UV-B Driven Metabolite Enrichment and Functional Bioactivity Enhancement in Allium cepa L.

IJEP 46(11): 1065-1075 : Vol. 46 Issue 11 (November 2026)

Pasupath Y Allasamy1, Shanthi Natarajan1* and Murugesan Subbiah2

1. Pachaiyappa’s College (Affiliated to University of Madras), P.G. and Research Department of Botany, Unit of Plant Stress Physiology, Chennai – 600 300, Tamil Nadu, India
2. Pachaiyappa’s College, P.G. and Research Department of Botany, Unit of Algal Biotechnology and Bionano- technology, Chennai – 600 030, Tamil Nadu, India

Abstract

This research examines the morphological, biochemical, phytochemical and proteomic responses of onion (Allium cepa L.) to ultraviolet-B (UV-B) radiation. In particular, UV-B-exposed plants showed greater morphological improvements, reflected in greater shoot extension, increased leaf count, increased bulb size and improved root structure, which are attributed to increased vigor and adaptive growth under UV-B stress. Biochemical testing showed increased chlorophyll, carotenoids, flavonoids and anthocyanins relative to controls, indicating UV-B-mediated stimulation of pigment biosynthesis and accumulation of secondary metabolites. High-performance liquid chromatography (HPLC) results showed an increase in water-soluble vitamins (C and B-complex) following UV-B irradiation and a decrease in fat-soluble vitamins (A, D, E and K), suggesting selective photostability under stress and metabolically regulated behaviour. Phytochemical analysis showed moderate increases in phenolic, flavonoid and alkaloid levels, consistent with activation of the phenylpropanoid pathway. Antimicrobial assays showed greater effectiveness against Bacillus pumilus and Candida albicans because of the increased levels of phenolic and flavonoid compounds. The SDS-PAGE analysis of chloroplast proteins showed that UV-B-treated plants produced stronger bands at ~35, ~45 and ~55 kDa, corresponding to proteins that help plants respond to stress and protect themselves from UV damage. The research results showed that moderate UV-B exposure helps onions develop better physical strength, increase pigment production and vitamin levels and enhance antimicrobial defense through biochemical and proteomic changes, demonstrating their ability to adapt and remain healthy.

Keywords

Allium cepa, UV-B radiation, morphological adaptation, secondary metabolites, chloroplast proteins, phenyl propanoid pathway, antimicrobial activity

