Tolerance of Landoltia punctata to arsenate: an evaluation of the potential use in phytoremediation programs

References

• Agency for Toxic Substances & Disease Registry [ATSDR]. 2019. Substance priority list Atlanta (GA) [accessed 2020 May 19]. https://www.atsdr.cdc.gov/spl/index.html.
   Google Scholar
• Ali S, Abbas Z, Rizwan M, Zaheer IE, Yavaş I, Ünay A, Abdel-Daim MM, Bin-Jumah M, Hasanuzzaman M, Kalderis D. 2020. Application of floating aquatic plants in phytoremediation of heavy metals polluted water: a review. Sustainability. 12(5):1927. doi:10.3390/su12051927.
   Web of Science ®Google Scholar
• Alscher RG, Erturk N, Heath LS. 2002. Role of superoxide dismutases (SODs) in controlling oxidative stress in plants. J Exp Bot. 53(372):1331–1341. doi:10.1093/jxb/53.372.1331.
   PubMed Web of Science ®Google Scholar
• Anderson JV, Davis DG. 2004. Abiotic stress alters transcript profiles and activity of glutathione S-transferase, glutathione peroxidase, and glutathione reductase in Euphorbia esula. Physiol Plant. 120(3):421–433. doi:10.1111/j.0031-9317.2004.00249.x.
   PubMed Web of Science ®Google Scholar
• Anderson MD, Prasad TK, Stewart CR. 1995. Changes in isozyme profiles of catalase, peroxidase, and glutathione reductase during acclimation to chilling in mesocotyls of maize seedlings. Plant Physiol. 109(4):1247–1257. doi:10.1104/pp.109.4.1247.
   PubMed Web of Science ®Google Scholar
• Apel K, Hirt H. 2004. Reactive oxygen species: metabolism, oxidative stress, and signal transduction. Annu Rev Plant Biol. 55:373–399. doi:10.1146/annurev.arplant.55.031903.141701.
   PubMed Web of Science ®Google Scholar
• Bali AS, Sidhu GPS, Kumar V. 2020. Root exudates ameliorate cadmium tolerance in plants: a review. Environ Chem Lett. 18(4):1243–1275. doi:10.1007/s10311-020-01012-x.
   Web of Science ®Google Scholar
• Barbosa AP, Gonçalves EC, Azevedo AA. 2015. Morpho-anatomical and growth alterations induced by arsenic in Cajanus cajan (L.) DC (Fabaceae). Environ Sci Pollut Res Int. 22(15):11265–11274. doi:10.1007/s11356-015-4342-9.
   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
• Bhaduri AM, Fulekar MH. 2012. Antioxidant enzyme responses of plants to heavy metal stress. Rev Environ Sci Biotechnol. 11(1):55–69. doi:10.1007/s11157-011-9251-x.
   Web of Science ®Google Scholar
• Borba RP, Figueiredo BR, Rawlins B, Matschullat J. 2000. Arsenic in water and sediment in the iron quadrangle, state of Minas Gerais, Brazil. RBG. 30(3):558–561. doi:10.25249/0375-7536.2000303558561.
   Google Scholar
• Boveris A. 1984. Determination of the production of superoxide radicals and hydrogen peroxide in mitochondria. Meth Enzymol. 105:429–435. doi:10.1016/s0076-6879(84)05060-6.
   PubMed Web of Science ®Google Scholar
• Bradford MM. 1976. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 72:248–254. doi:10.1006/abio.1976.9999.
   PubMed Web of Science ®Google Scholar
• Campos FV, de Oliveira JA, Silva AA, Ribeiro C, Farnese FS. 2019b. Phytoremediation of arsenite-contaminated environments: is Pistia stratiotes L. a useful tool?. Ecol Indic. 104:794–801. doi:10.1016/j.ecolind.2019.04.048.
   Web of Science ®Google Scholar
• Campos FV, de Oliveira JA, Silva AA, Ribeiro C, Montoya SG, Farnese FS. 2019a. Involvement of glutathione and glutathione metabolizing enzymes in Pistia stratiotes tolerance to arsenite. Int J Phytoremed. 22(4):404–411. doi:10.1080/15226514.2019.1667951.
   PubMed Web of Science ®Google Scholar
• Carlberg I, Mannervik B. 1985. Glutathione reductase. Meth Enzymol. 113:484–495. doi:10.1016/s0076-6879(85)13062-4.
   PubMed Web of Science ®Google Scholar
• Chance B, Maehley AC. 1955. Assay of catalase and peroxidase. Methods Enzymol. 2:764–755.
