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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...

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Detalles Bibliográficos
Autores principales: Liu, Ning, Shang, Fei, Xi, Lijun, Huang, Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
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.
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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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