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2019 | 72 | 2 |

Tytuł artykułu

EDTA reduces cadmium toxicity in mustard (Brassica juncea L.) by enhancing metal chelation, antioxidant defense and glyoxalase systems

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Warianty tytułu

PL
EDTA obniża toksyczność kadmu w gorczycy sarepskiej (Brassica juncea L.) poprzez zwiększenie chelatowania metalu oraz poprawę działania systemu antyoksydacyjnego i glioksalazowego

Języki publikacji

EN

Abstrakty

EN
To investigate the possible role of EDTA in mitigating cadmium (Cd) toxicity, we treated mustard (Brassica juncea L.) seedlings with CdCl2 (0.5 mM and 1.0 mM, 3 days) alone and in combination with 0.5 mM EDTA in a semihydroponic medium. In the absence of EDTA, mustard seedlings accumulated Cd in their roots and shoots in a concentration dependent manner. Overaccumulation of Cd boosted generation of hydrogen peroxide (H2O2) and superoxide anions (O2•−), increased lipoxygenase (LOX) activity, lipid peroxidation, and cytotoxic methylglyoxal (MG) content. It also disturbed components of the antioxidant defense and glyoxalase systems. Furthermore, Cd stress decreased growth, leaf relative water content (RWC) and chlorophyll (chl) content but augmented the proline (Pro) content. On the other hand, EDTA supplemented Cd-stressed seedlings improved the constituents of the AsA-GSH cycle with the upregulated activities of ascorbate peroxidase (APX), monodehydroascorbate reductase (MDHAR), dehydroascorbate reductase (DHAR), glutathione reductase (GR), glutathione peroxidase (GPX), superoxide dismutase (SOD), and catalase (CAT). Moreover, addition of EDTA to the Cd-stressed seedlings notably enhanced Gly I activity in contrast to the stress treatment. Ethylenediaminetetraacetic acid decreased Cd accumulation in the both shoots and roots, as well as increased other nonprotein thiols (NPTs) in leaves, including the phytochelatin (PC) content. It also decreased H2O2 and O2•− generation, lipid peroxidation and MG content but enhanced RWC, chl and Pro contents in the leaves, which confirmed the improved growth of seedlings. The findings of the study suggest that exogenous application of EDTA to the Cd-treated seedlings reduces Cd-induced oxidative injuries by restricting Cd uptake, increasing NPTs concentration and upregulating most of the components of their antioxidant defense and glyoxalase systems.
PL
W celu określenia roli EDTA (kwas edetynowy, acidum edeticum) w obniżaniu toksyczności kadmu (Cd), siewki gorczycy (Brassica juncea L.) traktowano CdCl2 (w stężeniach 0,5 i 1 mM przez 3 dni) w kombinacjach z lub bez dodatku 0,5 mM EDTA do semi-hydroponicznego podłoża. Rośliny uprawiane w obecności Cd bez EDTA akumulowały metal w korzeniach i częściach nadziemnych proporcjonalnie do zastosowanego stężenia Cd. Akumulacja Cd indukowała produkcję nadtlenku wodoru (H2O2) i anionu ponadtlenkowego (O2•−), zwiększała aktywność lipoksygenazy (LOX), peroksydację lipidów i poziom cytotoksycznego metyloglioksalu (MG). Kadm zakłócał również funkcjonowanie składników systemu antyoksydacyjnego i glioksalazowego. Ponadto, Cd negatywnie wpływał na wzrost roślin, względną zawartość wody w liściach (RWC) i stężenie chlorofilu, ale stymulował akumulację proliny (Pro). Dodatek EDTA do pożywki zawierającej Cd pozytywnie wpływał na funkcjonowanie cyklu glutationowo-askorbinianowego, zwiększając aktywność peroksydazy askorbinianowej (APX), reduktazy monodehydroaskorbinianowej (MDHAR), reduktazy dehydroaskorbinianowej (DHAR), reduktazy glutationowej (GR), peroksydazy glutationowej (GPX), a także dysmutazy ponadtlenkowej (SOD) i katalazy (CAT). Ponadto, dodanie EDTA do środowiska wzrostu roślin traktowanych Cd zwiększyło aktywność glioksalazy I (Gly I) w roślinach, czego nie stwierdzono w roślinach traktowanych wyłącznie Cd. EDTA ograniczył akumulację Cd zarówno w korzeniach, jak i w częściach nadziemnych, zwiększając jednocześnie poziom niebiałkowych tioli (NPT), w tym fitochelatyn (PC). Dodatkowo, w roślinach traktowanych Cd w obecności EDTA stwierdzono niższy poziom H2O2, O2•− i MG oraz obniżenie peroksydacji lipidów, ale wzrost RWC, a także stężenia chlorofilu i Pro, co wpłynęło na lepszy wzrost roślin. Uzyskane wyniki sugerują, że zastosowanie egzogennego EDTA razem z Cd obniża toksyczność metalu związaną z generowaniem stresu oksydacyjnego, poprzez ograniczenie pobierania Cd, zwiększenie stężenia NPT i pozytywny wpływ na aktywność większości składników systemu antyoksydacyjnego i glioksalazowego.

