Importance of fluctuations in light on plant photosynthetic acclimation

Plant Physiology

Volumn 173, Issue 4, 2017, Pages 2163-2179

  Vialet Chabrand, Silvere ^a   Matthews, Jack S A ^a   Simkin, Andrew J ^a   Raines, Christine A ^a   Lawson, Tracy ^a  

^a UNIVERSITY OF ESSEX   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ARABIDOPSIS PROTEIN; CARBON; CHLOROPHYLL;

ACCLIMATIZATION; ALGORITHM; ARABIDOPSIS; BIOLOGICAL MODEL; BIOMASS; CIRCADIAN RHYTHM; ELECTRON TRANSPORT; LIGHT; METABOLISM; PHOTOSYNTHESIS; PHYSIOLOGY; PLANT LEAF; RADIATION RESPONSE; TIME FACTOR; WESTERN BLOTTING;

ACCLIMATIZATION; ALGORITHMS; ARABIDOPSIS; ARABIDOPSIS PROTEINS; BIOMASS; BLOTTING, WESTERN; CARBON; CHLOROPHYLL; CIRCADIAN RHYTHM; ELECTRON TRANSPORT; LIGHT; MODELS, BIOLOGICAL; PHOTOSYNTHESIS; PLANT LEAVES; TIME FACTORS;

EID: 85016489794     PISSN: 00320889     EISSN: 15322548     Source Type: Journal    
DOI: 10.1104/pp.16.01767     Document Type: Article

References (73)

