The effect of NADPH oxidase inhibitor diphenyleneiodonium (DPI) and glutathione (GSH) on Isatis cappadocica, under Arsenic (As) toxicity

References

• Abbas G, Murtaza B, Bibi I, Shahid M, Niazi NK, Khan MI, Amjad M, Hussain M., Natasha  . 2018. Arsenic uptake, toxicity, detoxification, and speciation in plants: physiological, biochemical, and molecular aspects. Int J Environ Res Publ Health. 15(1):59. doi:10.3390/ijerph15010059.
   PubMed Web of Science ®Google Scholar
• Aebi H. 1984. Catalase in vitro. Methods Enzymol. 105:121–126.
   PubMed Web of Science ®Google Scholar
• Ahmad P, Ahanger MA, Egamberdieva D, Alam P, Alyemeni MN, Ashraf M. 2018. Modification of osmolytes and antioxidant enzymes by 24-epibrassinolide in chickpea seedlings under mercury (Hg) toxicity. J Plant Growth Regul. 37(1):309–322. doi:10.1007/s00344-017-9730-6.
   Web of Science ®Google Scholar
• Ahmad P, Alam P, Balawi TH, Altalayan FH, Ahanger MA, Ashraf M. 2020. Sodium nitroprusside (SNP) improves tolerance to arsenic (As) toxicity in Vicia faba through the modifications of biochemical attributes, antioxidants, ascorbate-glutathione cycle and glyoxalase cycle. Chemosphere. 244:125480. doi:10.1016/j.chemosphere.2019.125480.
   PubMed Web of Science ®Google Scholar
• Bates LS, Waldren RP, Teare ID. 1973. Rapid determination of free proline for water-stress studies. Plant Soil. 39(1):205–207. doi:10.1007/BF00018060.
   Web of Science ®Google Scholar
• Baxter A, Mittler R, Suzuki N. 2014. ROS as key players in plant stress signalling. J Exp Bot. 65(5):1229–1240. doi:10.1093/jxb/ert375.
   PubMed Web of Science ®Google Scholar
• Beauchamp C, Fridovich I. 1971. Superoxide dismutase: improved assays and an assay applicable to acrylamide gels. Anal Biochem. 44(1):276–287. doi:10.1016/0003-2697(71)90370-8.
   PubMed Web of Science ®Google Scholar
• Chance B, Maehly AC. 1955. Assay of catalases and peroxidases. Methods Enzymol. 2:764–775.
   Google Scholar
• Chandrakar V, Naithani SC, Keshavkant S. 2016. Arsenic-induced metabolic disturbances and their mitigation mechanisms in crop plants: a review. Biologia. 71(4):367–377. doi:10.1515/biolog-2016-0052.
   Web of Science ®Google Scholar
• Chen GX, Asada K. 1989. Ascorbate peroxidase in tea leaves: occurrence of two isozymes and the differences in their enzymatic and molecular properties. Plant Cell Physiol. 30:978–998. doi:10.1093/oxfordjournals.pcp.a077844.
   Web of Science ®Google Scholar
• Chen H-J, Huang C-S, Huang G-J, Chow T-J, Lin Y-H. 2013. NADPH oxidase inhibitor diphenyleneiodonium and reduced glutathione mitigate ethephon-mediated leaf senescence, H2O2 elevation and senescence-associated gene expression in sweet potato (Ipomoea batatas). J Plant Physiol. 170(17):1471–1483. doi:10.1016/j.jplph.2013.05.015.
   PubMed Web of Science ®Google Scholar
• Corpas FJ, Barroso JB. 2014. NADPH-generating dehydrogenases: their role in the mechanism of protection against nitro-oxidative stress induced by adverse environmental conditions. Front Environ Sci. 2:55. doi:10.3389/fenvs.2014.00055.
   Google Scholar
• Dal Santo S, Stampfl H, Krasensky J, Kempa S, Gibon Y, Petutschnig E, Rozhon W, Heuck A, Clausen T, Jonak C. 2012. Stress-induced GSK3 regulates the redox stress response by phosphorylating glucose-6-phosphate dehydrogenase in Arabidopsis. Plant Cell. 24(8):3380–3392. doi:10.1105/tpc.112.101279.
   PubMed Web of Science ®Google Scholar
• Dave R, Tripathi RD, Dwivedi S, Tripathi P, Dixit G, Sharma YK, Trivedi PK, Corpas FJ, Barroso JB, Chakrabarty D. 2013. Arsenate and arsenite exposure modulate antioxidants and amino acids in contrasting arsenic accumulating rice (Oryza sativa L.) genotypes. J Hazard Mater. 262:1123–1131. doi:10.1016/j.jhazmat.2012.06.049.
