Antioxidant Activity, γ-Aminobutyric Acid, and Genome Analysis of Lactiplantibacillus plantarum FL13-2 from Fermented Rice Flour
Keywords:
Fermented rice, γ-Aminobutyric acid, Limosilactobacillus fermentum, LactiplantibacillusAbstract
Ten rod-shaped isolates of lactic acid bacteria (LAB) from the traditional fermented rice flour, khao-khab were identified as belonging to the genus Lactobacillus based on phenotypic characteristics. Group I isolates (FL12-1, FL18-1, FL19-1S, FL23-1, FL24-1, FL25-1, and FL26-1) were closely related to Limosilactobacillus fermentum, exhibiting 16S rRNA gene sequence similarity of 99.4%–100%. Group II included FL13-2 and FL22-2 (Group IIA) and FL17B (Group IIB), closely related to Lactiplantibacillus plantarum (99.9%–100%) and Lactiplantibacillus pentosus (100%), respectively. All isolates demonstrated strong antioxidant potential, with 2,2-Diphenyl-1-picrylhydrazyl (DPPH) radical scavenging activity—measured by the standard DPPH assay—ranging from 78.49±1.01% to 91.18±3.95%, surpassing that of ascorbic acid. Strain FL13-2, identified as L. plantarum through genomic analysis (Average Nucleotide Identity (ANI) 98.5%, digital DNA-DNA hybridization (dDDH) 92.5%), produced 2.43 g/L of γ-aminobutyric acid (GABA). It harbored key biosynthesis and transport genes (gadB, gadC, gatABCD, pdxK). Phylogenetic analysis confirmed high sequence similarity of these genes with other LAB strains, supporting their functional roles. The gad system was implicated in acid resistance and GABA production under low pH conditions. Genome annotation revealed bacteriocin genes (Enterocin X β, Plantaricin E, and F) and indicated low pathogenicity and absence of virulence factors. Antimicrobial resistance genes (vanH, vanT, vanY) were detected; however, these are intrinsic to LAB and associated with essential cell wall biosynthesis rather than acquired resistance. Additionally, the presence of the qacJ efflux pump and hlyIII gene—both commonly found in probiotic strains—further supports the safety profile of FL13-2. These findingshighlight L. plantarum FL13-2 as a promising multifunctional probiotic candidate with potent antioxidative, GABA-producing, and antimicrobial properties.
References
Ahn, J., & Park, J.Y. (2023). Potential of γ-aminobutyric acid-producing Leuconostoc mesenteroides strains isolated from kimchi as a starter for high-γ-aminobutyric acid kimchi fermentation. Preventive Nutrition and Food Science, 28(4), 492–501.
Asun, A.C., Lin, S.T., Ng, H.S., & Lan, J.C.W. (2022). Production of gamma-aminobutyric acid (GABA) by Bacillus subtilis BBEL02 fermentation using nitrogen-rich industrial wastes as crude feedstocks. Biochemical Engineering Journal, 187, 108654.
Aziz, R.K., Bartels, D., Best, A.A., DeJongh, M., Disz, T., Edwards, R.A., Zagnitko, O. (2008). The RAST server: Rapid annotations using subsystems technology. BMC Genomics, 9(1), 75.
Aziz, R.K., Devoid, S., Disz, T., Edwards, R.A., Henry, C.S., Olsen, G.J., Xia, F. (2012). SEED Servers: Highperformance access to the SEED genomes, annotations, and metabolic models. PLoS One, 7, e48053.
Bankevich, A., Nurk, S., Antipov, D., Gurevich, A.A., Dvorkin, M., Kulikov, A.S., Pevzner, P.A. (2012). SPAdes: A new genome assembly algorithm and its applications to single-cell sequencing. Journal of Computational Biology, 19(5), 455–477.
Chan, M.Z.A., Lu, Y., & Liu, S.Q. (2021). In vitro bioactivities of coffee brews fermented with the probiotics Lacticaseibacillus rhamnosus GG and Saccharomyces boulardii CNCM-I745. Food Research International, 149, 110693.
Chittrakhani, C., Songsermpong, S., Trevanich, S., & Sukor, R. (2022). Effect of Levilactobacillus brevis TISTR 860 and Lactiplantibacillus plantarum TISTR 951 on gamma-aminobutyric acid content in fermented rice flour and rice noodles (Kanomjeen). International Journal of Food Science and Technology, 57(6), 3410–3418.