   Web of Science ®Google Scholar
• Clark RB. 1975. Characterization of phosphatase of intact maize roots. J Agric Food Chem. 23(3):458–460. doi:10.1021/jf60199a002.
   PubMed Web of Science ®Google Scholar
• Dai LP, Dong XJ, Ma HH. 2012. Antioxidative and chelating properties of anthocyanins in Azolla imbricata induced by cadmium. Pol J Environ Stud. 21:837–844.
   Web of Science ®Google Scholar
• Da-Silva CJ, Canatto RA, Cardoso AA, Ribeiro C, de Oliveira JA. 2018. Oxidative stress triggered by arsenic in a tropical macrophyte is alleviated by endogenous and exogenous nitric oxide. Braz J Bot. 41(1):21–28. doi:10.1007/s40415-017-0431-y.
   Web of Science ®Google Scholar
• Da-Silva CJ, Canatto RA, Cardoso AA, Ribeiro C, Oliveira JA. 2017. Arsenic-hyperaccumulation and antioxidant system in the aquatic macrophyte. Theor Exp Plant Physiol. 29(4):203–213. doi:10.1007/s40626-017-0096-8.
   Web of Science ®Google Scholar
• Duman F, Ozturk F, Aydin Z. 2010. Biological responses of duckweed (Lemna minor L.) exposed to the inorganic arsenic species As(III) and As(V): effects of concentration and duration of exposure. Ecotoxicology. 19(5):983–993. doi:10.1007/s10646-010-0480-5.
   PubMed Web of Science ®Google Scholar
• Durkee J, Bartrem C, Möller G. 2017. Legacy lead arsenate soil contamination at childcare centers in the Yakima Valley, Central Washington, USA. Chemosphere. 168:1126–1135. doi:10.1016/j.chemosphere.2016.10.094.
   PubMed Web of Science ®Google Scholar
• Farnese FS, Oliveira JA, Lima FS, Leão GA, Gusman GS, Silva LC. 2014. Evaluation of the potential of Pistia stratiotes L. (water lettuce) for bioindication and phytoremediation of aquatic environments contaminated with arsenic. Braz J Biol. 74:108–112.
   Web of Science ®Google Scholar
• Fayiga AO, Ma LQ, Cao X, Rathinasabapathi B. 2004. Effects of heavy metals on growth and arsenic accumulation in the arsenic hyperaccumulator Pteris vittata L. Environ Pollut. 132(2):289–296. doi:10.1016/j.envpol.2004.04.020.
   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
• Gay C, Gebicki JM. 2000. A critical evaluation of the effect of sorbitol on the ferric-xylenol orange hydroperoxide assay. Anal Biochem. 284(2):217–220. doi:10.1006/abio.2000.4696.
   PubMed Web of Science ®Google Scholar
• Geng A, Wang X, Li Q, Yang H, Chen Y, Liu W, Chen Y, Wang F. 2020. Mechanism of anthocyanins-mediated resistance to heavy metals stresses in plants: a review. J South Agr. 51(1):80–90.
   Google Scholar
• Giannopolitis CN, Ries SK. 1977. Superoxide dismutases: I. Occurrence in higher plants. Plant Physiol. 59(2):309–314. doi:10.1104/pp.59.2.309.
   PubMed Web of Science ®Google Scholar
• Gill SS, Tuteja N. 2010. Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiol Biochem. 48(12):909–930. doi:10.1016/j.plaphy.2010.08.016.
   PubMed Web of Science ®Google Scholar
• Gould KS, McKelvie J, Markham KR. 2002. Do anthocyanins function as antioxidants in leaves? Imaging of H2O2 in red and green leaves after mechanical injury. Plant Cell Environ. 25(10):1261–1269. doi:10.1046/j.1365-3040.2002.00905.x.
   Web of Science ®Google Scholar
• Guo L, Ding Y, Xu Y, Li Z, Jin Y, He K, Fang Y, Zhao H. 2017. Responses of Landoltia punctata to cobalt and nickel: removal, growth, photosynthesis, antioxidant system and starch metabolism. Aquat Toxicol. 190:87–93. doi:10.1016/j.aquatox.2017.06.024.
   PubMed Web of Science ®Google Scholar
• Hatje V, Pedreira RM, de Rezende CE, Schettini CF, de Souza GC, Marin DC, Hackspacher PC. 2017. The environmental impacts of one of the largest tailing dam failures worldwide. Sci Rep. 7(1):1–13. doi:10.1038/s41598-017-11143-x.
