Energy dissipation is an essential mechanism to sustain the viability of plants: The physiological limits of improved photosynthesis

Journal of Plant Physiology

Volumn 168, Issue 2, 2011, Pages 79-87

  Wilhelm, Christian ^a   Selmar, Dirk ^b  

^a UNIVERSITY OF LEIPZIG   (Germany)

^b TECHNICAL UNIVERSITY OF BRAUNSCHWEIG   (Germany)

Author keywords

Energy; Non photochemical quenching; Photorespiration; Photosynthesis; Vitamin E; Water water cycle; Xanthophyll cycle

Indexed keywords

ALPHA TOCOPHEROL; WATER; XANTHOPHYLL;

METABOLISM; PHOTOSYNTHESIS; PHYSIOLOGY; PLANT; REVIEW;

PHOTOSYNTHESIS; PLANTS; VITAMIN E; WATER; XANTHOPHYLLS;

EID: 78650004470     PISSN: 01761617     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jplph.2010.07.012     Document Type: Review

References (63)

1. Andersson B., Aro E.-M. Photodamage and D1-turnover in photosystem II. Regulation of photosynthesis 2001, 377-393. Kluwer Academic Press, Dordrecht, The Netherlands. B. Andersson, E.-M. Aro (Eds.).
2. Armstrong A.F., Badger M.R., Day D., Barthet M.M., Smith P.M.C., Millar H., et al. Dynamic changes in the mitochondrial electron transport chain underpinning cold acclimation of leaf respiration. Plant Cell Environ 2008, 31:1156-1169.
3. Asada K. The water-water cycle in chloroplasts: scavenging of active oxygens and dissipation of excess photons. Annu Rev Plant Physiol Mol Biol 1999, 50:601-639.
4. Bennoun P. Evidence for a respiratory chain in the chloroplast. Proc Natl Acad Sci USA 1982, 79:4352-4356.
5. 2-gas exchange and fluorescence measurements indicate differences in light energy dissipation between the wild type and the phytochrome-deficient aurea mutant of tomato during water stress. J Exp Bot 1997, 48:1439-1449.
6. Björkman O. Responses to different quantum flux densities, physiological plant ecology. Encyclopedia in plant physiology 1981, vol. 12A:58. Springer Verlag Heidelberg.
7. Bläsing O., Gibbon Y., Günther M., Höhne M., Morcuende R., Osuna D., et al. Sugars and circadian regulation make major contributions to the global regulation of diurnal gene expression in Arabidopsis. Plant Cell 2005, 17:3257-3281.
8. Carol P., Stevenson D., Bisanz C., Breitenbach J., Sandmann G., Mache R., et al. Mutations in the Arabidopsis gene IMMUTANS cause a variegated phenotype by inactivation a chloroplast terminal oxidase associated with phytoen dasaturation. Plant Cell 1999, 11:57-68.
9. Casano L.M., Zapata J.M., Martin M., Sabater B. Chlororespiration and poising of cyclic electron tran sport, plastoquinone as electron transporter between thylakoid NADH dehydrogenase and peroxidise. J Biol Chem 2000, 275:942-948.
10. Clifton R., Millar A.H., Whelan J. Alternative oxidases in Arabidopsis: a comparative analysis of differential expression in the gene family provides new insights into function of non-phosphorylating bypasses. Biochim Biophys Acta - Bioenerg 2006, 1757:730-741.
11. Cournac L., Redding K., Ravenel J., Rumeau D., Josse E.M., Kuntz M., et al. Electron flow between photosystem II and oxygen in chloroplasts of photosystem I-deficient algae is mediated by a quinol oxidase involved in chlororespiration. J Biol Chem 2000, 275:17256-17262.
12. Cruz S., Serodio J. Relationship of rapid light curves of variable fluorescence to photoacclimation and non-photochemical quenching in a benthic diatom. Aquat Bot 2008, 88:256-264.
13. 2 uptake in Arbutus unedo growing in Portugal. Planta 1989, 177:377-387.
14. 2 uptake in C3 and C4 plants. Plant Physiol 1977, 59:86-90.
15. 2 assimilation in leaves of C3 species. Planta 1980, 149:78-90.
16. Foyer C., Nocter G. Oxygen processing in photosynthesis: regulation and signalling. New Phytol 2000, 146:359-388.
17. Foyer C., Bloom A.J., Queval G., Noctor G. Photorespiratory metabolism: genes, mutants, energetics and redox signalling. Annu Rev Plant Biol 2009, 60:455-484.
18. Gilbert M., Domin A., Becker A., Wilhelm C. Estimation of pirmary productivity by chlorophyll a in vivo fluorescence in freshwater phytoplankton. Photosynthetica 2000, 38:111-126.
19. Goss R., Pinto E., Wilhelm C., Richter M. The importance of a highly active and pH-regulated diatoxanthin epoxidase for the regulation of the PS II antenna function in diadinoxanthin cycle containing algae. J Plant Physiology 2006, 163:1008-1021.
