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Arsenic and nutrient absorption characteristics and antioxidant response in different leaves of two ryegrass (Lolium perenne) species under arsenic stress


Autoři: Jinbo Li aff001;  Qian Zhao aff001;  Bohan Xue aff001;  Hongyan Wu aff001;  Guilong Song aff001;  Xunzhong Zhang aff002
Působiště autorů: Institute of Turfgrass Science, Beijing Forestry University, Beijing, China aff001;  School of Plant and Environmental Sciences, Virginia Polytechnic Institute and State University, Blacksburg, Virginia, United States of America aff002
Vyšlo v časopise: PLoS ONE 14(11)
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.pone.0225373

Souhrn

Arsenic (As), a heavy metal element, causes soil environmental concerns in many parts of the world, and ryegrass has been considered as an effective plant species for bioremediation of heavy metal pollution including As. This study was designed to investigate As content, nutrient absorption and antioxidant enzyme activity associated with As tolerance in the mature leaves, expanded leaves and emerging leaves of perennial ryegrass (Lolium perenne) and annual ryegrass (Lolium multiflorum) under 100 mg·kg-1 As treatment. The contents of As, calcium (Ca), magnesium (Mg), manganese (Mn) in the leaves of both ryegrass species were greatest in the mature leaves and least in the emerging leaves. The nitrogen (N), phosphorus (P), potassium (K) contents of both ryegrass species were greatest in the emerging leaves and least in the mature leaves. The As treatment reduced biomass more in the mature leaves and expanded leaves relative to the emerging leaves for annual ryegrass and reduced more in emerging leaves relative to the mature and expanded leaves for perennial ryegrass. Perennial ryegrass had higher As content than annual ryegrass in all three kinds of leaves. The As treatment increased hydrogen peroxide (H2O2) in expanded leaves of two ryegrass species, relative to the control. The As treatment increased the ascorbate peroxidase (APX) activity in the expanded leaves of perennial ryegrass and the mature leaves of annual ryegrass, the catalase (CAT) activity in the mature and expanded leaves of perennial ryegrass and the emerging leaves of annual ryegrass, relative to the control. The As treatment reduced peroxidase (POD) activity in all three kinds of leaves of annual ryegrass and superoxide dismutase (SOD) activity in expanded leaves of perennial ryegrass, relative to the control. The results of this study suggest that As tolerance may vary among different ages of leaf and reactive oxygen species (ROS) and antioxidant enzyme activity may be associated with As tolerance in the ryegrass.

Klíčová slova:

Grasses – Plant resistance to abiotic stress – Leaves – Heavy metals – Antioxidants – Species delimitation – Ryegrass – Hydrogen peroxide


Zdroje

1. Kamnev AA, Lelie D, Van Der. Chemical and biological parameters as tools to evaluate and improve heavy metal phytoremediation. Bioscience Reports. 2000;20(4):239–58. doi: 10.1023/a:1026436806319 11092247

2. Meharg AA, Williams PN, Eureka A, Lawgali YY, Claire D, Antia V, et al. Geographical variation in total and inorganic arsenic content of polished (white) rice. Environ Sci Technol. 2009;43(5):1612–7. doi: 10.1021/es802612a 19350943

3. Govarthanan M, Mythili R, Selvankumar T, Kamala-Kannan S, Kim H. Myco-phytoremediation of arsenic- and lead-contaminated soils by Helianthus annuus and wood rot fungi, Trichoderma sp. isolated from decayed wood. Ecotoxicol Environ Saf. 2018;151:279–84. doi: 10.1016/j.ecoenv.2018.01.020 29407561

4. Carbonell AA, Aarabi MA, DeLaune RD, Gambrell RP, Patrick WH. Bioavailability and uptake of arsenic by wetland vegetation: Effects on plant growth and nutrition. Journal of Environmental Science and Health, Part A:Toxic/Hazardous Substances and Environmental Engineering. 1998;33(1):45–66. http://dx.doi.org/10.1080/10934529809376717.

5. Tewari RK, Kumar P, Sharma PN, Bisht SS. Modulation of oxidative stress responsive enzymes by excess cobalt. Plant Science. 2002;162(3):381–8. https://doi.org/10.1016/S0168-9452(01)00578-7.

6. Singh R, Upadhyay AK, Singh DP. Regulation of oxidative stress and mineral nutrient status by selenium in arsenic treated crop plant Oryza sativa. Ecotoxicol Environ Saf. 2018;148:105–13. Epub 2017/10/17. doi: 10.1016/j.ecoenv.2017.10.008 29035752.

