journal article Open Access May 20, 2024

Exogenous melatonin prolongs raspberry postharvest life quality by increasing some antioxidant and enzyme activity and phytochemical contents

View at Publisher Save 10.1038/s41598-024-62111-1
Abstract
AbstractThere is a growing trend towards enhancing the post-harvest shelf life and maintaining the nutritional quality of horticultural products using eco-friendly methods. Raspberries are valued for their diverse array of phenolic compounds, which are key contributors to their health-promoting properties. However, raspberries are prone to a relatively short post-harvest lifespan. The present study aimed to investigate the effect of exogenous melatonin (MEL; 0, 0.001, 0.01, and 0.1 mM) on decay control and shelf-life extension. The results demonstrated that MEL treatment significantly reduced the fruit decay rate (P ≤ 0.01). Based on the findings, MEL treatment significantly increased titratable acidity (TA), total phenolics content (TPC), total flavonoid content (TFC), and total anthocyanin content (TAC). Furthermore, the MEL-treated samples showed increased levels of rutin and quercetin content, as well as antioxidant activity as measured by 2,2-diphenyl-1-picrylhydrazyl (DPPH) and ferric reduction activity potential (FRAP). Additionally, the samples exhibited higher levels of phenylalanine ammonia-lyase (PAL) and catalase (CAT) enzymes compared to the control samples. Moreover, the levels of pH, total soluble solids (TSS), and IC50 were decreased in the MEL-treated samples (P ≤ 0.01). The highest amount of TA (0.619 g/100 ml juice), rutin (16.722 µg/ml juice) and quercetin (1.467 µg/ml juice), and PAL activity (225.696 nm/g FW/min) was observed at 0.001 mM treatment, while, the highest amount of TAC (227.235 mg Cy-g/100 ml juice) at a concentration of 0.01 mM and CAT (0.696 u/g FW) and TAL activities (9.553 nm/100 g FW) at a concentration of 0.1 mM were obtained. Considering the lack of significant differences in the effects of melatonin concentrations and the low dose of 0.001 mM, this concentration is recommended for further research. The hierarchical cluster analysis (HCA) and principal component analysis (PCA) divided the treatments into three groups based on their characteristics. Based on the Pearson correlation between TPC, TFC, TAC, and TAA, a positive correlation was observed with antioxidant (DPPH and FRAP) and enzyme (PAL and CAT) activities. The results of this study have identified melatonin as an eco-friendly compound that enhances the shelf life of raspberry fruits by improving phenolic compounds, as well as antioxidant and enzyme activities.
Topics

No keywords indexed for this article. Browse by subject →

References
77
[1]
Faridi, M. R. & Sulphey, M. M. Food security as a prelude to sustainability: a case study in the agricultural sector, its impacts on the Al Kharj community in The Kingdom of Saudi Arabia. Entrepreneur. Sustain. 6(3), 1536. https://doi.org/10.9770/jesi.2019.6.3(34) (2019). 10.9770/jesi.2019.6.3(34)
[2]
Crop losses to pests