20. Hartmann F.C., Harpel M.R. Structure, function, regulation and assembly of D-ribulose-1,5 bisphosphate carboxilase oxygenase. Annu Rev Biochem 1994, 63:197-234.
21. Heber U. Irrungen, Wirrungen? The Mehler reaction in relation to cyclic electron transport in C3 plants. Photosynth. Res. 2002, 73:223-231.
22. Hihara Y., Sonoike K. Regulation, inhibition and protection of PSI. Regulation of photosynthesis 2001, 507-531. Kluwer Academic Press, Dordrecht, The Netherlands. B. Andersson, E.-M. Aro (Eds.).
23. Holzwarth A.R., Miloslavina Y., Nilkens M. Identification of two quenching sites active in the regulation of photosynthetic light-harvesting studied by time-resolved fluorescence. Chem Phys Lett 2009, 483:262-267.
24. 2-reduction in the absence of methyl viologen - indirect evidence for a regulatory role of superoxide protonation. Photosynth Res 1993, 37:69-80.
25. Ide R., Nakji T., Ogumua H. Assessment of canopy photosynthetic capacity and estimation of GPP by using spectral vegetation indices and the light-response function in a larch forest. Agricult Forst Meterol 2010, 150:389-398.
26. Jakob T., Wagner H., Stehfest K., Wilhelm C. Uncoupling of growth rates and biomass production under nitrate limitation in combination with dynamic light conditions in the diatom Phaeodactylum tricornutum. J Exp Bot 2007, 58:2101-2113.
27. Kebeish R., Niessen M., Krishanaveni T., Bari R., Hirsch H.J., Rosenkranz R., et al. Chloroplastic photorespiratory bypass increases photosynthesis and biomass production in Arabidopsis thaliana. Nat Biotechnol 2007, 25:593-599.
28. Kruk J., Szymanska R., Krupinska K. Tocopherol quinone content of green algae and higher plants revised by a new high-sensitive fluorescence detection method using HPLC - effects of high light stress and senescence. J Plant Physiol 2008, 165:1238-1247.
29. Langner U., Jakob T., Stehfest K., Wilhelm C. A complete energy balance for Chlamydomonas reinhardtii and Chlamydomonas acidophila under neutral and extremely acidic growth conditions. Plant Cell Environm 2009, 32:250-258.
30. Lemaire S.D., Michelet L., Zalfagnini M., Massot V., Issakidis-Bourget E. Thioredoxin in chloroplasts. Curr Genet 2007, 51:343-365.
31. Li D.H., Xie J., Zhao J.Q. Light-induced excitation energy redistribution in Spirulina platensis cells: " spillover" or " mobile PBSs" ?. Biochim. Biophys. Acta 2004, 1608:114-121.
32. Mattoo A.K., Edelman M. Intramembrane translocation and posttranslational palmitoylation of the chloroplast 32-KDa herbicide binding protein. Proc Natl Acad Sci 1987, 84:1497-1501.
33. Miyake C., Scheiber U., Hormann H., Sano S., Asada K. The FAD enzyme monodehydroascorbate radical reductase mediates photoproduction of superoxide radicals in spinach thylakoid membranes. Plant Cell Physiol 1995, 39:821-829.
34. Morandini P. Rethinking metabolic control. Plant Sci 2009, 176:441-451.
35. Nilkens M., Kress E., Labrev P., Miloslavina Y., Müller M., Holzwarth A., et al. Identifiction of a slowly inducible zeaxanthin-dependent component of non-photochemical quenching of chlorophyll fluorescence generated under steady state conditions in Arabidopsis. Biochim Biophys Acta 2010, 1797:466-475.
36. Nowak, M, Manderscheid R, Weigel H-J, Kleinwächter M, Selmar D. in press. Drought Stress Increases the Accumulation of Monoterpenes in Sage (Salvia officinalis), an Effect that is Compensated by Elevated Carbon Dioxide Concentration. Journal of Applied Botany.
37. Posten C. Design principles of photo-bioreactors for cultivation of microalgae. Eng Life Sci 2009, 9:165-177.
38. Quick W.P., Schurr U., Fichtner K., Schulze E.D., Wendler R., Leegood R.C., et al. Decreased ribulose-1,5 bisphosphate carboxilase-oxygenase in transgenic tobacco transformed with antisense rbcS. Impact on photosynthesis in condition of altered nitrogen supply. Planta 1992, 188:522-531.
39. Raines C.A. The Calvin cycle revisited. Photosynth Res 2003, 75:1-10.
40. Raven J.A., Giordano M., Beardall J. Insights into the evolution of CCMs from comparisons with other resource acquisition and assimilation processes. Physiol Plant 2008, 133:4-14.
