Abstract
Mechanically isolated Asparagus sprengeri Regel mesophyll cells were suspended in 1 millimolar CaSO4. Immediate alkalinization of the medium occured on the addition of 1 millimolar concentrations of l-glutamate (Glu) and its analog l-methionine-d,l-sulfoximine (l-MSO). d-Glu and the l isomers of the protein amino acids did not elicit alkalinization. l-Glu dependent alkalinization was transient and acidification resumed after approximately 30 to 45 minutes. At pH 6.0, 5 millimolar l-Glu stimulated initial rates of alkalinization that varied between 1.3 to 4.1 nmol H+/106 cells·minute. l-Glu dependent alkalinization was saturable, increased with decreasing pH, was inhibited by carbonyl cyanide-p-trichloromethoxyphenyl hydrazone (CCCP), and was not stimulated by light. Uptake of l-[U-14C]glutamate increased as the pH decreased from 6.5 to 5.5, and was inhibited by l-MSO. l-Glu had no influence on K+ efflux. Although evidence for multiple amino acid/proton cotransport systems has been found in other tissues, the present report indicates that a highly specific l-Glu/proton uptake process is present in Asparagus mesophyll cells.
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- Bennett A. B., Spanswick R. M. Derepression of amino Acid-h cotransport in developing soybean embryos. Plant Physiol. 1983 Jul;72(3):781–786. doi: 10.1104/pp.72.3.781. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bown A. W. An investigation into the roles of photosynthesis and respiration in h efflux from aerated suspensions of asparagus mesophyll cells. Plant Physiol. 1982 Sep;70(3):803–810. doi: 10.1104/pp.70.3.803. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bown A. W., Nicholls F. An investigation into the role of photosynthesis in regulating ATP levels and rates of h efflux in isolated meosphyll cells. Plant Physiol. 1985 Dec;79(4):928–934. doi: 10.1104/pp.79.4.928. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chapman J. S., Meeks J. C. Glutamine and glutamate transport by Anabaena variabilis. J Bacteriol. 1983 Oct;156(1):122–129. doi: 10.1128/jb.156.1.122-129.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Despeghel J. P., Delrot S. Energetics of Amino Acid Uptake by Vicia faba Leaf Tissues. Plant Physiol. 1983 Jan;71(1):1–6. doi: 10.1104/pp.71.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kanai R., Edwards G. E. Purification of enzymatically isolated mesophyll protoplasts from c(3), c(4), and crassulacean Acid metabolism plants using an aqueous dextran-polyethylene glycol two-phase system. Plant Physiol. 1973 Nov;52(5):484–490. doi: 10.1104/pp.52.5.484. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kinraide T. B., Etherton B. Electrical evidence for different mechanisms of uptake for basic, neutral, and acidic amino acids in oat coleoptiles. Plant Physiol. 1980 Jun;65(6):1085–1089. doi: 10.1104/pp.65.6.1085. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kinraide T. B., Newman I. A., Etherton B. A Quantitative Simulation Model for H-Amino Acid Cotransport To Interpret the Effects of Amino Acids on Membrane Potential and Extracellular pH. Plant Physiol. 1984 Nov;76(3):806–813. doi: 10.1104/pp.76.3.806. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Vogelmann T. C., Dickson R. E., Larson P. R. Comparative Distribution and Metabolism of Xylem-Borne Amino Compounds and Sucrose in Shoots of Populus deltoides. Plant Physiol. 1985 Feb;77(2):418–428. doi: 10.1104/pp.77.2.418. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wyse R. E., Komor E. Mechanism of amino Acid uptake by sugarcane suspension cells. Plant Physiol. 1984 Dec;76(4):865–870. doi: 10.1104/pp.76.4.865. [DOI] [PMC free article] [PubMed] [Google Scholar]