Shub D A
Mol Gen Genet. 1975;137(2):171-80. doi: 10.1007/BF00341683.
A cell free protein synthesizing system, derived from E. coli, is shown to be a quantitiative assay system for messenger RNA extracted from B. subtilis infected with bacteriophage SPO1. DNA-directed protein synthesis in this system is shown to be limited mostly to those proteins whose messages are contained in early RNA. A phage induced enzyme, dCMP deaminase, is shown to be dependent on appearance of a class mRNA made in vivo in response to new initiations of transcription dependent on prior synthesis of phage induced protein. Control of the enzyme synthesized in the cell free system is contrasted with in vivo control, and an estimate of "read-through" by RNA polymerase in vitro is presented.
一种源自大肠杆菌的无细胞蛋白质合成系统,被证明是用于定量分析从感染噬菌体SPO1的枯草芽孢杆菌中提取的信使RNA的分析系统。该系统中DNA指导的蛋白质合成主要限于那些其信息包含在早期RNA中的蛋白质。一种噬菌体诱导酶,dCMP脱氨酶,被证明依赖于体内合成的一类mRNA的出现,该mRNA是响应于依赖于噬菌体诱导蛋白质的先前合成的新转录起始而产生的。将无细胞系统中合成的酶的调控与体内调控进行了对比,并给出了RNA聚合酶体外“通读”的估计值。