Schell M A
Gene. 1985;36(3):301-9. doi: 10.1016/0378-1119(85)90185-4.
The positively regulated nah and sal operons of the NAH7 plasmid from Pseudomonas putida encode the enzymes for metabolism of naphthalene via salicylate. To study their coordinate regulation, a 6-kb DNA fragment containing the entire nahA gene (encoding naphthalene dioxygenase), the gene of the nah operon, was cloned into a RSF1010 plasmid derivative. Analysis of expression of nahA from the nah promoter in either Escherichia coli or Pseudomonas putida showed that a 1.6-kb DNA fragment from the nahR (nah operon regulatory locus) region was required in trans for (i) induction by salicylate; (ii) high-level expression of nahA, and (iii) complementation of nahR- mutants. Measurement of transcription in induced and uninduced P. putida showed that induction of the nah and sal operons occurred at the transcriptional level. The trans-acting positive regulatory gene, nahR, however, was constitutively transcribed.
恶臭假单胞菌NAH7质粒上正向调控的nah和sal操纵子编码通过水杨酸代谢萘的酶。为了研究它们的协同调控,将包含整个nahA基因(编码萘双加氧酶)的6 kb DNA片段,即nah操纵子的基因,克隆到RSF1010质粒衍生物中。对大肠杆菌或恶臭假单胞菌中nah启动子的nahA表达分析表明,来自nahR(nah操纵子调控位点)区域的1.6 kb DNA片段在反式作用中是必需的,用于:(i)水杨酸诱导;(ii)nahA的高水平表达,以及(iii)nahR突变体的互补。对诱导和未诱导的恶臭假单胞菌中的转录进行测量表明,nah和sal操纵子的诱导发生在转录水平。然而,反式作用的正向调控基因nahR是组成型转录的。