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PMID: 12546643 Published · ppublish English Lecture Research Support, U.S. Gov't, P.H.S.

Biochemical Society Special Lecture. Nitrate- and nitrite-responsive sensors NarX and NarQ of proteobacteria.

Biochemical Society transactions ·Vol. 31 ·No. Pt 1 ·2003-02-00 ·Pages 1-10

Stewart V

Abstract

Nitrate and nitrite are efficient respiratory oxidants for anaerobic growth. In Escherichia coli, the homologous nitrate reductase (Nar) two-component regulatory systems NarX-NarL and NarQ-NarP collaborate to control anaerobic respiratory gene expression in response to nitrate and nitrite. Several other species classified in the gamma and beta subdivisions of the proteobacteria contain only a single Nar two-component regulatory pair. This raises questions concerning the physiology of anaerobic respiration as well as the evolution, function and cross-regulation of two-component regulatory systems. Here, I focus on the sensor histidine kinases NarX and NarQ, and present a comparison of the deduced NarX and NarQ primary sequences from a broad sampling of proteobacteria. This comparison defines shared features, including a large central region of unknown function that appears to be unique to this family of sensor kinases. I then consider the phylogenetic distribution of narX and narQ genes in relation to anaerobic respiratory enzyme repertoire and physiological function. One noteworthy observation is that narXL genes are specifically associated with the structural genes for membrane-bound nitrate reductase, narGHJI, whereas organization and linkage of the narQ and narP genes is quite variable. I conclude with some speculative thoughts on the evolutionary and functional divergence of the NarX-NarL and NarQ-NarP regulatory systems. Overall, this analysis aims to provide a basis for future hypothesis and experimentation in this area.

MeSH Terms
Amino Acid Sequence Cysteine/chemistry Escherichia coli/metabolism Escherichia coli Proteins Membrane Proteins/physiology Molecular Sequence Data Phosphoproteins/physiology Phylogeny Protein Kinases/physiology Protein Structure, Tertiary Proteobacteria/metabolism Sequence Homology, Amino Acid
Chemicals
Escherichia coli Proteins Membrane Proteins Phosphoproteins narQ protein, E coli Protein Kinases narX protein, E coli Cysteine
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Stewart V
Section of Microbiology, University of California, 1 Shields Avenue, Davis, CA 95616-8665, USA. vjstewart@ucdavis.edu
Article Info
Journal
Biochemical Society transactions
Abbr.
Biochem Soc Trans
ISSN
0300-5127
Published
2003-02-00
Pages
1-10
Language
English
Region
England
NLM ID
7506897
Subset
IM
Grants
NIGMS NIH HHS · GM36877 · United States
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