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2012 | 34 | 4 |
Tytuł artykułu

Differential response of photosystem II photochemistry in young and mature leaves of Arabidopsis thaliana to the onset of drought stress

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EN
Abstrakty
EN
Photosystem II (PSII) photochemistry and oxidative stress of mature leaves (ML) and young leaves (YL) of 4-week-old Arabidopsis thaliana plants subjected to water deficit for 24 h was investigated. To the onset of drought, maximum quantum yield of PSII photochemistry (Fv/Fm), quantum efficiency of PSII photochemistry (ΦPSII), quantum yield for dissipation by down regulation (ΦNPQ) and electron transport rate decreased in ML more than in YL. These changes were accompanied by increased quantum yield of non-regulated energy dissipation (ΦNO) and increased excitation pressure (1 - qP) in ML more than in YL. The more excitation energy dissipated by nonphotochemical quenching (NPQ) in drought-stressed YL compared to ML seemed to be sufficient in scavenging reactive oxygen species, as it was evident by the decreased lipid peroxidation level measured as malondialdehyde content. The better PSII functioning of YL may reflect their capacity to acclimate better to the onset of drought stress, as revealed by the higher ΦPSII, the more excitation energy dissipated by NPQ and the decreased excitation pressure (1 – qP). Our results suggest that the dissipation of excess excitation energy in YL plays an important role in order to avoid possible photodamage to PSII under drought stress conditions.
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-
Rocznik
Tom
34
Numer
4
Opis fizyczny
p.1267-1276,fig.,ref.
Twórcy
autor
  • Department of Botany, School of Biology, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece
autor
  • Department of Botany, School of Biology, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece
Bibliografia
  • Alves AA, Guimarães LMS, Chaves ARM, DaMatta FM, Alfenas AC (2011) Leaf gas exchange and chlorophyll a fluorescence of Eucalyptus urophylla in response to Puccinia psidii infection. Acta Physiol Plant 33:1831–1839
  • Asada K (1999) The water–water cycle in chloroplasts: scavenging of active oxygen and dissipation of excess photons. Annu Rev Plant Physiol Plant Mol Biol 50:601–639
  • Asada K (2006) Production and scavenging of reactive oxygen species in chloroplasts and their functions. Plant Physiol 141:391–396
  • Baker NR, Rosenqvist E (2004) Applications of chlorophyll fluorescence can improve crop production strategies: an examination of future possibilities. J Exp Bot 55:1607–1621
  • Balakumar T, Hani Babu V, Paliwal K (1993) On the interaction of UV-B radiation (280–315 nm) with water stress in crop plants. Physiol Plantarum 87:217–222
  • Bolhar-Nordenkampf HR, Long SP, Baker NR, Öquist G, Schreiber U, Lechner EG (1989) Chlorophyll fluorescence as probe of the photosynthetic competence of leaves in the field: a review of current instrument. Funct Ecol 3:497–514
  • Calatayud A, Roca D, Martínez PF (2006) Spatial-temporal variations in rose leaves under water stress conditions studied by chlorophyll fluorescence imaging. Plant Physiol Biochem 44:564–573
  • Chaerle L, van der Straeten D (2001) Seeing is believing: imaging techniques to monitor plant health. Biochem Biophys Acta 1519:153–166
  • Chaves MM (1991) Effects of water deficits on carbon assimilation. J Exp Bot 42:1–16
  • Chaves MM, Flexas J, Pinheiro C (2009) Photosynthesis under drought and salt stress: regulation mechanisms from whole plant to cell. Ann Bot Lond 103:551–560