Cho, S.Y., Park, M.J., Kim, K.M., Ryu, J.H., & Park, H.J. (2011). Production of high γ-Aminobutyric acid (GABA) sour kimchi using lactic acid bacteria isolated from Mukherjee kimchi. Food Science and Biotechnology, 20, 403–408.
Corsetti, A., Lavermicocca, P., Morea, M., Baruzzi, F., Tosti, N., & Gobbetti, M. (2001). Phenotypic and molecular identification and clustering of lactic acid bacteria and yeasts from wheat (Triticum durum and Triticum aestivum) sourdough of Southern Italy. International Journal of Food Microbiology, 64, 95–104.
Davis, C.D., & Milner, J.A. (2009). Gastrointestinal microflora, food components, and colon cancer prevention. Journal of Nutritional Biochemistry, 20(10), 743–752.
De Marco, S., Sichetti, M., Muradyan, D., Piccioni, M., Traina, G., Pagiotti, R., & Pietrella, D. (2018). Probiotic cellfree supernatants exhibited anti-inflammatory and antioxidant activity on human gut epithelial cells and macrophages stimulated with LPS. Evidence-Based Complementary and Alternative Medicine, 2018(1), 1756308.
Dhakal, R., Bajpai, V.K., & Baek, K.H. (2012). Production of GABA (γ–aminobutyric acid) by microorganisms: A review. Brazilian Journal of Microbiology, 43(4), 1230–1241.
Felsenstein, J. (1985). Confidence limits on phylogenies: An approach using the bootstrap. Evolution, 39(4), 783–791.
Guerrero, R., Guevara, L., González, E., Ferrer, S., & Mesas, J.M. (2022). Biosynthesis of gamma-aminobutyric acid by Lactiplantibacillus plantarum K16: Optimization and application in agri-food by-products. Scientific Reports, 12(1), 22875.
Hamed, E. (2021). Isolation, characterization and identification of lactic acid bacteria as probiotic. Annals of Agricultural Science, Moshtohor, 59(5), 311–322.
Hammes, W.P., & Vogel, R.F. (1995). The genus Lactobacillus. In B.J.B. Wood & W.H. Holzapfel (Eds.), The genera of lactic acid bacteria (pp. 19–54). London, UK: Blackie Academic and Professional.
Hols, P., Defrenne, C., Ferain, T., Derzelle, S., Delplace, B., & Delcour, J. (1997). The alanine racemase gene is essential for growth of Lactobacillus plantarum. Journal of Bacteriology, 179(11), 3804–3807.
Jitpakdee, J., Kantachote, D., Kanzaki, H., & Nitoda, T. (2021). Selected probiotic lactic acid bacteria isolated from fermented foods for functional milk production: Lower cholesterol with more beneficial compounds. LWT - Food Science and Technology, 135, 110061.
Jitpakdee, S., Kaewsorn, P., Rangsiruji, A., Sukhoom, A., & Tanasupawat, S. (2022). Cholesterol-lowering potential and production of beneficial metabolites, including gamma-aminobutyric acid, by Lactiplantibacillus plantarum SPS109 isolated from fermented food. Journal of Applied Microbiology, 133(4), 2514–2529.
Kanklai, J., Somwang, T.C., Rungsirivanich, P., & Thongwai, N. (2021). Screening of GABA-producing lactic acid bacteria from Thai fermented foods and probiotic potential of Levilactobacillus brevis F064A for GABA-fermented mulberry juice production. Microorganisms, 9(1), 33.
Kim, H., Kim, J.S., Kim, Y., Jeong, Y., Kim, J.E., Paek, N.S., & Kang, C.H. (2020). Antioxidant and Probiotic properties of Lactobacilli and Bifidobacteria of human origins. Biotechnology and Bioprocess Engineering, 25(3), 421–430.
Kim, J., Choi, H., & Park, S. (2021). Gamma-aminobutyric acid production by Levilactobacillus brevis F109-MD3 isolated from kimchi. Journal of Microbiology and Biotechnology, 31(10), 1267–1275.
Kingkaew, E., Konno, H., Hosaka, Y., & Tanasupawat, S. (2023a). Probiogenomic analysis of Lactiplantibacillus sp. LM14-2 from fermented mussel (Hoi-Dong), and evaluation of its cholesterol-lowering and immunomodulation effects. Probiotics and Antimicrobial Proteins, 15(5), 1206–1220.