7. Williams PN, Shofiqul I, Rafiqul I, Jahiruddin M,., Eureka A, Soliaman ARM, et al. Arsenic limits trace mineral nutrition (selenium, zinc, and nickel) in Bangladesh rice grain. Environ Sci Technol. 2009;43(21):8430–6. doi: 10.1021/es901825t 19924980

8. Tu C, Ma LQ. Effects of arsenic on concentration and distribution of nutrients in the fronds of the arsenic hyperaccumulator Pteris vittata L. Environmental Pollution. 2005;135(2):333–40. doi: 10.1016/j.envpol.2004.03.026 15734593

9. Wang HB, He HB, Yang GD, Ye CY, Niu BH, Lin WX. Effects of two species of inorganic arsenic on the nutrient physiology of rice seedlings. Acta Physiologiae Plantarum. 2010;32(2):245–51. https://doi.org/10.1007/s11738-009-0399-8.

10. Paez PL, Bazan CM, Bongiovanni ME, Toneatto J, Albesa I, Becerra MC, et al. Oxidative stress and antimicrobial activity of chromium(III) and ruthenium(II) complexes on Staphylococcus aureus and Escherichia coli. Biomed Res Int. 2013;2013:906912. Epub 2013/10/05. doi: 10.1155/2013/906912 24093107; PubMed Central PMCID: PMC3777176.

11. Dizdaroglu M, Jaruga P. Mechanisms of free radical-induced damage to DNA. Free Radic Res. 2012;46(4):382–419. Epub 2012/01/27. doi: 10.3109/10715762.2011.653969 22276778.

12. Srivastava S, Tripathi RD, Dwivedi UN. Synthesis of phytochelatins and modulation of antioxidants in response to cadmium stress in Cuscuta reflexa—an angiospermic parasite. J Plant Physiol. 2004;161(6):665–74. Epub 2004/07/23. doi: 10.1078/0176-1617-01274 15266713.

13. Duan GL, Zhu YG, Tong YP, Cai C, Kneer R. Characterization of arsenate reductase in the extract of roots and fronds of Chinese brake fern, an arsenic hyperaccumulator. Plant Physiol. 2005;138(1):461–9. Epub 2005/04/19. doi: 10.1104/pp.104.057422 15834011; PubMed Central PMCID: PMC1104199.

14. Moller IM, Jensen PE, Hansson A. Oxidative modifications to cellular components in plants. Annu Rev Plant Biol. 2007;58:459–81. Epub 2007/02/10. doi: 10.1146/annurev.arplant.58.032806.103946 17288534.

15. Hartley-Whitaker J, Ainsworth G, Meharg AA. Copper- and arsenate-induced oxidative stress in Holcus lanatus L. cloneswith differential sensitivity. Plant Cell & Environment. 2001;24(7):713–22. https://doi.org/10.1046/j.0016-8025.2001.00721.x.

16. Lee Y, Kim H, Kim S, Park A, Kim Y-J, Han T, et al. The effects of silver and arsenic on antioxidant system in Lemna paucicostata: Different effects on glutathione system. Toxicol Environ Health Sci. 2016;8(5):332–40. https://doi.org/10.1007/s13530-016-0294-9.

17. Shri M, Kumar S, Chakrabarty D, Trivedi PK, Mallick S, Misra P, et al. Effect of arsenic on growth, oxidative stress, and antioxidant system in rice seedlings. Ecotoxicol Environ Saf. 2009;72(4):1102–10. Epub 2008/11/18. doi: 10.1016/j.ecoenv.2008.09.022 19013643.

18. Srivastava S, Sinha P, Sharma YK. Status of photosynthetic pigments, lipid peroxidation and anti-oxidative enzymes in Vigna mungoin presence of arsenic. Journal of Plant Nutrition. 2016;40(3):298–306. https://doi.org/10.1080/01904167.2016.1240189.

19. Wang MC, Chen YT, Chen SH, Chang Chien SW, Sunkara SV. Phytoremediation of pyrene contaminated soils amended with compost and planted with ryegrass and alfalfa. Chemosphere. 2012;87(3):217–25. Epub 2012/01/17. doi: 10.1016/j.chemosphere.2011.12.063 22245074.

20. Xu PX. Studies on cadmium tolerance and detoxification in tall fescue and kentucky bluegrass [dissertation]: Shanghai Jiaotong University; 2014.

21. Velikova V, Yordanov I, Edreva A. Oxidative stress and some antioxidant systems in acid rain-treated bean plants: Protective role of exogenous polyamines. Plant Science. 2000;151(1):59–66. https://doi.org/10.1016/S0168-9452(99)00197-1.

