DOI QR코드

DOI QR Code

Optimization of an Industrial Medium and Culture Conditions for Probiotic Weissella cibaria JW15 Biomass Using the Plackett-Burman Design and Response Surface Methodology

  • Yu, Hyung-Seok (Department of Food Science and Biotechnology of Animal Resources, Konkuk University) ;
  • Lee, Na-Kyoung (Department of Food Science and Biotechnology of Animal Resources, Konkuk University) ;
  • Kim, Won-Ju (Department of Food Science and Biotechnology of Animal Resources, Konkuk University) ;
  • Lee, Do-Un (Department of Food Science and Biotechnology of Animal Resources, Konkuk University) ;
  • Kim, Jong-Ha (Department of Food Science and Biotechnology of Animal Resources, Konkuk University) ;
  • Paik, Hyun-Dong (Department of Food Science and Biotechnology of Animal Resources, Konkuk University)
  • 투고 : 2022.02.15
  • 심사 : 2022.03.20
  • 발행 : 2022.05.28

초록

The objective of this study was to optimize industrial-grade media for improving the biomass production of Weissella cibaria JW15 (JW15) using a statistical approach. Eleven variables comprising three carbon sources (glucose, fructose, and sucrose), three nitrogen sources (protease peptone, yeast extract, and soy peptone), and five mineral sources (K2HPO4, potassium citrate, ⳑ-cysteine phosphate, MgSO4, and MnSO4) were screened by using the Plackett-Burman design. Consequently, glucose, sucrose, and soy peptone were used as significant variables in response surface methodology (RSM). The composition of the optimal medium (OM) was 22.35 g/l glucose, 15.57 g/l sucrose, and 10.05 g/l soy peptone, 2.0 g/l K2HPO4, 5.0 g/l sodium acetate, 0.1 g/l MgSO4·7H2O, 0.05 g/l MnSO4·H2O, and 1.0 g/l Tween 80. The OM significantly improved the biomass production of JW15 over an established commercial medium (MRS). After fermenting OM, the dry cell weight of JW15 was 4.89 g/l, which was comparable to the predicted value (4.77 g/l), and 1.67 times higher than that of the MRS medium (3.02 g/l). Correspondingly, JW15 showed a rapid and increased production of lactic and acetic acid in the OM. To perform a scale-up validation, batch fermentation was executed in a 5-l bioreactor at 37℃ with or without a pH control at 6.0 ± 0.1. The biomass production of JW15 significantly improved (1.98 times higher) under the pH control, and the cost of OM was reduced by two-thirds compared to that in the MRS medium. In conclusion, OM may be utilized for mass producing JW15 for industrial use.

키워드

과제정보

This paper was supported by Konkuk University Researcher Fund in 2020.

