Siehnel R J, Egli C, Hancock R E
Department of Microbiology, University of British Columbia, Vancouver, Canada.
Mol Microbiol. 1992 Aug;6(16):2319-26. doi: 10.1111/j.1365-2958.1992.tb01407.x.
The oprO gene of Pseudomonas aeruginosa codes for a polyphosphate-specific porin and terminates 458 bp upstream of the start codon for the phosphate-specific porin OprP. OprO was found to be expressed only under phosphate-starvation conditions in both wild-type and oprP::Tn501 mutant P. aeruginosa strains. However, unlike the rest of the genes of the Pho regulon, including oprP, expression of oprO required cells to be in the stationary growth phase in addition to phosphate starvation. Wild-type P. aeruginosa cells were grown in fermentor culture under these conditions and fractionated by selective solubilization in octylpolyoxyethylene detergent solution. Solubilized OprO was separated from OprP by application to a Mono Q FPLC column and elution with a salt gradient and shown to be functionally identical to cloned OprO produced in Escherichia coli. DNA sequencing of oprO showed the gene product to be highly homologous to OprP, with 76% identity and 16% conserved substitutions. Most genes of the Pho regulon possess a modified -35 region called the Pho box. Two such elements, separated by 4 bp were found in oprO. DNA sequencing also revealed a second Pho box in the oprP gene with the same spacing.
铜绿假单胞菌的oprO基因编码一种多聚磷酸盐特异性孔蛋白,位于磷酸盐特异性孔蛋白OprP起始密码子上游458 bp处终止。研究发现,在野生型和oprP::Tn501突变型铜绿假单胞菌菌株中,oprO仅在磷酸盐饥饿条件下表达。然而,与包括oprP在内的Pho调控子的其他基因不同,oprO的表达除了需要磷酸盐饥饿外,还要求细胞处于稳定生长期。野生型铜绿假单胞菌细胞在这些条件下进行发酵罐培养,并通过在辛基聚氧乙烯洗涤剂溶液中选择性增溶进行分级分离。通过应用Mono Q FPLC柱并用盐梯度洗脱,将增溶的OprO与OprP分离,结果表明其功能与在大肠杆菌中产生的克隆OprO相同。oprO的DNA测序显示该基因产物与OprP高度同源,同一性为76%,保守替换率为16%。Pho调控子的大多数基因都有一个称为Pho框的修饰-35区域。在oprO中发现了两个这样的元件,间隔4 bp。DNA测序还揭示了oprP基因中具有相同间隔的第二个Pho框。