Skip to main content
Log in

Adaptive Response of Bacillus sp. F26 to Hydrogen Peroxide and Menadione

  • Published:
Current Microbiology Aims and scope Submit manuscript

Abstract

The adaptive and cross-protection responses to oxidants were investigated in Bacillus sp. F26. The cells were treated with sublethal concentrations of either H2O2 or menadione (a superoxide-generating agent) to induce an adaptive response. The results showed that the cells treated with menadione exhibited cross-protection against, but in another case, those cells treated with H2O2 did not show significant resistance to menadione. It suggests that Bacillus sp. F26 possesses two separate adaptive responses that respond to the two different kinds of oxidants. The adaptability is regarded as that which is accompanied by the inductions of some antioxidant enzymes. It was found that catalase (CAT) production was increased about 1.6-fold after treatment with 600 μM H2O2, whereas the presence of 50 μM menadione induced CAT, superoxide dismutase (SOD), glucose-6-phosphate dehydrogenase (G6PD), and glutathione reductase (GR) by 2-, 2-, 2-, and 1.6-fold, respectively. The results can be used to explain why menadione-treated cells have higher adaptability to lethal concentrations of oxidants than that of those H2O2-treated. In addition, it was found that growing Bacillus sp. F26 in high-salinity media causes it to become more resistant to H2O2 and menadione stress, which may be partially due to the induction of CAT and SOD production under high NaCl concentration.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2

Similar content being viewed by others

Literature Cited

  1. Aebi H (1984) Catalase in vitro. Methods Enzymol 105:121–126

    CAS  PubMed  Google Scholar 

  2. Antelmann H, Engelmann S, Scmid R, Hecker M (1996) General and oxidative stress responses in Bacillus subtilis: cloning, expression, and mutation of the alkyl hydroperoxide reductase operon. J Bacteriol 178:6571–6578

    CAS  PubMed  Google Scholar 

  3. Boylan SA, Redfield AR, Brody MS, Price CW (1993) Stress-induced activation of the σB transcription factor of Bacillus subtilis. J Bacteriol 175:7931–7937

    CAS  PubMed  Google Scholar 

  4. Bradford M (1976) A rapid and sensitive method of the quantification of microgram quantities of protein using the principle of protein-dye binding. Anal Biochem 72:248–255

    Article  CAS  PubMed  Google Scholar 

  5. Demple B (1996) Redox signalling and gene control in the Escherichia coli soxRS oxidative stress regulon—a review. Gene 179:53–57

    Article  CAS  PubMed  Google Scholar 

  6. Dowds BCA, Murphy P, McConnell DJ, Devine KM (1987) Relationship of among oxidative stress, growth cycle, and sporulation in Bacillus subtilis. J Bacteriol 169:5771–5775

    CAS  PubMed  Google Scholar 

  7. Dowds BCA (1994) The oxidative stress response in Bacillus subtilis. FEMS Microbiol Lett 124:255–264

    CAS  PubMed  Google Scholar 

  8. Flattery-OBrain J, Collinson LP, Dawes IW (1993) Saccharomyces cerevisiae has an inducible response to menadione which differ from that of hydrogen peroxide. J Gen Microbiol 139:501–507

    Google Scholar 

  9. Fridovich I (1978) The biology of oxygen radicals. Science 201:875–880

    CAS  PubMed  Google Scholar 

  10. Jamieson DJ (1992) Saccharomyces cerevisiae has distinctive adaptive response to both hydrogen peroxide and menadione. J Bacteriol 174:6678–6681

    CAS  PubMed  Google Scholar 

  11. Jamieson DJ, Rivers SL, Stephen DWS (1994) Analysis of Saccharomyces cerevisiae proteins induced by peroxide and superoxide stress. Microbiology 140:3277–3283

    CAS  PubMed  Google Scholar 

  12. Jamieson DJ, Stephen DWS, Terriere EC (1996) Analysis of the adaptive stress response of Candida albicans. FEMS Microbiol Lett 138:83–88

    CAS  PubMed  Google Scholar 

  13. Kao SM, Hassan HM (1985) Biochemical characterization of a paraquat-tolerant mutant of Escherichia coli. J Biol Chem 260:10478–10481

    CAS  PubMed  Google Scholar 

  14. Kitzler J, Fridovich I (1986) Effects of salts on the lethality of paraquat. J Bacteriol 167:346–349

    CAS  PubMed  Google Scholar 

  15. Marklund S, Marklund G (1974) Involvement of the superoxide anion radical in the autoxidation of pyrogallol a convenient assay for Superoxide dismutase. Eur J Biochem 47:469–474

    Article  CAS  PubMed  Google Scholar 

  16. Mongkolsuk S, Vattanaviboon P, Praitaun W (1997) Induced adaptive and cross-protection responses against oxidative stress killing in a bacterial phytopathogen, Xanthomonas oryzae pv. oryzae. FEMS Microbiol Lett 146:217–221

    CAS  Google Scholar 

  17. Murphy P, Dowds BCA, McConnell DJ, Devine KM (1987) Oxidative stress and growth temperature in Bacillus subtilis. J Bacteriol 169:5766–5770

    CAS  PubMed  Google Scholar 

  18. Smith IK, Vierheller TL, Thorne CA (1988) Assay of glutathione reductase in crude tissue homogenates using 5, 5-dithiobis (2-nitrobenzoic acid). Anal Biochem 175:408–413

    Article  CAS  PubMed  Google Scholar 

  19. Storz G, Imlay JA (1999) Oxidative stress. Curr Opin Microbiol 2:188–194

    Article  CAS  PubMed  Google Scholar 

  20. Vattanaviboon P, Eiampuhngporn W, Mongkolsuk S (2003) Atypical adaptive and cross-protective response against peroxide killing in a bacterial plant pathogen, Agrobacterium tumefaciens. Curr Microbiol 47:323–326

    Article  CAS  PubMed  Google Scholar 

  21. Vattanaviboon P, Panmanee W, Mongkolsuk S (2003) Induction of peroxide and superoxide protective enzymes and physiological cross-protection against peroxide killing by a superoxide generator in Vibrio harveyi. FEMS Microbiol Lett 221:89–95

    Article  CAS  PubMed  Google Scholar 

  22. Yan GL, Hua ZZ, Liu DR, Li Y, Chen J (2005) Enhanced catalase synthesis by a novel combined system of photocatalytic reactor and fermenter. Biotechnol Lett 27:683–687

    Article  CAS  PubMed  Google Scholar 

  23. Zhang WZ, Xue YF, Ma YH, Grant WD, Ventosa A, Zhou PJ (2002) Marinospirillum alkaliphilum sp. nov, a new alkaliphilic helical bacterium from Haoji soda lake in Inner Mongolia Autonomous Region of China. Extremophiles 6:33–37

    Article  PubMed  Google Scholar 

  24. Zhao LQ, Cui SX, Zhang LX, Zhang CL (2004) The survival mechanism of dune reed (Phragmites communis) cultures under high sodium chloride concentration. Plant Cell Tiss Org 79:291–298

    CAS  Google Scholar 

Download references

Acknowledgments

This research was financially supported by Chinese National Programs for High Technology Research and Development (2003AA322050) and the Natural Science Foundation for Youth Project of Innovative Science and Technology of Jiangsu Province, China (BK2004401).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Zhaozhe Hua.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Yan, G., Hua, Z., Du, G. et al. Adaptive Response of Bacillus sp. F26 to Hydrogen Peroxide and Menadione. Curr Microbiol 52, 238–242 (2006). https://doi.org/10.1007/s00284-005-0313-6

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00284-005-0313-6

Keywords

Navigation