41. Reumann S., Weber A.P.M. Plant peroxisomes in the light: some gaps of the photorespiratory C2 cycle have become filled - others remain. Biochim. Biophys. Acta 2006, 1763:1496-1510.
42. Ritchie R.J. Fitting light saturation curves measured using modulated fluorometry. Photosynth Res 2008, 96:201-215.
43. Reddy M.M., Vani T., Raghavendra A. Light-enhanced dark respiration in mesophyll protoplasts from leaves of pea. Plant Physiol 1991, 96:1371-1388.
44. Raghavendra A., Padmasree K., Saradadevi K. Interdependence of photosynthesis and respiration in plant cells: interactions between chloroplasts and mitochondria. Plant Sci 1994, 97:1-14.
45. Rasmusson A.G., Escobar M.A. Light and diurnal regulation of plant respiratory gene expression. Physiol Plant 2007, 129:57-67.
46. Sato T., Yamada D., Hirabayashi S. Development of virtual photobioreactor for microalgae culture considering turbulent flow and flashing light effect. Energy Convers Manage 2010, 51:1196-1201.
47. Saroussi S., Beer S. Acclimations of macroalgae as reflected in photosynthetic parameters derived from PAM fluorometry, and possible implications for abundance patterns. Mar Ecol 1997, 28:377-383.
48. Scheibe R., Backhausen J.E., Emmerlich V. Strategies to maintain redox homeostasis during photosynthesis under changing conditions. J Exp Bot 2005, 56:1481-1489.
49. Schmetterer G., Alge D., Gregor W. Deletion of cytochrom C-oxidase genes from the cyanobacterium Synchocystis SP PCC 6803 - Evedence for alternative respiratory pathways. Photosynth Res 1994, 42:43-50.
50. Selmar D. Potential of salt and drought stress to increase pharmaceutical significant secondary compounds in plants. Landbauforschung 2008, 58:139-144.
51. Shahbazi M., Gilbert M., Labouré A.-M., Kuntz M. Dual role of the plastid terminal oxidase in tomato. Plant Physiol 2007, 145:691-702.
52. Siefermann D., Yamamoto H.Y. Properties of NADPH and oxygen-dependent zeaxanthin epoxidation in isolated chloroplasts. A transmembrane-model for the xanthophyll cycle. Arch. Biochem. Biophys. 1975, 171:70-77.
53. Stirbet A., Govindjee, Strasser B.J., Strasser R. Chlorophyll a fluorescence induction in higher plants: modelling and Numerical Simulation. J Theor Biol 1998, 193:131-151.
54. Szabó I., Bergantino E., Giocometti GM Light and oxygenic photosynthesis: energy dissipation as a protection mechanism against photo-oxidation. EMBO Reports 2005, 6:629-634.
55. Taniguchi M., Nagasaki J., Tomita Y. Does the malate valve prevent chloroplasts from excessive reducing power?. Plant Cell Physiol 2005, 46:6-16.
56. Tcherkez G.G., Farquhar G.D., Andrews T.J. Despite slow catalysis and confused substrate specificity, all ribulose bisphosphate carboxylases may be nearly perfectly optimized. Proc Natl Acad Sci USA 2006, 103:7246-7251.
57. van den Berg A.K., Vogelmann T.C., Perkins T.D. Anthocyanin influence on light absorption within juvenile and senescing sugar maple leaves - do anthocyanins function as photoprotective visible light screens? Funct. Plant Biol 2009, 36:793-800.
58. Wagner H., Jakob T., Wilhelm C. Balancing the energy flow from captured light to biomass under fluctuating light conditions. New Phytol 2005, 169:95-108.
59. Wild A. Physiologie der Photosynthese höherer Pflanzen. Ber Deutsch Bot Ges 1979, 92:345-368.
60. Wilhelm C., Wild A. The variability of the photosynthetic unit in Chlorella II. The effect of light intensity and cell development on photosynthesis, P-700 and cytochrome f in homocontinuous and synchronous cultures of Chlorella. J Plant Physiol 1984, 115:124-135.
61. Wilhelm C., Duval J.C. Fluorescence induction kinetics as a tool to detect chlororespiratorian activity in the prasinophycean alga Mantoniella squamata. Biochim Biophys Acta 1990, 1016:197-202.
62. Wilhelm C., Büchel C., Fisahn J., Goss R., Jakob T., Kroth P., et al. The regulation of carbon and nutrient assimilation in diatoms is significantly different from Green Algae, a putative consequence of secondary endosymbiosis. Protist 2006, 157:91-124.
63. Wu D., Wright D.A., Wetzel C., Voytas D.F., Rodermel S. The IMMUNANS variegation locus of Arabidopsis defines a mitochondrial alternative oxidase homologue that functions during early chloroplast biogenesis. Plant Cell 1999, 11:43-55.