Kingkaew, E., Woraprayote, W., Booncharoen, A., Niwasabutra, K., Janyaphisan, T., Vilaichone, R.K., ... Tanasupawat, S. (2023b). Functional genome analysis and antiHelicobacter pylori activity of a novel bacteriocinogenic Lactococcus sp. NH2-7C from Thai fermented pork (Nham). Scientific Reports, 13(1), 20362.
Kingkaew, E., Woraprayote, W., Sitdhipol, J., Vilaichone, R.K., Visessanguan, W., & Tanasupawat, S. (2025). Genomic assessment, metabolic profile mapping, and antiHelicobacter pylori activity of Lactococcus lactis SK2-659 from Thai fermented green mustard (Pakkad-dong). Probiotics and Antimicrobial Proteins, 1–17.
Komatsuzaki, N., Tsukahara, K., Toyoshima, H., Suzuki, T., Shimizu, N., & Kimura, T. (2007). Effect of soaking and germination on GABA content in germinated brown rice. Journal of Food Composition and Analysis, 20(4), 311–316.
Lane, D.J. (1991). 16S/23S rRNA sequencing. In E. Stackebrandt & M. Goodfellow (Eds.), Nucleic acid techniques in bacterial systematics (pp. 115–175). New York, USA: John Wiley & Sons.
Lee, K.W., Shim, J.M., Yao, Z., Kim, J.A., Park, J., & Kim, H.J. (2018). Enhanced production of gammaaminobutyric acid (GABA) in kimchi fermented by Lactobacillus zymae GU240 using monosodium glutamate and kelp extract powder as supplements. Food Science and Biotechnology, 27(3), 731–738.
Łepecka, A., Szymański, P., Okoń, A., & Zielińska, D. (2023). Antioxidant activity of environmental lactic acid bacteria strains isolated from organic raw fermented meat products. LWT-Food Science and Technology, 174, 114440.
Lin, M.Y., & Yen, C.L. (1999). Antioxidative ability of lactic acid bacteria. Journal of Agricultural and Food Chemistry, 47(4), 1460–1466.
Liwinski, T., Lang, U.E., Brühl, A.B., & Schneider, E. (2023). Exploring the therapeutic potential of gammaaminobutyric acid in stress and depressive disorders through the gut–brain axis. Biomedicines, 11(12), 3128.
Oh, S.H., Moon, Y.J., & Oh, C.H. (2003). γ-Aminobutyric acid (GABA) content of selected uncooked foods. Preventive Nutrition and Food Science, 8(1), 75–78.
Pakdeeto, A., Phuengjayaem, S., Arayakarn, T., Phitchayaphon, C., Tungkajiwangkoon, S., & Tanasupawat, S. (2022). Identification of gamma-aminobutyric acid (GABA)-producing lactic acid bacteria from plant-based Thai fermented foods and genome analysis of Lactobacillus brevis GPB7-4. ScienceAsia, 48(3), 254–262.
Park, S.Y., Kim, K.S., Lee, M.K., & Lim, S.D. (2013). Physiological characteristics and GABA production of Lactobacillus plantarum K255 isolated from kimchi. Food Science of Animal Resources, 33(5), 595–602.
Phuengjayaem, S., Pakdeeto, A., Kingkaew, E., Tunvongvinis, T., Somphong, A., & Tanasupawat, S. (2023). Genome sequences and functional analysis of Levilactobacillus brevis LSF9-1 and Pediococcus acidilactici LSF1-1 from fermented fish cake (Som-fak) with gammaaminobutyric acid (GABA) production. Functional and Integrative Genomics, 23(2), 158.
Phuengjayaem, S., Tanasupawat, S., & Teeradakorn, S. (2020). Characterization of a novel Clostridium sp. SP17-B1 and its application for succinic acid production from Hevea wood waste hydrolysate. Anaerobe, 61, 102096.
Rehman, A., Di Benedetto, G., Bird, J.K., Dabene, V., Vadakumchery, L., May, A., ... Mak, T.N. (2023). Development of a workflow for the selection, identification and optimization of lactic acid bacteria with high γ-aminobutyric acid production. Scientific Reports, 13(1), 13663.
Richter, M., Rosselló-Móra, R., Glöckner, F.O., & Peplies, J. (2016). JSpeciesWS: A web server for prokaryotic species circumscription based on pairwise genome comparison. Bioinformatics, 32(6), 929–931.
