Danilevich V N, Stepanshin Iu G, Volozhantsev N V, Amosenko F A, Golub E I
Antibiotiki. 1978 Apr;23(4):337-41.
Integration of R-factor RP4 with the chromosome of E. coli was studied with the use of replication thermosensitive mutant pEG1 of this factor. It was found that the frequency of integration of factor pEG1 containing the ampicillin transposone Tn1 with the chromosome of bacteria JC411 carrying transposone Tn1 previously inserted into it was very high and markedly exceeded that of its insertion into the same chromosome but not carrying this transposone. The frequency of factor pEG1 insertion into the chromosome of bacteria JC 1553 rec A defective with respect to genetic recombination was less than 2.10(-5) and did not depend on the presence of transposone Tn1 in it. Probably, insertion of factor RP4 into the bacterial chromosome may be realized through the rec A-dependent process of recombination between transposone Tn1 previously translocated into the chromosome and the same transposone contained in R-factor.
利用该因子的复制温度敏感突变体pEG1研究了R因子RP4与大肠杆菌染色体的整合。发现含有氨苄青霉素转座子Tn1的因子pEG1与先前已插入转座子Tn1的细菌JC411的染色体整合频率非常高,明显超过其插入同一但未携带该转座子的染色体的频率。因子pEG1插入在遗传重组方面有缺陷的细菌JC 1553 rec A染色体的频率小于2×10⁻⁵,且不依赖于其中转座子Tn1的存在。可能,因子RP4插入细菌染色体可通过先前易位到染色体中的转座子Tn1与R因子中所含相同转座子之间依赖rec A的重组过程来实现。