   PubMedGoogle Scholar
• Havir EA, Mchale NA. 1987. Biochemical and developmental characterization of multiple forms of catalase in tobacco leaves. Plant Physiol. 84(2):450–455. doi:10.1104/pp.84.2.450.
   PubMed Web of Science ®Google Scholar
• 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(4):604–611. doi:10.1007/s004250050524.
   Web of Science ®Google Scholar
• Islam A, Saha PK, Iqbal M, Islam MN, Nayeem M. 2016. Removal of arsenic by water hyacinth from arsenic contaminated water. Water Int. 1(2):36–41.
   Google Scholar
• Kamperidou I, Vasilakakis M. 2006. Effect of propagation material on some quality attributes of strawberry fruit (Fragaria × ananassa. Var. Selva). Sci Hortic. 107(2):137–142. doi:10.1016/j.scienta.2005.06.009.
   Web of Science ®Google Scholar
• Kar M, Mishra D. 1976. Catalase, peroxidase, and polyphenoloxidase activities during rice leaf senescence. Plant Physiol. 57(2):315–319. doi:10.1104/pp.57.2.315.
   PubMed Web of Science ®Google Scholar
• Koshiba T. 1993. Cytosolic ascorbate peroxidase in seedlings and leaves of maize (Zea mays). Plant Cell Physiol. 34(5):713–721. doi:10.1093/oxfordjournals.pcp.a078474.
   Web of Science ®Google Scholar
• Kumar V, Parihar RD, Sharma A, Bakshi P, Singh Sidhu GP, Bali AS, Karaouzas I, Bhardwaj R, Thukral AK, Gyasi-Agyei Y, et al. 2019a. Global evaluation of heavy metal content in surface water bodies: a meta-analysis using heavy metal pollution indices and multivariate statistical analyses. Chemosphere. 236:124364. doi:10.1016/j.chemosphere.2019.124364.
   PubMed Web of Science ®Google Scholar
• Kumar V, Sharma A, Kaur P, Sidhu GPS, Bali AS, Bhardwaj R, Thukral AK, Cerda A. 2019b. Pollution assessment of heavy metals in soils of India and ecological risk assessment: a state-of-the-art. Chemosphere. 216:449–462. doi:10.1016/j.chemosphere.2018.10.066.
   PubMed Web of Science ®Google Scholar
• Kuo CC, Moon KA, Wang S, Silbergeld E, Navas-Acien A. 2017. The association of arsenic metabolism with cancer, cardiovascular disease, and diabetes: a systematic review of the epidemiological evidence. Environ Health Perspect. 125(8):087001–087016. doi:10.1289/EHP577.
   PubMed Web of Science ®Google Scholar
• Kuo MC, Kao CH. 2003. Aluminum effects on lipid peroxidation and antioxidative enzyme activities in rice leaves. Biologia Plant. 46(1):149–152. doi:10.1023/A:1022356322373.
   Web of Science ®Google Scholar
• Lahive E, O'Callaghan MJA, Jansen MAK, O'Halloran J. 2011. Uptake and partitioning of zinc in Lemnaceae. Ecotoxicology. 20(8):1992–2002. doi:10.1007/s10646-011-0741-y.
   PubMed Web of Science ®Google Scholar
• Leão GA, Oliveira JAD, Felipe RTA, Farnese FS. 2017. Phytoremediation of arsenic-contaminated water: the role of antioxidant metabolism of Azolla caroliniana Willd. (Salviniales). Acta Bot Bras. 31(2):161–168. doi:10.1590/0102-33062016abb0407.
   Web of Science ®Google Scholar
• Li TY, Xiong ZT. 2004. Cadmium-induced colony disintegration of duckweed (Lemna paucicostata Hegelm.) and as biomarker of phytotoxicity. Ecotoxicol Environ Saf. 59(2):174–179. doi:10.1016/j.ecoenv.2003.11.007.
   PubMed Web of Science ®Google Scholar
• Lin YF, Aarts MG. 2012. The molecular mechanism of zinc and cadmium stress response in plants. Cell Mol Life Sci. 69(19):3187–3206. doi:10.1007/s00018-012-1089-z.
   PubMed Web of Science ®Google Scholar
• Malar S, Shivendra SV, Favas PJC, Perumal V. 2016. Lead heavy metal toxicity induced changes on growth and antioxidative enzymes level in water hyacinths [Eichhornia crassipes (Mart)]. Bot Stud. 55(1):11. doi:10.1186/s40529-014-0054-6.
   Google Scholar
• McGrath SP, Zhao FJ. 2003. Phytoextraction of metals and metalloids from contaminated soils. Curr Opin Biotechnol. 14(3):277–282. doi:10.1016/s0958-1669(03)00060-0.