Saito, H., & Miura, K.I. (1963). Preparation of transforming deoxyribonucleic acid by phenol treatment. Biochimica et Biophysica Acta (BBA)-Specialized Section on Nucleic Acids and Related Subjects, 72, 619–629.
Sanchart, C., Rattanaporn, O., Haltrich, D., Phukpattaranont, P., & Maneerat, S. (2017). Lactobacillus futsaii CS3, a new GABA-producing strain isolated from Thai fermented shrimp (Kung-Som). Indian Journal of Microbiology, 57(2), 211–217.
Stogios, P.J., & Savchenko, A. (2020). Molecular mechanisms of vancomycin resistance. Protein Science, 29(3), 654–669.
Tamura, K., Stecher, G., & Kumar, S. (2021). MEGA11: Molecular evolutionary genetics analysis version 11. Molecular Biology and Evolution, 38(7), 3022–3027.
Tanamool, V., Hongsachart, P., & Soemphol, W. (2019). Screening and characterisation of gamma-aminobutyric acid (GABA) producing lactic acid bacteria isolated from Thai fermented fish (Plaa-som) in Nong Khai and its application in Thai fermented vegetables
(Som-pak). Food Science and Technology, 40(2), 483–490.
Tanasupawat, S., & Komagata, K. (1995) Lactic acid bacteria in fermented foods in Thailand. World Journal of Microbiology and Biotechnology, 11(3), 253–256.
Tanasupawat, S., Ezaki, T., Suzuki, K., Okada, S., Komagata, K., & Kozaki, M. (1992). Characterization and identification of Lactobacillus pentosus and Lactobacillus plantarum strains from fermented foods in Thailand. Journal of General and Applied Microbiology, 38(2), 121–134.
Tanasupawat, S., Okada, S., & Komagata, K. (1998). Lactic acid bacteria found in fermented fish in Thailand. Journal of General and Applied Microbiology, 44(3), 193–200.
Tanasupawat, S., Thongsanit, J., Okada, S., & Komagata, K. (2002). Lactic acid bacteria isolated from soy sauce mash in Thailand. Journal of General and Applied Microbiology, 48(4), 201–209.
Tang, W., Li, C., He, Z., Pan, F., Pan, S., & Wang, Y. (2018). Probiotic properties and cellular antioxidant activity of Lactobacillus plantarum MA2 isolated from Tibetan kefir grains. Probiotics and Antimicrobial Proteins, 10(3), 523–533.
Thompson, J.D., Gibson, T.J., Plewniak, F., Jeanmougin, F., & Higgins, D.G. (1997). CLUSTAL_X windows interface: Flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Research, 25(24), 4876–4882.
Wan-Mohtar, W.A.A.Q.I., Sohedein, M.N.A., Ibrahim, M.F., Ab Kadir, S., Suan, O.P., Weng Loen, A.W., ... Ilham, Z. (2020). Isolation, identification, and optimization of γ-Aminobutyric acid (GABA)-producing Bacillus cereus strain KBC from a commercial soy sauce
moromi in submerged-liquid fermentation. Processes, 8(6), 652.
Yang, J., Dong, C., Ren, F., Xie, Y., Liu, H., Zhang, H., & Jin, J. (2021a). Lactobacillus paracasei M11-4 isolated from fermented rice demonstrates good antioxidant properties in vitro and in vivo. Journal of the Science of Food and Agriculture, 102, 3107–3118.
Yang, S.Y., Chae, S.A., Bang, W.Y., Lee, M., Ban, O.H., Kim, S.J., ... Yang, J. (2021b). Anti-inflammatory potential of Lactiplantibacillus plantarum IDCC 3501 and its safety evaluation. Brazilian Journal of Microbiology, 52(4), 2299–2306.
Zhang, Q., Xiang, J., Zhang, L., Zhu, X., Evers, J., van der Werf, W., & Duan, L. (2014). Optimizing soaking and germination conditions to improve gammaaminobutyric acid content in japonica and indica germinated brown rice. Journal of Functional Foods, 10, 283–291.
Zheng, J., Wittouck, S., Salvetti, E., Franz, C.M., Harris, H.M., Mattarelli, P., ... Lebeer, S. (2020). A taxonomic note on the genus Lactobacillus: Description of 23 novel genera, emended description of the genus Lactobacillus Beijerinck 1901, and union of Lactobacillaceae and Leuconostocaceae. International journal of systematic and evolutionary microbiology, 70(4), 2782–2858.
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