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Functional plasticity of photosynthetic apparatus and its resistance to photoinhibition in Plantago media

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Abstract

Morphological and functional characteristics of Plantago media L. leaves were compared for plants growing at different light regimes on limestone outcrops in Southern Timan (62°45′N, 55°49′E). The plants grown in open areas under exposure to full sunlight had small leaves with low pigment content and high specific leaf weight; these leaves exhibited high photosynthetic capacity and elevated water use efficiency at high irradiance. The maximum photochemical activity of photosystem II (F v/F m) in leaves of sun plants remained at the level of about 0.8 throughout the day. The photosynthetic apparatus of sun plants was resistant to excess photosynthetically active radiation, mostly due to non-photochemical quenching of chlorophyll fluorescence (qN). This quenching was promoted by elevated deepoxiation of violaxanthin cycle pigments. Accumulation of zeaxanthin, a photoprotective pigment in sun plant leaves was observed already in the morning hours. The plant leaves grown in the shade of dense herbage were significantly larger than the sun leaves, with pigment content 1.5–2.0 times greater than in sun leaves; these leaves had low qN values and did not need extensive deepoxidation of violaxanthin cycle pigments. The data reveal the morphophysiological plasticity of plantain plants in relation to lighting regime. Environmental conditions can facilitate the formation of the ecotype with photosynthetic apparatus resistant to photoinhibition. Owing to this adjustment, hoary plantain plants are capable of surviving in ecotopes with high insolation.

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Abbreviations

Ant:

antheraxanthin

β-Car:

β-carotene

Car:

carotenoids

Chl:

chlorophyll

Ft, F0, and Fm:

stationary minimum, and maximum yields of chlorophyll fluorescence, respectively

Fv/Fm:

variable to maximum fluorescence ratio, i.e., the maximum quantum yield of PSII

LCFA:

long-chain fatty acids

MDA:

malondialdehyde

PAR:

photosynthetically active radiation

P n :

rate of apparent (net) photosynthesis

PSII:

photosystem II

PSA:

photosynthetic apparatus

qP and qN:

coefficients of photochemical and non-photochemical fluorescence quenching, respectively

Vio:

violaxanthin

VXC:

violaxanthin cycle

Y:

effective quantum yield of PSII photochemistry, i.e., the part of light energy used by PSII for electron transport

Zea:

zeaxanthin

References

  1. Lyubimenko, V.N., Photosynthesis and Plant Adaptation to Light, Selected Works, vol. 1, Lyubimenko, V.N., Ed., Kiev: Akad. Nauk UkrSSR, 1963.

    Google Scholar 

  2. Bazzaz, F.A. and Carlson, R.W., Photosynthetic Acclimation to Variability in Light Environment of Early and Late Successional Plant, Oecologia, 1982, vol. 54, pp. 3313–3316.

    Article  Google Scholar 

  3. Osmond, B. and Forster, B., Photoinhibition: Then and Now, Photoprotection, Photoinhibition, Gene Regulation, and Environment, Demmig-Adams, B., Adams, W.W., III., and Mattoo, A.K., Eds., Dordrecht: Springer-Verlag, 2006, pp. 11–22.

    Chapter  Google Scholar 

  4. Murata, N., Takahashi, S., Nishiyama, Y., and Allakhverdiev, S.I., Photoinhibition of Photosystem II under Environmental Stress, Biochim. Biophys. Acta, 2007, vol. 1767, pp. 414–421.

    Article  PubMed  CAS  Google Scholar 

  5. Kuiper, D. and Smid, A., Genetic Differentiation and Phenotypic Plasticity in Plantago major ssp. major: 1. The Effect of Differences in Level of Irradiance on Growth, Photosynthesis, Respiration and Chlorophyll Content, Physiol. Plant., 1985, vol. 60, pp. 520–528.

    Article  Google Scholar 

  6. Lambers, H., Posthumus, F., Stulen, I., Lanting, I., van de Dijk, S.J., and Hofstra, R., Energy Metabolism of Plantago major ssp. major as Dependent on the Supply of Mineral Nutrients, Physiol. Plant., 1981, vol. 51, pp. 245–252.

    Article  CAS  Google Scholar 

  7. Mudrik, V., Kosobrukhov, A., Knyazeva, I., and Pigulevskaya, T., Changes in the Photosynthetic Characteristics of Plantago major Plants Caused by Soil Drought Stress, Plant Growth Regul., 2003, vol. 40, pp. 1–6.

    Article  CAS  Google Scholar 

  8. Garmash, E.V. and Golovko, T.K., CO2 Gas Exchange and Growth in Rhaponticum carthamoides under the Conditions of the Middle Taiga Subzone of Northeastern Europe: 1. Dependence of Photosynthesis and Respiration on Environmental Factors, Russ. J. Plant Physiol., 1997, vol. 44, pp. 737–745.

    CAS  Google Scholar 

  9. Krause, G.H. and Weis, E., Chlorophyll Fluorescence and Photosynthesis: The Basis, Annu. Rev. Plant Physiol. Plant Mol. Biol., 1991, vol. 42, pp. 313–349.

