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Cold Stress Makes Escherichia coli Susceptible to Glycopeptide Antibiotics by Altering Outer Membrane Integrity

机译:寒冷胁迫通过改变外膜完整性使大肠杆菌对糖肽类抗生素敏感

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A poor understanding of the mechanisms by which antibiotics traverse the outer membrane remains a considerable obstacle to the development of novel Gram-negative antibiotics. Herein, we demonstrate that the Gram-negative bacterium Escherichia coli becomes susceptible to the narrow-spectrum antibiotic vancomycin during growth at low temperatures. Heterologous expression of an Enterococcus vanHBX vancomycin resistance cluster in E. coli confirmed that the mechanism of action was through inhibition of peptidoglycan biosynthesis. To understand the nature of vancomycin permeability, we screened for strains of E. coli that displayed resistance to vancomycin at low temperature. Surprisingly, we observed that mutations in outer membrane biosynthesis suppressed vancomycin activity. Subsequent chemical analysis of lipopolysaccharide from vancomycin-sensitive and -resistant strains confirmed that suppression was correlated with truncations in the core oligosaccharide of lipopolysaccharide. These unexpected observations challenge the current understanding of outermembrane permeability, and provide new chemical insights into the susceptibility of E. coli to glycopeptide antibiotics.
机译:对抗生素穿越外膜的机制的了解不足,仍然是新型革兰氏阴性抗生素发展的一大障碍。在本文中,我们证明了革兰氏阴性细菌大肠杆菌在低温生长过程中对窄谱抗生素万古霉素敏感。大肠杆菌肠球菌vanHBX万古霉素耐药簇的异源表达证实了其作用机制是通过抑制肽聚糖的生物合成。为了了解万古霉素渗透性的本质,我们筛选了在低温下对万古霉素具有抗性的大肠杆菌菌株。令人惊讶地,我们观察到外膜生物合成中的突变抑制了万古霉素活性。随后对万古霉素敏感和耐药菌株的脂多糖进行化学分析,证实抑制作用与脂多糖核心寡糖的截短有关。这些意想不到的发现挑战了目前对外膜通透性的理解,并为大肠杆菌对糖肽抗生素的敏感性提供了新的化学见解。

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