Crop Science Research in Arid Regions

Crop Science Research in Arid Regions

The effect of foliar application of glycine betaine on biochemical, physiological, and agronomic traits of quinoa plant (Chenopodium quinoa Wild.) under different irrigation regimes

Document Type : Original Article

Author
Payame Noor University, Tehran, Iran
Abstract
Introduction: Quinoa (Chenopodium quinoa Wild.) is a pseudocereal that is one of the oldest crops in the Americas and a native plant in the Andes region. Compared to other grains, quinoa has more protein and a more balanced amino acid composition with 8-5% lysine and 1.5-2.4% methionine.
Drought, heat, salinity, etc. are types of abiotic stresses that reduce plant growth and cause a sharp drop in crop yield due to various changes at the physiological, morphological, and molecular levels. In addition, drought stress may cause the production of reactive oxygen species in plants, which damage lipid and protein structures and cause the cell membrane to lose permeability and selectivity. Leakage of intracellular ions leads to disturbance in metabolism, chloroplast decomposition, and reduction of chlorophyll content.
Glycine betaine not only acts as an osmotic regulator but also stabilizes the structure and activity of enzymes and protein complexes and maintains the integrity of membranes against the damaging effects of drought. Glycine betaine treatment increases the growth, survival, and tolerance of plants to different stress conditions by regulating different metabolic processes, improving the rate of absorption of pure CO2, maintaining proteins, enzymes, and lipids of the photosynthetic apparatus, and maintaining the flow of electrons through thylakoid membranes.
This research was conducted to investigate the effect of glycine betaine foliar application on agronomic, biochemical, and physiological traits of quinoa under water stress conditions.
Materials and Methods: The experiment of split plots based on randomized complete blocks design with three replications was performed at the station of Research in the 2020-2021 and 2021-2022 crop years, Agriculture and Natural Resources Center in Kerman province of Iran. The main factor included three levels of irrigation treatment (irrigation to the full maturity stage (control), irrigation to the beginning of the flowering stage, and irrigation to the beginning of the development stage) and the secondary factor included two levels of glycine betaine (0 and 3 mM). Biological and seed yields and harvest index, biochemical traits including proline and total phenol and flavonoid contents, and physiological traits including the activity of antioxidant enzymes such as catalase, ascorbate peroxidase, peroxidase, and polyphenol oxidase were measured. Variance analysis of all traits and LSD mean comparison test at five percent level was conducted with SAS software version 9.2.
Results and Discussion: The effect of irrigation factor and glycine betaine and their interaction effect on the most measured traits were significant. The highest biological and seed yields were observed in control condition and the application of glycine betaine. The lowest of them were in plants grown under irrigation condition to the beginning of the flowering stage and non-application of glycine betaine. Water stress was increased the content of proline and total phenol and flavonoid and the activity of antioxidant enzymes in both level of glycine betaine. The foliar application of glycine betaine caused an increase in the biological and seed yields and biochemical and physiological traits at all three irrigation conditions.
Conclusion: Under water stress conditions at both glycine betaine levels, the biological and seed yields decreased while the biochemical and physiological traits increased. These results show that the quinoa plant responds to water stress with enzymatic and non-enzymatic defense systems. The application of glycine betaine led to the improvement of biological and seed yields and biochemical and physiological traits in all three irrigation treatments. So, glycine betaine can be used to compensate for the harmful effects of water stress in quinoa.  
