Literature DB >> 9409151

Cell biology and molecular basis of denitrification.

W G Zumft1.   

Abstract

Denitrification is a distinct means of energy conservation, making use of N oxides as terminal electron acceptors for cellular bioenergetics under anaerobic, microaerophilic, and occasionally aerobic conditions. The process is an essential branch of the global N cycle, reversing dinitrogen fixation, and is associated with chemolithotrophic, phototrophic, diazotrophic, or organotrophic metabolism but generally not with obligately anaerobic life. Discovered more than a century ago and believed to be exclusively a bacterial trait, denitrification has now been found in halophilic and hyperthermophilic archaea and in the mitochondria of fungi, raising evolutionarily intriguing vistas. Important advances in the biochemical characterization of denitrification and the underlying genetics have been achieved with Pseudomonas stutzeri, Pseudomonas aeruginosa, Paracoccus denitrificans, Ralstonia eutropha, and Rhodobacter sphaeroides. Pseudomonads represent one of the largest assemblies of the denitrifying bacteria within a single genus, favoring their use as model organisms. Around 50 genes are required within a single bacterium to encode the core structures of the denitrification apparatus. Much of the denitrification process of gram-negative bacteria has been found confined to the periplasm, whereas the topology and enzymology of the gram-positive bacteria are less well established. The activation and enzymatic transformation of N oxides is based on the redox chemistry of Fe, Cu, and Mo. Biochemical breakthroughs have included the X-ray structures of the two types of respiratory nitrite reductases and the isolation of the novel enzymes nitric oxide reductase and nitrous oxide reductase, as well as their structural characterization by indirect spectroscopic means. This revealed unexpected relationships among denitrification enzymes and respiratory oxygen reductases. Denitrification is intimately related to fundamental cellular processes that include primary and secondary transport, protein translocation, cytochrome c biogenesis, anaerobic gene regulation, metalloprotein assembly, and the biosynthesis of the cofactors molybdopterin and heme D1. An important class of regulators for the anaerobic expression of the denitrification apparatus are transcription factors of the greater FNR family. Nitrate and nitric oxide, in addition to being respiratory substrates, have been identified as signaling molecules for the induction of distinct N oxide-metabolizing enzymes.

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Year:  1997        PMID: 9409151      PMCID: PMC232623          DOI: 10.1128/mmbr.61.4.533-616.1997

Source DB:  PubMed          Journal:  Microbiol Mol Biol Rev        ISSN: 1092-2172            Impact factor:   11.056


  716 in total

1.  Modelling heme d1. The spectral properties of copper(II) porphyrindiones.

Authors:  L A Andersson; T M Loehr; W S Wu; C K Chang; R Timkovich
Journal:  FEBS Lett       Date:  1990-07-16       Impact factor: 4.124

2.  Environment of copper in Pseudomonas fluorescens azurin: fluorometric approach.

Authors:  A Finazzi-Agrò; G Rotilio; L Avigliano; P Guerrieri; V Boffi; B Mondovì
Journal:  Biochemistry       Date:  1970-04-28       Impact factor: 3.162

3.  Nucleotide sequence of a Pseudomonas denitrificans 5.4-kilobase DNA fragment containing five cob genes and identification of structural genes encoding S-adenosyl-L-methionine: uroporphyrinogen III methyltransferase and cobyrinic acid a,c-diamide synthase.

Authors:  J Crouzet; L Cauchois; F Blanche; L Debussche; D Thibaut; M C Rouyez; S Rigault; J F Mayaux; B Cameron
Journal:  J Bacteriol       Date:  1990-10       Impact factor: 3.490

4.  Glutamyl-tRNA synthetases of Bacillus subtilis 168T and of Bacillus stearothermophilus. Cloning and sequencing of the gltX genes and comparison with other aminoacyl-tRNA synthetases.

