首页> 外文OA文献 >Overexpression of the waaZ Gene Leads to Modification of the Structure of the Inner Core Region of Escherichia coli Lipopolysaccharide, Truncation of the Outer Core, and Reduction of the Amount of O Polysaccharide on the Cell Surface
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Overexpression of the waaZ Gene Leads to Modification of the Structure of the Inner Core Region of Escherichia coli Lipopolysaccharide, Truncation of the Outer Core, and Reduction of the Amount of O Polysaccharide on the Cell Surface

机译:waaZ基因的过表达导致大肠杆菌脂多糖内核区域结构的修饰,外核的截断和细胞表面O多糖含量的减少

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摘要

The waa gene cluster is responsible for the biosynthesis of the lipopolysaccharide (LPS) core region in Escherichia coli and Salmonella. Homologs of the waaZ gene product are encoded by the waa gene clusters of Salmonella enterica and E. coli strains with the K-12 and R2 core types. Overexpression of WaaZ in E. coli and S. enterica led to a modified LPS structure showing core truncations and (where relevant) to a reduction in the amount of O-polysaccharide side chains. Mass spectrometry and nuclear magnetic resonance spectroscopy were used to determine the predominant LPS structures in an E. coli isolate with an R1 core (waaZ is lacking from the type R1 waa gene cluster) with a copy of the waaZ gene added on a plasmid. Novel truncated LPS structures, lacking up to 3 hexoses from the outer core, resulted from WaaZ overexpression. The truncated molecules also contained a KdoIII residue not normally found in the R1 core.
机译:waa基因簇负责大肠杆菌和沙门氏菌中脂多糖(LPS)核心区域的生物合成。 waaZ基因产物的同源物由肠炎沙门氏菌和大肠杆菌菌株(具有K-12和R2核心类型)的waa基因簇编码。 WaaZ在大肠杆菌和肠炎链球菌中的过表达导致修饰的LPS结构显示核心截短,并且(在相关情况下)导致O多糖侧链数量减少。使用质谱和核磁共振波谱法确定带有R1核心(R1 waa型基因簇中缺少waaZ)的大肠杆菌分离株中的主要LPS结构,并将waaZ基因的副本添加到质粒上。 WaaZ过度表达导致新型截短的LPS结构,从外部核心最多缺少3个己糖。截短的分子还包含Rdo核心中通常不存在的KdoIII残基。

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