E.-C. OERKE

The Journal of Agricultural Science 2006 10.1017/s0021859605005708
[3]
Chakraborty, S. & Newton, A. C. Climate change, plant diseases and food security: an overview. Plant Pathol. 60(1), 2–14. https://doi.org/10.1111/j.1365-3059.2010.02411.x (2011). 10.1111/j.1365-3059.2010.02411.x
[4]
Rahemi, M. Physiology of Postharvest An introduction to the physiology and handling of fruit, vegetables and ornamental plants 4th edn. (Shiraz University Press, 2005).
[5]
Tefera, T. et al. The metal silo: An effective grain storage technology for reducing post-harvest insect and pathogen losses in maize while improving smallholder farmers’ food security in developing countries. Crop Prot. 30(3), 240–245. https://doi.org/10.1016/j.cropro.2010.11.015 (2011). 10.1016/j.cropro.2010.11.015
[6]
Manandhar, A., Milindi, P. & Shah, A. An overview of the post-harvest grain storage practices of smallholder farmers in developing countries. Agriculture. 8(4), 57. https://doi.org/10.3390/agriculture8040057 (2018). 10.3390/agriculture8040057
[7]
Minhas, P. S., Ramos, T. B., Ben-Gal, A. & Pereira, L. S. Coping with salinity in irrigated agriculture: Crop evapotranspiration and water management issues. Agric. Water Manag. https://doi.org/10.1016/j.agwat.2019.105832 (2020). 10.1016/j.agwat.2019.105832
[8]
Lurie, S. Plant growth regulators for improving postharvest stone fruit quality. XI International Symposium on Plant Bioregulators in Fruit Production. Acta Hortic. 884, 189–197. https://doi.org/10.17660/ActaHortic.2010.884.21 (2009). 10.17660/actahortic.2010.884.21
[9]
Reid, M. S. & Jiang, C. Z. Postharvest biology and technology of cut flowers and potted plants. Hortic. Rev. 40, 1–54. https://doi.org/10.1002/9781118351871.ch1 (2012). 10.1002/9781118351871.ch1
[10]
Tan, D. X. et al. Mitochondria and chloroplasts as the original sites of melatonin synthesis: A hypothesis related to melatonin’s primary function and evolution in eukaryotes. J. Pineal Res. 54(2), 127–138. https://doi.org/10.1111/jpi.12026 (2013). 10.1111/jpi.12026
[11]
Tan, D. X., Manchester, L. C., Helton, P. & Reiter, R. J. Phytoremediative capacity of plants enriched with melatonin. Plant Signal. Behav. 2(6), 514–516. https://doi.org/10.4161/psb.2.6.4639 (2007). 10.4161/psb.2.6.4639
[12]
Li, C. et al. The mitigation effects of exogenous melatonin on salinity-induced stress in Malus hupehensis. J. Pineal Res. 53(3), 298–306. https://doi.org/10.1111/j.1600-079X.2012.00999.x (2012). 10.1111/j.1600-079x.2012.00999.x
[13]
Wang, Z. et al. Melatonin enhanced chilling tolerance and alleviated peel browning of banana fruit under low temperature storage. Postharvest Biol. Technol. https://doi.org/10.1016/j.postharvbio.2021.111571 (2021). 10.1016/j.postharvbio.2021.111571
[14]
Huang, K. et al. Melatonin enhances the resistance of ginger rhizomes to postharvest fungal decay. Postharvest Biol. Technol. https://doi.org/10.1016/j.postharvbio.2021.111706 (2021). 10.1016/j.postharvbio.2021.111706
[15]
El-Mogy, M. M., Ludlow, R. A., Roberts, C., Müller, C. T. & Rogers, H. J. Postharvest exogenous melatonin treatment of strawberry reduces postharvest spoilage but affects components of the aroma profile. J. Berry Res. 9(2), 297–307. https://doi.org/10.3233/JBR-180361 (2019). 10.3233/jbr-180361
[16]
Xin, D. D., Si, J. J. & Kou, L. P. Postharvest exogenous melatonin enhances quality and delays the senescence of cucumber. Acta Hortic. Sin. 44(5), 891–901. https://doi.org/10.16420/j.issn.0513-353x.2016-0888 (2017). 10.16420/j.issn.0513-353x.2016-0888
[17]
Wang, F., Zhang, X., Yang, Q. & Zhao, Q. Exogenous melatonin delays postharvest fruit senescence and maintains the quality of sweet cherries. Food Chem. https://doi.org/10.1016/j.foodchem.2019.125311 (2019). 10.1016/j.foodchem.2019.125311
[18]
Tan, X. L. et al. Exogenous melatonin maintains leaf quality of postharvest Chinese flowering cabbage by modulating respiratory metabolism and energy status. Postharvest Biol. Technol. https://doi.org/10.1016/j.postharvbio.2021.111524 (2021). 10.1016/j.postharvbio.2021.111524
[19]
Deng, B., Xia, C., Tian, S. & Shi, H. Melatonin reduces pesticide residue, delays senescence, and improves antioxidant nutrient accumulation in postharvest jujube fruit. Postharvest Biol. Technol. https://doi.org/10.1016/j.postharvbio.2020.111419 (2021). 10.1016/j.postharvbio.2020.111419
