Plant Biol (Stuttg) 2003; 5(4): 432-440
DOI: 10.1055/s-2003-42713
Original Paper

Georg Thieme Verlag Stuttgart · New York

High Temperature Effects on Light Sensitivity in the Two High Mountain Plant Species Soldanella alpina (L.) and Rannunculus glacialis (L.)

P. Streb 1 , 2 , S. Aubert 1 , 3 , R. Bligny 1
  • 1Station Alpine du Lautaret & Laboratoire de Physiologie Cellulaire Végétale, Unité Mixte de Recherche 5019 (Commissariat à l'Energie Atomique, Centre National de la Recherche Scientifique, Université Joseph Fourier), Département de Biologie Moléculaire et Structurale, CEA-Grenoble, Grenoble, France
  • 2Laboratoire d'Ecophysiologie Végétale, UFR Scientifique d'Orsay Université Paris XI, Paris, France
  • 3Laboratoire d'Ecologie Alpine (UMR UJF - CNRS 5553), Grenoble, France
Further Information

Publication History

Publication Date:
02 October 2003 (online)

Abstract

The susceptibility to high temperature-induced photoinhibition was investigated in leaves of two high mountain plant species, S. alpina and R. glacialis. In both species, PSII was similarly photoinactivated at 38 °C in the light. However, recovery from damage was much faster in S. alpina and depended on protein synthesis. In contrast, recovery was independent from protein synthesis in R. glacialis. Heat-induced photoinactivation in both species was accompanied by: (1) a decrease in relative photosynthetic electron transport rates, (2) an increase in non-photochemical chlorophyll fluorescence quenching, (3) a strong accumulation of zeaxanthin, (4) a marked decrease in soluble carbon metabolites and (5) an increase in lipid metabolism products, which was more pronounced in R. glacialis than in S. alpina. These results indicate that carbon assimilation was in„hibited and that membranes were affected. Lipid peroxidation and possible membrane disintegration might limit the repair of damaged PSII in R. glacialis, while S. alpina appears to be protected by carotenoids and antioxidants. A marked decrease in α-tocopherol content and an increase in reduced ascorbate indicated lipid peroxide scavenging activity in S. alpina. When zeaxanthin synthesis was impaired by DTT, photoinhibition increased and α-tocopherol accumulated in R. glacialis. The increased susceptibility of R. glacialis leaves to light-induced photoinhibition after growth at moderate temperature ([Streb et al., 2003a]) and the inability to repair heat-induced damage might limit the distribution of R. glacialis to lower altitudes in the Alps.

