Ballal Anand, Apte Shree Kumar
Molecular Biology Division, Bhabha Atomic Research Centre, Trombay, Mumbai, Maharashtra 400085, India.
Arch Biochem Biophys. 2008 Jun 1;474(1):65-71. doi: 10.1016/j.abb.2008.02.017. Epub 2008 Feb 23.
The potassium dependent adenosine triphosphatase (Kdp-ATPase), encoded by the kdp operon, is a potassium uptake system found in several prokaryotes. The cyanobacterium Anabaena sp. strain L-31 shows the presence of two kdp operons (kdp1 and kdp2) of which the kdp2 is predominantly induced in response to potassium limitation or desiccation stress. Two ORFs, encoding a sensor kinase and a response regulator, respectively, were identified upstream of the kdp2 operon in Anabaena sp. strain L-31. The response regulator protein, tagged with 6 additional C-terminal histidine residues, was over-expressed in Escherichia coli and purified by affinity chromatography. Employing the protein-specific antiserum, the response regulator protein was detected in Anabaena L-31 cytosolic fractions. The response regulator protein bound to the kdp2 promoter region with higher affinity than kdp1 promoter region. Addition of acetyl phosphate increased the ability of the protein to bind to kdp2 promoter region by several fold, suggesting a phosphorylation-dependent binding of response regulator to the promoter. These data implicate the response regulator protein in regulation of kdp2 expression in Anabaena sp. strain L-31.
由kdp操纵子编码的钾依赖性三磷酸腺苷酶(Kdp - ATPase)是在几种原核生物中发现的一种钾摄取系统。蓝藻鱼腥藻属L - 31菌株显示存在两个kdp操纵子(kdp1和kdp2),其中kdp2主要在钾限制或干燥胁迫下被诱导。在鱼腥藻属L - 31菌株的kdp2操纵子上游分别鉴定出两个分别编码传感激酶和反应调节蛋白的开放阅读框。带有6个额外C末端组氨酸残基的反应调节蛋白在大肠杆菌中过表达并通过亲和层析纯化。使用该蛋白特异性抗血清,在鱼腥藻L - 31的胞质组分中检测到反应调节蛋白。与kdp1启动子区域相比,反应调节蛋白与kdp2启动子区域结合的亲和力更高。添加乙酰磷酸使该蛋白与kdp2启动子区域结合的能力提高了几倍,表明反应调节蛋白与启动子的结合依赖于磷酸化。这些数据表明反应调节蛋白参与了鱼腥藻属L - 31菌株中kdp2表达的调控。