with the collaboration of Iranian Food Science and Technology Association (IFSTA)

Document Type : Research Article

Authors

1 Department of Horticultural Science, Faculty of Agriculture, Ilam University, Ilam, Iran.

2 , Department of Horticultural Science, Faculty of Agriculture, Ilam University, Ilam, Iran.

Abstract

Introduction: Button mushroom (Agaricus bisporus L.) is one of the most popular and widely consumed edible mushrooms that is grown all over the world. However, button mushrooms have a short shelf life of about 3 to 4 days after harvest and lose their commercial value within a few days due to browning of the tissue, water loss, aging and microbial attack. Tissue browning is caused by the activity of polyphenol oxidase (PPO) in plastids on phenolic compounds in the vacuoles as a substrate. Therefore, enzymatic browning is intensified by the loss of membrane integrity due to aging and tissue deterioration and as a result of physical connection between the enzyme and the substrate. The use of some techniques such as the chemicals and physical treatments gives promising results in delaying Browning and increasing the shelf life of edible mushrooms. Cinnamic acid (CA) is an organic acid that occurs naturally in plants and has low toxicity and a wide range of biological activities. Cinnamic acid and its derivatives are widely used in food industry. This compound acts as an inhibitor of polyphenol oxidase activity. On the other hand, cinnamic acid in low concentration has been proposed as an activator of the antioxidant system and its positive effects on reducing the effects of environmental stresses in various plants have been proven in several experiments. Therefore, in the present study, the effect of cinnamic acid treatment on reducing the browning of the tissue and maintaining the quality of white button mushrooms in the post-harvest period has been investigated.
 
Materials and Methods: Treatments included exogenous application of cinnamic acid at four levels (control, 100, 200 and 400 μM trans cinnamic acid) and storage time at five times (0, 4, 8, 12 and 16 days after storage). Cinnamic acid treatment at the mentioned concentrations was applied by top application 24 hours before mushroom harvest. Distilled water was used for control treatment. At the time of picking, infected, very large and small mushrooms were removed and the same mushrooms with a cap diameter of 40 to 45 mm were collected for each experimental treatment. After harvesting, the mushrooms were placed in a polyethylene box covered with cellophane and after weighing, they were transferred to an incubator at 4°C. In the post-harvest period, different traits were measured with a four day interva.
 
Results and Discussion: The results showed that by increasing storage time, the activity of polyphenol oxidase and peroxidase increased and consequently the browning of the tissue also had an increasing trend. Also, with increasing storage time, weight loss percentage, hydrogen peroxide and malondialdehyde increased and total phenol and total antioxidant capacity were decreased. The use of cinnamic acid treatment in all three concentrations (100, 200 and 400 μM) reduced the activity of peroxidase and polyphenol oxidase activities and reduced tissue browning. The application of cinnamic acid also improved the quality traits of edible mushrooms such as total phenol, total antioxidant capacity and visual quality index. These findings suggest that application of cinnamic acid, especially at a concentration of 400 μM, could have the potential of inhibiting tissue browning and thus maintaining the mushrooms quality at the postharvest period 

