Skip to main content
Plant Physiology logoLink to Plant Physiology
. 1989 Oct;91(2):679–684. doi: 10.1104/pp.91.2.679

Stromal Phosphate Concentration Is Low during Feedback Limited Photosynthesis 1

Thomas D Sharkey 1, Peter J Vanderveer 1
PMCID: PMC1062055  PMID: 16667087

Abstract

It has been hypothesized that photosynthesis can be feedback limited when the phosphate concentration cannot be both low enough to allow starch and sucrose synthesis at the required rate and high enough for ATP synthesis at the required rate. We have measured the concentration of phosphate in the stroma and cytosol of leaves held under feedback conditions. We used non-aqueous fractionation techniques with freeze-clamped leaves of Phaseolus vulgaris plants grown on reduced phosphate nutrition. Feedback was induced by holding leaves in low O2 or high CO2 partial pressure. We found 7 millimolar phosphate in the stroma of leaves in normal oxygen but just 2.7 millimolar phosphate in leaves held in low oxygen. Because 1 to 2 millimolar phosphate in the stroma may be metabolically inactive, we estimate that in low oxygen, the metabolically active pool of phosphate is between negligible and 1.7 millimolar. We conclude that halfway between these extremes, 0.85 millimolar is a good estimate of the phosphate concentration in the stroma of feedback-limited leaves and that the true concentration could be even lower. The stromal phosphate concentration was also low when leaves were held in high CO2, which also induces feedback-limited photosynthesis, indicating that the effect is related to feedback limitation, not to low oxygen per se. We conclude that the concentration of phosphate in the stroma is usually in excess and that it is sequestered to regulate photosynthesis, especially starch synthesis. The capacity for this regulation is limited by the coupling factor requirement for phosphate.

Full text

PDF
679

Selected References

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

  1. Foyer C., Walker D., Spencer C., Mann B. Observations on the phosphate status and intracellular pH of intact cells, protoplasts and chloroplasts from photosynthetic tissue using phosphorus-31 nuclear magnetic resonance. Biochem J. 1982 Feb 15;202(2):429–434. doi: 10.1042/bj2020429. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Gerhardt R., Heldt H. W. Measurement of subcellular metabolite levels in leaves by fractionation of freeze-stopped material in nonaqueous media. Plant Physiol. 1984 Jul;75(3):542–547. doi: 10.1104/pp.75.3.542. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Harris G. C., Cheesbrough J. K., Walker D. A. Effects of mannose on photosynthetic gas exchange in spinach leaf discs. Plant Physiol. 1983 Jan;71(1):108–111. doi: 10.1104/pp.71.1.108. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Itaya K., Ui M. A new micromethod for the colorimetric determination of inorganic phosphate. Clin Chim Acta. 1966 Sep;14(3):361–366. doi: 10.1016/0009-8981(66)90114-8. [DOI] [PubMed] [Google Scholar]
  5. Monson R. K., Fall R. Isoprene emission from aspen leaves : influence of environment and relation to photosynthesis and photorespiration. Plant Physiol. 1989 May;90(1):267–274. doi: 10.1104/pp.90.1.267. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Penney C. L. A simple micro-assay for inorganic phosphate. Anal Biochem. 1976 Sep;75(1):201–210. doi: 10.1016/0003-2697(76)90071-3. [DOI] [PubMed] [Google Scholar]
  7. Rebeille F., Bligny R., Martin J. B., Douce R. Relationship between the cytoplasm and the vacuole phosphate pool in Acer pseudoplatanus cells. Arch Biochem Biophys. 1983 Aug;225(1):143–148. doi: 10.1016/0003-9861(83)90017-6. [DOI] [PubMed] [Google Scholar]
  8. Sage R. F., Sharkey T. D. The Effect of Temperature on the Occurrence of O(2) and CO(2) Insensitive Photosynthesis in Field Grown Plants. Plant Physiol. 1987 Jul;84(3):658–664. doi: 10.1104/pp.84.3.658. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Santarius K. A., Heber U. Changes in the intracellular levels of ATP, ADP, AMP and P1 and regulatory function of the adenylate system in leaf cells during photosynthesis. Biochim Biophys Acta. 1965 May 25;102(1):39–54. doi: 10.1016/0926-6585(65)90201-3. [DOI] [PubMed] [Google Scholar]
  10. Schröppel-Meier G., Kaiser W. M. Ion Homeostasis in Chloroplasts under Salinity and Mineral Deficiency: II. Solute Distribution between Chloroplasts and Extrachloroplastic Space under Excess or Deficiency of Sulfate, Phosphate, or Magnesium. Plant Physiol. 1988 Aug;87(4):828–832. doi: 10.1104/pp.87.4.828. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Selman B. R., Selman-Reimer S. The steady state kinetics of photophosphorylation. J Biol Chem. 1981 Feb 25;256(4):1722–1726. [PubMed] [Google Scholar]
  12. Sharkey T. D. O(2)-insensitive photosynthesis in c(3) plants : its occurrence and a possible explanation. Plant Physiol. 1985 May;78(1):71–75. doi: 10.1104/pp.78.1.71. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Sharkey T. D., Seemann J. R., Berry J. A. Regulation of Ribulose-1,5-Bisphosphate Carboxylase Activity in Response to Changing Partial Pressure of O(2) and Light in Phaseolus vulgaris. Plant Physiol. 1986 Jul;81(3):788–791. doi: 10.1104/pp.81.3.788. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Sharkey T. D., Stitt M., Heineke D., Gerhardt R., Raschke K., Heldt H. W. Limitation of Photosynthesis by Carbon Metabolism : II. O(2)-Insensitive CO(2) Uptake Results from Limitation Of Triose Phosphate Utilization. Plant Physiol. 1986 Aug;81(4):1123–1129. doi: 10.1104/pp.81.4.1123. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Sharkey T. D., Vassey T. L. Low oxygen inhibition of photosynthesis is caused by inhibition of starch synthesis. Plant Physiol. 1989 Jun;90(2):385–387. doi: 10.1104/pp.90.2.385. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Vassey T. L., Sharkey T. D. Mild Water Stress of Phaseolus vulgaris Plants Leads to Reduced Starch Synthesis and Extractable Sucrose Phosphate Synthase Activity. Plant Physiol. 1989 Apr;89(4):1066–1070. doi: 10.1104/pp.89.4.1066. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Wintermans J. F., de Mots A. Spectrophotometric characteristics of chlorophylls a and b and their pheophytins in ethanol. Biochim Biophys Acta. 1965 Nov 29;109(2):448–453. doi: 10.1016/0926-6585(65)90170-6. [DOI] [PubMed] [Google Scholar]

Articles from Plant Physiology are provided here courtesy of Oxford University Press

RESOURCES