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TIP Revista Especializada en Ciencias Químico-Biológicas

2021, Number 1

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TIP Rev Esp Cienc Quim Biol 2021; 24 (1)

Application of GRAS compounds to control soft rot in jackfruit (Artocarpus heterophyllus L.) caused by Rhizopus stolonifer

Coronado-Partida LD, Serrano M, Romanazzi G, González-Estrada RR, Gutiérrez-Martínez P

Language: English
References: 30
Page:
PDF size: 250.96 Kb.


ABSTRACT

Jackfruit is affected by various pathogens in the post-harvest stage, among which is Rhizopus stolonifer, the causal agent of soft rot. To control this pathogen, fungicides are used which damage the environment and affect human health. This situation encourages the search for safe alternatives, among which is chitosan, which has fungicidal characteristics and controls the ripening of various fruits. Also, potassium sorbate is a compound that has traditionally been used to preserve food. In this study, chitosan (Chi) and potassium sorbate (PS) was applied to inhibit the development of R. stolonifer. Determining the mycelial growth, spore germination, sporulation, the severity of the disease, as well as the activity of enzymes involved in the defense of the fruit such as peroxidase (POD) and polyphenoloxidase (PPO). Obtaining a 100% reduction in mycelial growth and spore germination with the 1% Chi-1.0% PS combination. Furthermore, soft rot is not evident when the same treatment was applied to jackfruit, inducing the activity of POD and PPO. The application of chitosan combined with potassium sorbate may be a promising alternative against soft rot in jackfruit.


REFERENCES

  1. Ayala-Valencia, G. (2015). Efecto antimicrobiano del quitosano: una revisión de la literatura. Scientia Agroalimentaria, 2, 6–12.

  2. Bautista-Baños, S., Bosquez-Molina, E. & Barrera-Necha, L. (2014). Rhizopus stolonifer (Soft Rot). pp. 1-144. In: Postharvest Decay-Control Strategies, Bautista-Baños (ed.). Academic Press. San Diego, USA. https://doi.org/10.1016/ B978-0-12-411552-1.00001-6

  3. Bautista-Baños, S., Ventura-Aguilar, R. I., Correa-Pacheco, Z. & Corona-Rangel, M. L. (2017). Chitosan: a versatile antimicrobial polysaccharide for fruit and vegetables in postharvest-a review. Revista Chapingo Serie Horticultura, 23(2), 103–121.

  4. Benhamou, N. (1996). Elicitor-induced plant defence pathways. Trends in Plant Science, 1(7), 233–240. https://doi. org/10.1016/1360-1385(96)86901-9

  5. Berúmen-Varela, G., Coronado-Partida, L., Ochoa-Jiménez, A., Chacón-López, M. & Gutiérrez-Martínez, P. (2015). Effect of chitosan on the induction of disease resistance against Colletotrichum sp in mango (Mangifera indica L.) cv Tommy Atkins. Revista Investigación y Ciencia, 23(66),16–21.

  6. Blechert, S., Brodschelm, W., Hölder, S., Kammerer, L., Kutchan, T. M., Mueller, M. J. & Zenk, M. H. (1995). The octadecanoic pathway: Signal molecules for the regulation of secondary pathways. Proceedings of the National Academy of Sciences of the United States of America, 92(10), 4099–4105. https://doi.org/10.1073/ pnas.92.10.4099

  7. Bradford, M. M. (1976). A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Biochemistry, 72(1), 248–254. https://doi.org/10.1016/0003- 2697(76)90527-3

  8. Chance, B. & Maehly, A. C. (1955). Assay of catalases and peroxidases. Methods in Enzymology, 2(C), 764–775. https://doi.org/10.1016/S0076-6879(55)02300-8

  9. Chen, C., Bélanger, R. R., Benhamou, N. & Paulitz, T. C. (2000). Defense enzymes induced in cucumber roots by treatment with plant growth-promoting rhizobacteria (PGPR) and Pythium aphanidermatum. Physiological and Molecular Plant Pathology, 56(1), 13–23. https://doi.org/10.1006/ pmpp.1999.0243

  10. Chen, J., Zou, X., Liu, Q., Wang, F., Feng, W. & Wan, N. (2014). Combination effect of chitosan and methyl jasmonate on controlling Alternaria alternata and enhancing activity of cherry tomato fruit defense mechanisms. Crop Protection, 56, 31–36. https://doi.org/10.1016/j.cropro.2013.10.007

  11. Cortes-Rivera, H. J., Blancas-Benítez, F. J., Romero-Islas, L. d. C., Gutiérrez-Martínez, P. & González-Estrada, R. R. (2019). In vitro evaluation of residues of coconut (Cocos nucifera L.) aqueous extracts, against the fungus Penicillium italicum. Emirates Journal of Food and Agriculture, 31,613- 617. https://doi.org/https://doi.org/10.9755/ejfa.2019.v31. i8.1993

  12. García-Garrido, J. M. & Ocampo, J. A. (2002). Regulation of the plant defense response in arbuscular mycorrhizal symbiosis. Journal of Experimental Botany, 53(373), 1377–1386. https://doi.org/10.1093/jxb/53.373.1377

  13. González-Estrada, R. R., Vega-Arreguín, J., Robles-Villanueva, B. A., Velázquez-Estrada, R. M., Ramos-Guerrero, A. & Gutiérrez-Martínez, P. (2020). Evaluación in vitro de productos químicos no convencionales para el control de Penicillium citrinum. Polibotánica, 49, 161–172. https:// doi.org/10.18387/polibotanica.49.11

