Calero S, Garriga X, Barbé J
Department of Genetics and Microbiology, Autonomous University of Barcelona, Bellaterra, Spain.
FEMS Microbiol Lett. 1993 Jun 1;110(1):65-70. doi: 10.1111/j.1574-6968.1993.tb06296.x.
A fusion between the lexA gene of Pseudomonas aeruginosa and Pseudomonas putida and the lacZ gene was constructed in vitro and cloned in a mini-Tn5 transposon derivative to obtain chromosomal insertions which enable to quantitatively examine their transcriptional regulation in both Pseudomonas and E. coli. Analysis of DNA damage-mediated induction of these lexA-lacZ fusions showed that expression of P. putida and P. aeruginosa lexA genes was always higher and earlier than the expression of the lexA gene of E. coli. Furthermore, and in contrast to the lexA gene fusion of E. coli, the rates and extent of the induction of lexA gene fusion of P. putida and P. aeruginosa were largely independent of the UV doses applied. The behaviour of the lexA-lacZ fusions of two Pseudomonas species was the same regardless of whether they were inserted into their own chromosome or into E. coli.
体外构建了铜绿假单胞菌和恶臭假单胞菌的lexA基因与lacZ基因的融合体,并克隆到一个mini-Tn5转座子衍生物中,以获得染色体插入片段,从而能够在假单胞菌和大肠杆菌中定量检测它们的转录调控。对这些lexA-lacZ融合体的DNA损伤介导的诱导分析表明,恶臭假单胞菌和铜绿假单胞菌lexA基因的表达总是高于且早于大肠杆菌lexA基因的表达。此外,与大肠杆菌的lexA基因融合体不同,恶臭假单胞菌和铜绿假单胞菌lexA基因融合体的诱导速率和程度在很大程度上与所施加的紫外线剂量无关。两种假单胞菌的lexA-lacZ融合体,无论插入自身染色体还是大肠杆菌染色体,其行为都是相同的。