1. Alter P, Dreissen A, Luo FL, Matsubara S (2012) Acclimatory responses of Arabidopsis to fluctuating light environment: comparison of different sunfleck regimes and accessions. Photosynth Res 113: 221-237
2. Athanasiou K, Dyson BC, Webster RE, Johnson GN (2010) Dynamic acclimation of photosynthesis increases plant fitness in changing environments. Plant Physiol 152: 366-373
3. Bailey S, Horton P, Walters RG (2004) Acclimation of Arabidopsis thaliana to the light environment: the relationship between photosynthetic function and chloroplast composition. Planta 218: 793-802
4. Bailey S, Walters RG, Jansson S, Horton P (2001) Acclimation of Arabidopsis thaliana to the light environment: the existence of separate low light and high light responses. Planta 213: 794-801
5. Baker NR (2008) Chlorophyll fluorescence: a probe of photosynthesis in vivo. Annu Rev Plant Biol 59: 89-113
6. Bernacchi CJ, Bagley JE, Serbin SP, Ruiz-Vera UM, Rosenthal DM, Vanloocke A (2013) Modelling C3 photosynthesis from the chloroplast to the ecosystem. Plant Cell Environ 36: 1641-1657
7. Carmo-Silva AE, Salvucci ME (2013) The regulatory properties of Rubisco activase differ among species and affect photosynthetic induction during light transitions. Plant Physiol 161: 1645-1655
8. Chabot BF, Jurik TW, Chabot JF (1979) Influence of instantaneous and integrated light-flux density on leaf anatomy and photosynthesis. Am J Bot 66: 940-945
9. Chazdon RL, Pearcy RW (1991) The importance of sunflecks for forest understory plants. Bioscience 41: 760-766
10. Demmig-Adams B, Adams WW (1992) Photoprotection and other responses of plants to high light stress. Annu Rev Plant Physiol Plant Mol Biol 43: 599-626
11. Ernstsen J, Woodrow IE, Mott KA (1997) Responses of Rubisco activation and deactivation rates to variations in growth-light conditions. Photosynth Res 52: 117-125
12. Evans JR, Poorter H (2001) Photosynthetic acclimation of plants to growth irradiance: the relative importance of specific leaf area and nitrogen partitioning in maximizing carbon gain. Plant Cell Environ 24: 755-767
13. Foyer CH, Neukermans J, Queval G, Noctor G, Harbinson J (2012) Photosynthetic control of electron transport and the regulation of gene expression. J Exp Bot 63: 1637-1661
14. Foyer FH, Nurmi A, Dulieu H, Parry MAJ (1993) Analysis of two Rubiscodeficient tobacco mutants, h7 and sp25: evidence for the production of Rubisco large subunits in the sp25 mutant that form clusters and are inactive. J Exp Bot 44: 1445-1452
15. Frechilla S, Talbott LD, Zeiger E (2004) The blue light-specific response of Vicia faba stomata acclimates to growth environment. Plant Cell Physiol 45: 1709-1714
16. Garnier E, Salager JL, Laurent G, Sonié L (1999) Relationships between photosynthesis, nitrogen and leaf structure in 14 grass species and their dependence on the basis of expression. New Phytol 143: 119-129
17. Givnish TJ (1988) Adaptation to sun and shade: a whole-plant perspective. Aust J Plant Physiol 15: 63-92
18. Harley PC, Loreto F, Di Marco G, Sharkey TD (1992) Theoretical considerations when estimating the mesophyll conductance to CO2 flux by analysis of the response of photosynthesis to CO2. Plant Physiol 98: 1429-1436
19. Harrison EP, Willingham NM, Lloyd JC, Raines CA (1998) Reduced sedoheptulose-1,7-bisphosphatase levels in transgenic tobacco lead to decreased photosynthetic capacity and altered carbohydrate accumulation. Planta 204: 27-36
20. Henkes S, Sonnewald U, Badur R, Flachmann R, Stitt M (2001) A small decrease of plastid transketolase activity in antisense tobacco transformants has dramatic effects on photosynthesis and phenylpropanoid metabolism. Plant Cell 13: 535-551
21. Huxley PA (1969) The effect of fluctuating light intensity on plant growth. J Appl Ecol 6: 273-276
22. Kono M, Terashima I (2014) Long-term and short-term responses of the photosynthetic electron transport to fluctuating light. J Photochem Photobiol B 137: 89-99
23. Kono M, Terashima I (2016) Elucidation of photoprotective mechanisms of PSI against fluctuating light photoinhibition. Plant Cell Physiol 57: 1405-1414
24. Külheim C, Agren J, Jansson S (2002) Rapid regulation of light harvesting and plant fitness in the field. Science 297: 91-93
25. Lawson T, Kramer DM, Raines CA (2012) Improving yield by exploiting mechanisms underlying natural variation of photosynthesis. Curr Opin Biotech 23: 215-220
26. Lawson T, Blatt MR (2014) Stomatal size, speed, and responsiveness impact on photosynthesis and water use efficiency. Plant Physiol 164: 1556-1570