22. Schneider K,., Schlegel HG. Production of superoxide radicals by soluble hydrogenase from Alcaligenes eutrophus H16. Biochemical Journal. 1981;193(1):99–107. doi: 10.1042/bj1930099 6272708

23. Zhang J, Kirkham MB. Enzymatic responses of the ascorbate-glutathione cycle to drought in sorghum and sunflower plants. Plant Science. 1996;113(2):139–47. https://doi.org/10.1016/0168-9452(95)04295-4.

24. Giannopolitis CN, Ries SK. Superoxide dismutases: I. Occurrence in higher plants. Plant Physiology. 1977;59(2):309–14. doi: 10.1104/pp.59.2.309 16659839

25. Karimi N, Shayesteh LS, Ghasmpour H, Alavi M. Effects of Arsenic on Growth, Photosynthetic Activity, and Accumulation in Two New Hyperaccumulating Populations of Isatis cappadocica Desv. J Plant Growth Regul. 2013;32(4):823–30. https://doi.org/10.1007/s00344-013-9350-8.

26. Liu Q, Zheng C, Hu CX, Tan Q, Sun XC, Su JJ. Effects of high concentrations of soil arsenic on the growth of winter wheat (Triticum aestivum L.) and rape (Brassica napus). Plant Soil Environ. 2012;58(1):22–7. https://doi.org/10.2134/agronj2011.0260.

27. Ahsan N, Lee DG, Alam I, Kim PJ, Lee JJ, Ahn YO, et al. Comparative proteomic study of arsenic-induced differentially expressed proteins in rice roots reveals glutathione plays a central role during As stress. Proteomics. 2008;8(17):3561–76. Epub 2008/08/30. doi: 10.1002/pmic.200701189 18752204.

28. Ullrich-Eberius CI, Sanz A, Novacky AJ. Evaluation of Arsenate- and Vanadate-Associated Changes of Electrical Membrane Potential and Phosphate Transport in Lemna gibba G1. Journal of Experimental Botany. 1989;40(210):119–28. http://doi.org/10.1093/jxb/40.1.119.

29. Lefevre I, Vogel-Mikus K, Jeromel L, Vavpetic P, Planchon S, Arcon I, et al. Differential cadmium and zinc distribution in relation to their physiological impact in the leaves of the accumulating Zygophyllum fabago L. Plant Cell Environ. 2014;37(6):1299–320. Epub 2013/11/19. doi: 10.1111/pce.12234 24237383.

30. Baxter I, Dilkes BP. Elemental profiles reflect plant adaptations to the environment. Science. 2012;336(6089):1661–3. doi: 10.1126/science.1219992 22745418

31. Finnegan PM, Chen W. Arsenic toxicity: the effects on plant metabolism. Front Physiol. 2012;3(182):182. https://doi.org/10.3389/fphys.2012.00182.

32. Verbruggen N, Hermans C, Schat H. Mechanisms to cope with arsenic or cadmium excess in plants. Curr Opin Plant Biol. 2009;12(3):364–72. Epub 2009/06/09. doi: 10.1016/j.pbi.2009.05.001 19501016.

33. Duan G, Liu W, Chen X, Hu Y, Zhu Y. Association of arsenic with nutrient elements in rice plants. Metallomics. 2013;5(7). https://doi.org/10.1039/c3mt20277a.

34. Ghosh S, Saha J, Biswas AK. Interactive influence of arsenate and selenate on growth and nitrogen metabolism in wheat (Triticum aestivum L.) seedlings. Acta Physiologiae Plantarum. 2013;35(6):1873–85. https://doi.org/10.1007/s11738-013-1225-x.

35. Pigna M, Cozzolino V, Violante A, Meharg AA. Influence of Phosphate on the Arsenic Uptake by Wheat (Triticum durum L.) Irrigated with Arsenic Solutions at Three Different Concentrations. Water, Air, and Soil Pollution. 2009;197(1–4):371–80. https://doi.org/10.1007/s11270-008-9818-5.

36. Fayiga AO, Ma LQ. Using phosphate rock to immobilize metals in soil and increase arsenic uptake by hyperaccumulator Pteris vittata. Sci Total Environ. 2006;359(1–3):17–25. Epub 2005/06/30. doi: 10.1016/j.scitotenv.2005.06.001 15985282.

37. Cakmak I. The role of potassium in alleviating detrimental effects of abiotic stresses in plants. J Plant Nutr Soil Sci. 2005;168(4):521–30. https://doi.org/10.1002/jpln.200420485.

38. Lombi E, Zhao FJ, Fuhrmann M, Ma LQ, Mcgrath SP. Arsenic Distribution and Speciation in the Fronds of the Hyperaccumulator Pteris vittata. New Phytologist. 2002;156(2):195–203. http://doi.org/10.1046/j.1469-8137.2002.00512.x.

