FnrP and NNR of Paracoccus denitrificans are both members of the FNR family of transcriptional activators but have distinct roles in respiratory adaptation in response to oxygen limitation

Abstract

The Paracoccus denitrificansfnrP gene encoding a homologue of the Escherichia coli FNR protein was localized upstream of the gene cluster that encodes the high‐affinity cbb₃‐type oxidase. FnrP harbours the invariant cysteine residues that are supposed to be the ligands of the redox‐sensitive [4Fe–4S] cluster in FNR. NNR, another FNR‐like transcriptional regulator in P. denitrificans, does not. Analysis of FnrP and NNR single and double mutants revealed that the two regulators each exert exclusive control on the expression of a discrete set of target genes. In FnrP mutants, the expression of cytochrome c peroxidase was blocked, that of membrane‐bound nitrate reductase and the cbb₃‐type oxidase was significantly reduced, whilst the activity of the bb₃‐type quinol oxidase was increased. The amounts of the nitrite and nitric oxide reductases in these FnrP mutants were the same as in the wild type. NNR mutants, on the other hand, were disturbed exclusively in the concentrations of nitrite reductase and nitric oxide reductase. An FnrP.NNR double mutant combined the phenotypes of the single mutant strains. In all three mutants, the concentrations and/or activities of the aa₃‐type oxidase, cytochrome c₅₅₀, cytochrome c₅₅₂, and nitrous oxide reductase equalled those in the wild type. As the FNR boxes in front of the FnrP‐ and NNR‐regulated genes are highly similar to or even identical to each other, the absence of cross‐talk between the regulation by FnrP and NNR implies that as yet unidentified factors are important in the control. It is proposed that the redox state of an intracellular redox couple other than the oxygen/water couple is one of the factors that modulates the activity of FnrP.