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. 1992 May;99(1):291–297. doi: 10.1104/pp.99.1.291

Quantitation of Rates of Transport, Metabolic Fluxes, and Cytoplasmic Levels of Inorganic Carbon in Maize Root Tips during K+ Ion Uptake 1

Keejong Chang 1, Justin K M Roberts 1
PMCID: PMC1080438  PMID: 16668864

Abstract

Our aim was to determine whether fixation of inorganic carbon (Ci), due to phosphoenolpyruvate carboxylase activity, is limited by the availability of Ci in the cytoplasm of maize (Zea mays L.) root tips. Rates of Ci uptake and metabolism were measured during K2SO4 treatment, which stimulates dark Ci fixation. 13Ci uptake was followed by 13C-nuclear magnetic resonance (NMR); 5 millimolar K2SO4 had no significant effect on 13Ci influx. The contribution of respiratory CO2 production to cytoplasmic HCO3 was measured using in vivo 13C-NMR and 1H-NMR of cell extracts; K2SO4 treatment had no effect on respiratory CO2 production. The concentration of cytoplasmic HCO3 was estimated to be approximately 11 millimolar, again with K2SO4 having no significant effect. These experiments allowed us to determine the extent to which extracellularly supplied 14Ci was diluted in the cytoplasm by respiratory CO2 and thereby measure phosphoenolpyruvate (PEP) carboxylase activity in vivo using 14Ci. PEP carboxylase activity in root tips was enhanced approximately 70% over controls within 12 minutes of the addition of 5 millimolar K2SO4. The activity of carbonic anhydrase, which provides PEP carboxylase with Ci, was determined by saturation transfer 13C-NMR to be more than 200 times that of PEP carboxylase in vivo. The regulation of PEP carboxylase in K2SO4-treated roots is discussed.

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Selected References

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  1. Anderson M. P., Heichel G. H., Vance C. P. Nonphotosynthetic CO(2) Fixation by Alfalfa (Medicago sativa L.) Roots and Nodules. Plant Physiol. 1987 Sep;85(1):283–289. doi: 10.1104/pp.85.1.283. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Chang K., Roberts J. K. Cytoplasmic malate levels in maize root tips during K+ ion uptake determined by 13C-NMR spectroscopy. Biochim Biophys Acta. 1991 Mar 19;1092(1):29–34. doi: 10.1016/0167-4889(91)90174-v. [DOI] [PubMed] [Google Scholar]
  3. Chang K., Roberts J. K. Observation of Cytoplasmic and Vacuolar Malate in Maize Root Tips by C-NMR Spectroscopy. Plant Physiol. 1989 Jan;89(1):197–203. doi: 10.1104/pp.89.1.197. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Gadian D. G., Radda G. K., Brown T. R., Chance E. M., Dawson M. J., Wilkie D. R. The activity of creatine kinase in frog skeletal muscle studied by saturation-transfer nuclear magnetic resonance. Biochem J. 1981 Jan 15;194(1):215–228. doi: 10.1042/bj1940215. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Hatch M. D., Burnell J. N. Carbonic anhydrase activity in leaves and its role in the first step of c(4) photosynthesis. Plant Physiol. 1990 Jun;93(2):825–828. doi: 10.1104/pp.93.2.825. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Holtum J. A., Summons R., Roeske C. A., Comins H. N., O'Leary M. H. Oxygen-18 incorporation into malic acid during nocturnal carbon dioxide fixation in crassulacean acid metabolism plants. A new approach to estimating in vivo carbonic anhydrase activity. J Biol Chem. 1984 Jun 10;259(11):6870–6881. [PubMed] [Google Scholar]
  7. Jacoby B., Laties G. G. Bicarbonate Fixation and Malate Compartmentation in Relation to Salt-induced Stoichiometric Synthesis of Organic Acid. Plant Physiol. 1971 Apr;47(4):525–531. doi: 10.1104/pp.47.4.525. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Osmond C. B., Laties G. G. Compartmentation of malate in relation to ion absorption in beet. Plant Physiol. 1969 Jan;44(1):7–14. doi: 10.1104/pp.44.1.7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Overstreet R., Ruben S., Broyer T. C. The Absorption of Bicarbonate Ion by Barley Plants as Indicated by Studies with Radioactive Carbon. Proc Natl Acad Sci U S A. 1940 Dec 15;26(12):688–695. doi: 10.1073/pnas.26.12.688. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Roberts J. K. Observation of uridine triphosphate:glucose-1-phosphate uridylyltransferase activity in maize root tips by saturation transfer 31P-NMR. Estimation of cytoplasmic PP. Biochim Biophys Acta. 1990 Jan 23;1051(1):29–36. doi: 10.1016/0167-4889(90)90170-i. [DOI] [PubMed] [Google Scholar]
  11. Roberts J. K., Wemmer D., Jardetzky O. Measurement of mitochondrial ATPase activity in maize root tips by saturation transfer p nuclear magnetic resonance. Plant Physiol. 1984 Mar;74(3):632–639. doi: 10.1104/pp.74.3.632. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Saglio P. H., Pradet A. Soluble Sugars, Respiration, and Energy Charge during Aging of Excised Maize Root Tips. Plant Physiol. 1980 Sep;66(3):516–519. doi: 10.1104/pp.66.3.516. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Schuller K. A., Plaxton W. C., Turpin D. H. Regulation of Phosphoenolpyruvate Carboxylase from the Green Alga Selenastrum minutum: Properties Associated with Replenishment of Tricarboxylic Acid Cycle Intermediates during Ammonium Assimilation. Plant Physiol. 1990 Aug;93(4):1303–1311. doi: 10.1104/pp.93.4.1303. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Smith R. G., Vanlerberghe G. C., Stitt M., Turpin D. H. Short-Term Metabolite Changes during Transient Ammonium Assimilation by the N-Limited Green Alga Selenastrum minutum. Plant Physiol. 1989 Oct;91(2):749–755. doi: 10.1104/pp.91.2.749. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Ting I. P. CO(2) Metabolism in Corn Roots. III. Inhibition of P-enolpyruvate Carboxylase by l-malate. Plant Physiol. 1968 Dec;43(12):1919–1924. doi: 10.1104/pp.43.12.1919. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Ting I. P., Dugger W. M. CO(2) Metabolism in Corn Roots. I. Kinetics of Carboxylation and Decarboxylation. Plant Physiol. 1967 May;42(5):712–718. doi: 10.1104/pp.42.5.712. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Turpin D. H., Botha F. C., Smith R. G., Feil R., Horsey A. K., Vanlerberghe G. C. Regulation of Carbon Partitioning to Respiration during Dark Ammonium Assimilation by the Green Alga Selenastrum minutum. Plant Physiol. 1990 May;93(1):166–175. doi: 10.1104/pp.93.1.166. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Vanlerberghe G. C., Schuller K. A., Smith R. G., Feil R., Plaxton W. C., Turpin D. H. Relationship between NH(4) Assimilation Rate and in Vivo Phosphoenolpyruvate Carboxylase Activity : Regulation of Anaplerotic Carbon Flow in the Green Alga Selenastrum minutum. Plant Physiol. 1990 Sep;94(1):284–290. doi: 10.1104/pp.94.1.284. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Wedding R. T., Black M. K., Meyer C. R. Inhibition of phosphoenolpyruvate carboxylase by malate. Plant Physiol. 1990 Feb;92(2):456–461. doi: 10.1104/pp.92.2.456. [DOI] [PMC free article] [PubMed] [Google Scholar]

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