The Aer protein mediates aerotactic behavior in Escherichia coli. A growing list of other bacteria, including pathogens such as Vibrio cholerae and Yersinia pestis, have Aer homologs. The long-range goals of this project are to understand in molecular detail how the Aer protein senses changes in environmental oxygen levels and how that stimulus information is transmitted through the Aer molecule to control the cell's swimming movements. Aer appears to be located predominantly in the cytoplasm, but anchored to the inner face of the cytoplasmic membrane through a central segment of hydrophobic amino acids. To explore the role of membrane association in Aer function, the topology of the native molecule will be probed by accessibility to proteases and aqueous sulfhydryl modification reagents. Mutant proteins with deletions or substitutions in the hydrophobic segment will be tested for membrane association and aerotactic signaling ability in attempts to develop a soluble, active form of Aer. To identify conformational features that might play a role in Aer signal transduction, an extensive set of mutant proteins with single cysteine reporter residues will be constructed and used to examine intra- and intersubunit interactions between different regions of the native Aer molecule. Mutations that """"""""lock"""""""" Aer into a stimulus-insensitive or stimulus-mimicked state will be isolated and used to trace the path of signal transmission through the molecule. Preliminary studies have established that the N-terminus of Aer binds flavin adenine dinucleotide (FAD), which might serve as a prosthetic group to monitor the redox state of an electron transport component. To test the redox-sensing model, in vitro assays of Aer signaling activity will be developed. The redox potential of FAD in native Aer will also be determined to identify electron transport components that could conceivably interact with Aer during stimulus detection. These studies promise to shed new light on biological mechanisms of oxygen-sensing. Moreover, the existence of Aer homologs in pathogenic bacteria suggests that aerotactic behavior might play a role in virulence. Thus, a molecular understanding of Aer signal transduction could lead to new anti-infection agents.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM062940-03
Application #
6607010
Study Section
Microbial Physiology and Genetics Subcommittee 2 (MBC)
Program Officer
Deatherage, James F
Project Start
2001-07-01
Project End
2005-06-30
Budget Start
2003-07-01
Budget End
2004-06-30
Support Year
3
Fiscal Year
2003
Total Cost
$187,500
Indirect Cost
Name
University of Utah
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
009095365
City
Salt Lake City
State
UT
Country
United States
Zip Code
84112
del Carmen Buron-Barral, Maria; Gosink, Khoosheh K; Parkinson, John S (2006) Loss- and gain-of-function mutations in the F1-HAMP region of the Escherichia coli aerotaxis transducer Aer. J Bacteriol 188:3477-86
Wright, Stuart; Walia, Bharat; Parkinson, John S et al. (2006) Differential activation of Escherichia coli chemoreceptors by blue-light stimuli. J Bacteriol 188:3962-71
Gosink, Khoosheh K; Buron-Barral, Maria del Carmen; Parkinson, John S (2006) Signaling interactions between the aerotaxis transducer Aer and heterologous chemoreceptors in Escherichia coli. J Bacteriol 188:3487-93
Parkinson, John S; Ames, Peter; Studdert, Claudia A (2005) Collaborative signaling by bacterial chemoreceptors. Curr Opin Microbiol 8:116-21