   PubMed Web of Science ®Google Scholar
• Mkandawire M, Dudel EG. 2005. Accumulation of arsenic in Lemna gibba L. (duckweed) in tailing waters of two abandoned uranium mining sites in Saxony, Germany. Sci Total Environ. 336(1-3):81–89. doi:10.1016/j.scitotenv.2004.06.002.
   PubMed Web of Science ®Google Scholar
• Mohammadi M, Karr AL. 2001. Superoxide anion generation in effective and ineffective soybean root nodules. J Plant Physiol. 158(8):1023–1029. doi:10.1078/S0176-1617(04)70126-1.
   Web of Science ®Google Scholar
• Moller IM, Sweetlove LJ. 2010. ROS signalling-specificity is required. Trends Plant Sci. 15(7):370–374. doi:10.1016/j.tplants.2010.04.008.
   PubMed Web of Science ®Google Scholar
• Nagalakshmi N, Prasad M. 2001. Responses of glutathione cycle enzymes and glutathione metabolism to copper stress in Scenedesmus bijugatus. Plant Sci. 160(2):291–299. doi:10.1016/S0168-9452(00)00392-7.
   PubMed Web of Science ®Google Scholar
• Nakano Y, Asada K. 1981. Hydrogen peroxide is scavenged by ascorbate specific peroxidase in spinach chloroplasts. Plant Cell Physiol. 22:867–880. doi:10.1093/oxfordjournals.pcp.a076232.
   Web of Science ®Google Scholar
• Prado C, Pagano E, Prado F, Rosa M. 2012. Detoxification of Cr(VI) in Salvinia minima is related to seasonal-induced changes of thiols, phenolics and antioxidative enzymes. J Hazard Mater. 239-240:355–361. doi:10.1016/j.jhazmat.2012.09.010.
   PubMed Web of Science ®Google Scholar
• Rai PK. 2009. Heavy metal phytoremediation from aquatic ecosystems with special reference to macrophytes. Crit Rev Environ Sci Technol. 39(9):697–753. doi:10.1080/10643380801910058.
   Web of Science ®Google Scholar
• Rascio N, Navari-Izzo F. 2011. Heavy metal hyperaccumulating plants: how and why do they do it? And what makes them so interesting? Plant Sci. 180(2):169–181. doi:10.1016/j.plantsci.2010.08.016.
   PubMed Web of Science ®Google Scholar
• Rezania S, Taib SM, Md Din MF, Dahalan FA, Kamyab H. 2016. Comprehensive review on phytotechnology: heavy metals removal by diverse aquatic plants species from wastewater. J Hazard Mater. 318:587–599. doi:10.1016/j.jhazmat.2016.07.053.
   PubMed Web of Science ®Google Scholar
• Sidhu G. 2016. Heavy metal toxicity in soils: sources, remediation technologies and challenges. Adv Plants Agric Res. 5(1):445–446.
   Google Scholar
• Sidhu GPS, Bali AS, Singh HP, Batish D, Kohli RK. 2020. Insights into the tolerance and phytoremediation potential of Coronopus didymus L. (Sm) grown under zinc stress. Chemosphere. 244:125350. doi:10.1016/j.chemosphere.2019.125350.
   PubMed Web of Science ®Google Scholar
• Sidhu GPS, Bali AS, Singh HP, Batish DR, Kohli RK. 2018a. Ethylenediamine disuccinic acid enhanced phytoextraction of nickel from contaminated soils using Coronopus didymus (L.) Sm. Chemosphere. 205:234–243. doi:10.1016/j.chemosphere.2018.04.106.
   PubMed Web of Science ®Google Scholar
• Sidhu GPS, Bali AS, Singh HP, Batish DR, Kohli RK. 2018b. Phytoremediation of lead by a wild, non-edible Pb accumulator Coronopus didymus (L.) Brassicaceae. Int J Phytoremed. 20(5):483–489. doi:10.1080/15226514.2017.1374331.
   PubMed Web of Science ®Google Scholar
• Sidhu GPS, Singh HP, Batish DR, Kohli RK. 2016. Effect of lead on oxidative status, antioxidative response and metal accumulation in Coronopus didymus. Plant Physiol Biochem. 105:290–296. doi:10.1016/j.plaphy.2016.05.019.
   PubMed Web of Science ®Google Scholar
• Sidhu GPS, Singh HP, Batish DR, Kohli RK. 2017a. Tolerance and hyperaccumulation of cadmium by a wild, unpalatable herb Coronopus didymus (L.) Sm. (Brassicaceae). Ecotoxicol Environ Saf. 135:209–215. doi:10.1016/j.ecoenv.2016.10.001.
