Vinogradov E V, Shashkov A S, Knirel Y A, Kochetkov N K, Dabrowski J, Grosskurth H, Stanislavsky E S, Kholodkova E V
N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow.
Carbohydr Res. 1992 Jul 2;231:1-11. doi: 10.1016/0008-6215(92)84002-a.
The O-specific polysaccharide was obtained by mild degradation of the Salmonella arizonae O61 lipopolysaccharide with acid. It contained 2-acetamido-2-deoxy-D-glucose, 2-acetamidino-2,6-dideoxy-L-galactose (FucAm), and 7-acetamido-3,5,7,9-tetradeoxy-5-[(R)-3-hydroxybutyramido]-D- glycero-L-galacto-nonulosonic acid (Sug). On the basis of partial acid hydrolysis with 0.1 M HCl, solvolysis with anhydrous HF in methanol, and 1H- and 13C-NMR analysis (including 1H/13C inversely correlated spectroscopy for localisation of N-acyl substituents), it was concluded that the O-specific polysaccharide had the following structure. ----3)-alpha-L-FucAm-(1----3)-alpha-D-GlcNAc-(1----8)-beta-Sug+ ++-(2---- The O-antigen of S. arizonae O61 is structurally related to that of Pseudomonas aeruginosa O12, thus explaining the known serological cross-reactivity between these micro-organisms.
通过用酸对亚利桑那沙门氏菌O61脂多糖进行温和降解得到O-特异性多糖。它含有2-乙酰氨基-2-脱氧-D-葡萄糖、2-脒基-2,6-二脱氧-L-半乳糖(FucAm)和7-乙酰氨基-3,5,7,9-四脱氧-5-[(R)-3-羟基丁酰胺基]-D-甘油-L-半乳糖壬糖醛酸(Sug)。基于用0.1 M HCl进行部分酸水解、在甲醇中用无水HF进行溶剂解以及1H-和13C-NMR分析(包括用于N-酰基取代基定位的1H/13C反向相关光谱),得出O-特异性多糖具有以下结构。----3)-α-L-FucAm-(1----3)-α-D-GlcNAc-(1----8)-β-Sug+ ++-(2---- 亚利桑那沙门氏菌O61的O抗原在结构上与铜绿假单胞菌O12的O抗原相关,从而解释了这些微生物之间已知的血清学交叉反应。