Laban A, Cohen A
Mol Gen Genet. 1981;184(2):200-7. doi: 10.1007/BF00272905.
The construction of plasmids which facilitate the study of interplasmidic and intraplasmidic recombination is described. In this system, a single recombination event between two mutated Tcr genes on separate plasmids or on one plasmid leads to a change in the host phenotype from sensitivity to resistance to tetracycline. Recombination proficiencies have been determined for different E. coli K-12 strains: both interplasmidic and intraplasmidic recombination are independent of the recBC gene product. RecA mutations decrease the proficiency of plasmidic recombination 40 - 100 fold. Intraplasmidic and interplasmidic recombination via the recE pathway are more efficient than via the recBC pathway. Intraplasmidic recombination, but not interplasmidic recombination via the recE pathway is independent of a functional recA product.
本文描述了有助于研究质粒间和质粒内重组的质粒构建。在该系统中,位于不同质粒或同一质粒上的两个突变Tcr基因之间的单个重组事件会导致宿主表型从对四环素敏感变为耐药。已测定了不同大肠杆菌K-12菌株的重组效率:质粒间和质粒内重组均不依赖于recBC基因产物。RecA突变使质粒重组效率降低40至100倍。通过recE途径的质粒内和质粒间重组比通过recBC途径更有效。通过recE途径的质粒内重组(而非质粒间重组)不依赖于功能性recA产物。