Knirel' Iu A, Paramonov N A, Vinogradov E V, Shashkov A S, Dmitriev B A
Bioorg Khim. 1986 Dec;12(12):1649-57.
Mild acid degradation of lipopolysaccharide from Pseudomonas aeruginosa O(3a), 3d, 3f (Lányi classification) afforded O-specific polysaccharide containing N-acetyl-D-fucosamine, 2,3-diacetamido-2,3-dideoxy-D-mannuronic acid, 3-acetamidino-2-acetamido-2,3-dideoxy-L-guluronic and D-mannuronic acid as well as O-acetyl groups. On the basis of O-deacetylation, selective cleavage with anhydrous fluoride, chemical transformation of the oligosaccharides obtained (hydrolysis or reductive deamination of the acetamidino group into acetamido or ethylamino group, respectively) and analysis by 13C NMR spectroscopy, it was concluded that the polysaccharide is built up mainly by trisaccharide repeating units of types A and B in the ratio approximately 2:1: (Formula: see text). The units of both types most probably enter the same polymeric chain. If so, such a hybrid structure can be accounted for by incompleteness of epimerization at C5 of the acetamidino derivative of mannuronic acid at the polymer level in the course of biosynthesis of this polysaccharide.
对铜绿假单胞菌O(3a)、3d、3f(兰伊分类法)的脂多糖进行温和酸降解,得到了含有N-乙酰-D-岩藻糖胺、2,3-二乙酰氨基-2,3-二脱氧-D-甘露糖醛酸、3-脒基-2-乙酰氨基-2,3-二脱氧-L-古洛糖醛酸和D-甘露糖醛酸以及O-乙酰基的O-特异性多糖。基于O-脱乙酰化、用无水氟化物进行选择性裂解、对所得寡糖进行化学转化(分别将脒基水解或还原脱氨为乙酰氨基或乙氨基)以及通过13C NMR光谱分析,得出该多糖主要由A和B型三糖重复单元以大约2:1的比例构成(化学式:见原文)。两种类型的单元很可能进入同一聚合物链。如果是这样,这种杂化结构可以通过在该多糖生物合成过程中聚合物水平上甘露糖醛酸脒基衍生物C5处的差向异构化不完全来解释。