Michiels J, Vande Broek A, Vanderleyden J
F.A. Janssens Laboratory of Genetics, University of Leuven, Heverlee, Belgium.
Mol Gen Genet. 1991 Sep;228(3):486-90. doi: 10.1007/BF00260644.
A recombinant lambda phage carrying the recA gene of Rhizobium phaseoli was isolated from a R. phaseoli genomic library by complementation of the Fec- phenotype of the recombinant phage in Escherichia coli. When expressed in E. coli, the cloned recA gene was shown to restore resistance to both UV irradiation and the DNA alkylating agent methyl methanesulphonate (MMS). The R. phaseoli recA gene also promoted homologous recombination in E. coli. The cloned recA gene was only weakly inducible in E. coli recA strains by DNA damaging agents. The DNA sequence of the R. phaseoli recA gene was determined and compared with published recA sequences. No LexA-binding site was detected in the R. phaseoli recA upstream region.
通过重组噬菌体在大肠杆菌中对Fec-表型进行互补,从菜豆根瘤菌基因组文库中分离出携带菜豆根瘤菌recA基因的重组λ噬菌体。当在大肠杆菌中表达时,克隆的recA基因显示出能恢复对紫外线照射和DNA烷化剂甲磺酸甲酯(MMS)的抗性。菜豆根瘤菌recA基因也促进了大肠杆菌中的同源重组。在大肠杆菌recA菌株中,克隆的recA基因仅被DNA损伤剂微弱诱导。测定了菜豆根瘤菌recA基因的DNA序列,并与已发表的recA序列进行了比较。在菜豆根瘤菌recA上游区域未检测到LexA结合位点。