Document Type : Original Article

Authors

1 M.Sc. Student of Agricultural Biotechnology, Department of Plant Production and Genetics, Faculty of Agriculture and Natural Resources, University of Mohaghegh Ardabili, Ardabil, Iran

2 Associate Professor, Department of Plant Production and Genetics, Faculty of Agriculture and Natural Resources, University of Mohaghegh Ardabili, Ardabil, Iran

3 PhD Student of Agricultural Biotechnology, Department of Plant Production and Genetics, Faculty of Agriculture and Natural Resources, University of Mohaghegh Ardabili, Ardabil, Iran

Abstract

Introduction
Environmental pollution with heavy metals has spread in the world. The impact these pollutants on the human health and food chain, as one of the factors of economic and health concerns, needs more attention. Cadmium (cd) as one of the most important heavy metals compared to other metals is rapidly absorbed and accumulated in plant tissues, and its transfer to the food chain is the result of widespread contamination of the soil with cadmium. Nano-silicon (Si) is more effective than usual fertilizers in protecting plants against biotic and abiotic stresses. Medicinal plants are one of the most important sources of drug production that humans have used for many years, and their importance is expanding day by day. Many secondary metabolites of Borago officinalis and its products are consumed in the world pharmaceutical markets, so it requires special attention to improve the quality of culture, production efficiency, and health. This attention requires increasing knowledge about the physiological mechanisms of this plant affected by environmental factors such as cadmium stress. This study aimed to investigate the effect of nano-silicon on alleviating the detrimental effects of cadmium stress on physiological properties such as antioxidant enzyme activity in Borago officinalis.
Materials and methods
Treatment was performed by adding cadmium in the form of cadmium nitrate (Cd (NO3)2) and nano-silicon in hydroponic cultures of borage plants at the 7-8 leaf stage. This study was conducted as a factorial experiment based on a completely randomized design with three replications. Experimental factors were cadmium at three levels (0 (control), 25 mg L-1, and 75 mg L-1) and nano silicon at two different levels (0 and 1.5 mM). One day, one week, and two weeks after treatment, plant leaves were sampled and the amount of cadmium accumulation and biochemical and physiological properties were measured.
Results and discussion
The results showed that the accumulation of cadmium in the aerial parts of the borage plant was significantly increased with increasing the cadmium concentration in the hydroponic medium. The utilization of nano-silicon significantly reduced the amount of cadmium absorption and accumulation in borage plants.
Cadmium nitrate increased the amount of hydrogen peroxide compared to the control. The use of nano-silicon significantly reduced the amount of hydrogen peroxide under cadmium stress at one and two weeks after treatment. One of the important consequences of increasing the concentration of heavy metals in plants is increasing in the production and accumulation of reactive oxygen species (ROS) such as superoxide, hydroxyl and hydrogen peroxide (H2O2) radicals in the cells. This reactive oxygen species leads to the oxidation and destruction of macromolecules such as protein, DNA, cell membrane damage and ion leakage.
With increasing the concentration of cadmium, the amount of malondialdehyde (MDA) and proline in the cells were significantly increased. Malondialdehyde (MDA) and proline levels were significantly reduced by nano-silicon treatment. Heavy metals such as cadmium lead to the production of hydroxyl radicals, followed by lipid peroxidation. With increasing the lipid peroxidation, the cell membrane is destroyed and malondialdehyde levels increase. In the present study, the amount of malondialdehyde was significantly reduced under the influence of nano- silicon treatment. Proline accumulation in plants may also be a biomarker of cadmium stress, because proline can scavenge free radicals and protect the cells from their damaging effects.
With increasing the concentration of cadmium, the activity of polyphenol oxidase, peroxidase, and catalase enzymes was increased. In addition, the activity of these enzymes was reduced with the utilization of nano-silicon. The highest activities of these enzymes were recorded under cadmium concentration at 75 mg l-1 and the lowest activities of these enzymes were related to the treatment of nano-silicon and control. Increasing the level of antioxidant activity can sweep ROS produced by heavy metals, and protects the cell from the damaging effects of oxidative stress, which increases the plant's tolerance to environmental stresses, including heavy metals. The use of nano-silicon positively reduces cadmium accumulation in the plant maybe by maintaining the photosynthetic capacity and regulating the uptake and transfer of cadmium under cadmium stress conditions. On the other hand, nano-silicon reduces the amount of malondialdehyde (MDA) and reactive oxygen species (H2O2) may be through the reduction of cadmium uptake and accumulation in the plant cells and tissues as well as increase in the efficiency of enzymatic and non-enzymatic antioxidant systems.
Conclusions
The results of the present study showed that the accumulation of cadmium in the borage tissues under cadmium stress was reduced due to the application of nano-silicon. In other words, the use of nano-silicon improved the physiological characteristics of the borage plant by reducing the uptake and transfer of cadmium nitrate. This reduction in the amount of uptake and accumulation of cadmium nitrate in plant tissues is important for the health of agricultural products and human communities.

