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Journal of Zhejiang University SCIENCE B 2009 Vol.10 No.10 P.784~790


Cyclic electron flow around photosystem I is required for adaptation to high temperature in a subtropical forest tree, Ficus concinna

Author(s):  Song-heng JIN, Xue-qin LI, Jun-yan HU, Jun-gang WANG

Affiliation(s):  School of Forestry and Biotechnology, Zhejiang Forestry University, Lin’ more

Corresponding email(s):   shjin@zjfc.edu.cn

Key Words:  Ficus concinna, High-temperature stress, Chlorophyll fluorescence, Photosynthesis, Cyclic electron transport around photosystem I, Dissipation of excitation energy

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Song-heng JIN, Xue-qin LI, Jun-yan HU, Jun-gang WANG. Cyclic electron flow around photosystem I is required for adaptation to high temperature in a subtropical forest tree, Ficus concinna[J]. Journal of Zhejiang University Science B, 2009, 10(10): 784~790.

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%A Jun-gang WANG
%J Journal of Zhejiang University SCIENCE B
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%DOI 10.1631/jzus.B0820348

T1 - Cyclic electron flow around photosystem I is required for adaptation to high temperature in a subtropical forest tree, Ficus concinna
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A1 - Jun-gang WANG
J0 - Journal of Zhejiang University Science B
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DOI - 10.1631/jzus.B0820348

Dissipation mechanisms of excess photon energy under high-temperature stress were studied in a subtropical forest tree seedling, Ficus concinna. Net CO2 assimilation rate decreased to 16% of the control after 20 d high-temperature stress, and thus the absorption of photon energy exceeded the energy required for CO2 assimilation. The efficiency of excitation energy capture by open photosystem II (PSII) reaction centres (Fv′/Fm′) at moderate irradiance, photochemical quenching (qP), and the quantum yield of PSII electron transport (ΦPSII) were significantly lower after high-temperature stress. Nevertheless, non-photochemical quenching (qNP) and energy-dependent quenching (qE) were significantly higher under such conditions. The post-irradiation transient of chlorophyll (Chl) fluorescence significantly increased after the turnoff of the actinic light (AL), and this increase was considerably higher in the 39 °C-grown seedlings than in the 30 °C-grown ones. The increased post-irradiation fluorescence points to enhanced cyclic electron transport around PSI under high growth temperature conditions, thus helping to dissipate excess photon energy non-radiatively.

Darkslateblue:Affiliate; Royal Blue:Author; Turquoise:Article


[1] Berry, J.A., Björkman, O., 1980. Photosynthetic response and adaptation to temperature in higher plants. Annual Review of Plant Physiology, 31(1):491-543.

[2] Bukhov, N.G., Samson, G., Carpentier, R., 2000. Nonphotosynthetic reduction of the intersystem electron transport chain of chloroplasts following heat stress. Steady-state rate. Photochemistry and Photobiology, 72(3):351-357.

[3] Burrows, P.A., Sazanov, L.A., Svab, Z., Maliga, P., Nixon, P.J., 1998. Identification of a functional respiratory complex in chloroplasts through analysis of tobacco mutants containing disrupted plastid ndh genes. The EMBO Journal, 17(4):868-876.

[4] Chaitanya, K.V., Sundar, D., Masilamani, S., Ramachandra, R.A., 2002. Variation in heat stress-induced antioxidant enzyme activities among three mulberry cultivars. Plant Growth Regulation, 36(2):175-180.

[5] Demmig-Adams, B., Adams III, W.W., 1992. Photoprotection and other responses of plants to high light stress. Annual Review of Plant Physiology and Plant Molecular Biology, 43(1):599-626.

[6] Deng, Y., Ye, J., Mi, H., 2003. Effects of low CO2 on NAD(P)H dehydrogenase, a mediator of cyclic electron transport around photosystem I in the cyanobacterium Synechocystis PCC6803. Plant and Cell Physiology, 44(5):534-540.

[7] Feller, U., Crafts-Brandner, S.J., Salvucci, M.E., 1998. Moderately high temperatures inhibit ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) activase-mediated activation of Rubisco. Plant Physiology, 116(2): 539-546.

[8] Guo, Y.P., Zhou, H.F., Zhang, L.C., 2006. Photosynthetic characteristics and protective mechanisms against photooxidation during high temperature stress in two citrus species. Scientia Horticulturae, 108(3):260-267.

[9] Haldimann, P., Feller, U., 2004. Inhibition of photosynthesis by high temperature in oak (Quercus pubescens L.) leaves grown under natural conditions closely correlates with a reversible heat-dependent reduction of the activation state of ribulose-1,5-bisphosphate carboxylase/oxygenase. Plant Cell and Environment, 27(9):1169-1183.

