Wilson C R, Totten P A, Baldwin J N
Appl Environ Microbiol. 1978 Aug;36(2):368-74. doi: 10.1128/aem.36.2.368-374.1978.
A rapid, reproducible, mini-volume assay capable of detecting staphylococcal plasmid DNA in the range of 0.8 to 32 megadaltons has been developed. The assay employs lysostaphin-mediated lysis of cells followed by a short, low-speed centrifugation and does not require treatment with ribonuclease or protease or deproteinization with phenol. A period of only 24 h may be required to detect the presence and size of a plasmid once an organism has been isolated. This method has been used to study the plasmid ecology of Staphylococcus epidermidis and to correlate the presence or absence of plasmids with tetracycline, chloramphenicol, neomycin, penicillin, and cadmium resistances.
已开发出一种快速、可重复的微量检测方法,能够检测大小在0.8至32兆道尔顿范围内的葡萄球菌质粒DNA。该检测方法采用溶葡萄球菌素介导的细胞裂解,随后进行短时间低速离心,且不需要用核糖核酸酶或蛋白酶处理,也不需要用苯酚进行脱蛋白处理。一旦分离出微生物,检测质粒的存在和大小可能仅需24小时。该方法已用于研究表皮葡萄球菌的质粒生态学,并将质粒的存在与否与四环素、氯霉素、新霉素、青霉素和镉抗性相关联。