Knirel' Iu A, Kocharova N A, Shashkov A S, Dmitriev B A, Kochetkov N K
Bioorg Khim. 1986 Oct;12(10):1384-90.
Polysaccharide chains of P. aeruginosa O5a, b, c, O5a, b, d and O5a, d (Lányi classification) lipopolysaccharides contain D-xylose, N-acetyl-D-fucosamine (FucNAc) and a derivative of 5,7-diamino-3,5,7,9-tetradeoxy-L-glycero-L-manno-nonulosonic acid (pseudaminic acid, PseN2) carrying acetyl or (R)-3-hydroxybutyryl (Hb) and formyl (Fm) groups as N-acyl substituents. Degradation of the lipopolysaccharides with dilute acetic acid caused depolymerisation of the polysaccharide chains as a result of cleavage of glycosidic linkage of pseudaminic acid to give trisaccharides representing chemical repeating units of the polysaccharides. Basing on analysis of the trisaccharides using 1H and 13C NMR spectroscopy and mass-spectrometry, the following structures of the polysaccharide chains were established: (Formula: see text). O5a, d polysaccharide is identical to P. aeruginosa immunotype 6 O-specific polysaccharide.
铜绿假单胞菌O5a、b、c、O5a、b、d和O5a、d(兰伊分类法)脂多糖的多糖链含有D-木糖、N-乙酰-D-岩藻糖胺(FucNAc)以及5,7-二氨基-3,5,7,9-四脱氧-L-甘油-L-甘露-壬糖醛酸(假氨基糖酸,PseN2)的一种衍生物,该衍生物带有乙酰基或(R)-3-羟基丁酰基(Hb)和甲酰基(Fm)基团作为N-酰基取代基。用稀乙酸降解脂多糖会导致多糖链解聚,这是由于假氨基糖酸的糖苷键断裂,生成了代表多糖化学重复单元的三糖。基于使用1H和13C核磁共振光谱法以及质谱法对三糖的分析,确定了多糖链的以下结构:(化学式:见正文)。O5a、d多糖与铜绿假单胞菌免疫型6 O-特异性多糖相同。