Abstract
Due to their ability to act as antioxidants, many metabolites serve as plant defense chemicals. Holistic metabolomic analysis is a method to investigate UV-B radiation impacts because the metabolome directly represents the physiological state of the plant. In order to determine how the exposure to UV-B radiation affected the accumulation of primary metabolites (amino acids, organic acids), secondary metabolites (phenolic compounds, fatty acids), and their synergistic antioxidant capacity in Rhododendron chrysanthum Pall., this study used gas chromatography-time-of-flight mass spectrometry (GC-TOFMS). Metabolite analysis revealed that there were 444 metabolites in total. Most amino acids and organic acids, in particular, rose in concentration following being exposed to UV-B. Simultaneously, the levels of tricarboxylic acid cycle (TCA) intermediates and phenolic compounds grew steadily. Furthermore, after UV-B therapy, the amount of anthocyanins, which are known to be powerful antioxidants, rose. In terms of protein–protein interaction (PPI) and enzyme content, the experimental group demonstrated greater antioxidant ability. In reaction to UV-B radiation, the content of metabolites that act as antioxidants increased. This experiment proved that R. chrysanthum main and secondary metabolisms were altered by UV-B radiation. It sheds some information on the combined analysis of metabolomics and other omics in R. chrysanthum.
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The datasets generated during and/or analysed during the current study are available from the corresponding author on reasonable request.
References
Durand TC, Cueff G, Godin B, Valot B, Clément G, Gaude T, Rajjou L (2019) Combined proteomic and metabolomic profiling of the Arabidopsis thaliana vps29 mutant reveals pleiotropic functions of the retromer in seed development. Int J Mol Sci. https://doi.org/10.3390/ijms20020362
Elsheery NI, Cao K-F (2008) Gas exchange, chlorophyll fluorescence, and osmotic adjustment in two mango cultivars under drought stress. Acta Physiol Plant 30(6):769–777. https://doi.org/10.1007/s11738-008-0179-x
Elsheery NI, Sunoj VSJ, Wen Y, Zhu JJ, Muralidharan G, Cao KF (2020) Foliar application of nanoparticles mitigates the chilling effect on photosynthesis and photoprotection in sugarcane. Plant Physiol Biochem 149:50–60. https://doi.org/10.1016/j.plaphy.2020.01.035
Erb M, Kliebenstein DJ (2020) Plant secondary metabolites as defenses, regulators, and primary metabolites: The blurred functional trichotomy. Plant Physiol 184(1):39–52. https://doi.org/10.1104/pp.20.00433
Escobar-Bravo R, Klinkhamer PGL, Leiss KA (2017) Interactive effects of UV-B light with abiotic factors on plant growth and chemistry, and their consequences for defense against arthropod herbivores. Front Plant Sci. https://doi.org/10.3389/fpls.2017.00278
Gai QY, Lu Y, Jiao J, Fu JX, Xu XJ, Yao L, Fu YJ (2022) Application of UV-B radiation for enhancing the accumulation of bioactive phenolic compounds in pigeon pea [Cajanus cajan (l.) Millsp.] hairy root cultures. J Photochem Photobiol B. https://doi.org/10.1016/j.jphotobiol.2022.112406
Gould KS (2004) Nature’s swiss army knife: The diverse protective roles of anthocyanins in leaves. J Biomed Biotechnol 2004(5):314–320. https://doi.org/10.1155/s1110724304406147
Hayat S, Hayat Q, Alyemeni MN, Wani AS, Pichtel J, Ahmad A (2012) Role of proline under changing environments: A review. Plant Signal Behav 7(11):1456–1466. https://doi.org/10.4161/psb.21949
Hu J, Fang H, Wang J, Yue X, Su M, Mao Z, Zou Q, Jiang H, Guo Z, Yu L, Feng T, Lu L, Peng Z, Zhang Z, Wang N, Chen X (2020) Ultraviolet B-induced MdWRXY72 expression promotes anthocyanin synthesis in apple. Plant Sci 292:110377. https://doi.org/10.1016/j.plantsci.2019.110377
Kasote DM, Katyare SS, Hegde MV, Bae H (2015) Significance of antioxidant potential of plants and its relevance to therapeutic applications. Int J Biol Sci 11(8):982–991. https://doi.org/10.7150/ijbs.12096
Korkina LG (2007) Phenylpropanoids as naturally occurring antioxidants: From plant defense to human health. Cell Mol Biol 53(1):15–25
Liu Z, Liu F, Li G, Chi X, Wang Y, Wang H, Ma L, Han K, Zhao G, Guo X, Xu B (2020) Metabolite support of long-term storage of sperm in the spermatheca of honeybee (Apis mellifera) queens. Front Physiol 11:574856. https://doi.org/10.3389/fphys.2020.574856
López-Bucio J, Nieto-Jacobo MF, Ramírez-Rodríguez VV, Herrera-Estrella L (2000) Organic acid metabolism in plants: From adaptive physiology to transgenic varieties for cultivation in extreme soils. Plant Sci 160(1):1–13. https://doi.org/10.1016/s0168-9452(00)00347-2
Lyu J, Wang C, Liang DY, Liu L, Pandey LK, Xu HW, Zhou XF (2019) Sensitivity of wild and domesticated Rhododendron chrysanthum to different light regime (UVA, UVB, and PAR). Photosynthetica 57(3):841–849. https://doi.org/10.32615/ps.2019.098
