Tetrameric cation channels are widely conserved among all species. While bacterial cation channels are often used in structural and biophysical assays as models for their eukaryotic homologs, little is known about their physiological role in bacteria. Escherichia coli (E. coli) possesses a single tetrameric K+ channel, kch, which bears high sequence homology to eukaryotic K+ channels. The generation of a viable ?kch strain created as part of a large E. coli single-gene knockout collection led to kch being categorized as a non-essential protein, and the functional role of this putative K+ channel has remained unknown. Preliminary data demonstrates that Kch is actually an essential protein and that ?kch strains acquire suppressor mutations in order to remain viable. These suppressor mutations provide important clues as to which metabolic processes utilize the channel and has revealed a potential physiological role for Kch. Based on these results, the following aims are proposed: (1) to characterize the functional properties of the kch K+ channel; (2) to determine how Kch function affects E. coli physiology; and (3) to expand these findings to other bacteria to elucidate the conserved functions of bacterial cation channels. The results of this work will expand knowledge on the role of cation channels in bacterial physiology. Given the prevalence of these channels in pathogenic bacteria, understanding how cation channels benefit them may reveal how these proteins could be exploited as novel drug targets.

Public Health Relevance

) Tetrameric cation channels are found in nearly all species of bacteria, including major pathogens, yet very little is known about their physiological role. Experiments presented in this application demonstrate that these channels are essential to optimal growth, and we propose to elucidate the direct effects of the ion channel on bacterial physiology. Knowledge gained from this study could be used to help develop bacterial cation channels as novel antimicrobial targets.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
1R01GM132436-01
Application #
9713555
Study Section
Prokaryotic Cell and Molecular Biology Study Section (PCMB)
Program Officer
Gaillard, Shawn R
Project Start
2019-07-01
Project End
2023-06-30
Budget Start
2019-07-01
Budget End
2020-06-30
Support Year
1
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Texas A&M University
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
020271826
City
College Station
State
TX
Country
United States
Zip Code
77845