Skip to main content
Plant Physiology logoLink to Plant Physiology
. 1985 Oct;79(2):441–444. doi: 10.1104/pp.79.2.441

The Effect of Low Osmotic Potential on Nitrite Reduction in Intact Spinach Chloroplasts 1

Paul W Behrens 1,2, Fujuan Xu 1,3, Marisa Werner 1, Teresa Hoffman 1, Thomas V Marsho 1,4, A Bryan MacKay 1
PMCID: PMC1074904  PMID: 16664429

Abstract

The effect of water stress (reduced osmotic potential) on photosynthetic nitrite reduction was investigated using intact, isolated spinach (Spinacia oleracea) chloroplasts. Nitrite-dependent O2 evolution was inhibited 39% at −29.5 bars osmotic potential, relative to a control at −11 bars. In the presence of an uncoupler of photophosphorylation this inhibition was not seen. Reduced osmotic potential did not inhibit either methyl viologen reduction or photosynthetic O2 reduction. These results indicate that an inhibition of electron transport to ferredoxin cannot account for the observed inhibition of nitrite-dependent O2 evolution. In vitro assay of nitrite reductase activity showed that the interaction of the enzyme with nitrite was not affected by changes in the concentrations of ions or molecules that might be caused by water stress conditions. These results indicate that the most likely site for the effect of water stress on chloroplastic nitrite reduction is the interaction of ferredoxin with nitrite reductase.

Full text

PDF
441

Selected References

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

  1. Arnon D. I., Tsujimoto H. Y., McSwain B. D. Ferredoxin and photosynthetic phosphorylation. Nature. 1967 May 6;214(5088):562–566. doi: 10.1038/214562a0. [DOI] [PubMed] [Google Scholar]
  2. Behrens P. W., Marsho T. V., Radmer R. J. Photosynthetic o(2) exchange kinetics in isolated soybean cells. Plant Physiol. 1982 Jul;70(1):179–185. doi: 10.1104/pp.70.1.179. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Berkowitz G. A., Gibbs M. Effect of osmotic stress on photosynthesis studied with the isolated spinach chloroplast : generation and use of reducing power. Plant Physiol. 1982 Oct;70(4):1143–1148. doi: 10.1104/pp.70.4.1143. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Berkowitz G. A., Gibbs M. Effect of osmotic stress on photosynthesis studied with the isolated spinach chloroplast : site-specific inhibition of the photosynthetic carbon reduction cycle. Plant Physiol. 1982 Nov;70(5):1535–1540. doi: 10.1104/pp.70.5.1535. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Berkowitz G. A., Gibbs M. Reduced osmotic potential effects on photosynthesis : identification of stromal acidification as a mediating factor. Plant Physiol. 1983 Apr;71(4):905–911. doi: 10.1104/pp.71.4.905. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Heldt W. H., Werdan K., Milovancev M., Geller G. Alkalization of the chloroplast stroma caused by light-dependent proton flux into the thylakoid space. Biochim Biophys Acta. 1973 Aug 31;314(2):224–241. doi: 10.1016/0005-2728(73)90137-0. [DOI] [PubMed] [Google Scholar]
  7. 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]
  8. Ida S., Kobayakawa K., Morita Y. Ferredoxin-Sepharose affinity chromatography for the purification of assimilatory nitrite reductase. FEBS Lett. 1976 Jun 15;65(3):305–308. doi: 10.1016/0014-5793(76)80135-4. [DOI] [PubMed] [Google Scholar]
  9. Marsho T. V., Behrens P. W. Photosynthetic oxygen reduction in isolated intact chloroplasts and cells in spinach. Plant Physiol. 1979 Oct;64(4):656–659. doi: 10.1104/pp.64.4.656. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Marsho T. V., Sokolove P. M., Mackay A. B. Regulation of Photosynthetic Electron Transport in Intact Spinach Chloroplasts: I. INFLUENCE OF EXOGENOUS SALTS ON OXALOACETATE REDUCTION. Plant Physiol. 1980 Apr;65(4):703–706. doi: 10.1104/pp.65.4.703. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Plaut Z., Bravdo B. Response of carbon dioxide fixation to water stress: parallel measurements on isolated chloroplasts and intact spinach leaves. Plant Physiol. 1973 Jul;52(1):28–32. doi: 10.1104/pp.52.1.28. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Plaut Z., Lendzian K., Bassham J. A. Nitrite Reduction in Reconstituted and Whole Spinach Chloroplasts during Carbon Dioxide Reduction. Plant Physiol. 1977 Feb;59(2):184–188. doi: 10.1104/pp.59.2.184. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Radmer R. J., Kok B. Photoreduction of O(2) Primes and Replaces CO(2) Assimilation. Plant Physiol. 1976 Sep;58(3):336–340. doi: 10.1104/pp.58.3.336. [DOI] [PMC free article] [PubMed] [Google Scholar]

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

RESOURCES