PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
2015 | 37 | 03 |

Tytuł artykułu

Indole acetic acid modulates changes in growth, chlorophyll a fluorescence and antioxidant potential of Trigonella foenum-graecum L. grown under cadmium stress

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Indole acetic acid at low (IAAL, 10 lM) and high (IAAH, 100 lM) dose-induced responses on growth, chlorophyll a fluorescence and antioxidant potential of widely cultivated Trigonella foenum-graecum L. seedlings grown under cadmium (Cd1, 3 mg Cd Kg-1 soil and Cd2, 9 mg Cd Kg-1 soil) stress were investigated. Cadmium (Cd) at tested doses reduced the growth, pigment contents, photosynthetic (O2 evolution) and carbonic anhydrase (CA) activity which was accompanied with Cd accumulation in tissues. To quantify the performance of photosystem (PS) II, chlorophyll a fluorescence (JIP test) was analyzed and under Cd stress, the yield for primary photochemistry (uP0), yield of electron transport per trapped exciton (w0), quantum yield of electron transport (uE0) and performance index of PS II (PIABS) were decreased, while it induced significant rise in energy flux parameters. Foliar application of IAAL dose causes significant reduction in Cd accumulation and hence alleviated the toxic effects of Cd on these parameters appreciably; while at IAAH dose, Cd inducedeffects were further aggravated. Respiratory O2 uptake was increased progressively with rising concentration of Cd, while together with IAA, it showed reverse trend. Cd alone and together with IAAH enhanced the oxidative markers: O2•-, H2O2 and MDA contents despite of the significant increase in SOD and CAT activity; while with IAAL, these markers were declined significantly. Overall results suggest that application of IAAL reduced the Cd accumulation in tissues significantly; hence, increased activity of photosynthesis and antioxidant potential improved the growth performance of Trigonella seedlings grown under Cd stress.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

37

Numer

03

Opis fizyczny

Article: 49 [14 p.], fig.,ref.

Twórcy

autor
  • Ranjan Plant Physiology and Biochemistry Laboratory, Department of Botany, University of Allahabad (A Central University of India), Allahabat 211002, India
autor
  • Ranjan Plant Physiology and Biochemistry Laboratory, Department of Botany, University of Allahabad (A Central University of India), Allahabat 211002, India