  • Demmig-Adams B, Adams WW III (1992) Photoprotection and other responses of plants to high light stress. Ann Rev Plant Physiol Plant Mol Biol 43:599–626
  • Demmig-Adams B, Adams WW III (2006) Photoprotection in an ecological context: the remarkable complexity of thermal energy dissipation. New Phytol 172:11–21
  • Dillenburg LR, Sullivan JH, Teramura AH (1995) Leaf expansion and development of photosynthetic capacity and pigments in Liquidambar styraciflua. Am J Bot 82:433–440
  • Flexas J, Bota J, Loreto F, Cornic G, Sharkey TD (2004) Diffusive and metabolic limitations to photosynthesis under drought and salinity in C3 plants. Plant Biol 6:269–279
  • Flexas J, Barón M, Bota J, Ducruet JM, Gallé A, Galmés J, Jiménez M, Pou A, Ribas-Carbó M, Sajnani C, Tomàs M, Medrano H (2009) Photosynthesis limitations during water stress acclimation and recovery in the drought-adapted Vitis hybrid Richter-110 (V. berlandieri 9 V. rupestris). J Exp Bot 60:2361–2377
  • Foyer CH, Noctor G (2009) Redox regulation in photosynthetic organisms: signaling, acclimation, and practical implications. Antioxid Redox Signal 11:861–905
  • Gallé A, Haldimann P, Feller U (2007) Photosynthetic performance and water relations in young pubescent oak (Quercus pubescens) trees during drought stress and recovery. New Phytol 174:799–810
  • Galmés J, Abadia A, Medrano H, Flexas J (2007) Photosynthesis and photoprotection responses to water stress in the wild-extinct plant Lysimachia minoricensis. Environ Exp Bot 60:308–317
  • Garcia-Plazaola JI, Hernàndez A, Olano JM, Becerril JM (2003) The operation of the lutein epoxide cycle correlates with energy dissipation. Funct Plant Biol 30:319–324
  • Genty B, Briantais JM, Baker NR (1989) The relationship between the quantum yield of photosynthetic electron transport and quenching of chlorophyll fluorescence. Biochim Biophys Acta 990:87–92
  • Giannakoula A, Moustakas M, Syros T, Yupsanis T (2010) Aluminium stress induces up-regulation of an efficient antioxidant system in the Al-tolerant maize line but not in the Al-sensitive line. Environ Exp Bot 67:487–494
  • Graßes T, Pesaresi P, Schiavon F, Varotto C, Slamini F, Jahns P, Leister D (2002) The role of DpH-dependent dissipation of excitation energy in protecting photosystem II against lightinduced damage in Arabidopsis thaliana. Plant Physiol Biochem 40:41–49
  • Gray GR, Savitch LV, Ivanov AG, Huner NPA (1996) Photosystem II excitation pressure and development of resistance to photoinhibition. II. Adjustment of photosynthetic capacity in winter wheat and winter rye. Plant Physiol 110:61–71
  • Haimeirong, Kubota F (2003) The effects of drought stress and leaf ageing on leaf photosynthesis and electron transport in photosystem 2 in sweet potato (Ipomoea batatas Lam.) cultivars. Photosynthetica 41:253–258
  • Han H, Gao S, Li B, Dong XC, Feng HL, Meng QW (2010) Over expression of violaxanthin de-epoxidase gene alleviates photoinhibition of PSII and PSI in tomato during high light and chilling stress. J Plant Physiol 167:176–183
  • Havaux M, Strasser RJ, Greppin HA (1991) Theoretical and experimental analysis of the qP and qN coefficients of chlorophyll fluorescence quenching and their relation to photochemical and nonphotochemical events. Photosynth Res 27:41–55
  • Havaux M, Dall’Osto L, Bassi R (2007) Zeaxanthin has enhanced antioxidant capacity with respect to all other xanthophylls in Arabidopsis leaves and functions independent of binding to PSII antennae. Plant Physiol 145:1506–1520
  • Heath RL, Packer L (1968) Photoperoxidation in isolated chloroplasts I. Kinetics and stoichiometry of fatty acid peroxidation. Arch Biochem Biophys 125:189–198
