Photosynthetica 2006, 44(3):419-424 | DOI: 10.1007/s11099-006-0045-2

Effects of different irradiances on the photosynthetic process during ex-vitro acclimation of Anoectochilus plantlets

D. M. Pandey1,2, K. W. Yu1, R. Z. Wu1, E. J. Hahn1, K. Y. Paek1,*
1 Research Center for the Development of Advanced Horticultural Technology, Chungbuk National University, Cheong-ju, South Korea
2 Plant Molecular Biology Laboratory (Functional Genomics Lab), Department of Life Science, Sogang University, Seoul, South Korea

Six months old in vitro-grown Anoectochilus formosanus plantlets were transferred to ex-vitro acclimation under low irradiance, LI [60 µmol(photon) m-2 s-1], intermediate irradiance, II [180 µmol(photon) m-2 s-1], and high irradiance, HI [300 µmol(photon) m-2 s-1] for 30 d. Imposition of II led to a significant increase of chlorophyll (Chl) b content, rates of net photosynthesis (P N) and transpiration (E), stomatal conductance (g s), electron transfer rate (ETR), quantum yield of electron transport from water through photosystem 2 (ΦPS2), and activity of ribulose-1,5-bisphosphate carboxylase/ oxygenase (RuBPCO, EC 4.1.1.39). This indicates that Anoectochilus was better acclimated at II compared to LI treatment. On the other hand, HI acclimation led to a significant reduction of Chl a and b, P N, E, g s, photochemical quenching, dark-adapted quantum efficiency of open PS2 centres (Fv/Fm), probability of an absorbed photon reaching an open PS2 reaction centre (Fv'/Fm'), ETR, ΦPS2, and energy efficiency of CO2 fixation (ΦCO2PS2). This indicates that HI treatment considerably exceeded the photo-protective capacity and Anoectochilus suffered HI induced damage to the photosynthetic apparatus. Imposition of HI significantly increased the contents of antheraxanthin and zeaxanthin (ZEA), non-photochemical quenching, and conversion of violaxanthin to ZEA. Thus Anoectochilus modifies its system to dissipate excess excitation energy and to protect the photosynthetic machinery.

Additional key words: chlorophyll a fluorescence; electron transfer rate; photoinhibition; photosystem 2; ribulose-1,5-bisphosphate carboxylase, oxygenase; stomatal conductance; transpiration; xanthophylls

Received: September 5, 2005; Accepted: January 5, 2006; Published: September 1, 2006  Show citation

ACS AIP APA ASA Harvard Chicago Chicago Notes IEEE ISO690 MLA NLM Turabian Vancouver
Pandey, D.M., Yu, K.W., Wu, R.Z., Hahn, E.J., & Paek, K.Y. (2006). Effects of different irradiances on the photosynthetic process during ex-vitro acclimation of Anoectochilus plantlets. Photosynthetica44(3), 419-424. doi: 10.1007/s11099-006-0045-2
Download citation

