Effect of long-term grazing on the contents of phenolic compounds in Carex and Aster plants in Mongolia

Authors

  • Purevdorj Erdenetsogt Institute of Chemistry and Chemical Technology, Mongolian Academy of Sciences, Ulaanbaatar 13330, Mongolia
  • Nomin Munkhbat Institute of Chemistry and Chemical Technology, Mongolian Academy of Sciences, Ulaanbaatar 13330, Mongolia
  • Enkhriimaa Narmandakh Botanic Garden and Research Institute, Mongolian Academy of Sciences, Ulaanbaatar 13330, Mongolia
  • Tuvshintogtokh Idree Botanic Garden and Research Institute, Mongolian Academy of Sciences, Ulaanbaatar 13330, Mongolia
  • Chuan-Ming Yeh Institute of Molecular Biology, National Chung Hsing University, Taichung 40227, Taiwan
  • Munkhtsetseg Tsednee Institute of Chemistry and Chemical Technology, Mongolian Academy of Sciences, Ulaanbaatar 13330, Mongolia https://orcid.org/0000-0002-2878-0112

DOI:

https://doi.org/10.5564/mjc.v25i52.3582

Keywords:

Carex, Aster, Stipa baicalensis, grazing, phenol, lavonoid

Abstract

Long-term grazing changes the plant diversity and their growth significantly. At the metabolite level, the contents and compositions of the specialized metabolic compounds in plants could also be altered under long-term grazing conditions. To understand the metabolic changes caused by the grazing stress, in this study, we compared the contents and compositions of major phenolic compounds, together with total flavonoid contents, in two grazing-tolerant plants, Carex duriuscula and Aster hispidus, and two grazing-non-tolerant plants, Carex pediformus and Aster alphinus, and a local native plant Stipa baicalensus under long-term grazing conditions in Mongolia. Our results showed that long-term grazing has altered the contents and compositions of phenolic compounds and flavonoids both in above-ground tissues and roots of the analyzed five plants. Interestingly, such effects could appear to differ depending on plant species. These results provide the first comparative study of metabolite changes in grazing-tolerant and grazing-non-tolerant plants under overgrazing stress in the country.          

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References

1. Munkhzul O., Oyundelger K., Narantuya N., Tuvshintogtokh I., Oyuntsetseg B., et al. (2021) Grazing effects on Mongolian steppe vegetation - A systematic review of local literature. Front. Ecol. Evol., 9, 703220, 1-13. https://doi.org/10.3389/fevo.2021.703220

2. Ahlborn J., von Wehrden H., Lang B., Römermann C., Munkhzul O., et al. (2020) Climate - grazing interactions in Mongolian rangelands: Effects of grazing change along a large-scale environmental gradient. J. Arid. Environ., 173, 104043, 1-10. https://doi.org/10.1016/j.jaridenv.2019.104043

3. Yearly report of Mongolian pasture land (2016) Ministry of Environment and Tourism, Mongolia.

4. Tuvshintogtokh I. (2014) Grassland in Mongolia and their degradation indicator plants. In: International Symposium on the East Asia Environmental Problems (EAEP2014), Fukuoka, 8. https://www.researchgate.net/publication/271509448

5. Tuvshintogtokh I. (2014) The steppe vegetation of Mongolia. Bembi san printing, Ulaanbaatar, 610.

6. Tuvshintogtokh I., Ariungerel D. (2013) Degradation of Mongolian grassland vegetation under overgrazing by livestock and its recovery by protection from livestock grazing. In: Yamamura N., Fujita N., Maekawa A. (eds). The Mongolian Ecosystem Network: Environmental Issues under Climate and Social Changes. Ecological research monographs. Springer, Tokyo. 115-130. https: doi.org/10.1007/978-4-431-54052-6_10

7. Shulaev V., Cortes D., Miller G., Mittler R. (2008) Metabolomics for plant stress response. Physiol. Plant., 132(2), 199-208. https://doi.org/10.1111/j.1399-3054.2007.01025.x

8. Aguirre-Becerra H., Vazquez-Hernandez M.C., Saenz O.D., Alvarado-Mariana A., Guevara-Gonzalez R.G., et al. (2021) Role of stress and defense in plant secondary metabolites production. In: Pal D., Nayak A.K (eds) Bioactive Natural Products for Pharmaceutical Applications. Advanced structured materials, 140. Springer, Cham. 151-195. https://doi.org/10.1007/978-3-030-54027-2_5

9. Tsubo M., Nishihara E., Nakamatsu K., Cheng Y., Shinoda M. (2011) Plant volatiles inhibit restoration of plant species communities in dry grassland. Basic App. Ecol., 13(1), 76-84. https://doi.org/10.1016/j.baae.2011.11.005

10. Waśkiewicz A., Muzolf-Panek M., Goliński P. (2013) Phenolic content changes in plants under salt stress. In: Ahmad P., Azooz M., and Prasad M. (eds) Ecophysiology and Responses of Plants under Salt Stress. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-4747-4_11

