Siehnel R J, Worobec E A, Hancock R E
Department of Microbiology, University of British Columbia, Vancouver, Canada.
Mol Microbiol. 1988 May;2(3):347-52. doi: 10.1111/j.1365-2958.1988.tb00038.x.
Plasmids pPBP and pRS-XP containing the cloned genes for the Pseudomonas aeruginosa phosphate-starvation-inducible periplasmic phosphate-binding protein and outer membrane porin P (oprP), respectively, were introduced into various Escherichia coli Pho-regulon regulatory mutants. Using Western immunoblots and specific antisera, the production of both gene products was observed to be under the control of regulatory elements of the E. coli Pho regulon. Sequencing of the region upstream of the translational start site of the oprP gene revealed a 'Pho box' with strong homology to the E. coli consensus 'Pho box', the putative binding site of the PhoB activator. Since P. aeruginosa and E. coli belong to different families and have quite different GC contents, these data suggest strong evolutionary conservation of regulatory elements of the Pho regulon.
分别含有铜绿假单胞菌磷酸盐饥饿诱导型周质磷酸盐结合蛋白和外膜孔蛋白P(oprP)克隆基因的质粒pPBP和pRS-XP被导入各种大肠杆菌Pho调节子调节突变体中。使用Western免疫印迹和特异性抗血清,观察到两种基因产物的产生受大肠杆菌Pho调节子调节元件的控制。oprP基因翻译起始位点上游区域的测序揭示了一个与大肠杆菌共有“Pho框”具有高度同源性的“Pho框”,Pho框是PhoB激活剂的假定结合位点。由于铜绿假单胞菌和大肠杆菌属于不同的家族且GC含量差异很大,这些数据表明Pho调节子的调节元件具有很强的进化保守性。