Perel'man B V, Kolibaba L G, Shakulov R S
Biokhimiia. 1978 Dec;43(12):2183-8.
The synthesis of rRNA in the ribosome-free extracts S100 of E. coli cells was about 30 and 60% of total transcript when E. coli DNA and DNA of lambda rifd 18 phage were used respectively. The synthesis of rRNA with both types of DNA was inhibited in 5--6 times by 0.8 mM ppGpp, while the synthesis of total RNA decreased only two-fold. Selective action of ppGpp on rRNA synthesis is due to the intensive inhibition of the initiation of transcription of the appropriate genes. The rRNA synthesis and the inhibitory capacity of ppGpp was shown to dependend on the KCl concentration in S 100 extracts. These results indicate that ppGpp is the main factor controlling rRNA synthesis both in isolated RNA polymerase system and in cell-free extracts.
当分别使用大肠杆菌DNA和λrifd 18噬菌体DNA时,大肠杆菌细胞无核糖体提取物S100中rRNA的合成量分别约为总转录量的30%和60%。0.8 mM的ppGpp可使两种DNA的rRNA合成受到5至6倍的抑制,而总RNA合成仅下降两倍。ppGpp对rRNA合成的选择性作用是由于其对相应基因转录起始的强烈抑制。结果表明,rRNA合成及ppGpp的抑制能力取决于S100提取物中的KCl浓度。这些结果表明,ppGpp是在分离的RNA聚合酶系统和无细胞提取物中控制rRNA合成的主要因素。