Keywords

  1. Bondet, V., Brand-Williams, W., & Berset, C. L. W. T. (1997). Kinetics and mechanisms of antioxidant activity using the DPPH. Free radical method. LWT-Food Science and Technology30(6), 609-615. https://doi.org/10.1006/fstl.1997.0240
  2. Chomkitichai, W., Chumyam, A., Rachtanapun, P., Uthaibutra, J., & Saengnil, K. (2014). Reduction of reactive oxygen species production and membrane damage during storage of ‘Daw’longan fruit by chlorine dioxide. Scientia Horticulturae170, 143-149. https://doi.org/10.1016/j.scienta.2014.02.036
  3. Ding, Y., Zhu, Z., Zhao, J., Nie, Y., Zhang, Y., Sheng, J., & Tang, X. (2016). Effects of postharvest brassinolide treatment on the metabolism of white button mushroom (Agaricus bisporus) in relation to development of browning during storage. Food and Bioprocess Technology9(8), 1327-1334. https://doi.org/10.1007/s11947-016-1722-1
  4. Gao, H., Zhang, Z. K., Chai, H. K., Cheng, N., Yang, Y., Wang, D. N., & Cao, W. (2016). Melatonin treatment delays postharvest senescence and regulates reactive oxygen species metabolism in peach fruit. Postharvest Biology and Technology118, 103-110. https://doi.org/10.1016/j.postharvbio.2016.03.006
  5. Gao, M., Feng, L., & Jiang, T. (2014). Browning inhibition and quality preservation of button mushroom (Agaricus bisporus) by essential oils fumigation treatment. Food chemistry149, 107-113. https://doi.org/10.1016/j.foodchem.2013.10.073
  6. Hu, Y. H., Chen, C. M., Xu, L., Cui, Y., Yu, X. Y., Gao, H. J., ... & Chen, Q. X. (2015). Postharvest application of 4-methoxy cinnamic acid for extending the shelf life of mushroom (Agaricus bisporus). Postharvest Biology and Technology104, 33-41. https://doi.org/10.1016/j.postharvbio.2015.03.007
  7. Hu, Y. H., Chen, Q. X., Cui, Y., Gao, H. J., Xu, L., Yu, X. Y., & Wang, Q. (2016). 4-Hydroxy cinnamic acid as mushroom preservation: anti-tyrosinase activity kinetics and application. International Journal of Biological Macromolecules, 86, 489-495. https://doi.org/10.1016/j.ijbiomac.2016.01.070
  8. Jiang, T. (2013). Effect of alginate coating on physicochemical and sensory qualities of button mushrooms (Agaricus bisporus) under a high oxygen modified atmosphere. Postharvest biology and technology76, 91-97. https://doi.org/10.1016/j.postharvbio.2012.09.005
  9. Jiang, T., Zheng, X., Li, J., Jing, G., Cai, L., & Ying, T. (2011). Integrated application of nitric oxide and modified atmosphere packaging to improve quality retention of button mushroom (Agaricus bisporus). Food Chemistry126(4), 1693-1699. https://doi.org/10.1016/j.foodchem.2010.12.060
  10. Kalač, P. (2009). Chemical composition and nutritional value of European species of wild growing mushrooms: A review. Food chemistry113(1), 9-16. https://doi.org/10.1016/j.foodchem.2008.07.077
  11. Kar, M., and Mishra, D. 1976. Catalase, peroxidase, and polyphenoloxidase activities during rice leaf senescence. Plant physiology, 57(2): 315-319. https://doi.org/10.1104/pp.57.2.315
  12. Li, Q., Yu, B., Gao, Y., Dai, A. H., & Bai, J. G. (2011). Cinnamic acid pretreatment mitigates chilling stress of cucumber leaves through altering antioxidant enzyme activity. Journal of plant physiology168(9), 927-934. https://doi.org/10.1016/j.jplph.2010.11.025
  13. Li-Qin, Z., Jie, Z., Shu-Hua, Z., & Lai-Hui, G. (2009). Inhibition of browning on the surface of peach slices by short-term exposure to nitric oxide and ascorbic acid. Food Chemistry114(1), 174-179. https://doi.org/10.1016/j.foodchem.2008.09.036
  14. Mishra, K., Ojha, H., & Chaudhury, N. K. (2012). Estimation of antiradical properties of antioxidants using DPPH assay: A critical review and results. Food chemistry130(4), 1036-1043. https://doi.org/10.1016/j.foodchem.2011.07.127
  15. Morales, M., & Munné-Bosch, S. (2019). Malondialdehyde: Facts and artifacts. Plant physiology180(3), 1246-1250. https://doi.org/10.1104/pp.19.00405
  16. Ortiz‐Ruiz, C. V., Maria‐Solano, M. A., Garcia‐Molina, M. D. M., Varon, R., Tudela, J., Tomas, V., & Garcia‐Canovas, F. (2015). Kinetic characterization of substrate‐analogous inhibitors of tyrosinase. IUBMB life67(10), 757-767. https://doi.org/10.1002/iub.1432
  17. Plewa, M. J., Smith, S. R., and Wagner, E. D. 1991. Diethyldithio carbamate suppresses the plant activation of aromatic amines into mutagens by inhibiting tobacco cell peroxidase. Mutation research/fundamental and molecular mechanisms of mutagenesis, 247(1): 57-64. https://doi.org/10.1016/0027-5107(91)90033-K
  18. Serafini, M. (2006). The role of antioxidants in disease prevention. Medicine34(12), 533-535. https://doi.org/10.1053/j.mpmed.2006.09.007
  19. Sharma, A., Shahzad, B., Rehman, A., Bhardwaj, R., Landi, M., & Zheng, B. (2019). Response of phenylpropanoid pathway and the role of polyphenols in plants under abiotic stress. Molecules24(13), 2452. https://doi.org/10.3390/molecules24132452
  20. Shi, Y., Chen, Q. X., Wang, Q., Song, K. K., & Qiu, L. (2005). Inhibitory effects of cinnamic acid and its derivatives on the diphenolase activity of mushroom (Agaricus bisporus) tyrosinase. Food Chemistry, 92(4), 707-712. https://doi.org/10.1016/j.foodchem.2004.08.031
  21. Singh, P. K., Singh, R., & Singh, S. (2013). Cinnamic acid induced changes in reactive oxygen species scavenging enzymes and protein profile in maize (Zea mays) plants grown under salt stress. Physiology and Molecular Biology of Plants19(1), 53-59. https://doi.org/10.1007/s12298-012-0126-6
  22. Singleton, V. L., & Rossi, J. A. (1965). Colorimetry of total phenolics with phosphomolybdic-phosphotungstic acid reagents. American journal of Enology and Viticulture16(3), 144-158.
  23. Stewart, R. R., & Bewley, J. D. (1980). Lipid peroxidation associated with accelerated aging of soybean axes. Plant physiology65(2), 245-248. https://doi.org/10.1104/pp.65.2.245
  24. Yan, J., Ban, Z., Luo, Z., Yu, L., Wu, Q., Li, D., Zahedi, S, M., & Li, L. (2021). Variation in cell membrane integrity and enzyme activity of the button mushroom (Agaricus bisporus) during storage and transportation. Journal of Food Science and Technology58(5), 1655-1662. https://doi.org/10.1007/s13197-020-04674-1
  25. Ye, S. F., Zhou, Y. H., Sun, Y., Zou, L. Y., & Yu, J. Q. (2006). Cinnamic acid causes oxidative stress in cucumber roots, and promotes incidence of FusariumEnvironmental and Experimental Botany56(3), 255-262. https://doi.org/10.1016/j.envexpbot.2005.02.010

 

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