Tai J Y, Gotschlich E C, Lancefield R C
J Exp Med. 1979 Jan 1;149(1):58-66. doi: 10.1084/jem.149.1.58.
Group B streptococcus type Ib (strain H36B) was subjected to digestion with extracellular muralytic enzymes prepared from Streptomyces albus. Type Ib-specific polysaccharide antigen was isolated from the lysate by alcohol precipitation and Sepharose 6B chromatography. The purified type Ib antigen has a Kd value of 0.31 on a Sepharose 4B column and contains four sugars, galactose, glucose, N-acetyl glucosamine, and sialic acid in a molar ratio of 2.05:0.86:1.00:0.90. Acid treatment (pH 2.0) of this polysaccharide results in partial degradation of the antigen (Kd = 0.41 on Sepharose 4B) with the loss of 93% of the sialic acid. The molar ratio of the remaining sugars in the polysaccharide remains identical to that in the native one. This suggests that the sialic acid is at the terminal position in the molecule. Both intact and acid-treated antigen cross-react with some type Ia and type Ic antisera as a result of the common Iabc determinant, but not with type II and type III antisera. Absorption studies indicate that Ib-specific determinant and Iabc determinant are on the same molecule and that sialic acid is not the cross-reactive determinant.
B群Ib型链球菌(菌株H36B)用从白色链霉菌制备的细胞外壁溶解酶进行消化。通过乙醇沉淀和琼脂糖6B柱色谱法从裂解物中分离出Ib型特异性多糖抗原。纯化的Ib型抗原在琼脂糖4B柱上的Kd值为0.31,含有四种糖,半乳糖、葡萄糖、N-乙酰葡糖胺和唾液酸,摩尔比为2.05:0.86:1.00:0.90。对该多糖进行酸处理(pH 2.0)会导致抗原部分降解(在琼脂糖4B上Kd = 0.41),唾液酸损失93%。多糖中剩余糖的摩尔比与天然多糖中的相同。这表明唾液酸位于分子的末端位置。由于共同的Iabc决定簇,完整和酸处理的抗原都与一些Ia型和Ic型抗血清发生交叉反应,但不与II型和III型抗血清发生交叉反应。吸收研究表明,Ib特异性决定簇和Iabc决定簇在同一分子上,且唾液酸不是交叉反应决定簇。