Hase S, Rietschel E T
Eur J Biochem. 1976 Mar 16;63(1):101-7. doi: 10.1111/j.1432-1033.1976.tb10212.x.
A degradation procedure of lipopolysaccharides was worked out which allows the isolation of the reduced backbone of lipid A in a total yield of between 20 and 30%. This procedure was applied to lipopolysaccharides of S forms (Salmonella minnesota, Shigella flexneri 5b, Escherichia coli 086, E. coli 0111, Xanthomonas sinensis, Rhodopseudomonas gelatinosa) and R mutants (Salmonella minnesota, Shigella flexneri, 5b, E. coli BB9 and E. coli EH 100). Chemical analysis, reaction with beta-N-acetyl-glucosaminidase and application of methylation analysis revealed that the lipid A backbone of all strains contains beta 1', 6-linked glucosamine disaccharides carrying two phosphate groups, one in glycosidic and one in ester linkage, a structure, identified previously in the Salmonella minnesota Re mutant.
制定了一种脂多糖降解程序,该程序可分离出脂质A的还原主链,总产率在20%至30%之间。此程序应用于S型(明尼苏达沙门氏菌、福氏志贺氏菌5b、大肠杆菌O86、大肠杆菌O111、中华黄单胞菌、胶状红假单胞菌)和R突变体(明尼苏达沙门氏菌、福氏志贺氏菌5b、大肠杆菌BB9和大肠杆菌EH 100)的脂多糖。化学分析、与β-N-乙酰葡糖胺酶的反应以及甲基化分析的应用表明,所有菌株的脂质A主链均含有β1',6-连接的携带两个磷酸基团的葡糖胺二糖,一个处于糖苷键,一个处于酯键,该结构先前在明尼苏达沙门氏菌Re突变体中已得到确认。