Adlam C, Knights J M, Mugridge A, Lindon J C, Williams J M, Beesley J E
J Gen Microbiol. 1986 Apr;132(4):1079-87. doi: 10.1099/00221287-132-4-1079.
The serotype-specific capsular polysaccharide from two strains of Pasteurella haemolytica serotype A7 organisms was purified and characterized by chemical analysis and by 1H and 13C NMR spectroscopy using one- and two-dimensional methods. The polymer has the repeating unit----3)-beta-2-acetamido-2-deoxygalactopyranose-(1----3)-alpha- 2-acetamido- 2-deoxy-6-O-acetyl-glucopyranose-(1-phosphate----. It was immunogenic (capable of eliciting antibodies) for sheep. Chemical removal of O-acetyl groups destroyed both the ability of the polymer to adhere to sheep erythrocytes at neutral pH and the ability to form immune precipitates with specific antisera. Studies using the protein A-gold technique in the electron microscope showed the polysaccharide to be peripherally localized on the bacterial surface.
从两株溶血巴斯德氏菌A7型菌株中纯化出血清型特异性荚膜多糖,并通过化学分析以及使用一维和二维方法的1H和13C核磁共振光谱对其进行表征。该聚合物具有重复单元----3)-β-2-乙酰氨基-2-脱氧吡喃半乳糖-(1----3)-α-2-乙酰氨基-2-脱氧-6-O-乙酰基-吡喃葡萄糖-(1-磷酸----。它对绵羊具有免疫原性(能够引发抗体)。化学去除O-乙酰基既破坏了聚合物在中性pH下与绵羊红细胞结合的能力,也破坏了其与特异性抗血清形成免疫沉淀的能力。在电子显微镜下使用蛋白A-金技术进行的研究表明,多糖位于细菌表面的外周。