Owttrim G W, Coleman J R
J Bacteriol. 1987 May;169(5):1824-9. doi: 10.1128/jb.169.5.1824-1829.1987.
A recA-like gene isolated from the cyanobacterium Anabaena variabilis was cloned and partially characterized. When introduced into Escherichia coli recA mutants, the 7.5-kilobase-pair plasmid-borne DNA insert restored resistance to methyl methanesulfonate and UV irradiation, as well as recombination proficiency when measured by Hfr-mediated conjugation. The cyanobacterial recA gene restored spontaneous but not mitomycin C-induced prophage production. Restriction analysis and subcloning yielded a 1.5-kilobase-pair Sau3A fragment which also restored methylmethane sulfonate resistance and coded for a 38- to 40-kilodalton polypeptide when expressed in an in vitro transcription-translation system.
从多变鱼腥蓝细菌中分离出的一个类recA基因被克隆并进行了部分特性分析。当将其导入大肠杆菌recA突变体时,这个7.5千碱基对的质粒携带的DNA插入片段恢复了对甲磺酸甲酯和紫外线照射的抗性,以及通过高频重组(Hfr)介导的接合作用测定的重组能力。蓝细菌recA基因恢复了自发的原噬菌体产生,但未恢复丝裂霉素C诱导的原噬菌体产生。限制性分析和亚克隆产生了一个1.5千碱基对的Sau3A片段,该片段也恢复了对甲磺酸甲酯的抗性,并且在体外转录-翻译系统中表达时编码一种38至40千道尔顿的多肽。