  • Hodges DM, Delong JM, Forney CF, Prange RK (1999) Improving the thiobarbituric acid-reactive-substances assay for estimating lipid peroxidation in plant tissues containing anthocyanin and other interfering compounds. Planta 207:604–611
  • Janušauskaitė D, Auškalnienė O, Pšibišauskienė G (2011) Evaluation of chlorophyll fluorescence in different densities of spring barley. Acta Physiol Plant 33:2159–2167
  • Jiang CD, Li PM, Gao HY, Zou Q, Jiang GM, Li LH (2005) Enhanced photoprotection at the early stages of leaf expansion in field-grown soybean plants. Plant Sci 168:911–919
  • Jung S (2004) Variation in antioxidant metabolism of young and mature leaves of Arabidopsis thaliana subjected to drought. Plant Sci 166:459–466
  • Kramer DM, Johnson G, Kiirats O, Edwards GE (2004) New fluorescence parameters for the determination of QA redox state and excitation energy fluxes. Photosynth Res 79:209–218
  • Krause GH, Weis E (1991) Chlorophyll fluorescence and photosynthesis: the basics. Annu Rev Plant Physiol Plant Mol Biol 42:313–349
  • Lawlor DW, Cornic G (2002) Photosynthetic carbon assimilation and associated metabolism in relation to water deficits in higher plants. Plant Cell Environ 25:275–294
  • Lawlor DW, Tezara W (2009) Causes of decreased photosynthetic rate and metabolic capacity in water-deficient leaf cells: a critical evaluation of mechanisms and integration of processes. Ann Bot Lond 103:561–579
  • Lichtenthaler HK, Miehé JA (1997) Fluorescence imaging as a diagnostic tool for plant stress. Trends Plant Sci 2:316–320
  • Loreto F, Sharkey TD (1990) Low humidity can cause uneven photosynthesis in olive (Olea europea L.) leaves. Tree Physiol 6:409–415
  • Massacci A, Nabiev SM, Pietrosanti L, Nematov SK, Chernikova TN, Thor K, Leipner J (2008) Response of the photosynthetic apparatus of cotton (Gossypium hirsutum) to the onset of drought stress under field conditions studied by gas-exchange analysis and chlorophyll fluorescence imaging. Plant Physiol Biochem 46:189–195
  • Maxwell K, Johnson GN (2000) Chlorophyll fluorescence: a practical guide. J Exp Bot 51:659–668
  • Miller G, Suzuki N, Ciftci-Yilmaz S, Mittler R (2010) Reactive oxygen species homeostasis and signaling during drought and salinity stresses. Plant Cell Environ 33:453–467
  • Mittler R (2002) Oxidative stress, antioxidants and stress tolerance. Trends Plant Sci 7:405–410
  • Mittler R, Vanderauwera S, Gollery M, van Breusegem F (2004) Reactive oxygen gene network of plants. Trends Plant Sci 9:490–498
  • Molinari HBC, Marur CJ, Daros E, De Campos MKF, De Carvalho JFRP, Filho JCB, Pereira LFP, Vieira LGE (2007) Evaluation of the stress-inducible production of proline in transgenic sugarcane (Saccharum spp.): osmotic adjustment, chlorophyll fluorescence and oxidative stress. Physiol Plant 130:218–229
  • Moustakas M, Ouzounidou G (1994) Increased non-photochemical quenching in leaves of aluminium-stressed wheat plants is due to Al³⁺-induced elemental loss. Plant Physiol Biochem 32:527–532
  • MoustakasM, Sperdouli I, Kouna T, Antonopoulou CI, Therios I (2011) Exogenous proline induces soluble sugar accumulation and alleviates drought stress effects on photosystem II functioning of Arabidopsis thaliana leaves. Plant Growth Regul 65:315–325
  • Müller P, Li XP, Niyogi KK (2001) Non-photochemical quenching. A response to excess light energy. Plant Physiol 125:1558–1566
  • Munné-Bosch S, Alegre L (2003) Drought-induced changes in the redox state of alpha-tocopherol, ascorbate, and the diterpene carnosic acid in chloroplasts of Labiatae species differing in carnosic acid contents. Plant Physiol 131:1816–1825
