Effect of aqueous extracts from Ceriporiopsis subvermispora-biotreated wood on the decolorization of Azure B by Fenton-like reactions

International Biodeterioration and Biodegradation

Volumn 74, Issue , 2012, Pages 61-66

  Aguiar, André ^a,b   Ferraz, André ^a  

^a UNIVERSITY OF SÃO PAULO   (Brazil)

^b FEDERAL UNIVERSITY OF SÃO JOÃO DEL REI   (Brazil)

Author keywords

Ceriporiopsis subvermispora; Dyes; Fenton reaction; Hydroxyl radical; Wood biodegradation

Indexed keywords

AQUEOUS EXTRACTS; CERIPORIOPSIS SUBVERMISPORA; FENTON LIKES; FENTON REACTIONS; HYDROXYL RADICALS; OH RADICAL; PRO-OXIDANT PROPERTIES; PROOXIDANT; RECALCITRANT DYE; REDUCING ACTIVITY; WHITE ROT FUNGI; WOOD EXTRACTS;

BIODEGRADATION; DYES; FREE RADICALS; PHENOLS;

WOOD;

ANTIOXIDANT; AQUEOUS SOLUTION; BIODEGRADATION; CATION; COPPER; DYE; FUNGUS; HYDROXYL RADICAL; IRON; OXIDANT; PHENOL; POLLUTANT REMOVAL; WOOD;

BIODEGRADATION; DYES; PHENOLS; WOOD;

CERIPORIOPSIS SUBVERMISPORA; CORIOLACEAE; FUNGI;

EID: 84864917701     PISSN: 09648305     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ibiod.2012.07.010     Document Type: Article

References (43)