11. Corso M., Perreau F., Mouille G., Lepiniec L. (2020) Specialized phenolic compounds in seeds: Structures, functions, and regulations. Plant Sci., 296, 10471. https://doi.org/10.1016/j.plantsci.2020.110471

12. Tsednee M., Mak Y.W., Chen Y.R., Yeh K.C. (2012) A sensitive LC‐ESI‐Q‐TOF‐MS method reveals novel phytosiderophores and phytosiderophore-iron complexes in barley. New Phytol., 195(4), 951-961. https://doi.org/10.1111/j.1469-8137.2012.04206.x

13. Tsednee M., Yang S.C., Lee D.C., Yeh K.C. (2014) Root-secreted nicotianamine from Arabidopsis halleri facilitates zinc hypertolerance by regulating zinc bioavailability. Plant Physiol., 166(2), 839-852. https://doi.org/10.1104/pp.114.241224

14. Oidovsambuu S., Tsagaantsooj T., Bekh-Ochir D., Maygmar N., Batkikh I., et al. (2024) Cytotoxicity screening of 114 Mongolian plant extracts on liver, colon, breast, and cervix cancer cell lines. Mong. J. Chem., 25(51), 11-17. https://doi.org/10.5564/mjc.v25i51.2934

15. Selenge D., Jamyansan Ya., Javzan S., Delegmaa M., Dumaa M., Gerelt-Od Ya., Solongo A., Nyamsuren E., Mungunshagai B. (2018) Alkaloids from some Mongolian medicinal plants. Bull. Inst. Chem. Chem. Technol., (6), 10-20. https://doi.org/10.5564/bicct.v0i6.1095

16. Method standard for quantification of phenolic compounds using spectrophotometer (2020) The Institute of Chemistry and Chemical Technology, Mongolian Academy of Sciences, CAS-01-01:2020

17. Ayele D.T., Akele L.M., Melese A.T. (2022) Analysis of total phenolic contents, flavonoids, antioxidant and antibacterial activities of Croton macrostachyus root extracts. BMC Chem., 16(30), 1-12. https://doi.org/10.1186/s13065-022-00822-0

18. Gendaram O. (2019) Phytochemicals in leaves of Cotoneaster mongolica, their antioxidative, and acetylcholinesterase inhibitory activity. Mong. J. Chem., 20(46), 1-6. https://doi.org/10.5564/mjc.v20i46.1235

19. Qu K., Cheng Y., Gao K., Ren W., Fry E., et al. (2022) Growth-defense trade-offs induced by long-term overgrazing could act as a stress memory. Front. Plant Science, 13, 917354. https://doi.org/10.3389/fpls.2022.917354

20. Csepregi K., Hideg E. (2018) Phenolic compound diversity explored in the context of photo-oxidative stress protection. Phytoch. Anal., 29, 129-136. https://doi.org/10.1002/pca.2720

21. Marchiosi R., dos Santos W.D., Constantin R.P., de Lima R.B., Soares A.R., et al. (2020) Biosynthesis and metabolic actions of simple phenolic acids in plants. Phytochem. Rev., 19, 865-906. https://doi.org/10.1007/s11101-020-09689-2

22. Tsednee M., Tanaka M., Giehl R.F., von Wirén N., Fujiwara T. (2022) Involvement of NGATHA-Like 1 transcription factor in boron transport under low and high boron conditions. Plant Cell Physiol., 63(9), 1242-1252. https://doi.org/10.1093/pcp/pcac099

23. Vives-Peris V., de Ollas C., Gómez-Cadenas A., Pérez-Clemente R.M. (2020) Root exudates: from plant to rhizosphere and beyond. Plant Cell Rep., 39, 3-17. https://doi.org/10.1007/s00299-019-02447-5

24. Yu R.P., Zhang W.P., Yu Y.C., Yu S.B., Lambers H., et al. (2020) Linking shifts in species composition induced by grazing with root traits for phosphorus acquisition in a typical steppe in Inner Mongolia. Sci. Total Environ., 712, 136495, 1-10. https://doi.org/10.1016/j.scitotenv.2020.136495

25. Li B., Fan R., Sun G., Sun T., Fan Y., et al. (2021) Flavonoids improve drought tolerance of maize seedlings by regulating the homeostasis of reactive oxygen species. Plant Soil, 461, 389-405. https://doi.org/10.1007/s11104-020-04814-8

26. Gourlay G., Hawkins B.J., Albert A., Schnitzler J.P., Peter C.C. (2022) Condensed tannins as antioxidants that protect poplar against oxidative stress from drought and UV-B. Plant Cell Environmen., 45(2), 362-377. https://doi.org/10.1111/pce.14242

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Published

2024-12-27

How to Cite

Erdenetsogt, P., Munkhbat, N., Narmandakh, E., Idree, T., Yeh, C.-M., & Tsednee, M. (2024). Effect of long-term grazing on the contents of phenolic compounds in Carex and Aster plants in Mongolia. Mongolian Journal of Chemistry, 25(52), 43–50. https://doi.org/10.5564/mjc.v25i52.3582

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