   PubMed Web of Science ®Google Scholar
• de Freitas-Silva L, Rodríguez-Ruiz M, Houmani H, da Silva LC, Palma JM, Corpas FJ. 2017. Glyphosate-induced oxidative stress in Arabidopsis thaliana affecting peroxisomal metabolism and triggers activity in the oxidative phase of the pentose phosphate pathway (OxPPP) involved in NADPH generation. J Plant Physiol. 218:196–205. doi:10.1016/j.jplph.2017.08.007.
   PubMed Web of Science ®Google Scholar
• Dixit G, Singh AP, Kumar A, Singh PK, Kumar S, Dwivedi S, Trivedi PK, Pandey V, Norton GJ, Dhankher OP, et al. 2015. Sulfur mediated reduction of arsenic toxicity involves efficient thiol metabolism and the antioxidant defense system in rice. J Hazard Mater. 298:241–251. doi:10.1016/j.jhazmat.2015.06.008.
   PubMed Web of Science ®Google Scholar
• Duan G-L, Hu Y, Liu W-J, Kneer R, Zhao F-J, Zhu Y-G. 2011. Evidence for a role of phytochelatins in regulating arsenic accumulation in rice grain. Environ Exp Bot. 71:416–421. doi:10.1016/j.envexpbot.2011.02.016.
   Web of Science ®Google Scholar
• Ellman GL. 1959. Tissue sulfhydryl groups. Arch Biochem Biophys. 82(1):70–77. doi:10.1016/0003-9861(59)90090-6.
   PubMed Web of Science ®Google Scholar
• Farooq MA, Niazi AK, Akhtar J, Saifullah Farooq M, Souri Z, Karimi N, Rengel Z. 2019. Acquiring control: the evolution of ROS-Induced oxidative stress and redox signaling pathways in plant stress responses. Plant Physiol Biochem. 141:353–369. doi:10.1016/j.plaphy.2019.04.039.
   PubMed Web of Science ®Google Scholar
• Flora SJS. 2011. Arsenic-induced oxidative stress and its reversibility. Free Radic Biol Med. 51(2):257–281. doi:10.1016/j.freeradbiomed.2011.04.008.
   PubMed Web of Science ®Google Scholar
• Foyer CH, Halliwell B. 1976. The presence of glutathione and glutathione reductase in chloroplasts: a proposed role in ascorbic acid metabolism. Planta. 133(1):21–25. doi:10.1007/bf00386001.
   PubMed Web of Science ®Google Scholar
• Foyer CH, Noctor G. 2003. Redox sensing and signalling associated with reactive oxygen in chloroplasts, peroxisomes and mitochondria. Physiol Plantarum. 119(3):355–364. doi:10.1034/j.1399-3054.2003.00223.x.
   Web of Science ®Google Scholar
• Foyer CH, Noctor G. 2005. Redox homeostasis and antioxidant signaling: a metabolic interface between stress perception and physiological responses. Plant Cell. 17(7):1866–1875. doi:10.1105/tpc.105.033589.
   PubMed Web of Science ®Google Scholar
• Frederickson Matika DE, Loake GJ. 2014. Redox regulation in plant immune function. Antioxid Redox Signal. 21(9):1373–1388. doi:10.1089/ars.2013.5679.
   PubMed Web of Science ®Google Scholar
• Freeman JL, Persans MW, Nieman K, Albrecht C, Peer W, Pickering IJ, Salt DE. 2004. Increased glutathione biosynthesis plays a role in nickel tolerance in thlaspi nickel hyperaccumulators. Plant Cell. 16(8):2176–2191. doi:10.1105/tpc.104.023036.
   PubMed Web of Science ®Google Scholar
• Ghiani A, Fumagalli P, Nguyen Van T, Gentili R, Citterio S. 2014. The combined toxic and genotoxic effects of Cd and As to plant bioindicator Trifolium repens L. PLoS One. 9(6):e99239. doi:10.1371/journal.pone.0099239.
   PubMed Web of Science ®Google Scholar
• Gill SS, Anjum NA, Hasanuzzaman M, Gill R, Trivedi DK, Ahmad I, Pereira E, Tuteja N. 2013. Glutathione and glutathione reductase: a boon in disguise for plant abiotic stress defense operations. Plant Physiol Biochem. 70:204–212. doi:10.1016/j.plaphy.2013.05.032.
