Increase of Trigonelline in Trigonella persica Plant under Drought Stress

Authors

  • Fatemeh Zarinkamar Department of Plant Biology, Faculty of Biological Biology, Tarbiat Modares University, Tehran, Iran
  • Maryam Rezayian Department of Plant Biology, Faculty of Biological Biology, Tarbiat Modares University, Tehran, Iran
  • Reyhaneh Medhat Department of Plant Biology, Faculty of Biological Biology, Tarbiat Modares University, Tehran, Iran

DOI:

https://doi.org/10.30564/jbr.v4i2.4512

Abstract

Trigonella persica is a valuable medicinal plant which comprises trigonelline that is secondary metabolite and important component in cosmetic and medicine. This research was conducted in order to evaluation the drought stress effect on growth parameters, root anatomical changes and trigonelline content in T. persica. Plants were grown under soil moisture corresponding to 100%, 75%, 50% and 25% field capacity for two weeks. The data showed that drought stress was significantly decreased fresh weight and dry weight of shoot and root. In addition, leaf area was declined due to drought stress. Interestingly, root length was enhanced by drought stress. Root microscopic study demonstrated that drought stress increased thickness of epidermal, endodermal, vascular bundle, central cylinder and parenchyma in T. persica. Drought stress caused a significant increment in alkaloid and trigonelline content in aerial parts and roots of T. persica. These results revealed that T. persica responded to drought stress by increasing the alkaloid and trigonelline, as well as the anatomical changes in root. Considering the importance of trigonline and alkaloids, this work may open prospects for production of the pharmaceutically valuable secondary metabolites thereby drought stress.

Keywords:

Anatomical changes, Drought, Root, Trigonella persica, Trigonelline

References

[1] Khan, M.A., Iqbal, M., Akram, M., et al., 2013. Recent advances in molecular tool development for drought tolerance breeding in cereal crops: a review. Zemdirbyste-Agriculture. 100(3), 325-334.

[2] Wen, W., Li, K., Alseek, S., et al., 2015. Genetic determinants of the network of primary metabolism and their relationships to plant performance in a maize recombinant inbred line population. Plant Cell. 27(7), 1839-1856.

[3] Edreva, A., Velikova, V., Tsonev, T., et al., 2008. Stress-protective role of secondary metabolites: diversity of functions and mechanisms. General & Applied Plant Physiology. 34(1-2), 67-78.

[4] Selmar, D., Kleinwächter, M., 2013. Influencing the product quality by deliberately applying drought stress during the cultivation of medicinal plants. Industrial Crops and Products. 42, 558-566.

[5] Paulsen, J., Selmar, D., 2016. Case study: the difficulty of correct reference values when evaluating the effects of drought stress: a case study with Thymus vulgaris. Journal of Applied Botany & Food Quality. 89, 287-289.

[6] de Matos Nunes, J., Bertodo, L.O.O., Da Rosa, L.M.G., et al., 2014. Stress induction of valuable secondary metabolites in Hypericum polyanthemum acclimatized plants. South African Journal of Botany. 94, 182-189.

[7] Niinemets, Ü., 2016. Uncovering the hidden facets of drought stress: secondary metabolites make the difference. Tree Physiology. 36(2), 129-132.

[8] Debnath, B., Singha, W.S., Dasa, M., et al., 2018. Role of plant alkaloids on human health: A review of biological activities. Materials Today Chemistry. 9, 56-72.

[9] Wu, X., Yuan, J., Luo, A., et al., 2016. Drought stress and re-watering increase secondary metabolites and enzyme activity in dendrobium moniliforme. Industrial Crops & Products. 94, 385-393.

[10] Yahyazadeh, M., Meinen, R., Hänsch, R., et al., 2018. Impact of drought and salt stress on the biosynthesis of alkaloids in Chelidonium majus L. Phytochemistry. 152, 204-212.