Keywords

Abd Elhamid, E.M., Sadak, M. Sh, Ezzo, M.I. and Abdalla, A.M., 2021. Impact of glycine betaine on drought tolerance of maringa oleifera plant grown under sandy soil. Asian Journal of Plant Sciences, 20, pp.578-589. doi: 10.3923/ajps.2021.578.589
Akram, N.A., Shafiq, F. and Ashraf, M., 2017. Ascorbic acid a potential oxidant scavenger and its role in plant development and abiotic stress tolerance. Frontiers in Plant Science, 8, 613. doi: 10.3389/fpls2017.00613
Alqudah, A.M., Samarah, N.H. and Mullen, R.E., 2011. Drought stress effect on crop pollination, seed yield and quality. In Alternative Farming Systems, Biotechnology, Drought Stress and Ecological Fertilisation; Lichtfouse, E., Ed.; Springer: Dordrecht, The Netherlands, pp.193-213. doi.10.1007/978_94_007_0186_1_6
Ardestani, A. and Yazdanparast, R., 2007. Antioxidant and free radical scavenging potential of Achillea santolina extracts. Food Chemistry, 104, pp.21-29. doi: 10.1016/j.foodchem.2006.10.066
Arora, A., Sairam, R.K. and Srivastava, G.C., 2002. Oxidative stress and antioxidative systems in plants. Current Science, 82, pp.1227-1238. doi: 10.016/j.envexpbot.2005.12.006
Ashraf, M. and Foolad, M.A., 2007. Improving plant abiotic stress resistance by exogenous application of osmoprotectants glycine betaine and proline. Environmental and Experimental Botany, 59, pp.206-216. doi: 1016/j.envexphot.2005.12.006
Aziz, A., Akram, N.A. and Ashraf, M., 2018. Influence of natural and synthetic vitamin C (ascorbic acid) on primary and secondary metabolites and associated metabolism in quinoa (Chenopodium quinoa Wild.) plants under water deficit regimes. Plant Physiology and Biochemistry, 123, pp.192-203. doi: 10.1016/j.plaphy.2017.12.004
Bates, L.S., Waldern, R.P. and Tear, I.D., 1973. Rapid determination of free proline for water stress studies. Plant Soil, 39, pp.205-207. doi: 10.1007/bf00018060
Beebs, S., Ramirez, J. Javis, A., Rao, I.M., Mosquera, G. and Bueno, J.M., 2011. Genetic improvement of common beans and the challenges of climate change. Crop Adaptation to Climate Change, 10, pp.356-369. doi: 10.1002/9780470960929.ch25
Beers, G.R. and sizer, I.W., 1952. A spectrophotometric method for measuring the breakdown of hydrogen peroxide by catalase. Biological Chemistry, 195, pp.133-140. doi.org/10.1016/s0021_9258(19)50881_x
Chao, Y.Y. and Hsueh, I.E., 2019. Insights into physiological mechanisms of salt stress tolerance in djulis (Chenopodium formosanum koidz) sprouts. Journal of Plant Physiology, 62, pp.263-273. doi: 10.1007/s/2374-019-0053-y
Elewa, T.A., Sadak, M.Sh. and Saad, A.M., 2017. Proline treatment improves physiological responses in quinoa plants under drought stress. Bioscience Research, 14, pp.21-33. doi: 10.1080/00103624.2046036
Fahad, S., Bajwa, A.A., Nazir, U., Amjum, S.A., Farooq, A., Zohaib, A. et al., 2017. Crop production under drought and heat stress: Plant responses and management options. Frontiers in Plant Science, 8, pp.40-50 doi: 103389/fpls.2017.01147
Fang, Y. and Xiong, L., 2015. General mechanisms of drought response and their application in drought resistance improvement in plants. Cell Mol. Life Science, 72, pp.673-689. doi: 10.1007/s00018-014-1767-0
Farooq, M., Wahid, A., Lee, D.J., Cheema, S.A. and Aziz, T., 2010. Drought stress comparative time course action of the foliar applied glycine betaine, salicylic acid, nitrous oxide, brassinosteroids and spermine in improving drought resistance of rice. Journal of Agronomy Crop and Science, 196, pp.336-345. doi: 10.1111/j.1439-037x.2010. 00422.x
