Department of Applied Chemistry, National Defense Academy, Hashirimizu, Yokosuka, Japan.
Mol Genet Genomics. 2010 Sep;284(3):197-205. doi: 10.1007/s00438-010-0559-y. Epub 2010 Jul 17.
In response to environmental phosphate limitation, the transcriptional activator PhoB of Escherichia coli (E. coli) activates transcription of the phosphate regulon (pho regulon) genes that are involved in phosphate utilization. At least 31 of pho regulon genes have been identified and well characterized in E. coli by numerous studies using non-pathogenic K-12 derivative strains. In this study, we searched for PhoB-regulated promoters from a lacZ-fused genomic library of the E. coli O157:H7 Sakai in an attempt to find novel pho regulon genes in the strain. A promoter region located upstream of a gene cluster (ecs0540-ecs0544) that mapped within one of the strain-specific chromosomal regions of the E. coli O157:H7 was identified. By further in vivo analysis with various subclones of the 5'-flanking region, it was suggested that the ecs0540 transcription was regulated by at least two promoters, an upstream PhoB-regulated promoter and a downstream constitutive promoter. S1 mapping and footprinting experiments revealed two transcription start sites and a sequence similar to the consensus sequence of PhoB binding, respectively. Bioinformatic analysis of the ecs0540-ecs0544 genes showed that these genes were highly homologous to the Escherichia fergusonii (E. fergusonii) siiCA-DA operon encoding a 718 kDa giant protein (SiiEA) and its cognate type I secretion system. In addition, a highly repetitive region and motifs that are shared among RTX (repeats in toxin) toxin family were found in the amino acid sequence of these giant proteins. Our finding is the first example of a member of the pho regulon identified in the O157:H7 strain-specific chromosomal region.
针对环境磷酸盐限制,大肠杆菌(E. coli)的转录激活因子 PhoB 激活参与磷酸盐利用的磷酸盐调节基因(pho 调节基因)的转录。通过使用非致病性 K-12 衍生株进行的多项研究,已经在大肠杆菌中鉴定和充分表征了至少 31 个 pho 调节基因。在这项研究中,我们从大肠杆菌 O157:H7 Sakai 的 lacZ 融合基因组文库中搜索 PhoB 调节启动子,试图在该菌株中找到新的 pho 调节基因。鉴定了一个位于基因簇(ecs0540-ecs0544)上游的启动子区域,该基因簇位于大肠杆菌 O157:H7 的菌株特异性染色体区域之一内。通过进一步用该 5'侧翼区域的各种亚克隆进行体内分析,表明 ecs0540 转录受到至少两个启动子的调节,一个上游 PhoB 调节启动子和一个下游组成型启动子。S1 作图和足迹实验分别揭示了两个转录起始位点和一个类似于 PhoB 结合的保守序列。ecs0540-ecs0544 基因的生物信息学分析表明,这些基因与 Escherichia fergusonii(E. fergusonii) siiCA-DA 操纵子高度同源,该操纵子编码一个 718 kDa 的巨大蛋白(SiiEA)及其同源的 I 型分泌系统。此外,在这些巨大蛋白的氨基酸序列中发现了高度重复的区域和 RTX(毒素重复)毒素家族共有的基序。我们的发现是在 O157:H7 菌株特异性染色体区域中鉴定出 pho 调节基因成员的首例。