首页> 外文期刊>Applied and Environmental Microbiology >Characterization of TsaR, an Oxygen-Sensitive LysR-Type Regulator for the Degradation of p-Toluenesulfonate in Comamonas testosteroni T-2
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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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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型调节剂,编码降解 p -甲苯磺酸盐(TSA)的第一步)在 Comamonas testosteroni T-2中。转座子诱变被用于敲除 tsaR 。所得突变体缺乏与TSA和 p -甲苯甲酸(TCA)一起生长的能力。在表达载体上重新引入 tsaR ,并用TSA和TCA重建生长。将 tsaR 基因克隆到具有C末端His标签的大肠杆菌中,并过表达为TsaR His 。 TsaR His 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TsaR His 是溶液中的单体。过表达的TsaR His 特异地绑定到发散转录的 tsaR tsaMBCD 启动子之间的三个区域。整个启动子区域的解离常数( K D )约为0.9μM,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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