[11] Gowda, V.R.P., Henry, A., Yamauchi, A., et al., 2011. Root biology and genetic improvement for drought avoidance in rice. Field Crops Research. 122(1), 1-13.

[12] Lynch, J.P., 2015. Root phenes that reduce the metabolic costs of soil exploration: opportunities for 21st century agriculture. Plant, Cell & Environment. 38(9), 1775-1784.

[13] da Cunha Cruz, Y., Scarpa, A.L.M., Pereira, M.P., et al., 2020. Root anatomy and nutrient uptake of the cattail Typha domingensis Pers.(Typhaceae) grown under drought condition. Rhizosphere. 16, 100253.

[14] Balodi, B., 1991. The genus Trigonella L.(Fabaceae) in the northwest Himalaya. Journal of Economic and Taxonomic Botany. 5, 11-16.

[15] Al-Habori, M., Raman, A., 2002. Pharmalogical properties in Fenugreek: The genus Trigonella. Petropoulos, GA. Taylor and Francis. London.

[16] Bano, D., Tabassum, H., Ahmad, A., et al., 2016. The medicinal significance of the bioactive compounds of Trigonella foenum-graecum: a review. International Journal of Research in Ayurveda and Pharmacy. 7, 84-91.

[17] Rechinger, K.H., 1984. Rumex (Polygonaceae) in Australia: a reconsideration. Nuytsia.

[18] Mehrafarin, A., Ghaderi, A., Rezazadeh, S.H., et al., 2010. Bioengineering of important secondary metabolites and metabolic pathways in fenugreek (Trigonella foenum-graecum L.).

[19] Evans, L.S., Tramontano, W.A., 1984. Trigonelline and promotion of cell arrest in G2 of various legumes. Phytochemistry. 23(9), 1837-1840.

[20] Altinkut, A., Kazan, K., Ipekci, Z., et al., 2001. Tolerance to paraquat is correlated with the traits associated with water stress tolerance in segregating F2 populations of barley and wheat. Euphytica. 121(1), 81-86.

[21] Shailajan, S., Sayed, N., Menon, S., et al., 2011. A validated RP-HPLC method for quantitation of trigonelline from herbal formulations containing Trigonella foenum-graecum (L.) seeds. Pharmaceutical Methods. 2(3), 157-160.

[22] Rahimi, Y., Taleei, A., Ranjbar, M., 2017. Changes in the expression of key genes involved in the biosynthesis of menthol and menthofuran in Mentha piperita L. under drought stress. Acta Physiologiae Plantarum. 39(9), 1-9.

[23] Karimi, S., Yadollahi, A., Arzani, K., et al., 2015. Gas-exchange response of almond genotypes to water stress. Photosynthetica. 53(1), 29-34.

[24] Hossain, M.S., Li, J., Sikdar, A., et al., 2020. Exogenous melatonin modulates the physiological and biochemical mechanisms of drought tolerance in tartary buckwheat (Fagopyrum tataricum (L.) Gaertn). Molecules. 25(12), 2828.

[25] Rezayian, M., Niknam, V., Ebrahimzadeh, H., 2018. Positive effects of Penconazole on growth of Brassica napus under drought stress. Archives of Agronomy and Soil Science. 64(13), 1791-1806. DOI: https://doi.org/10.1080/03650340.2018.1458095

[26] Narayanan, S., Mohan, A., Gill, K.S., et al., 2014. Variability of root traits in spring wheat germplasm. PLoS One. 9(6), e100317.

[27] Comas, L.H., Mueller, K.E., Taylor, L.L., et al., 2012. Evolutionary patterns and biogeochemical significance of angiosperm root traits. International Journal of Plant Sciences. 173(6), 584-595.

[28] Comas, L., Becker, S., Cruz, V.M.V., et al., 2013. Root traits contributing to plant productivity under drought. Frontiers in Plant Science. 4, 442.

