Javascript must be enabled to continue!
Potassium-mediated bacterial chemotactic response
View through CrossRef
Abstract
Bacteria in biofilms secrete potassium ions to attract free swimming cells. However, the basis of chemotaxis to potassium remains poorly understood. Here, using a microfluidic device, we found that Escherichia coli can rapidly accumulate in regions of high potassium concentration on the order of millimoles. Using a bead assay, we measured the dynamic response of individual flagellar motors to stepwise changes in potassium concentration, finding that the response resulted from the chemotaxis signaling pathway instead of the motor response to changes in the proton motive force (PMF). To characterize the chemotactic response to potassium, we exposed the bacteria to a range of potassium concentrations and measured the dose-response curve and adaptation kinetics via a FRET assay, finding that the chemotaxis pathway exhibited a sensitive response and fast adaptation to potassium. We further found that the two major chemoreceptors Tar and Tsr respond differently to potassium. Tar receptors exhibit a biphasic response, whereas Tsr receptors respond to potassium as an attractant. These different responses were consistent with the responses of the two receptors to intracellular pH changes. Therefore, bacteria may sense the change in potassium concentration by sensing the change in intracellular pH. The sensitive response and fast adaptation allow bacteria to sense and localize small changes in potassium concentration. As the ratio of the two major chemoreceptors changes with bacterial growth stages, the differential responses of Tar and Tsr receptors to potassium suggest that cells at different growth stages respond differently to potassium and may have different requirements for potassium.
Title: Potassium-mediated bacterial chemotactic response
Description:
Abstract
Bacteria in biofilms secrete potassium ions to attract free swimming cells.
However, the basis of chemotaxis to potassium remains poorly understood.
Here, using a microfluidic device, we found that Escherichia coli can rapidly accumulate in regions of high potassium concentration on the order of millimoles.
Using a bead assay, we measured the dynamic response of individual flagellar motors to stepwise changes in potassium concentration, finding that the response resulted from the chemotaxis signaling pathway instead of the motor response to changes in the proton motive force (PMF).
To characterize the chemotactic response to potassium, we exposed the bacteria to a range of potassium concentrations and measured the dose-response curve and adaptation kinetics via a FRET assay, finding that the chemotaxis pathway exhibited a sensitive response and fast adaptation to potassium.
We further found that the two major chemoreceptors Tar and Tsr respond differently to potassium.
Tar receptors exhibit a biphasic response, whereas Tsr receptors respond to potassium as an attractant.
These different responses were consistent with the responses of the two receptors to intracellular pH changes.
Therefore, bacteria may sense the change in potassium concentration by sensing the change in intracellular pH.
The sensitive response and fast adaptation allow bacteria to sense and localize small changes in potassium concentration.
As the ratio of the two major chemoreceptors changes with bacterial growth stages, the differential responses of Tar and Tsr receptors to potassium suggest that cells at different growth stages respond differently to potassium and may have different requirements for potassium.
Related Results
Potassium-mediated bacterial chemotactic response
Potassium-mediated bacterial chemotactic response
Abstract
Bacteria in biofilms secrete potassium ions to attract free swimming cells. However, the basis of chemotaxis to potassium remains poorly understood. Here, using a microflu...
Potassium-mediated bacterial chemotactic response
Potassium-mediated bacterial chemotactic response
Abstract
Bacteria in biofilms secrete potassium ions to attract free swimming cells. However, the basis of chemotaxis to potassium remains poorly understood. Here, using a microflu...
Potassium-mediated bacterial chemotactic response
Potassium-mediated bacterial chemotactic response
AbstractBacteria in biofilms secrete potassium ions to attract free swimming cells. However, the basis of chemotaxis to potassium remains poorly understood. Here, using a microflui...
A C5 Fragment with Chemotactic Activity for Tumor Cells
A C5 Fragment with Chemotactic Activity for Tumor Cells
Abstract
The chemotactic behavior of several animal tumor cells (Novikoff hepatoma cells, Walker carcinosarcoma cells, and murine mastocytoma cells) was studied in m...
Monocyte Chemotactic Activity in Sera after Hypnotically Induced Emotional States
Monocyte Chemotactic Activity in Sera after Hypnotically Induced Emotional States
In a number of studies it has been shown that psychological factors in general and specifically emotional factors can be correlated to changes in immunological function and defence...
Sodium, potassium intake and urinary sodium-to-potassium ratio in rheumatoid arthritis: association with markers of cardiovascular dysfunction and disease-related parameters
Sodium, potassium intake and urinary sodium-to-potassium ratio in rheumatoid arthritis: association with markers of cardiovascular dysfunction and disease-related parameters
Abstract
Introduction/objectives
Patients with rheumatoid arthritis (RA) are at increased cardiovascular risk. Rather than either sodium or potas...
Revisiting Chemoaffinity Theory:Chemotactic Implementation of Topographic Axonal Projection
Revisiting Chemoaffinity Theory:Chemotactic Implementation of Topographic Axonal Projection
AbstractNeural circuits are wired by chemotactic migration of growth cones guided by extracellular guidance cue gradients. How growth cone chemotaxis builds the macroscopic structu...
Selective Inhibition of Potassium Contracture in Presence of Intact Twitch
Selective Inhibition of Potassium Contracture in Presence of Intact Twitch
If a sartorius muscle of frog is pretreated for 30 min. with a hyposmotic Ringer's (called "hyposmotic potassium chloride") in which all sodium chloride is replaced by 23 mM potass...


