Register      Login
Functional Plant Biology Functional Plant Biology Society
Plant function and evolutionary biology
RESEARCH ARTICLE

Research note: Energy partitioning in photosystem II complexes subjected to photoinhibitory treatment

Dmytro Kornyeyev A B and Luke Hendrickson C D
+ Author Affiliations
- Author Affiliations

A Institute of Plant Physiology and Genetics, Vasylkivska St. 31/17, 03022, Kyiv, Ukraine.

B Department of Biological Sciences, Texas Tech University, Lubbock, TX 79409, USA.

C ARC Centre for Excellence in Plant Energy Biology, Research School of Biological Sciences, Australian National University, GPO Box 475, Canberra, ACT 2601, Australia.

D Corresponding author. Email: luke.hendrickson@anu.edu.au

Functional Plant Biology 34(3) 214-220 https://doi.org/10.1071/FP06327
Submitted: 11 December 2006  Accepted: 14 February 2007   Published: 22 March 2007

Abstract

Chlorophyll a fluorescence measured in vivo is frequently used to study the role of different processes influencing the distribution of excitation energy in PSII complexes. Such studies are important for understanding the regulation of photosynthetic electron transport. However, at the present time, there is no unified methodology to analyse the energy partitioning in PSII. In this article, we critically assess several approaches recently developed in this area of research and propose new simple equations, which can be used for de-convolution of non-photochemical energy quenching in PSII complexes.

Additional keywords: Capsicum annuum, photoinactivation, thermal dissipation.


Acknowledgements

D. K. was funded by USDA grant #99-35100-7630 (National Research Initiative Grants Program) to A. S. Holaday, B. A. Logan, R. Allen (PIs). L. H. was funded by the Australian Research Council Centre for Excellence in Plant Energy Biology.


References


Bilger W, Björkman O (1994) Relationship among violaxanthin de-epoxidation, thylakoid membrane conformation, and non-photochemical chlorophyll fluorescence quenching in leaves of cotton (Gossypium hirsutum L.). Planta 193, 238–246.
Crossref | GoogleScholarGoogle Scholar | open url image1

Cailly AL, Rizza F, Genty B, Harbinson J (1996) Fate of excitation at PSII in leaves: The non-photochemical side. Plant Physiology and Biochemistry special issue , 86. open url image1

Demmig-Adams B, Adams WW, Baker DH, Logan BA, Bowling DR, Verhoeven AS (1996) Using chlorophyll fluorescence to assess the fraction of absorbed light allocated to thermal dissipation of excess excitation. Physiologia Plantarum 98, 253–264.
Crossref | GoogleScholarGoogle Scholar | open url image1

Demmig-Adams B, Moeller DL, Logan BA, Adams WW (1998) Positive correlation between levels of retained zeaxanthin + zeaxanthin and degree of photoinhibition in shade leaves of Schefflera arboricola. Planta 205, 367–374.
Crossref | GoogleScholarGoogle Scholar | open url image1

Demmig-Adams B, Ebbert V, Mellman DL, Mueh KE, Schaffer L, Funk C, Zarter CR, Adamska I, Jansson S, Adams WW (2006) Modulation of PsbS and flexible vs sustained energy dissipation by light environment in different species. Physiologia Plantarum 127, 670–680.
Crossref | GoogleScholarGoogle Scholar | open url image1

Genty B, Briantais JM, Baker NR (1989) The relationship between the quantum yield of photosynthetic electron transport and quenching of chlorophyll fluorescence. Biochimica et Biophysica Acta 990, 87–90. open url image1

Golding AJ, Johnson GN (2003) Down-regulation of linear and activation of cyclic electron transport during drought. Planta 218, 107–114.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

He J, Chow WS (2003) The rate coefficient of repair of photosystem II after photoinactivation. Physiologia Plantarum 118, 297–304.
Crossref | GoogleScholarGoogle Scholar | open url image1

Hendrickson L, Furbank RT, Chow WS (2004) A simple alternative approach to assessing the fate of absorbed light energy using chlorophyll fluorescence. Photosynthesis Research 82, 73–81.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Hendrickson L, Förster B, Pogson BJ, Chow WS (2005) A simple chlorophyll fluorescence parameter that correlates with the rate coefficient of photoinactivation of photosystem II. Photosynthesis Research 84, 43–49.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Hikosaka K, Kato MC, Hirose T (2004) Photosynthetic rates and partitioning of absorbed light energy in photoinhibited leaves. Physiologia Plantarum 121, 699–708.
Crossref | GoogleScholarGoogle Scholar | open url image1

Ivanov AG, Sane PV, Hurry V, Król M, Sveshnikov D, Huner NPA, Öquist G (2003) Low-temperature modulation of the redox properties of the acceptor side of photosystem II: photoprotection through reaction centre quenching of excess energy. Physiologia Plantarum 119, 376–383.
Crossref | GoogleScholarGoogle Scholar | open url image1

