Periplasmic nitrate-reducing system of the phototrophic bacterium Rhodobacter sphaeroides DSM 158: transcriptional and mutational analysis of the napKEFDABC gene cluster
Open Access
- 1 May 1998
- journal article
- research article
- Published by Portland Press Ltd. in Biochemical Journal
- Vol. 331 (3) , 897-904
- https://doi.org/10.1042/bj3310897
Abstract
The phototrophic bacterium Rhodobacter sphaeroidesDSM 158 is able to reduce nitrate to nitrite by means of a periplasmic nitrate reductase which is induced by nitrate and is not repressed by ammonium or oxygen. Recently, a 6.8 kb PstI DNA fragment carrying the napABCgenes coding for this periplasmic nitrate-reducing system was cloned [Reyes, Roldán, Klipp, Castillo and Moreno-Vivián (1996) Mol. Microbiol. 19, 1307–1318]. Further sequence and genetic analyses of the DNA region upstream from the napABCgenes reveal the presence of four additional napgenes. All these R. sphaeroidesgenes seem to be organized into a napKEFDABCtranscriptional unit. In addition, a partial open reading frame similar to the Azorhizobium caulinodans yntCgene and the Escherichia coli yjcCand yhjKgenes is present upstream from this napgene cluster. The R. sphaeroides napKgene codes for a putative 6.3 kDa transmembrane protein which is not similar to known proteins and the napEgene codes for a 6.7 kDa transmembrane protein similar to the Thiosphaera pantotrophaNapE. The R. sphaeroides napFgene product is a 16.4 kDa protein with four cysteine clusters that probably bind four [4Fe-4S] centres. This iron–sulphur protein shows similarity to the NapF and NapG proteins of E. coliand Haemophilus influenzae.Finally, the napDgene product is a 9.4 kDa soluble protein which is also found in E. coliand T. pantotropha. The 5´ end of the naptranscript has been determined by primer extension, and a δ70-like promoter has been identified upstream from the napKgene. The same transcriptional start site is found for cells growing aerobically or anaerobically with nitrate. Different mutant strains carrying defined polar and non-polar insertions in each napgene were constructed. Characterization of these mutant strains demonstrates the participation of the napgene products in the periplasmic nitrate reduction in R. sphaeroides.Keywords
This publication has 39 references indexed in Scilit:
- Regulation of the ndh gene of Escherichia coli by integration host factor and a novel regulator, ArrMicrobiology, 1997
- Nitrate and Nitrite Regulation of the Fnr-dependentaeg-46.5Promoter ofEscherichia coliK-12 is Mediated by Competition Between Homologous Response Regulators (NarL and NarP) for a Common DNA-binding SiteJournal of Molecular Biology, 1995
- The purified SoxABCD quinol oxidase complex of Sulfolobus acidocaldarius contains a novel haemMolecular Microbiology, 1994
- Molecular analysis of dimethylsulfoxide reductase: a complex iron-sulfur molybdoenzyme of Escherichia coliBiochimica et Biophysica Acta (BBA) - Bioenergetics, 1992
- Membrane protein structure predictionJournal of Molecular Biology, 1992
- The identification of cytochromes involved in the transfer of electrons to the periplasmic NO−3 reductase of Rhodobacter capsulatus and resolution of a soluble NO−3 ‐reductase − cytochrome‐c552 redox complexEuropean Journal of Biochemistry, 1990
- FNR and its role in oxygen-regulated gene expression inEscherichia coliFEMS Microbiology Letters, 1990
- Molecular genetic analysis of FNR‐dependent promotersMolecular Microbiology, 1989
- A family of high-copy-number plasmid vectors with single end-label sites for rapid nucleotide sequencingGene, 1988
- A simple method for displaying the hydropathic character of a proteinJournal of Molecular Biology, 1982