Physiological responses of Plantago algarbiensis and P. almogravensis shoots and plantlets to low pH and aluminum stress

• Autorzy: Martins N , Osorio M. L. , Goncalves S. , Osorio J. , Palma T. , Romano A.
• Języki publikacji: EN

Abstrakty

EN

We investigated the impact of low pH and aluminum (Al) stress on the growth, nutrients concentration, chlorophyll a fluorescence, photosynthetic pigment contents, proline and carbohydrate accumulation in shoots and plantlets (leaves and roots) of Plantago almogravensis and P. algarbiensis. Both species accumulated considerable and similar amounts of Al in their tissues, mainly in the roots. The presence of Al caused a significant reduction on root elongation in P. algarbiensis. Low pH and Al induced significant changes on nutrient accumulation, but no significant alterations on the maximum efficiency of PSII (Fv/Fm), quantum yield of PSII photochemistry (ØPSII), quantum yield of regulated energy dissipation (ØNPQ) and quantum yield of non-regulated energy dissipation (ØNO) were detected in both species in response to these stresses. However, Al increased significantly the nonphotochemical quenching and the chlorophyll b content and decreased the PSII excitation pressure (1 - qp) in P. almogravensis leaves. Both stress treatments induced carbohydrate accumulation in the shoots and roots of this species, but not in leaves. In P. algarbiensis, low pH and Al decreased the photosynthetic pigment contents in the shoots, whereas Al stimulated the carbohydrate accumulation in the leaves. Although our data showed that both species are tolerant to Al3+ and H+, P. almogravensis appeared to be more adapted to maintain cellular physiology and growth under those conditions.

• Wydawca: -
• Czasopismo: Acta Physiologiae Plantarum
• Rocznik: 2013
• Tom: 35
• Numer: 02
• Opis fizyczny: p.615-625,fig.,ref.

Twórcy

autor

Martins N

• Faculty of Sciences and Technology, Institute for Biotechnology and Bioengineering, Centre of Genomics and Biotechnology (IBB/CGB), University of Algarve, Campus de Gambelas, Ed. 8, 8005-139 Faro, Portugal

autor

Osorio M. L.

• Faculty of Sciences and Technology, Institute for Biotechnology and Bioengineering, Centre of Genomics and Biotechnology (IBB/CGB), University of Algarve, Campus de Gambelas, Ed. 8, 8005-139 Faro, Portugal

autor

Goncalves S.

• Faculty of Sciences and Technology, Institute for Biotechnology and Bioengineering, Centre of Genomics and Biotechnology (IBB/CGB), University of Algarve, Campus de Gambelas, Ed. 8, 8005-139 Faro, Portugal

autor

Osorio J.

• Faculty of Sciences and Technology, Institute of Mediterranean Agricultural and Environment Sciences (ICAAM), University of Algarve, Campus de Gambelas, Ed. 8, 8005-139 Faro, Portugal

autor

Palma T.

• Faculty of Sciences and Technology, Institute for Biotechnology and Bioengineering, Centre of Genomics and Biotechnology (IBB/CGB), University of Algarve, Campus de Gambelas, Ed. 8, 8005-139 Faro, Portugal

autor

Romano A.

• Faculty of Sciences and Technology, Institute for Biotechnology and Bioengineering, Centre of Genomics and Biotechnology (IBB/CGB), University of Algarve, Campus de Gambelas, Ed. 8, 8005-139 Faro, Portugal