   PubMed Web of Science ®Google Scholar
• Gomes MP, Moreira Duarte D, Silva Miranda PL, Carvalho Barreto L, Matheus MT, Garcia QS. 2012. The effects of arsenic on the growth and nutritional status of Anadenanthera peregrina, a Brazilian savanna tree. Z Pflanzenernähr Bodenk. 175(3):466–473. doi:10.1002/jpln.201100195.
   Google Scholar
• Guo J, Xu W, Ma M. 2012. The assembly of metals chelation by thiols and vacuolar compartmentalization conferred increased tolerance to and accumulation of cadmium and arsenic in transgenic Arabidopsis thaliana. J Hazard Mater. 199–200:309–313. doi:10.1016/j.jhazmat.2011.11.008.
   PubMed Web of Science ®Google Scholar
• Gupta DK, Inouhe M, Rodríguez-Serrano M, Romero-Puertas MC, Sandalio LM. 2013. Oxidative stress and arsenic toxicity: role of NADPH oxidases. Chemosphere. 90(6):1987–1996. doi:10.1016/j.chemosphere.2012.10.066.
   PubMed Web of Science ®Google Scholar
• Habiba U, Ali S, Rizwan M, Ibrahim M, Hussain A, Shahid MR, Alamri SA, Alyemeni MN, Ahmad P. 2019. Alleviative role of exogenously applied mannitol in maize cultivars differing in chromium stress tolerance. Environ Sci Pollut Res Int. 26(5):5111–5121. doi:10.1007/s11356-018-3970-2.
   PubMed Web of Science ®Google Scholar
• Hare V, Chowdhary P, Kumar B, Sharma DC, Baghel VS. 2018. Arsenic toxicity and its remediation strategies for fighting the environmental threat. In: Emerging and eco-friendly approaches for waste management. Singapore: Springer; p. 143–170.
   Google Scholar
• Hasanuzzaman M, Nahar K, Anee TI, Fujita M. 2017. Glutathione in plants: biosynthesis and physiological role in environmental stress tolerance. Physiol Mol Biol Plants. 23(2):249–268. doi:10.1007/s12298-017-0422-2.
   PubMed Web of Science ®Google Scholar
• Hasanuzzaman M, Nahar K, Rahman A, Mahmud JA, Alharby HF, Fujita M. 2018. Exogenous glutathione attenuates lead-induced oxidative stress in wheat by improving antioxidant defense and physiological mechanisms. J Plant Interact. 13(1):203–212. doi:10.1080/17429145.2018.1458913.
   Web of Science ®Google Scholar
• Hassinen VH, Tervahauta AI, Schat H, Kärenlampi SO. 2011. Plant metallothioneins-metal chelators with ROS scavenging activity? Plant Biol (Stuttg). 13(2):225–232. doi:10.1111/j.1438-8677.2010.00398.x.
   PubMed Web of Science ®Google Scholar
• Hayashi S, Tanikawa H, Kuramata M, Abe T, Ishikawa S. 2020. Domain exchange between Oryza sativa phytochelatin synthases reveals a region that determines responsiveness to arsenic and heavy metals. Biochem Biophys Res Commun. 523(2):548–553. doi:10.1016/j.bbrc.2019.12.093.
   PubMed Web of Science ®Google Scholar
• He J, Li H, Ma C, Zhang Y, Polle A, Rennenberg H, Cheng X, Luo Z-B. 2015. Overexpression of bacterial γ-glutamylcysteine synthetase mediates changes in cadmium influx, allocation and detoxification in poplar. New Phytol. 205(1):240–254. doi:10.1111/nph.13013.
   PubMed Web of Science ®Google Scholar
• Huang Y, Hatayama M, Inoue C. 2011. Characterization of As efflux from the roots of As hyperaccumulator Pteris vittata L. Planta 234(6):1275–1284.
   PubMed Web of Science ®Google Scholar
• Huang J, Zhang Y, Peng J-S, Zhong C, Yi H-Y, Ow DW, Gong J-M. 2012. Fission yeast HMT1 lowers seed cadmium through phytochelatin-dependent vacuolar sequestration in Arabidopsis. Plant Physiol. 158(4):1779–1788. doi:10.1104/pp.111.192872.
   PubMed Web of Science ®Google Scholar
• Huang Y, Zhu Z, Wu X, Liu Z, Zou J, Chen Y, Su N, Cui J. 2019. Lower cadmium accumulation and higher antioxidative capacity in edible parts of Brassica campestris L. seedlings applied with glutathione under cadmium toxicity. Environ Sci Pollut Res Int. 26(13):13235–13245. doi:10.1007/s11356-019-04745-7.
