Analysis of changes in growth parameters and primary root architecture of Arabidopsis thaliana under the influence of copper and iron oxide nanoparticles

Authors

  • Maryia I. Aliakseyeva Belarusian State University, 4 Niezaliezhnasci Avenue, Minsk 220030, Belarus
  • Anna O. Muravitskaya Belarusian State University, 4 Niezaliezhnasci Avenue, Minsk 220030, Belarus
  • Viera S. Mackievic Belarusian State University, 4 Niezaliezhnasci Avenue, Minsk 220030, Belarus
  • Veranika V. Samokhina Belarusian State University, 4 Niezaliezhnasci Avenue, Minsk 220030, Belarus
  • Veranika V. Tarima Belarusian State University, 4 Niezaliezhnasci Avenue, Minsk 220030, Belarus
  • Palina A. Muchinskaya Belarusian State University, 4 Niezaliezhnasci Avenue, Minsk 220030, Belarus
  • Natalia L. Pshybytko Belarusian State University, 4 Niezaliezhnasci Avenue, Minsk 220030, Belarus
  • Vadim V. Demidchik V. F. Kuprevich Institute of Experimental Botany, National Academy of Sciences of Belarus, 27 Akademichnaja Street, Minsk 220072, Belarus

Keywords:

iron oxide nanoparticles, copper oxide nanoparticles, Arabidopsis thaliana, plant growth and development, plant root, nanofertilisers
Supporting Agencies
This work was carried out with financial support from the Belarusian Republican Foundation for Fundamental Research within the framework of projects B25KI-086 and B24-060-1, as well as assignment 2.04.5 «Establishing the patterns of toxic effects of metal-containing atmospheric nanopollutants on physiological processes in higher plants» of the state programme of scientific research «Natural resources and environment» for 2021–2025 (state registration No. 20211705).

Abstract

Nanoparticles containing copper and iron oxides are increasingly used in agriculture as nanofertilisers. Despite this, the question of their toxicity for plant organism remains unresolved. To address this, it is necessary to conduct researches on model objects under standardised conditions. This paper presented the results of experiments on the effect of copper oxide nanoparticles (here and further – CuO-NPs) and iron oxide nanoparticles (here and further – Fe3O4-NPs) on the growth parameters and primary root architecture of Arabidopsis thaliana (L.) Heynh. in vertical culture in vitro. Treatment with CuO-NPs at concentrations of 10 and 30 mg/L and Fe3O4-NPs at concentrations of 30; 100 and 300 mg/L stimulated the primary root growth of A. thaliana, while application of CuO-NPs at concentrations above 100 mg/L and Fe3O4-NPs at concentrations above 300 mg/L inhibited this process. It was found that CuO-NPs exhibit lower toxicity than the ionic form Cu2+ (CuCl2) introduced into the gel medium at the same concentrations as the mentioned nanoparticles. Treatment with the studied nanoparticles led to a modification of the primary root architecture: the diameter of the primary root in the mature epidermis zone, the length of the elongation zone of this organ and its diameter in the division zone decreased after the application of CuO-NPs and increased after treatment with Fe3O4-NPs. It was concluded that CuO-NPs and Fe3O4-NPs used for the production of nanofertilisers exhibit relatively low toxicity, while Fe3O4-NPs demonstrate a strong root-stimulating effect under the treatment at a wide range of concentrations.

Author Biographies

  • Maryia I. Aliakseyeva, Belarusian State University, 4 Niezaliezhnasci Avenue, Minsk 220030, Belarus

    postgraduate student at the department of plant cell biology and bioengineering, faculty of biology

  • Anna O. Muravitskaya, Belarusian State University, 4 Niezaliezhnasci Avenue, Minsk 220030, Belarus

    postgraduate student at the department of plant cell biology and bioengineering, faculty of biology

  • Viera S. Mackievic, Belarusian State University, 4 Niezaliezhnasci Avenue, Minsk 220030, Belarus

    senior lecturer at the department of plant cell biology and bioengineering, faculty of biology