Bibliografia

• Ali B, Hasan SA, Hayat S, Hayat Q, Yadav S, Fariduddin Q, Ahmad A (2008) A role for brassinosteroids in the amelioration of aluminium stress through antioxidant system in mung bean (Vigna radiate L. Wilczek). Environ Exp Bot 62:153–159
• Ali S, Zeng F, Qiu B, Cai S, Qiu L, Wu F, Zhang G (2011) Interactive effects of aluminum and chromium stresses on the uptake of nutrients and the metals in barley. Soil Sci Plant Nutr 57:68–79
• A.O.A.C. (1990) Official Methods of Analysis, Association of Official Agricultural Chemists, Washington, DC Barcelo´ J, Poschenrieder C (2002) Fast root growth responses, root exudates, and internal detoxification as clues to the mechanisms of aluminium toxicity and resistance: a review. Environ Exp Bot 48:75–92
• Bilger W, Schreiber U (1986) Energy-dependent quenching of dark level chlorophyll fluorescence in intact leaves. Photosynth Res 10:303–308
• Bjo¨rkman O, Demmig B (1987) Photon yield of O2 evolution and chlorophyll fluorescence characteristics at 77 K among vascular plants of diverse origin. Planta 170:489–504
• Bowyer JB, Leegood RC (1997) Photosynthesis. In: Dey PM, Harborne JB (eds) Plant biochemistry. Academic Press, San Diego, pp 49–110
• Branquinho C, Serrano HC, Pinto MJ, Martins-Louc¸a˜o MA (2007) Revisiting the plant hyperaccumulation criteria to rare plants and earth abundant elements. Environ Pollut 146:437–443
• Chen L-S, Qi Y-P, Liu X-H (2005a) Effects of aluminum on light energy utilization and photoprotective systems in citrus leaves. Ann Bot 96:35–41
• Chen L-S, Qi Y-P, Smith BR, Liu X-H (2005b) Aluminum-induced decrease in CO2 assimilation in citrus seedlings is unaccompanied by decreased activities of key enzymes involved in CO2 assimilation. Tree Physiol 25:317–324
• Chen Z, Cuin TA, Zhou M, Twomey A, Naidu BP, Shabala S (2007) Compatible solute accumulation stress-mitigating affects in barley genotypes contrasting in their salt tolerance. J Exp Bot 58:4245–4255
• Chen L-S, Qi Y-P, Jiang H-X, Yang L-T, Yang G-H (2010) Photosynthesis and photoprotective systems of plants in response to aluminum toxicity. Afr J Biotechnol 9:9237–9247
• Chen YM, Tsao TM, Liu CC, Lin KC, Wang MK (2011) Aluminium and nutrients induce changes in the profiles of phenolic substances in tea plants (Camellia sinensis CV TTES, No.12 (TTE)). J Sci Food Agric 91:1111–1117
• Choudhary AK, Singh D (2011) Screening of pigeonpea genotypes for nutrient uptake efficiency under aluminium toxicity. Physiol Mol Biol Plants 17:145–152
• Cornic G (1994) Drought stress and high effects on leaf photosynthesis. In: Baker NR, Bowyer JR (eds) Photoinhibition of photosynthesis: from molecular mechanisms to the field. BIOS Scientific Publishers, Oxford, pp 297–313
• Demmig-Adams B, Adams WW, Czygan F-C, Schreiber U, Lange OL (1990) Differences in the capacity for radiationless energy dissipation in the photochemical apparatus of green and bluegreen alga1 lichens associated with differences in carotenoid composition. Planta 180:582–589
• Dreywood R (1946) Qualitative test for carbohydrate material. Ind Eng Chem (Anal ed) 18:499
• Ezaki B, Nagao E, Yamamoto Y, Nakashima S, Enomoto T (2008) Wild plants, Andropogon virginicus L. and Miscanthus sinensis Anders, are tolerant to multiple stresses including aluminum, heavy metals and oxidative stresses. Plant Cell Rep 27:951–961
• Foy CD (1984) Physiological effects of hydrogen, aluminium and manganese toxicities in acid soil. In: Pearson RW, Adams F (eds) Soil acidity and liming, 2nd edn. American Society of Agronomy, Wisconsin, pp 57–97
• 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, Mylona P, Papadakis I, Yupsanis T (2008) Aluminum tolerance in maize is correlated with increased levels of mineral nutrients, carbohydrates and proline and decreased levels of lipid peroxidation and Al accumulation. J Plant Physiol 165:385–396
• Gonc¸alves S, Martins N, Romano A (2009) Micropropagation and conservation of endangered species Plantago algarbiensis and P. almogravensis. Biol Plant 53:774–778
• He G, Zhang J, Hu X, Wu J (2011) Effect of aluminum toxicity and phosphorus deficiency on the growth and photosynthesis of oil tea (Camellia oleifera Abel.) seedlings in acidic red soils. Acta Physiol Plant 33:1285–1292
• Jiang H-X, Chen L-S, Zheng JG, Han S, Tang N, Smith BR (2008) Aluminum-induced effects on photosystem II photochemistry in citrus leaves assessed by the chlorophyll a fluorescence transient. Tree Physiol 28:1863–1871
• Jin SH, Li XQ, Jia XL (2011) Genotypic differences in the responses of gas exchange, chlorophyll fluorescence, and antioxidant enzymes to aluminum stress in Festuca arundinacea. Russ J Plant Physiol 58:560–566
• KatoMC,HikosakaK,Hirotsu N,Makino A, HiroseT (2003)The excess light energy that is neither utilized in photosynthesis nor dissipated by photoprotective mechanisms determines the rate of photoinactivation in photosystem II. Plant Cell Physiol 44:318–325
• Kornyeyev D, Hendrickson L (2007) Energy partitioning in photosystem II complexes subjected to photoinhibitory treatment. Funct Plant Biol 34:214–220
• Kornyeyev D, Logan BA, Holaday AS (2010) Excitation pressure as a measure of the sensitivity of photosystem II to photoinactivation. Funct Plant Biol 37:943–951