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Czasopismo

Rocznik

Tom

72

Numer

2

Opis fizyczny

Article: 1772 [17 p.], fig.,ref.

Twórcy

autor
  • Department of Agroforestry and Environmental Science, Faculty of Agriculture, Sher-e-Bangla Agricultural University, Sher-e-Bangla Nagar, Dhaka 1207, Bangladesh
  • Department of Agronomy, Faculty of Agriculture, Sher-e-Bangla Agricultural University, Sher-e-Bangla Nagar, Dhaka 1207, Bangladesh
autor
  • Department of Agricultural Botany, Faculty of Agriculture, Sher-e-Bangla Agricultural University, Sher-e-Bangla Nagar, Dhaka 1207, Bangladesh
autor
  • Department of Agronomy, Faculty of Agriculture, Sher-e-Bangla Agricultural University, Sher-e-Bangla Nagar, Dhaka 1207, Bangladesh
autor
  • Laboratory of Plant Stress Responses, Department of Applied Biological Science, Faculty of Agriculture, Kagawa University, Miki-cho, Kita-gun, Kagawa 761-0795, Japan

Bibliografia

  • Campbell PGC. Cadmium – a priority pollutant. Environ Chem. 2006;3:387–388. https://doi.org/10.1071/EN06075
  • Popova LP, Maslenkova LT, Yordanova RY, Ivanova AP, Krantev AP, Szalai G, et al. Exogenous treatment with salicylic acid attenuates cadmium toxicity in pea seedlings. Plant Physiol Biochem. 2009;47:224–231. https://doi.org/10.1016/j.plaphy.2008.11.007
  • Hasanuzzaman M, Fujita M. Heavy metals in the environment: current status, toxic effects on plants and possible phytoremediation. In: Anjum NA, Pereira MA, Ahmad I, Duarte AC, Umar S, Khan NA, editors. Phytotechnologies: remediation of environmental contaminants. Boca Raton, FL: CRC Press; 2012. p. 7–73. https://doi.org/10.1201/b12954-4
  • Benavides MP, Gallego SM, Tomaro ML. Cadmium toxicity in plants. Braz J Plant Physiol. 2005;17:21–34. https://doi.org/10.1590/S1677-04202005000100003
  • Gill SS, Tuteja N. Cadmium stress tolerance in crop plants: probing the role of sulfur. Plant Signal Behav. 2011;6:215–222. https://doi.org/10.4161/psb.6.2.14880
  • Hasanuzzaman M, Hossain MA, Teixeira da Silva JA, Fujita M. Plant responses and tolerance to abiotic oxidative stress: antioxidant defense is a key factor. In: Bandi V, Shanker, AK, Shanker C, Mandapaka M, editors. Crop stress and its management: perspectives and strategies. Berlin: Springer; 2012. p. 261–316. https://doi.org/10.1007/978-94-007-2220-0_8
  • Sigfridsson KGV, Bernát G, Mamedov F, Styring S. Molecular interference of Cd2+ with photosystem II. Biochim Biophys Acta. 2004;1659:19–31. https://doi.org/10.1016/j.bbabio.2004.07.003
  • Hall JL. Cellular mechanisms for heavy metal detoxification and tolerance. J Exp Bot. 2002;53:1–11. https://doi.org/10.1093/jexbot/53.366.1
  • Gratão PL, Polle A, Lea PJ, Azevedo RA. Making the life of heavy metal stressed plants a little easier. Funct Plant Biol. 2005;32:481–494. https://doi.org/10.1071/FP05016
  • Gill SS, Tuteja N. Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiol Biochem. 2010;48:909–930. https://doi.org/10.1016/j.plaphy.2010.08.016
