | Liu, Ning Shang, Fei Xi, Lijun Huang, Ying |
author_facet | Liu, Ning Shang, Fei Xi, Lijun Huang, Ying |
author_sort | Liu, Ning |
collection | PubMed |
description | Two new oxazole/thiazole derivatives, named tetroazolemycins A (1) and B (2), have been isolated from the acetone extract of the mycelium of Streptomyces olivaceus FXJ8.012 derived from deep-sea water, together with three known compounds, spoxazomicins A–C (3–5), isolated from the fermentation supernatant. The planar structure and relative configuration of tetroazolemycins were elucidated by a combination of spectroscopic analyses, including 1D- and 2D-NMR techniques, and showed to be new pyochelin-type antibiotics. Both compounds showed metal ion-binding activity and their Zn(2+) complexes exhibited weak activity against pathogenic bacteria Klebsiella pneumoniae. |
format | Online Article Text |
id | pubmed-3707159 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-37071592013-07-10 Tetroazolemycins A and B, Two New Oxazole-Thiazole Siderophores from Deep-Sea Streptomyces olivaceus FXJ8.012 Liu, Ning Shang, Fei Xi, Lijun Huang, Ying Mar Drugs Article Two new oxazole/thiazole derivatives, named tetroazolemycins A (1) and B (2), have been isolated from the acetone extract of the mycelium of Streptomyces olivaceus FXJ8.012 derived from deep-sea water, together with three known compounds, spoxazomicins A–C (3–5), isolated from the fermentation supernatant. The planar structure and relative configuration of tetroazolemycins were elucidated by a combination of spectroscopic analyses, including 1D- and 2D-NMR techniques, and showed to be new pyochelin-type antibiotics. Both compounds showed metal ion-binding activity and their Zn(2+) complexes exhibited weak activity against pathogenic bacteria Klebsiella pneumoniae. MDPI 2013-05-09 /pmc/articles/PMC3707159/ /pubmed/23665958 http://dx.doi.org/10.3390/md11051524 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 Liu, Ning Shang, Fei Xi, Lijun Huang, Ying Tetroazolemycins A and B, Two New Oxazole-Thiazole Siderophores from Deep-Sea Streptomyces olivaceus FXJ8.012 |
title | Tetroazolemycins A and B, Two New Oxazole-Thiazole Siderophores from Deep-Sea Streptomyces olivaceus FXJ8.012 |
title_full | Tetroazolemycins A and B, Two New Oxazole-Thiazole Siderophores from Deep-Sea Streptomyces olivaceus FXJ8.012 |
title_fullStr | Tetroazolemycins A and B, Two New Oxazole-Thiazole Siderophores from Deep-Sea Streptomyces olivaceus FXJ8.012 |
title_full_unstemmed | Tetroazolemycins A and B, Two New Oxazole-Thiazole Siderophores from Deep-Sea Streptomyces olivaceus FXJ8.012 |
title_short | Tetroazolemycins A and B, Two New Oxazole-Thiazole Siderophores from Deep-Sea Streptomyces olivaceus FXJ8.012 |
title_sort | tetroazolemycins a and b, two new oxazole-thiazole siderophores from deep-sea streptomyces olivaceus fxj8.012 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3707159/ https://www.ncbi.nlm.nih.gov/pubmed/23665958 http://dx.doi.org/10.3390/md11051524 |
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