Comparative lactic acid bacteria (LAB) profiles during dadih fermentation with spontaneous and back-slopping methods, as identified by terminal-restriction fragment length polymorphism (T-RFLP)

https://doi.org/10.22146/ijbiotech.61164

Chandra Utami Wirawati(1*), Mirnawati Bachrum Sudarwanto(2), Denny Widaya Lukman(3), Ietje Wientarsih(4), Eko Agus Srihanto(5)

(1) Food Technology Department, Politeknik Negeri Lampung, Jl. Soekarno Hatta Rajabasa 10, Bandar Lampung 35141, Indonesia
(2) Department of Animal Diseases and Veterinary Public Health, Faculty of Veterinary Medicine, Bogor Agricultural University, Jl. Raya Dramaga, Bogor, Jawa Barat 16680, Indonesia
(3) Department of Animal Diseases and Veterinary Public Health, Faculty of Veterinary Medicine, Bogor Agricultural University, Jl. Raya Dramaga, Bogor, Jawa Barat 16680, Indonesia
(4) Departement of Veterinary Clinic Reproduction and Pathology Faculty of Veterinary Medicine, Bogor Agricultural University, Jl. Raya Dramaga, Bogor, Jawa Barat 16680, Indonesia
(5) Lampung Veterinary Office, General Directorate Animal Husbandry and Healthiness, Agricultural Ministry Republic of Indonesia, Bandar Lampung 35141, Indonesia
(*) Corresponding Author

Abstract


The diversity of lactic acid bacteria (LAB) present during the manufacture of traditional fermented buffalo milk from West Sumatra, known as dadih, was studied via a culture-independent approach using terminal-restriction fragment length polymorphism (T-RFLP) to compare the dynamic diversity in back-slopping and spontaneous fermentation methods. Total LAB and pH were measured in freshly prepared buffalo milk and in \textit{dadih} fermented for 24 and 48 hours. The results indicated significant differences between the fermentation methods, with higher total LAB, and greater phylotype richness and relative abundance being identified in the back-slopping method. Terminal fragment lengths (TRFs) of 68 and 310 bp were common to both techniques, similar to those of Lactobacillus fermentum, Fructobacillus pseudoficulneus, Leuconostoc citreum, Leuconostoc kimchii, and Leuconostoc sp. The changes in phylotype number (species number) and relative abundances of LAB communities identified are expected to produce data needed to formulate the best fermentation process for dadih manufacturing. A 24-hour back-slopping fermentation method is recommended, as fermentation time of longer than 24 hours reduced viable LAB significantly. Our results also indicated that the T-RFLP technique is not only clearly sensitive enough and adequate for segregating LAB diversity in both fermentation methods, but that it also provides good information regarding the structure of microbial communities and their composition change during the fermentation process.

Keywords


Dadih; lactic acid bacteria (LAB); dynamic diversity; T-RFLP

Full Text:

PDF


References

Ao X, Zhang X, Zhang X, Shi L, Zhao K, Yu J, Dong L, Cao Y, Cai Y. 2012. Identification of lactic acid bacteria in traditional fermented yak milk and evaluation of their application in fermented milk products. J Dairy Sci. 95(3):1073–1084. doi:10.3168/jds.2011­4224.

Baniyah L, Nur Jannah S, Rukmi I, Sugiharto. 2018. Molecular diversity of lactic acid bacteria on ileum broiler chicken fed by bran and bran fermentation. J Phys Conf Ser. 1025(1). doi:10.1088/1742­ 6596/1025/1/012049.

Bintsis T. 2018. Lactic acid bacteria as starter cultures: An update in their metabolism and genetics. AIMS Microbiol. 4(4):665–684. doi:10.3934/microbiol.2018.4.665.

Chakoosari MMD, Ghasemi MF, Masiha A. 2014. Antimicrobial Activities of Lactic Acid Bacteria. Bull Environ Pharmacol Life Sci. 3(2):275–278.

de Oliveira MN. 2014. Fermented Milks: Fermented Milks and Yogurt. In: Encyclopedia of Food Microbiology: Second Edition. p. 908–922. doi:10.1016/B978­0­12­384730­0.00121­X.

Dervisoglu M, Aydemir O. 2007. Physicochemical and microbiological characteristics of Kulek cheese made from raw and heat­treated milk. World J Microbiol Biotechnol. 23(4):451–460. doi:10.1007/s11274­ 006­9246­x.

