The goal of the proposed research is to understand biological energy transduction between the cytoplasmic and outer membranes of Gram-negative bacteria, using Escherichia coli as the model system. in E. coli, cytoplasmic membrane energy is coupled to the active transport of important nutrients (iron-siderophore complexes and vitamin Bl2) across the outer membrane. Although we know that energy transduction is energized by the cytoplasmic membrane electrochemical potential, and that the proteins TonB, ExbB, and ExbD participate in that process, the molecular mechanism of energy transduction and the role of ExbB and ExbD are unclear. The role of TonB as energy transducer has been established, however, the molecular details of its interactions with other energy transduction proteins have not been elucidated. Furthermore, recent data suggest the participation of additional proteins which have been defined only biochemically, and not genetically.
The aims of this proposal are to 1.) define, both genetically and biochemically, the protein components of the energy transduction machinery; 2.) determine the function(s) of specific amino acid residues in the amino terminus of the energy transducer, TonB. These are the regions of TonB believed to be in direct contact with the energy generating machinery in the cytoplasmic membrane. 3.) Investigate the role of ExbB in energy transduction, focusing on its proposed recycling activity and the function of its cytoplasmic domains.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM042146-07
Application #
2459397
Study Section
Microbial Physiology and Genetics Subcommittee 2 (MBC)
Project Start
1991-08-01
Project End
1999-07-31
Budget Start
1997-08-01
Budget End
1998-07-31
Support Year
7
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Washington State University
Department
Microbiology/Immun/Virology
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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