References

  1. Jenkins, G. I. 2017. Photomorphogenic responses to ultraviolet-B light. Plant, Cell Env., 40(11): 2544–2557. DOI: 10.1111/pce.12934.
  2. Wang, Y., Zhu, H. and Fang, X. 2024. Moderate UV-B radiation acts as a eustress factor improving growth and phytochemical accumulation in onions. Photochem. Photobiol., 100(2): 342–353. DOI: 10. 1111/php.13895.
  3. Turner, B.L., Li, C. and Jenkins, G.I. 2025. Integrative photoreceptor signaling networks under UV-B exposure: Regulation of stress adaptation in higher plants. Trends Plant Sci., 30(2): 145–159. DOI: 10.1016/j.tplants.2024.09.005.
  4. Zlatev, Z., Lidon, F.C. and Ramalho, J.C. 2023. UV-B radiation as a plant eustressor: Mechanisms, regulation and agricultural potential. Plant Stress. 8: 100149. DOI: 10.1016/j. stress.2023.100149.
  5. Reilly, K. 2013. Onion and garlic. In Nutritional composition of fruit cultivars. Ed Simmonds, M.S.J. and Preesy, V.R. Academic Press.
  6. Abdellatif, F.M. and Al-Senosy, A.E. 2018. Phyto-chemical composition, antioxidant and antimicrobial activities of onion (Allium cepa L.) extracts. J. Appl. Pharmaceutical Sci., 8(5): 112–118. DOI: 10.7324/JAPS.2018.8520.
  7. Griffiths, G., Trueman, L., Crowther, T., Thomas, B. and Smith, B. 2020. Onions—A global benefit to health. Phytotherapy Res., 34(8): 1852–1863. DOI: 10.1002/ptr.6660.
  8. Li, X., Wang, Y., Liu, Y. and Wang, J. 2015. UV-induced accumulation of Quercetin derivatives and antioxidant capacity in onion bulbs. J. Photochem. Photobiol. B: Biol., 142: 78–84. DOI: 10.1016/j.jphotobiol.2014.12.018
  9. Marzouk, M.M., Soliman, F.M., Badawy, M.A. and El-Gengaihi, S.E. 2018. Polyphenolic profile and antioxidant activity of Allium cepa L. extracts. J. Appl. Pharmaceutical Sci., 8(2): 105–113.
  10. Neugart, S. and Schreiner, M. 2018. UV-B in controlled environment agriculture—Influence on plant secondary metabolites, composition and relevance for human health. Front. Plant Sci., 9: 1225. DOI: 10.3389/fpls.2018.01225.
  11. Li, X., Wang, L. and Zhang, Q. 2023. Modulation of UV-B-induced antioxidant response and flavonoid biosynthesis in onion leaves. Photochem. Photobiol. B: Biol., 248: 113488. DOI: 10.1016/j.jphotobiol. 2023.113488.
  12. Chen, X., Li, H., Zhang, Y. and Wang, Q. 2024. UV-B radiation enhances photosynthetic pigment biosynthesis and antioxidant activity in spinach leaves. Plant Physiol. Biochem., 210: 108245. DOI: 10. 1016/j.plaphy.2024.108245.
  13. Zhu, Y., Zhang, X. and Li, H. 2025. UV-B-induced chloroplast proteome remodeling enhances stress tolerance in onions (Allium cepa L.). J. Proteomics. 305: 104993. DOI: 10.1016/j.jprot. 2025.104993.
  14. Caldwell, M.M. 1971. Solar ultraviolet radiation and the growth and development of higher plants. Photo-physiol., 6: 131–177. DOI: 10.1016/B978-0-12-564106-2.50009-6.
  15. Arnon, D. I. 1949. Copper enzymes in isolated chloroplasts: Polyphenol oxidase in Beta vulgaris. Plant Physiol., 24(1): 1–15. DOI: 10.1104/pp.24.1.1.
  16. Mancinelli, A.L. 1975. The photoregulation of anthocyanin synthesis. Botanical Review. 41(4): 407–429. DOI: 10.1007/BF02860836.
  17. Mirecki, R.M. and Teramura, A.H. 1984. Effects of ultraviolet-B irradiance on soybean. V. The dependence of plant sensitivity on the photosynthetic photon flux density during and after leaf expansion. Plant Physiol., 74(3): 475–480. DOI: 10.1104/pp. 74.3.475.
  18. Chang, C., Yang, M., Wen, H. and Chern, J. 2002. Estimation of total flavonoid content in Propolis by two complementary colorimetric methods. J. Food Drug Analysis. 10(3): 178–182.
  19. Marzouk, M., and Koutb, N. 2018. Identification of bioactive compounds in UV-treated samples using peak analysis. Biosci. Res., 15(4): 3768–3774.
