Yamada M, Makino K, Amemura M, Shinagawa H, Nakata A
Department of Experimental Chemotherapy, Osaka University, Japan.
J Bacteriol. 1989 Oct;171(10):5601-6. doi: 10.1128/jb.171.10.5601-5606.1989.
The phoB gene product of Escherichia coli is the transcriptional activator for the genes in the phosphate regulon as well as for phoB itself, all of which are induced by phosphate starvation. The phoR gene product modulates PhoB function in response to the phosphate concentrations in the medium. We quantitatively compared the levels of expression of the phoA, phoB, phoE, and pstS genes in several phoB mutants with different phenotypes by constructing operon fusions of these genes with the gene for chloramphenicol acetyltransferase. Although all the phoB mutants examined had little activator function for phoA, three among the four mutants showed various levels of the activator function for phoB, pstS, and phoE. To study the functional motifs of the PhoB and PhoR proteins, we cloned and sequenced the four classical phoB and six phoR mutant genes. All of the phoB mutations and one of the phoR mutations were missense mutations, and most of the altered amino acids were in the highly conserved amino acids among the regulatory proteins homologous to PhoB or PhoR protein, such as the OmpR, SfrA, and VirG proteins or the EnvZ, CpxA, and VirA proteins. The other five phoR mutations were nonsense mutations.
大肠杆菌的phoB基因产物是磷酸盐调节子中各基因以及phoB自身的转录激活因子,所有这些基因均由磷酸盐饥饿诱导产生。phoR基因产物根据培养基中的磷酸盐浓度调节PhoB的功能。我们通过构建这些基因与氯霉素乙酰转移酶基因的操纵子融合体,定量比较了几种具有不同表型的phoB突变体中phoA、phoB、phoE和pstS基因的表达水平。尽管所检测的所有phoB突变体对phoA几乎没有激活功能,但四个突变体中的三个对phoB、pstS和phoE表现出不同水平的激活功能。为了研究PhoB和PhoR蛋白的功能基序,我们克隆并测序了四个经典的phoB突变基因和六个phoR突变基因。所有的phoB突变和一个phoR突变都是错义突变,大多数改变的氨基酸位于与PhoB或PhoR蛋白同源的调节蛋白中高度保守的氨基酸区域,如OmpR、SfrA和VirG蛋白或EnvZ、CpxA和VirA蛋白。其他五个phoR突变是无义突变。