The goal of the proposed research is to understand biological energy transduction between membranes using the Gram-negative bacterium E. coli as the model system. In E. coli, cytoplasmic membrane energy is coupled to the active transport of important nutrients (iron-bearing sideropheres and vitamin B12) across the outer membrane. The mechanism of energy transduction remains to be elucidated. Several proteins have been shown genetically to participate in the phenomenon, most likely in the form of energy transduction complexes. Emphasizing TonB protein, the protein most directly involved in energy transduction, we will attempt to characterize the structure, function, and regulation of energy transduction complexes.
The specific aims of this project are 1.) to determine the composition and stoichiometries of TonB-dependent energy transduction complexes. 2.) to elucidate the role of chemical modifications in TonB-dependent energy transduction. 3.) to delineate the mechanism of coupling between the cytoplasmic membrane proton-motive force and the energy-requiring processes of the outer membrane. 4.) to characterize the mechanisms of transcriptional regulation of TonB. Research in this area will have important ramifications for understanding energy transduction, protein-protein interactions, and membrane phenomena in general.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM042146-03
Application #
3300695
Study Section
Microbial Physiology and Genetics Subcommittee 2 (MBC)
Project Start
1991-08-01
Project End
1995-07-31
Budget Start
1993-08-01
Budget End
1994-07-31
Support Year
3
Fiscal Year
1993
Total Cost
Indirect Cost
Name
Washington State University
Department
Type
Schools of Arts and Sciences
DUNS #
041485301
City
Pullman
State
WA
Country
United States
Zip Code
99164
Gresock, Michael G; Postle, Kathleen (2017) Going Outside the TonB Box: Identification of Novel FepA-TonB Interactions In Vivo. J Bacteriol 199:
Baker, Kristin R; Postle, Kathleen (2013) Mutations in Escherichia coli ExbB transmembrane domains identify scaffolding and signal transduction functions and exclude participation in a proton pathway. J Bacteriol 195:2898-911
Bulathsinghala, Charles M; Jana, Bimal; Baker, Kristin R et al. (2013) ExbB cytoplasmic loop deletions cause immediate, proton motive force-independent growth arrest. J Bacteriol 195:4580-91
Ollis, Anne A; Postle, Kathleen (2012) ExbD mutants define initial stages in TonB energization. J Mol Biol 415:237-47
Ollis, Anne A; Kumar, Aruna; Postle, Kathleen (2012) The ExbD periplasmic domain contains distinct functional regions for two stages in TonB energization. J Bacteriol 194:3069-77
Ollis, Anne A; Postle, Kathleen (2012) Identification of functionally important TonB-ExbD periplasmic domain interactions in vivo. J Bacteriol 194:3078-87
Ollis, Anne A; Postle, Kathleen (2011) The same periplasmic ExbD residues mediate in vivo interactions between ExbD homodimers and ExbD-TonB heterodimers. J Bacteriol 193:6852-63
Jana, Bimal; Manning, Marta; Postle, Kathleen (2011) Mutations in the ExbB cytoplasmic carboxy terminus prevent energy-dependent interaction between the TonB and ExbD periplasmic domains. J Bacteriol 193:5649-57
Swayne, Cheryl; Postle, Kathleen (2011) Taking the Escherichia coli TonB transmembrane domain ""offline""? Nonprotonatable Asn substitutes fully for TonB His20. J Bacteriol 193:3693-701
Postle, Kathleen; Kastead, Kyle A; Gresock, Michael G et al. (2010) The TonB dimeric crystal structures do not exist in vivo. MBio 1:

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