Ouchane S, Kaplan S
Department of Microbiology and Molecular Genetics, University of Texas Medical School, Houston, Texas 77030, USA.
J Biol Chem. 1999 Jun 11;274(24):17290-6. doi: 10.1074/jbc.274.24.17290.
Photosynthesis gene expression in Rhodobacter sphaeroides is controlled in part by the two-component (Prr) regulatory system composed of a membrane-bound sensor kinase (PrrB) and a response regulator (PrrA). Hydropathy profile-based computer analysis predicted that the PrrB polypeptide could contain six membrane-spanning domains at its amino terminus and a hydrophilic, cytoplasmic carboxyl terminus. Both the localization and the topology of the PrrB sensor kinase have been studied by generating a series of gene fusions with the Escherichia coli periplasmically localized alkaline phosphatase and the cytoplasmic beta-galactosidase. Eighteen prrB-phoA and five prrB-lacZ fusions were constructed and expressed in both E. coli and R. sphaeroides. Enzymatic activity assays and immunoblot analyses were performed to identify and to localize the different segments of PrrB in the membrane. The data obtained in E. coli generally correlated with the data obtained in R. sphaeroides and support the computer predictions. On the basis of the theoretical model and the results provided by these studies, a topological model for the membrane localization of the PrrB polypeptide is proposed.
球形红杆菌中的光合作用基因表达部分受由膜结合传感器激酶(PrrB)和响应调节因子(PrrA)组成的双组分(Prr)调节系统控制。基于亲水性图谱的计算机分析预测,PrrB多肽在其氨基末端可能含有六个跨膜结构域和一个亲水性的胞质羧基末端。通过产生一系列与大肠杆菌周质定位的碱性磷酸酶和胞质β-半乳糖苷酶的基因融合体,对PrrB传感器激酶的定位和拓扑结构进行了研究。构建了18个prrB-phoA和5个prrB-lacZ融合体,并在大肠杆菌和球形红杆菌中表达。进行了酶活性测定和免疫印迹分析,以鉴定和定位PrrB在膜中的不同片段。在大肠杆菌中获得的数据通常与在球形红杆菌中获得的数据相关,并支持计算机预测。基于这些研究提供的理论模型和结果,提出了PrrB多肽膜定位的拓扑模型。