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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Main Authors: Ying Huang, Lijun Xi, Fei Shang, Ning Liu
Format: Article
Language:English
Published: MDPI AG 2013-05-01
Series:Marine Drugs
Subjects:
Online Access:http://www.mdpi.com/1660-3397/11/5/1524
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author Ying Huang
Lijun Xi
Fei Shang
Ning Liu
author_facet Ying Huang
Lijun Xi
Fei Shang
Ning Liu
author_sort Ying Huang
collection DOAJ
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 Zn2+ complexes exhibited weak activity against pathogenic bacteria Klebsiella pneumoniae.
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spelling doaj.art-ef9baf31302745229326ccfd60d5b08e2022-12-22T02:22:11ZengMDPI AGMarine Drugs1660-33972013-05-011151524153310.3390/md11051524Tetroazolemycins A and B, Two New Oxazole-Thiazole Siderophores from Deep-Sea Streptomyces olivaceus FXJ8.012Ying HuangLijun XiFei ShangNing LiuTwo 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 Zn2+ complexes exhibited weak activity against pathogenic bacteria Klebsiella pneumoniae.http://www.mdpi.com/1660-3397/11/5/1524deep-sea waterStreptomyces olivaceustetroazolemycinsiderophore
spellingShingle Ying Huang
Lijun Xi
Fei Shang
Ning Liu
Tetroazolemycins A and B, Two New Oxazole-Thiazole Siderophores from Deep-Sea Streptomyces olivaceus FXJ8.012
Marine Drugs
deep-sea water
Streptomyces olivaceus
tetroazolemycin
siderophore
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 deep-sea water
Streptomyces olivaceus
tetroazolemycin
siderophore
url http://www.mdpi.com/1660-3397/11/5/1524
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