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Deciphering lead tolerance mechanisms in a population of the plant species Biscutella auriculata L. from a mining area: Accumulation strategies and antioxidant defenses

Peco, J.D., Higueras, P., Campos, J.A., Olmedilla, A., Romero-Puertas, M.C., Sandalio, L.M.·2020·Chemosphere
DOI 10.1016/j.chemosphere.2020.127721
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Research works printed but not linked: 96

  1. Alarcón, 2019, Auxin modulated initiation of lateral roots is linked to pericycle cell length in maize, Front. Plant Sci., 10, 1, 10.3389/fpls.2019.00011 · DOI
  2. Ali, 2013, Phytoremediation of heavy metals-Concepts and applications, Chemosphere, 91, 869, 10.1016/j.chemosphere.2013.01.075 · DOI · Paper page
  3. Alscher, 2002, Role of superoxide dismutases (SODs) in controlling oxidative stress in plants, J. Exp. Bot., 53, 1331, 10.1093/jexbot/53.372.1331 · DOI · Paper page
  4. Andra, 2009, Induction of lead-binding phytochelatins in vetiver grass [Vetiveria zizanioides (L.)], J. Environ. Qual., 38, 868, 10.2134/jeq2008.0316 · DOI
  5. Bai, 2014, Effects of lead and nitric oxide on photosynthesis, antioxidative ability, and mineral element content of perennial ryegrass, Biol. Plant. (Prague), 59, 163, 10.1007/s10535-014-0476-8 · DOI
  6. Batista, 2017, Induced changes in the growth of four plant species due to lead toxicity, Rev. Bras. Eng. Agrícola Ambient., 21, 327, 10.1590/1807-1929/agriambi.v21n5p327-332 · doi:10.1590/1807-1929/agriambi.v21n5p327-332
  7. Beauchamp, 1971, Superoxide dismutase: improved assays and an assay applicable to acrylamide gels, Anal. Biochem., 44, 276, 10.1016/0003-2697(71)90370-8 · DOI · Paper page
  8. Benavides, 2005, Cadmium toxicity in plants. Toxic metals in plants, Braz. J. Plant Physiol., 17, 21, 10.1590/S1677-04202005000100003 · DOI · Paper page
  9. Bezerril, 2017, Effect of lead on physiological and antioxidant responses in two Vigna unguiculata cultivars differing in Pb-accumulation, Chemosphere, 176, 397, 10.1016/j.chemosphere.2017.02.072 · doi:10.1016/j.chemosphere.2017.02.072
  10. Bradford, 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, 10.1016/0003-2697(76)90527-3 · DOI · Paper page
  11. Buege, 1978, Microsomal lipid peroxidation, Methods Enzymol., 52, 302, 10.1016/S0076-6879(78)52032-6 · DOI · Paper page
  12. Calabrese, 2009, Hormesis and plant biology, Environ. Pollut., 157, 42, 10.1016/j.envpol.2008.07.028 · DOI · Paper page
  13. Chandrasekhar, 2019, Lead accumulation, growth responses and biochemical changes of three plant species exposed to soil amended with different concentrations of lead nitrate, Ecotoxicol. Environ. Saf., 171, 26, 10.1016/j.ecoenv.2018.12.058 · DOI
  14. Chatterjee, 2004, Detrimental effects of lead phytotoxicity on growth, yield, and metabolism of rice, Commun. Soil Sci. Plant Anal., 35, 255, 10.1081/CSS-120027648 · DOI
  15. Cutright, 2012, Evaluation of the phytoextraction potential at an acid-mine-drainage-impacted site, Soil Sediment Contam., 21, 970, 10.1080/15320383.2012.712070 · doi:10.1080/15320383.2012.712070
  16. del Río, 1991, Nutritional effect and expression of SODs: induction and gene expression; diagnostics; prospective protection against oxygen toxicity, Free Radic. Res. Commun., 12–13, 819, 10.3109/10715769109145863 · doi:10.3109/10715769109145863