Qiu Y, Cai G, Zhou B, Li D, Zhao A, Xie G, Li H, Cai S, Xie D, Huang C, Ge W, Zhou Z, Xu LX, Jia W, Zheng S, Yen Y, Jia W (2014) A distinct metabolic signature of human colorectal cancer with prognostic potential. Clin Cancer Res 20(8):2136–2146. https://doi.org/10.1158/1078-0432.Ccr-13-1939
Rizzini L, Favory JJ, Cloix C, Faggionato D, O’Hara A, Kaiserli E, Baumeister R, Schäfer E, Nagy F, Jenkins GI, Ulm R (2011) Perception of UV-B by the Arabidopsis UVR8 protein. Science 332(6025):103–106. https://doi.org/10.1126/science.1200660
Shen JJ, Chen QS, Li ZF, Zheng QX, Xu YL, Zhou HN, Mao HY, Shen Q, Liu PP (2022) Proteomic and metabolomic analysis of Nicotiana benthamiana under dark stress. FEBS Open Bio 12(1):231–249. https://doi.org/10.1002/2211-5463.13331
Stepansky A, Galili G (2003) Synthesis of the Arabidopsis bifunctional lysine-ketoglutarate reductase/saccharopine dehydrogenase enzyme of lysine catabolism is concertedly regulated by metabolic and stress-associated signals. Plant Physiol 133(3):1407–1415. https://doi.org/10.1104/pp.103.026294
Sun Q, Liu M, Cao K, Xu H, Zhou X (2022) UV-B irradiation to amino acids and carbohydrate metabolism in Rhododendron chrysanthum leaves by coupling deep transcriptome and metabolome analysis. Plants (basel). https://doi.org/10.3390/plants11202730
Tohge T, Perez de Souza L, Fernie AR (2018) On the natural diversity of phenylacylated-flavonoid and their in planta function under conditions of stress. Phytochem Rev 17(2):279–290. https://doi.org/10.1007/s11101-017-9531-3
Xia J, Wishart DS (2010) Metpa: A web-based metabolomics tool for pathway analysis and visualization. Bioinformatics 26(18):2342–2344. https://doi.org/10.1093/bioinformatics/btq418
Yadav A, Singh D, Lingwan M, Yadukrishnan P, Masakapalli SK, Datta S (2020) Light signaling and UV-B-mediated plant growth regulation. J Integr Plant Biol 62(9):1270–1292. https://doi.org/10.1111/jipb.12932
Yang B, Wang X, Gao C, Chen M, Guan Q, Tian J, Komatsu S (2016) Proteomic and metabolomic analyses of leaf from Clematis terniflora DC. exposed to high-level ultraviolet-b irradiation with dark treatment. J Proteome Res 15(8):2643–2657. https://doi.org/10.1021/acs.jproteome.6b00206
Zaynab M, Fatima M, Sharif Y, Zafar MH, Ali H, Khan KA (2019) Role of primary metabolites in plant defense against pathogens. Microb Pathog 137:103728. https://doi.org/10.1016/j.micpath.2019.103728
Zhang X, Ding X, Ji Y, Wang S, Chen Y, Luo J, Shen Y, Peng L (2018) Measurement of metabolite variations and analysis of related gene expression in Chinese liquorice (Glycyrrhiza uralensis) plants under UV-B irradiation. Sci Rep 8(1):6144. https://doi.org/10.1038/s41598-018-24284-4
Zhang Q, Li Y, Sun L, Chu S, Xu H, Zhou X (2023) Integration of transcriptomic and proteomic analyses of Rhododendron chrysanthum Pall. in response to cold stress in the Changbai Mountains. Mol Biol Rep 50(4):3607–3616. https://doi.org/10.1007/s11033-022-08114-5
Zhao CL, Yu YQ, Chen ZJ, Wen GS, Wei FG, Zheng Q, Wang CD, Xiao XL (2017) Stability-increasing effects of anthocyanin glycosyl acylation. Food Chem 214:119–128. https://doi.org/10.1016/j.foodchem.2016.07.073
Zhou X, Chen S, Wu H, Yang Y, Xu H (2017) Biochemical and proteomics analyses of antioxidant enzymes reveal the potential stress tolerance in Rhododendron chrysanthum Pall. Biol Direct 12(1):10. https://doi.org/10.1186/s13062-017-0181-6
Zhou X, Lyu J, Sun L, Dong J, Xu H (2021) Metabolic programming of Rhododendron chrysanthum leaves following exposure to UVB irradiation. Funct Plant Biol 48(11):1175–1185. https://doi.org/10.1071/fp20386
Zou S, Wu J, Shahid MQ, He Y, Lin S, Liu Z, Yang X (2020) Identification of key taste components in loquat using widely targeted metabolomics. Food Chem 323:126822. https://doi.org/10.1016/j.foodchem.2020.126822
Acknowledgements
We are grateful to Jingjie PTM Biolab (Hangzhou, China) Co., Ltd. for providing mass spectrometry support.
Funding
This work was supported by the Jilin Provincial Science and Technology Development Program project (Grant numbers: YDZJ202301ZYTS517).
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Writing—original draft preparation, F.G. and X.Z.; writing—review and editing, K.C., H.X. and X.Z.; methodology, F.G.; software, F.G. and X.Z.; visualization, F.G. and X.Z.; supervision, K.C. and X.Z.; project administration, H.X. and X.Z. All authors have read and agreed to the published version of the manuscript.
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Gong, F., Zhou, X., Cao, K. et al. Analyses of the metabolism and assessment of antioxidant activity in Rhododendron chrysanthum Pall. after UV-B Irradiation. Plant Growth Regul 103, 525–537 (2024). https://doi.org/10.1007/s10725-024-01119-z
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DOI: https://doi.org/10.1007/s10725-024-01119-z