Journals / Alınteri Zirai Bilimler Dergisi / 2019 / Cilt: 34 - Sayı: 1

Salt Stress Triggered Changes in Osmoregulation and Antioxidants in Herbaceous Perennial Inula Plants (Asteraceae)

Pages
39–46
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Salt tolerance mechanisms of this rich bioresourse needs to be further studied in detail for herbal medicines in pharma sector.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Global demand to cure ailments is a growing need.
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Key Findings & Data:Both salt stress treatments caused photosynthetic pigments’ degradation, increase in the leaf levels of osmolytes, and induction of oxidative stress indicated by the malondialdehyde (MDA).
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Conclusion & Impact:Salt tolerance mechanisms of this rich bioresourse needs to be further studied in detail for herbal medicines in pharma sector.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Özet

Global demand to cure ailments is a growing need. Inula genus extensively holds hundreds of species in warmer regions of Europe and Asia. It is being well-known for its phytochemical and pharmacological applications in industry thanks to its anti-inflammatory and antimicrobial interests. However, growth and production of Inula in the cuttingedge industry is commonly influenced by salt stress except for the halophyte species such as the Inula crithmoides. Salt tolerance level by means of changes in osmoregulation and antioxidant systems in an herbaceous perennial Inula plant has been biochemically evaluated here. Both salt stress treatments caused photosynthetic pigments’ degradation, increase in the leaf levels of osmolytes, and induction of oxidative stress indicated by the malondialdehyde (MDA). Higher hydrogen peroxide (H2O2) amount was recorded in high salt concentration than low salt. High salinity caused an increase in ascorbate (ASC) and glutathione (GSH) contents besides target enzymes of Inula leaves. NaCl tolerance of Inula also was found comprehensible through the higher concentrations of proline and to a lesser extent, total soluble sugar. Salt tolerance mechanisms of this rich bioresourse needs to be further studied in detail for herbal medicines in pharma sector.

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Cite This Article

GEDİK, N. P., GÜLER, N. S. (2019). Salt Stress Triggered Changes in Osmoregulation and Antioxidants in Herbaceous Perennial Inula Plants (Asteraceae). Alınteri Zirai Bilimler Dergisi, Cilt: 34 - Sayı: 1, 39–46. https://ajindex.com/articles/143477

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References (12)

  1. AbdElgawad, H., Zinta, G., Hegab, M. M., Pandey, R., Asard, H., and Abuelsoud, W., 2016. High salinity induces different oxidative stress and antioxidant responses in maize seedlings organs. Frontiers in Plant Science 7: 276. Arnon, D. I., 1949. Copper enzymes in isolated chloroplasts, polyphenoxidase in Beta vulgaris. Plant physiology 24: 1-15.
  2. Ashraf, M., and Foolad, M., 2007. Roles of glycine betaine and proline in improving plant abiotic stress resistance. Environmental and Experimental Botany 59(2): 206-216.
  3. Bates, L., Waldren, R. P., Teare, I. D., 1973. Rapid determination of free proline for water-stress studies. Plant and Soil 39: 205-207.
  4. Demiral, T., and Türkan, I., 2005. Comparative lipid peroxidation, antioxidant defense systems and proline content in roots of two rice cultivars differing in salt tolerance. Environmental and Experimental Botany 53: 247-257.
  5. Dhindsa, R. S., and Matowe, W., 1981. Drought tolerance in two mosses: correlated with enzymatic defence against lipid peroxidation. Journal of Experimental Botany 32: 79-91.
  6. Foyer, C. H., Rowell, J., Walker, D., 1983. Measurement of the ascorbate content of spinach leaf protoplasts and chloroplasts during illumination. Planta 157:239-244
  7. Foyer, C. H., and Noctor, G., 2009. Redox regulation in photosynthetic organisms: signaling, acclimation, and practical implications. Antioxidants & Redox Signaling 11(4): 861-905.
  8. Foyer, C. H., Halliwell, B., 1976. Presence of glutathione and glutathione reductase in chloroplast: a proposed role in ascorbic acid metabolism. Planta 133: 21-25.
  9. Griffith, O. W., 1980. Determination of glutathione and glutathione disulfide using glutathione reductase and 2- vinylpyridine. Analytical Biochemistry 106: 207-212.
  10. Hayes, J. D., McLellan, L. I., 1999. Glutathione and glutathione-dependent enzymes represent a coordinately regulated defence against oxidative stress. Free Radical Research 31: 273-300.
  11. Hossain, M. S., and Dietz, K. J., 2016. Tuning of Redox Regulatory Mechanisms, Reactive Oxygen Species and Redox Homeostasis under Salinity Stress. Frontiers in plant science, 7: 548. Katarina, S., Jajoo, A., Guruprasad, K. N., 2014. Impact of increasing Ultraviolet-B (UV-B) radiation on photosynthetic processes. J. Photochem. Journal of Photochemistry and Photobiology B: Biology 137: 55-66.
  12. Karimi, H., Yusef-Zadeh, H., 2013. The effect of salinity level on the morphological and physiological traits of two grape [Vitis vinifera L.] cultivars. International Journal of Agro