Keywords

Main Subjects

 
Aksoy, M., Ssechln Dlnler, B., 2012. Changes in pysiological parameters and some antioxidant enzymes activities of soybean (Glycine max L. Merr.) leaves under cadmium and salt stress. Journal of Stress Physiology & Biochemistry. 8, 179-190.
Alizadeh Oskooi, P., Ali Asgharzad, N., Shariatmedari, H., Asgharzadeh, S., 2009. The effect of two species of mycorrhizal fungi on reducing cadmium toxicity in tomato plants with different levels of phosphorus. Journal of Soil Research (Soil and Water Sciences). 23, 15-29. [In Persian with English summary].
Ashraf, M., 2009. Biotechnological approach of improving plant salt tolerance using antioxidants as markers. Biotechnology Advances. 27, 84-93.
Bates, L.S., Waldren, R.P., Teare. I.D., 1973. Rapid determination of free proline for water-stress studies. Plant and Soil. 39, 205-207.
Bian, Z.H., Cheng, R.F., Yang, Q.C., Wang, J., Lu. C.G., 2016. Continuous light from red, blue, and green light- emitting diodes reduces nitrate content and enhances phytochemical concentrations and antioxidant capacity in lettuce. Journal of American Society for Horticultural Science. 141, 186–195.
Bradford, M.M., 1976. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Biochemistry. 72, 248-254.
Brecht, M., Krauss, A., Muhammad, S., Sinai Esfahani, L., Bellanca, S., Margrie, T.W., 2004. Organization of rat vibrissa motor cortex and adjacent areas according to cytoarchitectonics, microstimulation, and intracellular stimulation of identified cells. Journal of Comparative Neurology. 479, 360-373.
Bienert, G.P., Schűssler, M.D., Jahn, T.P., 2008. Metalloids: essential, beneficial or toxic? Major intrinsic proteins sort it out. Trends in Biochemical Sciences, 33, 20–26.
Chang, C.J., Koa, C.H., 1988. H2O2 metabolism during senescence of rice leaves changes in enzyme activities in light and darkness. Plant Growth Regulation. 25, 11-15.
Clemens, S., Aarts, M.G., Thomine, S., Verbruggen, N., 2013. Plant science: the key to preventing slow cadmium poisoning. Trends in Plant Science. 18, 92-99.
Gallego, S.M., Pena, L.B., Barcia, R.A., Azpilicueta, C.E., Iannone, M.F., Rosales, E.P., Benavides. M.P.. 2012. Unravelling cadmium toxicity and tolerance in plants: insight into regulatory mechanisms. Environmental and Experimental Botany. 83, 33-46.
Hajiboland, R., Cheraghvareh, L., 2014. Influence of Si supplementation on growth and some physiological and biochemical parameters in salt- stressed tobacco (Nicotiana rustica L.) plants. Journal of Sciences. 25, 205-217.
Heath, R.L., Packer, L., 1968. Photoperoxidation in isolated chloroplast, kinetics and stoichiometry of fatty acid peroxidation. Biochemistry Biophysics. 125, 189-198.
Hegedus, A.S., Horvath, G., 2001. Comparative studies of H2O2 detoxifying enzymes in green and greening barley seedling under cadmium stress. Plant Science. 160, 1085- 1093.
Hoagland, D.R., Arnon, D.I., 1950. The water-culture method for growing plants without soil. Circular. California Agricultural Experiment Station. 347p.
Hossain, M.A., Piyatida, P., da Silva, J.A.T., Fujita, M., 2012. Molecular mechanism of heavy metal toxicity and tolerance in plants: central role of glutathione in detoxification of reactive oxygen species and methylglyoxal and in heavy metal chelation. Journal of Botany. 32, 1–37.
Hussain, I., Ashraf, M.A., Rasheed, R., Asghar, A. Sajid, M.A., Iqbal, M., 2015. Exogenous application of silicon at the boot stage decreases accumulation of cadmium in wheat (Triticum aestivum L.) grains. Brazilian Journal of Botany 38, 223-234.
John, R., Ahmad, P., Gadgil, K., Sharma, S., 2008. Effect of cadmium and lead on growth, biochemical parameters and uptake in Lemna polyrrhiza L. Plant, Soil and Environment. 54, 262–270.