  20. Laemmli, U.K. 1970. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 227(5259): 680–685. DOI: 10.1038/227680a0.
  21. Calabrese, E.J. and Baldwin, L.A. 2003. Hormesis: The dose-response revolution. Annual Review Pharmacol. Toxicol., 43: 175–197. DOI: 10.1146/annurev.pharmtox.43.100901.140223.
  22. Nashnoush, N. and Rodgers, C. 2020. Prolonged UV-B exposure induces growth inhibition and oxidative stress in crop plants. Photochem. Photobiol. Sci., 19(9): 1241–1252. DOI: 10.1039/ D0PP0011 1A.
  23. Xu, Q., Chen, X. and Li, H. 2024. UV-B intensity-dependent modulation of growth and antioxidant responses in horticultural plants. Front. Env. Sci., 12: 1365859. DOI: 10.3389/fenvs.2024. 1365859
  24. Li, H., Li, J., Chen, X. and Zhang, Y. 2023. Controlled UV-B exposure enhances photosynthetic efficiency and antioxidant capacity in greenhouse onions (Allium cepa L.). Env. Experimental Botany. 211: 105070. DOI: 10.1016/j.envexpbot.2023. 105070.
  25. Yadav, A., Singh, P. and Raghav, R. 2020. UVR8-mediated signaling regulates hormone balance and stress responses in plants. Plant Signal. Behaviour. 15(9): 1772551. DOI: 10.1080/15592 324.2020.1772551.
  26. Terry, M.J. 2013. Ultraviolet B radiation impacts on plant pigment biosynthesis. Annual Review Plant Biol., 64: 601–626. DOI: 10.1146/annurev-arplant-050312-120125.
  27. Liaqat, M., Khan, M.A. and Hussain, M. 2024. Modulation of phenolic and flavonoid profiles under UV-B radiation in horticultural crops. J. Photochem. Photobiol. B: Biol., 247: 112481. DOI: 10.1016/j.jphotobiol.2024.112481.
  28. Liu, J., Zhang, Q. and Luo, X. 2023. UV-B radiation enhances ascorbic acid accumulation through the stimulation of biosynthetic enzymes in lettuce. Plant Sci., 334: 111648. DOI: 10.1016/ j.plantsci.2023. 111648.
  29. Moyo-Bonnet, L., Farrant, J.M. and Krüger, G.H.J. 2017. Impact of UV-B radiation on carotenoid composition and photoprotection in tobacco leaves. Plant Physiol. Biochem., 118: 171–178. DOI: 10.1016j. plaphy.2017.06.009
  30. Zhang, X., He, J., Song, L. and Zheng, Y. 2023. Regulation of phenolic metabolism under UV-B radiation in higher plants. Env. Experimental Botany. 202: 105045. DOI: 10.1016/j.envexpbot. 2023.105045.
  31. Yang, L., Zhang, H. and Zheng, Y. 2024. UV-B-induced phenylpropanoid metabolism and antioxidant responses in buckwheat sprouts. J. Agric. Food Chem., 72(11): 4571–4582. DOI: 10.1021/acs. jafc.3c07426.
  32. Zhen, S., Tu, Y., Lin, X., Xu, W., Fu, J. and Han, L. 2022. UV-B exposure enhances phenolic synthesis and oxidative stress protection in plants. Plant Sci., 320: 111295. DOI: 10.1016/ j.plantsci.2022.111 295.
  33. Robson, T.M. and Klemen, B. 2021. Differential accumulation of photosynthetic proteins under UV-B radiation in higher plants. Plant, Cell Env., 44(7): 2203–2217. DOI: 10.1111/pce.14041.
  34. Jansen, M.A.K., Gaba, V. and Greenberg, B.M. 2023. Higher plants and UV-B radiation: Balancing damage, repair and acclimation. Physiol. Plantarum. 175(1): e13976. DOI: 10.1111/ppl.13976.
  35. Hideg, É., Jansen, M.A.K. and Strid, Å. 2020. UV-B exposure, ROS and stress management. Plant Physiol. Biochem., 152: 106–112. DOI: 10.1016/j.plaphy.2020.04.039.
  36. Jenkins, G.I. 2014. The UV-B photoreceptor UVR8: From structure to physiology. Plant Cell. 26(1): 21–37. DOI: 10.1105/tpc.113.119446.
  37. Kusumi, K., Sakurada, M. and Watanabe, M. 2023. UV-B-induced chloroplast proteome remodeling enhances photoprotection and stress tolerance in rice. Front. Plant Sci., 14: 1154362. DOI: 10.3389/fpls.2023.1154362.
  38. Zhu, H., Fang, X. and Yin, Y. 2024. Balancing growth and defense: UV-B radiation reshapes plant metabolism. Plant Stress. 12: 100276. DOI: 10.1016/j. stress.2024.100276.