참고문헌

  1. Lee NK, Ha KJ, Son SH, Eom SJ, Lee SK, Paik HD. 2015. Multifunctional effect of probiotic Lactococcus lactis KC24 isolated from kimchi. LWT-Food Sci. Technol. 64: 1036-1041. https://doi.org/10.1016/j.lwt.2015.07.019
  2. Sonnenburg JL, Backhed F. 2016. Diet-microbiota interactions as moderators of human metabolism. Nature 535: 56-64. https://doi.org/10.1038/nature18846
  3. Choi GH, Lee NK, Paik HD. 2021. optimization of medium composition for biomass production of Lactobacillus plantarum 200655 using response surface methodology. J. Microbiol. Biotechnol. 31: 717-725. https://doi.org/10.4014/jmb.2103.03018
  4. Jang HJ, Lee NK, Paik HD. 2019. Probiotic characterization of Lactobacillus brevis KU15153 showing antimicrobial and antioxidant effect isolated from kimchi. Food Sci. Biotechnol. 28: 1521-1528. https://doi.org/10.1007/s10068-019-00576-x
  5. Gao X, Qiao S, Lu W. 2009. Determination of an economical medium for growth of Lactobacillus fermentum using response surface methodology. Lett. Appl. Microbiol. 49: 556-561. https://doi.org/10.1111/j.1472-765X.2009.02705.x
  6. Polak-Berecka M, Wasko A, Kordowska-Wiater M, Podlesny M, Targonski Z, Kubik-Komar A. 2010. Optimization of medium composition for enhancing growth of Lactobacillus rhamnosus PEN using response surface methodology. Pol. J. Microbiol. 59: 113-118. https://doi.org/10.33073/pjm-2010-017
  7. Asan-Ozusaglam M, Gunyakti A. 2019. Lactobacillus fermentum strains from human breast milk with probiotic properties and cholesterol-lowering effects. Food Sci. Biotechnol. 28: 501-509. https://doi.org/10.1007/s10068-018-0494-y
  8. Khan I, Kang SC. 2016. Probiotic potential of nutritionally improved Lactobacillus plantarum DGK-17 isolated from Kimchi-A traditional Korean fermented food. Food Control 60: 88-94. https://doi.org/10.1016/j.foodcont.2015.07.010
  9. Silva MS, Ramos CL, Gonzalez-Avila M, Gschaedler A, Arrizon J, Schwan RF, Dias DR. 2017. Probiotic properties of Weissella cibaria and Leuconostoc citreum isolated from tejuino-A typical Mexican beverage. LWT-Food Sci. Technol. 86: 227-232. https://doi.org/10.1016/j.lwt.2017.08.009
  10. Li S, Zhao Y, Zhang L, Zhang X, Huang L, Li D, Niu C, Yang Z, Wang Q. 2012. Antioxidant activity of Lactobacillus plantarum strains isolated from traditional Chinese fermented foods. Food Chem. 135: 1914-1919. https://doi.org/10.1016/j.foodchem.2012.06.048
  11. Yu, H.S., Jang HJ, Lee NK, Paik HD. 2019. Evaluation of the probiotic characteristics and prophylactic potential of Weissella cibaria strains isolated from kimchi. LWT-Food Sci. Technol. 112: 108229. https://doi.org/10.1016/j.lwt.2019.05.127
  12. Unger MM, Spiegel J, Dillmann KU, Grundmann D, Philippeit H, Burmann J, et al. 2016. Short chain fatty acids and gut microbiota differ between patients with Parkinson's disease and age-matched controls. Parkinsonism Relat. Disord. 32: 66-72. https://doi.org/10.1016/j.parkreldis.2016.08.019
  13. Yeo S, Shin HS, Lee HW, Hong D, Park H, Holzapfel W, Kim EB, Huh CS. 2018. Determination of optimized growth medium and cryoprotective additives to enhance the growth and survival of Lactobacillus salivarius. J. Microbiol. Biotechnol. 28: 718-731. https://doi.org/10.4014/jmb.1801.01059
  14. Sreekumar G, Krishnan S. 2010. Enhanced biomass production study on probiotic Bacillus subtilis SK09 by medium optimization using response surface methodology. Afr. J. Biotechnol. 9: 8078-8084. https://doi.org/10.5897/AJB10.1283
  15. Park HE, Lee WK. 2018. Immune enhancing effects of Weissella cibaria JW15 on BALB/c mice immunosuppressed by cyclophosphamide. J. Funct. Foods 49: 518-525. https://doi.org/10.1016/j.jff.2018.09.003
  16. Yu HS, Lee NK, Choi AJ, Choe JS, Bae CH, Paik HD. 2018. Antagonistic and antioxidant effect of probiotic Weissella cibaria JW15. Food Sci. Biotechnol. 28: 851-855. https://doi.org/10.1007/s10068-018-0519-6
  17. Yu HS, Lee NK, Choi AJ, Choe JS, Bae CH, Paik HD. 2019. Anti-inflammatory potential of probiotic strain Weissella cibaria JW15 isolated from kimchi through regulation of NF-κB and MAPKs pathways in LPS-induced RAW 264.7 cells. J. Microbiol. Biotechnol. 29: 1022-1032. https://doi.org/10.4014/jmb.1903.03014
  18. Kim HY, Bae WY, Yu HS, Chang KH, Hong YH, Lee NK, Paik HD. 2019. Inula britannica fermented with probiotic Weissella cibaria D30 exhibited anti-inflammatory effect and increased viability in RAW 264.7 cells. Food Sci. Biotechnol. 29: 569-578. https://doi.org/10.1007/s10068-019-00690-w
  19. Kamal MM, Ali MR, Shishir MRI, Saifullah M, Haque MR, Mondal SC. 2019. Optimization of process parameters for improved production of biomass protein from Aspergillus niger using banana peel as a substrate. Food Sci. Biotechnol. 28: 1693-1702. https://doi.org/10.1007/s10068-019-00636-2
  20. Coghetto CC, Vasconcelos CB, Brinques GB, Ayuba MAZ. 2016. Lactobacillus plantarum BL011 cultivation in industrial isolated soybean protein acid residue. Braz. J. Microbiol. 47: 941-948. https://doi.org/10.1016/j.bjm.2016.06.003
  21. Lim HS, Roh SW, Seo, MJ. 2017. Enhanced production of gamma-aminobutyric acid by optimizing culture conditions of Lactobacillus brevis HYE1 isolated from kimchi, a Korean fermented food. J. Microbiol. Biotechnol. 27: 450-459. https://doi.org/10.4014/jmb.1610.10008
  22. Fonteles TV, Costa MGM, de Jesus ALT, Rodrigues S. 2012. Optimization of the fermentation of cantaloupe juice by Lactobacillus casei NRRL B-442. Food Bioproc. Tech. 5: 2819-2826. https://doi.org/10.1007/s11947-011-0600-0
  23. Mataragas M, Drosinos EH, Tsakalidou E, Metaxopouloset J. 2004. Influence of nutrients on growth and bacteriocin production by Leuconostoc mesenteroides L124 and Lactobacillus curvatus L442. Antonie Van Leeuwenhoek 85: 191-198. https://doi.org/10.1023/B:ANTO.0000020291.01957.a2
  24. Okano K, Sato Y, Hama S, Tanaka T, Noda H, Kondo A, Honda K. 2022. L-Lactate oxidase-mediated removal of L-lactic acid derived from fermentation medium for the production of optically pure D-lactic acid. Biotechnol. J. 2022: 2100331.
  25. Brinques GB, Peralba MC, Ayub MAZ. 2010. Optimization of probiotic and lactic acid production by Lactobacillus plantarum in submerged bioreactor systems. J. Ind. Microbiol. Biotechnol. 37: 205-212. https://doi.org/10.1007/s10295-009-0665-1
  26. Ricciardi A, Parente E, Zotta T. 2009. Modelling the growth of Weissella cibaria as a function of fermentation conditions. J. Appl. Microbiol. 107: 1528-1535. https://doi.org/10.1111/j.1365-2672.2009.04335.x
  27. Champagne CP, Gardner N, Doyon G. 1989. Production of Leuconostoc oenos biomass under pH control. Appl. Environ. Microbiol. 55: 2488-2492. https://doi.org/10.1128/aem.55.10.2488-2492.1989
  28. Rehman M, Kesharvani S, Dwivedi G, Suneja KG. 2022. Impact of cultivation conditions on microalgae biomass productivity and lipid content. Materials Today: Proceedings.