Platz A, Sjöberg B M
J Bacteriol. 1980 Aug;143(2):561-8. doi: 10.1128/jb.143.2.561-568.1980.
Recombinant plasmids containing all or part of the genetic region of Escherichia coli coding for the two subunits of ribonucleoside diphosphate reductase (proteins B1 and B2) were constructed with the aid of the multicopy plasmid pBR322. Two of these plasmids (pPS1 and pPS2) appeared to carry both a regulator and the complete structural information for the enzyme and, after transformation of E. coli, directed a 10- to 20-fold overproduction of both proteins B1 and B2. The other plasmids (pPS101 and pPS201) carried structural information for only protein B2. Cells carrying pPS1 and pPS2 showed a 5- to 500-fold increased resistance against the drug hydroxyurea. This establishes that in E. coli the inhibition of deoxyribonucleic acid synthesis by hydroxyurea is fully explained by its action on ribonucleotide reductase.
借助多拷贝质粒pBR322构建了含有大肠杆菌编码核糖核苷二磷酸还原酶两个亚基(蛋白质B1和B2)的全部或部分遗传区域的重组质粒。其中两个质粒(pPS1和pPS2)似乎携带了该酶的一个调节子和完整的结构信息,在转化大肠杆菌后,指导蛋白质B1和B2两者过量产生10到20倍。其他质粒(pPS101和pPS201)仅携带蛋白质B2的结构信息。携带pPS1和pPS2的细胞对药物羟基脲的抗性提高了5到500倍。这表明在大肠杆菌中,羟基脲对脱氧核糖核酸合成的抑制完全可以由其对核糖核苷酸还原酶的作用来解释。