  17. Dickinson, 2016, Phytoremediation. Encycl. Appl. Plant Sci., 3, 327
  18. El-Zohri, 2005, Quantification of phytochelatins in plants by reversed-phase HPLC–ESI–MS–MS, Anal. Bioanal. Chem., 382, 1871, 10.1007/s00216-005-3331-0 · doi:10.1007/s00216-005-3331-0
  19. Escarré, 2011, Heavy metal concentration survey in soils and plants of the les malines mining district (southern France): implications for soil restoration. Water, Air, Soil Pollut, 216, 485, 10.1007/s11270-010-0547-1 · DOI · Paper page
  20. Fahr, 2013, Effect of lead on root growth, Front. Plant Sci., 4, 175, 10.3389/fpls.2013.00175 · DOI · Paper page
  21. Farooq, 2013, Alleviation of cadmium toxicity by silicon is related to elevated photosynthesis, antioxidant enzymes; suppressed cadmium uptake and oxidative stress in cotton, Ecotoxicol. Environ. Saf., 96, 242, 10.1016/j.ecoenv.2013.07.006 · DOI · Paper page
  22. Fellet, 2012, Metallophytes and thallium hyperaccumulation at the former Raibl lead/zinc mining site (Julian Alps, Italy), Plant Biosyst., 146, 1023, 10.1080/11263504.2012.703250 · DOI
  23. Fischer, 2014, Analysis of plant Pb tolerance at realistic submicromolar concentrations demonstrates the role of phytochelatin synthesis for Pb detoxification, Environ. Sci. Technol., 48, 7552, 10.1021/es405234p · DOI
  24. Flores-Cáceres, 2015, Specific mechanisms of tolerance to copper and cadmium are compromised by a limited concentration of glutathione in alfalfa plants, Plant Sci., 233, 165, 10.1016/j.plantsci.2015.01.013 · DOI
  25. García, 2017, Response of Lupinus albus to Pb–EDTA indicates relatively high tolerance, Toxicol. Environ. Chem., 99, 1378, 10.1080/02772248.2017.1387263 · DOI · Paper page
  26. Gill, 2013, Importance of nitric oxide in cadmium stress tolerance in crop plants, Plant Physiol. Biochem., 63, 254, 10.1016/j.plaphy.2012.12.001 · DOI · Paper page
  27. Gupta, 2009, Antioxidant defense mechanism in hydroponically grown Zea mays seedlings under moderate lead stress, J. Hazard Mater., 172, 479, 10.1016/j.jhazmat.2009.06.141 · DOI · Paper page
  28. Habig, 1974, Glutathione S-transferases the first enzymatic step in mercapturic acid formation, J. Biol. Chem., 249, 7130, 10.1016/S0021-9258(19)42083-8 · DOI · Paper page
  29. Hadi, 2010, The improved phytoextraction of lead (Pb) and the growth of maize (Zea mays L.): the role of plant growth regulators (GA3 and IAA) and EDTA alone and in combinations, Chemosphere, 80, 457, 10.1016/j.chemosphere.2010.04.020 · DOI · Paper page
  30. Hafsi, 2010, Moderate salinity enhances the antioxidative response in the halophyte Hordeum maritimum L. under potassium deficiency, Environ. Exp. Bot., 69, 129, 10.1016/j.envexpbot.2010.04.008 · DOI
  31. Hernández, 2009, How relevant are flavonoids as antioxidants in plants?, Trends Plant Sci., 14, 125, 10.1016/j.tplants.2008.12.003 · DOI · Paper page
  32. Hoagland, 1950, The water-culture method for growing plants without soil, Circ. Calif. Agric. Exp. Stn., 347, 32
  33. Islam, 2008, Effect of Pb toxicity on leaf growth, physiology and ultrastructure in the two ecotypes of Elsholtzia argyi, J. Hazard Mater., 154, 914, 10.1016/j.jhazmat.2007.10.121 · DOI · Paper page
  34. Jiménez-Escrig, 2003, In vitro antioxidant activities of edible artichoke (Cynara scolymus L.) and effect on biomarkers of antioxidants in rats, J. Agric. Food Chem., 51, 5540, 10.1021/jf030047e · DOI · Paper page