Kar, M., Mishra, D., 1976. Catalase, peroxidase, and polyphenoloxidase activities during rice leaf senescence. Plant Physiology. 57, 315-319.
Khan, M.H., Panda, S.K., 2008. Alterations in root lipid peroxidation and antioxidative responses in two rice cultivars under NaCl-salinity stress. Plant Physiology. 30, 81-89.
Liu, D., Jiang, W., Gao, X., 2003. Effects of cadmium on root growth, cell division and nucleoli in root tip cells of garlic. Biologia Plantarum. 47, 79-83.
Lutts, S., Majerus, V., Kinet, J.M., 1999. NaCl effects on proline metabolism in rice (Oryza sativa) seedlings. Physiologia Plantarum. 105, 450–458.
Matejovic, I., Durackova, A., 1994. Comparison of microwave digestion, wet and dry mineralization, and solubilization of plant sample for determination of calcium, magnesium, potassium, phosphorus, sodium, iron, zinc, copper, and manganese. Communications in soil science and plant analysis. 25(9-10), 1277-1288.
Moghadam Ali, M.A., Ramezani, A., Mansuri Far, S., Aslani, K.S., Moradi-Ghahderijani, M.M., Jamian, S.S., 2013. Application of silicon ameliorates salinity stress in sunflower (Helianthus annuus L.) plants. International Journal of Agriculture and Crop Sciences. 6, 1367-1372.
Mohsenzadeh, S., Shahrtash, M., Mohabatkar, H., 2011. Interactive effects of salicylic acid and silicon on some physiological responses of cadmium-stressed maize seedlings. Iranian Journal of Science and Technology Transaction A- Science. 201, 57-60.
Pei, Z.F., Ming, D.F., Liu, D., Wan, G.L., Geng, X.X., Gong, H.J., Zhou, W.J., 2010. Silicon improves the tolerance to water-deficit stress induced by polyethylene glycol in wheat (Triticum aestivum L.) seedling. Journal Plant Growth Regulation. 29, 106-115.
Rizwan, M., Ali, S., Rehman, M.Z., Rinklebe, J., Tsang, D.C., Bashir, A., Maqbool, A., Tack, F.M., Ok, Y.S., 2018. Cadmium phytoremediation potential of Brassica crop species: a review. Science of the Total Environment. 631, 1175–1191.
Sheikhzadeh, P., Zare, N., Mahmoudi, F., 2020. The synergistic effects of hydro and hormone priming on seed germination, antioxidant activity and cadmium tolerance in borage. Acta Botanica Croatica. 80, https://doi.org/10.37427/botcro-2021-007
Shi, G.R., Cai, Q.S., Liu, C.F., Wu, L., 2010. Silicon alleviates cadmium toxicity in peanut plants in relation to cadmium distribution and stimulation of antioxidative enzymes. Plant Growth Regulation. 61, 45-52.
Song, A., Li, Z., Zhang, J., Xue, G., Fan, F., Liang, Y., 2009. Silicon-enhanced resistance to cadmium toxicity in Brassica chinensis L. is attributed to Si-suppressed cadmium uptake and transport and Si enhanced antioxidant defense capacity. Journal of Hazardous Materials. 172, 74-83.
Spurvey, S. A., Shahidi, F., 2000. Concentration of gamma linolenic acid (GLA) from borage oil by urea complexation: optimization of reaction conditions. Journal of Food Lipids, 7, 163-174.
Velikova, V., Yordanov, I., Edreva, A., 2000. Oxidative stress and some antioxidant systems in acid rain-treated bean plants: protective role of exogenous polyamines. Plant Science. 151, 59-66.
Wang, L., Zhou, Q., Ding, L., Sun, Y., 2008. Effect of cadmium toxicity on nitrogen metabolism in leaves of Solanum nigrum L. Journal of Hazard Mater. 154, 818-825.
Zofan, P., Nissi, E., Rastgarzade, S., 2019. Assessment of some growth indices and Cd accumulation in shoots and roots of Malva parviflora L. under hydroponic system. Journal of Plant Research, 31, 316-331.
Zhu, G.X., Guo, Q.J., Xiao, H.Y., Chen, T.B., Yang, J., 2017. Multivariate statistical and lead isotopic analyses approach to identify heavy metal sources in topsoil from the industrial zone of Beijing capital iron and steel factory. Environmental Science and Pollution Research. 24, 14877–14888.