Cells sense changes in their environment and respond, often in an all-or-none fashion, modulating motility, growth, developmental fate, or synaptic efficacy. Bacterial chemotaxis is a pre-eminent model system for studies of sensory transduction, where mechanisms can be understood in atomic detail. E. coli is a nanotechnological marvel, with cells only a micron in size propelled by several helical filaments, each driven at its base by a rotary motor 50 nm in diameter powered by a proton flux. When the filaments spin counterclockwise (CCW), a cell "runs" steadily forward. When one or more filaments spin clockwise (CW), the cell "tumbles" and changes course. A cell counts molecules of interest in its environment and extends runs deemed favorable. The counting is done by receptors that regulate the activity of a kinase that phosphorylates a response regulator that, when phosphorylated, diffuses across the cytoplasm and binds to the base of the flagellar motors, increasing the probability that they spin CW. The kinase activity is depressed by attractant binding and restored, during adaptation, by methylation. Using fluorescence resonance energy transfer (FRET) between fluorescent fusion proteins in vivo, we will study responses of cells to time-varying stimuli as a test of a model in which methylation rate is specified by kinase activity, and we will assess mechanisms for motor switching. Using fluorescence bleaching, we will study the relative motion of internal motor components. Using light scattered from nano-gold spheres attached to motors in cells without flagellar filaments, we will study the behavior of the motor near zero load, a domain in which movement of protons and mechanical components are rate limiting. By analyzing mutants that allow transformations in flagellar shape that are normally forbidden, we will learn more about the mechanics of flagellar propulsion. While this effort is directly relevant to microbial virulence, it is meant as a study of fundamental biological processes: chemoreception, intracellular signaling, and conversion of chemiosmotic energy to mechanical work.
Motile bacteria measure the concentrations of chemicals in their surroundings and move toward regions that they deem more favorable. Cells with flagella do this by controlling the direction of rotation of motors that drive helical propellers. The goal is to understand the genetics, biochemistry, and physiology of this system in molecular detail, i.e., to understand in a simple model system how cells interact with their environment, a process basic to all living things.
|Hosu, Basarab G; Nathan, Vedavalli S J; Berg, Howard C (2016) Internal and external components of the bacterial flagellar motor rotate as a unit. Proc Natl Acad Sci U S A 113:4783-7|
|Lele, Pushkar P; Roland, Thibault; Shrivastava, Abhishek et al. (2016) The flagellar motor of Caulobacter crescentus generates more torque when a cell swims backward. Nat Phys 12:175-178|
|Shrivastava, Abhishek; Roland, Thibault; Berg, Howard C (2016) The Screw-Like Movement of a Gliding Bacterium Is Powered by Spiral Motion of Cell-Surface Adhesins. Biophys J 111:1008-13|
|Lele, Pushkar P; Shrivastava, Abhishek; Roland, Thibault et al. (2015) Response thresholds in bacterial chemotaxis. Sci Adv 1:e1500299|
|Shrivastava, Abhishek; Berg, Howard C (2015) Towards a model for Flavobacterium gliding. Curr Opin Microbiol 28:93-7|
|Shrivastava, Abhishek; Lele, Pushkar P; Berg, Howard C (2015) A rotary motor drives Flavobacterium gliding. Curr Biol 25:338-41|
|Fahrner, Karen A; Berg, Howard C (2015) Mutations That Stimulate flhDC Expression in Escherichia coli K-12. J Bacteriol 197:3087-96|
|Lele, Pushkar P; Berg, Howard C (2015) Switching of bacterial flagellar motors [corrected] triggered by mutant FliG. Biophys J 108:1275-80|
|Ping, Liyan; Wu, Yilin; Hosu, Basarab G et al. (2014) Osmotic pressure in a bacterial swarm. Biophys J 107:871-8|
|Branch, Richard W; Sayegh, Michael N; Shen, Chong et al. (2014) Adaptive remodelling by FliN in the bacterial rotary motor. J Mol Biol 426:3314-24|
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