  35. Kim, 2002, Pb and Cd uptake in rice roots, Physiol. Plantarum, 116, 368, 10.1034/j.1399-3054.2002.1160312.x · DOI · Paper page
  36. Kopittke, 2007, Toxic effects of Ni2+ on growth of cowpea (Vigna unguiculata), Plant Soil, 292, 283, 10.1007/s11104-007-9226-4 · doi:10.1007/s11104-007-9226-4
  37. Kuhn, 2011, Flavonols accumulate asymmetrically and affect auxin transport in Arabidopsis, Plant Physiol., 156, 585, 10.1104/pp.111.175976 · DOI · Paper page
  38. Kumar, 2015, Heavy metal lead inflective toxicity and its assessment in phytoremediating plants - a Review, Water Air Soil Pollut., 226, 324, 10.1007/s11270-015-2547-7 · DOI
  39. Kumar, 2018, Plant-lead interactions: transport, toxicity, tolerance and detoxification mechanisms, Ecotoxicol. Environ. Saf., 166, 401, 10.1016/j.ecoenv.2018.09.113 · DOI · Paper page
  40. LaCoste, 1999, The phytoremediation potential of thallium-contaminated soils using Iberis and Biscutella species, Int. J. Phytoremediation, 1, 327, 10.1080/15226519908500023 · DOI
  41. León, 2002, Antioxidative enzymes in cultivars of pepper plants with different sensitivity to cadmium, Plant Physiol. Biochem., 40, 813, 10.1016/S0981-9428(02)01444-4 · DOI · Paper page
  42. Li, 2019, GSNOR provides plant tolerance to iron toxicity via preventing iron-dependent nitrosative and oxidative cytotoxicity, Nat. Commun., 10, 1
  43. Lichtenthaler, 2001, Chlorophylls and carotenoids: measurement and characterization by UV-VIS spectroscopy, Curr. Protoc. Food Anal. Chem., 1, F4.3.1, 10.1002/0471142913.faf0403s01 · DOI · Paper page
  44. Mahdavian, 2016, Pb accumulation, Pb tolerance, antioxidants, thiols, and organic acids in metallicolous and non-metallicolous Peganum harmala L. under Pb exposure, Environ. Exp. Bot., 126, 21, 10.1016/j.envexpbot.2016.01.010 · DOI · Paper page
  45. Małecka, 2008, Accumulation of lead in root cells of Pisum sativum, Acta Physiol. Plant., 30, 629, 10.1007/s11738-008-0159-1 · DOI
  46. Melo, 2009, Accumulation of arsenic and nutrients by castor bean plants grown on an As-enriched nutrient solution, J. Hazard Mater., 168, 479, 10.1016/j.jhazmat.2009.02.048 · DOI
  47. Meyers, 2008, Uptake and localisation of lead in the root system of Brassica juncea, Environ. Pollut., 153, 323, 10.1016/j.envpol.2007.08.029 · DOI · Paper page
  48. Michniewicz, 2019, Transporter of IBA1 links auxin and cytokinin to influence root architecture, Dev. Cell, 50, 599, 10.1016/j.devcel.2019.06.010 · doi:10.1016/j.devcel.2019.06.010
  49. Mohtadi, 2012, A comparison of lead accumulation and tolerance among heavy metal hyperaccumulating and non-hyperaccumulating metallophytes, Plant Soil, 352, 267, 10.1007/s11104-011-0994-5 · DOI
  50. Mroczek-Zdyrska, 2012, The influence of selenium on root growth and oxidative stress induced by lead in Vicia faba L. minor plants, Biol. Trace Elem. Res., 147, 320, 10.1007/s12011-011-9292-6 · DOI · Paper page
  51. Nakatsubo, 1998, Direct evidence of nitric oxide production from bovine aortic endothelial cells using new fluorescence indicators: Diaminofluoresceins, FEBS Lett., 427, 263, 10.1016/S0014-5793(98)00440-2 · DOI · Paper page
  52. Ortega-Galisteo, 2012, S-Nitrosylated proteins in pea (Pisum sativum L.) leaf peroxisomes: changes under abiotic stress, J. Exp. Bot., 63, 2089, 10.1093/jxb/err414 · DOI · Paper page