   PubMed Web of Science ®Google Scholar
• Iori V, Pietrini F, Massacci A, Zacchini M. 2012. Induction of metal binding compounds and antioxidative defence in callus cultures of two black poplar (P. nigra) clones with different tolerance to cadmium. Plant Cell Tiss Organ Cult. 108(1):17–26. doi:10.1007/s11240-011-0006-8.
   Web of Science ®Google Scholar
• Jakubowska D, Janicka-Russak M, Kabała K, Migocka M, Reda M. 2015. Modification of plasma membrane NADPH oxidase activity in cucumber seedling roots in response to cadmium stress. Plant Sci. 234:50–59. doi:10.1016/j.plantsci.2015.02.005.
   PubMed Web of Science ®Google Scholar
• Janků M, Luhová L, Petřivalský M. 2019. On the origin and fate of reactive oxygen species in plant cell compartments. Antioxidants (Basel). 8(4):105. doi:10.3390/antiox8040105.
   Google Scholar
• Jozefczak M, Remans T, Vangronsveld J, Cuypers A. 2012. Glutathione is a key player in metal-induced oxidative stress defenses. Int J Mol Sci. 13(3):3145–3175. doi:10.3390/ijms13033145.
   PubMed Web of Science ®Google Scholar
• Jung H-I, Kong M-S, Lee B-R, Kim T-H, Chae M-J, Lee E-J, Jung G-B, Lee C-H, Sung J-K, Kim Y-H. 2019. Exogenous glutathione increases arsenic translocation into shoots and alleviates arsenic-induced oxidative stress by sustaining ascorbate-glutathione homeostasis in rice seedlings. Front Plant Sci. 10:1089–1089. doi:10.3389/fpls.2019.01089.
   PubMed Web of Science ®Google Scholar
• Karimi N, Ghaderian SM, Maroofi H, Schat H. 2010. Analysis of arsenic in soil and vegetation of a contaminated area in Zarshuran, Iran. Int J Phytoremediation. 12(2):159–173. doi:10.1080/15226510903213977.
   PubMed Web of Science ®Google Scholar
• Karimi N, Ghaderian SM, Raab A, Feldmann J, Meharg AA. 2009. An arsenic-accumulating, hypertolerant brassica, Isatis capadocica. New Phytol. 184(1):41–47. doi:10.1111/j.1469-8137.2009.02982.x.
   PubMed Web of Science ®Google Scholar
• Karimi N, Souri Z. 2015. Effect of phosphorus on arsenic accumulation and detoxification in arsenic hyperaccumulator, Isatis cappadocica. J Plant Growth Regul. 34(1):88–95. doi:10.1007/s00344-014-9445-x.
   Web of Science ®Google Scholar
• Karimi N, Souri Z. 2016. Antioxidant enzymes and compounds complement each other during arsenic detoxification in shoots of Isatis cappadocica Desv. Chem Ecol. 32(10):937–951. doi:10.1080/02757540.2016.1236087.
   Web of Science ®Google Scholar
• Karimi N, Vakilipak F, Souri Z, Farooq MA, Akhtar J. 2019. The role of selenium on mitigating arsenic accumulation, enhancing growth and antioxidant responses in metallicolous and non-metallicolous population of Isatis cappadocica Desv. and Brassica oleracea L. Environ Sci Pollut Res Int. 26(21):21704–21716. doi:10.1007/s11356-019-05392-8.
   PubMed Web of Science ®Google Scholar
• Kaur G, Sharma A, Guruprasad K, Pati PK. 2014. Versatile roles of plant NADPH oxidases and emerging concepts. Biotechnol Adv. 32(3):551–563. doi:10.1016/j.biotechadv.2014.02.002.
   PubMed Web of Science ®Google Scholar
• Kaya C, Okant M, Ugurlar F, Alyemeni MN, Ashraf M, Ahmad P. 2019. Melatonin-mediated nitric oxide improves tolerance to cadmium toxicity by reducing oxidative stress in wheat plants. Chemosphere. 225:627–638. doi:10.1016/j.chemosphere.2019.03.026.
   PubMed Web of Science ®Google Scholar
• Kim Y-O, Bae H-J, Cho E, Kang H. 2017. Exogenous glutathione enhances mercury tolerance by inhibiting mercury entry into plant cells. Front Plant Sci. 8:683–683. doi:10.3389/fpls.2017.00683.
