Verbenko V N, Kuznetsova L V, Krup'ian E P, Shalguev V I
Genetika. 2009 Oct;45(10):1353-60.
Plasmids pKS5 and pKSrec30 carrying normal and mutant alleles of Deinococcus radiodurans recA gene controlled by the lactose promoter slightly increase radioresistance of Escherichia coli cells with mutations at genes recA and ssb. The RecA protein of D. radiodurans is expressed in E. coli cells, and its synthesis can be supplementary induced. The radioprotective effect of the xenologic protein does not exceed 1.5 times and is essentially to the contribution of plasmid pUC 19-recA1.1 harboring the E. coli recA+ gene in the recovery of resistance of the deltarecA deletion mutant. These data suggest that the expression of D. radiodurans recA gene in E. coli cells does not complement mutations at gene recA in the chromosome possibly due to structural and functional peculiarities of the D. radiodurans RecA protein.
携带受乳糖启动子控制的耐辐射奇异球菌recA基因的正常和突变等位基因的质粒pKS5和pKSrec30,会使recA和ssb基因发生突变的大肠杆菌细胞的辐射抗性略有增加。耐辐射奇异球菌的RecA蛋白在大肠杆菌细胞中表达,其合成可被额外诱导。这种异种蛋白的辐射防护作用不超过1.5倍,并且在很大程度上与携带大肠杆菌recA+基因的质粒pUC 19-recA1.1对δrecA缺失突变体抗性恢复的贡献相当。这些数据表明,耐辐射奇异球菌recA基因在大肠杆菌细胞中的表达可能由于耐辐射奇异球菌RecA蛋白的结构和功能特性,无法弥补染色体上recA基因的突变。