Journal of Experimental Botany, Vol. 54, No. 392, pp. 2419-2430,
November 1, 2003
© 2003 Oxford University Press
Chlorophyll thermoluminescence of leaf discs: simple instruments and progress in signal interpretation open the way to new ecophysiological indicators
Received 20 May 2003; Accepted 14 July 2003
1 Service de Bioénergétique, Bât 532, INRA/CEA Saclay, 91191 Gif-sur-Yvette cedex, France
2 Equipe Photosynthèse et Télédétection, LURE, Université Paris-Sud, 91898 Orsay, France
* Address correspondence to Gif-sur-Yvette. Fax: 33 1 69 08 68 38. E-mail: ducruet{at}dsvidf.cea.fr
Abbreviations: A band, Z+Qa; AG, afterglow (luminescence bounce); B band, S2Qb (B2) and S3Qb (B1); C band, D+Qa; DLE, delayed light emission; HTL, high temperature thermoluminescence (> 60 °C); LED, light emitting diodes; PSII, photosystem II; PSI, photosystem I; PMT, photomultiplier tube; TL, thermoluminescence; Tm, temperature of the maximum of a TL band (here corresponding to a 0.5 °C s1 heating rate).
Luminescence from photosynthetic material observed in darkness following illumination is a delayed fluorescence produced by a recombination of charge pairs stored in photosystem II, i.e. the back-reaction of photosynthetic charge separation. Thermolumi nescence (TL) is a technique consisting of a rapid cooling followed by the progressive warming of a preilluminated sample to reveal the different types of charge pairs as successive emission bands, which are resolved better than the corresponding decay phases recorded at constant temperatures. Progress in thermoelectric Peltier elements and in compact light detectors made the development of simple, affordable and transportable instruments possible. These instruments take advantage of multifurcated light guides for combined TL, fluorescence and absorbance/reflectance measurements. Meanwhile, experiments on unfrozen leaf discs, with excitation by single turn-over flashes or far red light and infiltration by specific inhibitors/uncouplers, have led to a better understanding of in vivo TL signals. Much like chlorophyll fluorescence and in a complementary way, TL in the 060 °C temperature range not only informs on the state of photosystem II in leaf tissues and its possible alterations, but also gives a broader insight into the energetic state inside the chloroplast by probing (1) the light-induced or dark-stable thylakoid proton gradient through the protonation of the Mn oxygen-evolving complex, (2) the induction of cyclic/chlororespiratory electron flow towards the plastoquinone pool, (3) the [NADPH+ATP] assimilatory potential. By a different mechanism, warming above 60 °C without preillumination reveals chemiluminescence high temperature thermoluminescence (HTL) bands due to the radiative thermolysis of peroxides, which are indicators of oxidative stress in leaves.
Key words: Delayed fluorescence, instrument, luminescence, photosynthesis, photosystem II.
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
J. Flexas, M. Baron, J. Bota, J.-M. Ducruet, A. Galle, J. Galmes, M. Jimenez, A. Pou, M. Ribas-Carbo, C. Sajnani, et al. Photosynthesis limitations during water stress acclimation and recovery in the drought-adapted Vitis hybrid Richter-110 (V. berlandierixV. rupestris) J. Exp. Bot., May 1, 2009; 60(8): 2361 - 2377. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. Ishida, M. Sugiura, F. Rappaport, T.-L. Lai, A. W. Rutherford, and A. Boussac Biosynthetic Exchange of Bromide for Chloride and Strontium for Calcium in the Photosystem II Oxygen-evolving Enzymes J. Biol. Chem., May 9, 2008; 283(19): 13330 - 13340. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Havaux, L. Dall'Osto, and R. Bassi Zeaxanthin Has Enhanced Antioxidant Capacity with Respect to All Other Xanthophylls in Arabidopsis Leaves and Functions Independent of Binding to PSII Antennae Plant Physiology, December 1, 2007; 145(4): 1506 - 1520. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Shahbazi, M. Gilbert, A.-M. Laboure, and M. Kuntz Dual Role of the Plastid Terminal Oxidase in Tomato Plant Physiology, November 1, 2007; 145(3): 691 - 702. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Fufezan, C. M. Gross, M. Sjodin, A. W. Rutherford, A. Krieger-Liszkay, and D. Kirilovsky Influence of the Redox Potential of the Primary Quinone Electron Acceptor on Photoinhibition in Photosystem II J. Biol. Chem., April 27, 2007; 282(17): 12492 - 12502. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. Umate, S. Schwenkert, I. Karbat, C. D. Bosco, L. Mlcochova, S. Volz, H. Zer, R. G. Herrmann, I. Ohad, and J. Meurer Deletion of PsbM in Tobacco Alters the QB Site Properties and the Electron Flow within Photosystem II J. Biol. Chem., March 30, 2007; 282(13): 9758 - 9767. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Schwenkert, P. Umate, C. D. Bosco, S. Volz, L. Mlcochova, M. Zoryan, L. A. Eichacker, I. Ohad, R. G. Herrmann, and J. Meurer PsbI Affects the Stability, Function, and Phosphorylation Patterns of Photosystem II Assemblies in Tobacco J. Biol. Chem., November 10, 2006; 281(45): 34227 - 34238. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. Ossenbuhl, M. Inaba-Sulpice, J. Meurer, J. Soll, and L. A. Eichacker The Synechocystis sp PCC 6803 Oxa1 Homolog Is Essential for Membrane Integration of Reaction Center Precursor Protein pD1 PLANT CELL, September 1, 2006; 18(9): 2236 - 2246. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Havaux, F. Eymery, S. Porfirova, P. Rey, and P. Dormann Vitamin E Protects against Photoinhibition and Photooxidative Stress in Arabidopsis thaliana PLANT CELL, December 1, 2005; 17(12): 3451 - 3469. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Kirilovsky, M. Roncel, A. Boussac, A. Wilson, J. L. Zurita, J.-M. Ducruet, H. Bottin, M. Sugiura, J. M. Ortega, and A. W. Rutherford Cytochrome c550 in the Cyanobacterium Thermosynechococcus elongatus: STUDY OF REDOX MUTANTS J. Biol. Chem., December 17, 2004; 279(51): 52869 - 52880. [Abstract] [Full Text] [PDF] |
||||



