Knirel Yuriy A, Qian Chengqian, Senchenkova Sofya N, Guo Xi, Shashkov Alexander S, Chizhov Alexander O, Perepelov Andrei V, Liu Bin
N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 119991 Moscow, Russia.
Key Laboratory of Molecular Microbiology and Technology, Ministry of Education, TEDA Institute of Biological Sciences and Biotechnology, Nankai University, TEDA, 300457 Tianjin, China.
Int J Biol Macromol. 2016 Jul;88:578-85. doi: 10.1016/j.ijbiomac.2016.04.025. Epub 2016 Apr 13.
Fine structure of the O-polysaccharide chain of the lipopolysaccharide (O-antigen) defines the serospecificity of bacterial cells, which is the basis for O-serotyping of medically and agriculturally important gram-negative bacteria including Escherichia coli. In order to obtain the O-polysaccharide for structural analysis, the lipopolysaccharide was isolated from cells of E. coli O84a by phenol/water extraction and degraded with mild acid. However, the O-polysaccharide was cleaved at a highly acid-labile β-l-fucopyranosyl phosphate (β-l-Fucp-1-P) linkage to give mainly a pentasaccharide that corresponded to the O-polysaccharide repeat. Therefore, the lipopolysaccharide and the pentasaccharide as well as their O-deacylated derivatives were studied using sugar analysis, NMR spectroscopy, and (for oligosaccharides) ESI HR MS, and the O84-polysaccharide structure was established. The O-polysaccharide is distinguished by the presence of β-l-Fucp-1-P and randomly di-O-acetylated 6-deoxy-d-talose, which are found for the first time in natural carbohydrates. The gene cluster for the O84-antigen biosynthesis was analysed and its content was found to be consistent with the O-polysaccharide structure.
脂多糖(O抗原)的O-多糖链的精细结构决定了细菌细胞的血清特异性,这是对包括大肠杆菌在内的医学和农业上重要的革兰氏阴性菌进行O-血清分型的基础。为了获得用于结构分析的O-多糖,通过苯酚/水萃取从大肠杆菌O84a细胞中分离出脂多糖,并用弱酸进行降解。然而,O-多糖在高度酸不稳定的β-L-岩藻糖基磷酸酯(β-L-Fucp-1-P)键处断裂,主要生成一种与O-多糖重复序列相对应的五糖。因此,利用糖分析、核磁共振光谱以及(针对寡糖的)电喷雾高分辨质谱对脂多糖和五糖及其O-脱酰基衍生物进行了研究,并确定了O84-多糖的结构。O-多糖的特点是存在β-L-Fucp-1-P和随机二-O-乙酰化的6-脱氧-D-塔罗糖,这些在天然碳水化合物中首次被发现。对O84-抗原生物合成的基因簇进行了分析,发现其内容与O-多糖结构一致。