Antifungal ability of chitosan biofilms containing lactic acid bacteria
DOI:
https://doi.org/10.19230/jonnpr.3545Keywords:
Lactobacillus plantarum, MTT, Colletotrichum gloeosporioides, response surface designAbstract
Introduction. There are reports of the use of biofilms as a support for the incorporation of beneficial microorganisms, however, there are scarce the reports where the antimicrobial capacity of biofilms containing lactic acid bacteria (LAB) is evaluated.
Objective. Optimize the components of an edible biofilm based on chitosan to preserve the viability and antifungal capacity of the LAB Lactobacillus plantarum CDBB-B-1091 for 28 days.
Methods. Through a design Plackett-Burman of 8 treatments, two levels of 7 factors (componente) were evaluated (glucose, lactose, glycerol, starch, relative humidity, pH, BAL concentration). Of the factors that showed effect, the concentration was optimized using the response surface methodology based on a Box-Benhken arrangement.
Results. It was found that cell concentration (A), starch concentration (B) and glucose concentration (C) are the most determining biofilm components to maintain viability and antifungal ability against the phytopathogenic fungus Colletotrichum gloeosporioides. Optimal values were obtained by response surface analysis to maintain the viability of the bacteria for 28 days, the values being 7.009164 log CFU/g film for factor A, 1.997712% for B and 0.10750016 M for factor C. According to ANOVA the concentration of cells being the most influential factor. However, for the antifungal capacity it was only possible to obtain 100% inhibition with freshly made films, for this day the optimal values of 8.9004 log (CFU/g) for factor A, 2.0% for B and 0.0850143 M for C.
Conclusion. The antifungal capacity of the biofilms containing BAL was decreasing as the storage of the biofilms passed. Even with the above, regression models are proposed to predict the viability values and the antifungal capacity of biofilms containing the bacterium Lactobacillus plantarum CDBB-B-1091.
Downloads
References
Hernández A, Márquez C, Restrepo CE, Cano JA, Patiño JH. Aplicación de tratamiento térmico, recubrimiento comestible y baño químico como tratamiento poscosecha para la conservación de hortalizas mínimamente procesadas. Acta Agron. 2014; 63: 1-10.
Girard AL, Teferra T, Awika JM. Effects of condensed vs hydrolysable tannins on gluten film strength and stability. Food Hidrocoll. 89: 36:43.
Bergo P, Sobral PJA. Effects of plasticizer on physical properties of pigskin gelatin films. Food Hydrocolloid. 2007; 21: 1285-1289.
González A, Gastélu G, Barrera GN, Ribbota PD, Álvarez ICI. Food Hidrocoll. 2019; 89: 758-764.
Aloui H, Baraket K, Sendon R, Sanches SA, Khwaldia K. Development and characterization of novel composite glycerol-plasticized films based on sodium caseinate and lipid fraction of tomato pomace by-product. Int. J. Biol. Macrobiol. 2019; 139: 128-138.
Tavassoli-Kafrani E, Shekarchizadeh H, Masoudpour-Behabadi M. Development of edible films and coatings from alginates and carrageenans. Carbohyd. Polym. 2016; 137: 360-374.
Cazon P, Velázquez G, Ramírez JA, Vázquez M. Polysaccharide-based films and coatings for food packaging: A review. Food Hydrocoll. 2017; 68: 136-148.
Bolívar-Monsalve J, Ramírez-Toro C, Bolívar G, Ceballos-González C. Mechanisms of action of novel ingredients used in edible films to preserve microbial quality and oxidative stability in sausages - A review. Trends Food Sci. Tech. 2019; 89: 100-109.
Salvador-Figueroa M, Castillo-López D, Adriano-Anaya L, Gálvez-López D, Rosas-Quijano R, Vázquez-Ovando A. Chitosan composite films: physicochemical characterization and their use as coating in papaya Maradol stored at room temperature. Emir. J. Food Agric. 2017; 29: 779-791.
Monzón-Ortega K, Salvador-Figueroa M, Gálvez-López D, Rosas-Quijano R, Ovando-Medina I, Vázquez- Ovando A. Characterization of Aloe vera-chitosan composite films and their use for reducing the disease caused by fungi in papaya Maradol. J. Food Sci. Tech. 2018; 55: 4747-4757.
