Enhanced Survival of Lactobacillus Lg71 from Mangrove Sediment Under Simulated Gastric and Intestinal Conditions
DOI:
https://doi.org/10.34310/jbsh.v3.i1.291Keywords:
alginate encapsulation, functional foods, Lactobacillus, mangrove sediment, probioticAbstract
Background: For a probiotic to offer health benefits, it must stay viable through the tough environment of the human gastrointestinal tract. This study assesses the effectiveness of sodium alginate encapsulation in improving the survival of Lactobacillus LG71, a new strain from mangrove sediment, under simulated gastric and intestinal conditions. Objective: This study aims to evaluate the effectiveness of sodium alginate encapsulation in enhancing the viability and survival of Lactobacillus LG71, a probiotic strain isolated from mangrove sediment, during cold storage and under simulated gastric and intestinal conditions. Methods: Lactobacillus LG71 was encapsulated in sodium alginate beads. The viability of both encapsulated and free (non-encapsulated) cells was assessed over a 4-week storage period at 4 °C and during sequential exposure to simulated gastric and intestinal environments. Results: Encapsulation significantly improved survival rates compared to free cells (p < 0.05). Although both groups experienced a decline during the first week of storage, encapsulated cells maintained a high viability of approximately 107 CFU/mL, losing only 2.51 log CFU/g over four weeks. Most notably, encapsulated Lactobacillus LG71 demonstrated greater resilience during digestion, retaining populations of 2.21 log CFU/mL in gastric simulations and 1.00 log CFU/mL in intestinal simulations. In contrast, free cells were much more vulnerable to these acidic and enzymatic conditions. Conclusion: Sodium alginate encapsulation effectively protects Lactobacillus LG71 from environmental and biological stressors. These findings indicate that encapsulation is a crucial step for the commercial application of mangrove-derived probiotics, ensuring that a viable dose of living cells reaches the host's lower gastrointestinal tract to promote health benefits.
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Afzaal, M., Khan, A. U., Saeed, F., Ahmed, A., Ahmad, M. H., Maan, A. A., Tufail, T., Anjum, F. M., & Hussain, S. (2019). Functional exploration of free and encapsulated probiotic bacteria in yogurt and simulated gastrointestinal conditions. Food Science & Nutrition, 7(12), 3931-3940. https://doi.org/10.1002/fsn3.1254
Andriamanantoanina, H. & Rinaudo, M. (2010). Relationship between the molecular structure of alginates and their gelation in acidic conditions. Polymer International, 59(11), 1531-1541. https://doi.org/10.1002/pi.2943
Ayama, H., Sumpavapol, P., & Chanthachum, S. (2014). Effect of encapsulation of selected probiotic cell on survivalin simulated gastrointestinal tract condition. Songklanakarin Journal of Science and Technology, 36(3), 291-299.
Binda, S., Hill, C., Johansen, E., Obis, D., Pot, B., Sanders, M. E., Tremblay, A., & Ouwehand, A. C. (2020). Criteria to Qualify Microorganisms as 'Probiotic' in Foods and Dietary Supplements. Frontiers in Microbiology, 11, 1662. https://doi.org/10.3389/fmicb.2020.01662
Catozzi, C., Cusco, A., Lecchi, C., Talenti, A., Martucciello, A., Cappelli, G., Bonastre, A. S., Francino, O., & Ceciliani, F. (2019). Short communication: Intra- and inter-individual milk microbiota variability in healthy and infected water buffalo udder quarters. Journal of Dairy Science, 102(8), 7476-7482. https://doi.org/10.3168/jds.2019-16352
Champagne, C. P., Ross, R. P., Saarela, M., Hansen, K. F., & Charalampopoulos, D. (2011). Recommendations for the viability assessment of probiotics as concentrated cultures and in food matrices. International Journal of Food Microbiology, 149(3), 185-193. https://doi.org/10.1016/j.ijfoodmicro.2011.07.005
Damodharan, K., Palaniyandi, S. A., Yang, S. H., & Suh, J. W. (2017). Co-encapsulation of lactic acid bacteria and prebiotic with alginate-fenugreek gum-locust bean gum matrix: Viability of encapsulated bacteria under simulated gastrointestinal condition and during storage time. Biotechnology and Bioprocess Engineering, 22(3), 265-271. https://doi.org/10.1007/s12257-017-0096-1
Hwanhlem, N., Chobert, J., & H-Kittikun, A. (2014). Bacteriocin-producing lactic acid bacteria isolated from mangrove forests in southern Thailand as potential bio-control agents in food: Isolation, screening and optimization. Food Control, 41, 202-211. https://doi.org/10.1016/J.FOODCONT.2014.01.021
Jumazhanova, M., Kakimova, Z., Zharykbasov, Y., Kassymov, S., Zhumadilova, G., Muratbayev, A., Tashybayeva, M., & Suychinov, A. (2023). Effect of the encapsulation process on the viability of probiotics in a simulated gastrointestinal tract model medium. Processes, 11(9), 2757. https://doi.org/10.3390/pr11092757