  • Yadav SK, Singla-Pareek SL, Sopory SK. An overview on the role of methylglyoxal and glyoxalases in plants. Drug Metabol Drug Interact. 2008;23:51–68. https://doi.org/10.1515/DMDI.2008.23.1-2.51
  • Hasanuzzaman M, Nahar K, Hossain MS, Mahmud JA, Rahman A, Inafuku M, et al. Coordinated actions of glyoxalase and antioxidant defense systems in conferring abiotic stress tolerance in plants. Int J Mol Sci. 2017;18:200. https://doi.org/10.3390/ijms18010200
  • Salt DE, Smith RD, Raskin I. Phytoremediation. Annu Rev Plant Physiol Plant Mol Biol. 1998;49:643–668. https://doi.org/10.1146/annurev.arplant.49.1.643
  • Hernández-Allica J, Garbisu C, Barrutia O, Becerril JM. EDTA-induced heavy metal accumulation and phytotoxicity in cardoon plants. Environ Exp Bot. 2007;60:26–32. https://doi.org/10.1016/j.envexpbot.2006.06.006
  • Chigbo C, Batty L. Effect of EDTA and citric acid on phytoremediation of Cr-B[a]P-co-contaminated soil. Environ Sci Pollut Res Int. 2013;20:8955–8963. https://doi.org/10.1007/s11356-013-1883-7
  • Farid M, Ali S, Ishaque W, Shakoor MB, Niazi NK, Bibi I, et al. Exogenous application of ethylenediamminetetraacetic acid enhanced phytoremediation of cadmium by Brassica napus L. International Journal of Environmental Science and Technology. 2015;12:3981–3992. https://doi.org/10.1007/s13762-015-0831-0
  • Evangelou MWH, Bauer U, Ebel M, Schaeffer A. The influence of EDDS and EDTA on the uptake of heavy metals of Cd and Cu from soil with tobacco (Nicotiana tabacum). Chemosphere. 2007;68:345–353. https://doi.org/10.1016/j.chemosphere.2006.12.058
  • Agbadah EE, Nwachukwu KC, Okoh MP. Biochemical effects of ethylene diamine tetra-acetic acid (EDTA) on cadmium treated maize (Zea mays L.) and cowpea (Vigna unguiculata L.). Afr J Biotechnol. 2016;15:593–600. https://doi.org/10.5897/AJB2015.14841
  • Xu W, Li Y, He J, Ma O, Zhang X, Chen G, et al. Cd uptake in rice cultivars treated with organic acids and EDTA. Journal of Environmental Sciences. 2010;22:441–447. https://doi.org/10.1016/S1001-0742(09)60127-3
  • Greger M, Lindberg S. Effects of Cd2+ and EDTA on young sugar beets (Beta vulgaris). I. Cd2+ uptake and sugar accumulation. Physiol Plant. 1986;66:69–74. https://doi.org/10.1111/j.1399-3054.1986.tb01235.x
  • Hardiman RT, Jacoby B. Absorption and translocation of Cd in bush beans (Phaseolus vulgaris). Physiol Plant. 1984;61:670–674. https://doi.org/10.1111/j.1399-3054.1984.tb05189.x
  • Xu W, Li W, He J, Singh B, Xiong Z. Effects of insoluble Zn, Cd, and EDTA on the growth, activities of antioxidant enzymes and uptake of Zn and Cd in Vetiveria zizanioides. Journal of Environmental Sciences. 2009;21:186–192. https://doi.org/10.1016/S1001-0742(08)62249-4
  • Heath RL, Packer L. Photoperoxidation in isolated chloroplast: I. Kinetics and stoichiometry of fatty acid per oxidation. Arch Biochem Biophys. 1968;125:189–198. https://doi.org/10.1016/0003-9861(68)90654-1
