Abstract
[U-14C]glycine uptake into barley (Hordeum vulgare cv Hasso) vacuoles was investigated. Glycine (2 millimolar) transport was stimulated two- to fourfold by NaATP. Stimulation was saturable with respect to ATP (1 millimolar) and linear up to 20 millimolar glycine. Stimulation by NaATP was suppressed by Mg2+ in equimolar amounts. Neither MgATP nor Mg-inorganic pyrophosphate had any effect on basal transport rate. Thus, the proton motive force can be excluded as the driving force. Uncouplers (valinomycine/carbonylcyanide-m-chlorophenylhydrazone) inhibited the basal rate up to 30% but had no influence on NaATP-stimulated uptake. Vanadate had no effect on either basal or NaATP-stimulated uptake. Nonhydrolyzable ATP analogs (adenylyl(β, γ-methylen)-diphosphate or adenylyl-imidodiphosphate) stimulated comparable to NaATP. Other nucleotides (UTP, ADP) had no effect. Some evidence exists that other amino acids (arginine, alanine, isoleucine, phenylalanine) are transported to a certain extent by a similar mechanism. The results indicate a high capacity channel-like translocator that is regulated but not energized by ATP.
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- Arnon D. I. COPPER ENZYMES IN ISOLATED CHLOROPLASTS. POLYPHENOLOXIDASE IN BETA VULGARIS. Plant Physiol. 1949 Jan;24(1):1–15. doi: 10.1104/pp.24.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Blackwell R. D., Murray A. J., Lea P. J. Photorespiratory mutants of the mitochondrial conversion of glycine to serine. Plant Physiol. 1990 Nov;94(3):1316–1322. doi: 10.1104/pp.94.3.1316. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dietz K. J., Jäger R., Kaiser G., Martinoia E. Amino Acid Transport across the Tonoplast of Vacuoles Isolated from Barley Mesophyll Protoplasts : Uptake of Alanine, Leucine, and Glutamine. Plant Physiol. 1990 Jan;92(1):123–129. doi: 10.1104/pp.92.1.123. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Driessen A. J., Hellingwerf K. J., Konings W. N. Mechanism of energy coupling to entry and exit of neutral and branched chain amino acids in membrane vesicles of Streptococcus cremoris. J Biol Chem. 1987 Sep 15;262(26):12438–12443. [PubMed] [Google Scholar]
- Fischer E., Lüttge U. Membrane Potential Changes Related to Active Transport of Glycine in Lemna gibba G1. Plant Physiol. 1980 May;65(5):1004–1008. doi: 10.1104/pp.65.5.1004. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Garbarino J., Dupont F. M. Rapid induction of na/h exchange activity in barley root tonoplast. Plant Physiol. 1989 Jan;89(1):1–4. doi: 10.1104/pp.89.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Homeyer U., Litek K., Huchzermeyer B., Schultz G. Uptake of Phenylalanine into Isolated Barley Vacuoles Is Driven by Both Tonoplast Adenosine Triphosphatase and Pyrophosphatase : Evidence for a Hydrophobic l-Amino Acid Carrier System. Plant Physiol. 1989 Apr;89(4):1388–1393. doi: 10.1104/pp.89.4.1388. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Huchzermeyer B., Strotmann H. Acid/base-induced exchange of adenine nucleotides on chloroplast coupling factor (CF1). Z Naturforsch C. 1977 Sep-Oct;32(9-10):803–809. doi: 10.1515/znc-1977-9-1024. [DOI] [PubMed] [Google Scholar]
- Martinoia E., Schramm M. J., Kaiser G., Kaiser W. M., Heber U. Transport of anions in isolated barley vacuoles : I. Permeability to anions and evidence for a cl-uptake system. Plant Physiol. 1986 Apr;80(4):895–901. doi: 10.1104/pp.80.4.895. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Martinoia E., Thume M., Vogt E., Rentsch D., Dietz K. J. Transport of arginine and aspartic Acid into isolated barley mesophyll vacuoles. Plant Physiol. 1991 Oct;97(2):644–650. doi: 10.1104/pp.97.2.644. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Oliver D. J., Neuburger M., Bourguignon J., Douce R. Interaction between the Component Enzymes of the Glycine Decarboxylase Multienzyme Complex. Plant Physiol. 1990 Oct;94(2):833–839. doi: 10.1104/pp.94.2.833. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schumaker K. S., Sze H. Solubilization and reconstitution of the oat root vacuolar h/ca exchanger. Plant Physiol. 1990 Feb;92(2):340–345. doi: 10.1104/pp.92.2.340. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Skulachev V. P. Integrating functions of biomembranes. Problems of lateral transport of energy, metabolites and electrons. Biochim Biophys Acta. 1980 Dec 31;604(3):297–310. doi: 10.1016/0005-2736(80)90576-3. [DOI] [PubMed] [Google Scholar]
- Villalobo A. Reconstitution of ion-motive transport ATPases in artificial lipid membranes. Biochim Biophys Acta. 1990 May 15;1017(1):1–48. doi: 10.1016/0005-2728(90)90176-5. [DOI] [PubMed] [Google Scholar]
- Wang Y., Leigh R. A., Kaestner K. H., Sze H. Electrogenic h-pumping pyrophosphatase in tonoplast vesicles of oat roots. Plant Physiol. 1986 Jun;81(2):497–502. doi: 10.1104/pp.81.2.497. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wang Y., Sze H. Similarities and differences between the tonoplast-type and the mitochondrial H+-ATPases of oat roots. J Biol Chem. 1985 Sep 5;260(19):10434–10443. [PubMed] [Google Scholar]