H+/Ca2+ exchange driven by the plasma membrane Ca2+-ATPase of Arabidopsis thaliana reconstituted in proteoliposomes after calmodulin-affinity purification
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Luoni, L
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Univ Milan, Dipartimento Biol L Gorini, CNR, Ctr Studio Biol Cellulare & Mol Piante, I-20133 Milan, ItalyUniv Milan, Dipartimento Biol L Gorini, CNR, Ctr Studio Biol Cellulare & Mol Piante, I-20133 Milan, Italy
Luoni, L
[1
]
Bonza, MC
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Univ Milan, Dipartimento Biol L Gorini, CNR, Ctr Studio Biol Cellulare & Mol Piante, I-20133 Milan, ItalyUniv Milan, Dipartimento Biol L Gorini, CNR, Ctr Studio Biol Cellulare & Mol Piante, I-20133 Milan, Italy
Bonza, MC
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De Michelis, MI
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Univ Milan, Dipartimento Biol L Gorini, CNR, Ctr Studio Biol Cellulare & Mol Piante, I-20133 Milan, ItalyUniv Milan, Dipartimento Biol L Gorini, CNR, Ctr Studio Biol Cellulare & Mol Piante, I-20133 Milan, Italy
De Michelis, MI
[1
]
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[1] Univ Milan, Dipartimento Biol L Gorini, CNR, Ctr Studio Biol Cellulare & Mol Piante, I-20133 Milan, Italy
The plasma membrane Ca2+-ATPase was purified from Arabidopsis thaliana cultured cells by calmodulin (CaM)-affinity chromatography and reconstituted in proteoliposomes by the freeze-thaw sonication procedure. The reconstituted enzyme catalyzed CaM-stimulated Ca-45(2+) accumulation and H+ ejection, monitored by the increase of fluorescence of the pH probe pyranine entrapped in the liposomal lumen during reconstitution. Proton ejection was immediately reversed by the protonophore FCCP, indicating that it is not electrically coupled to Ca2+ uptake, but it is a primary event linked to Ca2+ uptake in the form of countertransport. (C) 2000 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.