  • Hasanuzzaman M, Hossain MA, Fujita M. Exogenous selenium pretreatment protects rapeseed from cadmium-induced oxidative stress by upregulating antioxidant defense and methylglyoxal detoxification systems. Biol Trace Elem Res. 2012;149:248–261. https://doi.org/10.1007/s12011-012-9419-4
  • Yu CW, Murphy TM, Lin CH. Hydrogen peroxide-induces chilling tolerance in mung beans mediated through ABA-independent glutathione accumulation. Funct Plant Biol. 2003;30:955–963. https://doi.org/10.1071/fp03091
  • Nahar K, Hasanuzzaman M, Alam MM, Rahman A, Suzuki T, Fujita M. Polyamine and nitric oxide crosstalk: antagonistic effects on cadmium toxicity in mung bean plants through upregulating the metal detoxification, antioxidant defense, and methylglyoxal detoxification systems. Ecotoxicol Environ Saf. 2016;126:245–255. https://doi.org/10.1016/j.ecoenv.2015.12.026
  • Arnon DT. Copper enzymes in isolated chloroplasts. Polyphenol oxidase in Beta vulgaris. Plant Physiol. 1949;24:1–15. https://doi.org/10.1104/pp.24.1.1
  • Bates LS, Waldren RP, Teari D. Rapid determination of free proline for water stress studies. Plant Soil. 1973;39:205–207. https://doi.org/10.1007/BF00018060
  • Wild R, Ooi L, Srikanth V, Münch G. A quick, convenient and economical method for the reliable determination of methylglyoxal in millimolar concentrations: the N-acetyl-l-cysteine assay. Anal Bioanal Chem. 2012;403:2577–2581. https://doi.org/10.1007/s00216-012-6086-4
  • Huang C, He W, Guo J, Chang X, Su P, Zhang L. Increased sensitivity to salt stress in ascorbate deficient Arabidopsis mutant. J Exp Bot. 2005;56:3041–3049. https://doi.org/10.1093/jxb/eri301
  • Bradford M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976;72:248–254. https://doi.org/10.1016/0003-2697(76)90527-3
  • Doderer A, Kokkelink I, van der Veen S, Valk B, Schram A, Douma A. Purification and characterization of two lipoxygenase isoenzymes from germinating barley. Biochim Biophys Acta. 1992;112:97–104. https://doi.org/10.1016/0167-4838(92)90429-H
  • El-Shabrawi H, Kumar B, Kaul T, Reddy MK, Singla-Pareek SL, Sopory SK. Redox homeostasis, antioxidant defense, and methylglyoxal detoxification as markers for salt tolerance in Pokkali rice. Protoplasma. 2010;245:85–96. https://doi.org/10.1007/s00709-010-0144-6
  • Nakano Y, Asada K. Hydrogen peroxide is scavenged by ascorbate-specific peroxidase in spinach chloroplasts. Plant Cell Physiol. 1981;22:867–880. https://doi.org/10.1093/oxfordjournals.pcp.a076232
  • Hossain MA, Nakano Y, Asada K. Monodehydroascorbate reductase in spinach chloroplasts and its participation in the regeneration of ascorbate for scavenging hydrogen peroxide. Plant Cell Physiol. 1984;25:385–395. https://doi.org/10.1093/oxfordjournals.pcp.a076726
  • Elia AC, Galarini R, Taticchi MI, Dorr AJM, Mantilacci L. Antioxidant responses and bioaccumulation in Ictalurus melas under mercury exposure. Ecotoxicol Environ Saf. 2003;55:162–167. https://doi.org/10.1016/S0147-6513(02)00123-9
