Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, 119991, Russia.
Biochemistry (Mosc). 2010 Jan;75(1):19-24. doi: 10.1134/s0006297910010037.
On mild acid degradation of the lipopolysaccharide of Escherichia coli O108, the O-polysaccharide was isolated and studied by sugar analysis and one- and two-dimensional 1H- and 13C-NMR spectroscopy. The polysaccharide was found to contain an unusual higher sugar, 5,7-diacetamido-3,5,7,9-tetradeoxy-l-glycero-d-galacto-non-2-ulosonic acid (di-N-acetyl-8-epilegionaminic acid, 8eLeg5Ac7Ac). The following structure of the tetrasaccharide repeating unit of the polysaccharide was established: -->4)-alpha-8eLegp5Ac7Ac-(2-->6)-alpha-D-Galp-(1-->3)-alpha-L-FucpNAc-(1-->3)-alpha-D-GlcpNAc-(1-->. Functions of the E. coli O108 antigen biosynthetic genes, including seven putative genes for synthesis of 8eLeg5Ac7Ac, were assigned by sequencing the O-antigen gene cluster along with comparison with gene databases and known biosynthetic pathways for related nonulosonic acids.
在温和的酸性条件下降解大肠杆菌 O108 的脂多糖,分离并研究了 O-多糖。通过糖分析和一维及二维 1H 和 13C-NMR 光谱研究。发现多糖含有一种不寻常的更高的糖,5,7-二乙酰氨基-3,5,7,9-四脱氧-l-甘油-d-半乳糖-壬-2-酮酸(二-N-乙酰-8-表莱格氨酸酸,8eLeg5Ac7Ac)。多糖的四糖重复单元的结构如下:-->4)-α-8eLegp5Ac7Ac-(2-->6)-α-D-Galp-(1-->3)-α-L-FucpNAc-(1-->3)-α-D-GlcpNAc-(1-->. 通过测序 O-抗原基因簇,并与基因数据库和相关非酮糖酸的已知生物合成途径进行比较,确定了大肠杆菌 O108 抗原生物合成基因的功能,包括 7 个可能用于合成 8eLeg5Ac7Ac 的基因。