Wiethaus Jessica, Schubert Britta, Pfänder Yvonne, Narberhaus Franz, Masepohl Bernd
Lehrstuhl für Biologie der Mikroorganismen, Fakultät für Biologie, Ruhr-Universität Bochum, 44780 Bochum, Germany.
J Bacteriol. 2008 Jan;190(2):487-93. doi: 10.1128/JB.01510-07. Epub 2007 Nov 2.
Rhodobacter capsulatus can efficiently grow with taurine as the sole sulfur source. The products of the tpa-tauR-xsc gene region are essential for this activity. TauR, a MocR-like member of the GntR superfamily of transcriptional regulators, activates tpa transcription, as shown by analysis of wild-type and tauR mutant strains carrying a tpa-lacZ reporter fusion. Activation of the tpa promoter requires taurine but is not inhibited by sulfate, which is the preferred sulfur source. TauR directly binds to the tpa promoter, as demonstrated by DNA mobility shift assays. As expected for a transcriptional activator, the TauR binding site is located upstream of the transcription start site, which has been determined by primer extension. Site-directed promoter mutations reveal that TauR binds to direct repeats, an unusual property that has to date been shown for only one other member of the MocR subfamily, namely, GabR from Bacillus subtilis. In contrast, all other members of the GntR family analyzed so far bind to inverted repeats.
荚膜红细菌能够以牛磺酸作为唯一硫源高效生长。tpa-tauR-xsc基因区域的产物对于该活性至关重要。TauR是转录调节因子GntR超家族中类似MocR的成员,如对携带tpa-lacZ报告基因融合体的野生型和tauR突变株分析所示,它可激活tpa转录。tpa启动子的激活需要牛磺酸,但不受硫酸盐抑制,硫酸盐是更优的硫源。DNA迁移率变动分析表明,TauR可直接结合到tpa启动子上。正如转录激活因子所预期的那样,TauR结合位点位于转录起始位点上游,这已通过引物延伸法确定。定点启动子突变表明,TauR结合到直接重复序列上,这是一种不同寻常的特性,迄今为止仅在MocR亚家族的另一个成员(即枯草芽孢杆菌的GabR)中发现过。相比之下,到目前为止分析的GntR家族的所有其他成员都结合到反向重复序列上。