   PubMed Web of Science ®Google Scholar
• Kong FX, Hu W, Chao SY, Sang WL, Wang LS. 1999. Physiological responses of the lichen Xanthoparmelia mexicana to oxidative stress of SO2. Environ Exp Bot. 42(3):201–209. doi:10.1016/S0098-8472(99)00034-9.
   Web of Science ®Google Scholar
• Kushwaha BK, Singh S, Tripathi DK, Sharma S, Prasad SM, Chauhan DK, Kumar V, Singh VP. 2019. New adventitious root formation and primary root biomass accumulation are regulated by nitric oxide and reactive oxygen species in rice seedlings under arsenate stress. J Hazard Mater. 361:134–140. doi:10.1016/j.jhazmat.2018.08.035.
   PubMed Web of Science ®Google Scholar
• Lin A, Zhang X, Zhu YG, Zhao FJ. 2008. Arsenate-induced toxicity: effects on antioxidative enzymes and DNA damage in Vicia faba. Environ Toxicol Chem. 27(2):413–419. doi:10.1897/07-266R.1.
   PubMed Web of Science ®Google Scholar
• Liu D, Li TQ, Jin XF, Yang XE, Islam E, Mahmood Q. 2008. Lead induced changes in the growth and antioxidant metabolism of the lead accumulating and non-accumulating ecotypes of Sedum alfredii. J Integr Plant Biol. 50(2):129–140. doi:10.1111/j.1744-7909.2007.00608.x.
   PubMed Web of Science ®Google Scholar
• Liu J, Wang X, Hu Y, Hu W, Bi Y. 2013. Glucose-6-phosphate dehydrogenase plays a pivotal role in tolerance to drought stress in soybean roots. Plant Cell Rep. 32(3):415–429. doi:10.1007/s00299-012-1374-1.
   PubMed Web of Science ®Google Scholar
• Liu S, Cheng Y, Zhang X, Guan Q, Nishiuchi S, Hase K, Takano T. 2007. Expression of an NADP-malic enzyme gene in rice (Oryza sativa. L) is induced by environmental stresses; over-expression of the gene in Arabidopsis confers salt and osmotic stress tolerance. Plant Mol Biol. 64(1–2):49–58. doi:10.1007/s11103-007-9133-3.
   PubMed Web of Science ®Google Scholar
• Mahimairaja S, Bolan NS, Adriano DC, Robinson B. 2005. Arsenic contamination and its risk management in complex environmental settings. Adv Agronomy. 86:1–82.
   Web of Science ®Google Scholar
• Marino D, Dunand C, Puppo A, Pauly N. 2012. A burst of plant NADPH oxidases. Trends Plant Sci. 17(1):9–15. doi:10.1016/j.tplants.2011.10.001.
   PubMed Web of Science ®Google Scholar
• Marino D, González EM, Frendo P, Puppo A, Arrese-Igor C. 2007. NADPH recycling systems in oxidative stressed pea nodules: a key role for the NADP+ -dependent isocitrate dehydrogenase. Planta. 225(2):413–421. doi:10.1007/s00425-006-0354-5.
   PubMed Web of Science ®Google Scholar
• Mishra S, Dwivedi S, Mallick S, Tripathi RD. 2019. Redox homeostasis in plants under arsenic stress. In: Panda S, Yamamoto Y, editors. Redox Homeostasis in Plants. Signaling and communication in plants. Cham: Springer; p. 179–198.
   Google Scholar
• Mohamed AA, Castagna A, Ranieri A, Sanità di Toppi L. 2012. Cadmium tolerance in Brassica juncea roots and shoots is affected by antioxidant status and phytochelatin biosynthesis. Plant Physiol Biochem. 57:15–22. doi:10.1016/j.plaphy.2012.05.002.
   PubMed Web of Science ®Google Scholar
• Mostofa MG, Seraj ZI, Fujita M. 2014. Exogenous sodium nitroprusside and glutathione alleviate copper toxicity by reducing copper uptake and oxidative damage in rice (Oryza sativa L.) seedlings. Protoplasma. 251(6):1373–1386. doi:10.1007/s00709-014-0639-7.
   PubMed Web of Science ®Google Scholar
• Ngole-Jeme VM, Fantke P. 2017. Ecological and human health risks associated with abandoned gold mine tailings contaminated soil. PLoS One. 12(2):e0172517. doi:10.1371/journal.pone.0172517.
   PubMed Web of Science ®Google Scholar
• Noctor G, Queval G, Gakière B. 2006. NAD(P) synthesis and pyridine nucleotide cycling in plants and their potential importance in stress conditions. J Exp Bot. 57(8):1603–1620. doi:10.1093/jxb/erj202.
