Estrogenic Reduction of Styrene Monomer Degraded by Phanerochaete chrysosporium KFRI 20742

  • Lee Jae-Won (Department of Forest Sciences, College of Agriculture and Life Sciences, Seoul National University) ;
  • Lee Soo-Min (Department of Forest Sciences, College of Agriculture and Life Sciences, Seoul National University) ;
  • Hong Eui-Ju (College of Veterinary, Chungbuk National University) ;
  • Jeung Eui-Bae (College of Veterinary, Chungbuk National University) ;
  • Kang Ha-Young (Department of Wood Chemistry and Microbiology, Korea Forest Research Institute) ;
  • Kim Myung-Kil (Department of Wood Chemistry and Microbiology, Korea Forest Research Institute) ;
  • Choi In-Gyu (Department of Forest Sciences, College of Agriculture and Life Sciences, Seoul National University)
  • Published : 2006.04.01

Abstract

The characteristic biodegradation of monomeric styrene by Phanerochaete chrysosporium KFRI 20742, Trametes versicolor KFRI 20251 and Daldinia concentrica KFRI 40-1 was carried out to examine the resistance, its degradation efficiency and metabolites analysis. The estrogenic reduction effect of styrene by the fungi was also evaluated. The mycelium growth of fungi differentiated depending on the concentration levels of styrene. Additionally P. chrysosporium KFRI 20742 showed superior mycelium growth at less than 200 mg/l, while D. concentrica KFRI 40-1 was more than 200 mg/l. The degradation efficiency reached 99 % during one day of incubation for all the fungi. Both manganese-dependent peroxidase and laccase activities in liquid medium were the highest at the initial stage of incubation, whereas the lowest was after the addition of styrene. However, both activities were gradually recovered after. The major metabolites of styrene by P. chrysosporium KFRI 20742 were 2-phenyl ethanol, benzoic acid, cyclohexadiene-1,4-dione, butanol and succinic acid. From one to seven days of incubating the fungi, the expression of pS2 mRNA widely known as an estrogen response gene was decreased down to the level of baseline after one day. Also, the estrogenic effect of styrene completely disappeared after treatment with supernatant of P. chrysosporium KFRI 20742 from one week of culture down to the levels of vehicle.

