Characterization of TsaR, an Oxygen-Sensitive LysR-Type Regulator for the Degradation of p-Toluenesulfonate in Comamonas testosteroni T-2 |
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| Authors: | Tewes Tralau, J rg Mampel, Alasdair M. Cook, Jü rgen Ruff |
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| Affiliation: | Tewes Tralau, Jörg Mampel, Alasdair M. Cook, and Jürgen Ruff |
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| Abstract: | 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. |
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