  53. Pavoni, 2017, Bioaccumulation of thallium and other trace metals in Biscutella laevigata nearby a decommissioned zinc-lead mine (Northeastern Italian Alps), J. Environ. Manag., 186, 214
  54. Pawlak-Sprada, 2011, Activation of phenylpropanoid pathway in legume plants exposed to heavy metals . Part I . Effects of cadmium and lead on phenylalanine ammonia-lyase gene expression , enzyme activity and lignin content, Acta Biochim. Pol., 58, 211, 10.18388/abp.2011_2267 · DOI
  55. Peco, 2020, Characterization of mechanisms involved in tolerance and accumulation of Cd in Biscutella auriculata L, Ecotoxicol. Environ. Saf., 201, 110784, 10.1016/j.ecoenv.2020.110784 · DOI
  56. Pena, 2015, Early response of wheat seminal roots growing under copper excess, Plant Physiol. Biochem., 87, 115, 10.1016/j.plaphy.2014.12.021 · doi:10.1016/j.plaphy.2014.12.021
  57. Pereira, 2016, Cadmium tolerance in Schinus molle trees is modulated by enhanced leaf anatomy and photosynthesis, Trees Struct. Funct., 30, 807, 10.1007/s00468-015-1322-0 · DOI
  58. Pielichowska, 2004, Uptake and localization of cadmium by Biscutella laevigata, a cadmium hyperaccumulator, Acta Biol. Cracoviensia, 46, 57
  59. Poschenrieder, 2013, Do toxic ions induce hormesis in plants?, Plant Sci., 212, 15, 10.1016/j.plantsci.2013.07.012 · DOI · Paper page
  60. Pošćić, 2013, Hyperaccumulation of thallium is population-specific and uncorrelated with caesium accumulation in the thallium hyperaccumulator, Biscutella laevigata, Plant Soil, 365, 81, 10.1007/s11104-012-1384-3 · doi:10.1007/s11104-012-1384-3
  61. Pourrut, 2011, Lead uptake, toxicity, and detoxification in plants, Rev. Environ. Contam. Toxicol., 213, 113
  62. Rodríguez, 2009, Heavy metal distribution and chemical speciation in tailings and soils around a Pb-Zn mine in Spain, J. Environ. Manag., 90, 1106
  63. Romero-Puertas, 2018, Reactive oxygen and nitrogen species as key indicators of plant responses to Cd stress, Environ. Exp. Bot., 161, 107, 10.1016/j.envexpbot.2018.10.012 · DOI
  64. Romero-Puertas, 2004, Cadmium-induced subcellular accumulation of O2·− and H2O2 in pea leaves, Plant Cell Environ., 27, 1122, 10.1111/j.1365-3040.2004.01217.x · DOI · Paper page
  65. Ruiz, 2009, Phytoextraction of metal polluted soils around a Pb-Zn mine by crop plants, Int. J. Phytoremediation, 11, 360, 10.1080/15226510802565568 · DOI
  66. Sadeghipour, 2017, Nitric oxide increases Pb tolerance by lowering Pb uptake and translocation as well as phytohormonal changes in cowpea (Vigna unguiculata (L.) Walp.), Sains Malays., 46, 189, 10.17576/jsm-2017-4602-02 · doi:10.17576/jsm-2017-4602-02
  67. Saleem, 2018, Impact of lead tolerant plant growth promoting rhizobacteria on growth, physiology, antioxidant activities, yield and lead content in sunflower in lead contaminated soil, Chemosphere, 195, 606, 10.1016/j.chemosphere.2017.12.117 · DOI
  68. Sanz-Fernández, 2017, Screening Arabidopsis mutants in genes useful for phytoremediation, J. Hazard Mater., 335, 143, 10.1016/j.jhazmat.2017.04.021 · DOI
  69. Seregin, 2011, Histochemical methods for detection of heavy metals and strontium in the tissues of higher plants, Russ. J. Plant Physiol., 58, 721, 10.1134/S1021443711040133 · DOI
