Papkova S V, Tarasov V A, Abilev S K
Genetika. 1993 Jun;29(6):914-21.
The recA gene from Escherichia coli and Propionibacterium shermanii and lexA gene from E. coli were cloned of the plasmid pBI101 with a broad host range. The correlation of induction of the SOS function and the dose of UV-light, MMS and 4-NQO was studied in E. coli cells carrying the plasmid pJE43. The level of SOS response in recA cells carrying the plasmid pBI101::recA E. coli and pBI101::recA P. shermanii was higher than a SOS response level in EC1000 with a normal recA gene. However, no complete complementation of the SOS function was observed in recA cells when pBI101 with recA and lexA genes was incorporated and under the action of all mutagenic factors.
将来自大肠杆菌和费氏丙酸杆菌的recA基因以及来自大肠杆菌的lexA基因克隆到具有广泛宿主范围的质粒pBI101中。在携带质粒pJE43的大肠杆菌细胞中研究了SOS功能诱导与紫外线、甲基磺酸甲酯(MMS)和4-硝基喹啉-1-氧化物(4-NQO)剂量之间的相关性。携带质粒pBI101::recA大肠杆菌和pBI101::recA费氏丙酸杆菌的recA细胞中的SOS反应水平高于具有正常recA基因的EC1000中的SOS反应水平。然而,当含有recA和lexA基因的pBI101被导入并在所有诱变因素作用下时,在recA细胞中未观察到SOS功能的完全互补。