Research Articles
Vol. 9 No. sp3 (2022)
Effects of drought stress on growth and flavonoid accumulation of fish mint (Houttuynia cordata Thumb.)
Vietnam National University
Abstract
Fish mint (Houttuynia cordata Thumb.) is a popular medicinal plant grown primarily because of its pharmacological values. Drought stress has on the relationship between growth and physio-biochemical changes, especially flavonoid content. The impacts of various drought stress conditions on the fish mint development were investigated, including 85% of field capacity (FC), 75% FC, 65% FC and 55% FC in 14, 21 and 28 days. Agronomic, physiological and biochemical parameters during the growth of fish mint plants under drought stress conditions were assessed. According to the results of variance analysis, drought stress results in a considerable drop in the measured parameters (shoot height, leaf number, leaf area and fresh weight). Similarly, all of the above-mentioned parameters were also decreased with increasing the number of drought days. Furthermore, drought period and level caused a drop in respiration, photosynthetic rate, chlorophyll and starch content. The concentration of carotenoids and flavonoids, on the other hand, increased dramatically as drought stress periods and levels increased. In comparison to the control, the drought treatment (65% FC) in 7 days maintained the growth rate and increased flavonoid accumulation from 2.42 mg to 3.04 mg. These findings might give a scientific foundation for growing fish mint plants under drought stress to boost flavonoid content.
References
- Wu Z, Deng X, Hu Q, Xiao X, Jiang J, Ma X, Wu M. Houttuynia cordata Thunb.: An Ethnopharmacological Review. Frontiers in Pharmacology. 2021;12. https://doi.org/10.3389/fphar.2021.714694
- Wang XP, Ye MR, Zhang XP, Zhang LF, Jing NN, Su W. Physiological adaptation of Houttuynia cordata to substrate moisture change under shading condition. Wetland Science. 2016;14(3):446-50.
- Wei W, Li C, Yuming W, Zehong Y. Genetic diversity among the germplasm resources of the genus Houttuynia Thunb. in China based on RAMP markers. Genetic Resources and Crop Evolution. 2005;52(4):473-82. https://doi.org/10.1007/s10722-005-2261-1
- Lau KM, Lee KM, Koon CM, Cheung CS, Lau CP, Ho HM et al. Immunomodulatory and anti-SARS activities of Houttuynia cordata. Journal of Ethnopharmacology. 2008;118(1):79-85. https://doi.org/10.1016/j.jep.2008.03.018
- Nuengchamnong N, Krittasilp K, Ingkaninan K. Rapid screening and identification of antioxidants in aqueous extracts of Houttuynia cordata using LC–ESI–MS coupled with DPPH assay. Food Chemistry. 2009;117(4):750-56. https://doi.org/10.1016/j.foodchem.2009.04.071
- Shingnaisui K, Dey T, Manna P, Kalita J. Therapeutic potentials of Houttuynia cordata Thunb. against inflammation and oxidative stress: A review. Journal of Ethnopharmacology. 2018;220:35-43. https://doi.org/10.1016/j.jep.2018.03.038
- Jiang N, Doseff AI, Grotewold E. Flavones: from biosynthesis to health benefits. Plants. 2016;5(2):27. https://doi.org/10.3390/plants5020027
- Barrs HD, Weatherley PE. A re-examination of the relative turgidity technique for estimating water deficits in leaves. Australian Journal of Biological Sciences. 1962;15(3):413-28. https://doi.org/10.1071/BI9620413
- Lichtenthaler HK. Chlorophylls and carotenoids: pigments of photosynthetic biomembranes. In: Methods in Enzymology. Academic Press. 1987:350-82. https://doi.org/10.1016/0076-6879(87)48036-1
- Thang TT. Effects of sodium silicate on the growth and starch content in seeds of mungbean (Vigna radiata L.) under salt stress. The Bach Khoa Youths Science and Technology Conference. 2022;33.
- Hedge JE, Hofreiter BT, Whistler RL. Carbohydrate chemistry. Academic Press, New York. 1962;17:371-80.
- Ábrahám E, Hourton-Cabassa C, Erdei L, Szabados L. Methods for determination of proline in plants. In: Plant Stress Tolerance. 2010:317-31. Humana Press. https://doi.org/10.1007/978-1-60761-702-0_20
- Chang CC, Yang MH, Wen HM, Chern JC. Estimation of total flavonoid content in propolis by two complementary colorimetric methods. Journal of Food and Drug Analysis. 2002;10(3). https://doi.org/10.38212/2224-6614.2748
- Yang X, Lu M, Wang Y, Wang Y, Liu Z, Chen S. Response mechanism of plants to drought stress. Horticulturae. 202;7(3):50. https://doi.org/10.3390/horticulturae7030050
- Shen C, Zhang Y, Li Q, Liu S, He F, An Y et al. PdGNC confers drought tolerance by mediating stomatal closure resulting from NO and H2O2 production via the direct regulation of PdHXK1 expression in Populus. New Phytologist. 2021;230(5):1868-82. https://doi.org/10.1111/nph.17301
- Lawson T, Vialet?Chabrand S. Speedy stomata, photosynthesis and plant water use efficiency. New Phytologist. 2019;221(1):93-98. https://doi.org/10.1111/nph.15330
- Fitzpatrick D, Aro EM, Tiwari A. True oxygen reduction capacity during photosynthetic electron transfer in thylakoids and intact leaves. Plant Physiology. 2022. https://doi.org/10.1093/plphys/kiac058
- Baccari S, Elloumi O, Chaari-Rkhis A, Fenollosa E, Morales M, Drira N et al. Linking leaf water potential, photosynthesis and chlorophyll loss with mechanisms of photo-and antioxidant protection in juvenile olive trees subjected to severe drought. Frontiers in Plant Science. 2020;11:2011. https://doi.org/10.3389/fpls.2020.614144
- Barickman TC, Adhikari B, Sehgal A, Walne CH, Reddy KR, Gao W. Drought and elevated CO2 impacts photosynthesis and biochemicals of basil (Ocimum basilicum L.). Stresses. 2021;1(4):223-37. https://doi.org/10.3390/stresses1040016
- Vanlerberghe GC, Martyn GD, Dahal K. Alternative oxidase: a respiratory electron transport chain pathway essential for maintaining photosynthetic performance during drought stress. Physiologia Plantarum. 2016;157(3):322-37. https://doi.org/10.1111/ppl.12451
- Liang X, Zhang L, Natarajan SK, Becker DF. Proline mechanisms of stress survival. Antioxidants and redox signaling. 2013;19(9):998-1011. https://doi.org/10.1089/ars.2012.5074
- Furlan AL, Bianucci E, Giordano W, Castro S, Becker DF. Proline metabolic dynamics and implications in drought tolerance of peanut plants. Plant Physiology and Biochemistry. 2020;151:566-78. https://doi.org/10.1016/j.plaphy.2020.04.010
- Nguyen VT, Le VM, Vo TS, Bui LM, Anh HL, Danh VT. Preliminary phytochemical screening and determination of total polyphenols and flavonoids content in the leaves of Houttuynia cordata Thunb. In IOP Conference Series: Materials Science and Engineering 2020 (Vol. 736, No. 6, p. 062013). IOP Publishing. https://doi.org/10.1088/1757- 899X/736/6/062013
- Lu N, Takagaki M, Yamori W, Kagawa N. Flavonoid productivity optimized for green and red forms of Perilla frutescens via environmental control technologies in plant factory. Journal of Food Quality. 2018;2018. https://doi.org/10.1155/2018/4270279
Downloads
Download data is not yet available.