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Photosynthetic electron transport and carbon-reduction-cycle enzyme activities under long-term drought stress in Casuarina equisetifolia Forst. & Forst.

Abstract

The inhibition of photosynthetic electron transport and the activity of photosynthetic carbon reduction cycle (PCR) enzymes under long-term water stress after slow dehydration was studied in non-nodulated Casuarina equisetifolia Forst. & Forst. plants. Initially, drought increased the fraction of closed Photosystem II (PS II) reaction centres (lowered qP) and decreased the quantum yield of PS II electron transport (ΦPSII) with no enhancement of non-radiative dissipation of light energy (qN) because it increased the efficiency of electron capture by open PS II centres (F′v/F′m). As drought progressed, F′v/F′m fell and the decrease in ΦPSII was associated with an increased qN. The kinetics of dark relaxation of fluorescence quenching pointed to an increase in a slowly-relaxing component under drought, in association with increased contents of zeaxanthin and antheraxanthin. Total NADP-dependent malate dehydrogenase activity increased and total stromal fructose-1,6-bisphosphatase activity decreased under drought, while the activation state of these enzymes remained unchanged. Water stress did not alter the activity and the activation state of ribulose bisphosphate carboxylase oxygenase.

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References

  • Arnon DI (1949) Copper enzymes in isolated chloroplasts. Polyphenol oxidase in Beta vulgaris. Plant Physiol 73: 681–686

    Google Scholar 

  • Boyer JS (1976) Water deficits and photosynthesis. In: Kozlowski TT (ed) Water Deficits and Plant Growth, Vol 4, pp 153–190. Academic Press, New York

    Google Scholar 

  • Boyer JS and Younis HM (1983) Molecular aspects of photosynthesis at low leaf water potentials. In: Marcelle R, Clijsters H and van Poucke M (eds) Effects of Stress on Photosynthesis, pp 29–34. Martinus Nijhoff/Dr. W Junk Publishers, The Hague, the Netherlands

    Google Scholar 

  • Brestic M, Cornic G, Fryer MJ and Baker NR (1995) Does photorespiration protect the photosynthetic apparatus in French bean leaves from photoinhibition during drought stress? Planta 196: 450–457

    Article  Google Scholar 

  • Chaumont M, Morot-Gaudry J-F and Foyer CH (1995) Effects of photoinhibitory treatment on CO2 assimilation, the quantum yield of CO2 assimilation, D1 protein, ascorbate, glutathione and xanthophyll contents and the electron transport rate in vine leaves. Plant Cell Environ 18: 1358–1366

    Google Scholar 

  • Cornic G (1994) Drought stress and high light effects on leaf photosynthesis. In: Baker NR and Bowyer JR (eds) Photoinhibition of Photosynthesis. From Molecular Mechanisms to the field, pp 297–313. Bios Scientific Publishers, Oxford, UK

    Google Scholar 

  • Demmig-Adams B (1990) Carotenoids and photoprotection in plants: A role for the xanthophyll zeaxanthin. Biochim Biophys Acta 1020: 1–24

    Google Scholar 

  • Demmig-Adams B and Adams WW (1996) Xanthophyll cycle and light stress in nature: Uniform response to excess direct sunlight among higher plant species. Planta 198: 460–470.

    Google Scholar 

  • Demmig B, Winter K, Krüger A and Czygan FC (1988) Zeaxanthin and the heat dissipation of excess light energy in Nerium oleander exposed to a combination of high light and water stress. Plant Physiol 87: 17–24

    Google Scholar 

  • Genty B, Briantais J-M and Baker NR (1989) The relationship between the quantum yield of photosynthetic electron transport and quenching of chlorophyll fluorescence. Biochim Biophys Acta 990: 87–92

    Google Scholar 

  • Giardi MT, Cona A, Geiken B, Kucera T, Masojídek J and Mattoo AK (1996) Long-term drought stress induces structural and functional reorganization of Photosystem II. Planta 199: 118–125

    Article  Google Scholar 

  • Gilmore AM and Yamamoto HY (1991) Resolution of lutein and zeaxanthin using a non-endcapped, lightly carbon-loaded C18 high-performance liquid chromatographic column. J Chromatogr 543: 137–145

    Article  Google Scholar 

  • Gimenez C, Mitchell VJ and Lawlor DW (1992) Regulation of photosynthetic rate of two sunflower hybrids under water stress. Plant Physiol 98: 516–524

    Google Scholar 

  • Gunasekera D and Berkowitz GA (1993) Use of transgenic plants with ribulose-1,5-bisphosphate carboxylase/oxygenase antisense DNA to evaluate the rate limitation of photosynthesis under water stress. Plant Physiol 103: 629–635

    PubMed  Google Scholar 

  • Harbinson J and Foyer CH (1991) Relationships between the efficiencies of Photosystems I and II and stromal redox state in CO2-free air. Evidence for cyclic electron flow in vivo. Plant Physiol 97: 41–49

    Google Scholar 

  • Harbinson J, Genty B and Foyer CH (1990) Relationship between photosynthetic electron transport and stromal enzyme activity in pea leaves. Toward an understanding of the nature of photosynthetic control. Plant Physiol 94: 545–553

