Sens D, Natter W, Garvin R T, James E
Mol Gen Genet. 1977 Sep 21;155(1):7-18. doi: 10.1007/BF00268555.
The cell-free transcription of the argF and argI genes of the arginine biosynthetic regions is described using an S-30 system capable of coupled in vitro transcription-translation. Template DNA isolated from two independently isolated arginine transducing phages was used in this work. Steady state mRNA synthesis was observed which was attributed to RNAase degradation. Regulation of argF mRNA synthesis, directed by the argF gene carried on the specialized transducing phage phi80dargF is effected to the extent of at least 95% by the arginine holorepressor at the transcriptional stage and at least 80% of the regulation of the expression of the argI gene is mediated at the transcriptional stage. Evidence is presented which indicates that the arginine holorepressor prevents RNA polymerase from binding to the arginine promoter and suggests that the operator and promoter sites may overlap.
利用能够进行体外转录-翻译偶联的S-30系统,描述了精氨酸生物合成区域中argF和argI基因的无细胞转录。本研究使用了从两个独立分离的精氨酸转导噬菌体中分离得到的模板DNA。观察到了稳态mRNA合成,这归因于RNA酶的降解。由特殊转导噬菌体phi80dargF携带的argF基因指导的argF mRNA合成的调节,在转录阶段至少95%受精氨酸全阻遏物的影响,并且argI基因表达调节的至少80%在转录阶段介导。提供的证据表明精氨酸全阻遏物可阻止RNA聚合酶与精氨酸启动子结合,并表明操纵子和启动子位点可能重叠。