Effect of Lactic Acid Bacteria on D- and L-Lactic Acid Contents of Kimchi

  • Jin, Qing (Department of Food Science and Technology, Research Center for Bioresource and Health (RCBH), Chungbuk National University) ;
  • Yoon, Hyang-Sik (Team for Food Research and Development, Chungcheongbuk-do Agricultural Research and Extension Services) ;
  • Han, Nam-Soo (Department of Food Science and Technology, Research Center for Bioresource and Health (RCBH), Chungbuk National University) ;
  • Lee, Jun-Soo (Department of Food Science and Technology, Research Center for Bioresource and Health (RCBH), Chungbuk National University) ;
  • Han, Jin-Soo (College of Veterinary Medicine, Konkuk University)
  • Published : 2006.12.31

Abstract

The D-form of lactic acid is frequently detected in fermented foods, and an excessive dietary intake of D-lactic acid may induce metabolic stress in both infants and patients. This work was carried out to determine the prevailing microorganisms relevant to the accumulation of D-lactic acid in kimchi. Leuconostoc (Leuc.) mesenteroides and Leuc. citreum primarily synthesized D-lactate with a small quantity of L-form. Leuc. gelidum and Leuc. inhae evidenced patterns similar to this. Lactobacillus (Lb.) plantarum and Lb. brevis were shown to convert glucose into a balanced mixture of D-/L-lactic acid, whereas Lb. casei principally synthesized L-lactic acid and a very small quantity of D-lactic acid. When kimchi was incubated at 8 or $22^{\circ}C$, D-lactic acid was over-produced than L-form. Leuconostoc was determined as the primary producer between the initial to mid-phase of fermentation and Lb. plantarum or Lb. brevis seemed to boost D-lactic acid content during later stage of acid accumulation.