• 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
• Lichtenthaler HK (1987) Chlorophylls and carotenoids: pigments of photosynthetic biomembranes. Methods Enzymol 148:350–382
• Lidon FC, Barreiro MG, Ramalho JC, Lauriano JA (1999) Effects of aluminum toxicity on nutrient accumulation in maize shoots: implications on photosynthesis. J Plant Nutr 22:397–416
• Liu P, Yang YA (2000) Effects of molybdenum and boron on membrane lipid peroxidation and endogenous protective systems of soybean leaves. Acta Bot Sin 42:461–466
• Liu P, Yang YS, Xu G, Guo S, Zheng X, Wang M (2006) Physiological responses of four herbaceous plants to aluminum stress in South China. Front Biol China 3:295–302
• Magne´ C, Larher F (1992) High sugar content of extracts interferes with colorimetric determination of aminoacid and free proline. Anal Biochem 200:115–118
• Martins N, Gonc¸alves S, Palma T, Romano A (2011) The influence of low pH on in vitro growth and biochemical parameters of Plantago almogravensis and P. algarbiensis. Plant Cell, Tissue Organ Cult 107:113–121
• Matsumoto H (2000) Cell biology of aluminum toxicity and tolerance in higher plants. Int Rev Cytol 200:1–46
• Maxwell DP, Falk S, Hunner NPA (1995) Photosystem II excitation pressure and development of resistance to photoinhibition. Plant Physiol 107:687–694
• Mihailovic N, Drazic G, Vucinic Z (2008) Effects of aluminium on photosynthetic performance in Al-sensitive and Al-tolerant maize inbred lines. Photosynthesis 46:476–480
• Mishra P, Dubey RS (2008) Effect of aluminium on metabolism of starch and sugars in growing rice seedlings. Acta Physiol Plant 30:265–275
• Moustakas M, Ouzounidou G, Lannoye R (1995) Aluminum effects on photosynthesis and elemental uptake in an aluminum-tolerant and non-tolerant wheat cultivars. J Plant Nutr 18:669–683
• Moustakas M, Ouzounidou G, Eleftheriou EP, Lannoye R (1996) Indirect effects of aluminium stress on the function of the photosynthetic apparatus. Plant Physiol Biochem 34:553–560
• Mu¨ller P, Li X-P, Niyogi KK (2001) Non-photochemical quenching. A response to excess light energy. Plant Physiol 125:1558–1566
• Murashige T, Shoog F (1962) A revised medium for rapid growth and bio-assays with tobacco tissue cultures. Physiol Plant 15:473–497
• Papageorgiou GC, Govindjee A (2004) Chlorophyll a fluorescence: a signature of photosynthesis. Springer, Dordrecht, pp 447–461
• Paul MJ, Foyer CH (2001) Sink regulation of photosynthesis. J Exp Bot 52:1383–1400
• Peixoto HP, Da Matta FM, Da Matta JC (2002) Responses of the photosynthetic apparatus to aluminum stress in two sorghum cultivars. J Plant Nutr 25:821–832
• Pereira WE, Siqueira DL, Martı´nez CA, Puiatti M (2000) Gas exchange and chlorophyll fluorescence in four citrus rootstocks under aluminium stress. J Plant Physiol 157:513–520
• Poschenrieder C, Llugany M, Barcelo J (1995) Short-term effects of pH and aluminum on mineral-nutrition in maize varieties differing in proton and aluminum tolerance. J Plant Nutr 18:1495–1507
• Reyes-Diaz M, Inostroza-Blancheteau C, Millaleo R, Cruces E, Wulff-Zottele C, Alberdi M, Mora MD (2010) Long-term aluminum exposure effects on physiological and biochemical features of highbush blueberry cultivars. J Am Soc Hortic Sci 135:212–222
• Samac DA, Tesfaye M (2003) Plant improvement for tolerance to aluminum in acid soils: a review. Plant Cell, Tissue Organ Cult 75:189–207
• Schroth G, Lehmann J, Barrios E (2003) Soil nutrient availability and acidity. In: Schroth G, Sinclair FL (eds) Trees, crops and soil fertility. CAB International, New York, pp 93–130
• Serrano HC, Pinto MJ, Martins-Louc¸a˜o MA, Branquinho C (2011) How does an Al-hyperaccumulator plant respond to a natural field gradient of soil phytoavailable Al? Sci Tot Environ 409: 3749–3756
• Shaff JE, Schultz BA, Craft EJ, Clark RT, Kochian LV (2010) GEOCHEM-EZ: a chemical speciation program with greater power and flexibility. Plant Soil 330:207–214
• Silva S, Pinto-Carnide O, Martins-Lopes P, Matos M, Guedes-Pinto H, Santos C (2010) Differential aluminium changes on nutrient accumulation and root differentiation in an Al sensitive vs. tolerant wheat. Environ Exp Bot 68:91–98
• Silva S, Pinto G, Dias MC, Correia CM, Moutinho-Pereira J, Pinto-Carnide O, Santos C (2012) Aluminium long-term stress differently affects photosynthesis in rye genotypes. Plant Physiol Biochem 54:105–112
• Tabuchi A, Kikuia S, Matsumoto H (2004) Differential effects of aluminum on osmotic potential and sugar accumulation in the root cells of Al-resistant and Al-sensitive wheat. Physiol Plant 120:106–112
• Troll W, Lindsley J (1955) A photometric method for the determination of proline. J Biol Chem 215:655–660
• von Uexku¨ll HR, Mutert E (1995) Global extent, development and economic impact of acid soils. Plant Soil 171:1–15
• Yemm EW, Willis AJ (1954) The estimation of carbohydrates in plant extracts by anthrone. Biochem J 57:508–514
• Zhang X-B, Liu P, Yang YS, Xu GD (2007) Effect of Al in soil on photosynthesis and related morphological and physiological characteristics of two soybean genotypes. Bot Stud 48:435–444

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