Ferrando-May E, Brustmann B, Oesterhelt D
Max-Planck-Institut für Biochemie, Martinsried, Germany.
Mol Microbiol. 1993 Sep;9(5):943-53. doi: 10.1111/j.1365-2958.1993.tb01224.x.
Expression of the gene encoding the halobacterial photoreceptor sensory rhodopsin I (SRI), sopI, was studied by means of homologous gene targeting. A sopI- Halobacterium salinarium mutant strain was constructed by homologous replacement of sopI with a novobiocin-resistant gyrB from Haloferax Aa 2.2. Cells bearing gyrB were resistant to novobiocin, indicating that the Haloferax gene is functional in H. salinarium. Complementation of this deletion strain with sopI fused to the bacterio-opsin promoter resulted in the recovery of all phenotypical attributes of SRI. This establishes the first direct correlation between sopI and the function of its gene product. In the complemented deletion strain, functional expression of sopI occurred from the bop locus, where sopI had integrated by homologous recombination. This shows that cotranscription of sopI and the gene encoding the SRI signal transducer, htrI, which is found in the wild type, is not a prerequisite for photosensory activity. Deletion of the last 43 bp at the 3' end of sopI resulted in a 10-fold increase in the amount of SRI, without affecting the activity of the pigment. The mRNA level of the truncated gene was not affected as compared to that of the wild type. We propose that regulation occurs at the protein level, probably through a negative determinant of protein stability located in the C-terminus of SRI. Replacement of the last 28 amino acids of bacteriorhodopsin by the last 29 amino acids of SRI results in a decrease of the bacteriorhodopsin, supporting our observations. The C-terminus of SRI is the first domain with a downregulating influence on protein levels thus far identified in H. salinarium. The system for SRI overexpression we present here greatly facilitates biochemical and biophysical studies on the photoreceptor and allows investigation of the molecular interactions underlying the signal transduction chain of halobacterial phototaxis.
通过同源基因靶向方法研究了编码嗜盐菌光感受器视紫红质I(SRI)的基因sopI的表达。通过用来自嗜盐栖热菌Aa 2.2的新霉素抗性gyrB同源替换sopI,构建了sopI - 盐生盐杆菌突变株。携带gyrB的细胞对新霉素具有抗性,这表明嗜盐栖热菌基因在盐生盐杆菌中具有功能。用与细菌视紫红质启动子融合的sopI对该缺失菌株进行互补,导致SRI的所有表型特征得以恢复。这建立了sopI与其基因产物功能之间的第一个直接关联。在互补的缺失菌株中,sopI的功能性表达发生在bop位点,sopI通过同源重组整合到该位点。这表明sopI与编码SRI信号转导器的基因htrI(在野生型中发现)的共转录不是光感受活性的先决条件。sopI 3'端最后43 bp的缺失导致SRI量增加10倍,而不影响色素的活性。与野生型相比,截短基因的mRNA水平未受影响。我们提出调控发生在蛋白质水平,可能是通过位于SRI C末端的蛋白质稳定性负决定因素。用SRI的最后29个氨基酸替换细菌视紫红质的最后28个氨基酸导致细菌视紫红质减少,支持了我们的观察结果。SRI的C末端是迄今为止在盐生盐杆菌中鉴定出的第一个对蛋白质水平有下调影响的结构域。我们在此展示的SRI过表达系统极大地促进了对光感受器的生化和生物物理研究,并允许研究嗜盐菌趋光性信号转导链背后的分子相互作用。