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Laccase Activity and Azo Dye Decolorization Potential of Podoscypha elegans

  • Pramanik, Satadru (Mycology and Plant Pathology Section, Department of Botany, University of Kalyani) ;
  • Chaudhuri, Sujata (Mycology and Plant Pathology Section, Department of Botany, University of Kalyani)
  • Received : 2017.09.18
  • Accepted : 2018.01.10
  • Published : 2018.03.31

Abstract

Azo dyes containing effluents from different industries pose threats to the environment. Though there are physico-chemical methods to treat such effluents, bioremediation is considered to be the best eco-compatible technique. In this communication, we discuss the decolorization potentiality of five azo dyes by Podoscypha elegans (G. Mey.) Pat., a macro-fungus, found growing on the leaf-litter layer of Bethuadahari Wildlife Sanctuary in West Bengal, India. The fungus exhibited high laccase and very low manganese peroxidase activities under different culture conditions. Decolorization of five high-molecular weight azo dyes, viz., Orange G, Congo Red, Direct Blue 15, Rose Bengal and Direct Yellow 27 by the fungus was found to be positive in all cases. Maximum and minimum mean decolorization percentages were recorded in Rose Bengal (70.41%) and Direct Blue 15 (24.8%), respectively. This is the first record of lignolytic study and dye decolorization by P. elegans.

