Abstract
Whole-cell patch clamp recordings were done on giant protoplasts of Escherichia coli. The pressure sensitivity of the protoplasts was studied. Two different unit conductance mechanosensitive channels, 1100 +/- 25 pS and 350 +/- 14 pS in 400 mM symmetric KCl solution, were observed upon either applying positive pressure to the interior of the cells or down shocking the cells osmotically. The 1100 pS conductance channel discriminated poorly among the monovalent ions tested and it was permeable to Ca2+ and glutamate-. Both of the two channels were sensitive to the osmotic gradient across the membrane; the unit conductances of the channels remained constant while the mean current of the cell was increased by increasing the osmotic gradient. Both of the channels were voltage sensitive. Voltage-ramp results showed that the pressure sensitivity of protoplasts was voltage dependent: there were more channels active upon depolarization than hyperpolarization. The mechanosensitive channels were reversibly blocked by gadolinium ion. Also they could reversibly be inhibited by protons. Mutations in two of the potassium efflux systems, KefB and KefC, did not affect the channel activity, while a null mutation in the gene for KefA changed the channel activity significantly. This indicates a potential modulation of these channels by KefA.
MeSH Terms
Antiporters/physiology
Bacterial Proteins/physiology
Calcium/metabolism
Cytoplasm/physiology
Escherichia coli/physiology
Escherichia coli Proteins
Gadolinium/pharmacology
Glutamic Acid/metabolism
Intracellular Membranes/physiology
Ion Channel Gating/physiology
Mechanoreceptors/physiology
Osmotic Pressure
Patch-Clamp Techniques
Potassium/metabolism
Potassium Channels/physiology
Potassium-Hydrogen Antiporters
Protons
Protoplasts/physiology
Chemicals
Antiporters
Bacterial Proteins
Escherichia coli Proteins
Potassium Channels
Potassium-Hydrogen Antiporters
Protons
KefC protein, E coli
Glutamic Acid
Gadolinium
Potassium
Calcium
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Cui C
Department of Biochemistry, University of Wisconsin-Madison 53706, USA.
Smith D O
Adler J
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