Facultative anaerobes, such as Escherichia coli, possess a genetic regulatory network to capitalize on the best mode of energy extraction under different environments. The most efficient mode is aerobic respiration. Expression of many genes in this process is controlled by a two-component regulatory system in which ArcB (the membrane sensor protein) communicates the signal to ArcA (the cytoplasmic response regulator) by phosphorylation. ArcA-P in turn regulates the expression of its target promoters. The family of target operons includes those that encode numerous primary dehydrogenases of the flavoprotein class, members of the citric acid cycle, and the aerobic electron transport chain. We propose to continue our investigation of the Arc system, focussing on the following problems. l) We will focus on the plasma membrane both as a source of a signal and a medium for transmitting the information to ArcB. 2) We will analyze the catalytic interactions between the various domains of the two regulatory proteins and the physiological significance of the structures. 3) The mechanisms by which ArcA-P represses the negatively controlled sdh operon (encoding succinate dehydrogenase) and activates the positively controlled cyd operon (encoding 02 scavenging cytochrome d) will be characterized. In particular we wish to discover the DNA consensus sequence in the target promoters recognized by ArcA-P (i.e., to determine the """"""""Arc Box""""""""). 4) Studies on another two-component system, Cpx, will be continued, because there is reason to think that its function is also related to regulation of membrane bioenergetics. In addition, the Cpx system might have some important role in membrane organization.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM040993-06A1
Application #
2180643
Study Section
Microbial Physiology and Genetics Subcommittee 2 (MBC)
Project Start
1988-12-01
Project End
1998-11-30
Budget Start
1994-12-06
Budget End
1995-11-30
Support Year
6
Fiscal Year
1995
Total Cost
Indirect Cost
Name
Harvard University
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
082359691
City
Boston
State
MA
Country
United States
Zip Code
02115
Liu, Xueqiao; De Wulf, Peter (2004) Probing the ArcA-P modulon of Escherichia coli by whole genome transcriptional analysis and sequence recognition profiling. J Biol Chem 279:12588-97
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Nunez, Maria Felisa; Kwon, Ohsuk; Wilson, T Hastings et al. (2002) Transport of L-Lactate, D-Lactate, and glycolate by the LldP and GlcA membrane carriers of Escherichia coli. Biochem Biophys Res Commun 290:824-9
Echave, Pedro; Esparza-Ceron, M Angel; Cabiscol, Elisa et al. (2002) DnaK dependence of mutant ethanol oxidoreductases evolved for aerobic function and protective role of the chaperone against protein oxidative damage in Escherichia coli. Proc Natl Acad Sci U S A 99:4626-31
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Georgellis, D; Kwon, O; Lin, E C (2001) Quinones as the redox signal for the arc two-component system of bacteria. Science 292:2314-6
Georgellis, D; Kwon, O; Lin, E C et al. (2001) Redox signal transduction by the ArcB sensor kinase of Haemophilus influenzae lacking the PAS domain. J Bacteriol 183:7206-12
Pernestig, A K; Melefors, O; Georgellis, D (2001) Identification of UvrY as the cognate response regulator for the BarA sensor kinase in Escherichia coli. J Biol Chem 276:225-31
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Kwon, O; Georgellis, D; Lin, E C (2000) Phosphorelay as the sole physiological route of signal transmission by the arc two-component system of Escherichia coli. J Bacteriol 182:3858-62

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