[20]
de Ancos, B., Gonzales, E. M. & Cano, M. P. Differentiation of raspberry varieties according to anthocyanin composition. Z. Lebensm. Unters. Forsch. 208, 33–38. https://doi.org/10.1007/s002170050371 (1999). 10.1007/s002170050371
[21]
Kalt, W., Forney, C. F., Martin, A. & Prior, R. L. Antioxidant capacity, vitamin C, phenolics, and anthocyanins after fresh storage of small fruits. J. Agric. Food Chem. 47(11), 4638–4644. https://doi.org/10.1021/jf990266t (1999). 10.1021/jf990266t
[22]
Wang, S. Y. & Lin, H. S. Antioxidant activity in fruit and leaves of blackberry, raspberry, and strawberry varies with cultivar and developmental stage. J. Agric. Food Chem. 48(2), 140–146. https://doi.org/10.1021/jf9908345 (2000). 10.1021/jf9908345
[23]
Mullen, W. et al. Ellagitannins, flavonoids, and other phenolics in red raspberries and their contribution to antioxidant capacity and vasorelaxation properties. J. Agric. Food Chem. 50(18), 5191–5196. https://doi.org/10.1021/jf020140n (2002). 10.1021/jf020140n
[24]
Beekwilder, J. et al. Antioxidants in raspberry: on-line analysis links antioxidant activity to a diversity of individual metabolites. J. Agric. Food Chem. 53, 3313–3320. https://doi.org/10.1021/jf047880b (2005). 10.1021/jf047880b
[25]
Protagente, A. R. et al. The antioxidant activity of regularly consumed fruit and vegetable reflects their phenolic and vitamin C composition. Free Radic. Res. 36, 217–233. https://doi.org/10.1080/10715760290006484 (2002). 10.1080/10715760290006484
[26]
Tezotto-Uliana, J. V., Fargoni, G. P., Geerdink, G. M. & Kluge, R. A. Chitosan applications pre-or post-harvest prolong raspberry shelf-life quality. Postharvest Biol. Technol. 91, 72–77. https://doi.org/10.1016/j.postharvbio.2013.12.023 (2014). 10.1016/j.postharvbio.2013.12.023
[27]
Mass, L. L. Post harvest diseases of strawberry. In The Strawberry Cultivars to Marketing (ed. Childers, N. F.) 329–353 (Horticultural publications. University of Florida, 1981).
[28]
Reddy, M. V. B., Belkacemi, K., Corcuff, R., Castaigne, F. & Arul, J. Effect of preharvest chitosan sprays on post-harvest infection by Botrytis cinerea and quality of strawberry fruit. Postharvest Biol. Technol. 20, 39–51. https://doi.org/10.1016/S0925-5214(00)00108-3 (2000). 10.1016/s0925-5214(00)00108-3
[29]
Schieber, A., Keller, P. & Carle, R. Determination of phenolic acids and flavonoids of apple and pear by high-performance liquid chromatography. J. Chromatogr. 910, 265–273. https://doi.org/10.1016/S0021-9673(00)01217-6 (2001). 10.1016/s0021-9673(00)01217-6
[30]
Slinkard, K. & Singleton, V. L. Total phenol analysis: automation and comparison with manual methods. Am. J. Enol. Vitic. 28, 49–55. https://doi.org/10.5344/ajev.1977.28.1.49 (1977). 10.5344/ajev.1977.28.1.49
[31]
Shin, Y., Liu, R. H., Nock, J. F., Holliday, D. & Watkins, C. B. Temperature and relative humidity effects on quality, total ascorbic acid, phenolics and flavonoid concentrations, and antioxidant activity of strawberry. Postharvest Biol. Technol. 45, 349–357. https://doi.org/10.1016/j.postharvbio.2007.03.007 (2007). 10.1016/j.postharvbio.2007.03.007
[32]
Giusti, M. M. & Wrolstad, R. E. Anthocyanins: characterization and measurement with UV-visible spectroscopy. In Current Protocols in Food Analytical Chemistry (eds Wrolstad, R. E. & Schwartz, S. J.) (Wiley, 2001).
[33]
Bor, J. Y., Chen, H. Y. & Yen, G. C. Evaluation of antioxidant activity and inhibitory effect on nitric oxide production of some common vegetables. J. Agric. Food Chem. 54(5), 1680–1686. https://doi.org/10.1021/jf0527448 (2006). 10.1021/jf0527448
[34]
Nakajima, J., Tanaka, I., Seo, S., Yamazaki, M. & Saito, K. LC/PDA/ESI-MS profiling and radical scavenging activity of anthocyanins in various berries. J. Biomed. Biotechnol. 5, 241–247. https://doi.org/10.1155/S1110724304404045 (2004). 10.1155/s1110724304404045
[35]
Asghari, M. & Hasanlooe, A. R. Interaction effects of salicylic acid and methyl jasmonate on total antioxidant content, catalase and peroxidase enzymes activity in Sabrosa strawberry fruit during storage. Sci. Hortic. 197, 490–495. https://doi.org/10.1016/j.scienta.2015.10.009 (2015). 10.1016/j.scienta.2015.10.009
[36]
