Skip to main content
Log in

The Effect of Some Factors of Polluted Environment on Catalase Responses and Resistance of Microbial Isolates Against Toxic Oxidative Stress

  • Published:
Current Microbiology Aims and scope Submit manuscript

Abstract

The properties of bacterial isolates from polluted environments which are characterized by increased levels of oxidative stress do not reflect only the level of contaminants, but also arise as a consequence of many permanently changed conditions. The survival rate of Comamonas terrigena N3H isolates from an environment with elevated levels of H2O2 is correlated with stimulation of catalase. The response of bacterial catalase to the effect of phenol in exogenous conditions was affected by the presence of an additional contaminant, Cd2+. An isolate of Aspergillus niger selected from river sediment containing 363 mg/kg As, 93 mg/kg Sb at pH 5.2–4.8 grew on Czapek-Dox agar ~1.6 times faster than an isolate of the same species from coal dust sediment with approximately the same level of pollution (400 mg/kg As) but somewhat lower pH (3.3–2.8). It also exhibited differences in the microscopic characteristics of its mycelial structures. Both isolates exhibited a higher tolerance to the exogenic toxic effects of metals (As5+, Cd2+, and Cu2+ at 5, 25, or 50 mg/L) than a control culture, but the differences in tolerance between them were only slight. These laboratory results suggest that there are complicated relationships which may exist in the “in situ” environment.

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

References

  1. Baker KH, Herson DS (1994) Microbiology and biodegradation. In: Baker KH, Herson DS (eds) Bioremediation. McGraw-Hill, New York, pp 9–60

    Google Scholar 

  2. Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72:248–250

    Article  PubMed  CAS  Google Scholar 

  3. Bučková M, Godočíková J, Šimonovičová A, Polek B (2005) Production of catalases by Aspergillus niger isolates as a response to pollutant stress by heavy metals. Curr Microbiol 50:175–179

    Article  PubMed  Google Scholar 

  4. Bučková M, Godočíková J, Polek B (2007) Responses in the mycelial growth of Aspergillus niger isolates to arsenic contaminated environments and their resistance to exogenic metal stress. J Basic Microbiol 47:295–300

    Article  PubMed  Google Scholar 

  5. Bučková M, Godočíková J, Zámocký M, Polek B (2010) Screening of bacterial isolates from polluted soils exhibiting catalase and peroxidase activity and diversity of their responses to oxidative stress. Curr Microbiol 61:241–247

    Article  PubMed  Google Scholar 

  6. Bučková M, Godočíková J, Zámocký M, Polek B (2010) Isolates of Comamonas spp. exhibiting catalase and peroxidase activities and diversity of their responses to oxidative stress. Ecotoxicol Environ Saf 73:1511–1516

    Article  PubMed  Google Scholar 

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

    PubMed  CAS  Google Scholar 

  8. Godočíková J, Boháčová V, Zámocký M, Polek B (2005) Production of catalases by Comamonas spp. and resistance to oxidative stress. Folia Microbiol 50:113–118

    Article  Google Scholar 

  9. Godočíková J, Zámpocký, Bučková M, Obinger C, Polek B (2010) Molecular diversity of katG genes in the soil bacteria Comamonas. Arch Microbiol 192:175–184

    Article  PubMed  Google Scholar 

  10. Ferianc P, Polek B, Godočíková J, Tóth D (1995) Metabolic activity of cadmium-stressed and/or starved Vibrio sp. Folia Microbiol 40:443–446

    Article  CAS  Google Scholar 

  11. Ichise N, Hirota K, Ichihashi D, Nodasaka Y, Morita N, Okuyama H, Yumoto I (2008) H2O2 tolerance of Vibrio S-1(T) is attributable to the cellular catalase activity. J Biosci Bioeng 106:39–46

    Article  PubMed  CAS  Google Scholar 

  12. Jenkins DE, Schultz JE, Matin A (1988) Starvation-induced cross-protection against heat and H2O2 challenge in Escherichia coli. J Bacteriol 170:3910–3914

    PubMed  CAS  Google Scholar 

  13. Paar A, Costa S, Tzanov T, Gudelj M, Robra KH, Cavaco-Paulo A, Gubitz GM (2001) Thermo-alkali-stable catalases from newly isolated Bacillus sp. for the treatment and recycling of textile bleaching effluents. J Biotechnol 89:147–153

    Article  PubMed  CAS  Google Scholar 

  14. Prokšová M, Vrbanová A, Augustín J (1996) Enrichment, isolation and characterization of dialkyl sulfosuccinate degrading bacteria Comamonas terrigena N3H and Comamonas terrigena N1C. Folia Microbiol 42:635–639

    Article  Google Scholar 

  15. Roggenkamp R, Sahm H, Wagner F (1974) Microbial assimilation of methanol induction and function of catalase in Candida boidinii. FEBS Lett 41:283–286

    Article  PubMed  CAS  Google Scholar 

  16. Sharpley AN (1991) Effect of soil pH on cation and anion solubility. Commun Soil Sci Plant Anal 22:1391–1399

    Article  Google Scholar 

  17. Stohs SJ, Bagchi D (1995) Oxidative mechanisms in the toxicity of metal ions. Free Radic Biol Med 18:321–336

    Article  PubMed  CAS  Google Scholar 

  18. Stojnev T, Harichová J, Ferianc P, Nyström T (2007) Function of a novel cadmium-induced YodA protein in Escherichia coli. Curr Microbiol 55:99–104

    Article  PubMed  CAS  Google Scholar 

  19. Takenaka S, Mulyono S, Sasano Y, Takahashi Y, Murakami S, Aoki K (2006) Microbial transformation of aniline derivates: regioselective biotransformation and detoxification of 2-phenylenediamine by Bacillus cereus strain PDa-1. J Biosci Bioeng 102:21–27

    Article  PubMed  CAS  Google Scholar 

  20. Zámocký M, Godočíková J, Koller F, Polek B (2001) Potential application of catalase-peroxidase from Comamonas terrigena N3H in the biodegradation of phenolic compounds. Antonie Van Leeuwenhoek 256:169–182

    Google Scholar 

Download references

Acknowledgments

This study was supported by the Grant 2/0149/11 of VEGA (Slovak Science fund).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Bystrík Polek.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Polek, B., Godočíková, J. The Effect of Some Factors of Polluted Environment on Catalase Responses and Resistance of Microbial Isolates Against Toxic Oxidative Stress. Curr Microbiol 65, 345–349 (2012). https://doi.org/10.1007/s00284-012-0163-y

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00284-012-0163-y

Keywords

Navigation