References

  1. Amâncio, S., Rebordão, J.P., Chaves, M.M.: Improvement of acclimatization of micropropagated grapevine: photosynthetic competence and carbon allocation.-Plant Cell Tissue Organ Cult. 58: 31-37, 1999. Go to original source...
  2. Bertamini, M., Nedunchezhian, N.: Decline of photosynthetic pigments, ribulose-1,5-bisphosphate carboxylase and soluble protein contents, nitrate reductase and photosynthetic activities, and changes in thylakoid membrane protein pattern in canopy shade grapevine (Vitis vinifera L. cv. Moscato giallo) leaves.-Photosynthetica 39: 529-537, 2001. Go to original source...
  3. Borland, A.M., Técsi, L.I., Leegood, R.C., Walker, R.P.: Inducibility of crassulacean acid metabolism (CAM) in Clusia species; physiological/biochemical characterisation and intracellular localization of carboxylation and decarboxylation processes in three species which exhibit different degrees of CAM.-Planta 205: 342-351, 1998. Go to original source...
  4. Bradford, M.M.: A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye-binding.-Anal. Biochem.73: 248-254, 1976. Go to original source...
  5. Chang, D.C.N, Chou, L.C., Lee, K.C.: New cultivation methods for Anoectochilus formosanus Hayata.-In: Third International Conference on Mycorrhizas. P. 1. Adelaide Convention Centre, Adelaide 2001.
  6. de las Rivas, J., Abadía, A., Abadía, J.: A new reversed phase-HPLC method resolving all major higher plant photosynthetic pigments.-Plant Physiol. 91: 190-192, 1989. Go to original source...
  7. Demmig-Adams, B., Adams, W.W., III: The carotenoid zeaxanthin and "high-energy-state quenching" of chlorophyll fluorescence.-Photosynth. Res. 25: 187-197, 1990. Go to original source...
  8. Demmig-Adams, B., Adams, W.W., III: Photoprotection and other responses of plants to high light stress.-Annu. Rev. Plant Physiol. Plant mol. Biol. 43: 599-626, 1992. Go to original source...
  9. Fryer, M.J., Andrews, J.R., Oxborough, K., Blowers, D.A., Baker, N.R.: Relationship between CO2 assimilation, photosynthetic electron transport and active O2 metabolism in leaves of maize in the field during periods of low temperature.-Plant Physiol. 116: 571-580, 1998. Go to original source...
  10. Genty, B., Briantais, J.-M., Baker, N.R.: The relationship between the quantum yield of photosynthetic electron transport and quenching of chlorophyll fluorescence.-Biochim. biophys. Acta 990: 87-92, 1989. Go to original source...
  11. Grout, B.W.W., Aston, M.J.: Transplanting of cauliflower plants regenerated from meristem culture. II. Carbon dioxide fixation and development of photosynthetic ability.-Hort. Res. 17: 65-71, 1978.
  12. Havaux, M., Niyogi, K.K.: The violaxanthin cycle protects plants from photooxidative damage by more than one mechanism.-Proc. nat. Acad. Sci. USA 96: 8762-8767, 1999. Go to original source...
  13. Hymus, G.J., Ellsworth, D.S., Baker, N.R., Long, S.P.: Does free-air carbon dioxide enrichment affect photochemical energy use by evergreen trees in different seasons? A chlorophyll fluorescence study of mature loblolly pine.-Plant Physiol. 120: 1183-1191, 1999. Go to original source...
  14. Ito, H., Tanaka, Y., Tsuji, H., Tanaka, A.: Conversion of chlorophyll b to chlorophyll a in isolated cucumber etioplasts.-Arch. Biochem. Biophys. 306: 148-151, 1993. Go to original source...
  15. Kornyeyev, D., Holaday, S., Logan, B.: Predicting the extent of photosystem II photoinactivation using chlorophyll a fluorescence parameters measured during illumination.-Plant Cell Physiol. 44: 1064-1070, 2003. Go to original source...
  16. Kozai, T.: Micropropagation under photoautotrophic conditions.-In: Debergh, P.C., Zimmerman, R.H. (ed.): Micropropagation: Technology and Application. Pp. 447-469. Kluwer Academic Publ., Dordrecht-Boston-London 1991. Go to original source...
  17. Krause, G.H.: Photoinhibition of photosynthesis. An evaluation of damaging and protective mechanisms.-Physiol. Plant. 74: 566-574, 1988. Go to original source...
  18. Pandey, D.M., Kang, K.-H., Yeo, U.-D.: Effects of excessive photon on the photosynthetic pigments and violaxanthin deepoxidase activity in the xanthophylls cycle of spinach leaf.-Plant Sci. 168: 161-166, 2005. Go to original source...
  19. Pandey, D.M., Wu, R.Z., Hahn, E.-J., Paek, K.-Y.: Drought effect on electrophoretic protein pattern of Anoectochilus formosanus.-Sci. Hort. 107: 205-209, 2006. Go to original source...
  20. Pell, E.J., Eckardt, N.A., Glick, R.E.: Biochemical and molecular basis for impairment of photosynthetic potential.-Photosynth. Res. 39: 453-462, 1994. Go to original source...
  21. Pfündel, E., Bilger, W.: Regulation and possible function of the violaxanthin cycle.-Photosynth. Res. 42: 89-109, 1994. Go to original source...
  22. Piel, C., Frak, E., Le Roux, X., Genty, B.: Effect of local irradiance on CO2 transfer conductance of mesophyll in walnut.-J. exp. Bot. 53: 2423-2430, 2002. Go to original source...
  23. Powles, S.B.: Photoinhibition of photosynthesis induced by visible light.-Annu. Rev. Plant Physiol. 35: 15-44, 1984. Go to original source...
  24. Ramalho, J.C., Pons, T.L., Groeneveld, H.W., Azinheira, H.G., Nunes, M.A.: Photosynthetic acclimation to high light conditions in mature leaves of Coffea arabica L.: Role of xanthophylls, quenching mechanisms and nitrogen nutrition.-Aust. J. Plant Physiol. 27: 43-51, 2000. Go to original source...
  25. Rosenqvist, E., van Kooten, O.: Chlorophyll fluorescence: A general description and nomenclature.-In: DeEll, J.R., Toivonen, P.M.A. (ed.): Practical Applications of Chlorophyll Fluorescence in Plant Biology. Pp. 32-77. Kluwer Academic Publ., Dordrecht 2003. Go to original source...
  26. Ruban, A.V., Horton, P.: An investigation of the sustained component of nonphotochemical quenching of chlorophyll fluorescence in isolated chloroplasts and leaves of spinach.-Plant Physiol. 108: 721-726, 1995. Go to original source...
  27. Slesak, I., Karpinska, B., Surowka, E., Miszalski, Z., Karpinski, S.: Redox changes in the chloroplast and hydrogen peroxide are essential for regulation of C3-CAM transition and photooxidative stress responses in the facultative CAM plant Mesembryanthemum crystallinum L.-Plant Cell Physiol. 44: 573-581, 2003. Go to original source...
  28. Woitsch, S., Römer, S.: Expression of xanthophyll biosynthetic genes during light-dependent chloroplast differentiation.-Plant Physiol. 132: 1508-1517, 2003. Go to original source...