Authors:  R Breton; D Watson; M Yaguchi; J Lapointe
Journal:  J Biol Chem       Date:  1990-10-25       Impact factor: 5.157

5.  The evolution of nitrogen cycling.

Authors:  R L Mancinelli; C P McKay
Journal:  Orig Life Evol Biosph       Date:  1988       Impact factor: 1.950

6.  The nitric oxide reductase of Paracoccus denitrificans.

Authors:  G J Carr; S J Ferguson
Journal:  Biochem J       Date:  1990-07-15       Impact factor: 3.857

7.  Nitrate and nitrite regulation of the Fnr-dependent aeg-46.5 promoter of Escherichia coli K-12 is mediated by competition between homologous response regulators (NarL and NarP) for a common DNA-binding site.

Authors:  A J Darwin; V Stewart
Journal:  J Mol Biol       Date:  1995-08-04       Impact factor: 5.469

Review 8.  Protein folding in the periplasm of Escherichia coli.

Authors:  C Wülfing; A Plückthun
Journal:  Mol Microbiol       Date:  1994-06       Impact factor: 3.501

9.  Cloning and characterization of the Escherichia coli hemN gene encoding the oxygen-independent coproporphyrinogen III oxidase.

Authors:  B Troup; C Hungerer; D Jahn
Journal:  J Bacteriol       Date:  1995-06       Impact factor: 3.490

10.  Nitric oxide and nitrous oxide production and cycling during dissimilatory nitrite reduction by Pseudomonas perfectomarina.

Authors:  O C Zafiriou; Q S Hanley; G Snyder
Journal:  J Biol Chem       Date:  1989-04-05       Impact factor: 5.157

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  726 in total

1.  The napF and narG nitrate reductase operons in Escherichia coli are differentially expressed in response to submicromolar concentrations of nitrate but not nitrite.

Authors:  H Wang; C P Tseng; R P Gunsalus
Journal:  J Bacteriol       Date:  1999-09       Impact factor: 3.490

2.  Genetic identification of three ABC transporters as essential elements for nitrate respiration in Haloferax volcanii.

Authors:  C Wanner; J Soppa
Journal:  Genetics       Date:  1999-08       Impact factor: 4.562

3.  Two nitrate/nitrite transporters are encoded within the mobilizable plasmid for nitrate respiration of Thermus thermophilus HB8.

Authors:  S Ramírez; R Moreno; O Zafra; P Castán; C Vallés; J Berenguer
Journal:  J Bacteriol       Date:  2000-04       Impact factor: 3.490

Review 4.  Prokaryotic nitrate reduction: molecular properties and functional distinction among bacterial nitrate reductases.

Authors:  C Moreno-Vivián; P Cabello; M Martínez-Luque; R Blasco; F Castillo
Journal:  J Bacteriol       Date:  1999-11       Impact factor: 3.490

5.  The periplasmic nitrate reductase in Pseudomonas sp. strain G-179 catalyzes the first step of denitrification.

Authors:  L Bedzyk; T Wang; R W Ye
Journal:  J Bacteriol       Date:  1999-05       Impact factor: 3.490

6.  A comprehensive phylogenetic analysis of Rieske and Rieske-type iron-sulfur proteins.

Authors:  C L Schmidt; L Shaw
Journal:  J Bioenerg Biomembr       Date:  2001-02       Impact factor: 2.945

7.  Purification, characterization, and genetic analysis of Cu-containing dissimilatory nitrite reductase from a denitrifying halophilic archaeon, Haloarcula marismortui.

Authors:  H Ichiki; Y Tanaka; K Mochizuki; K Yoshimatsu; T Sakurai; T Fujiwara
Journal:  J Bacteriol       Date:  2001-07       Impact factor: 3.490

8.  Diversity of nitrite reductase (nirK and nirS) gene fragments in forested upland and wetland soils.

Authors:  Anders Priemé; Gesche Braker; James M Tiedje
Journal:  Appl Environ Microbiol       Date:  2002-04       Impact factor: 4.792

Review 9.  Nitrogen cycling in the ocean: new perspectives on processes and paradigms.

Authors:  Jonathan P Zehr; Bess B Ward
Journal:  Appl Environ Microbiol       Date:  2002-03       Impact factor: 4.792

10.  Transcriptional regulation of the cpr gene cluster in ortho-chlorophenol-respiring Desulfitobacterium dehalogenans.

Authors:  H Smidt; M van Leest; J van der Oost; W M de Vos
Journal:  J Bacteriol       Date:  2000-10       Impact factor: 3.490

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