  • Veranika V. Samokhina, Belarusian State University, 4 Niezaliezhnasci Avenue, Minsk 220030, Belarus

    senior lecturer at the department of plant cell biology and bioengineering, faculty of biology

  • Veranika V. Tarima, Belarusian State University, 4 Niezaliezhnasci Avenue, Minsk 220030, Belarus

    student at the faculty of biology

  • Palina A. Muchinskaya, Belarusian State University, 4 Niezaliezhnasci Avenue, Minsk 220030, Belarus

    student at the faculty of biology

  • Natalia L. Pshybytko, Belarusian State University, 4 Niezaliezhnasci Avenue, Minsk 220030, Belarus

    PhD (biology), docent; deputy dean for scientific work, faculty of biology

  • Vadim V. Demidchik, V. F. Kuprevich Institute of Experimental Botany, National Academy of Sciences of Belarus, 27 Akademichnaja Street, Minsk 220072, Belarus

    doctor of science (biology), сorresponding member of the National Academy of Sciences of Belarus, full professor; chief researcher at the laboratory of plant growth and development

References

  1. Zhang P, Ma Y, Zhang Z. Interactions between engineered nanomaterials and plants phytotoxicity uptake translocation, and biotransformation. In: Siddiqui MH, Al-Whaibi MH, Mohammad F, editors. Nanotechnology and plant sciences: nanoparticles and their impact on plants. Berlin: Springer; 2015. p. 77–99. DOI: 10.1007/978-3-319-14502-0_5.
  2. Wang P, Lombi E, Zhao F, Kopittke PM. Nanotechnology: a new opportunity in plant sciences. Trends in Plant Science. 2016;21(8):699–712. DOI: 10.1016/j.tplants.2016.04.005.
  3. Thiruvengadam M, Chi HY, Kim S-H. Impact of nanopollution on plant growth, photosynthesis, toxicity, and metabolism in the agricultural sector: an updated review. Plant Physiology and Biochemistry. 2024;207:108370. DOI: 10.1016/j.plaphy.2024.108370.
  4. Khan MU, Ullah H, Honey Sh, Talib Z, Abbas M, Umar A, et al. Metal nanoparticles: synthesis approach, types and applications – a mini review. Nano-Horizons. 2023;2:1–21. DOI: 10.25159/NanoHorizons.87a973477e35.
  5. Duman H, Eker F, Akdaşçi E, Witkowska AM, Bechelany M, Karav S. Silver nanoparticles: a comprehensive review of synthesis methods and chemical and physical properties. Nanomaterials. 2024;14(18):1527. DOI: 10.3390/nano14181527.
  6. Peters R, Brandhoff P, Weigel S, Marvin HJP, Bouwmeester H, Aschberger K, et al. Inventory of nanotechnology applications in the agricultural, feed and food sector. EFSA Supporting Publications. 2014;11(7):621E. DOI: 10.2903/sp.efsa.2014.EN-621.
  7. Toksha BG, Sonawale VAM, Vanarase A, Bornare DT, Tonde Sh, Hazra Ch, et al. Nanofertilizers: a review on synthesis and impact of their use on crop yield and environment. Environmental Technology & Innovation. 2021;24:101986. DOI: 10.1016/j.eti. 2021.101986.
  8. Grillo R, Mattos BD, Antunes DR, Forini MML, Monikh FA, Rojas OJ. Foliage adhesion and interactions with particulate delivery systems for plant nanobionics and intelligent agriculture. Nano Today. 2024;37:101078. DOI: 10.1016/j.nantod.2021.101078.
  9. Kah M, Tufenkji N, White JC. Nano-enabled strategies to enhance crop nutrition and protection. Nature Nanotechnology. 2019;14(6):532–540. DOI: 10.1038/s41565-019-0439-5.
  10. Vega-Vásquez P, Mosier NS, Irudayaraj J. Nanoscale drug delivery systems: from medicine to agriculture. Frontiers in Bioengineering and Biotechnology. 2020;8:79. DOI: 10.3389/fbioe.2020.00079.