Keywords

References

  1. Braum-Lullemann, A., A. Majcherczyk, and A. Hüttermann. 1997. Degradation of styrene by white-rot fungi. Appl. Microbiol. Biotechnol. 47, 150-155 https://doi.org/10.1007/s002530050904
  2. Choi, I.G. 1999. Biodegradation of Chlorinated Phenols, Pentachlorophenol and 4, 5,6-Trichloroguaiacol, by Lignin -Degrading Basidiomycetes, Grammothele fuligo, and Phanerochaete crassa. KFRI Journal of Forest Sciences 62, 53-66
  3. Choi, I.G., and S.H. Ahn. 1998. Biodegradation of pentachlorophenol by wood rot fungi. Mokchaekonghak 26, 53-62
  4. Cripps, R.E., P.W. Trudgill, and J.G. Whateley. 1978. The metabolism of 1-phenylethanol and acetophenone by Nocardia T5 and an Arthrobacter sp. Eur. J. Biochem. 86, 175-186 https://doi.org/10.1111/j.1432-1033.1978.tb12297.x
  5. Gbric-Gallic, D., N. Churchman-Eisel, and I. Markovic. 1990. Microbial transformation of styrene by anaerobic consortia. J. Appl. Bacteriol. 69, 247-260 https://doi.org/10.1111/j.1365-2672.1990.tb01516.x
  6. Han M.J., H.T. Choi, G.S. Song. 2004. Degradation of phenanthrene by Trametes versicolor and its laccase. J. Microbiol. 42, 94-98
  7. Hartmans, S., J.P. Smits, M.J. van der Werf, F. Volkering, and J.A.M. de Bont. 1989. Metabolism of styrene oxide and 2-phenylethanol in the styrene degrading Xanthobacter strain 124X. Appl. Environ. Microbiol. 55, 2850-2855
  8. Heinfling, A., M. Bergbauer, and U. Szewzyk. 1997. Biodegradation of azo and phthalocyanine dyes by Trametes versicolor and Bjerkandera adusta. Appl. Microbiol. Biotechnol. 48, 261-266 https://doi.org/10.1007/s002530051048
  9. Jakowlew, S.B., R. Breathnach, J.M. Jeltsch, P. Masiakowski, and P. Chambon. 1984. Sequence of the pS2 mRNA induced by estrogen in the human breast cancer cell line MCF-7. Nucleic Acids Res. 12, 2861-78 https://doi.org/10.1093/nar/12.6.2861
  10. Johannes, C., A. Majcherczyk, and A. Hüttermann. 1998. Oxidation of acenaphthene and acenaphthylene by laccase of Trametes versicolor in a laccase-mediator system. J. Biotechnol. 61, 151-156 https://doi.org/10.1016/S0168-1656(98)00030-3
  11. Kirk, T.K., S. Croan, M. Tien, K.E. Murtagh, and R.L. Farrell. 1986. Production of multiple ligninases by Phanerochaete chrysosporium: effect of selected growth conditions and use of a mutant strain. Enzyme Micro. Tech. 8, 27-32 https://doi.org/10.1016/0141-0229(86)90006-2
  12. Lee, S.M., B.W. Koo, S.S. Lee, M.K. Kim, D.H. Choi, E.J. Hong, E.B. Jeung, and I.G. Choi. 2004. Biodegradation of dibutylphthalate by white rot fungi and evaluation on its estrogenic activity. Enzyme Micro. Tech. 35, 417-423 https://doi.org/10.1016/j.enzmictec.2004.06.001
  13. Levin, L., A. Viale, and A. Forchiassin. 2003. Degradation of organic pollutants by the white rot basidiomycete Trametes trogii. Int. Biodeterioration Biodegrad. 52, 1-5 https://doi.org/10.1016/S0964-8305(02)00091-4
  14. Li, K., F. Xu, and E-K. Eriksson. 1999. Comparison of fungal laccases and redox mediators in oxidation of a nonphenolic lignin model compound. Appl. Environ. Microbiol. 65, 2654-2660
  15. Lu, C.S., M.R. Lin, and J.C. Lin. 2001. Removal of styrene vapor from waste gases by a trickle-bed air biofilter. Journal of Hazardrous Materials B82, 233-245
  16. Mario, Z., Emilio, P., Luciane S., Attilio, C., Marco, D.B., 2001. Toluene and styrene removal from air in biofilters. Process Biochem. 37, 423-429 https://doi.org/10.1016/S0032-9592(01)00228-X
  17. Masiakowski, P., R. Breathnach, J. Bloch, F. Gannon, A. Krust, and P. Chambon. 1982. Cloning of cDNA sequences of hormone-regulated genes from the MCF-7 human breast cancer cell line. Nucleic Acids Res. 10, 7895-7903 https://doi.org/10.1093/nar/10.24.7895
  18. O'Conner, K.E., C.M. Buckely, S. Hartmans, and A.D.W. Dobson. 1995. Possible regulatory role for non-aromatic carbon sources in styrene degradation by Pseudomonas putida CA-3. Appl. Environ. Microbiol. 61, 544-548
  19. O'Conner, K.E., and A.D.W. Dobson. 1996. Microbial degradation of alkenylbenzenes. World J. Microbiol. Biotechnol. 12, 207-212 https://doi.org/10.1007/BF00360916
  20. Ohyama, K.I., F. Nagai, and Y. Tsuchiya. 2001. Certain styrene oligomers have proliferative activity on MCF-7 human breast tumor cells and binding affinity for human estrogen receptor. Environ. Health Perspect.109, 699-703 https://doi.org/10.1289/ehp.01109s5699
  21. Sato, A., H. Justicia, J.W. Wray, and C. Sonnenschein. 1991. p-nonyl-phenol: an estrogenic xenobiotic released from 'modified' polystyrene. Environ. Health Perspect. 92, 167-173 https://doi.org/10.2307/3431154
  22. Schutzendübel, A., A. Majcherczyk, C. Johannes, and A. Hüttermann. 1999. Degradation of fluorene, anthracene, phenanthrene, fluoranthene, and pyrene lacks connection to the production of extracellular enzymes by Pleurotus ostreatus and Bjerkandera adusta. Int. Biodeterioration Biodegrad. 43, 93-100 https://doi.org/10.1016/S0964-8305(99)00035-9
  23. Shin, K.S. 2004. The role of enzymes produced by white-rot fungus Irpex lacteus in the decolorization of the textile industry effluent. J. Microbiol. 42, 37-41
  24. Skehan, P., R. Storeng, D. Scudiero, A. Monks, J. Mcmahon, D. Vistica, J.T. Warren, H. Bokesch, S. Kenney, and M.R. Boyd. 1990. New colorimetric cytotoxicity assay for anticancer-drug screening. J. Natl. Cancer Inst, 82, 1107- 1112 https://doi.org/10.1093/jnci/82.13.1107
  25. Soto, A.M., C. Sonnenschein, K.L. Chung, M.F. Fernandez, N. Olea, and F.O. Serrano. 1995. The E-SCREEN assay as a tool to identify estrogens: an update on estrogenic environmental pollutants. Environ. Health Perspect. 103, 113-122 https://doi.org/10.1289/ehp.95103s7113
  26. Stahl, D.P., and M.J. Klug. 1996. Characterization and differentiation of filamentous fungi based on fatty acid composition. Appl. Environ. Microbiol. 62, 4136-4146
  27. Warhurst, A.M., K.F. Clarke, R.A. Hill, R.A. Holt, and C.A. Fewson. 1994. Metabolism of styrene by Rhodococcus rhodochrous NCIMB13259. Appl. Environ. Microbiol. 60, 1137-1145
  28. Wariishi, H., K. Valli, and M.H Gold. 1992. Manganese (II) oxidation by manganese peroxidase from the basidiomycete Phanerochaete chrysosporium. J. Biol. Chem. 267, 23688-23695
  29. While, R., S. Jobling, S. Hoare, J.P. Sumpter, and M.G. Parker. 1994. Environmentally persistent alkylphenolic compounds are estrogenic. Endocrinol. 135, 175-182 https://doi.org/10.1210/en.135.1.175
  30. Yamada, T., M. Tanaka, S. Hirano, Y. Nagao, K. Kobayashi, T. Sakurai, Y. Furukawa, and Y. Nobuhara. 2000. Determination of styrene oligomers in instant noodles contained in a polystyrene container. Bunseki Kagaku 49, 857-867 https://doi.org/10.2116/bunsekikagaku.49.857