Yamada M, Makino K, Shinagawa H, Nakata A
Department of Experimental Chemotherapy, Osaka University, Japan.
Mol Gen Genet. 1990 Feb;220(3):366-72. doi: 10.1007/BF00391740.
The phoR gene is a bifunctional regulatory gene for the phosphate regulon of Escherichia coli. It acts as a negative regulator in the presence of excess phosphate and as a positive regulator with limited phosphate, through modification of PhoB protein. We constructed several phoR genes, with various deletions in the 5' regions, which were regulated by the trp-lac hybrid promoter. The PhoR1084 and PhoR1159 proteins that lack the 83 and 158 N-terminal amino acids, respectively, retained the positive function for the expression of phoA that codes for alkaline phosphatase, but lacked the negative function. The PhoR1263 protein that lacks the 262 N-terminal amino acids was deficient in both functions. An antiserum against PhoR1084 protein was prepared. Western blot analysis of the subcellular fractions obtained by differential centrifugation indicated that the intact PhoR and PhoR1084 proteins are located in the inner membrane and cytoplasmic fractions, respectively. The results suggest that PhoR protein is anchored to the cytoplasmic membrane by the amino-terminal region.
phoR基因是大肠杆菌磷酸盐调节子的双功能调节基因。在磷酸盐过量存在时,它作为负调节子起作用;在磷酸盐有限时,它通过修饰PhoB蛋白作为正调节子起作用。我们构建了几个在5'区域有不同缺失的phoR基因,这些基因由trp-lac杂合启动子调控。分别缺失83个和158个N端氨基酸的PhoR1084和PhoR1159蛋白,保留了对编码碱性磷酸酶的phoA表达的正功能,但缺乏负功能。缺失262个N端氨基酸的PhoR1263蛋白在这两种功能上均有缺陷。制备了针对PhoR1084蛋白的抗血清。对通过差速离心获得的亚细胞组分进行的蛋白质免疫印迹分析表明,完整的PhoR蛋白和PhoR1084蛋白分别位于内膜和细胞质组分中。结果表明,PhoR蛋白通过其氨基末端区域锚定在细胞质膜上。