Effect of Bacillus polyfermenticus SCD and Its Bacteriocin on MNNG-induced DNA Damage

Park, Eun-Ju;Park, Jun-Seok;Paik, Hyun-Dong

  • Published : 20041000

Abstract

Bacillus polyfermenticus SCD and its bacteriocin were investigated in vitro to examine their potential to deactivate carcinogen N-methyl-$N^{t}$-nitro-N-nitrosoguanidine (MNNG). Using the comet assay to detect DNA damage in CHO-$K_{1}$ cells, we found that B. polyfermenticus SCD and its bacteriocin deactivated MNNG and then protected the cells from MNNG-induced DNA damage. No protective effects were observed when they were treated simultaneously with MNNG without any preincubation process or when they were given before MNNG. Therefore, the action mechanisms could be due to a binding of reactive intermediates before they reach the DNA. These results indicate that B. polyfermenticus SCD and its bacteriocin have the potential to inhibit carcinogen-induced DNA damage.

Keywords

References

  1. J. Korean Soc. Food Sci. Nutr. v.28 Microbiological identification of medical probiotic bispan strain Jun, K.D.;Lee, K.H.;Kim, W.S.;Paik, R.D.
  2. Letters in Applied Microbiology v.32 no.3 Partial characterization of polyfermenticin SCD, a newly identified bacteriocin of Bacillus polyfennenticus Lee, K.H.;Jun, K.D.;Kim, W.S.;Paik, H.D. https://doi.org/10.1046/j.1472-765x.2001.00876.x
  3. J. Korean Soc. Food Sci. Nutr. v.34 Development of a culture medium for growth and sporulation of Bacillus polyfennenticus SCD Lee, K.H.;Park, K.Y.;Kim, S.M.;Kim, W.S.;Paik, H.D.
  4. Bacteriol. Rev. v.40 Bacteriocins of Gram- positive bacteria Tagg, J.R.;Dajani, A.S.;Wannamaker, L.W.
  5. Urol. Int. v.49 BPL Study Group. Prophylactic effect of a Lactobacillus casei preparation on the recurrence of superficial bladder cancer Aso, Y.;Akazan, H. https://doi.org/10.1159/000282409
  6. J. Nutr. v.130 The role of probiotic cultures in the prevention of colon cancer Brady, L.J.;Gallaher, D.D.;Busta, F.F. https://doi.org/10.1093/jn/130.2.410S
  7. European Journal of Nutrition v.40 no.6 Effect of lactobacilli, bifidobacteria and inulin on the formation of aberrant crypt foci in rats Bolognani, F.C.;Rumney, J.;Pool-Zobel, B.L.;Rowland, I.R. https://doi.org/10.1007/s394-001-8359-7
  8. International Journal of Antimicrobial Agents v.16 no.4 The use of probiotics in medical practice Mombelli, B.;Gismondo, M.R. https://doi.org/10.1016/S0924-8579(00)00322-8
  9. Cancer Res. v.310 The origins of human cancer; molecular mechanisms and their implications for cancer prevention and treatment Weinstein, l.B.
  10. Food Sci. Biotechnol. v.13 Determination of oxidative DNA damage in cancer research: biological significance and methods of analysis Hwang, E.S.
  11. Brit. J. Cancer v.55 Cigarette smoke and the involvement of free radical reactions in chemical carcinogenesis Pryor, W.A.
  12. Annals of the New York Academy of Sciences v.686 no.1 tobacco smoki Cigarette smoke-induced DNA damage in cultured human lung cells Leanderson, P. https://doi.org/10.1111/j.1749-6632.1993.tb39183.x
  13. Journal of Molecular Medicine v.74 no.6 Cancer risk and oxidative DNA damage in man Loft, S.;Poulsen, H.E. https://doi.org/10.1007/BF00207507
  14. Mutat. Res. v.485 Effect of phytoestrogen and antioxidant supplementation on oxidative DNA damage assessed using the comet assay Sierens, J.;Hartley, J.A.;Campbell, M.J.;Leathem, A.J.;Woodside, J.V. https://doi.org/10.1016/S0921-8777(00)00069-0
  15. Nutrition and Cancer v.20 no.3 Antigenotoxic properties of lactic acid bacteria in vivo in the gastrointestinal tract of rats Pool-Zobel, B.L.;Bertram, B.;Knoll, M.;Lambertz, R.;Neudecker, C.;Schillinger, U.;Schmezer, P.;Holzapfel, W.H. https://doi.org/10.1080/01635589309514295
  16. Korean J. Food. Sci. Technol. v.31 Antigenotoxic effect of dominant bacterial isolates from Kimchi in vitro Choi, J.W.;Park, J.H.;Ji, S.T.;Choi, O.B.;Shin, H.K.
  17. Experimental Cell Research v.175 no.1 A simple technique for quantitation of low levels of DNA damage in individual cells Singh, P.N.;McCoy, M.T.;Tice, R.R.;Schneider, E.L. https://doi.org/10.1016/0014-4827(88)90265-0
  18. Mutat. Res. v.238 Antimutagenicity profiles for some model compounds Waters, M.D.;Brady, A.L.;Stack, H.F.;Brockman, H.E. https://doi.org/10.1016/0165-1110(90)90039-E
  19. Cancer Res. v.45 Chemoprevention of cancer Wattenberg, L.W. https://doi.org/10.1016/S0065-230X(08)60265-1
  20. J. Dairy Sci. v.74 Binding of mutagens by fractions of the cell wall skeleton of lactic acid bacteria on mutagens Zhang, X.B.;Ohta, Y. https://doi.org/10.3168/jds.S0022-0302(91)78306-9
  21. Milchwissenschaft v.45 Binding properties of lactic acid bacteria from kefir milk with mutagenic amino acid pyrolyzates Hosono, A.;Tanabe, T.;Otani, H.