Rodriguez R L, West R W
J Bacteriol. 1984 Mar;157(3):764-71. doi: 10.1128/jb.157.3.764-771.1984.
The control region for the histidine operon of Klebsiella pneumoniae was cloned and analyzed with the Escherichia coli promoter-probe plasmid pPV33. A restriction fragment which contained the his control region was identified by its ability to activate the tetracycline resistance (Tcr) gene on this vector. Expression of Tcr by bacteria containing the his promoter-active plasmid was found to be under the attenuation control of the his promoter. DNA sequence analysis of the his control region revealed a base sequence homology of approximately 86% of the analogous DNA sequences of E. coli and Salmonella typhimurium. Most of the base alterations in the K. pneumoniae DNA sequence were found to reside in regions flanking the transcriptional and translational regulatory sites.
利用大肠杆菌启动子探针质粒pPV33对肺炎克雷伯菌组氨酸操纵子的调控区进行了克隆和分析。通过其激活该载体上四环素抗性(Tcr)基因的能力,鉴定出一个含有组氨酸调控区的限制性片段。发现含有组氨酸启动子活性质粒的细菌中Tcr的表达受组氨酸启动子的衰减控制。组氨酸调控区的DNA序列分析显示,其与大肠杆菌和鼠伤寒沙门氏菌的类似DNA序列的碱基序列同源性约为86%。肺炎克雷伯菌DNA序列中的大多数碱基变化位于转录和翻译调控位点两侧的区域。