Huber T W, Schuhardt V T
J Bacteriol. 1970 Jul;103(1):116-9. doi: 10.1128/jb.103.1.116-119.1970.
Staphylococcus aureus FDA 209P cells when suspended in 24% (w/v) NaCl were rendered osmotically fragile by exposure to lysostaphin for time intervals ranging from 2 to 60 min. Such cells were analyzed chemically and serologically for evidence of residual cell wall material, were plated in hypertonic sucrose medium to determine revertibility to normal, and were subjected to manometric studies to determine metabolic capabilities. Most of the cells (95%) which were exposed to lysostaphin (0.5 or 1.0 unit/ml) for 2 min, although osmotically fragile, retained their cell wall hexosamine and were capable of reverting to osmotically normal cells when plated in hypertonic medium. Cells exposed to lysostaphin for 5 and 10 min also retained much of their cell wall hexosamine, but lost their ability to revert to normal staphylococci. Cells exposed to lysostaphin for 2 to 10 min continued to react with staphylococcus anti-k antiserum. Complete removal of cell wall hexosamine was attained only after exposure to lysostaphin for 20 min or more; these cells failed to react with k antiserum. Lysostaphin-induced L-type colonies were extremely rare in our experiments, even if incubation times and media were optimal for their detection. Lysostaphin-induced staphylococcal protoplasts were as active metabolically in manometric studies as were untreated staphylococci.
金黄色葡萄球菌FDA 209P细胞悬浮于24%(w/v)氯化钠中时,通过暴露于溶葡萄球菌素2至60分钟的不同时间间隔而变得渗透压敏感。对这些细胞进行化学和血清学分析,以寻找残留细胞壁物质的证据,接种于高渗蔗糖培养基中以确定恢复正常的能力,并进行压力测量研究以确定代谢能力。大多数暴露于溶葡萄球菌素(0.5或1.0单位/毫升)2分钟的细胞,尽管渗透压敏感,但仍保留其细胞壁己糖胺,并且接种于高渗培养基中时能够恢复为渗透压正常的细胞。暴露于溶葡萄球菌素5分钟和10分钟的细胞也保留了大部分细胞壁己糖胺,但失去了恢复为正常葡萄球菌的能力。暴露于溶葡萄球菌素2至10分钟的细胞继续与葡萄球菌抗k抗血清发生反应。仅在暴露于溶葡萄球菌素20分钟或更长时间后才完全去除细胞壁己糖胺;这些细胞不与k抗血清发生反应。在我们的实验中,溶葡萄球菌素诱导的L型菌落极其罕见,即使培养时间和培养基对其检测最为适宜。溶葡萄球菌素诱导的葡萄球菌原生质体在压力测量研究中的代谢活性与未处理的葡萄球菌相同。