27. Lefebvre S, Lawson T, Zakhleniuk OV, Lloyd JC, Raines CA, Fryer M (2005) Increased sedoheptulose-1,7-bisphosphatase activity in transgenic tobacco plants stimulates photosynthesis and growth from an early stage in development. Plant Physiol 138: 451-460
28. Li XP, Björkman O, Shih C, Grossman AR, Rosenquist M, Jansson S, Niyogi KK (2000) A pigment-binding protein essential for regulation of photosynthetic light harvesting. Nature 403: 391-395
29. Li XP, Gilmore AM, Caffarri S, Bassi R, Golan T, Kramer D, Niyogi KK (2004) Regulation of photosynthetic light harvesting involves intrathylakoid lumen pH sensing by the PsbS protein. J Biol Chem 279: 22866-22874
30. Li Z, Wakao S, Fischer BB, Niyogi KK (2009) Sensing and responding to excess light. Annu Rev Plant Biol 60: 239-260
31. Long SP, Bernacchi CJ (2003) Gas exchange measurements, what can they tell us about the underlying limitations to photosynthesis? Procedures and sources of error. J Exp Bot 54: 2393-2401
32. López-Juez E, Jarvis RP, Takeuchi A, Page AM, Chory J (1998) New Arabidopsis cue mutants suggest a close connection between plastidand phytochrome regulation of nuclear gene expression. Plant Physiol 118: 803-815
33. Matsubara S, Naumann M, Martin R, Nichol C, Rascher U, Morosinotto T, Bassi R, Osmond B (2005) Slowly reversible de-epoxidation of luteinepoxide in deep shade leaves of a tropical tree legume may ‘lock-in’ lutein-based photoprotection during acclimation to strong light. J Exp Bot 56: 461-468
34. McAusland L, Vialet-Chabrand S, Davey P, Baker NR, Brendel O, Lawson T (2016) Effects of kinetics of light-induced stomatal responses on photosynthesis and water-use efficiency. New Phytol 211: 1209-1220
35. Medlyn BE (1998) Physiological basis of the light use efficiency model. Tree Physiol 18: 167-176
36. Müller P, Li XP, Niyogi KK (2001) Non-photochemical quenching: a response to excess light energy. Plant Physiol 125: 1558-1566
37. Mullineaux PM, Karpinski S, Baker NR (2006) Spatial dependence for hydrogen peroxide-directed signaling in light-stressed plants. Plant Physiol 141: 346-350
38. Murchie EH, Horton P (1997) Acclimation of photosynthesis to irradiance and spectral quality in British plant species: chlorophyll content, photosynthetic capacity and habitat preference. Plant Cell Environ 20: 438-448
39. Murchie EH, Hubbart S, Peng S, Horton P (2005) Acclimation of photosynthesis to high irradiance in rice: gene expression and interactions with leaf development. J Exp Bot 56: 449-460
40. Murchie EH, Lawson T (2013) Chlorophyll fluorescence analysis: a guide to good practice and understanding some new applications. J Exp Bot 64: 3983-3998
41. Naumburg E, Ellsworth DS (2002) Short-term light and leaf photosynthetic dynamics affect estimates of daily understory photosynthesis in four tree species. Tree Physiol 22: 393-401
42. Niinemets U (2007) Photosynthesis and resource distribution through plant canopies. Plant Cell Environ 30: 1052-1071
43. Niinemets Ü (2010) A review of light interception in plant stands from leaf to canopy in different plant functional types and in species with varying shade tolerance. Ecol Res 25: 693-714
44. Oguchi R, Hikosaka K, Hiura T, Hirose T (2008) Costs and benefits of photosynthetic light acclimation by tree seedlings in response to gap formation. Oecologia 155: 665-675
45. Okegawa Y, Long TA, Iwano M, Takayama S, Kobayashi Y, Covert SF, Shikanai T (2007) A balanced PGR5 level is required for chloroplast development and optimum operation of cyclic electron transport around photosystem I. Plant Cell Physiol 48: 1462-1471
46. Ort DR, Merchant SS, Alric J, Barkan A, Blankenship RE, Bock R, Croce R, Hanson MR, Hibberd JM, Long SP, et al (2015) Redesigning photosynthesis to sustainably meet global food and bioenergy demand. Proc Natl Acad Sci USA 112: 8529-8536
47. Parsons R, Weyers JDB, Lawson T, Godber IM (1998) Rapid and straightforward estimates of photosynthetic characteristics using a portable gas exchange system. Photosynthetica 34: 265-279
48. Paul MJ, Foyer CH (2001) Sink regulation of photosynthesis. J Exp Bot 52: 1383-1400
49. Paul MJ, Pellny TK (2003) Carbon metabolite feedback regulation of leaf photosynthesis and development. J Exp Bot 54: 539-547
50. Pearcy R (2007) Responses of plants to heterogeneous light environments. In F Valladares, F Pugnaire, eds, Functional Plant Ecology, Ed 2. CRC Press, Boca Raton, FL, pp 213-246
51. Pearcy RW (1990) Sunflecks and photosynthesis in plant canopies. Annu Rev Plant Physiol Plant Mol Biol 41: 421-453
