Modulation of the vacuolar H+-ATPase by adenylates as basis for the transient CO2-dependent acidification of the leaf vacuole upon illumination

Dietz K-J, Heber U, Mimura T (1998)
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES 1373(1): 87-92.

Zeitschriftenaufsatz | Veröffentlicht | Englisch
 
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Autor*in
Dietz, Karl-JosefUniBi; Heber, U; Mimura, T
Abstract / Bemerkung
Using tonoplast vesicles, we have investigated the activity of the vacuolar H+-ATPase which is the dominant proton pump at the tonoplast of mesophyll cells. Bafilomycin-sensitive ATP hydrolysis or acidification of tonoplast vesicles in the presence of ATP were measured at varying ATP, ADP and P-i concentrations, and in the presence of oxidized or reduced glutathione. Increased ATP/ADP ratios as reported for the extrachloroplast cytoplasm during the induction phase of photosynthesis at high or low CO2 (P. Gardestrom, Biochim. Biophys. Acta 1183 (1993) 327-332) increased the activity of the V-ATPase in simulation experiments with vesicles. Depending on reported subsequent decreases in cytoplasmic ATP/ADP ratios in the presence of high or low CO2, the ATPase activity of tonoplast vesicles changed in simulation experiments to lower values. More than 10 mM phosphate was required to decrease the ATPase activity in vesicles significantly at ATP/ADP ratios of 3 or higher, indicating that ATPase activity is controlled more by ratios of ATP to ADP than by phosphorylation potentials (ATP)/(ADP)(P-i). Oxidized glutathione was inhibitory. The results permit interpretation of the observation that on illumination of previously darkened leaves the pH of the vacuoles of mesophyll cells decreases indicating energized transport of protons across the tonoplast into acidic vacuoles, and that the extent of vacuolar acidification depends on the CO2 concentration of the surrounding air (Z.-H. Yin, S. Neimanis, U. Heber, Planta 182 (1990) 253-261). We conclude that short term control of tonoplast ATPase activity in leaves during dark/light transients can essentially be understood on the basis of reported changes in cytoplasmic ATP/ADP ratios, with a possible participation of redox modulation. (C) 1998 Elsevier Science B,V. All rights reserved.
Stichworte
proton pumping; pH homeostasis; ATPase; tonoplast; redox control
Erscheinungsjahr
1998
Zeitschriftentitel
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES
Band
1373
Ausgabe
1
Seite(n)
87-92
ISSN
0005-2736
Page URI
https://pub.uni-bielefeld.de/record/1625003

Zitieren

Dietz K-J, Heber U, Mimura T. Modulation of the vacuolar H+-ATPase by adenylates as basis for the transient CO2-dependent acidification of the leaf vacuole upon illumination. BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES. 1998;1373(1):87-92.
Dietz, K. - J., Heber, U., & Mimura, T. (1998). Modulation of the vacuolar H+-ATPase by adenylates as basis for the transient CO2-dependent acidification of the leaf vacuole upon illumination. BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1373(1), 87-92. https://doi.org/10.1016/S0005-2736(98)00094-7
Dietz, Karl-Josef, Heber, U, and Mimura, T. 1998. “Modulation of the vacuolar H+-ATPase by adenylates as basis for the transient CO2-dependent acidification of the leaf vacuole upon illumination”. BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES 1373 (1): 87-92.
Dietz, K. - J., Heber, U., and Mimura, T. (1998). Modulation of the vacuolar H+-ATPase by adenylates as basis for the transient CO2-dependent acidification of the leaf vacuole upon illumination. BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES 1373, 87-92.
Dietz, K.-J., Heber, U., & Mimura, T., 1998. Modulation of the vacuolar H+-ATPase by adenylates as basis for the transient CO2-dependent acidification of the leaf vacuole upon illumination. BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1373(1), p 87-92.
K.-J. Dietz, U. Heber, and T. Mimura, “Modulation of the vacuolar H+-ATPase by adenylates as basis for the transient CO2-dependent acidification of the leaf vacuole upon illumination”, BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, vol. 1373, 1998, pp. 87-92.
Dietz, K.-J., Heber, U., Mimura, T.: Modulation of the vacuolar H+-ATPase by adenylates as basis for the transient CO2-dependent acidification of the leaf vacuole upon illumination. BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES. 1373, 87-92 (1998).
Dietz, Karl-Josef, Heber, U, and Mimura, T. “Modulation of the vacuolar H+-ATPase by adenylates as basis for the transient CO2-dependent acidification of the leaf vacuole upon illumination”. BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES 1373.1 (1998): 87-92.

17 Zitationen in Europe PMC

Daten bereitgestellt von Europe PubMed Central.

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Vacuolar compartmentalization as indispensable component of heavy metal detoxification in plants.
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Inorganic phosphate uptake in intact vacuoles isolated from suspension-cultured cells of Catharanthus roseus (L.) G. Don under varying Pi status.
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PMID: 16955272
Transcript level regulation of the vacuolar H(+)-ATPase subunit isoforms VHA-a, VHA-E and VHA-G in Arabidopsis thaliana.
Hanitzsch M, Schnitzer D, Seidel T, Golldack D, Dietz KJ., Mol Membr Biol 24(5-6), 2007
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Evidence for major structural changes in subunit C of the vacuolar ATPase due to nucleotide binding.
Armbrüster A, Hohn C, Hermesdorf A, Schumacher K, Börsch M, Grüber G., FEBS Lett 579(9), 2005
PMID: 15792803
Mapping of C-termini of V-ATPase subunits by in vivo-FRET measurements.
Seidel T, Golldack D, Dietz KJ., FEBS Lett 579(20), 2005
PMID: 16061227
Isolation of intact vacuoles and proteomic analysis of tonoplast from suspension-cultured cells of Arabidopsis thaliana.
Shimaoka T, Ohnishi M, Sazuka T, Mitsuhashi N, Hara-Nishimura I, Shimazaki K, Maeshima M, Yokota A, Tomizawa K, Mimura T., Plant Cell Physiol 45(6), 2004
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Subcellular distribution of the V-ATPase complex in plant cells, and in vivo localisation of the 100 kDa subunit VHA-a within the complex.
Kluge C, Seidel T, Bolte S, Sharma SS, Hanitzsch M, Satiat-Jeunemaitre B, Ross J, Sauer M, Golldack D, Dietz KJ., BMC Cell Biol 5(), 2004
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Inhibition of the yeast V-type ATPase by cytosolic ADP.
Kettner C, Obermeyer G, Bertl A., FEBS Lett 535(1-3), 2003
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Significance of the V-type ATPase for the adaptation to stressful growth conditions and its regulation on the molecular and biochemical level.
Dietz KJ, Tavakoli N, Kluge C, Mimura T, Sharma SS, Harris GC, Chardonnens AN, Golldack D., J Exp Bot 52(363), 2001
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The functions of inter- and intracellular glutathione transport systems in plants.
Foyer CH, Theodoulou FL, Delrot S., Trends Plant Sci 6(10), 2001
PMID: 11590068
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