    Article  CAS  Google Scholar 

  10. Lichtenthaler, H., Buschmann, C., and Knapp, M., Measurement of Chlorophyll Fluorescence Kinetics (Kautsky Effect) and the Chlorophyll Fluorescence Decrease Ratio (RFD-Values) with the PAM-Fluorometer, Analytical Methods in Plant Stress Biology, Filek, M., Biesaga-Kos-cielniak, J., and Marcin-ska, I., Eds., Krako-w: Inst. Plant Physiol., Polish Acad. Sci., 2004, pp. 93–111.

    Google Scholar 

  11. Maslova, T.G., Popova, I.A., and Popova, O.F., Spectrophotometry for Carotenoid Quantification: Critical Evaluation, Sov. Plant Physiol., 1986, vol. 33, pp. 615–619.

    CAS  Google Scholar 

  12. Kornyushenko, G.A. and Sapozhnikov, D.I., Determination of Carotenoids in Green Leaf Using Thin-Layer Chromatography, Metody kompleksnogo izucheniya fotosinteza (Methods for Complex Investigation of Photosynthesis), Leningrad: Vses. Inst. Rastenievod., 1969, pp. 181–192.

    Google Scholar 

  13. Schindler, C. and Lichtenthaler, H.K., Photosynthetic CO2-Assimilation, Chlorophyll Fluorescence and Zeaxanthin Accumulation in Field Grown Maple Trees in the Course of a Sunny and Cloudy Day, J. Plant Physiol., 1996, vol. 148, pp. 399–412.

    CAS  Google Scholar 

  14. Glyad, V.M., Determination of Monosaccharides, Disaccharides, and Oligosaccharides in the Same Plant Sample by High-Performance Liquid Chromatography, Russ. J. Plant Physiol., 2002, vol. 49, pp. 277–282.

    Article  CAS  Google Scholar 

  15. Lukatkin, A.S. and Golovanova, V.S., Lipid Peroxidation Intensity in Chilled Leaves of Thermophyte Plants, Sov. Plant Physiol., 1988, vol. 35, pp. 773–780.

    CAS  Google Scholar 

  16. Aro, E.-M., Virgin, I., and Andersson, B., Photoinhibition of Photosystem II: Inactivation, Protein Damage, and Turnover, Biochim. Biophys. Acta, 1993, vol. 1143, pp. 113–134.

    Article  PubMed  CAS  Google Scholar 

  17. Krasnovsky, A.A., Singlet Oxygen: Mechanisms of Development and Pathways of Deactivation in Biological Systems, Biofizika, 1994, vol. 39, pp. 236–250.

    Google Scholar 

  18. Polesskaya, O.G., Rastitel’naya kletka i aktivnye formy kisloroda (Plant Cell and Reactive Oxygen Species), Moscow: Knizhn. Dom Univ., 2007.

    Google Scholar 

  19. Adams, W.W., III, Zarter, C.R., Much, K.E., Amiard, V., and Demmig-Adams, B., Energy Dissipation and Photoinhibition: A Continuum of Photoprotection, Photoprotection, Photoinhibition, Gene Regulation, and Environment, Demmig-Adams, B., Adams, W.W., III., and Mattoo, A.K., Eds., Dordrecht: Springer-Verlag, 2006, pp. 49–64.

    Chapter  Google Scholar 

  20. Demmig-Adams, B., Linking the Xanthophyll Cycle with Thermal Energy Dissipation, Photosynth. Res., 2003, vol. 76, pp. 73–80.

    Article  PubMed  CAS  Google Scholar 

  21. Genty, B., Briantais, J.M., and Baker, N.R., The Relationship between the Quantum Yield of Photosynthetic Electron Transport and Quenching of Chlorophyll Fluorescence, Biochim. Biophys. Acta, 1989, vol. 990, pp. 87–92.

    CAS  Google Scholar 

  22. Rmiki, N.-E., Lemoine, Y., and Schoefs, B., Carotenoids and Stress in Higher Plants and Algae, Handbook of Plant and Crop Stress, Pessarakli, M., Ed., New York: Marcel Dekker, 1999, pp. 465–482.

    Chapter  Google Scholar 

  23. Gruszeski, W.I., Carotenoids in Membranes, Advances in Photosynthesis, vol. 8, The Photochemistry of Carotenoids, Frank, H.A., Young, A.J., Britton, G., and Cogdell, R.J., Eds., The Netherlands: Kluwer, 1999, pp. 363–379.

    Google Scholar 

  24. Dymova, O.A. and Golovko, T.K., Light Adaptation of Photosynthetic Apparatus in Ajuga reptans L., a Shade-Tolerant Plants as an Example, Russ. J. Plant Physiol., 2007, vol. 54, pp. 440–446.

    Article  Google Scholar 

  25. Adams, W.W., Demmig-Adams, B., Rosenstiel, T.N., Brightwell, A.K., and Ebbert, V., Photosynthesis and Photoprotection in Overwintering Plants, Plant Biol., 2002, vol. 4, pp. 545–557.

    Article  Google Scholar 

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Correspondence to O. V. Dymova.

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Original Russian Text © T.K. Golovko, I.V. Dalke, I.G. Zakhozhiy, O.V. Dymova, G.N. Tabalenkova, 2011, published in Fiziologiya Rastenii, 2011, Vol. 58, No. 4, pp. 490–501.

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Golovko, T.K., Dalke, I.V., Zakhozhiy, I.G. et al. Functional plasticity of photosynthetic apparatus and its resistance to photoinhibition in Plantago media . Russ J Plant Physiol 58, 549–559 (2011). https://doi.org/10.1134/S1021443711040054

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