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马勒菌素途径的可塑性及其对人病原细菌中铁载体作用的影响。

Plasticity of the malleobactin pathway and its impact on siderophore action in human pathogenic bacteria.

机构信息

Department of Biomolecular Chemistry, Leibniz Institute for Natural Product Research and Infection Biology (HKI), Beutenbergstr. 11a, 07745 Jena (Germany).

Chair of Natural Product Chemistry, Friedrich Schiller University, Jena (Germany).

出版信息

Chemistry. 2015 May 26;21(22):8010-4. doi: 10.1002/chem.201500757. Epub 2015 Apr 14.

Abstract

The human pathogenic bacteria Burkholderia mallei, Burkholderia pseudomallei, and Burkholderia thailandensis harbor a highly conserved gene cluster coding for the biosynthesis of the long sought-after malleobactins. Four new, unexpected congeners of the malleobactin family that were isolated and fully characterized in this study feature unusual deviations from the parent, ornibactin-like architecture. Thus, the malleobactin non-ribosomal peptide synthetase (NRPS) has a rare flexibility that yields diverse peptide backbones, of which one candidate confers pronounced siderophore activity (EC50: 8.4 μM, CAS assay). These findings not only unveil a highly diverse assembly line but also are an important addition to the knowledgebase of the pathogens' metabolomes.

摘要

人类病原菌鼻疽伯克霍尔德菌、类鼻疽伯克霍尔德菌和泰国伯克霍尔德菌拥有一个高度保守的基因簇,用于编码长期以来备受追捧的马勒菌素的生物合成。本研究中分离并充分表征的马勒菌素家族的四个新的、意想不到的同系物,其特征是与母体奥尼宾菌素样结构存在不寻常的偏差。因此,马勒菌素非核糖体肽合酶 (NRPS) 具有罕见的灵活性,可产生多种肽骨架,其中一种候选物具有明显的铁载体活性 (EC50:8.4 μM,CAS 测定)。这些发现不仅揭示了一个高度多样化的装配线,而且也是对病原体代谢组学知识库的重要补充。

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