  11. Servin A, Elmer W, Mukherjee A, de la Torre-Roche R, Hamdi H, White JC, et al. A review of the use of engineered nanomaterials to suppress plant disease and enhance crop yield. Journal of Nanoparticle Research. 2015;17(2):92. DOI: 10.1007/s11051-015-2907-7.
  12. Rastogi A, Zivcak M, Sytar O, Kalaji HM, He X, Mbarki S, et al. Impact of metal and metal oxide nanoparticles on plant: a critical review. Frontiers in Chemistry. 2017;5:10.3389. DOI: 10.3389/fchem.2017.00078.
  13. Francis DV, Abdalla AK, Mahakham W, Sarmah AK, Ahmed ZFR. Interaction of plants and metal nanoparticles: exploring its molecular mechanisms for sustainable agriculture and crop improvement. Environment International. 2024;190(2):108859. DOI: 10.1016/j.envint.2024.108859.
  14. Sosan A, Svistunenko D, Straltsova D, Tsiurkina K, Smolich I, Lawson T, et al. Engineered silver nanoparticles are sensed at the plasma membrane and dramatically modify the physiology of Arabidopsis thaliana plants. Plant Journal. 2016;85(2):245–257. DOI: 10.1111/tpj.13105.
  15. Javaid A, Munir N, Abideen Z, Duarte B, Siddiqui ZSh, Haq R, et al. The potential effects of nanoparticles in gene regulation and expression in mammalian, bacterial and plant cells – a comprehensive review. Plant Nano Biology. 2025;11:100145. DOI: 10.1016/j.plana.2025.100145.
  16. Zanella D, Bossi E, Gornati R, Faria N, Powell J, Bernardini G. The direct permeation of nanoparticles through the plasma membrane transiently modifies its properties. Biochimica et Biophysica Acta (BBA) – Biomembranes. 2019;1861(10):182997. DOI: 10.1016/j.bbamem.2019.05.019.
  17. Nair PMG, Chung IM. Impact of copper oxide nanoparticles exposure on Arabidopsis thaliana growth, root system development, root lignification, and molecular level changes. Environmental Science and Pollution Research. 2014;21(22):12709–12722. DOI: 10.1007/s11356-014-3210-3.
  18. Nair PMG, Chung IM. Evaluation of stress effects of copper oxide nanoparticles in Brassica napus L. seedlings. 3 Biotech. 2017;7(5):293. DOI: 10.1007/s13205-017-0929-9.
  19. Wang X, Xie H, Wang P, Yin H. Nanoparticles in plants: uptake, transport and physiological activity in leaf and root. Materials. 2023;16(8):3097. DOI: 10.3390/ma16083097.
  20. Naz S, Gul A, Zia M. Toxicity of copper oxide nanoparticles: a review study. IET Nanobiotechnology. 2020;14(1):1–13. DOI: 10.1049/iet-nbt.2019.0176.
  21. Chung IM, Venkidasamy B, Thiruvengadam M. Nickel oxide nanoparticles cause substantial physiological, phytochemical, and molecular-level changes in Chinese cabbage seedlings. Plant Physiology and Biochemistry. 2019;139:92–101. DOI: 10.1016/j.plaphy.2019.03.010.
  22. Ali Sh, Mehmood A, Khan N. Uptake, translocation, and consequences of nanomaterials on plant growth and stress adaptation. Journal of Nanomaterials. 2021;1:1–17. DOI: 10.1155/2021/6677616.
  23. Демидчик ВВ, Соколик АИ, Юрин ВМ. Токсичность избытка меди и толерантность к нему растений. Успехи современной биологии. 2001;121(5):511–525. EDN: YXZQIH.
  24. Lequeux H, Hermans Ch, Lutts S, Verbruggen N. Response to copper excess in Arabidopsis thaliana: impact on the root system architecture, hormone distribution, lignin accumulation and mineral profile. Plant Physiology and Biochemistry. 2010;48(8):673–682. DOI: 10.1016/j.plaphy.2010.05.005.