  70. Seregin, 2004, Distribution and toxic effects of cadmium and lead on maize roots, Russ. J. Plant Physiol., 51, 525, 10.1023/B:RUPP.0000035747.42399.84 · DOI · Paper page
  71. Sharma, 2012, Reactive Oxygen Species, oxidative damage, and antioxidative defense mechanism in plants under stressful conditions, J. Bot., Le, 1
  72. Sidhu, 2016, Effect of lead on oxidative status, antioxidative response and metal accumulation in Coronopus didymus, Plant Physiol. Biochem., 105, 290, 10.1016/j.plaphy.2016.05.019 · DOI
  73. Sidhu, 2018, Phytoremediation of lead by a wild, non-edible Pb accumulator Coronopus didymus (L.) Brassicaceae, Int. J. Phytoremediation, 20, 483, 10.1080/15226514.2017.1374331 · doi:10.1080/15226514.2017.1374331
  74. Sima, 2012, Determination of peroxidase activity, total phenolic and flavonoid compounds due to lead toxicity in Medicago sativa L, Adv. Environ. Biol., 6, 2357
  75. Sims, 2002, Relationships between leaf pigment content and spectral reflectance across a wide range of species, leaf structures and developmental stages, Remote Sens. Environ., 81, 337, 10.1016/S0034-4257(02)00010-X · DOI · Paper page
  76. Singleton, 1965, Colorimetry of total phenolics with phosphomolybdic-phosphotungstic acid reagents, Am. J. Enol. Vitic., 16, 144, 10.5344/ajev.1965.16.3.144 · DOI · Paper page
  77. Sinha, 2006, Alteration in uptake and translocation of essential nutrients in cabbage by excess lead, Chemosphere, 65, 651, 10.1016/j.chemosphere.2006.01.068 · DOI
  78. Souri, 2020, Nitric oxide improves tolerance to arsenic stress in Isatis cappadocica desv. Shoots by enhancing antioxidant defenses, Chemosphere, 239, 124523, 10.1016/j.chemosphere.2019.124523 · DOI
  79. Srivalli, 2001, Induction of new isoforms of superoxide dismutase and catalase enzymes in the flag leaf of wheat during monocarpic senescence, Biochem. Biophys. Res. Commun., 288, 1037, 10.1006/bbrc.2001.5843 · doi:10.1006/bbrc.2001.5843
  80. Sytar, 2013, Heavy metal-induced oxidative damage, defense reactions, and detoxification mechanisms in plants, Acta Physiol. Plant., 35, 985, 10.1007/s11738-012-1169-6 · DOI · Paper page
  81. Terrón-Camero, 2019, Role of nitric oxide in plant responses to heavy metal stress: exogenous application versus endogenous production, J. Exp. Bot., 70, 4477, 10.1093/jxb/erz184 · DOI
  82. Terrón-Camero, 2020, Low endogenous NO levels in roots and antioxidant systems are determinants for the resistance of Arabidopsis seedlings grown in Cd, Environ. Pollut., 256, 113411, 10.1016/j.envpol.2019.113411 · DOI
  83. Thakur, 2012, Leaf temperature as thermal bio-indicator of heavy metal pollutants, J. Agric. Sci. Technol., 2, 131
  84. Turull, 2017, Phytochelatin synthesis in response to Hg uptake in aquatic plants near a chlor-alkali factory, Chemosphere, 176, 74, 10.1016/j.chemosphere.2017.02.092 · doi:10.1016/j.chemosphere.2017.02.092
  85. Venkatachalam, 2017, Accumulation efficiency, genotoxicity and antioxidant defense mechanisms in medicinal plant Acalypha indica L. under lead stress, Chemosphere, 171, 544, 10.1016/j.chemosphere.2016.12.092 · DOI
  86. Weryszko-Chmielewska, 2005, Lead-Induced histological and ultrastructural changes in the leaves of Soybean (Glycine max (L.) Merr.), Soil Sci. Plant Nutr., 51, 203, 10.1111/j.1747-0765.2005.tb00024.x · DOI
  87. Whitacre, 2015, Lead uptake, toxicity, and detoxification in plants, In: Rev. Environ. Contam. Toxicol. D.M. Whitacre (ed.),, 233, 113