   PubMed Web of Science ®Google Scholar
• PÉRez-Chaca MV, RodrÍGuez-Serrano M, Molina AS, Pedranzani HE, Zirulnik F, Sandalio LM, Romero-Puertas MC. 2014. Cadmium induces two waves of reactive oxygen species in Glycine max (L.) roots. Plant Cell Environ. 37(7):1672–1687. doi:10.1111/pce.12280.
   PubMed Web of Science ®Google Scholar
• Qiu B, Zeng F, Cai S, Wu X, Haider SI, Wu F, Zhang G. 2013. Alleviation of chromium toxicity in rice seedlings by applying exogenous glutathione. J Plant Physiol. 170(8):772–779. doi:10.1016/j.jplph.2013.01.016.
   PubMed Web of Science ®Google Scholar
• Rahman A, Mostofa MG, Alam MM, Nahar K, Hasanuzzaman M, Fujita M. 2015. Calcium mitigates arsenic toxicity in rice seedlings by reducing arsenic uptake and modulating the antioxidant defense and glyoxalase systems and stress markers. Biomed Res Int. 2015:340812–340812. doi:10.1155/2015/340812.
   PubMed Web of Science ®Google Scholar
• Remans T, Opdenakker K, Smeets K, Mathijsen D, Vangronsveld J, Cuypers A. 2010. Metal-specific and NADPH oxidase dependent changes in lipoxygenase and NADPH oxidase gene expression in Arabidopsis thaliana exposed to cadmium or excess copper. Functional Plant Biol. 37(6):532. doi:10.1071/FP09194.
   Web of Science ®Google Scholar
• Rizwan M, Ali S, Ur Rehman MZ, Malik S, Adrees M, Qayyum MF, Alamri SA, Alyemeni MN, Ahmad P. 2019. Effect of foliar applications of silicon and titanium dioxide nanoparticles on growth, oxidative stress, and cadmium accumulation by rice (Oryza sativa). Acta Physiol Plant. 41:35. doi:10.1007/s11738-019-2828-7.
   Web of Science ®Google Scholar
• Rohman MM, Hossain MD, Suzuki T, Takada G, Fujita M. 2009. Quercetin-4′-glucoside: a physiological inhibitor of the activities of dominant glutathione S-transferases in onion (Allium cepa L.) bulb. Acta Physiol Plant. 31(2):301–309. doi:10.1007/s11738-008-0234-7.
   Web of Science ®Google Scholar
• Sakai Y, Watanabe T, Wasaki J, Senoura T, Shinano T, Osaki M. 2010. Influence of arsenic stress on synthesis and localization of low-molecular-weight thiols in Pteris vittata. Environ Pollut. 158(12):3663–3669. doi:10.1016/j.envpol.2010.07.043.
   PubMed Web of Science ®Google Scholar
• Scharte J, Schön H, Tjaden Z, Weis E, von Schaewen A. 2009. Isoenzyme replacement of glucose-6-phosphate dehydrogenase in the cytosol improves stress tolerance in plants. Proc Natl Acad Sci U S A. 106(19):8061–8066. doi:10.1073/pnas.0812902106.
   PubMed Web of Science ®Google Scholar
• Sedlak J, Lindsay RH. 1968. Estimation of total, protein-bound, and nonprotein sulfhydryl groups in tissue with Ellman’s reagent. Anal Biochem. 25(1):192–205. doi:10.1016/0003-2697(68)90092-4.
   PubMed Web of Science ®Google Scholar
• Seth CS, Remans T, Keunen E, Jozefczak M, Gielen H, Opdenakker K, Weyens N, Vangronsveld J, Cuypers A. 2012. Phytoextraction of toxic metals: a central role for glutathione. Plant Cell Environ. 35(2):334–346. doi:10.1111/j.1365-3040.2011.02338.x.
   PubMed Web of Science ®Google Scholar
• Shahid MA, Balal RM, Khan N, Zotarelli L, Liu GD, Sarkhosh A, Fernández-Zapata JC, Martínez Nicolás JJ, Garcia-Sanchez F. 2019. Selenium impedes cadmium and arsenic toxicity in potato by modulating carbohydrate and nitrogen metabolism. Ecotoxicol Environ Saf. 180:588–599. doi:10.1016/j.ecoenv.2019.05.037.
   PubMed Web of Science ®Google Scholar
• Sharma I. 2012. Arsenic induced oxidative stress in plants. Biologia. 67(3):447–453. doi:10.2478/s11756-012-0024-y.
