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Genetic Analysis of Lipooligosaccharide Core Biosynthesis in Campylobacter jejuni 81-176

机译:空肠弯曲菌81-176中脂寡糖核心生物合成的遗传分析

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摘要

We report isolation and characterization of Campylobacter jejuni 81-176 lgtF and galT lipooligosaccharide (LOS) core mutants. It has been suggested that the lgtF gene of C. jejuni encodes a two-domain glucosyltransferase that is responsible for the transfer of a β-1,4-glucose residue on heptosyltransferase I (Hep I) and for the transfer of a β-1,2-glucose residue on Hep II. A site-specific mutation in the lgtF gene of C. jejuni 81-176 resulted in expression of a truncated LOS, and complementation of the mutant in trans restored the core mobility to that of the wild type. Mass spectrometry and nuclear magnetic resonance of the truncated LOS confirmed the loss of two glucose residues, a β-1,4-glucose on Hep I and a β-1,2-glucose on Hep II. Mutation of another gene, galT, encoding a glycosyltransferase, which maps outside the region defined as the LOS biosynthetic locus in C. jejuni 81-176, resulted in loss of the β-(1,4)-galactose residue and all distal residues in the core. Both mutants invaded intestinal epithelial cells in vitro at levels comparable to the wild-type levels, in marked contrast to a deeper inner core waaC mutant. These studies have important implications for the role of LOS in the pathogenesis of Campylobacter-mediated infection.
机译:我们报告了空肠弯曲菌81-176 lgtF和galT脂寡糖(LOS)核心突变体的分离和表征。已经提出,空肠弯曲杆菌的lgtF基因编码一个双结构域的葡糖基转移酶,其负责转移庚糖基转移酶I(Hep I)上的β-1,4-葡萄糖残基和转移β-1。 Hep II上的-2-葡萄糖残基。空肠弯曲杆菌81-176的lgtF基因中的位点特异性突变导致截短的LOS的表达,并且突变体的反式互补将核心迁移率恢复为野生型。截短的LOS的质谱和核磁共振证实了两个葡萄糖残基的损失,Hep I上的一个β-1,4-葡萄糖和Hep II上的一个β-1,2-葡萄糖。编码糖基转移酶的另一个基因galT的突变位于空肠弯曲杆菌81-176中定义为LOS生物合成基因座的区域之外,导致β-(1,4)-半乳糖残基和所有末端残基的丢失核心。两种突变体均以与野生型水平相当的水平在体外侵袭肠上皮细胞,与更深的内在核心waaC突变体形成鲜明对比。这些研究对LOS在弯曲杆菌介导的感染的发病机理中的作用具有重要意义。

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