  14. Gutiérrez-Martínez, P., Ramos-Guerrero, A., Rodríguez-Pereida, C., Coronado-Partida, L., Angulo-Parra, J. & González- Estrada, R. R. (2018). Chitosan for Postharvest Disinfection of Fruits and Vegetables. pp. 231–241. In: Postharvest Disinfection of Fruits and Vegetables. Siddiqui (ed.). Academic Press, San Diego, USA. https://doi.org/https:// doi.org/10.1016/B978-0-12-812698-1.00012-1

  15. Jukanti, A. (2017). Physicochemical properties of polyphenol oxidases, pp. 33–56. In Polyphenol oxidases (PPOs) in plants. Jukanti A. (ed). Springer Singapore, Singapore. https://doi.org/10.1007/978-981-10-5747-2

  16. Kazan, K., Murray, F. R., Goulter, K. C., Llewellyn D. J. & Manners, J. M. (1998). Induction of cell death in transgenic plants expressing a fungal glucose oxidase. Molecular Plant-Microbe Interactions, 11(6), 555–562. https://doi. org/10.1094/MPMI.1998.11.6.555

  17. Liu, J., Tian, S., Meng, X. & Xu. (2007). Effects of chitosan on control of postharvest diseases and physiological responses of tomato fruit. Postharvest Biology and Technology, 44(3), 300–306. https://doi.org/10.1016/j. postharvbio.2006.12.019

  18. Montesinos-Herrero, C., Moscoso-Ramírez, P. A. & Palou, L. (2016). Evaluation of sodium benzoate and other food additives for the control of citrus postharvest green and blue molds. Postharvest Biology and Technology, 115, 72–80. https://doi.org/10.1016/j.postharvbio.2015.12.022

  19. Palou, L., Ali, A., Fallik, E. & Romanazzi, G. (2016). Postharvest Biology and Technology GRAS, plant- and animal-derived compounds as alternatives to conventional fungicides for the control of postharvest diseases of fresh horticultural produce. Postharvest Biology andTechnology, 122, 41–52. https://doi.org/10.1016/j.postharvbio.2016.04.017

  20. Peng, M. & Kuc, J. (1992). Peroxidase-generated hydrogen peroxide as a source of antifungal activity in vitro and on tobacco leaf disks. Phytopathology, 82(6), 696-699. https:// doi.org/10.1094/phyto-82-696

  21. Ramos-Guerrero, A., González-Estrada, R. R., Hanako-Rosas, G., Bautista-Baños, S., Acevedo-Hernández, G., Tiznado- Hernández, M. E. & Gutiérrez-Martínez, P. (2018). Use of inductors in the control of Colletotrichum gloeosporioides and Rhizopus stolonife isolated from soursop fruits: in vitro tests. Food Science Biotechnology, 27, 755–763.

  22. SIAP. (2019). Anuario Estadístico de la Producción Agrícola. México. https://nube.siap.gob.mx/cierreagricola / Accessed Ag. 10, 2020.

  23. Singh, D. & Sharma, R. R. (2018). Postharvest Diseases of Fruits and Vegetables and Their Management. pp. 1-52. In: Postharvest Disinfection of Fruits and Vegetables. Siddiqui (ed.). Academic Press, San Diego, USA. https:// doi.org/10.1016/b978-0-12-812698-1.00001-7

  24. Smilanick, J. L., Mansour, M. F., Gabler, F. M. & Sorenson, D. (2008). Control of citrus postharvest green mold and sour rot by potassium sorbate combined with heat and fungicides. Postharvest Biology and Technology, 47(2), 226–238. https://doi.org/10.1016/j. postharvbio.2007.06.020

  25. Soliva, R. C., Elez, P., Sebastián, M. & Martín, O. (2000). Evaluation of browning effect on avocado purée preserved by combined methods. Innovative Food Science and Emerging Technologies, 1(4), 261–268. https://doi. org/10.1016/S1466-8564(00)00033-3

  26. Sommer, K. A., Petersen, G. & Bautz, E. K. F. (1994). The gene upstream of DmRP128 codes for a novel GTP-binding protein of Drosophila melanogaster. Molecular Genetics and Genomics, 242(4), 391–398. https://doi.org/10.1007/ BF00281788

  27. Velázquez-del Valle, M. G., Bautista-Baños, S., Hernández- Lauzardo, A. N., Guerra-Sánchez, M. G. & Amora-Lazcano, E. (2008). Estrategias de Control de Rhizopus stolonifer Ehrenberg (Ex Fr.) Lind, Agente Causal de Pudriciones Postcosecha en Productos Agrícolas. Revista Mexicana de Fitopatología, 26(1), 49-55.

  28. Weir, T. L., Park, S. W. & Vivanco, J. M. (2004). Biochemical and physiological mechanisms mediated by allelochemicals. Current Opinion in Plant Biology, 7(4), 472–479. https:// doi.org/10.1016/j.pbi.2004.05.007

  29. Yin, L., Zou, Y., Ke, X., Liang, D., Du, X., Zhao, Y. & Ma, F. (2013). Phenolic responses of resistant and susceptible Malus plants induced by Diplocarpon mali. Scientia Horticulturae, 164, 17-23. https://doi.org/10.1016/j. scienta.2013.08.037

  30. Yue-Ming, J. (1999). Purification and some properties of polyphenol oxidase of longan fruit. Food Chemistry, 66(1), 75–79.




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