Keywords

References

  1. Wang ZW, Liang JS, Liang Y. Decolorization of reactive black 5 by a newly isolated bacterium Bacillus sp. YZU1. Int Biodeter Biodegr. 2013;76:41-48. https://doi.org/10.1016/j.ibiod.2012.06.023
  2. Jin XC, Liu GQ, Xu ZH, et al. Decolorization of a dye industry effluent by Aspergillus fumigatus XC6. Appl Microbiol Biotechnol. 2007;74:239-243. https://doi.org/10.1007/s00253-006-0658-1
  3. Leechart P, Nakbanpote W, Thiravetyan P. Application of 'waste' wood-shaving bottom ash for adsorption of azo reactive dye. J Environ Sci. 2009;90:912-920.
  4. Gupta VK, Jain R, Mittal A, et al. Photochemical degradation of the hazardous dye safranin-T using TiO2 catalyst. J Colloid Interface Sci. 2007;309:464-469. https://doi.org/10.1016/j.jcis.2006.12.010
  5. Sriram N, Reetha D, Saranraj P. Biological degradation of reactive dyes by using bacteria isolated from dye effluent contaminated soil. Middle-East J Sci Res. 2013;17:1695-1700.
  6. Gomi N, Yoshida S, Matsumoto K, et al. Degradation of the synthetic dye amaranth by the fungus Bjerkandera adusta Dec 1: inference of the degradation pathway from an analysis of decolorized products. Biodegradation. 2011;22:1239-1245. https://doi.org/10.1007/s10532-011-9478-9
  7. Kolekar YM, Nemade HN, Markad VL, et al. Decolorization and biodegradation of azo dye, reactive blue 59 by aerobic granules. Bioresour Technol. 2012;104:818-822. https://doi.org/10.1016/j.biortech.2011.11.046
  8. Sannino F, Nuzzo A, Ventorino V, et al. Effective degradation of organic pollutants in aqueous media by microbial strains isolated from soil of a contaminated industrial site. Chem Biol Technol Agric. 2016;3:2. https://doi.org/10.1186/s40538-016-0052-x
  9. Steffen KT, Hofrichter M, Hatakka A. Mineralisation of 14C-labelled synthetic lignin and ligninolytic enzyme activities of litter-decomposing basidiomycetous fungi. Appl Microbiol Biotechnol. 2000;54:819-825. https://doi.org/10.1007/s002530000473
  10. Steffen KT, Schubert S, Tuomela M, et al. Enhancement of bioconversion of high-molecular mass polycyclic aromatic hydrocarbons in contaminated non-sterile soil by litter-decomposing fungi. Biodegradation. 2007;18:359-369. https://doi.org/10.1007/s10532-006-9070-x
  11. Liers C, Pecyna MJ, Kellner H, et al. Substrate oxidation by dye-decolorizing peroxidases (DyPs) from wood-and litter-degrading agaricomycetes compared to other fungal and plant heme-peroxidases. Appl Microbiol Biotechnol. 2013;97:5839-5849. https://doi.org/10.1007/s00253-012-4521-2
  12. Pramanik S, Chaudhuri S. Macrofungal diversity in the forest litter of Nadia District, West Bengal, India. Afr J Microbiol Res. 2017;11:927-944. https://doi.org/10.5897/AJMR2017.8559
  13. Kirk TK, Schultz E, Connors WJ, et al. Influence of culture parameters on lignin metabolism by Phanerochaete chrysosporium. Arch Microbiol. 1978;117:277-285. https://doi.org/10.1007/BF00738547
  14. Katagiri N, Tsutsumi Y, Nishida T. Correlation of brightening with cumulative enzyme activity related to lignin biodegradation during biobleaching of kraft pulp by white rot fungi in the solidstate fermentation system. Appl Environ Microbiol. 1995;61:617-622.
  15. Arora DS, Gill PK. Comparison of two assay procedures for lignin peroxidase. Enzyme Microb Technol. 2001;28:602-605. https://doi.org/10.1016/S0141-0229(01)00302-7
  16. Sun SJ, Liu JZ, Hu KH, et al. The level of secreted laccase activity in the edible fungi and their growing cycles are closely related. Curr Microbiol. 2011;62:871-875. https://doi.org/10.1007/s00284-010-9794-z
  17. Tien M, Kirk TK. Lignin peroxidase of Phanerochaete chrysosporium. Methods Enzymol. 1988;161:238-249.
  18. Glenn JK, Gold MH. Purification and characterization of an extracellular Mn(II)-dependent peroxidase from the lignin-degrading basidiomycete, Phanerochaete chrysosporium. Arch Biochem Biophys. 1985;242:329-341. https://doi.org/10.1016/0003-9861(85)90217-6
  19. Rasera K, Ferla J, Dillon AJP, et al. Immobilization of laccase from Pleurotus sajor-caju in polyamide membranes. Desalination. 2009;245:657-661. https://doi.org/10.1016/j.desal.2009.02.033
  20. Baldrian P. Fungal laccases - occurrence and properties. FEMS Microbiol Rev. 2005;30:215-242.
  21. Leonowicz A, Edgehill RU, Bollag JM. The effect of pH on the transformation of syringic and vanillic acids by the laccases of Rhizoctonia praticola and Trametes versicolor. Arch Microbiol. 1884;137:89-96.
  22. Mayer AM. Polyphenol oxidases in plants-recent progress. Phytochemistry. 1986;26:11-20. https://doi.org/10.1016/S0031-9422(00)81472-7
  23. Sharma A, Thakur VV, Shrivastava A, et al. Xylanase and laccase based enzymatic kraft pulp bleaching reduces adsorbable organic halogen (AOX) in bleach effluents: a pilot scale study. Bioresour Technol. 2014;169:96-102. https://doi.org/10.1016/j.biortech.2014.06.066
  24. Ko EM, Leem YE, Choi H. Purification and characterization of laccase isozymes from the white-rot basidiomycete Ganoderma lucidum. Appl Microbiol Biotechnol. 2001;57:98-102. https://doi.org/10.1007/s002530100727
  25. Dekker RF, Barbosa AM. The effects of aeration and veratryl alcohol on the production of two laccases by the ascomycete Botryosphaeria sp. Enzyme Microb Technol. 2001;28:81-88. https://doi.org/10.1016/S0141-0229(00)00274-X
  26. Saraiva JA, Tavares APM, Xavier AMRB. Effect of the inducers veratryl alcohol, xylidine, and ligninosulphonates on activity and thermal stability and inactivation kinetics of laccase from Trametes versicolor. Appl Biochem Biotechnol. 2012;167:685-693. https://doi.org/10.1007/s12010-012-9719-3
  27. Kumar VV, Kirupha SD, Periyaraman P, et al. Screening and induction of laccase activity in fungal species and its application in dye decolorization. Afr J Microbiol Res. 2011;5:1261-1267. https://doi.org/10.5897/AJMR10.894

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