Venkatesh T V, Reddy M A, Das H K
Genetic Engineering Unit, Jawaharlal Nehru University, New Delhi, India.
Mol Gen Genet. 1990 Dec;224(3):482-6. doi: 10.1007/BF00262444.
The recA gene of Azotobacter vinelandii was isolated from a genomic library by heterologous complementation of an Escherichia coli recA mutation for resistance to UV radiation. The A. vinelandii recA gene was localized on adjacent PstI fragments of 1.3 and 1.7 kb. The cloned A. vinelandii recA gene was functionally analogous to the E. coli recA gene. It was also able to complement the E. coli recA mutation for homologous recombination. A recA deletion mutant of A. vinelandii was constructed. This mutant was sensitive to DNA-damaging agents like UV rays, methyl methane sulfonate (MMS) and nalidixic acid and was deficient in homologous recombination.
通过对大肠杆菌recA突变体进行紫外线辐射抗性的异源互补,从基因组文库中分离出了棕色固氮菌(Azotobacter vinelandii)的recA基因。棕色固氮菌recA基因定位在相邻的1.3 kb和1.7 kb的PstI片段上。克隆的棕色固氮菌recA基因在功能上类似于大肠杆菌recA基因。它也能够互补大肠杆菌recA突变体进行同源重组。构建了棕色固氮菌recA缺失突变体。该突变体对紫外线、甲基磺酸甲酯(MMS)和萘啶酸等DNA损伤剂敏感,并且在同源重组方面存在缺陷。