Journals / Eurasian Journal of Biological and Chemical Sciences / 2025 / Volume: 8 Issue: 2

Phenolic acid and flavonoid diversity in four Eucalyptus species

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Publication Date
2025-12-29
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AI Summary & Key Takeaways

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

E. botryoides was evaluated as a natural source for catechin, E. citriodora for t-ferulic acid and rosmarinic acid, and E. tereticornis for gallic acid were evaluated as rich sources.

📌 3 Key Takeaways

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Objective & Hypothesis:The economic importance of Eucalyptus trees is due to their rapid growth and high biomass productivity, as well as the beneficial chemical compounds found in their various tissues.
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Key Findings & Data:The highest total phenolic amounts were found in E. botryoides (160.56 mg g-1DW), followed by E. tereticornis (66.47 mg g⁻¹ DW) and E. citriodora (64.02 mg g⁻¹ DW).
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Conclusion & Impact:E. botryoides was evaluated as a natural source for catechin, E. citriodora for t-ferulic acid and rosmarinic acid, and E. tereticornis for gallic acid were evaluated as rich sources.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Polyphenol · Eucalypthus · HPLC

Abstract

The economic importance of Eucalyptus trees is due to their rapid growth and high biomass productivity, as well as the beneficial chemical compounds found in their various tissues. Eucalyptus cultivation is common in the southern part of Turkey, especially in the coastal areas of the Mediterranean. In this study, phenolic acids and flavonoids were analyzed in methanol extracts leaf tissues of four eucalyptus species by HPLC. Fifteen different phenolic compounds were determined in the leaf tissues of the four Eucalyptus species examined. The highest total phenolic amounts were found in E. botryoides (160.56 mg g-1DW), followed by E. tereticornis (66.47 mg g⁻¹ DW) and E. citriodora (64.02 mg g⁻¹ DW). Twelve different compounds were determined in E. botryoides and E. citriodora species, 10 in the hybrid E. camaldulensis x grandis and 9 in E. tereticornis. E. botryoides was evaluated as a natural source for catechin, E. citriodora for t-ferulic acid and rosmarinic acid, and E. tereticornis for gallic acid were evaluated as rich sources.

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Cite This Article

Albayrak, F. O., Aytar, F., Keleş, Y. (2025). Phenolic acid and flavonoid diversity in four Eucalyptus species. Eurasian Journal of Biological and Chemical Sciences, Volume: 8 Issue: 2. https://doi.org/10.46239/ejbcs.1772538

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References (23)