Fielding, J.L. and Hall. J., 1978. A biochemical and cytochemical Study of peroxidase activity in root pea. Journal of Experimental Botany, 29, pp.978-989. doi: 10.1093/jxb/29.4.983
Fischer, S., Wilckens, R., Jara, J. and Aranda, M., 2013. Variation in antioxidant capacity of quinoa (Chenopodium quinoa Will) subjected to drought stress. Industrial Crops and Products, 46, pp.341-349. doi: 10.1016/j.indcrop.2013.01/037
Ghosh, U.K., Islam, M.N., Siddiqui, M.N. and Khan, Md. A. R.,. 2021. Understanding the roles of osmolytes for acclimatizing plants to changing environment: a review of potential mechanism. Plant Signaling and Behavior, e1913306, pp.1-15. doi: 10.1080/15592324.2021.1913306
Gorinstein, S. and Lojek, A., 2008. Comparison of composition and antioxidant capacity of some cereals and pseudocereals. International Journal of Food Science and Technology, 43, pp.629-637. doi: 10.1111/j.1365-2621.2007.01498.x
Hirose, Y., Fujita, T., Ishii, T. and Ueno, N., 2010. Antioxidative properties and flavonoid composition of Chenopodium quinoa seeds cultivated in Japan. Food Chemistry, 119, pp.1300-1306. doi: 10.1016/j.foodchem.2009.09.008
Iqbal, N., Ashraf, M. and Ashraf, M.Y., 2008. Glycinebetaine, an osmolyte of interest to improve water stress tolerance in sunflower (Helianthus annuus L.): water relations and yield. South African Journal of Botany, 74, pp.274-281. doi: 10.1016/j.sajb.2007.11.016
Janovitz-Klapp, A.H., Richard, F.C., Goupy, P.M. and Nicolas, J.J., 1990. Inhibition studies on apple polyphenol oxadase. Journal of Agricultural Food Chemistry, 38, pp.926–931. doi: 10.1021/jf00094a002
Korkmaz, A., Deger, O. and Kocacinar, F., 2015. Alleviation of water stress effects on pepper seedlings by foliar application of glycinebetaine. New Zealand Journal of Crop and Horticultural, 43, pp.18-31. doi: 10.1080/0114067.2014.936945
Liaqat, S., Masroor, A., Ghafoor, F., Magqsood, Z., Tasleem, W. and Ghafoor, A., 2020. Effect of glycine betaine as a growth promoter and stress mitigator in Brassica oleracea Var. Italica. Journal La Lifescience, 1, pp.31-35. doi: 10.37899/j0urnallalifesci.v1i4.206
Lin, M., Han, P., Li, Y., Wang, W., Lai, D. and Zhou, L., 2019. Quinoa secondary metabolites and their biological activities or functions: A review. Molecules, 24, pp.22512. doi: 10.3390/molecules24132512
Lin, P.H. and Chao, Y.Y., 2021. Different drought-tolerant mechanisms in quinoa (Chenopodium quinoa Wild) and djulis (Chenopodium formosanum Koidz.) based on physiological analysis. Plants, 10, pp.2279. doi: 10.3390/plants10112279
Mahmood, K.T., Mugal, T. and Haq, I.U., 2010. Moringa oliefera. A natural gift-A review. Journal of Pharmaceutical Sciences and Research, 2, pp.775-781. doi: 10.25081/rip. 2014.v14.8807
Maqsood, M.F., Shahbaz, M., Arfan, M. and Basra, S.M.A., 2021. Presowing seed treatment with glycine betaine confers NaCl tolerance in quinoa by modulating some physiological processes and antioxidant machinery. Turkish Journal of Botany, 45, pp.1-14. doi: 10.3906/bot-2009-13
Matiacevich, S., Castellion, M., Maldonado, S. and Buera, P., 2006. Water-dependent thermal transitions in quinoa embryos. Thermochimica Acta, 448, pp.117-122. doi: 10.1016/j.tca.2006.06.016
Mohammadi, F., Maleki, A. and Fathi, A., 2021. Effects of drought stress and humic acid on plant growth, yield quality and its components of quinoa (Chenopodium quinoa Wild). Journal of Crop Nutrition, 7, pp.11-23. doi: 10.22059/jci.2021.312419.2469