Kusharyati, D. F., Ariaputri, F. J., Pramono, H., & Rovik, A. (2023). Lactic acid bacteria from mangrove sediment produce bacteriocins active against Gram-positive and -negative bacteria. Jurnal Biodjati, 8(1), 151-162. https://doi.org/10.15575/biodjati.v8i1.24856
Kusharyati, D. F., Pramono, H., Ryandini, D., Manshur, T. A., Dewi, M. A., Khatimah, K., & Rovik, A. (2020). Bifidobacterium from infant stool: The diversity and potential screening. Biodiversitas Journal of Biological Diversity, 21(6). https://doi.org/10.13057/biodiv/d210623
Kusharyati, D. F., Oedjijono, Satwika, T. D., Yulianti, D. M., Mariana, A., & Rovik, A. (2023). Bacteriocinogenic lactic acid bacteria isolated from mangrove sediment in Indonesia: growth optimization, bacteriocin production, and its application in food preservation. HAYATI Journal of Biosciences, 30(6), 1121-1131. https://doi.org/10.4308/hjb.30.6.1121-1131
Kusharyati, D. F., Satwika, T. D., Mariana, A., & Rovik, A. (2021). Potential screening of bacteriocinogenic-lactic acid bacteria from mangrove sediment of Logending beach for fisheries product preservation. Journal of Tropical Biodiversity and Biotechnology, 6(1), 61927. https://doi.org/10.22146/jtbb.61927
Le Morvan De Sequeira, C., Hengstberger, C., Enck, P., & Mack, I. (2022). Effect of probiotics on psychiatric symptoms and central nervous system functions in human health and disease: a systematic review and meta-analysis. Nutrients, 14(3), 621. https://doi.org/10.3390/nu14030621
Litocha, A., Michalczyk, A., Miastkowska, M., & Sikora, E. (2024). Effect of encapsulation of lactobacillus casei in alginate-tapioca flour microspheres coated with different biopolymers on the viability of probiotic bacteria. ACS Applied Materials & Interfaces, 16(39), 52878-52893. https://doi.org/10.1021/acsami.4c10187
Luca, L. & Oroian, M. (2021). Influence of different prebiotics on viability of Lactobacillus casei, Lactobacillus plantarum and Lactobacillus rhamnosus encapsulated in alginate microcapsules. Foods, 10(4), 710. https://doi.org/10.3390/foods10040710
Pradeep Prasanna, P. H. & Charalampopoulos, D. (2019). Encapsulation in an alginate-goats' milk-inulin matrix improves survival of probiotic Bifidobacterium in simulated gastrointestinal conditions and goats' milk yoghurt. International Journal of Dairy Technology, 72(1), 132-141. https://doi.org/10.1111/1471-0307.12568
Qi, W., Liang, X., Yun, T., & Guo, W. (2019). Growth and survival of microencapsulated probiotics prepared by emulsion and internal gelation. Journal of Food Science and Technology, 56(3), 1398-1404. https://doi.org/10.1007/s13197-019-03616-w
Rovik, A., & Kusharyati, D. F. (2025). Mapping the landscape: Indonesian fermented foods, probiotics, and cardiovascular disease prevention-a bibliometric and scoping review. BIO Web of Conferences, 190, 01031. https://doi.org/10.1051/bioconf/202519001031
Sarita, B., Samadhan, D., Hassan, M. Z., & Kovaleva, E. G. (2025). A comprehensive review of probiotics and human health-current prospective and applications. Frontiers in Microbiology, 15, 1487641. https://doi.org/10.3389/fmicb.2024.1487641
Shi, L.-E., Li, Z.-H., Li, D.-T., Xu, M., Chen, H.-Y., Zhang, Z.-L., & Tang, Z.-X. (2013). Encapsulation of probiotic Lactobacillus bulgaricus in alginate-milk microspheres and evaluation of the survival in simulated gastrointestinal conditions. Journal of Food Engineering, 117(1), 99-104. https://doi.org/10.1016/j.jfoodeng.2013.02.012
Sornplang, P. & Piyadeatsoontorn, S. (2016). Probiotic isolates from unconventional sources: A review. Journal of Animal Science and Technology, 58(1), 26. https://doi.org/10.1186/s40781-016-0108-2
Wang, X., Gao, S., Yun, S., Zhang, M., Peng, L., Li, Y., & Zhou, Y. (2022). Microencapsulating alginate-based polymers for probiotics delivery systems and their application. Pharmaceuticals, 15(5), 644. https://doi.org/10.3390/ph15050644
Wang, Y., Ding, W., Qiao, F., Wang, S., Li, J., Li, Y., Zhao, W., Gong, P., De Souza, C., Zhang, L., & Lin, K. (2025). Electrostatic spraying encapsulation of probiotic-loaded W/O/W emulsion in sodium alginate microspheres to enhance probiotic survival stability. International Journal of Biological Macromolecules, 284, 138005. https://doi.org/10.1016/j.ijbiomac.2024.138005
Yeung, T. W., Arroyo-Maya, I. J., McClements, D. J., & Sela, D. A. (2016). Microencapsulation of probiotics in hydrogel particles: enhancing Lactococcus lactis subsp. cremoris LM0230 viability using calcium alginate beads. Food & Function, 7(4), 1797-1804. https://doi.org/10.1039/C5FO00801H
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