52. Pearcy RW, Way DA (2012) Two decades of sunfleck research: looking back to move forward. Tree Physiol 32: 1059-1061
53. Poorter H, Fiorani F, Pieruschka R, Wojciechowski T, van der Putten WH, Kleyer M, Schurr U, Postma J (2016) Pampered inside, pestered outside? Differences and similarities between plants growing in controlled conditions and in the field. New Phytol 212: 838-855
54. Porcar-Castell A, Garcia-Plazaola JI, Nichol CJ, Kolari P, Olascoaga B, Kuusinen N, Fernández-Marín B, Pulkkinen M, Juurola E, Nikinmaa E (2012) Physiology of the seasonal relationship between the photochemical reflectance index and photosynthetic light use efficiency. Oecologia 170: 313-323
55. Retkute R, Smith-Unna SE, Smith RW, Burgess AJ, Jensen OE, Johnson GN, Preston SP, Murchie EH (2015) Exploiting heterogeneous environments: does photosynthetic acclimation optimize carbon gain in fluctuating light? J Exp Bot 66: 2437-2447
56. Rosenthal DM, Locke AM, Khozaei M, Raines CA, Long SP, Ort DR (2011) Over-expressing the C3 photosynthesis cycle enzyme sedoheptulose-1-7bisphosphatase improves photosynthetic carbon gain and yield under fully open air CO2 fumigation (FACE). BMC Plant Biol 11: 123
57. Sharkey TD, Bernacchi CJ, Farquhar GD, Singsaas EL (2007) Fitting photosynthetic carbon dioxide response curves for C3 leaves. Plant Cell Environ 30: 1035-1040
58. Simkin AJ, Lopez-Calcagno PE, Davey PA, Headland LR, Lawson T, Timm S, Bauwe H, Raines CA (2017) Simultaneous stimulation of sedoheptulose 1,7-bisphosphatase, fructose 1,6-bisphophate aldolase and the photorespiratory glycine decarboxylase H-protein increases CO2 assimilation, vegetative biomass and seed yield in Arabidopsis. Plant Biotechnol J http://dx.doi.org/10.1111/pbi.12676
59. Simkin AJ, McAusland L, Headland LR, Lawson T, Raines CA (2015) Multigene manipulation of photosynthetic carbon assimilation increases CO2 fixation and biomass yield in tobacco. J Exp Bot 66: 4075-4090
60. Sinclair TR, Muchow RC (1999) Radiation use efficiency. Adv Agron 65: 215-265
61. Suorsa M, Järvi S, Grieco M, Nurmi M, Pietrzykowska M, Rantala M, Kangasjärvi S, Paakkarinen V, Tikkanen M, Jansson S, et al (2012) PROTON GRADIENT REGULATION5 is essential for proper acclimation of Arabidopsis photosystem I to naturally and artificially fluctuating light conditions. Plant Cell 24: 2934-2948
62. Terashima I, Hanba YT, Tazoe Y, Vyas P, Yano S (2006) Irradiance and phenotype: comparative eco-development of sun and shade leaves in relation to photosynthetic CO2 diffusion. J Exp Bot 57: 343-354
63. Tikkanen M, Grieco M, Kangasjärvi S, Aro EM (2010) Thylakoid protein phosphorylation in higher plant chloroplasts optimizes electron transfer under fluctuating light. Plant Physiol 152: 723-735
64. Walker B, Ariza LS, Kaines S, Badger MR, Cousins AB (2013) Temperature response of in vivo Rubisco kinetics and mesophyll conductance in Arabidopsis thaliana: comparisons to Nicotiana tabacum. Plant Cell Environ 36: 2108-2119
65. Walters R, Horton P (1994) Acclimation of Arabidopsis thaliana to the light environment: changes in composition of the photosynthetic apparatus. Planta 195: 248-256
66. Watling J, Ball M, Woodrow I (1997) The utilization of lightflecks for growth in four Australian rainforest species. Funct Ecol 11: 231-239
67. Weraduwage SM, Chen J, Anozie FC, Morales A, Weise SE, Sharkey TD (2015) The relationship between leaf area growth and biomass accumulation in Arabidopsis thaliana. Front Plant Sci 6: 167
68. Weston E, Thorogood K, Vinti G, López-Juez E (2000) Light quantity controls leaf-cell and chloroplast development in Arabidopsis thaliana wild type and blue-light-perception mutants. Planta 211: 807-815
69. Wright IJ, Reich PB, Westoby M (2001) Strategy-shifts in leaf physiology, structure and nutrient content between species of high and low rainfall, and high and low nutrient habitats. Funct Ecol 15: 423-434
70. Yamori W (2016) Photosynthetic response to fluctuating environments and photoprotective strategies under abiotic stress. J Plant Res 129: 379-395
71. Yin ZH, Johnson GN (2000) Photosynthetic acclimation of higher plants to growth in fluctuating light environments. Photosynth Res 63: 97-107
72. Zapata M, Rodríguez F, Garrido JL (2000) Separation of chlorophylls and carotenoids from marine phytoplankton, a new HPLC method using a reversed phase C8 column and phridine-containing mobile phases. Mar Ecol Prog Ser 195: 29-45
73. Zhu XG, Long SP, Ort DR (2010) Improving photosynthetic efficiency for greater yield. Annu Rev Plant Biol 61: 235-261