1. 2+-reduction by phenol derivatives associated with Azure B degradation in Fenton-like reaction. Chemosphere 2007, 66:947-954.
2. Aguiar A., Ferraz A. Relevance of extractives and wood transformations products on the biodegradation of Pinus taeda by Ceriporiopsis subvermispora. International Biodeterioration & Biodegradation 2008, 61:182-188.
3. Aguiar A., Ferraz A. Mechanisms involved in the biodegradation of lignocellulosic materials and related technological applications. Química Nova 2011, 34:1729-1738.
4. Aguiar A., Ferraz A. Effects of exogenous calcium or oxalic acid on Pinus taeda treatment with the white-rot fungus Ceriporiopsis subvermispora. International Biodeterioration & Biodegradation 2012, 72:88-93.
5. 3+-reduction activity and oxidative enzymes detected in culture extracts recovered from Pinus taeda wood chips biotreated by Ceriporiopsis subvermispora. Enzyme and Microbial Technology 2006, 38:873-878.
6. Aguiar A., Ferraz A., Contreras D., Rodríguez J. Mechanism and applications of the Fenton reaction assisted by iron-reducing phenolic compounds. Química Nova 2007, 30:623-628.
7. Ajila C.M., Brar S.K., Verma M., Tyagi R.D., Valéro J.R. Solid-state fermentation of apple pomace using Phanerochaete chrysosporium - Liberation and extraction of phenolic antioxidants. Food Chemistry 2011, 126:1071-1080.
8. Arantes V., Milagres A.M.F. The effect of a catecholate chelator as a redox agent in Fenton-based reactions on degradation of lignin model substrates and on COD removal from effl{ligature}uent of an ECF kraft pulp mill. Journal of Hazardous Materials 2007, 141:273-279.
9. Arantes V., Milagres A.M.F., Filley T.R., Goodell B. Lignocellulosic polysaccharides and lignin degradation by wood decay fungi: the relevance of nonenzymatic Fenton-based reactions. Journal of Industrial Microbiology and Biotechnology 2011, 38:541-555.
10. Arnow L.E. Colorimetric determination of the components of 3,4-dihydroxyphenylamine-tyrosine mixtures. Journal of Biological Chemistry 1937, 118:531-537.
11. Arora D.S., Sharma R.K., Chandra P. Biodelignifi{ligature}cation of wheat straw and its effect on in vitro digestibility and antioxidant properties. International Biodeterioration & Biodegradation 2011, 65:352-358.
12. Contreras D., Rodríguez J., Freer J., Schwederski B., Kaim W. Enhanced hydroxyl radical production by dihydroxybenzene-driven Fenton reactions: implications for wood biodegradation. Journal of Biological Inorganic Chemistry 2007, 12:1055-1061.
13. Contreras D., Oviedo C., Valenzuela R., Freer J., Rojo K., Rodríguez J. Tribromophenol degradation by a catechol-driven Fenton reaction. Journal of Chilean Chemical Society 2009, 54:141-143.
14. Cunha G.G.S., Masarin F., Norambuena M., Freer J., Ferraz A. Linoleic acid peroxidation and lignin degradation by enzymes produced by Ceriporiopsis subvermispora grown on wood or in submerged liquid cultures. Enzyme and Microbial Technology 2010, 46:262-267.
15. Eggert C., Temp U., Dean J.F.D., Eriksson K.E.L. A fungal metabolite mediates degradation of non-phenolic lignin structures and synthetic lignin by laccase. FEBS Letters 1996, 391:144-148.
16. 3+ reduction and enzymatic activities in cultures of Ganoderma australe growing on Drimys winteri wood. FEMS Microbiology Letters 2006, 260:112-118.
17. Enoki M., Honda H., Kuwahara M., Watanabe T. Chemical synthesis, iron redox interactions and charge transfer complex formation of alkylitaconic acids from Ceriporiopsis subvermispora. Chemistry and Physics of Lipids 2002, 120:9-20.
18. Ferraz A., Rodriguez J., Freer J., Baeza J. Estimating the chemical composition of biodegraded pine and eucalyptus wood by DRIFT spectroscopy and multivariate analysis. Bioresource Technology 2000, 74:201-212.
19. Ferraz A., Parra C., Freer J., Baeza J., Rodríguez J. Occurrence of iron-reducing compounds in biodelignifi{ligature}ed "palo podrido" wood samples. International Biodeterioration & Biodegradation 2001, 47:203-208.
20. Goodell B., Qian Y., Jellison J., Richard M. Decolorization and degradation of dyes with mediated Fenton reaction. Water Environmental Research 2004, 76:2703-2707.
21. Goodell B., Daniel G., Jellison J., Qian Y.H. Iron-reducing capacity of low-molecular-weight compounds produced in wood by fungi. Holzforschung 2006, 60:630-636.
22. Goodell B. Overview of white-rot research: where we are today. Wood Deterioration and Preservation - Advances in our Changing World, ACS Symposium Series 2003, vol. 845:97-118. American Chemical Society, Washington, DC.
23. Gutiérrez A., del Rio J.C., Martínez-Inigo M.J., Martínez M.J., Martínez A.T. Production of new unsaturated lipids during wood decay by ligninolytic basidiomycetes. Applied and Environmental Microbiology 2002, 68:1344-1350.
24. Henry W.P. Non-enzymatic iron, manganese and copper chemistry of potential importance in wood decay. Wood Deterioration and Preservation - Advances in our Changing World, ACS Symposium Series 2003, vol. 845:175-195. American Chemical Society, Washington, DC.
25. 3+-reducing compounds recovered from Eucalyptus grandis biotreated with Ceriporiopsis subvermispora. International Biodeterioration & Biodegradation 2011, 65:164-171.
26. Kapich A.N., Jensen K.A., Hammel K.E. Peroxyl radicals are potential agents of lignin biodegradation. FEBS Letters 1999, 461:115-119.
27. Kerem Z., Jensen K.A., Hammel K.E. Biodegradative mechanism of the brown-rot basidiomycete Gloeophyllum trabeum: evidence for an extracellular hydroquinone-driven Fenton reaction. FEBS Letters 1999, 446:49-54.
28. Koenigs J.W. Production of hydrogen peroxide by wood-rotting fungi in wood and its correlation with weight loss, depolymerization, and pH changes. Archives of Microbiology 1974, 99:129-145.
29. Lateef A., Oloke J.K., Kana G.E.B., Oyeniyi S.O., Onifade O.R., Oyeleye A.O., Oladosu O.C., Oyelami A.O. Improving the quality of agro-wastes by solid state fermentation: enhanced antioxidant activities and nutritional qualities. World Journal of Microbiology and Biotechnology 2008, 24:2369-2374.
30. 2 in photo-Fenton reactions using metavanadate. Talanta 2005, 66:86-91.
31. Oviedo C., Contreras D., Freer J., Rodríguez J. Degradation of Fe(II)-ethylenediamine tetraacetic acid (EDTA) complex by a catechol-driven Fenton reaction. Fresenius Environmental Bulletin 2003, 12:1323-1327.
32. Paszczynski A., Crawford R., Funk D., Goodell B. De novo synthesis of 4,5-dimethoxycatechol and 2,5-dimethoxyhydroquinone by the brown rot fungus Gloeophyllum trabeum. Applied and Environmental Microbiology 1999, 65:674-679.
33. Qian Y., Goodell B., Jellison J., Felix C.C. The effect of hydroxyl radical generation on free-radical activation of TMP fi{ligature}bers. Journal of Polymers and the Environment 2004, 12:147-155.
34. Rodríguez J., Contreras D., Parra C., Freer J., Baeza J., Durán N. Pulp mill effluent treatment by Fenton-type reactions catalyzed by iron complexes. Water Science and Technology 1999, 40:351-355.
35. Smith G.F., McCardy W.H. 2,9-dimethyl-1,10-phenanthroline - new specifi{ligature}c spectrophotometric determination of copper. Analytical Chemistry 1954, 24:371-373.
36. Spiteller G. Peroxyl radicals: inductors of neurodegenerative and other infl{ligature}ammatory diseases. Their origin and how they transform cholesterol, phospholipids, plasmalogens, polyunsaturated fatty acids, sugars, and proteins into deleterious products. Free Radical Biology & Medicine 2006, 41:362-387.
37. Stookey L.L. Ferrozine - a new spectrophotometric reagent for iron. Analytical Chemistry 1970, 42:779-781.
38. Tornberg K., Olsson S. Detection of hydroxyl radicals produced by wood decomposing fungi. FEMS Microbiology Ecology 2002, 40:13-20.
39. Valenzuela R., Contreras D., Oviedo C., Freer J., Rodríguez J. Copper catechol-driven Fenton reactions and their potential role in wood degradation. International Biodeterioration & Biodegradation 2008, 61:345-350.
40. Varela W., Tien M. Effect of pH and oxalate on hydroquinone-derived hydroxyl radical formation during brown rot wood degradation. Applied and Environmental Microbiology 2003, 69:6025-6031.
41. Verma P., Baldrian P., Gabriel J., Trnka T., Nerud F. Copper-ligand complex for the decolorization of synthetic dyes. Chemosphere 2004, 57:1207-1211.
42. Xu C., Ma F., Zhang X. Lignocellulose degradation and enzyme production by Irpex lacteus CD2 during solid-state fermentation of corn stover. Journal of Bioscience and Bioengineering 2009, 108:372-375.
43. Zanta C.L.P.S., Friedrich L.C., Machulek A., Higa K.M., Quina F.H. Surfactant degradation by a catechol-driven Fenton reaction. Journal of Hazardous Materials 2010, 178:258-263.