    Google Scholar 

  • Hewitt EJ (1966) Sand and water culture methods used in the study of plant nutrition. Technical communication no. 22, 2nd ed, pp 430–472. Commonwealth Agricultural Bureau. Farnham Royal, UK

    Google Scholar 

  • Hodges M, Cornic G and Briantais J-M (1989) Chlorophyll fluorescence from spinach leaves: Resolution of non-photochemical quenching. Biochim Biophys Acta 974: 289–293

    Google Scholar 

  • Holaday AS, Martindale W, Alred R, Brooks AL and Leegood RC (1992) Changes in activities of enzymes of carbon metabolism in leaves during exposure of plants to low temperature. Plant Physiol 98: 1105–1114

    Google Scholar 

  • Horton P and Hague A (1988) Studies on the induction of chlorophyll fluorescence in isolated barley protoplasts. IV. Resolution of non-photochemical quenching. Biochim Biophys Acta 932: 107–115

    Google Scholar 

  • Horton P and Ruban A (1994) The role of light-harvesting complex II in energy quenching. In: Baker NR and Bowyer JR (eds) Photoinhibition of Photosynthesis. From Molecular Mechanisms to the Field, pp 111–128. Bios Scientific Publishers, Oxford, UK

    Google Scholar 

  • Horton P, Ruban A and Walters RG (1994) Regulation of light harvesting in green plants. Indication by nonphotochemical quenching of chlorophyll fluorescence. Plant Physiol 106: 415–420

    PubMed  Google Scholar 

  • Krause GH (1994) Photoinhibition caused by low temperatures. In: Baker NR and Bowyer JR (eds) Photoinhibition of Photosynthesis. From Molecular Mechanisms to the Field, pp 331–348. Bios Scientific Publishers, Oxford, UK

    Google Scholar 

  • Krause GH, Somersalo S, Zumbusch E, Weyers B and Laasch H (1990) On the mechanism of photoinhibition in chloroplasts. Relationship between changes in fluorescence and activity of Photosystem II. J Plant Physiol 136: 472–479

    Google Scholar 

  • Krause GH, Virgo A and Winter K (1995) High susceptibility to photoinhibition of young leaves of tropical forest trees. Planta 197: 583–591

    Article  Google Scholar 

  • Ortiz-Lopez A, Ort DR and Boyer JS (1991) Photophosphorylation in attached leaves of Helianthus annuus at low water potentials. Plant Physiol 96: 1018–1025

    Google Scholar 

  • Osmond CB (1994) What is photoinhibition? Some insights from comparisons of shade and sun plants. In: Baker NR and Bowyer JR (eds) Photoinhibition of Photosynthesis. From Molecular Mechanisms to the Field, pp 1–24. Bios Scientific Publishers, Oxford, UK

    Google Scholar 

  • Pitel JA and Cheliak WM (1985) Methods to extract NAD+-malate dehydrogenase efficiently from white spruce needles. Physiol Plant 65: 129–134

    Google Scholar 

  • Ruban AV, Young AJ and Horton P (1993) Induction of nonphotochemical energy dissipation and absorbance changes in leaves. Evidence for changes in the state of the light-harvesting system of Photosystem II in vivo. Plant Physiol 102: 741–750

    PubMed  Google Scholar 

  • Scheibe R and Stitt M (1988) Comparison of NADP-malate dehydrogenase activation, QA, reduction and O2 evolution in spinach leaves. Plant Physiol Biochem 26: 473–481.

    Google Scholar 

  • Scheibe R, Fickenscher K and Ashton AR (1986) Studies on the mechanisms of the reductive activation of NADP-malate dehydrogenase by thioredoxinm and low molecular weight thiols. Biochim Biophis Acta 870: 191–197

    Google Scholar 

  • Skarkey TD and Seemann JR (1989) Mild water stress effects on carbon-reduction cycle intermediates, ribulose bisphosphate carboxylase activity, and spatial homogeneity of photosynthesis in intact leaves. Plant Physiol 89: 1060–1065.

    Google Scholar 

  • Sharkey TD, Savitch LV and Butz ND (1991) Photometric method for routine determination of kcat and carbamylation of rubisco. Photosynth Res 28: 41–48

    Article  Google Scholar 

  • Turner NC (1981) Techniques and experimental approaches for the measurement of plant water status. Plant and Soil 58: 339–366

    Google Scholar 

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Sánchez-Rodriguez, J., Martínez-Carrasco, R. & Pérez, P. Photosynthetic electron transport and carbon-reduction-cycle enzyme activities under long-term drought stress in Casuarina equisetifolia Forst. & Forst.. Photosynthesis Research 52, 255–262 (1997). https://doi.org/10.1023/A:1005878307607

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  • DOI: https://doi.org/10.1023/A:1005878307607

  • chlorophyll fluorescence
  • fructose bisphosphatase
  • NADP-malate dehydrogenase
  • Photosystem II
  • ribulose bisphosphate carboxylase
  • water stress