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Electron Microscopy and Viability of Lysostaphin-induced Staphylococcal Spheroplasts Protoplast-like Bodies and Protoplasts

机译:电镜和溶葡萄球菌素诱导的葡萄球菌原生质体原生质体样体和原生质体的生存力。

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摘要

The cell walls of a selected isolate of Staphylococcus aureus FDA 209P were observed undergoing progressive disintegration when exposed to lysostaphin (1 unit/ml) in 24% NaCl solution. Electron micrographs of ultrathin sections of test cells after exposure to lysostaphin for 2 min showed only superficial evidence of lytic damage. However, an average of 89% of these cells were osmotically fragile, and 21% were damaged beyond their capacity to regenerate cell walls and to grow as normal staphylococci. The 68% (average) of the osmotically fragile cells which retained the capacity to revert to normal staphylococci were designated spheroplasts. Neither perforations of the cell walls nor separation of the cell walls from the plasma membranes were observed in the micrographs of these 2-min spheroplasts. Thus, it appears that the osmotic fragility of these and possibly all lysostaphin-induced staphylococcal spheroplasts results from the hydrolysis of a critical number of the pentapeptide cross-linkages of the murein of the cell wall. Electron micrographs of cells exposed to lysostaphin for 5 to 10 min showed perforations and more extensive damage, including the separation of walls from the plasma membranes and the disintegration of large sections of the walls. Smaller numbers of spheroplasts (21 and 8%) were recovered from these 5- and 10-min preparations; those recovered probably represent cells which were attacked more slowly than the majority by the lytic enzyme. The nonrevertible, osmotically fragile cells that retained segments of cell wall were designated protoplast-like bodies. After 20-min exposure to lysostaphin, all of the cell wall was digested away from most of the cells, and true staphylococcal protoplasts were produced. These lysostaphin-induced, osmotically fragile forms appear to have different osmotic properties from the staphylococcal “protoplasts” reported by other investigators and should serve as the basis for a variety of fundamental investigations.
机译:当暴露于24%NaCl溶液中的溶葡萄球菌素(1单位/毫升)时,观察到所选金黄色葡萄球菌FDA 209P分离株的细胞壁进行性崩解。暴露于溶葡萄球菌素2分钟后,测试细胞超薄切片的电子显微照片仅显示了溶血性损伤的表面证据。但是,这些细胞中平均有89%处于渗透脆性状态,其中21%的细胞超出了其再生细胞壁并以正常葡萄球菌生长的能力而受到破坏。保留了恢复正常葡萄球菌能力的渗透压脆弱细胞的68%(平均)称为原生质球。在这些2分钟原生质球的显微照片中,既未观察到细胞壁的穿孔也未观察到细胞壁与质膜的分离。因此,似乎这些和可能的溶葡萄球菌素诱导的葡萄球菌原生质球的渗透脆性是由细胞壁中的鼠李糖蛋白的关键数目的五肽交联的水解引起的。暴露于溶葡萄球菌素5至10分钟的细胞的电子显微照片显示出穿孔和更大范围的损害,包括从质膜上分离壁和壁的大部分分解。从5分钟和10分钟的制剂中回收的原生质球数量较少(21和8%);那些被回收的细胞可能代表比大多数裂解酶攻击慢的细胞。保留了细胞壁部分的不可逆的渗透性脆性细胞称为原生质体样体。暴露于溶葡萄球菌素20分钟后,所有细胞壁都被大部分细胞消化掉,并产生了真正的葡萄球菌原生质体。这些溶葡萄球菌素诱导的渗透性脆性形式似乎具有与其他研究者报告的葡萄球菌“原生质体”不同的渗透特性,并应作为各种基础研究的基础。

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