Kitajima M, Butler WL (1975) Quenching of chlorophyll fluorescence and primary photochemistry in chloroplasts by dibromothymoquinone. Biochimica et Biophysica Acta 376, 105–115.
Crossref | PubMed |
open url image1

van Kooten O, Snel JFH (1990) The use of chlorophyll fluorescence nomenclature in plant stress physiology. Photosynthesis Research 25, 147–150.
Crossref | GoogleScholarGoogle Scholar | open url image1

Kornyeyev D, Logan BA, Payton P, Allen RD, Holaday AS (2001) Enhanced photochemical light utilization and decreased chilling-induced photoinactivation of photosystem II in cotton over-expressing genes encoding chloroplast-targeted antioxidant enzymes. Physiologia Plantarum 113, 323–331.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Kornyeyev D, Logan BA, Tissue DT, Allen RD, Holaday AS (2006) Compensation for photosystem II photoinactivation by regulated non-photochemical dissipation influences the impact of photoinactivation on electron transport and CO2 assimilation. Plant and Cell Physiology 47, 437–446.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Kramer D, Johnson G, Kiirats O, Edwards GE (2004) New fluorescence parameters for the determination of QA redox state and excitation energy fluxes. Photosynthesis Research 79, 209–218.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Laisk A, Oja V, Rasulov B, Eichelmann H, Sumberg A (1997) Quantum yield and rate constant of photochemical and non-photochemical excitation quenching. Experiment and model. Plant Physiology 115, 803–815.
PubMed |
open url image1

Lee H-Y, Chow WS, Hong Y-N (1999) Photoinactivation of photosystem II in leaves of Capsicum annuum. Physiologia Plantarum 105, 376–383.
Crossref | GoogleScholarGoogle Scholar | open url image1

Lee H-Y, Hong Y-N, Chow WS (2001) Photoinactivation of photosystem II complexes and photoprotection by non-functional neighbours in Capsicum annuum L. leaves. Planta 212, 332–342.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Matsubara S, Chow WS (2004) Populations of photoinactivated photosystem II characterized by Chl fluorescence lifetime in vivo. Proceedings of the National Academy of Sciences of the USA 101, 18234–18239.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Melkonian J, Owens TG, Wolfe DW (2004) Gas-exchange and co-regulation of photochemical and non-photochemical quenching in bean during chilling at ambient and elevated carbon dioxide. Photosynthesis Research 79, 71–82.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Niyogi KK, Li X-P, Rosenberg V, Jung H-S (2005) Is PsbS the site of non-photochemical quenching in photosynthesis? Journal of Experimental Botany 56, 375–382.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Oxborough K, Baker NR (2000) An evaluation of the potential triggers of photoinactivation of photosystem II in the context of a Stern–Volmer model for down-regulation and the reversible radical pair equilibrium model. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences 355, 1489–1498.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Pascal AA, Liu Z, Broess K, van Oort B, van Amerongen H, Wang C, Horton P, Robert B, Chang W, Ruban A (2005) Molecular basis of photoprotection and control of photosynthetic light harvesting. Nature 436, 134–137.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Quick P, Stitt M (1989) An examination of the factors contributing to non-photochemical quenching of chlorophyll fluorescence in barley leaves. Biochimica et Biophysica Acta 977, 287–296.
Crossref |
open url image1

Roháček K (2002) Chlorophyll fluorescence parameters: the definitions, photosynthetic meaning, and mutual relationships. Photosynthetica 40, 13–29.
Crossref |
open url image1

Schreiber U, Schliwa U, Bilger W (1986) Continuous recording of photochemical chlorophyll fluorescence quenching with a new type of modulation fluorometer. Photosynthesis Research 10, 51–62.
Crossref | GoogleScholarGoogle Scholar | open url image1

Shinkarev VP,, Govindjee (1993) Insight into the relationship of chlorophyll a fluorescence yield to the concentration of its natural quenchers in oxygenic photosynthesis. Proceedings of the National Academy of Sciences USA 90, 7466–7469.
Crossref |
open url image1

Trissl H-W, Lavergne J (1995) Fluorescence induction from photosystem II: analytical equations for the yields of photochemistry and fluorescence derived from analysis of a model including exciton-radical pair equilibrium and restricted energy transfer between photosynthetic units. Australian Journal of Plant Physiology 22, 183–193. open url image1

Walters RG, Horton P (1993) Theoretical assessment of alternative mechanisms for non-photochemical quenching of PSII fluorescence in barley leaves. Photosynthesis Research 36, 119–139.
Crossref | GoogleScholarGoogle Scholar | open url image1

Weis E, Lechtenberg D (1989) Fluorescence analysis during steady-state photosynthesis. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences 323, 253–268.
Crossref | GoogleScholarGoogle Scholar | open url image1

Wünschmann G, Brand JJ (1992) Rapid turnover of a component required for photosynthesis explains temperature dependence and kinetics of photoinactivation in a cyanobacterium, Synechococcus 6301. Planta 186, 426–433.
Crossref | GoogleScholarGoogle Scholar | open url image1