ABSTRACT
In Paracoccus denitrificans, electrons pass from the membrane-bound cytochrome bc
1 complex to the periplasmic nitrite reductase, cytochrome cd
1. The periplasmic protein cytochrome c
550 has often been implicated in this electron transfer, but its absence, as a consequence of mutation, has previously been shown to result in almost no attenuation in the ability of the nitrite reductase to function in intact cells. Here, the hypothesis that cytochrome c
550 and pseudoazurin are alternative electron carriers from the cytochrome bc
1 complex to the nitrite reductase was tested by construction of mutants of P. denitrificans that are deficient in either pseudoazurin or both pseudoazurin and cytochrome c
550. The latter organism, but not the former (which is almost indistinguishable in this respect from the wild type), grows poorly under anaerobic conditions with nitrate as an added electron acceptor and accumulates nitrite in the medium. Growth under aerobic conditions with either succinate or methanol as the carbon source is not significantly affected in mutants lacking either pseudoazurin or cytochrome c
550 or both these proteins. We concluded that pseudoazurin and cytochrome c
550 are the alternative electron mediator proteins between the cytochrome bc
1 complex and the cytochrome cd
1-type nitrite reductase. We also concluded that expression of pseudoazurin is mainly controlled by the transcriptional activator FnrP.
SERR Spectroelectrochemical Study of Cytochrome cd1 Nitrite Reductase Co-Immobilized with Physiological Redox Partner Cytochrome c552 on Biocompatible Metal Electrodes