Yang J, Pittard J
Department of Microbiology, University of Melbourne, Parkville, Victoria, Australia.
J Bacteriol. 1987 Oct;169(10):4710-5. doi: 10.1128/jb.169.10.4710-4715.1987.
The tyrB gene from Escherichia coli K-12 was cloned and sequenced, and the transcriptional start point of tyrB was determined by primer extension. By using a fusion plasmid in which the lacZ structural gene is transcribed from the tyrB promoter, it was shown that the expression of tyrB is controlled at the transcriptional level by the TyrR protein, with tyrosine as corepressor. The fusion plasmid was used to isolate mutants in which the repression of tyrB had been abolished. The tyrB promoter-operator region of these mutants was sequenced, and the tyrB operator was identified. A comparison between the tyrB operator and those of the other genes belonging to the tyrR regulon is presented.
克隆并测序了来自大肠杆菌K-12的tyrB基因,通过引物延伸法确定了tyrB的转录起始点。利用一种融合质粒,其中lacZ结构基因由tyrB启动子转录,结果表明tyrB的表达在转录水平上受TyrR蛋白控制,酪氨酸作为共阻遏物。该融合质粒用于分离tyrB阻遏作用已被消除的突变体。对这些突变体的tyrB启动子-操纵子区域进行了测序,并鉴定出tyrB操纵子。本文对tyrB操纵子与tyrR调节子中其他基因的操纵子进行了比较。