  1. Albayrak FÖ, Özdeniz E, Kurt L, Keleş Y. 2021. Variation of phenolic and pigment composition depending on soil type in three serpentinovag plant species. Int J Second Metabol. 8:1–10. doi:10.21448/ijsm.765645
  2. Almeida IF, Fernandes E, Lima JLFC, Valentão P, Andrade PB, Seabra RM, Costa PC, Bahia MF. 2009. Oxygen and nitrogen reactive species are effectively scavenged by Eucalyptus globulus leaf water extract. J Med Food. 12:175–183.
  3. Álvarez X, Cancela Á, Merchán Y, Sánchez Á. 2021. Anthocyanins, phenolic compounds, and antioxidants from extractions of six Eucalyptus species. Appl Sci. 11:9818. doi:10.3390/app11219818
  4. Caponio F, Alloggio V, Gomes T. 1999. Phenolic compounds of virgin olive oil: influence of paste preparation techniques. Food Chem. 64:203–209. doi:10.1016/S0308-8146(98)00146-0
  5. Chamali S, Bendaoud H, Bouajila J, Camy S, Saadaoui E, Condoret JS, Romdhane M. 2023. Optimization of accelerated solvent extraction of bioactive compounds from Eucalyptus intertexta using response surface methodology and evaluation of its phenolic composition and biological activities. J Appl Res Med Aromat Plants. 35:100464. doi:10.1016/j.jarmap.2023.100464
  6. Çekiç FÖ, Özdeniz E, Öktem M, Kurt L, Keleş Y. 2018. The role of biochemical regulation on the adaptation of gypsophile and gypsovag species. Biochem Syst Ecol. 81:12–16. doi:10.1016/j.bse.2018.09.007
  7. Cheng LC, Murugaiyah V, Chan KL. 2015. Flavonoids and phenylethanoid glycosides from Lippia nodiflora as promising antihyperuricemic agents and elucidation of their mechanism of action. J Ethnopharmacol. 176:485–493. doi:10.1016/j.jep.2015.11.025
  8. Elansary HO, Salem MZM, Ashmawy NA, Yessoufou K, El-Settawy AAA. 2017. In vitro antibacterial, antifungal and antioxidant activities of Eucalyptus spp. leaf extracts related to phenolic composition. Nat Prod Res. 31:2927–2930. doi:10.1080/14786419.2017.1303698
  9. Elbouzidi A, Haddou M, Baraich A, Taibi M, El Hachlafi N, Pareek A, Mesnard F, Addi M. 2025. Biochemical insights into specialized plant metabolites: Advancing cosmeceutical applications for skin benefits. J Agric Food Res. 19:101651. doi:10.1016/j.jafr.2025.101651
  10. Goldsmith C, Vuong Q, Stathopoulos C, Roach P, Scarlett C. 2014. Optimization of the aqueous extraction of phenolic compounds from olive leaves. Antioxidants. 3:700–712. doi:10.3390/antiox3040700
  11. Gullón P, Gullón B, Astray G, Munekata PES, Pateiro M, Lorenzo JM. 2020. Value-added compound recovery from invasive forest for biofunctional applications: Eucalyptus species as a case study. Molecules. 25:4227. doi:10.3390/molecules25184227
  12. Lee JE, Jayakody JTM, Kim JI, Jeong JW, Choi KM, Kim TS, Seo C, Azimi I, Hyun JM, Ryu BM. 2024. The influence of solvent choice on the extraction of bioactive compounds from Asteraceae: A comparative review. Foods. 13(19):3151. doi: 10.3390/foods13193151.
  13. Limam H, Ezzine Y, Tammar S, Ksibi N, Selmi S, Del Re G, Ksouri R, Msaada K. 2021. Phenolic composition and antioxidant activities of thirteen Eucalyptus species cultivated in North East of Tunisia. Plant Biosyst. 155:587–597. doi:10.1080/11263504.2020.1762791
  14. Moges GW, Manahelohe GM, Asegie MA. 2024. Phenolic and flavonoid contents, antioxidant and antibacterial activity of selected Eucalyptus species: review. Biol Med Nat Prod Chem. 13:147–157. doi:10.14421/biomedich.2024.131.147-157
  15. Nasr A, Zhou X, Liu T, Yang J, Zhu GP. 2019. Acetone-water mixture is a competent solvent to extract phenolics and antioxidants from four organs of Eucalyptus camaldulensis. Turk J Biochem. 44:231–239. doi:10.1515/tjb-2018-0438
  16. Öncel I, Yurdakulol E, Keleş Y, Kurt L, Yıldız A. 2004. Role of antioxidant defense system and biochemical adaptation on stress tolerance of high mountain and steppe plants. Acta Oecol. 26:211–218. doi:10.1016/j.actao.2004.04.004
  17. Park JY, Kim JY, Son YG, Kang SD, Lee SW, Kim KD, Kim JY. 2023. Characterization of chemical composition and antioxidant activity of Eucalyptus globulus leaves under different extraction conditions. Appl Sci. 13:9984. doi:10.3390/app13179984
  18. Santos SAO, Vilela C, Freire CSR, Neto CP, Silvestre AJD. 2013. Ultra-high performance liquid chromatography coupled to mass spectrometry applied to the identification of valuable phenolic compounds from Eucalyptus wood. J Chromatogr B. 938:65–74. doi:10.1016/j.jchromb.2013.08.034
  19. Tyagi AK, Malik A. 2011. Antimicrobial potential and chemical composition of Eucalyptus globulus oil in liquid and vapour phase against food spoilage microorganisms. Food Chem. 126:228–235. doi:10.1016/j.foodchem.2010.11.002
  20. Wagay NA, Rafiq S, Khan A, Kaloo ZA, Malik AR, Pulate PV 2023. Impact of phenolics on drought stress and expression of phenylpropanoid pathway genes. In: Lone, R., Khan, S., Mohammed Al-Sadi, A. (eds) Plant Phenolics in Abiotic Stress Management. Springer, Singapore. doi:10.1007/978-981-19-6426-8_13
  21. Wingfield MJ, Roux J, Slippers B, Hurley BP, Garnas J, Myburg AA, Wingfield BD. 2013. Established and new technologies reduce increasing pest and pathogen threats to Eucalypt plantations. For Ecol Manag. 301:35–42. doi:10.1016/j.foreco.2012.09.002
  22. Zhu H, Song D, Zhao X. 2021. Potential applications and preliminary mechanism of action of dietary polyphenols against hyperuricemia: a review. Food Biosci. 43:101297. doi:10.1016/j.fbio.2021.101297
  23. Zhou G, Xu R, Groth T, Wang Y, Yuan X, Ye H, Dou X. 2024. The combination of bioactive herbal compounds with biomaterials for regenerative medicine. Tissue Eng Part B Rev. 30:607–630. doi:10.1089/ten.teb.2024.0002