Mujtaba M, Morsi RE, Kerch G, Elsabee MZ, Kaya M, Labidi J, Khawar KM. Current advancements in chitosan- based film production for food technology; A review. Int. J. Biol. Macrobiol. 2019; 121: 889-904.
Wilson MD, Stanley RA, Eyles A, Ross T. Innovative processes and technologies for modified atmosphere packaging of fresh and fresh-cut fruits and vegetables. Crit. Rev. Food Sci. Nutr. 2019; 59: 411-422.
Aloui H, Licciardello F, Khwaldia K, Hamdi M, Restuccia C. Physical properties and antifungal activity of bioactive films containing Wickerhamomyces anomalus killer yeast and their application for preservation of oranges and control of postharvest green mold caused by Penicillium digitatum. Int. J. Food Microbiol. 2015; 4: 22-30.
Maldonado Z, Vázquez-Ovando A. Viabilidad de bacterias del ácido láctico incorporadas en películas de quitosán. Tesis de licenciatura. Instituto de Biociencias, Universidad Autónoma de Chiapas. Tapachula, Chiapas, México. 2015. 17p.
Pereira JO, Soares J, Sousa S, Madureira AR, Gomes A, Pintado M. Edible films as carrier for lactic acid bacteria. LWT – Food Sci. Technol. 2016, 73: 543-550.
Hartmann A, Wilke T, Erdmann R. Efficacy of bacteriocin-containing cell-free culture supernatants from lactic acid bacteria to control Listeria monocytogenes in food. Int. J. Food Microbiol. 2011; 146: 192-199.
Concha A, Schobitz R, Brito C, Fuentes R. Lactic acid bacteria in alginate film inhibit Listeria monocytogenes growth on smoked salmon. Food Control 2010; 22: 485-489.
Schmidt CA. Antagonismo en contra de Listeria monocytogenes de nisina y de una cepa láctica, encapsuladas en alginato. Tesis de licenciatura. Universidad Austral de Chile. 2007. 53p.
Cheong EYL, Sandhu A, Jayabalan J, Kieu-Le TT, Thi-Nhiep N, My-Ho HT, Zwielehner T, Bansala N, Turner MS. Isolation of lactic acid bacteria with antifungal activity against the common cheese spoilage mould Penicillium commune and their potential as biopreservatives in cheese. Food Control 2014; 46: 91-97.
Ndagano D, Lamoureux T, Dortu C, Vandermoten S, Thonart P. Antifungal activity of 2 lactic acid bacteria of the Weissella genus isolated from food. J. Food Sci. 2011; 76: 305-311.
Vázquez-Ovando A, López-Hilerio H, Salvador-Figueroa M, Adriano-Anaya L, Rosas-Quijano R, Gálvez-López D. Uso combinado de radiación UV-C y biorecubrimiento de quitosán con aceites esenciales para el control de hongos en papaya Maradol. Rev. Bras. de Frutic. 2018; 40(3): e-688.
Magnusson J, Ströma K, Roos S, Sjögren J, Schnürer J. Broad and complex antifungal activity among environmental isolates of lactic acid bacteria. FEMS Microbiol. Lett. 2003; 219: 129-135.
Binsi PK, Ravishankar CN, Srinivasa-Gopal TK. Development and characterization of an edible composite film based on chitosan and virgin coconut oil with improved moisture sorption properties. J. Food Sci. 2013; 70: 526- 534.
Hegyi F, Zalán Z, Halasz A. Improved 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) colorimetric assay for measuring the viability of lactic acid bacteria. Acta Aliment. 2012; 41: 506-512.
Egusa M, Iwamoto R, Izawa H, Morimoto M, Saimoto H, Kaminaka H, Ifuku S. Characterization of chitosan nanofiber sheets for antifungal application. Int. J. Mol. Sci. 2015; 16: 26202-26210.
Arasu M, Jung MW, Ilavenil S, Jane M, Kim DH, Lee KD, Park HS, Hur TY, Choi GJ, Lim YC, Al-Dhabi NA, Choi KC. Isolation and characterization of antifungal compound from Lactobacillus plantarum KCC-10 from forage silage with potential beneficial properties. J. Appl. Microbiol. 2013; 115(5): 1172-1185.