  • Papageorgiou GC, Govindjee (eds) (2004) Chlorophyll a fluorescence: a signature of photosynthesis. Advances in photosynthesis and respiration, vol 19. Springer, Dordrecht
  • Pereira JS, Chaves MM (1993) Plant water deficits in Mediterranean ecosystems. In: Smith JAC, Griffiths H (eds) Plant responses to water deficits-from cell to community. BIOS Scientific, Oxford, pp 237–251
  • Pinheiro C, Chaves MM (2011) Photosynthesis and drought: can we make metabolic connections from available data? J Exp Bot 62:869–882
  • Pinheiro C, António C, Ortuño MF, Dobrev PI, Hartung W, Thomas-Oates J, Ricardo CP, Vanková R, Chaves MM, Wilson JC (2011) Initial water deficit effects on Lupinus albus photosynthetic performance, carbon metabolism, and hormonal balance: metabolic reorganization prior to early stress responses. J Exp Bot 62:4965–4974
  • Posch S, Bennett LT (2009) Photosynthesis, photochemistry and antioxidative defence in response to two drought severities and with re-watering in Allocasuarina luehmannii. Plant Biol 11(S1):83–93
  • Reddy RA, Chaitanya KV, Vivekanandan M (2004) Drought-induced responses of photosynthesis and antioxidant metabolism in higher plants. J Plant Physiol 161:1189–1202
  • Rowan BA, Oldenburg DJ, Bendich AJ (2007) A high-throughput method for detection of DNA in chloroplasts using flow cytometry. Plant Methods 3:5
  • Skirycz A, de Bodt S, Obata T, de Clercq I, Claeys H, de Rycke R, Andriankaja M, van Aken O, van Breusegem F, Fernie AR, Inze D (2010) Developmental stage specificity and the role of mitochondrial metabolism in the response of Arabidopsis leaves to prolonged mild osmotic stress. Plant Physiol 152:226–244
  • Souza BD, Meiado MV, Rodrigues BM, Santos MG (2010) Water relations and chlorophyll fluorescence responses of two leguminous trees from the Caatinga to different watering regimes. Acta Physiol Plant 32:235–244
  • Sperdouli I, Moustakas M (2012) Spatio-temporal heterogeneity in Arabidopsis thaliana leaves under drought stress. Plant Biol 14:118–128
  • Suzuki K, Ohmori Y, Ratel E (2011) High root temperature blocks both linear and cyclic electron transport in the dark during chilling of the leaves of rice seedlings. Plant Cell Physiol 52:1697–1707
  • Szabo I, Bergantino E, Giacometti GM (2005) Light and oxygenic photosynthesis: energy dissipation as a protection mechanism against photo-oxidation. EMBO Rep 6:629–634
  • Triantaphylidès C, Krischke M, Hoeberichts FA, Ksas B, Gresser G, Havaux M, Van Breusegem F, Mueller MJ (2008) Singlet oxygen is the major reactive oxygen species involved in photooxidative damage to plants. Plant Physiol 148:960–968
  • Urban O, Šprtová M, Košvancová M, Tomášková I, Lichtenthaler HK, Marek MV (2008) Comparison of photosynthetic induction and transient limitations during the induction phase in young andmature leaves from three poplar clones. Tree Physiol 28:1189–1197
  • Verslues PE, Agarwal M, Katiyar-Agarwal S, Zhu J, Zhu JK (2006) Methods and concepts in quantifying resistance to drought, salt and freezing, abiotic stresses that affect plant water status. Plant J 45:523–539
  • Woo NS, Badger MR, Pogson BJ (2008) A rapid, non-invasive procedure for quantitative assessment of drought survival using chlorophyll fluorescence. Plant Methods 4:27
  • Xu Z, Zhou G, Han G, Li Y (2011) Photosynthetic potential and its association with lipid peroxidation in response to high temperature at different leaf ages in maize. J Plant Growth Regul 30:41–50
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