Gealt M A, Chai M D, Alpert K B, Boyer J C
Appl Environ Microbiol. 1985 Apr;49(4):836-41. doi: 10.1128/aem.49.4.836-841.1985.
Laboratory strains of Escherichia coli containing plasmid pBR325 (or pBR322) were coincubated with a mobilizer strain of E. coli (containing the conjugative plasmid R100-1) and a recipient strain of bacteria. Bacterial strains isolated from raw wastewater or a plasmid-free E. coli laboratory strain served as recipients. Transfer of the pBR plasmid into the recipient strain occurred during a 25-h coincubation in either L broth or sterilized wastewater; transfer frequencies were several orders of magnitude lower in wastewater. After the coincubation, recipients exhibited both plasmid-encoded phenotypic characteristics and an altered plasmid profile, as shown by agarose gel electrophoresis of purified plasmid DNA.
含有质粒pBR325(或pBR322)的大肠杆菌实验室菌株与大肠杆菌的一个动员菌株(含有接合质粒R100-1)和一个细菌受体菌株共同孵育。从原废水中分离出的细菌菌株或无质粒的大肠杆菌实验室菌株用作受体。在L肉汤或灭菌废水中进行25小时的共同孵育期间,pBR质粒转移到受体菌株中;在废水中的转移频率要低几个数量级。共同孵育后,受体表现出质粒编码的表型特征以及改变的质粒图谱,这通过纯化质粒DNA的琼脂糖凝胶电泳得以显示。