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. 1985 May;78(1):41–45. doi: 10.1104/pp.78.1.41

Energetics of Sucrose Transport into Protoplasts from Developing Soybean Cotyledons 1

Willy Lin 1
PMCID: PMC1064672  PMID: 16664205

Abstract

The accumulation of tetraphenylphosphonium (TPP+), 5,5′-dimethyl-oxazolidine-2,4-dione (DMO), and a micro pH electrode were used to measure membrane potential, intracellular and extracellular pH, respectively, upon the addition of exogenous sucrose to soybean cotyledon protoplasts. Addition of sucrose caused a specific and transient (a) depolarization of the membrane potential (measured by TPP+ accumulation), (b) acidification of the intracellular pH (measured by DMO accumulation), and (c) alkalization of the external medium (measured by a micro pH electrode). The time course for all these changes was similar (i.e. 5 to 10 minutes). Based on the rate of sucrose uptake and alkalization of the external medium, a stoichiometry of 1.02 to 1.10 for proton to sucrose was estimated. These data strongly support a proton/sucrose cotransporting mechanism in soybean cotyledon cells.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Addanki A., Cahill F. D., Sotos J. F. Determination of intramitochondrial pH and intramitochondrial-extramitochondrial pH gradient of isolated heart mitochondria by the use of 5,5-dimethyl-2,4-oxazolidinedione. I. Changes during respiration and adenosine triphosphate-dependent transport of Ca++, Mg++, and Zn++. J Biol Chem. 1968 May 10;243(9):2337–2348. [PubMed] [Google Scholar]
  2. Harold F. M., Papineau D. Cation transport and electrogenesis by Streptococcus faecalis. I. The membrane potential. J Membr Biol. 1972;8(1):27–44. doi: 10.1007/BF01868093. [DOI] [PubMed] [Google Scholar]
  3. Komor E., Tanner W. The determination of the membrane ptoential of Chlorella vulgaris. Evidence for electrogenic sugar transport. Eur J Biochem. 1976 Nov 1;70(1):197–204. doi: 10.1111/j.1432-1033.1976.tb10970.x. [DOI] [PubMed] [Google Scholar]
  4. Lichtner F. T., Spanswick R. M. Electrogenic sucrose transport in developing soybean cotyledons. Plant Physiol. 1981 Apr;67(4):869–874. doi: 10.1104/pp.67.4.869. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Lichtshtein D., Kaback H. R., Blume A. J. Use of a lipophilic cation for determination of membrane potential in neuroblastoma-glioma hybrid cell suspensions. Proc Natl Acad Sci U S A. 1979 Feb;76(2):650–654. doi: 10.1073/pnas.76.2.650. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Lin W. Corn Root Protoplasts: ISOLATION AND GENERAL CHARACTERIZATION OF ION TRANSPORT . Plant Physiol. 1980 Oct;66(4):550–554. doi: 10.1104/pp.66.4.550. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Lin W., Hanson J. B. Increase in electrogenic membrane potential with washing of corn root tissue. Plant Physiol. 1974 Nov;54(5):799–801. doi: 10.1104/pp.54.5.799. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Lin W. Responses of corn root protoplasts to exogenous reduced nicotinamide adenine dinucleotide: Oxygen consumption, ion uptake, and membrane potential. Proc Natl Acad Sci U S A. 1982 Jun;79(12):3773–3776. doi: 10.1073/pnas.79.12.3773. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Lin W., Schmitt M. R., Hitz W. D., Giaquinta R. T. Sugar transport into protoplasts isolated from developing soybean cotyledons : I. Protoplast isolation and general characteristics of sugar transport. Plant Physiol. 1984 Aug;75(4):936–940. doi: 10.1104/pp.75.4.936. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Roos A., Boron W. F. Intracellular pH. Physiol Rev. 1981 Apr;61(2):296–434. doi: 10.1152/physrev.1981.61.2.296. [DOI] [PubMed] [Google Scholar]
  11. Rubinstein B. Use of lipophilic cations to measure the membrane potential of oat leaf protoplasts. Plant Physiol. 1978 Dec;62(6):927–929. doi: 10.1104/pp.62.6.927. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Schmitt M. R., Hitz W. D., Lin W., Giaquinta R. T. Sugar Transport into Protoplasts Isolated from Developing Soybean Cotyledons : II. Sucrose Transport Kinetics, Selectivity, and Modeling Studies. Plant Physiol. 1984 Aug;75(4):941–946. doi: 10.1104/pp.75.4.941. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Schuldiner S., Kaback H. R. Membrane potential and active transport in membrane vesicles from Escherichia coli. Biochemistry. 1975 Dec 16;14(25):5451–5461. doi: 10.1021/bi00696a011. [DOI] [PubMed] [Google Scholar]
  14. Spanswick R. M., Miller A. G. Measurement of the Cytoplasmic pH in Nitella translucens: Comparison of Values Obtained by Microelectrode and Weak Acid Methods. Plant Physiol. 1977 Apr;59(4):664–666. doi: 10.1104/pp.59.4.664. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Thorne J. H. Characterization of the active sucrose transport system of immature soybean embryos. Plant Physiol. 1982 Oct;70(4):953–958. doi: 10.1104/pp.70.4.953. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Volokita M., Kaplan A., Reinhold L. Evidence for Mediated HCO(3) Transport in Isolated Pea Mesophyll Protoplasts. Plant Physiol. 1981 Jun;67(6):1119–1123. doi: 10.1104/pp.67.6.1119. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. WADDELL W. J., BUTLER T. C. Calculation of intracellular pH from the distribution of 5,5-dimethyl-2,4-oxazolidinedione (DMO); application to skeletal muscle of the dog. J Clin Invest. 1959 May;38(5):720–729. doi: 10.1172/JCI103852. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Warth J., Desforges J. F. Intraerythrocyte pH and physiochemical homogeneity. Proc Soc Exp Biol Med. 1978 Oct;159(1):136–138. doi: 10.3181/00379727-159-40299. [DOI] [PubMed] [Google Scholar]

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