Department of Biochemistry and Biophysics, Arrhenius Laboratories for Natural Sciences, Stockholm University, SE-106 91 Stockholm, Sweden.
BMC Biochem. 2011 Sep 1;12:49. doi: 10.1186/1471-2091-12-49.
The transcriptional regulators DntR, NagR and NtdR have a high sequence identity and belong to the large family of LysR type transcriptional regulators (LTTRs). These three regulators are all involved in regulation of genes identified in pathways for degradation of aromatic compounds. They activate the transcription of these genes in the presence of an inducer, but the inducer specificity profiles are different.
The results from this study show that NtdR has the broadest inducer specificity, responding to several nitro-aromatic compounds. Mutational studies of residues that differ between DntR, NagR and NtdR suggest that a number of specific residues are involved in the broader inducer specificity of NtdR when compared to DntR and NagR. The inducer response was also investigated as a function of the experimental conditions and a number of parameters such as the growth media, plasmid arrangement of the LTTR-encoding genes, promoter and gfp reporter gene, and the presence of a His6-tag were shown to affect the inducer response in E.coli DH5α. Furthermore, the response upon addition of both salicylate and 4-nitrobenzoate to the growth media was larger than the sum of responses upon addition of each of the compounds, which suggests the presence of a secondary binding site, as previously reported for other LTTRs.
Optimization of the growth conditions and gene arrangement resulted in improved responses to nitro-aromatic inducers. The data also suggests the presence of a previously unknown secondary binding site in DntR, analogous to that of BenM.
转录调控因子 DntR、NagR 和 NtdR 具有高度的序列同一性,属于 LysR 型转录调控因子(LTTRs)大家族。这三个调节剂都参与了芳香族化合物降解途径中鉴定的基因的调控。它们在诱导物存在的情况下激活这些基因的转录,但诱导物特异性谱不同。
本研究结果表明,NtdR 具有最广泛的诱导特异性,可响应几种硝基芳香族化合物。DntR、NagR 和 NtdR 之间差异的残基突变研究表明,与 DntR 和 NagR 相比,许多特定残基参与了 NtdR 更广泛的诱导特异性。还研究了诱导物响应作为实验条件的函数,许多参数,如生长培养基、LTTR 编码基因的质粒排列、启动子和 gfp 报告基因以及 His6 标签的存在,都显示出影响大肠杆菌 DH5α 中的诱导物响应。此外,向生长培养基中添加水杨酸盐和 4-硝基苯甲酸的响应大于添加每种化合物的响应之和,这表明存在以前报道的其他 LTTRs 中的二级结合位点。
优化生长条件和基因排列可提高对硝基芳香族诱导物的响应。数据还表明,DntR 中存在以前未知的二级结合位点,类似于 BenM 的结合位点。