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Characterization of TsaR, an Oxygen-Sensitive LysR-Type Regulator for the Degradation of p-Toluenesulfonate in Comamonas testosteroni T-2

机译:TsaR的表征,氧敏感的LysR型调节剂,用于降解睾丸激素T-2中对甲苯磺酸盐

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摘要

TsaR is the putative LysR-type regulator of the tsa operon (tsaMBCD) which encodes the first steps in the degradation of p-toluenesulfonate (TSA) in Comamonas testosteroni T-2. Transposon mutagenesis was used to knock out tsaR. The resulting mutant lacked the ability to grow with TSA and p-toluenecarboxylate (TCA). Reintroduction of tsaR in trans on an expression vector reconstituted growth with TSA and TCA. The tsaR gene was cloned into Escherichia coli with a C-terminal His tag and overexpressed as TsaRHis. TsaRHis was subject to reversible inactivation by oxygen, which markedly influenced the experimental approaches used. Gel filtration showed TsaRHis to be a monomer in solution. Overexpressed TsaRHis bound specifically to three regions within the promoter between the divergently transcribed tsaR and tsaMBCD. The dissociation constant (KD) for the whole promoter region was about 0.9 μM, and the interaction was a function of the concentration of the ligand TSA. A regulatory model for this LysR-type regulator is proposed on the basis of these data.
机译:TsaR是tsa操纵子(tsaMBCD)的公认LysR型调节子,它编码Comamonas testosteroni T-2中对甲苯磺酸酯(TSA)降解的第一步。转座子诱变用于敲除tsaR。所得突变体缺乏与TSA和对甲苯甲酸酯(TCA)一起生长的能力。在表达载体上反式导入tsaR,用TSA和TCA重建生长。将tsaR基因克隆到具有C端His标签的大肠杆菌中,并以TsaRHis的形式过表达。 TsaRHis受到氧气的可逆灭活作用,这显着影响了所用的实验方法。凝胶过滤显示TsaRHis是溶液中的单体。过表达的TsaRH与发散转录的tsaR和tsaMBCD之间的启动子内的三个区域特异性结合。整个启动子区域的解离常数(KD)约为0.9μM,且相互作用是配体TSA浓度的函数。在这些数据的基础上,提出了此LysR型调节剂的调节模型。

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