  25. Xu E, Liu Y, Gu D, Zhan X, Li J, Zhou K, et al. Molecular mechanisms of plant responses to copper: from deficiency to excess. International Journal of Molecular Sciences. 2024;25(13):6993. DOI: 10.3390/ijms25136993.
  26. Кирисюк ЮВ, Демидчик ВВ. Влияние наночастиц меди на рост каллусной культуры, полученной из незрелых зародышей Triticum aestivum L. Журнал Белорусского государственного университета. Биология. 2017;1:23–30.
  27. Feigl G. The impact of copper oxide nanoparticles on plant growth: a comprehensive review. Journal of Plant Interactions. 2023;18(1):2243098. DOI: 10.1080/17429145.2023.2243098.
  28. Festa RA, Thiele DJ. Copper: an essential metal in biology. Current Biology. 2011;21(21):R877 – R883. DOI: 10.1016/j.cub.2011.09.040.
  29. Kopittke PM, Dart PJ, Menzies NW. Toxic effects of low concentrations of Cu on nodulation of cowpea (Vigna unguiculata). Environmental Pollution. 2007;145(1):309–315. DOI: 10.1016/j.envpol.2006.03.007.
  30. Shaw AK, Ghosh S, Kalaji HM, Bosa K, Brestic M, Zivcak M, et al. Nano-CuO stress induced modulation of antioxidative defense and photosynthetic performance of Syrian barley (Hordeum vulgare L.). Environmental and Experimental Botany. 2014;102:37–47. DOI: 10.1016/j.envexpbot.2014.02.016.
  31. Song G, Hou W, Gao Y, Wang Y, Lin L, Zhang Z, et al. Effects of CuO nanoparticles on Lemna minor. Botanical Studies. 2016;57:3. DOI: 10.1186/s40529-016-0118-x.
  32. Rui M, Ma Ch, Hao Y, Guo J, Rui Y, Tang X, et al. Iron oxide nanoparticles as a potential iron fertilizer for peanut (Arachis hypogaea). Section Plant Nutrition. 2016;7:815. DOI: 10.3389/fpls.2016.00815.
  33. Feng Y, Kreslavski VD, Shmarev AN, Ivanov AA, Zharmukhamedov SK, Kosobryukhov A, et al. Effects of iron oxide nanoparticles (Fe3O4) on growth, photosynthesis, antioxidant activity and distribution of mineral elements in wheat (Triticum aestivum) plants. Plants. 2022;11(14):1894. DOI: 10.3390/plants11141894.
  34. Zia-ur-Rehman M, Naeem A, Khalid H, Rizwan M, Ali S, Azhar M. Responses of plants to iron oxide nanoparticles. Nanomaterials in Plants, Algae, and Microorganisms. 2018;1:221–238. DOI: 10.1016/B978-0-12-811487-2.00010-4.
  35. Marschner H. Mineral nutrition of higher plants. London: Academic Press; 1995. XV, 889 p.
  36. Bergmann W, editor. Nutritional disorders of plants: development, visual and analytical diagnosis. Jena: Gustav Fischer; 1992. 788 p.
  37. Kim J-H, Lee Y, Kim E-J, Gu S, Sohn E, Seo YS, et al. Exposure of iron nanoparticles to Arabidopsis thaliana enhances root elongation by triggering cell wall loosening. Environmental Science & Technology. 2014;48(6):3477–3485. DOI: 10.1021/es4043462.
  38. Bombin S, LeFebvre M, Sherwood J, Xu Y, Bao Y, Ramonell KM. Developmental and reproductive effects of iron oxide nanoparticles in Arabidopsis thaliana. International Journal of Molecular Sciences. 2015;16(10):24174–24193. DOI: 10.3390/ijms161024174.

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Published

2025-11-04

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Section

Physiology and Сell Biology

How to Cite

Aliakseyeva, M. I., Muravitskaya, A. O., Mackievic, V. S., Samokhina, V. V., Tarima, V. V., Muchinskaya, P. A., Pshybytko, N. L., & Demidchik, V. V. (2025). Analysis of changes in growth parameters and primary root architecture of Arabidopsis thaliana under the influence of copper and iron oxide nanoparticles. Experimental Biology and Biotechnology, 2, 25-35. https://doi.org/10.33581/2957-5060-2025-2-%p