Bibliografia

  • Aebi H (1984) Catalase in vitro. Methods Enzymol 105:121–126
  • Allen SE, Grimshaw HM, Rowland AP (1986) Chemical analysis. In: Moore PD, Chapman SB (eds) Methods in plant ecology. Blackwell Scientific Publication, Oxford, pp 285–344
  • Basch E, Ulbricht C, Kuo G, Szapary P, Smith M (2003) Therapeutic applications of fenugreek. Alt Med Rev 8:20–27
  • Buschmann C, Lichtenthaler HK (1977) Hill-activity and P700 concentration of chloroplasts isolated from radish seedlings treated with-indole acetic acid, kinetin and gibberellic acid. Z Naturforsch C Bio Sci 32:798–802
  • Chaoui A, Ferjani EE (2005) Effects of cadmium and copper on antioxidant capacities, lignification and auxin degradation in leaves of pea (Pisum sativum L.) seedlings. Plant Biol Pathol 328:23–31
  • Di Cagno R, Guidi L, De Gara L, Soldatini GF (2001) Combined cadmium and ozone treatments affect photosynthesis and ascorbate-dependent defenses in sunflower. New Phytol 151:627–636
  • Durand TC, Sergeant K, Planchon S, Carpin S, Label P, Morabito D, Hausman JF, Renaut J (2010) Acute metal stress in Populus tremula 9 P. alba (717-1B4 genotype): leaf and cambial proteome changes induced by Cd2+. Proteomics 10:349–368
  • Elstner EF, Heupel A (1976) Inhibition of nitrite formation from hydroxylaminonium chloride: a simple assay for superoxide dismutase. Anal Biochem 70:616–620
  • Fang Z, Bouwkamp JC, Solomos T (1998) Chlorophyllase activities and chlorophyll degradation during leaf senescence in nonyellowing mutant and wild type of Phaseolus vulgaris L. J Exp Bot 49:503–510
  • Fässler E, Robinson BH, Stauffer W, Gupta SK, Papritz A, Schulin R (2010) Phytomanagement of metal-contaminated agricultural land using sunflower, maize and tobacco. Agric Ecosyst Environ 136:49–58
  • Giannopolitis CN, Ries SK (1977) Superoxide dismutase I: occurrence in higher plants. Plant Physiol 59:309–314
  • Gill SS, Tuteja N (2010) Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiol Biochem 48:909–930
  • Gomes-Junior RA, Moldes CA, Delite FS, Pompeu GB, Gratao PL, Mazzafera P, Lea PJ, Azevedo RA (2006) Antioxidant metabolism of coffee cell suspension cultures in response to cadmium. Chemosphere 65:1330–1337
  • Gonzalez-Mendoza D, Espadasy Gil F, Santamaria JM, Zapata-Perez O (2007) Multiple effects of cadmium on the photosynthetic apparatus of Avicennia germinans L. as probed by OJIP chlorophyll fluorescence measurements. Z Naturfors C 62:265–272
  • Govindjee (1995) Sixty-three years since Kautsky: chlorophyll a fluorescence. Aust J Plant Physiol 22:131–160
  • Gupta N, Khan DK, Santra SC (2008) An assessment of heavy metal contamination in vegetables grown in wastewater-irrigated areas of Titagarh, West Bengal, India. Bull Environ Contamin Toxicol 80:115–118
  • Heath RL, Packer L (1968) Photoperoxidation in isolated chloroplasts I. Kinetics and stoichiometry of fatty acid peroxidation. Arch Biochem Biophys 125:189–198
  • Heyno E, Klose C, Krieger-Liszkay A (2008) Origin of cadmium induced reactive oxygen species production: mitochondrial electron transfer versus plasma membrane NADPH oxidase. New Phytol 179:687–699
  • Iglesias MJ, Terrile MC, Bartoli CG, D’Ippólito S, Casalongue CA (2010) Auxin signaling participates in the adaptative response against oxidative stress and salinity by interacting with redox metabolism in Arabidopsis. Plant Mol Biol 74:215–222
  • Jain M, Khurana JP (2009) Transcript profiling reveals diverse roles of auxin-responsive genes during reproductive development and abiotic stress in rice. FEBS Lett 276:3148–3162
  • Kurra-Hotta M, Satoh K, Katoh S (1987) Relationship between photosynthesis and chlorophyll content during leaf senescence of rice seedlings. Plant Cell Physiol 28:1321–1329
  • Lichtenthaler HK (1987) Chlorphylls and carotenoids: pigments of photosynthetic biomembranes. Methods Enzymol 148:350–382
  • Marinos NG (1956) Responses of Avena coleoptile sections to high concentrations of auxins. Aust J Biol Sci 10:147–163
  • McCarthy I, Romero-Puertas MC, Palma JM, Sandalio LM, Corpas FJ, Gómez M, del Río LA (2001) Cadmium induces senescence symptoms in leaf peroxisomes of pea plants. Plant Cell Environ 24:1065–1073
  • Mendoza-Cozatl DG, Moreno-Sanchez R (2006) Control of glutathione and phytochelatin synthesis under cadmium stress. Pathway modeling for plants. J Theor Biol 36:238–919
  • Mittler R (2002) Oxidative stress, antioxidants and stress tolerance. Trends Plant Sci 7:405–410
