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半乳糖醛酸在肺炎克雷伯菌外膜稳定性中的作用。

The role of galacturonic acid in outer membrane stability in Klebsiella pneumoniae.

作者信息

Frirdich Emilisa, Bouwman Catrien, Vinogradov Evgeny, Whitfield Chris

机构信息

Department of Molecular and Cellular Biology, University of Guelph, Guelph Ontario N1G 2W1, Canada.

出版信息

J Biol Chem. 2005 Jul 29;280(30):27604-12. doi: 10.1074/jbc.M504987200. Epub 2005 Jun 1.

Abstract

In most members of the Enterobacteriaceae, including Escherichia coli and Salmonella, the lipopolysaccharide core oligosaccharide backbone is modified by phosphoryl groups. The negative charges provided by these residues are important in maintaining the barrier function of the outer membrane. Mutants lacking the core heptose region and the phosphate residues display pleiotrophic defects collectively known as the deep-rough phenotype, characterized by changes in outer membrane structure and function. Klebsiella pneumoniae lacks phosphoryl residues in its core, but instead contains galacturonic acid. The goal of this study was to determine the contribution of galacturonic acid as a critical source of negative charge. A mutant was created lacking all galacturonic acid by targeting UDP-galacturonic acid precursor synthesis through a mutation in gla(KP). Gla(KP) is a K. pneumoniae UDP-galacturonic acid C4 epimerase providing UDP-galacturonic acid for core synthesis. The gla(KP) gene was inactivated and the structure of the mutant lipopolysaccharide was determined by mass spectrometry. The mutant displayed characteristics of a deep-rough phenotype, exhibiting a hypersensitivity to hydrophobic compounds and polymyxin B, an altered outer membrane profile, and the release of the periplasmic enzyme beta-lactamase. These results indicate that the negative charge provided by the carboxyl groups of galacturonic acid do play an equivalent role to the core oligosaccharide phosphate residues in establishing outer membrane integrity in E. coli and Salmonella.

摘要

在大多数肠杆菌科成员中,包括大肠杆菌和沙门氏菌,脂多糖核心寡糖主链会被磷酸基团修饰。这些残基提供的负电荷对于维持外膜的屏障功能很重要。缺乏核心庚糖区域和磷酸残基的突变体表现出多种缺陷,统称为深粗糙表型,其特征是外膜结构和功能发生变化。肺炎克雷伯菌的核心中缺乏磷酸残基,但含有半乳糖醛酸。本研究的目的是确定半乳糖醛酸作为关键负电荷来源的作用。通过在gla(KP)中引入突变来靶向UDP-半乳糖醛酸前体合成,从而创建了一个缺乏所有半乳糖醛酸的突变体。Gla(KP)是一种肺炎克雷伯菌UDP-半乳糖醛酸C4差向异构酶,为核心合成提供UDP-半乳糖醛酸。使gla(KP)基因失活,并通过质谱法确定突变体脂多糖的结构。该突变体表现出深粗糙表型的特征,对疏水化合物和多粘菌素B高度敏感,外膜轮廓改变,以及周质酶β-内酰胺酶的释放。这些结果表明,半乳糖醛酸羧基提供的负电荷在建立大肠杆菌和沙门氏菌外膜完整性方面确实发挥了与核心寡糖磷酸残基相当的作用。

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