Cold acclimation and photoinhibition of photosynthesis in Scots pine |
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Authors: | Alla Krivosheeva Da-Li Tao Christina Ottander Gunnar Wingsle Sylvain L. Dube Gunnar Öquist |
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Affiliation: | (1) Department of Plant Physiology, University of Umeå, S-901 87 Umeå, Sweden;(2) Department of Biophysics, Ural Forest Technology Institute, 620032 Ekaterinburg, Russia;(3) Institute of Applied Ecology, Academia Sinica, P.O. Box 417, 110015 Shenyang, China;(4) Department of Forest Genetics and Plant Physiology, Faculty of Forestry, Swedish University of Agricultural Sciences, S-901 83, Umeå, Sweden;(5) Department of Plant Physiology, University of Lund, S-220 27 Lund, Sweden;(6) Present address: Horticulture Research Center, University Lavai, G1K 7P4 Québec, Canada |
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Abstract: | Cold acclimation of Scots pine did not affect the susceptibility of photosynthesis to photoinhibition. Cold acclimation did however cause a suppression of the rate of CO2 uptake, and at given light and temperature conditions a larger fraction of the photosystem II reaction centres were closed in cold-acclimated than in nonacclimated pine. Therefore, when assayed at the level of photosystem II reaction centres, i.e. in relation to the degree of photosystem closure, cold acclimation caused a significant increase in resistance to photoinhibition; at given levels of photosystem II closure the resistance to photoinhibition was higher after cold acclimation. This was particularly evident in measurements at 20° C. The amounts and activities of the majority of analyzed active oxygen scavengers were higher after cold acclimation. We suggest that this increase in protective enzymes and compounds, particularly Superoxide dismutase, ascorbate peroxidase, glutathione reductase and ascorbate of the chloroplasts, enables Scots pine to avoid excessive photoinhibition of photosynthesis despite partial suppression of photosynthesis upon cold acclimation. An increased capacity for light-induced de-epoxidation of violaxanthin to zeaxanthin upon cold acclimation may also be of significance.Abbreviations APX ascorbate peroxidase - DHA dehydroascorbate - DHAR dehydroascorbate reductase - Fm maximal fluorescence when all reaction centres are closed - Fv/Fm maximum photochemical yield of PSII - GR glutathione reductase - GSH reduced glutathione - Je rate of photosynthetic electron transport - MDAR monodehydroascorbate reductase - qN nonphotochemical quenching of fluorescence - qP photochemical quenching of fluorescence - SOD superoxide dismutaseThis work was supported by the Swedish Natural Science Research Council and the National Natural Science Foundation of China. |
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Keywords: | Frost hardening Low temperature Photoinhibition Photosystem II Pinus Scavenging |
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