Efriwati, Suwanto A, Rahayu G, Nuraida L. 2013. Population Dynamics of Yeasts and Lactic Acid Bacteria (LAB) During Tempeh Production. HAYATI J Biosci. 20(2):57–64. doi:10.4308/hjb.20.2.57.

Ercolini D. 2013. High­Throughput Sequencing and Metagenomics: Moving Forward in the CultureIndependent Analysis of Food Microbial Ecology. Appl Environ Microbiol. 79(10):3148–3155. doi:10.1128/aem.00256­13.

Fugl A, Berhe T, Kiran A, Hussain S, Laursen MF, Bahl MI, Hailu Y, Sørensen KI, Guya ME, Ipsen R, Hansen EB. 2017. Characterisation of lactic acid bacteria in spontaneously fermented camel milk and selection of strains for fermentation of camel milk. International Dairy Journal 73:19–24. doi:10.1016/j.idairyj.2017.04.007.

Hayek SA, Ibrahim SA. 2013. Current Limitations and Challenges with Lactic Acid Bacteria: A Review. Food Nutr Sci. 04(11):73–87. doi:10.4236/fns.2013.411a010.

Jannah SN, Dinoto A, Wiryawan KG, Rusmana I. 2016. Molecular diversity pattern of intestinal lactic acid bacteria in Cemani chicken, Indonesian native chicken, as revealed by terminal restriction fragment length polymorphisms. Malays J Microbiol. 12(1):102–111. doi:10.21161/mjm.73815.

Jernberg C, Sullivan Å, Edlund C, Jansson JK. 2005. Monitoring of antibiotic­induced alterations in the human intestinal microflora and detection of probiotic strains by use of terminal restriction fragment length polymorphism. Appl Environ Microbiol. 71(1):501–506. doi:10.1128/AEM.71.1.501­506.2005.

Kim DH, Jeong D, Song KY, Seo KH. 2018. Comparison of traditional and backslopping methods for kefir fermentation based on physicochemical and microbiological characteristics. Lwt. 97:503–507. doi:10.1016/j.lwt.2018.07.023.

Kimaryo VM, Massawe GA, Olasupo NA, Holzapfel WH. 2000. The use of a starter culture in the fermentation of cassava for the production of ’kivunde’, a traditional Tanzanian food product. International Journal of Food Microbiology 56(2­3):179– 190. doi:10.1016/S0168­1605(00)00159­8.

Lackey KA, Williams JE, Price WJ, Carrothers JM, Brooker SL, Shafii B, McGuire MA, McGuire MK. 2017. Comparison of commercially­available preservatives for maintaining the integrity of bacterial DNA in human milk. J Microbiol Methods. 141:73–81. doi:10.1016/j.mimet.2017.08.002.

Moran CA, Scholten RHJ, Tricarico JM, Brooks PH, Verstegen MWA. 2006. Fermentation of wheat: Effects of backslopping different proportions of prefermented wheat on the microbialand chemical com­position. Archives of Animal Nutrition 60(2):158– 169. doi:10.1080/17450390600562700.

Mulyawati AI, Jatmiko YD, Mustafa I, Ardyati T, Suharjono. 2019. Diversity of lactic acid bacteria isolated from fermented mare’s milk products based on PCRRFLP analysis. P Conf Ser Earth Environ Sci. 230(1). doi:10.1088/1755­1315/230/1/012104.

Mustopa AZ, Fatimah F. 2014. Diversity of Lactic Acid Bacteria Isolated from Indonesian Traditional Fermented Foods. Microbiol Indones. 8(2):48–57. doi:10.5454/mi.8.2.2.

Nduko JM, Matofari JW, Nandi ZO, Sichangi MB. 2017. Spontaneously fermented kenyan milk products: A review of the current state and future perspectives. African J Food Sci. 11(1):1–11. doi:10.5897/ajfs2016.1516.

Prakash O, Pandey PK, Kulkarni GJ, Mahale KN, Shouche YS. 2014. Technicalities and Glitches of Terminal Restriction Fragment Length Polymorphism (T­RFLP). Indian J Microbiol. 54(3):255–261. doi:10.1007/s12088­014­0461­0.

Rademaker JL, Peinhopf M, Rijnen L, Bockelmann W, Noordman WH. 2005. The surface microflora dynamics of bacterial smear­ripened Tilsit cheese determined by T­RFLP DNA population fingerprint analysis. Int Dairy J. 15(6­9):785–794. doi:10.1016/j.idairyj.2004.08.027.