  88. Wierzbicka, 2004, Adaptation of Biscutella laevigata L, a metal hyperaccumulator, to growth on a zinc–lead waste heap in southern Poland: I: differences between waste-heap and mountain populations, Chemosphere, 54, 1663, 10.1016/j.chemosphere.2003.08.031 · doi:10.1016/j.chemosphere.2003.08.031
  89. Wierzbicka, 2016, Thallium hyperaccumulation in polish populations of Biscutella laevigata (Brassicaceae), Acta Biol. Cracoviensia s. Bot., 58
  90. Wojas, 2010, The role of subcellular distribution of cadmium and phytochelatins in the generation of distinct phenotypes of AtPCS1- and CePCS3-expressing tobacco, J. Plant Physiol., 167, 981, 10.1016/j.jplph.2010.02.010 · DOI
  91. Wuana, 2014, Heavy metals in contaminated soils: a review of sources, chemistry, risks, and best available strategies for remediation, Heavy Met. Contam. Water Soil Anal. Assessment, Remediat. Strateg., 2011, 1
  92. Xiong, 2009, Exogenous nitric oxide enhances cadmium tolerance of rice by increasing pectin and hemicellulose contents in root cell wall, Planta, 230, 755, 10.1007/s00425-009-0984-5 · DOI · Paper page
  93. Yu, 2012, Lead-induced nitric oxide generation plays a critical role in lead uptake by Pogonatherum crinitum root cells, Plant Cell Physiol., 53, 1728, 10.1093/pcp/pcs116 · DOI
  94. Zafari, 2017, Nitric oxide production shifts metabolic pathways toward lignification to alleviate Pb stress in Prosopis farcta, Environ. Exp. Bot., 141, 41, 10.1016/j.envexpbot.2017.06.011 · doi:10.1016/j.envexpbot.2017.06.011
  95. Zheng, 2012, Pb-induced ultrastructural alterations and subcellular localization of Pb in two species of Lespedeza by TEM-coupled electron energy loss spectroscopy, Environ. Exp. Bot., 77, 196, 10.1016/j.envexpbot.2011.11.018 · DOI
  96. Zhishen, 1999, The determination of flavonoid contents in mulberry and their scavenging effects on superoxide radicals, Food Chem., 64, 555, 10.1016/S0308-8146(98)00102-2 · DOI · Paper page

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Metadata

Authors
Peco, J. D., Higueras, P., Campos, J. A., Olmedilla, A., Romero-Puertas, M. C., & Sandalio, L. M.
Venue
Chemosphere
Publisher
Elsevier BV
Published
2020-12
Volume
261
Pages
127721
ISSN
0045-6535
DOI
10.1016/j.chemosphere.2020.127721
Cited by
32
References
1
Language
en
Licence
  • www.elsevier.com/tdm/userlicense/1.0/ (tdm)
  • www.elsevier.com/legal/tdmrep-license (tdm)
Funders
Ministerio de Ciencia, Innovación y Universidades (PGC 2018-098372-B-100, CGL 2015-67644-R, SBPLY/17/180501/000273)

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CoChat. (2026). Citation check: Deciphering lead tolerance mechanisms in a population of the plant species Biscutella auriculata L. from a mining area: Accumulation strategies and antioxidant defenses. https://app.cochat.ai/papers/10.1016/j.chemosphere.2020.127721
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Peco, J. D., Higueras, P., Campos, J. A., Olmedilla, A., Romero-Puertas, M. C., & Sandalio, L. M. (2020). Deciphering lead tolerance mechanisms in a population of the plant species Biscutella auriculata L. from a mining area: Accumulation strategies and antioxidant defenses. Chemosphere. https://doi.org/10.1016/j.chemosphere.2020.127721

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