Ström K, Sjögren J, Broberg A, Schnürer J. Lactobacillus plantarum MiLAB 393 produces the antifungalcyclic dipeptides cyclo (L-Phe-L-Pro) and cyclo (L-Phe-trans-4-OH-L-Pro) and phenyl lactic acid. Appl. Environ. Microb. 2002; 68: 4322–4327.
Dalié DKD, Deschamps AM, Richard-Forget F. Lactic acid bacteria potential for control of mould growth and mycotoxins: A review. Food Control 2010; 21: 370-380. 29. Barrios-Roblero C, Rosas-Quijano R, Salvador-Figueroa M, Gálvez-López D, Vázquez-Ovando A. Antifungal lactic acid bacteria isolated from fermented beverages with activity against Colletotrichum gloeosporioides. Food Biosci. 2019; 29: 47-54.
Rodrigues D, Sousa S, Rocha-Santos T, Silva J, Lobo JS, Costa P. Influence of Lcysteine, oxygen and relative humidity upon survival throughout storage of probiotic bacteria in whey protein-based microcapsules. Int. Dairy J. 2011; 21: 869-876.
Romano N, Tavera-Quiroz M, Bertola N, Mobili P, Pinotti A, Gómez-Zavaglia A. Edible methylcellulose-based films containing fructo-oligosaccharides as vehicles for lactic acid bacteria. Food Res. Int. 2014; 64: 560-566.
Nguyen HT, Truong DH, Kouhoundé S, Ly S, Razafindralambo H, Delvigne F. Biochemical engineering approaches for increasing viability and functionality of probiotic bacteria. Int. J. Mol. Sci. 2016; 17: 867.
Piermaria J, Diosma G, Aquino C, Garrote G, Abraham A. Edible kefiran films as vehicle for probiotic microorganisms. Innov. Food Sci. Emerg. Technol. 2015; 32: 193-199.
Pereira JO, Soares J, Sousa S, Madureira A, Gomes A, Pintado M. Edible films as carrier for lactic acid bacteria. LWT Food Sci. Technol. 2016; 73: 543-550.
Sánchez-González L. Quintero-Saavedra JI, Chiralt A. Physical properties and antilisterial activity of bioactive edible films containing Lactobacillus plantarum. Food Hydrocolloid. 2014; 33: 92-98.
Muynck C, Leroy A, Maeseneire S, Arnaut F, Soetaert W, Vandamme EJ. Potential of selected lactic acid bacteria to produce food compatible antifungal metabolites. Microbiol. Res. 2004; 159: 339-346.
Marín A, Atarés L, Cháfer M, Chriralt A. Properties of biopolymer dispersions and films used as carriers of the biocontrol agent Candida sake CPA-1. LWT Food Sci. Technol. 2017; 79: 60-69.
Kanmani P, Lim ST. Development and characterization of novel probiotic-residing pullulan/starch edible films. Food Chem. 2013; 141: 1041-1049.
Published
Issue
Section
License
All accepted originals remain the property of JONNPR. In the event of publication, the authors exclusively transfer their rights of reproduction, distribution, translation and public communication (by any sound, audiovisual or electronic medium or format) of their work. To do so, the authors shall sign a letter transferring these rights when sending the paper via the online manuscript management system.
The articles published in the journal are freely used under the terms of the Creative Commons BY NC SA license, therefore.
You are free to:
Share — copy and redistribute the material in any medium or format
Adapt — remix, transform, and build upon the material
The licensor cannot revoke these freedoms as long as you follow the license terms.
Under the following terms:
Attribution — You must give appropriate credit, provide a link to the license, and indicate if changes were made. You may do so in any reasonable manner, but not in any way that suggests the licensor endorses you or your use.
NonCommercial — You may not use the material for commercial purposes.
ShareAlike — If you remix, transform, or build upon the material, you must distribute your contributions under the same license as the original.
No additional restrictions — You may not apply legal terms or technological measures that legally restrict others from doing anything the license permits.
This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License