Schiefer H G, Krauss H, Brunner H, Gerhardt U
J Bacteriol. 1976 Jul;127(1):461-8. doi: 10.1128/jb.127.1.461-468.1976.
Anionic sites on mycoplasma membranes were visualized in the electron microscope by a polycationized ferritin derivative. The technique of thin sectioning was used. Staining prior to fixation led to clustering of ferritin granules on the mycoplasma cell surface. On glutaraldehyde-fixed Mycoplasma mycoides subsp. capri, M. gallisepticum, M. pneumoniae, and Acholeplasma laidlawii, the anionic sites were uniformly distributed over the entire membrane surface. M. hominis did not bind the polycationic ferritin label. Chemical and enzymatic treatments of the mycoplasmas indicated that the anionic sites may be lipid phosphate groups. Isolated M. mycoides subsp. capri membranes were labeled exclusively on only one membrane surface, presumably the outer one. Liposomes prepared from diphosphatidylglycerol and phosphatidylcholine were also labeled by the polycationic ferritin.
通过一种聚阳离子化铁蛋白衍生物在电子显微镜下观察到支原体膜上的阴离子位点。采用了超薄切片技术。固定前染色导致铁蛋白颗粒聚集在支原体细胞表面。在戊二醛固定的蕈状支原体山羊亚种、鸡毒支原体、肺炎支原体和莱氏无胆甾原体上,阴离子位点均匀分布在整个膜表面。人型支原体不结合聚阳离子铁蛋白标记。对支原体的化学和酶处理表明,阴离子位点可能是脂质磷酸基团。分离的蕈状支原体山羊亚种膜仅在一个膜表面被标记,推测是外表面。由二磷脂酰甘油和磷脂酰胆碱制备的脂质体也被聚阳离子铁蛋白标记。