Livshits V A, Shakulov R S, Zaigraeva G G, Gusiatiner M M, Zhdanova N I
Genetika. 1978 Jun;14(6):947-56.
The substitution of the relA gene mutant allele with wild type allele of this gene in strictly auxotrophic strain of Escherichia coli K-12 GT25, carrying thr B1007 mitation, results in the appearance of the partial dependence of the bacterial growth upon threonine. On the other hand, the introduction of relA mutation into genome of incomplete threonine auxotroph, which was isolated as pseudorevertant from the strict threonine auxotroph CP78, recovered the strict dependency of the growth on the presence of threonine in the medium. The introduction of relA mutation into genome of partial isoleucine auxotroph, carrying a mutation in ilvA gene, reduces the residual activity of threonine deaminase under the conditions of derepression and results in the appearance of strict dependency of bacterial growth on the presence of isoleucine. These data indicate that operons, which control the biosynthesis of threonine and isoleucine, are positively regulated by the product of relA gene. The possibility of using leaky mutations, which lead to incomplete block of these amino acids synthesis, for testing allelic state of relA gene is discussed.
在携带苏氨酸B1007突变的大肠杆菌K - 12 GT25严格营养缺陷型菌株中,将relA基因突变等位基因替换为该基因的野生型等位基因,会导致细菌生长对苏氨酸出现部分依赖性。另一方面,将relA突变引入从不严格苏氨酸营养缺陷型CP78分离出的假回复突变体——不完全苏氨酸营养缺陷型的基因组中,恢复了生长对培养基中苏氨酸存在的严格依赖性。将relA突变引入携带ilvA基因突变的部分异亮氨酸营养缺陷型的基因组中,在去阻遏条件下会降低苏氨酸脱氨酶的残余活性,并导致细菌生长对异亮氨酸的存在出现严格依赖性。这些数据表明,控制苏氨酸和异亮氨酸生物合成的操纵子受到relA基因产物的正调控。讨论了使用导致这些氨基酸合成不完全受阻的渗漏突变来检测relA基因等位基因状态的可能性。