Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow.
Biochemistry (Mosc). 2011 Jul;76(7):774-9. doi: 10.1134/S0006297911070078.
The O-polysaccharide (O-antigen) of Salmonella enterica O51 was isolated by mild acid degradation of the lipopolysaccharide and its structure was established using sugar analysis and NMR spectroscopy. The O-antigen of Escherichia coli O23, whose structure was elucidated earlier, possesses a similar structure and differs only in the presence of an additional lateral α-D-Glcp residue at position 6 of the GlcNAc residue in the main chain. Sequencing of the O-antigen gene clusters of S. enterica O51 and E. coli O23 revealed the same genes with a high-level similarity. By comparison with opened gene databases, all genes expected for the synthesis of the common structure of the two O-antigens were assigned functions. It is suggested that the gene clusters of both bacteria originated from a common ancestor, whereas the O-antigen modification in E. coli O23, which, most probably, is induced by prophage genes outside the gene cluster, could be introduced after the species divergence.
肠沙门氏菌 O51 的 O-多糖(O-抗原)通过脂多糖的温和酸降解分离得到,并通过糖分析和 NMR 光谱确定其结构。大肠杆菌 O23 的 O-抗原结构较早被阐明,其结构相似,仅在主链中 GlcNAc 残基的 6 位上存在额外的侧向α-D-Glcp 残基。肠沙门氏菌 O51 和大肠杆菌 O23 的 O-抗原基因簇的测序揭示了具有高度相似性的相同基因。通过与开放基因数据库的比较,为两种 O-抗原的共同结构合成预期的所有基因都被赋予了功能。这表明这两种细菌的基因簇都起源于一个共同的祖先,而大肠杆菌 O23 的 O-抗原修饰,很可能是由基因簇外的噬菌体基因诱导的,可能是在物种分化后引入的。