   PubMed Web of Science ®Google Scholar
• Sidhu GPS, Singh HP, Batish DR, Kohli RK. 2017b. Appraising the role of environment friendly chelants in alleviating lead by Coronopus didymus from Pb-contaminated soils. Chemosphere. 182:129–136. doi:10.1016/j.chemosphere.2017.05.026.
   PubMed Web of Science ®Google Scholar
• Silva AA, de Oliveira JA, Campos FV, Ribeiro C, Farnese FS, Costa AC. 2018. Phytoremediation potential of Salvinia molesta for arsenite contaminated water: role of antioxidant enzymes. Theor Exp Plant Physiol. 30(4):275–286. doi:10.1007/s40626-018-0121-6.
   Web of Science ®Google Scholar
• Silva AA, de Oliveira JA, Campos FV, Ribeiro C, Farnese FS. 2017. Role of glutathione in tolerance to arsenite in Salvinia molesta, an aquatic fern. Acta Bot Bras. 31(4):657–664. doi:10.1590/0102-33062017abb0087.
   Web of Science ®Google Scholar
• Singh HP, Batish DR, Kohli RK, Arora K. 2007. Arsenic-induced root growth inhibition in mung bean (Phaseolus aureus Roxb.) is due to oxidative stress resulting from enhanced lipid peroxidation. Plant Growth Regul. 53(1):65–73. doi:10.1007/s10725-007-9205-z.
   Web of Science ®Google Scholar
• Skladanka J, Adam V, Zitka O, Krystofova O, Beklova M, Kizek R, Havlicek Z, Slama P, Nawrath A. 2012. Investigation into the effect of molds in grasses on their content of low molecular mass thiols. IJERPH. 9(11):3789–3805. doi:10.3390/ijerph9113789.
   Google Scholar
• Souri Z, Cardoso AA, Da-Silva CJ, Oliveira LM, Dari B, Sihi D, Karimi1 N. 2019. Heavy metals and photosynthesis. In: Ahmad P, Ahanger MA, Alyemeni MN, Alam P, editors. Photosynthesis, productivity, and environmental stress. Chichester: John Wiley & Sons Ltd. p. 107–134.
   Google Scholar
• Tang J, Chen C, Chen L, Daroch M, Cui Y. 2017. Effects of pH, initial Pb2+ concentration, and polyculture on lead remediation by three duckweed species. Environ Sci Pollut Res Int. 24(30):23864–23871. doi:10.1007/s11356-017-0004-4.
   PubMed Web of Science ®Google Scholar
• Tippery NP, Les DH. 2020. Tiny plants with enormous potential: phylogeny and evolution of duckweeds. In: Cao X, Fourounjian P, Wang W, editors. The duckweed genomes. compendium of plant genomes. New York: Springer. p. 19–38.
   Google Scholar
• Tripathi RD, Srivastava S, Mishra S, Singh N, Tuli R, Gupta DK, Maathuis F. 2007. Arsenic hazards: strategies for tolerance and remediation by plants. Trends Biotechnol. 25(4):158–165. doi:10.1016/j.tibtech.2007.02.003.
   PubMed Web of Science ®Google Scholar
• Vergilio CDS, Lacerda D, Oliveira BCV, Sartori E, Campos GM, Pereira ALS, Aguiar DB, Souza TS, Almeida MG, Thompson F, et al. 2020. Metal concentrations and biological effects from one of the largest mining disasters in the world (Brumadinho, Minas Gerais). Sci Rep. 10(1):1–12. doi:10.1038/s41598-020-62700-w.
   PubMed Web of Science ®Google Scholar
• WHO. 2017. Guidelines for drinking-water quality: fourth edition incorporating the first addendum. Geneva.
   Google Scholar
• Xu H, Yu C, Xia X, Li M, Li H, Wang Y, Wang S, Wang C, Ma Y, Zhou G. 2018. Comparative transcriptome analysis of duckweed (Landoltia punctata) in response to cadmium provides insights into molecular mechanisms underlying hyperaccumulation. Chemosphere. 190:154–165. doi:10.1016/j.chemosphere.2017.09.146.
   PubMed Web of Science ®Google Scholar
• Zhao FJ, McGrath SP, Meharg AA. 2010. Arsenic as a food chain contaminant: mechanisms of plant uptake and metabolism and mitigation strategies. Annu Rev Plant Biol. 61:535–559. doi:10.1146/annurev-arplant-042809-112152.
   PubMed Web of Science ®Google Scholar