Yang G C, Schrank G D, Freeman B A
J Bacteriol. 1977 Feb;129(2):1121-8. doi: 10.1128/jb.129.2.1121-1128.1977.
A procedure is described for the purification of the cores of flagella sheared from Vibrio cholerae. V. cholerae is a monotrichous organism whose flagellar core (FC) is enclosed within a sheath. The purification procedure consists of several cycles of differential centrifugation and cesium chloride density-gradient ultracentrifugation in the presence of a neutral detergent, Triton X-100. Purity of the FC preparations is assessed by electron microscopy, polyacrylamide gel electrophoresis, and chemical analysis. The purified FC preparations are devoid of flagellar sheaths and free from detectable cell wall and cytoplasmic contamination. Antibody prepared in rabbits against purified FC reacts with the flagellum of intact V. cholerae or purified FC as seen by ferritin-labeled antibody studies. Purified FC is composed of a single protein subunit with an estimated molecular weight of 45,000 g/mol and a density of about 1.3 g/cm3.
本文描述了一种从霍乱弧菌中纯化剪切鞭毛核心的方法。霍乱弧菌是一种单鞭毛菌,其鞭毛核心(FC)被包裹在鞘中。纯化过程包括在中性去污剂Triton X-100存在下进行的几个循环的差速离心和氯化铯密度梯度超速离心。通过电子显微镜、聚丙烯酰胺凝胶电泳和化学分析评估FC制剂的纯度。纯化的FC制剂没有鞭毛鞘,且没有可检测到的细胞壁和细胞质污染。通过铁蛋白标记抗体研究发现,用兔制备的针对纯化FC的抗体与完整霍乱弧菌的鞭毛或纯化的FC发生反应。纯化的FC由单个蛋白质亚基组成,估计分子量为45,000 g/mol,密度约为1.3 g/cm³。