References

  • 1 Arnon D. I.. Copper enzymes in isolated chloroplasts. Polyphenoloxidase in Beta vulgaris. .  Plant Physiology. (1949);  24 1-15
  • 2 Aubert S., Curien G., Bligny R., Gout E., Douce R.. Transport, compartmentation, and metabolism of homoserine in higher plant cells.  Plant Physiology. (1998);  116 547-557
  • 3 Aubert S., Gout E., Bligny R., Marty-Mazars D., Barrieu F., Alabouvette J., Marty F., Douce R.. Ultrastructural and biochemical characterization of autophagy in higher plant cells subjected to carbon deprivation: control by the supply of mitochondria with respiratory substrates.  The Journal of Cell Biology. (1996);  133 1251-1263
  • 4 Buettner G. R.. The pecking order of free radicals and antioxidants: lipid peroxidation, α-tocopherol, and ascorbate.  Archives of Biochemistry and Biophysics. (1993);  300 535-543
  • 5 Chas E.. Atlas de la flore des Hautes-Alpes. Conservatoire Botanique National Alpin de Gap-Charance. (1994): 158/384
  • 6 Demmig-Adams B., Adams III., W. W.. Photoprotection and other responses of plants to high light stress.  Annual Review of Plant Physiology and Plant Molecular Biology. (1992);  99 599-626
  • 7 Falk S., Maxwell D. P., Laudenbach D. E., Huner N. P. A.. Photosynthetic adjustment to temperature. Baker, N. R., ed. Advances in Photosynthesis, Vol. 5: Photosynthesis and the Environment. Dordrecht; Kluwer Academic Publishers (1996): 367-385
  • 8 Feierabend J., Schaan C., Hertwig B.. Photoinactivation of catalase occurs under both high- and low-temperature stress conditions and accompanies photoinhibition of PSII.  Plant Physiology. (1992);  100 1554-1561
  • 9 Friend A. D., Woodward F. I.. Evolutionary and ecophysiological responses of mountain plants to the growing season environment.  Advances in Ecological Research. (1990);  20 59-124
  • 10 Fryer M. J.. The antioxidant effects of thylakoid vitamin E (α-tocopherol).  Plant Cell and Environment. (1992);  15 381-392
  • 11 Gauslaa Y.. Heat resistance and energy budget in different Scandinavian plants.  Holarctic Ecology. (1984);  7 1-78
  • 12 Havaux M.. Stress tolerance of photosystem II in vivo. Antagonistic effects of water, heat, and photoinhibition stresses.  Plant Physiology. (1992);  100 424-423
  • 13 Havaux M.. Characterization of thermal damage to the photosynthetic electron transport system in potato leaves.  Plant Science. (1993);  94 19-33
  • 14 Havaux M.. Carotenoids as membrane stabilizers in chloroplasts.  Trends in Plant Science. (1998);  3 147-151
  • 15 Havaux M., Greppin H., Strasser R. J.. Functioning of photosystems I and II in pea leaves exposed to heat stress in the presence or absence of light.  Planta. (1991);  186 88-98
  • 16 Hertwig B., Streb P., Feierabend J.. Light dependence of catalase synthesis and degradation in leaves and the influence of interfering stress conditions.  Plant Physiology. (1992);  100 1547-1553
  • 17 Körner C.. Alpine plant life. Berlin, Heidelberg; Springer Verlag (1999)
  • 18 Körner C., Larcher W.. Plant life in cold climates. Long, S. P. and Woodward, F. J., eds. Plants and Temperature, Vol. 42. Cambridge; Society of Experimental Biology (1988): 25-57
  • 19 Kozaki A., Takeba G.. Photorespiration protects C3 plants from photooxidation.  Nature. (1996);  384 557-560
  • 20 Larcher W., Wagner J., Lütz C.. The effect of heat on photosynthesis, dark respiration and cellular ultrastructure of the arctic-alpine psychrophyte Rannuculus glacialis. .  Photosynthetica. (1997);  34 219-232
  • 21 Leegood R. C., Edwards G. E.. Carbon metabolism and photorespiration: Temperature dependence in relation to other environmental factors. Baker, N. R., ed. Advances in Photosynthesis, Vol. 5: Photosynthesis and the Environment. Dordrecht; Kluwer Academic Publishers (1996): 191-221
  • 22 Mishra R. K., Singhal G. S.. Function of photosynthetic apparatus of intact wheat leaves under high light and heat stress and its relationship with peroxidation of thylakoid lipids.  Plant Physiology. (1992);  98 1-6
  • 23 Mishra R. K., Singhal G. S.. Photosynthetic activity and peroxidation of thylakoid lipids during photoinhibition and high temperature treatment of isolated wheat chloroplasts.  Journal of Plant Physiology. (1993);  141 286-292
  • 24 Moser W., Brzoska W., Zachhuber K., Larcher W.. Ergebnisse des IBP-Projekts “Hoher Nebelkogel 3184 m”. Sitzungsberichte der Österreichischen Akademie der Wissenschaften (Wien).  Mathematisch-Naturwissenschaftliche Klasse, Abteilung I. (1997);  186 387-419
  • 25 Müller P., Li X.-P., Niyogi K. K.. Non-photochemical quenching. A response to excess light energy.  Plant Physiology. (2001);  125 1558-1566
  • 26 Neuner G., Braun V., Buchner O., Taschler D.. Leaf rosette closure in the alpine rock species Saxifrage paniculata Mill.: significance for survival of drought and heat under high irradiation.  Plant Cell and Environment. (1999);  22 1539-1548
  • 27 Neuner G., Buchner O., Braun V.. Short-term changes in heat tolerance in the alpine cushion plant Silene acaulis ssp. excapa (All.)  J. Braun at different altitudes. Plant Biology. (2000);  2 677-683
  • 28 Powles S. B.. Photoinhibition of photosynthesis induced by visible light.  Annual Review of Plant Physiology. (1984);  35 15-44
  • 29 Streb P., Aubert S., Gout E., Bligny R.. Reversibility of cold- and light-stress tolerance and accompanying changes of metabolite and antioxidant levels in the two high mountain plant species Soldanella alpina and Ranunculus glacialis. .  Journal of Experimental Botany. (2003 a);  54 405-418
  • 30 Streb P., Aubert S., Gout E., Bligny R.. Cold- and light-induced changes of metabolite and antioxidant levels in two high mountain plant species Soldanella alpina and Ranunculus glacialis and a lowland species Pisum sativum. .  Physiologia Plantarum. (2003 b);  118 96-104
  • 31 Streb P., Feierabend J.. Significance of antioxidants and electron sinks for the cold-hardening-induced resistance of winter rye leaves to photo-oxidative stress.  Plant Cell and Environment. (1999);  22 1225-1237
  • 32 Streb P., Feierabend J. J., Bligny R.. Resistance to photoinhibition of photosystem II and catalase and antioxidative protection in high mountain plants.  Plant Cell and Environment. (1997);  20 1030-1040
  • 33 Streb P., Shang W., Feierabend J.. Resistance of cold-hardened winter rye leaves (Secale cereale L.) to photo-oxidative stress.  Plant Cell and Environment. (1999);  22 1211-1223
  • 34 Streb P., Shang W., Feierabend J., Bligny R.. Divergent strategies of photoprotection in high-mountain plants.  Planta. (1998);  207 313-324
  • 35 Tardy F., Havaux M.. Thylakoid membrane fluidity and thermostability during the operation of the xanthophyll cycle in higher-plant chloroplasts.  Biochimica et Biophysica Acta. (1997);  1330 179-193
  • 36 Thayer S. S., Björkman O.. Leaf xanthophyll content and composition in sun and shade determined by HPLC.  Photosynthesis Research. (1990);  23 331-343
  • 37 Weis E., Berry J. A.. Plants and high temperature stress. Long, S. P. and Woodward, F. J., eds. Plants and Temperature, Vol. 42. Cambridge; Society of Experimental Botany (1988): 329-346
  • 38 Wildi B., Lütz C.. Antioxidant composition of selected high alpine plant species from different altitudes.  Plant Cell and Environment. (1996);  19 138-146
  • 39 Wise R. R.. Chilling-enhanced photooxidation: The production, action and study of reactive oxygen species produced during chilling in the light.  Photosynthesis Research. (1995);  45 79-97

P. Streb

Laboratoire d'Ecophysiologie Végétale
Bâtiment 362
UFR Scientifique d'Orsay Université Paris XI

91405 Orsay Cedex

France

Email: peter.streb@eco.u-psud.fr

Section Editor: M. Riederer

    >