Enterobacteria such as Escherichia coli and Salmonella enterica are facultative aerobes, and when cultured in the absence of oxygen can use a variety of alternative respiratory oxidants. Nitrate and nitrite are the preferred alternatives, and anaerobic respiratory enzyme gene expression is tightly controlled in response to their availability. This control is mediated by dual interacting two-component regulatory systems. Nitrate and nitrite control the autophosphorylation of two cytoplasmic membrane-bound sensor-kinases, the NarX and NarQ proteins, which in turn control the phosphorylation of two DNA-binding response regulators, the NarL and NarP proteins. Thus, transcription initiation at more than one dozen operons is activated or repressed according to electron acceptor availability. The Nar regulatory network is unique to enterobacteria; other species of proteobacteria (including several human pathogens) contain only the NarQ-NarP system (e.g., Vibrio cholerae) or the NarX-NarL system (e.g., Pseudomonas aeruginosa). The proposed studies therefore broadly inform our understanding of anaerobic physiology for many species within the gamma and beta subdivisions of the proteobacteria. Work proposed here comprises five specific aims: (1) We must characterize cross-regulation in vitro in biochemical detail in order to evaluate and extend models based primarily on in vivo observations. (2) In collaboration with E. P. Baldwin, we will study cooperative DMA binding by the response regulator NarL. (3) In collaboration with P. J. Kiley, we will study transcription activation by the response regulator NarP. (4) We continue to explore response to defined regulatory signals by the sensors NarX and NarQ. (5) In collaboration with M. M. Igo, we will identify previously- unknown target genes whose expression is controlled by the NarX-NarL or NarQ-NarP systems. Our overall goal is to integrate both in vivo and in vitro approaches to better understand the physiology of anaerobic metabolism. The relevance to public health of this fundamental research is in the realm of anaerobic physiology and metabolism. Most pathogenic species within the proteobacteria are facultative aerobes or facultative anaerobes, and many infectious diseases involve colonization of anaerobic environments such as the mammalian intestine. Thus, results from the model species E. coli enhance understanding for a broad range of pathogens that significantly impact public health.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM036877-20
Application #
7352777
Study Section
Prokaryotic Cell and Molecular Biology Study Section (PCMB)
Program Officer
Anderson, James J
Project Start
1986-07-01
Project End
2010-01-31
Budget Start
2008-02-01
Budget End
2009-01-31
Support Year
20
Fiscal Year
2008
Total Cost
$317,628
Indirect Cost
Name
University of California Davis
Department
Microbiology/Immun/Virology
Type
Schools of Arts and Sciences
DUNS #
047120084
City
Davis
State
CA
Country
United States
Zip Code
95618
Huynh, TuAnh Ngoc; Lin, Hsia-Yin; Noriega, Chris E et al. (2015) Cross Talk Inhibition Nullified by a Receiver Domain Missense Substitution. J Bacteriol 197:3294-306
Huynh, TuAnh Ngoc; Chen, Li-Ling; Stewart, Valley (2015) Sensor-response regulator interactions in a cross-regulated signal transduction network. Microbiology 161:1504-15
Huynh, TuAnh Ngoc; Noriega, Chris E; Stewart, Valley (2013) Missense substitutions reflecting regulatory control of transmitter phosphatase activity in two-component signalling. Mol Microbiol 88:459-72
Huynh, TuAnh Ngoc; Stewart, Valley (2011) Negative control in two-component signal transduction by transmitter phosphatase activity. Mol Microbiol 82:275-86
Stewart, Valley; Chen, Li-Ling (2010) The S helix mediates signal transmission as a HAMP domain coiled-coil extension in the NarX nitrate sensor from Escherichia coli K-12. J Bacteriol 192:734-45
Noriega, Chris E; Lin, Hsia-Yin; Chen, Li-Ling et al. (2010) Asymmetric cross-regulation between the nitrate-responsive NarX-NarL and NarQ-NarP two-component regulatory systems from Escherichia coli K-12. Mol Microbiol 75:394-412
Stewart, Valley; Bledsoe, Peggy J; Chen, Li-Ling et al. (2009) Catabolite repression control of napF (periplasmic nitrate reductase) operon expression in Escherichia coli K-12. J Bacteriol 191:996-1005
Noriega, Chris E; Schmidt, Radomir; Gray, Michael J et al. (2008) Autophosphorylation and dephosphorylation by soluble forms of the nitrate-responsive sensors NarX and NarQ from Escherichia coli K-12. J Bacteriol 190:3869-76
Stewart, Valley; Bledsoe, Peggy J (2008) Substitutions at auxiliary operator O3 enhance repression by nitrate-responsive regulator NarL at synthetic lac control regions in Escherichia coli K-12. J Bacteriol 190:428-33
Cruz-Garcia, Claribel; Murray, Alison E; Klappenbach, Joel A et al. (2007) Respiratory nitrate ammonification by Shewanella oneidensis MR-1. J Bacteriol 189:656-62

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