Adlam C, Knights J M, Mugridge A, Lindon J C, Baker P R, Beesley J E, Spacey B, Craig G R, Nagy L K
J Gen Microbiol. 1984 Sep;130(9):2415-26. doi: 10.1099/00221287-130-9-2415.
The serotype-specific capsular polysaccharide from two strains of Pasteurella haemolytica serotype A1 organisms was purified and characterized by chemical analysis and NMR spectroscopy. The polymer has the structure----3)-O-(2-acetamido-2-deoxy-4-O-acetyl-beta-D-mannopyranos yluronic acid)-(1----4)-O-(2-acetamido-2-deoxy-beta-D-mannopyranose)-(1----. The polysaccharide was immunogenic (able to evoke production of antibodies) for sheep but not for rabbits. Immuno electron-microscopy studies using the Protein A-gold technique showed the polysaccharide to be peripherally located on the bacterial surface. Reduction, oxidation and de-O-acetylation of the polymer did not appear to alter its immunological precipitability with specific antiserum, but all three treatments destroyed its ability to adhere to sheep erythrocytes at neutral pH. De-N-acetylation of the polymer destroyed both immunological precipitability and erythrocyte adherence.
从两株溶血巴斯德氏菌A1型菌株中纯化出血清型特异性荚膜多糖,并通过化学分析和核磁共振光谱对其进行表征。该聚合物具有以下结构:----3)-O-(2-乙酰氨基-2-脱氧-4-O-乙酰基-β-D-甘露糖醛酸)-(1----4)-O-(2-乙酰氨基-2-脱氧-β-D-甘露糖)-(1----。这种多糖对绵羊具有免疫原性(能够诱发抗体产生),但对兔子没有免疫原性。使用蛋白A-金技术进行的免疫电子显微镜研究表明,该多糖位于细菌表面的外周。聚合物的还原、氧化和去O-乙酰化似乎并未改变其与特异性抗血清的免疫沉淀性,但这三种处理均破坏了其在中性pH下与绵羊红细胞结合的能力。聚合物的去N-乙酰化破坏了免疫沉淀性和红细胞结合能力。