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Transfer of plasmids pBR322 and pBR325 in wastewater from laboratory strains of Escherichia coli to bacteria indigenous to the waste disposal system.

机译:将废水中的质粒pBR322和pBR325从大肠杆菌的实验室菌株转移到废物处理系统固有的细菌中。

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摘要

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.
机译:将含有质粒pBR325(或pBR322)的大肠杆菌实验室菌株与大肠杆菌的动员菌株(含有结合质粒R100-1)和细菌的受体菌株共同培养。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均作为受体。将pBR质粒转移到受体菌株中的过程是在L肉汤或灭菌废水中共孵育25小时的过程中发生的。废水中的转移频率要低几个数量级。共孵育后,受体表现出质粒编码的表型特征和改变的质粒图谱,如纯化质粒DNA的琼脂糖凝胶电泳所示。

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