Beaudoin-Eagan, L. D. & Thorpe, T. A. Tyrosine and phenylalanine ammonia lyase activities during shoot initiation in tobacco callus cultures. Plant Physiol. 78(3), 438–441. https://doi.org/10.1104/pp.78.3.438 (1985). 10.1104/pp.78.3.438
[37]
Chance, B. & Maehly, A. C. Assay of catalases and peroxidases. Meth. Enzymol. 2, 764–775. https://doi.org/10.1016/S0076-6879(55)02300-8 (1955). 10.1016/s0076-6879(55)02300-8
[38]
Hassanpour, H. Effect of Aloe vera gel coating on antioxidant capacity, antioxidant enzyme activities and decay in raspberry fruit. LWT - Food Sci. Technol. 60(1), 495–501. https://doi.org/10.1016/j.lwt.2014.07.049 (2015). 10.1016/j.lwt.2014.07.049
[39]
Zhu, L. L., Hu, H. L., Luo, S. F., Wu, Z. X. & Li, P. X. Melatonin delaying senescence of postharvest broccoli by regulating respiratory metabolism and antioxidant activity. Trans. Chin. Soc. Agric. 34(3), 300–308. https://doi.org/10.11975/j.issn.1002-6819.2018.03.040 (2018). 10.11975/j.issn.1002-6819.2018.03.040
[40]
Gao, H. et al. Melatonin treatment delays postharvest senescence and regulates reactive oxygen species metabolism in peach fruit. Postharvest Biol. Technol. 118, 103–110. https://doi.org/10.1016/j.postharvbio.2016.03.006 (2016). 10.1016/j.postharvbio.2016.03.006
[41]
Aghdam, M. S. & Fard, J. R. Melatonin treatment attenuates postharvest decay and maintains nutritional quality of strawberry fruits (Fragaria x anannasa cv. Selva) by enhancing GABA shunt activity. Food Chem. 221, 1650–1657. https://doi.org/10.1016/j.foodchem.2016.10.123 (2017). 10.1016/j.foodchem.2016.10.123
[42]
Li, S. et al. Melatonin treatment inhibits gray mold and induces disease resistance in cherry tomato fruit during postharvest. Postharvest Biol. Technol. https://doi.org/10.1016/j.postharvbio.2019.110962 (2019). 10.1016/j.postharvbio.2019.110962
[43]
Sun, C. et al. Improving the biocontrol efficacy of Meyerozyma guilliermondii Y-1 with melatonin against postharvest gray mold in apple fruit. Postharvest Biol. Technol. https://doi.org/10.1016/j.postharvbio.2020.111351 (2021). 10.1016/j.postharvbio.2020.111351
[44]
Yuan, X. et al. Biochemical and proteomic analysis of ‘Kyoho’grape (Vitis labruscana) berries during cold storage. Postharvest Biol. Technol. 88, 79–87. https://doi.org/10.1016/j.postharvbio.2013.10.001 (2014). 10.1016/j.postharvbio.2013.10.001
[45]
Asghari, M. & Zahedipour, P. 24-epibrassinolide acts as a growth-promoting and resistance-mediating factor in strawberry plants. J. Plant Growth Regul. 35(3), 22–729. https://doi.org/10.1007/s00344-016-9577-2 (2018). 10.1007/s00344-016-9577-2
[46]
Zhang, Y. Y. et al. Delay of postharvest browning in litchi fruit by melatonin via the enhancing of antioxidative processes and oxidation repair. J. Agric. Food Chem. 66(28), 7475–7484. https://doi.org/10.1021/acs.jafc.8b01922 (2018). 10.1021/acs.jafc.8b01922
[47]
González-Paramás, A. M. et al. Flavanol–anthocyanin condensed pigments in plant extracts. Food Chem. 94(3), 428–436. https://doi.org/10.1016/j.foodchem.2004.11.037 (2006). 10.1016/j.foodchem.2004.11.037
[48]
Santos-Buelga, C., Mateus, N. & De Freitas, V. Anthocyanins. Plant pigments and beyond. J. Agric. Food Chem. 62, 6879–6884. https://doi.org/10.1021/jf501950s (2014). 10.1021/jf501950s
[49]
Pantelidis, G. E., Vasilakakis, M., Manganaris, G. A. & Diamantidis, G. R. Antioxidant capacity, phenol, anthocyanin and ascorbic acid contents in raspberries, blackberries, red currants, gooseberries and Cornelian cherries. Food Chem. 102(3), 777–783. https://doi.org/10.1016/j.foodchem.2006.06.021 (2007). 10.1016/j.foodchem.2006.06.021
[50]
Crecente-Campo, J., Nunes-Damaceno, M., Romero-Rodríguez, M. A. & Vázquez-Odériz, M. L. Color, anthocyanin pigment, ascorbic acid and total phenolic compound determination in organic versus conventional strawberries (Fragaria× ananassa Duch, cv Selva). J. Food Compos. Anal. 28(1), 23–30. https://doi.org/10.1016/j.jfca.2012.07.004 (2012). 10.1016/j.jfca.2012.07.004

Showing 50 of 77 references

Metrics
9
Citations
77
References
Details
Published
May 20, 2024
Vol/Issue
14(1)
License
View
Cite This Article
Shirin Rahmanzadeh-Ishkeh, Habib Shirzad, Zahra Tofighi, et al. (2024). Exogenous melatonin prolongs raspberry postharvest life quality by increasing some antioxidant and enzyme activity and phytochemical contents. Scientific Reports, 14(1). https://doi.org/10.1038/s41598-024-62111-1