Keywords

References

  1. Hudson M, Pocknee R, Mowat NA. D-Lactic acidosis in short bowel syndrome-an examination of possible mechanism. Q. J. Med. 74: 157-163 (1990)
  2. Urirarri J, Oh MS, Carrol HJ. D-Lactate acidosis: a review of clinical presentation, biochemical features, and pathophysiologic mechanisms. Medicine 77: 73-82 (1998) https://doi.org/10.1097/00005792-199803000-00001
  3. FAO/WHO. Toxicological evaluation of certain food additives with a review of general principles and of specifications. Report of the 17th Joint FAO-WHO Expert Committee on Food Additives. WHO Tech. Rep. Ser. 539: 1-40 (1974)
  4. Stolberg L, Rolfe R, Gitlin N, Merritt J, Mann L, Linder J, Finegold S. D-Lactic acidosis due to abnormal gut flora. diagnosis and treatment of two cases. New Engl. J. Med, 306: 1344-1348 (1982) https://doi.org/10.1056/NEJM198206033062207
  5. FAO/WHO. Specifications for the identity and purity of food additives and their toxicological evaluation: some emulsifiers and stabilizers and certain other substances. Report of the 10th Joint FAO-WHO Expert Committee on Food Additives. WHO Tech. Rep. Ser. 373: 5-47 (1967)
  6. FAO/WHO. Codex Alimentarius. 2nd ed. Foods for Special Dietary Used (including Foods for Infants and Children). Food and Agriculture Organization (FAO) and the World Health Organization (WHO) of the United Nations (UNO), Geneva, Switzerland (1994)
  7. Park ID, Hong YH. D(-)- and L(+)-Lactic acids contents of commercial yogurts. Korean J. Food Sci. Technol. 23: 520-522 (1991)
  8. Olieman C, Devries ES. Determination of D-, L-lactic acid in fermented dairy products with HPLC. Neth. Milk Dairy J. 42: 111-120 (1988)
  9. Yoon HS, Son YJ, Han JS, Lee JS, Han NS. Comparison of D- and L-lactic acid contents in commercial kimchi and sauerkraut. Food Sci. Biotechnol. 14: 64-67 (2005)
  10. Bongaerts G, Tolboom J, Naber T, Bakkeren J, Severijnen R, Willems H. D-Lactic academia and aciduria in pediatric and adult patients with short bowel syndrome. Clin. Chem. 41: 107-110 (1995)
  11. Satoh T, Narisawa K, Konno T, Katoh T, Fujiyama J, Tomoe A, Metoki K, Hayasaka K, Tada K, Ishibashi M, Yamane N, Mitsuoka T, Benno Y. D-Lactic acidosis in two patients with short bowel syndrome: bacteriological analyses of the fecal flora. Eur. J. Pediatr. 138: 324-326 (1982) https://doi.org/10.1007/BF00442509
  12. Ferain T, Hobbs IN Jr, Richardson J, Bernard N, Garmyn D, Hols P, Allen NE, Delcour J. Knockout of the two ldh genes has a major impact on peptidoglycan precursor synthesis in Lactobacillus plantarum. J. Bacteriol. 178: 5431-5437 (1996) https://doi.org/10.1128/jb.178.18.5431-5437.1996
  13. Choi HJ, Shin YJ, Yu JH, Yoon SS. A new selective medium for the isolation and the detection of leuconostocs in foodstuffs. Korean J. Food Sci. Technol. 28: 279-284 (1996)
  14. Okubo S, Mashige F, Omori M, Hashimoto Y, Nakahara K, Kanazawa H, Matsushima Y. Enantiometric determination L. and Dlactic acid in human cerebrospinal fluid by chiral ligand exchange high-performance liquid chromatography. Biomed. Chromatogr. 14: 474-477 (2000) https://doi.org/10.1002/1099-0801(200011)14:7<474::AID-BMC995>3.0.CO;2-3
  15. Lee CW, Ko CY, Ha DM. Microfloral changes of the lactic acid bacteria during kimchi fermentation and identification of the isolates. Korean J. Appl. Microbiol. Biotechnol. 20: 102-109 (1992)
  16. Kim BJ, Lee HJ, Park SY, Kim J, Han HU. Identification and characterization of Leuconostoc gelidum, isolated from kimchi, a fermented cabbage product. J. Microbiol. 38: 132-136 (2000)
  17. Choi IK, Jung SH, Kim BJ, Park SY, Kim J and Han HU. Novel Leuconostoc citreum starter culture system for the fermentation of kimchi, a fermented cabbage product. Anton Leeuw. Int. J. G. 84: 247-253 (2003) https://doi.org/10.1023/A:1026050410724
  18. McDonald LC, Fleming HP, Hassan HM. Acid tolerance of Leuconostoc mesenteroides and Lactobacillus plantarum. Appl. Environ. Microbiol. 56: 2120- 2124 (1990)
  19. Lim CR, Park HK, Han HU. Reevaluation of isolation and identification of Gram-positive bacteria in kimchi. Korean J. Microbiol. 27: 404-414 (1989)
  20. Han HU, Lim CR, Park HK. Determination of microbial community as an indicator of kimchi fermentation. Korean J. Food Sci. Technol. 22: 26-32 (1990)
  21. Scheele C. (1782). In: The Collected Papers of Carl Wilhelm Scheele. Bell G (ed). London, UK (1931)
  22. Flick MJ, Konieczny SF. Identification of putative mammalian Dlactate dehydrogenase enzymes. Biochem. Bioph. Res. Co. 295: 910-916 (2002) https://doi.org/10.1016/S0006-291X(02)00768-4
  23. Stock DW, Quattro JM, Whitt GS, Powers DA. Lactate dehydrogenase (LDH) gene duplication during chordate evolution: The cDNA sequence of the LDH of the tunicate Styela plicata. Mol. Biol. Evol. 14: 1273-1284 (1997) https://doi.org/10.1093/oxfordjournals.molbev.a025737
  24. Malleret C, Lauret R, Ehrlich, Morel-Deville F, Zagorec M. Disruption of the sole IdhL gene in Lactobacillus sakei prevents the production of both L- and D-lactate. Microbiology 144: 3327-3333 (1998) https://doi.org/10.1099/00221287-144-12-3327
  25. Nancib N, Nancib A, Boudjelal A, Benslimane C, Blanchard F, Boudrant J. The effect of supplementation by different nitrogen sources on the production of lactic acid from date juice by Lactobacillus casei subsp. Rhamnosus. Bioresource Technol. 78: 149-153 (2001) https://doi.org/10.1016/S0960-8524(01)00009-8
  26. Senthuran A, Senthuran V, Hatti-Kaul R, Mattiasson B. Lactic acid production by immobilized Lactobacillus casei in recycle batch reactor: A step towards optimization. J. Biotechnol. 73: 61-70 (1999) https://doi.org/10.1016/S0168-1656(99)00133-9
  27. Lerch HP, Blocker H, Kallwass H, Hoppe J, Tsai H, Collins J. Cloning, sequencing and expression in Escherichia coli of the D-2-hydroxyisocaproate dehydrogenase gene of Lactobacillus casei. Gene 78: 47-57 (1989) https://doi.org/10.1016/0378-1119(89)90313-2
  28. Garvie, EI. The production of L(+)- and D(-)-Iactic acid in cultures of some lactic acid bacteria, with a special study of Lactobacillus acidophilus NCDO 2. J. Dairy Res. 34: 31-38 (1967) https://doi.org/10.1017/S0022029900012115
  29. Hontebeyrie M, Gasser F. Comparative immunological relationships of two distinct sets of isofunctional dehydrogenases in the genus Leuconostoc. Int. J. Syst. Bacteriol. 25: 1-6 (1975) https://doi.org/10.1099/00207713-25-1-1
  30. Schmitt P, Vasseur C, Phalip V, Huang DQ, Divies C, Prevost H. Diacetyl and acetoin production from the cometabolism of citrate and xylose by Leuconostoc mesenteroides subsp. mesenteroides. Appl. Microbiol. Biot. 47: 715-718 (1997) https://doi.org/10.1007/s002530051000
  31. Bourel G, Henini S, Krantar K, Oraby M, Divies C, Garmyn D. Sugar citrate cometabolism in Leuconostoc mesenteroides. Lait 81: 75-82 (2001) https://doi.org/10.1051/lait:2001113
  32. Gordon GL, Doelle HW. Production of racemic lactic acid in Pediococcus cerevisiae cultures by two lactate dehydrogenases. J. Bacteriol. 121: 600-607 (1975)
  33. Aamikunnas J, VonWeymam N, Ronnholm K, Leisola M, PaIva A. Metabolic engineering of Lactobacillusfermentum for production of mannitol and pure L-lactic acid or pyruvate. Biotechnol. Bioeng. 82: 653-663 (2003) https://doi.org/10.1002/bit.10615
  34. KylaNikkila K, Hujanen M, Leisola M, Paiva A. Metabolic engineering of Lactobacillus helveticus CNRZ32 for production of pure L-(+)-lactic acid. Appl. Environ. Microbiol. 66: 3835-3841 (2000) https://doi.org/10.1128/AEM.66.9.3835-3841.2000
  35. Lapierre L, Germond JE, Ott A, Delley M, Mollet B. D-Lactate dehydrogenase gene (ldhD) inactivation and resulting metabolic effects in the Lactobacillus johnsonii strains La1 and N312. Appl. Environ. Microbiol. 65: 4002-4007 (1999)