  • Ouzounidou G, Ilias I (2005) Hormone-induced protection of sunflower photosynthetic apparatus against copper stress. Plant Biol 49:223–228
  • Pagnussat GC, Lanteri ML, Lamattina L (2003) Nitric oxide and cyclic GMP are messengers in the indole acetic acid-induced adventitious rooting process. Plant Physiol 132:1241–1248
  • Pandey DM, Goswami CL, Kumar B, Jain S (2000) Hormonal regulation of photosynthetic enzymes in cotton under water stress. Photosynthetica 38:403–407
  • Popova LP, Maslenkova LT, Yordanova RY, Ivanova AP, Krantev AP, Szalai G, Janda T (2009) Exogenous treatment with salicylic acid attenuates cadmium toxicity in pea seedlings. Plant Physiol Biochem 47:224–231
  • Prasad SM, Zeeshan M (2005) UV-B radiation and cadmium induced changes in growth, photosynthesis, and antioxidant enzymes of cyanobacterium Plectonema boryanum. Plant Biol 49:229–236
  • Qian H, Li J, Sun L, Chen W, Sheng GD, Liu W, Fu Z (2009) Combined effect of copper and cadmium on Chlorella vulgaris growth and photosynthesis-related gene transcription. Aquat Toxicol 94:56–61
  • Sabater B, Rodrguez MT (1978) Control of chlorophyll degradation in detached leaves of barley and oat through effect of kinetin on chlorophyllase levels. Physiol Plant 43:274–276
  • Sandalio LM, Dalurzo HC, Gomez M, Romero-Puertas MC, del Río LA (2001) Cadmium-induced changes in the growth and oxidative metabolism of pea plants. J Exp Bot 52:2115–2126
  • Sharma RK, Agrawal M, Marshall FM (2006) Heavy metal contamination in vegetables grown in wastewater irrigated areas of Varanasi, India. Bull Environ Contam Toxicol 77:312–318
  • Shi GR, Cai QS, Liu QQ, Wu L (2009) Salicylic acid-mediated alleviation of cadmium toxicity in hemp plants in relation to cadmium uptake, photosynthesis, and antioxidant enzymes. Acta Physiol Plant 31:969–977
  • Strasser RJ, Srivastava A, Tsimilli-Michael M (2000) The fluorescence transient as a tool to characterize and screen photosynthetic samples. In: Yunus M, Pathre U, Mohanty P (eds) Probing photosynthesis: mechanisms, regulation and adaptation. Taylor & Francis, London, pp 445–483
  • Talukdar D (2013) Arsenic-induced oxidative stress in the common bean legume, Phaseolus vulgaris L. seedlings and its amelioration by exogenous nitric oxide. Physiol Mol Biol Plants 19:69–79
  • Tiwari BS, Belenghi B, Levine A (2002) Oxidative stress increased respiration and generation of reactive oxygen species, resulting in ATP depletion, opening of mitochondrial permeability transition, and programmed cell death. Plant Physiol 128:1271–1281
  • Tiwari A, Kumar P, Singh S, Ansari SA (2005) Carbonic anhydrase in relation to higher plants. Photosynthetica 43:1–9
  • Valko M, Leibfritz D, Moncol J, Cronin MT, Mazur M, Telser J (2007) Free radicals and antioxidants in normal physiological functions and human disease. Int J Biochem Cell Biol 39:44–84
  • Vanneste S, Friml J (2009) Auxin: a trigger for change in plant development. Cell 136:1005–1016
  • Velikova V, Yordanov I, Edreva A (2000) Oxidative stress and some antioxidant systems in acid rain-treated bean plants. Plant Sci 151:59–66
  • Verbruggen N, Hermans C, Schat H (2009) Mechanisms to cope with arsenic or cadmium excess in plants. Curr Opin Plant Biol 12:364–372
  • Wang Y, Fang J, Leonard SS, Rao KMK (2004) Cadmium inhibits the electron transfer chain and induces reactive oxygen species. Free Radical Bio Med 36:1434–1443
  • Wang H, Shan X, Wen B, Owens G, Fang J, Zhang S (2007) Effect of indole-3-acetic acid on lead accumulation in maize (Zea mays L.) seedlings and the relevant antioxidant response. Environ Exp Bot 61:246–253
  • Wang BL, Tang XY, Cheng LY, Zhang AZ, Zhang WH, Zhang FS, Liu JQ, Cao Y, Allan DL, Vance CP, Shen JB (2010) Nitric oxide is involved in phosphorus deficiency-induced cluster-root development and citrate exudation in white lupin. New Phytol 187:1112–1123
  • Wilbur KM, Anderson NG (1948) Electrometric and colorimetric determination of carbonic anhydrase. J Biol Chem 176:147–154
  • Xu J, Wang WY, Yin HX, Liu XJ, Sun H, Mi Q (2010) Exogenous nitric oxide improves antioxidative capacity and reduces auxin degradation in roots of Medicago truncatula seedlings under cadmium stress. Plant Soil 326:321–330
  • Zhao FJ, Jiang RF, Dunham SJ, McGrath SP (2006) Cadmium uptake, translocation and tolerance in the hyperaccumulator Arabidopsis halleri. New Phytol 172:646–654

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

bwmeta1.element.agro-d4ba338d-6dfa-496a-9568-697f3553f039
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.