[29] Thangthong, N., Jogloy, S., Pensuk, V., et al., 2016. Distribution patterns of peanut roots under different durations of early season drought stress. Field Crops Research. 198, 40-49.

[30] North, G.B., Nobel, P.S., 1992. Drought‐induced changes in hydraulic conductivity and structure in roots of Ferocactus acanthodes and Opuntia ficus‐ indica. New Phytologist. 120(1), 9-19.

[31] Bao, Y., Aggarwal, P., Robbins, N.E., et al., 2014. Plant roots use a patterning mechanism to position lateral root branches toward available water,” Proceedings of the National Academy of Sciences. 111(25), 9319-9324.

[32] Richards, R.A., Condon, A.G., Rebetzke, G.J., 2001. Traits to improve yield in dry environments. Application of Physiology in Wheat Breeding.

[33] Wasson, A.P., Richards, R.A., Chatrath, R., et al., 2012. Traits and selection strategies to improve root systems and water uptake in water-limited wheat crops. Journal of Experimental Botany. 63(9), 3485- 3498.

[34] Kashiwagi, J., Krishnamurthy, L., Crouch, J.H., et al., 2006. Variability of root length density and its contributions to seed yield in chickpea (Cicer arietinum L.) under terminal drought stress. Field Crops Research. 95(2-3), 171-181.

[35] Ghorbanpour, M., Hatami, M., Khavazi, K., 2013. Role of plant growth promoting rhizobacteria on antioxidant enzyme activities and tropane alkaloid production of Hyoscyamus niger under water deficit stress. Turkish Journal of Biology. 37(3), 350-360.

[36] Kleinwächter, M., Paulsen, J., Bloem, E., et al., 2015. Moderate drought and signal transducer induced biosynthesis of relevant secondary metabolites in thyme (Thymus vulgaris), greater celandine (Chelidonium majus) and parsley (Petroselinum crispum). Industrial Crops & Products. 64, 158-166.

[37] Falk, K.L., Tokuhisa, J.G., Gershenzon, J., 2007. The effect of sulfur nutrition on plant glucosinolate content: physiology and molecular mechanisms. Plant Biology. 9(5), 573-581.

[38] Liu, Y., Meng, Q., Duan, X., et al., 2017. Effects of PEG-induced drought stress on regulation of indole alkaloid biosynthesis in Catharanthus roseus. Journal of Plant Interactions. 12(1), 87-91.

[39] Keshavarz Afshar, R., Chaichi, M.R., Ansari Jovini, M., et al., 2015. Accumulation of silymarin in milk thistle seeds under drought stress. Planta. 242(3), 539-543.

[40] Cho, Y., Lightfoot, D.A., Wood, A.J., 1999. Trigonelline concentrations in salt stressed leaves of cultivated Glycine max. Phytochemistry. 52(7), 1235-1238.

[41] Rajasekaran, L.R., Aspinall, D., Jones, G.P., et al., 2001. Stress metabolism. IX. Effect of salt stress on trigonelline accumulation in tomato. Canadian Journal of Plant Science. 81(3), 487-498.

[42] Dadrasan, M., Chaichi, M.R., Pourbabaee, A.A., et al., 2015. Deficit irrigation and biological fertilizer influence on yield and trigonelline production of fenugreek. Industrial Crops & Products. 77, 156-162.

[43] Zamani, Z., Amiri, H., Ismaili, A., 2020. Improving drought stress tolerance in fenugreek (Trigonella foenum-graecum) by exogenous melatonin. Plant Biosystems An International Journal Dealing with All Aspects of Plant Biology. 154(5), 643-655.

Downloads

How to Cite

Zarinkamar, F., Rezayian, M., & Medhat, R. (2022). Increase of Trigonelline in Trigonella persica Plant under Drought Stress. Journal of Botanical Research, 4(2), 19–25. https://doi.org/10.30564/jbr.v4i2.4512

Issue

Article Type

Articles