Schütte UM, Abdo Z, Bent SJ, Shyu C, Williams CJ, Pierson JD, Forney LJ. 2008. Advances in the use of terminal restriction fragment length polymorphism (TRFLP) analysis of 16S rRNA genes to characterize microbial communities. Appl Microbiol Biotechnol. 80(3):365–380. doi:10.1007/s00253­008­1565­4.

Shyu C, Soule T, Bent SJ, Foster JA, Forney LJ. 2007. MiCA: A web­based tool for the analysis of microbial communities based on terminal­restriction fragment length polymorphisms of 16S and 18S rRNA genes. Microb Ecol. 53(4):562–570. doi:10.1007/s00248­ 006­9106­0.

Surono IS. 2003. In vitro probiotic properties of indigenous dadih lactic acid bacteria. Asian­Australas J Anim Sci. 16(5):726–731. doi:10.5713/ajas.2003.726.

Syukur S, Rijal F, Jamsari, Purwati E. 2014. Isolation and molecular characterization of lactic acid bacteria by using 16s rRNA from fermented buffalo milk (Dadih) in Sijunjung, West Sumatera. Res J Pharm, Biol Chem Sci. 5(6):871–876.

Teniola OD, Holzapfel WH, Odunfa SA. 2005. Comparative assessment of fermentation techniques useful in the processing of ogi. World J Microbiol Biotechnol. 21(1):39–43. doi:10.1007/s11274­004­1549­1.

Uroić K, Novak J, Hynönen U, Pietilä TE, Leboš Pavunc A, Kant R, Kos B, Palva A, Šušković J. 2016. The role of S­layer in adhesive and immunomodulating properties of probiotic starter culture Lactobacillus brevis D6 isolated from artisanal smoked fresh cheese. LWT ­ Food Sci Technol. 69:623–632. doi:10.1016/j.lwt.2016.02.013.

Venema K, Surono IS. 2019. Microbiota composition of dadih – a traditional fermented buffalo milk of West Sumatra. Letters in Applied Microbiology 68(3):234– 240. doi:10.1111/lam.13107.

Wanangkarn A, Liu DC, Swetwiwathana A, Jindaprasert A, Phraephaisarn C, Chumnqoen W, Tan FJ. 2014. Lactic acid bacterial population dynamics during fermentation and storage of Thai fermented sausage according to restriction fragment length polymorphism analysis. Int J Food Microbiol. 186:61–67. doi:10.1016/j.ijfoodmicro.2014.06.015.

Wang YC, Yu RC, Chou CC. 2002. Growth and survival of bifidobacteria and lactic acid bacteria during the fermentation and storage of cultured soymilk drinks. Food Microbiol. 19(5):501–508. doi:10.1006/fmic.2002.0506.

Wirawati CU, Sudarwanto MB, Lukman DW, Wientarsih I, Srihanto EA. 2019. Diversity of lactic acid bacteria in dadih produced by either back­slopping or spontaneous fermentation from two different regions of West Sumatra, Indonesia. Vet World. 12(6):823–829. doi:10.14202/vetworld.2019.823­829.

Yu J, Wang WH, Menghe BL, Jiri MT, Wang HM, Liu WJ, Bao QH, Lu Q, Zhang JC, Wang F, Xu HY, Sun TS, Zhang HP. 2011. Diversity of lactic acid bacteria associated with traditional fermented dairy products in Mongolia. J Dairy Sci. 94(7):3229–3241. doi:10.3168/jds.2010­3727.

Zafar SB, Siddiqui NN, Shahid F, Qader SAU, Aman A. 2018. Bioprospecting of indigenous resources for the exploration of exopolysaccharide producing lactic acid bacteria. J Genet Eng Biotechnol. 16(1):17–22. doi:10.1016/j.jgeb.2017.10.015.

Zhang J, Wang X, Huo D, Li W, Hu Q, Xu C, Liu S, Li C. 2016. Metagenomic approach reveals microbial diversity and predictive microbial metabolic pathways in Yucha, a traditional Li fermented food. Sci Rep. 6. doi:10.1038/srep32524.



DOI: https://doi.org/10.22146/ijbiotech.61164

Article Metrics

Abstract views : 2907 | views : 2663

Refbacks

  • There are currently no refbacks.


Copyright (c) 2021 The Author(s)

Creative Commons License
This work is licensed under a Creative Commons Attribution-ShareAlike 4.0 International License.