   Web of Science ®Google Scholar
• Sharma SS, Dietz K-J. 2009. The relationship between metal toxicity and cellular redox imbalance. Trends Plant Sci. 14(1):43–50. doi:10.1016/j.tplants.2008.10.007.
   PubMed Web of Science ®Google Scholar
• Shri M, Kumar S, Chakrabarty D, Trivedi PK, Mallick S, Misra P, Shukla D, Mishra S, Srivastava S, Tripathi RD, et al. 2009. Effect of arsenic on growth, oxidative stress, and antioxidant system in rice seedlings. Ecotoxicol Environ Saf. 72(4):1102–1110. doi:10.1016/j.ecoenv.2008.09.022.
   PubMed Web of Science ®Google Scholar
• Shukla D, Kesari R, Mishra S, Dwivedi S, Tripathi RD, Nath P, Trivedi PK. 2012. Expression of phytochelatin synthase from aquatic macrophyte Ceratophyllum demersum L. enhances cadmium and arsenic accumulation in tobacco. Plant Cell Rep. 31(9):1687–1699. doi:10.1007/s00299-012-1283-3.
   PubMed Web of Science ®Google Scholar
• Siddappaji MH, Scholes DR, Bohn M, Paige KN. 2013. Overcompensation in response to herbivory in Arabidopsis thaliana: the role of glucose-6-phosphate dehydrogenase and the oxidative pentose-phosphate pathway. Genetics. 195(2):589–598. doi:10.1534/genetics.113.154351.
   PubMed Web of Science ®Google Scholar
• Sil P, Das P, Biswas S, Mazumdar A, Biswas AK. 2019. Modulation of photosynthetic parameters, sugar metabolism, polyamine and ion contents by silicon amendments in wheat (Triticum aestivum L.) seedlings exposed to arsenic. Environ Sci Pollut Res Int. 26(13):13630–13648. doi:10.1007/s11356-019-04896-7.
   PubMed Web of Science ®Google Scholar
• Singh AP, Dixit G, Kumar A, Mishra S, Singh PK, Dwivedi S, Trivedi PK, Chakrabarty D, Mallick S, Pandey V, et al. 2015. Nitric oxide alleviated arsenic toxicity by modulation of antioxidants and thiol metabolism in rice (Oryza sativa L.). Front Plant Sci. 6:1272–1272. doi:10.3389/fpls.2015.01272.
   PubMed Web of Science ®Google Scholar
• Son K-H, Kim D-Y, Koo N, Kim K-R, Kim J-G, Owens G. 2012. Detoxification through phytochelatin synthesis in Oenothera odorata exposed to Cd solutions. Environ Exp Bot. 75:9–15. doi:10.1016/j.envexpbot.2011.08.011.
   Web of Science ®Google Scholar
• Souri Z, Karimi N, de Oliveira LM. 2018. Antioxidant enzymes responses in shoots of arsenic hyperaccumulator, Isatis cappadocica Desv., under interaction of arsenate and phosphate. Environ Technol. 39(10):1316–1327. doi:10.1080/09593330.2017.1329349.
   PubMed Web of Science ®Google Scholar
• Souri Z, Karimi N, Farooq MA, Sandalio LM. 2020. Nitric oxide improves tolerance to arsenic stress in Isatis cappadocica desv. Shoots by enhancing antioxidant defenses. Chemosphere. 239:124523. doi:10.1016/j.chemosphere.2019.124523.
   PubMed Web of Science ®Google Scholar
• Souri Z, Karimi N, Sandalio LM. 2017. Arsenic hyperaccumulation strategies: an overview. Front Cell Dev Biol. 5:67–67. doi:10.3389/fcell.2017.00067.
   PubMed Web of Science ®Google Scholar
• Souri Z, Karimi N. 2017. Enhanced phytoextraction by as hyperaccumulator Isatis cappadocica spiked with sodium nitroprusside. Soil Sediment Contam Int J. 26(4):457–468. doi:10.1080/15320383.2017.1326457.
   Web of Science ®Google Scholar
• Stoeva N, Berova M, Zlatev Z. 2005. Effect of arsenic on some physiological parameters in bean plants. Biologia Plant. 49(2):293–296. doi:10.1007/s10535-005-3296-z.
   Web of Science ®Google Scholar
• Sytykiewicz H. 2016. Deciphering the role of NADPH oxidase in complex interactions between maize (Zea mays L.) genotypes and cereal aphids. Biochem Biophys Res Commun. 476(2):90–95. doi:10.1016/j.bbrc.2016.05.050.
