Birnbaum S E, Affronti L F
J Bacteriol. 1968 Feb;95(2):559-64. doi: 10.1128/jb.95.2.559-564.1968.
The identity of a heteropolysaccharide from cell walls of Mycobacterium tuberculosis H37Ra with Seibert's tuberculopolysaccharide I was demonstrated by thin-layer chromatography, chemical analysis, and antigenic tests. The polysaccharide of M. kansasii was shown to be identical with that of M. tuberculosis. Defatted cells were disintegrated by ultrasonic treatment in the presence of glass beads; cell walls were obtained by differential ultracentrifugation. Ethyl alcohol-precipitated carbohydrate extracts were analyzed for protein and nucleic acid; these impurities were removed. Tuberculopolysaccharide I from the mycobacterial culture filtrate is probably derived from a lipopolysaccharide of the cell wall, which is partially removed by chloroform in the intact state. Alkaline extraction releases additional polysaccharide, in varying degrees of association with cell wall murein.
通过薄层色谱法、化学分析和抗原测试证实,结核分枝杆菌H37Ra细胞壁中的一种杂多糖与赛伯特结核多糖I具有相同的特性。堪萨斯分枝杆菌的多糖被证明与结核分枝杆菌的多糖相同。在玻璃珠存在的情况下,通过超声处理使脱脂细胞破碎;通过差速超速离心获得细胞壁。对乙醇沉淀的碳水化合物提取物进行蛋白质和核酸分析;去除这些杂质。分枝杆菌培养滤液中的结核多糖I可能来源于细胞壁的脂多糖,在完整状态下,脂多糖会被氯仿部分去除。碱性提取会释放出额外的多糖,其与细胞壁胞壁质的结合程度各不相同。