Kliachko E V, Bochkanov S S, Shakulov R S
Biokhimiia. 1983 Jul;48(7):1095-102.
The threonine biosynthetic operon transcription in E. coli cells during balanced growth was studied. The rate of threonine-mRNA synthesis was measured by hybridization of impulse-labelled RNA with pYN 1107 DNA carrying the structural threonine genes A, B, C. It was shown that threonine-mRNA synthesis depends on bacterial growth rate being maximal at mu = 0.8 doublings per hour. The influence of the ppGpp on the bacterial growth rate and threonine-mRNA synthesis rate was demonstrated, using spoT-mutants and strains with several relA gene copies. The rate of threonine-mRNA synthesis is maximal at the ppGpp level of about 50-60 pmole/A450. The deviation from this ppGpp optimum level results in inhibition of the threonine-mRNA synthesis. Thus, ppGpp appears to be involved in metabolic regulation of operon transcription. A mechanism of negative regulation of threonine-mRNA synthesis by high concentrations of ppGpp is discussed.
对大肠杆菌细胞在平衡生长期间苏氨酸生物合成操纵子转录进行了研究。通过脉冲标记的RNA与携带苏氨酸结构基因A、B、C的pYN 1107 DNA杂交来测量苏氨酸 - mRNA的合成速率。结果表明,苏氨酸 - mRNA的合成取决于细菌生长速率,在μ = 0.8次/小时的倍增率时达到最大值。利用spoT突变体和具有多个relA基因拷贝的菌株,证明了ppGpp对细菌生长速率和苏氨酸 - mRNA合成速率的影响。在ppGpp水平约为50 - 60 pmole/A450时,苏氨酸 - mRNA的合成速率最大。偏离此ppGpp最佳水平会导致苏氨酸 - mRNA合成受到抑制。因此,ppGpp似乎参与了操纵子转录的代谢调控。讨论了高浓度ppGpp对苏氨酸 - mRNA合成的负调控机制。