[10] Haldimann, P., Feller, U., 2005. Growth at moderately elevated temperature alters the physiological response of the photosynthetic apparatus to heat stress in pea (Pisum sativum L.) leaves. Plant Cell and Environment, 28(3): 302-317.

[11] Havaux, M., Tardy, F., Ravenel, J., Chanu, D., Parot, P., 1996. Thylakoid membrane stability to heat stress studied by flash spectroscopic measurements of the electrochromic shift in intact potato leaves: influence of the xanthophylls content. Plant Cell and Environment, 19(12):1359-1368.

[12] Isoda, A., Wang, P., 2002. Leaf temperature and transpiration of field grown cotton and soybean under arid and humid conditions. Plant Production Science, 5(3):224-228.

[13] Jin, S.H., Wang, D., Zhu, F.Y., Li, X.Q., Sun, J.W., Jiang, D.A., 2008. Up-regulation of cyclic electron flow and down-regulation of linear electron flow in antisense-rca mutant rice. Photosynthetica, 46(4):506-510.

[14] Kramer, D.M., Johnson, G., Kiirats, O., Edwards, G.E., 2004. New fluorescence parameters for the determination of QA redox state and excitation energy fluxes. Photosynthesis Research, 79(2):209-218.

[15] Lu, K.X., Yang, Y., He, Y., Jiang, D.A., 2008. Induction of cyclic electron flow around photosystem 1 and state transition are correlated with salt tolerance in soybean. Photosynthetica, 46(1):10-16.

[16] Maxwell, K., Johnson, G.N., 2000. Chlorophyll fluorescence: a practical guide. Journal of Experimental Botany, 51(345):659-668.

[17] Munné-Bosch, S., Shikanai, T., Asada, K., 2005. Enhanced ferredoxin-dependent cyclic electron flow around photosystem I and α-tocopherol quinone accumulation in water-stressed ndhB-inactivated tobacco mutants. Planta, 222(3):502-511.

[18] Peltier, G., Cournac, L., 2002. Chlororespiration. Annual Review of Plant Biology, 53(1):523-550.

[19] Quick, W.P., Stitt, M., 1989. An examination of factors contributing to non-photochemical quenching of chlorophyll fluorescence in barley leaves. Biochimica et Biophysica Acta (BBA)-Bioenergetics, 977(3):287-296.

[20] Salvucci, M.E., Crafts-Brandner, S.J., 2004. Relationship between the heat tolerance of photosynthesis and the thermal stability of rubisco activase in plants from contrasting thermal environments. Plant Physiology, 134(4): 1460-1470.

[21] Shikanai, T., 2007. Cyclic electron transport around photosystem I: genetic approaches. Annual Review of Plant Biology, 58(1):199-217.

[22] Shikanai, T., Endo, T., Hashimoto, T., Yamada, Y., Asada, K., Yokota, A., 1998. Directed disruption of the tobacco ndhB gene impairs cyclic electron flow around photosystem I. Proceedings of the National Academy of Sciences of the United States of America, 95(16):9705-9709.

[23] Shikanai, T., Munekage, Y., Kimura, K., 2002. Regulation of proton-to-electron stoichiometry in photosynthetic electron transport: physiological function in photoprotection. Journal of Plant Research, 115(1):3-10.

[24] Štroch, M., Špunda, V., Kurasová, I., 2004. Non-radiative dissipation of absorbed excitation energy within photosynthetic apparatus of higher plants. Photosynthetica, 42(3):323-337.

[25] Thiele, A., Krause, G.H., 1994. Xanthophyll cycle and thermal energy dissipation in photosystem II: relationship between zeaxanthin formation, energy-dependent quenching and photoinhibition. Journal of Plant Physiology, 144(3):324-332.

[26] Wang, P., Duan, W., Takabayashi, A., Endo, T., Shikanai, T., Ye, J.Y., Mi, H.L., 2006. Chloroplastic NAD(P)H dehydrogenase in tobacco leaves functions in alleviation of oxidative damage caused by temperature stress. Plant Physiology, 141(2):465-474.

[27] Yamori, W., Noguchi, K., Hanba, Y.T., Terashima, I., 2006. Effects of internal conductance on the temperature dependence of the photosynthetic rate in spinach leaves from contrasting growth temperatures. Plant and Cell Physiology, 47(8):1069-1080.

[28] Yang, Y., Yan, C.Q., Cao, B.H., Xu, H.X., Chen, J.P., Jiang, D.A., 2007. Some photosynthetic responses to salinity resistance are transferred into the somatic hybrid descendants from the wild soybean Glycine cyrtoloba ACC547. Physiologia Plantarum, 129(3):658-669.

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