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waaY、waaQ和waaP在大肠杆菌脂多糖修饰中的作用及其在稳定外膜形成中的作用

Involvement of waaY, waaQ, and waaP in the modification of Escherichia coli lipopolysaccharide and their role in the formation of a stable outer membrane.

作者信息

Yethon J A, Heinrichs D E, Monteiro M A, Perry M B, Whitfield C

机构信息

Department of Microbiology, University of Guelph, Guelph, Ontario N1G 2W1, Canada.

出版信息

J Biol Chem. 1998 Oct 9;273(41):26310-6. doi: 10.1074/jbc.273.41.26310.

DOI:10.1074/jbc.273.41.26310
PMID:9756860
Abstract

The waaY, waaQ, and waaP genes are located in the central operon of the waa (formerly rfa) locus on the chromosome of Escherichia coli. This locus contains genes whose products are involved in the assembly of the core region of the lipopolysaccharide molecule. In the R1 core prototype strain, E. coli F470, there are nine genes in this operon, and all but waaY, waaQ, and waaP have been assigned function. In this study, the waaY, waaQ, and waaP genes were independently mutated by insertion of a non-polar antibiotic resistance cassette, and the structures of the resulting mutant core oligosaccharides were determined by chemical analyses and phosphorus-nuclear magnetic resonance spectroscopy. All three of these mutations were shown to affect the modification of the heptose region of the core, a region whose structure is critical to outer membrane stability. Mutation of waaY resulted in a core oligosaccharide devoid of phosphate on HepII. Mutation of waaQ resulted in loss of the branch HepIII residue on HepII and impeded the activity of WaaY. Mutation of waaP resulted in loss of phosphoryl substituents on HepI and obviated WaaQ and WaaY activity. Only mutation of waaP resulted in hypersensitivity to novobiocin and sodium dodecyl sulfate, a characteristic of deep-rough mutations.

摘要

waaY、waaQ和waaP基因位于大肠杆菌染色体上waa(以前称为rfa)位点的中央操纵子中。该位点包含其产物参与脂多糖分子核心区域组装的基因。在R1核心原型菌株大肠杆菌F470中,该操纵子中有九个基因,除waaY、waaQ和waaP外,其他基因的功能均已确定。在本研究中,通过插入非极性抗生素抗性盒使waaY、waaQ和waaP基因独立突变,并通过化学分析和磷核磁共振光谱法确定所得突变核心寡糖的结构。结果表明,所有这三种突变均影响核心庚糖区域的修饰,该区域的结构对外膜稳定性至关重要。waaY突变导致核心寡糖在HepII上没有磷酸基团。waaQ突变导致HepII上的分支HepIII残基缺失,并阻碍了WaaY的活性。waaP突变导致HepI上的磷酰取代基缺失,并消除了WaaQ和WaaY的活性。只有waaP突变导致对新生霉素和十二烷基硫酸钠过敏,这是深度粗糙突变的一个特征。

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