Stepanov A I, Zimina M S, Khlebalina O I, Rabinovich P M, Beburov M I
Genetika. 1976;12(11):162-4.
Hybrid plasmid RP4-ColE1 was obtained by joining DNA plasmids RP4 and ColE1, each of which possessed only one site of restriction for EcoR1. These plasmid molecules were restricted by endonuclease EcoR1 and then treated by ligase. The hybrid plasmid retained the property of transmissibility typical for drug factor resistance RP4. Non-transmissible mutant of the hybrid plasmid selected by the character of the resistance of Escherichia coli C600 (RP4-ColE1) to the phage PRR1 is used for subsequent investigations.
杂种质粒RP4 - ColE1是通过连接DNA质粒RP4和ColE1获得的,这两种质粒对EcoR1都只有一个限制位点。这些质粒分子用核酸内切酶EcoR1进行切割,然后用连接酶处理。杂种质粒保留了耐药因子RP4典型的可转移性。通过大肠杆菌C600(RP4 - ColE1)对噬菌体PRR1的抗性特征筛选出的杂种质粒非转移性突变体用于后续研究。