39. Shaibur MR, Sera K, Kawai S. Effect of arsenic on concentrations and translocations of mineral elements in the xylem of rice. Journal of Plant Nutrition. 2015;39(3):365–76. http://dx.doi.org/10.1080/01904167.2015.1016171.

40. Shaibur MR, Kitajima N, Huq SMI, Kawai S. Arsenic–iron interaction: Effect of additional iron on arsenic-induced chlorosis in barley grown in water culture. Soil Science and Plant Nutrition. 2009;55(6):739–46. https://doi.org/10.1111/j.1747-0765.2009.00414.x.

41. Jutamanee K, Ngennoy S. Effect of Magnesium and Manganese Sprays on SPAD Readings and Chlorophyll Content of Chlorotic Leaves of Jackfruit. Acta Hort. 2013;984(984):163–9. https://doi.org/10.17660/ActaHortic.2013.984.17.

42. Stovea N, Berova M, Zlatev Z. Effect of arsenic on some physiological parameters in bean plants. Biologia Plantarum. 2005;49(2):293–6. https://doi.org/10.1007/s10535-005-3296-z.

43. Shaibur MR, Kitajima N, Sugawara R, Kondo T, Huq SMI, Kawai S. Effect of arsenic on phytosiderophores and mineral nutrition of barley seedlings grown in iron-depleted medium. Soil Science and Plant Nutrition. 2009;55(2):283–93. https://doi.org/10.1111/j.1747-0765.2009.00360.x.

44. Gunes A, Pilbeam DJ, Inal A. Effect of arsenic–phosphorus interaction on arsenic-induced oxidative stress in chickpea plants. Plant and Soil. 2008;314(1–2):211–20. http://doi.org/10.1007/s11104-008-9719-9.

45. Souri Z, Karimi N, Sandalio LM. Arsenic Hyperaccumulation Strategies: An Overview. Front Cell Dev Biol. 2017;5:67. Epub 2017/08/05. doi: 10.3389/fcell.2017.00067 28770198; PubMed Central PMCID: PMC5513893.

46. Molassiotis AN, Sotiropoulos T, Tanou G, Kofidis G, Diamantidis G, Therios I. Antioxidant and anatomical responses in shoot culture of the apple rootstock MM 106 treated with NaCl, KCl, mannitol or sorbitol. Biologia Plantarum. 2006;50(3):331–8. https://doi.org/10.1007/s10535-005-0075-9.

47. Imtiaz M, Tu S, Xie Z, Han D, Ashraf M, Rizwan MS. Growth, V uptake, and antioxidant enzymes responses of chickpea (Cicer arietinum L.) genotypes under vanadium stress. Plant and Soil. 2015;390(1–2):17–27. https://doi.org/10.1007/s11104-014-2341-0.

48. Mittler R. Oxidative stress, antioxidants and stress tolerance. Trends in Plant Science. 2002;7(9):405–10. doi: 10.1016/s1360-1385(02)02312-9 12234732

49. Mylona PV, Polidoros AN, Scandalios JG. Modulation of antioxidant responses by arsenic in maize. Free Radical Biology & Medicine. 1998;25(4–5):576–85. http://doi.org/10.1016/S0891-5849(98)00090-2.

50. Srivastava M, Ma LQ, Singh N, Singh S. Antioxidant responses of hyper-accumulator and sensitive fern species to arsenic. J Exp Bot. 2005;56(415):1335–42. Epub 2005/03/23. doi: 10.1093/jxb/eri134 15781440.

51. Ghosh M, Singh SP. A comparative study of cadmium phytoextraction by accumulator and weed species. Environ Pollut. 2005;133(2):365–71. Epub 2004/11/03. doi: 10.1016/j.envpol.2004.05.015 15519467.

52. Sabreen S, Sugiyama SI. Cadmium Phytoextraction Capacity in Eight C3 Herbage Grass Species. Grassland Science. 2010;54(1):27–32. http://doi.org/10.1111/j.1744-697X.2008.00101.x.

53. Guo J, Feng R, Ding Y, Wang R. Applying carbon dioxide, plant growth-promoting rhizobacterium and EDTA can enhance the phytoremediation efficiency of ryegrass in a soil polluted with zinc, arsenic, cadmium and lead. J Environ Manage. 2014;141(2014):1–8. Epub 2014/04/26. doi: 10.1016/j.jenvman.2013.12.039 24762567.

54. Hartley W, Lepp NW. Effect of in situ soil amendments on arsenic uptake in successive harvests of ryegrass (Lolium perenne cv Elka) grown in amended As-polluted soils. Environ Pollut. 2008;156(3):1030–40. Epub 2008/06/06. doi: 10.1016/j.envpol.2008.04.024 18524441.


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