   PubMed Web of Science ®Google Scholar
• Talukdar D. 2011. Effect of arsenic-induced toxicity on morphological traits of Trigonella foenum-graecum L. and Lathyrus sativus L. during germination and early seedling growth. Curr Res J Biol Sci. 3(2):116–123.
   Google Scholar
• Talukdar D. 2012. Exogenous calcium alleviates the impact of cadmium-induced oxidative stress in Lens culinaris medic. Seedlings through modulation of antioxidant enzyme activities. J Crop Sci Biotechnol. 15(4):325–334. doi:10.1007/s12892-012-0065-3.
   Google Scholar
• 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(1):69–79. doi:10.1007/s12298-012-0140-8.
   PubMed Web of Science ®Google Scholar
• Tripathi P, Mishra A, Dwivedi S, Chakrabarty D, Trivedi PK, Singh RP, Tripathi RD. 2012. Differential response of oxidative stress and thiol metabolism in contrasting rice genotypes for arsenic tolerance. Ecotoxicol Environ Saf. 79:189–198. doi:10.1016/j.ecoenv.2011.12.019.
   PubMed Web of Science ®Google Scholar
• Tripathi RD, Tripathi P, Dwivedi S, Dubey S, Chatterjee S, Chakrabarty D, Trivedi PK. 2012. Arsenomics: omics of arsenic metabolism in plants. Front Physiol. 3:275–275. doi:10.3389/fphys.2012.00275.
   PubMed Web of Science ®Google Scholar
• Velikova V, Yordanov I, Edreva A. 2000. Oxidative stress and some antioxidant systems in acid rain-treated bean plants. Plant Sci. 151(1):59–66. doi:10.1016/S0168-9452(99)00197-1.
   Web of Science ®Google Scholar
• Venkatachalam P, Jayaraj M, Manikandan R, Geetha N, Rene ER, Sharma NC, Sahi SV. 2017. Zinc oxide nanoparticles (ZnONPs) alleviate heavy metal-induced toxicity in Leucaena leucocephala seedlings: a physiochemical analysis. Plant Physiol Biochem. 110:59–69. doi:10.1016/j.plaphy.2016.08.022.
   PubMed Web of Science ®Google Scholar
• Wang F, Chen F, Cai Y, Zhang G, Wu F. 2011. Modulation of exogenous glutathione in ultrastructure and photosynthetic performance against Cd Stress in the two barley genotypes differing in Cd tolerance. Biol Trace Elem Res. 144(1–3):1275–1288. doi:10.1007/s12011-011-9121-y.
   PubMed Web of Science ®Google Scholar
• Wang G-F, Li W-Q, Li W-Y, Wu G-L, Zhou C-Y, Chen K-M. 2013. Characterization of Rice NADPH oxidase genes and their expression under various environmental conditions. Int J Mol Sci. 14(5):9440–9458. doi:10.3390/ijms14059440.
   PubMed Web of Science ®Google Scholar
• Wang M, Zhao X, Xiao Z, Yin X, Xing T, Xia G. 2016. A wheat superoxide dismutase gene TaSOD2 enhances salt resistance through modulating redox homeostasis by promoting NADPH oxidase activity. Plant Mol Biol. 91(1–2):115–130. doi:10.1007/s11103-016-0446-y.
   PubMed Web of Science ®Google Scholar
• Yao Y, Xu G, Mou D, Wang J, Ma J. 2012. Subcellular Mn compartation, anatomic and biochemical changes of two grape varieties in response to excess manganese. Chemosphere. 89(2):150–157. doi:10.1016/j.chemosphere.2012.05.030.
   PubMed Web of Science ®Google Scholar
• Yuan H, Zhang Y, Huang S, Yang Y, Gu C. 2015. Effects of exogenous glutathione and cysteine on growth, lead accumulation, and tolerance of Iris lactea var. Chinensis. Environ Sci Pollut Res Int. 22(4):2808–2816. doi:10.1007/s11356-014-3535-y.
   PubMed Web of Science ®Google Scholar
• Zhao F-J, McGrath SP, Meharg AA. 2010. Arsenic as a food chain contaminant: mechanisms of plant uptake and metabolism and mitigation strategies. Annu Rev Plant Biol. 61(1):535–559. doi:10.1146/annurev-arplant-042809-112152.
   PubMed Web of Science ®Google Scholar
• Zlobin IE, Kartashov AV, Shpakovski GV. 2017. Different roles of glutathione in copper and zinc chelation in Brassica napus roots. Plant Physiol Biochem. 118:333–341. doi:10.1016/j.plaphy.2017.06.029.
   PubMed Web of Science ®Google Scholar