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Membrane effects of 2,4-dichlorophenoxyacetic acid in motor cells of Mimosa pudica L.
Authors:Christelle Moyen  Janine Bonmort  Gabriel Roblin
Institution:1. Range Ecologist, Arctic Slope Regional Corporation Research & Technology Solutions, Contractor to US Geological Survey (USGS) Earth Resources Observation and Science (EROS) Center, Sioux Falls, SD 57198, USA;;2. Professor, Department of Natural Resource Management, South Dakota State University, Brookings, SD 57007, USA;3. Research Physical Scientist, US Geological Survey (USGS) Earth Resources Observation and Science (EROS) Center, Sioux Falls, SD 57198, USA.;1. Range Ecologist, Arctic Slope Regional Corporation Research & Technology Solutions, Contractor to US Geological Survey Earth Resources Observation and Science Center, Sioux Falls, SD 57198, USA;2. Professor, Department of Natural Resource Management, South Dakota State University, Brookings, SD 57007, USA;3. Research Physical Scientist, US Geological Survey Earth Resources Observation and Science Center, Sioux Falls, SD 57198, USA;4. Graduate Research Assistant, Department of Natural Resource Management, South Dakota State University, Brookings, SD 57007, USA.
Abstract:2,4-dichlorophenoxyacetic acid applied to excised leaves of Mimosa pudica L. inhibited in a dose-dependent manner the shock-induced pulvinar movement. This inhibition was negatively correlated with the amount of (14)C] 2,4-dichlorophenoxyacetic acid present in the vicinity of the motor cells. Although 2,4-dichlorophenoxyacetic acid is a weak acid, its greatest physiological efficiency was obtained with pH values close to neutrality. This observation opens the question of its mode of action which may be through external signaling or following internal transport by a specific anionic form transporter. The effect was related to molecular structure since 2,4-dichlorophenoxyacetic acid>3,4-dichlorophenoxyacetic acid>2,3-dichlorophenoxyacetic acid. An essential target of 2,4-dichlorophenoxyacetic acid action lies at the plasmalemma as indicated by the induced hyperpolarization of the cell membrane. Compared to indole-3-acetic acid and fusicoccin, it induced a complex effect on H(+) fluxes. Applied to plasma membrane vesicles purified from motor organs, 2,4-dichlorophenoxyacetic acid enhanced proton pumping, but, unlike fusicoccin, it did not increase the H(+)-ATPase catalytic activity in our experimental conditions. Taken together, the data suggest that 2,4-dichlorophenoxyacetic acid acts on cell turgor variation and the concomittant ion migration, in particular K(+), by a mechanism involving specific steps compared to indole-3-acetic acid and fusicoccin.
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