Literature DB >> 12823811

Electron transport to periplasmic nitrate reductase (NapA) of Wolinella succinogenes is independent of a NapC protein.

Jörg Simon1, Monica Sänger, Stephan C Schuster, Roland Gross.   

Abstract

The rumen bacterium Wolinella succinogenes grows by respiratory nitrate ammonification with formate as electron donor. Whereas the enzymology and coupling mechanism of nitrite respiration is well known, nitrate reduction to nitrite has not yet been examined. We report here that intact cells and cell fractions catalyse nitrate and chlorate reduction by reduced viologen dyes with high specific activities. A gene cluster encoding components of a putative periplasmic nitrate reductase system (napA, G, H, B, F, L, D) was sequenced. The napA gene was inactivated by inserting a kanamycin resistance gene cassette. The resulting mutant did not grow by nitrate respiration and did not reduce nitrate during growth by fumarate respiration, in contrast to the wild type. An antigen was detected in wild-type cells using an antiserum raised against the periplasmic nitrate reductase (NapA) from Paracoccus pantotrophus. This antigen was absent in the W. succinogenes napA mutant. It is concluded that the periplasmic nitrate reductase NapA is the only respiratory nitrate reductase in W. succinogenes, although a second nitrate-reducing enzyme is apparently induced in the napA mutant. The nap cluster of W. succinogenes lacks a napC gene whose product is thought to function in quinol oxidation and electron transfer to NapA in other bacteria. The W. succinogenes genome encodes two members of the NapC/NirT family, NrfH and FccC. Characterization of corresponding deletion mutants indicates that neither of these two proteins is required for nitrate respiration. A mutant lacking the genes encoding respiratory nitrite reductase (nrfHA) had wild-type properties with respect to nitrate respiration. A model of the electron transport chain of nitrate respiration is proposed in which one or more of the napF, G, H and L gene products mediate electron transport from menaquinol to the periplasmic NapAB complex. Inspection of the W. succinogenes genome sequence suggests that ammonia formation from nitrate is catalysed exclusively by periplasmic respiratory enzymes.

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Year:  2003        PMID: 12823811     DOI: 10.1046/j.1365-2958.2003.03544.x

Source DB:  PubMed          Journal:  Mol Microbiol        ISSN: 0950-382X            Impact factor:   3.501


  14 in total

1.  Site-directed modifications indicate differences in axial haem c iron ligation between the related NrfH and NapC families of multihaem c-type cytochromes.

Authors:  Roland Gross; Robert Eichler; Jörg Simon
Journal:  Biochem J       Date:  2005-09-15       Impact factor: 3.857

2.  Deep-sea hydrothermal vent Epsilonproteobacteria encode a conserved and widespread nitrate reduction pathway (Nap).

Authors:  Costantino Vetriani; James W Voordeckers; Melitza Crespo-Medina; Charles E O'Brien; Donato Giovannelli; Richard A Lutz
Journal:  ISME J       Date:  2014-01-16       Impact factor: 10.302

3.  NapGH components of the periplasmic nitrate reductase of Escherichia coli K-12: location, topology and physiological roles in quinol oxidation and redox balancing.

Authors:  T Harma C Brondijk; Arjaree Nilavongse; Nina Filenko; David J Richardson; Jeffrey A Cole
Journal:  Biochem J       Date:  2004-04-01       Impact factor: 3.857

4.  Genomics of a phototrophic nitrite oxidizer: insights into the evolution of photosynthesis and nitrification.

Authors:  James Hemp; Sebastian Lücker; Joachim Schott; Laura A Pace; Jena E Johnson; Bernhard Schink; Holger Daims; Woodward W Fischer
Journal:  ISME J       Date:  2016-04-19       Impact factor: 10.302

5.  Genome of the epsilonproteobacterial chemolithoautotroph Sulfurimonas denitrificans.

Authors:  Stefan M Sievert; Kathleen M Scott; Martin G Klotz; Patrick S G Chain; Loren J Hauser; James Hemp; Michael Hügler; Miriam Land; Alla Lapidus; Frank W Larimer; Susan Lucas; Stephanie A Malfatti; Folker Meyer; Ian T Paulsen; Qinghu Ren; Jörg Simon
Journal:  Appl Environ Microbiol       Date:  2007-12-07       Impact factor: 4.792

6.  Substrate specificity of three cytochrome c haem lyase isoenzymes from Wolinella succinogenes: unconventional haem c binding motifs are not sufficient for haem c attachment by NrfI and CcsA1.

Authors:  Melanie Kern; Florian Eisel; Juliane Scheithauer; Robert G Kranz; Jörg Simon
Journal:  Mol Microbiol       Date:  2009-11-17       Impact factor: 3.501

7.  Four PCR primers necessary for the detection of periplasmic nitrate reductase genes in all groups of Proteobacteria and in environmental DNA.

Authors:  Tobias Klatte; Laura Evans; Rebekah N Whitehead; Jeffrey A Cole
Journal:  Biochem Soc Trans       Date:  2011-01       Impact factor: 5.407

8.  Metagenomic insights into S(0) precipitation in a terrestrial subsurface lithoautotrophic ecosystem.

Authors:  Trinity L Hamilton; Daniel S Jones; Irene Schaperdoth; Jennifer L Macalady
Journal:  Front Microbiol       Date:  2015-01-08       Impact factor: 5.640

9.  Dissimilatory nitrate reduction by a freshwater cable bacterium.

Authors:  Ugo Marzocchi; Casper Thorup; Ann-Sofie Dam; Andreas Schramm; Nils Risgaard-Petersen
Journal:  ISME J       Date:  2021-07-02       Impact factor: 10.302

10.  Redundancy and modularity in membrane-associated dissimilatory nitrate reduction in Bacillus.

Authors:  Kim Heylen; Jan Keltjens
Journal:  Front Microbiol       Date:  2012-10-18       Impact factor: 5.640

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