Hill J C, Peterson N R, Weiss E
Infect Immun. 1972 Apr;5(4):612-21. doi: 10.1128/iai.5.4.612-621.1972.
Spheroplast membranes (spheroplast envelopes) of strain 2091 of group B Neisseria meningitidis were prepared by a procedure that included lysozyme treatment of the cells and osmotic lysis of the resulting spheroplasts. Electron microscopy revealed that the membranes consisted of two unit layers, generally parallel to each other. The membrane preparation migrated as a single component in a 40 to 70% sucrose gradient and consisted of 62% protein, 28% lipid, 9% ribonucleic acid, small amounts of carbohydrate, hexosamine, and deoxyribonucleic acid. When 1 or 10 mug (dry weight) was injected intravenously into rabbits, a mild pyrogenic reaction was elicited. In immunodiffusion tests, immune rabbit serum prepared against spheroplast membranes produced three major precipitin lines, with the homologous antigen solubilized with sodium dodecyl sulfate, and a single line with untreated antigen. The immune serum also reacted with a cell wall antigen, and to a lesser extent with some of the cytoplasmic antigens. Succinate dehydrogenase and reduced nicotinamide adenine dinucleotide (NADH) oxidase activities were found to be associated with the spheroplast membranes. NADH dehydrogenase also was associated with the membranes but was gradually released and recovered in other fractions. Glutamate-oxaloacetate transaminase, glutamate, glucose-6-phosphate, and isocitrate dehydrogenase activities were not found in the membrane preparation. About one-third of these enzymatic activities were recovered in the supernatant fluid after the sedimentation of the spheroplasts and two-thirds were recovered in the cytoplasmic fraction. N-acetylneuraminic acid (NAN)-condensing enzyme and cytidine monophosphate-NAN synthesizing enzyme also were identified in this organism. These enzymes were not associated with the membranes and were recovered from extracts from whole cells, spheroplasts, or cells exposed to osmotic shock, as well as from spheroplast supernatant and shock fluids. It is concluded that the spheroplast membranes of the strain of meningococci used in these studies are typical of those recovered from gram-negative bacteria.
B群脑膜炎奈瑟菌2091菌株的原生质球膜(原生质球包膜)通过包括用溶菌酶处理细胞以及对所得原生质球进行渗透裂解的程序制备。电子显微镜显示这些膜由通常彼此平行的两个单位层组成。膜制剂在40%至70%的蔗糖梯度中作为单一成分迁移,由62%的蛋白质、28%的脂质、9%的核糖核酸、少量的碳水化合物、己糖胺和脱氧核糖核酸组成。当1或10微克(干重)静脉注射到兔子体内时,会引发轻微的发热反应。在免疫扩散试验中,针对原生质球膜制备的免疫兔血清产生了三条主要沉淀线,其中同源抗原用十二烷基硫酸钠溶解,与未处理抗原产生一条沉淀线。免疫血清还与细胞壁抗原反应,并且在较小程度上与一些细胞质抗原反应。发现琥珀酸脱氢酶和还原型烟酰胺腺嘌呤二核苷酸(NADH)氧化酶活性与原生质球膜相关。NADH脱氢酶也与膜相关,但逐渐释放并在其他组分中回收。在膜制剂中未发现谷氨酸 - 草酰乙酸转氨酶、谷氨酸、葡萄糖 - 6 - 磷酸和异柠檬酸脱氢酶活性。这些酶活性的约三分之一在原生质球沉淀后的上清液中回收,三分之二在细胞质组分中回收。在该生物体中还鉴定出N - 乙酰神经氨酸(NAN)缩合酶和胞苷单磷酸 - NAN合成酶。这些酶与膜无关,并且从全细胞、原生质球或经受渗透休克的细胞提取物以及原生质球上清液和休克液中回收。结论是,这些研究中使用的脑膜炎球菌菌株的原生质球膜是从革兰氏阴性细菌中回收的典型膜。