Amemura M, Makino K, Shinagawa H, Kobayashi A, Nakata A
J Mol Biol. 1985 Jul 20;184(2):241-50. doi: 10.1016/0022-2836(85)90377-8.
The pstA(=phoT), pstB and phoU genes are situated at 84 minutes on the Escherichia coli genetic map. All of them are involved in the negative regulation of the phosphate regulon, and all of them except for phoU are required for the binding-protein-mediated, highly specific phosphate transport. We have determined the DNA sequence of about 4 X 10(3) bases of chromosomal segment containing these genes. Four translational reading frames (TRFs) were detected in the region. We attempted to assign the TRFs to the mutant alleles. Plasmids were constructed so that each contained only one of the TRFs, downstream from the lac promoter, to be used for the complementation tests. By this test, TRF-2, TRF-3 and TRF-4 were identified with the pstA(=phoT), pstB and phoU genes, respectively. Alkaline phosphatase-constitutive mutations of the two strains in our collection were complemented by the plasmid with the TRF-1 region. Therefore, we propose to designate the allele phoW. The order of the genes in this region has been established to be phoS-phoW-pstA(=phoT)-pstB-phoU counterclockwise on the E. coli genetic map.
pstA(=phoT)、pstB和phoU基因位于大肠杆菌遗传图谱的84分钟处。它们都参与磷酸盐调节子的负调控,除phoU外,其余基因都是结合蛋白介导的高度特异性磷酸盐转运所必需的。我们测定了包含这些基因的约4×10³个碱基的染色体片段的DNA序列。在该区域检测到四个翻译阅读框(TRF)。我们试图将这些TRF与突变等位基因进行匹配。构建了质粒,使每个质粒仅包含一个位于lac启动子下游的TRF,用于互补试验。通过该试验,分别将TRF-2、TRF-3和TRF-4与pstA(=phoT)、pstB和phoU基因进行了匹配。我们收集的两个菌株的碱性磷酸酶组成型突变由含有TRF-1区域的质粒互补。因此,我们提议将该等位基因命名为phoW。已确定该区域基因在大肠杆菌遗传图谱上按逆时针方向的顺序为phoS-phoW-pstA(=phoT)-pstB-phoU。