Praba, M.L., Cairns, J.E., Babu, R.C. and Laffite, H.R., 2009. Identification of physiological traits underlying cultivar differences in drought tolerance in rice and wheat. Journal of Agronomy and Crop Science, 195, pp.30-46. doi: 10.1111/j.1439-037x.2008.00341.x
Quan, R., Shang, M., Zhang, H., Zhao, Y. and Zhang, J., 2004. Engineering of enhanced glycine betaine synthesis improves drought tolerance in maize. Plant Biotechnology, 2, pp.477-486. doi: 10.1111/j.1467-7652.2004. 00093.x
Quiroga, G., Erice, G., Aroca, R., Zamarreno, A.M., Garcia-Mina, J.M. and Ruiz-Lozano, A., 2020. Radical water transport in arbuscular mycorrhizal maize plants under drought stress conditions is affected by indol-acetic acid (IAA) application. Journal of Plant Physiology, 1, pp.246-247. doi: 1016/j.jplph.2020.153115
Rajput, V.D., Harish, H., Singh, R.K., Verma, K.K., Sharma, L., Quiroz-Figueroa, F.R., et al., 2021.Recent developments in enzymatic antioxidant defense mechanism in plants with special reference to abiotic stress: A review. Biology, 10, 267. doi: 10.3390/bilogy10040267
Raza, S.H., Athar, H.R., Ashraf, M. and Hameed, A., 2007. Glycine betaine- induced modulation of antioxidant enzymes activities and ion accumulation in two wheat cultivars differing in salt tolerance. Environmental and Experimental Botany, 60, pp.368-376. doi: 10.1016/j.envexpbot.2006.12.009
Richards, R.A., Condon, A.G. and Rebetzke, G.J., 2001. Traits to improve yield in dry environments. Application of Physiology in Wheat Breeding (CYMMYT.). 240 pp. doi: 10.3389/fpls.2021.684205
Sadak, M.S., El-Bassiouny, H.M.S. and Dwood, M.G., 2019. Role of trehalose on antioxidant defense system and some osmolytes of quinoa plants under water deficit. Bulletin of the National Research Centre, 43, pp.5-10. doi: 10.1186/s42269-018-0039-9
Sakamoto, A. and Murata, M., 2002. The role of glycine betaine in the protection of plants from stress: clues from transgenic plants. Plant, Cell and Environment, 25, pp.163-171.doi: 10.1046/j.0016-8025.2001.007 
Schneider, C., 2005. Chemistry and biology of vitamin E. Molecular Nutrition and Food Research, 49, pp.7-30. doi: 10.1002/mnfr.200400049
Shafiq, S., Akram, N.A., Ashraf, M., Garcia-Caparros, P., Ali, O.M. and Latef, A.A.H.A., 2021. Influence of glycine betaine (natural and synthetic) on growth, metabolism and yield production of drought-stressed maize (Zea mays L.) plants. Plants, 10, 2540. doi: 10.3390/plants10112540
Shehzadi, A., Akram, N.A., Ali, A. and Ashraf, M., 2019. Exogenously applied glycine betaine induced alteration in some key physio-biochemical attributes and plant anatomical features in water stressed oat (Avena sativa L.) plants. Journal of Arid Land, 11, pp.292-305. doi: 10.1007/s40333-019-0007-8
Yoshimura, K., Yabute, Y., Ishikawa, T. and Shigeoka, S., 2000. Expression of spinach ascorbate peroxidase isoenzymes in response to oxidative stresses. Plant Physiology, 123, pp.223-233. doi: 10.1104/pp.123.1.223
Zhang, D.Y., Yao, X.H., Duan, M.H., Wei, F.Y., Wu, G.H. and Li, L., 2015. Variation of essential oil content and antioxidant activity of Lonicera species in different sites of China. Industrial Crops and Products, 77, pp.772-779. doi: 10.1016/j.indcrop.2015.09.048
Zeinab, Q., Tanees, C.M., Xiongming, D.U. Lori, H. and Tehseen, M.A., 2021. Review of oxidative stress and antioxidative defense mechanisms in Gossipum Hirsutum L. in response to extreme abiotic conditions. Journal of Cotton Research, 4, pp.1-9. doi: 10.1186/s42397-021-00086-4
Volume 6, Issue 3 - Serial Number 14
Autumn 2024
Pages 139-155

  • Receive Date 03 June 2024
  • Revise Date 01 July 2024
  • Accept Date 05 July 2024