| Autor: |
Kuhns M; Molecular Microbiology & Bioenergetics, Institute of Molecular Biosciences, Johann Wolfgang Goethe University Frankfurt Main, Max-von-Laue-Str. 9, 60438, Frankfurt, Germany., Trifunović D; Molecular Microbiology & Bioenergetics, Institute of Molecular Biosciences, Johann Wolfgang Goethe University Frankfurt Main, Max-von-Laue-Str. 9, 60438, Frankfurt, Germany., Huber H; Department of Microbiology, University of Regensburg, Universitätsstraße 31, 93053, Regensburg, Germany., Müller V; Molecular Microbiology & Bioenergetics, Institute of Molecular Biosciences, Johann Wolfgang Goethe University Frankfurt Main, Max-von-Laue-Str. 9, 60438, Frankfurt, Germany. vmueller@bio.uni-frankfurt.de. |
| Abstrakt: |
rnf genes are widespread in bacteria and biochemical and genetic data are in line with the hypothesis that they encode a membrane-bound enzyme that oxidizes reduced ferredoxin and reduces NAD and vice versa, coupled to ion transport across the cytoplasmic membrane. The Rnf complex is of critical importance in many bacteria for energy conservation but also for reverse electron transport to drive ferredoxin reduction. However, the enzyme has never been purified and thus, ion transport could not be demonstrated yet. Here, we have purified the Rnf complex from the anaerobic, fermenting thermophilic bacterium Thermotoga maritima and show that is a primary Na + pump. These studies provide the proof that the Rnf complex is indeed an ion (Na + ) translocating, respiratory enzyme. Together with a Na + -F 1 F O ATP synthase it builds a simple, two-limb respiratory chain in T. maritima. The physiological role of electron transport phosphorylation in a fermenting bacterium is discussed. |
