Skip to main content
Plant Physiology logoLink to Plant Physiology
. 1984 Apr;74(4):956–961. doi: 10.1104/pp.74.4.956

Permeability of Chloroplast Envelopes to Mg2+1

Effects on Protein Synthesis

Raymond J Deshaies 1,2, Leonard E Fish 1,3, Andre T Jagendorf 1
PMCID: PMC1066800  PMID: 16663541

Abstract

When suspended in media lacking free Mg2+, chloroplasts from young pea plants (Pisum sativum CV Progress No. 9) lose 25 to 75% of their stromal Mg2+ content to the medium, without breakage. This effect amounts for the inhibition of protein synthesis in the dark by ATP in excess of the Mg2+ provided, since free ATP chelates Mg2+. The rate of loss is from 1 to 4.5 microgram-atoms Mg2+/milligram Chl/hour; and depleted chloroplasts take up Mg2+ from the medium at even faster rates, to a total amount not much more than that present originally (0.8 to 1.8 microgram-atoms/milligram Chl with an average of 1.33 ± 0.32 μg-atoms/mg Chl). Leakage is completely prevented by 0.25 to 0.40 millimolar external Mg2+. Addition of Mg2+ at a level sufficient to prevent leakage from intact chloroplasts results in approximately 20% stimulation in light-driven protein synthesis.

Full text

PDF
957

Selected References

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

  1. 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]
  2. Avron M., Gibbs M. Carbon dioxide fixation in the light and in the dark by isolated spinach chloroplasts. Plant Physiol. 1974 Feb;53(2):140–143. doi: 10.1104/pp.53.2.140. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bottomley W., Spencer D., Whitfeld P. R. Protein synthesis in isolated spinach chloroplasts: comparison of light-driven and ATP-driven synthesis. Arch Biochem Biophys. 1974 Sep;164(1):106–117. doi: 10.1016/0003-9861(74)90012-5. [DOI] [PubMed] [Google Scholar]
  4. Heber U., Santarius K. A. Direct and indirect transfer of ATP and ADP across the chloroplast envelope. Z Naturforsch B. 1970 Jul;25(7):718–728. doi: 10.1515/znb-1970-0714. [DOI] [PubMed] [Google Scholar]
  5. Huber S. C., Maury W. Effects of Magnesium on Intact Chloroplasts: I. EVIDENCE FOR ACTIVATION OF (SODIUM) POTASSIUM/PROTON EXCHANGE ACROSS THE CHLOROPLAST ENVELOPE. Plant Physiol. 1980 Feb;65(2):350–354. doi: 10.1104/pp.65.2.350. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Markwell M. A., Haas S. M., Bieber L. L., Tolbert N. E. A modification of the Lowry procedure to simplify protein determination in membrane and lipoprotein samples. Anal Biochem. 1978 Jun 15;87(1):206–210. doi: 10.1016/0003-2697(78)90586-9. [DOI] [PubMed] [Google Scholar]
  7. Piazza G. J., Gibbs M. Influence of adenosine phosphates and magnesium on photosynthesis in chloroplasts from peas, sedum, and spinach. Plant Physiol. 1983 Mar;71(3):680–687. doi: 10.1104/pp.71.3.680. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Portis A. R. Evidence of a Low Stromal Mg Concentration in Intact Chloroplasts in the Dark: I. STUDIES WITH THE IONOPHORE A23187. Plant Physiol. 1981 May;67(5):985–989. doi: 10.1104/pp.67.5.985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Portis A. R., Jr, Heldt H. W. Light-dependent changes of the Mg2+ concentration in the stroma in relation to the Mg2+ dependency of CO2 fixation in intact chloroplasts. Biochim Biophys Acta. 1976 Dec 6;449(3):434–436. doi: 10.1016/0005-2728(76)90154-7. [DOI] [PubMed] [Google Scholar]
  10. Telfer A., Barber J. Dual action of ionophore A23187 on intact chloroplasts. Biochim Biophys Acta. 1978 Jan 11;501(1):94–102. doi: 10.1016/0005-2728(78)90098-1. [DOI] [PubMed] [Google Scholar]

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

RESOURCES