  • Principato GB, Rosi G, Talesa V, Govannini E, Uolila L. Purification and characterization of two forms of glyoxalase II from rat liver and brain of Wistar rats. Biochim Biophys Acta. 1987;911:349–355. https://doi.org/10.1016/0167-4838(87)90076-8
  • Ellman G. Tissue sulfhydryl groups. Arch Biochem Biophys. 1959;32:70–77. https://doi.org/10.1016/0003-9861(59)90090-6
  • Addinsoft. XLSTAT v. 2017: data analysis and statistics software for Microsoft Excel [Software]. Paris: Addinsoft; 2017.
  • Szollosi R, Varga IS, Erdei L, Mihalik E. Cadmium-induced oxidative stress and antioxidative mechanisms in germinating Indian mustard (Brassica juncea L.) seeds. Ecotoxicol Environ Saf. 2009;72:1337–1342. https://doi.org/10.1016/j.ecoenv.2009.04.005
  • Zheng G, Lv HP, Gao S, Wang SR. Effects of cadmium on growth and antioxidant responses in Glycyrrhiza uralensis seedlings. Plant Soil Environ. 2010;56:508–515. https://doi.org/10.17221/30/2010-PSE
  • Uruç K, Yilmaz DD. Effect of cadmium, lead and nickel on imbibition, water uptake and germination for the seeds of different plants. Dumlupınar Üniversitesi Fen Bilimleri Enstitüsü. 2008;17:1–10.
  • Najmanova J, Neumannova E, Leonhardt T, Zitka O, Kizek R, Macek T, et al. Cadmium-induced production of phytochelatins and speciation of intracellular cadmium in organs of Linum usitatissimum seedlings. Ind Crop Prod. 2012;36:536–542. https://doi.org/10.1016/j.indcrop.2011.11.008
  • Clemens S. Toxic metal accumulation, responses to exposure and mechanisms of tolerance in plants. Biochimie. 2006;88:1707–1719. https://doi.org/10.1016/j.biochi.2006.07.003
  • Niakan M, Kaghazloo F. Effect of ethylene diamine tetra acetic acid chelator in the presence of chromium on growth and some physiological characteristics of sunflower. Iranian Journal of Plant Physiology. 2016;6:1659–1665.
  • Miller G, Shulaev V, Mitter R. Reactive oxygen signaling and abiotic stress. Physiol Plant. 2008;133:481–489. https://doi.org/10.1111/j.1399-3054.2008.01090.x
  • Custos J, Moyne C, Treillon T, Sterckeman T. Contribution of Cd-EDTA complexes to cadmium uptake by maize: a modelling approach. Plant Soil. 2014;374:497–512. https://doi.org/10.1007/s11104-013-1906-7
  • Jiang XJ, Luo YM, Zhao QG, Baker AJM, Christie P, Wong MH. Soil Cd availability to Indian mustard and environmental risk following EDTA addition to Cd contaminated soil. Chemosphere. 2003;50:813–818. https://doi.org/10.1016/S0045-6535(02)00224-2
  • Vatamaniuk OK, Mari S, Lu Y, Rea PA. Mechanism of heavy metal ion activation of phytochelatin (PC) synthase. J Biol Chem. 2000;275:31451–31459. https://doi.org/10.1074/jbc.M002997200
  • Zagorchev L, Seal CE, Kranner I, Odjakova M. A central role for thiols in plant tolerance to abiotic stress. Int J Mol Sci. 2013;14:7405–7432. https://doi.org/10.3390/ijms14047405

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