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Function of the iron-binding chelator produced by Coriolus versicolor in lignin biodegradation

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Abstract

An ultrafiltered low-molecular-weight preparation of chelating compounds was isolated from a wood-containing culture of the white-rot basidiomycete Coriolus versicolor. This preparation could chelate Fe3+ and reduce Fe3+ to Fe2+, demonstrating that the substance may serve as a ferric chelator, oxygen-reducing agent, and redox-cycling molecule, which would include functioning as the electron transport carrier in Fenton reaction. Lignin was treated with the iron-binding chelator and the changes in structure were investigated by 1H-NMR, 13C-NMR, difference spectrum caused by ionization under alkaline conditions and nitrobenzene oxidation. The results indicated that the iron-binding chelator could destroy the β-O-4 bonds in etherified lignin units and insert phenolic hydroxyl groups. The low-molecular-weight chelator secreted by C. versicolor resulted in new phenolic substructures in the lignin polymer, making it susceptible to attack by laccase or manganese peroxidase. Thus, the synergic action of the iron-binding chelator and the lignocellulolytic enzymes made the substrate more accessible to degradation.

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References

  1. Kirk T K, Farrell R L. Enzymatic “combustion”: The microbial degradation of lignin. Annu Rev Microbiol, 1987, 41: 465–505

    Article  PubMed  CAS  Google Scholar 

  2. Shingo k, Masanori A, Noriko O, et al. Degradation of a non-phenolic β-O-4 substructure and of polymeric lignin model compounds by laccase of Coriolus versicolor in the presence of 1-hydroxybenzotriazole. FEMS Lett, 1999, 170(1): 51–57

    Google Scholar 

  3. Enoki A, Tanaka H, Fuse G. Relationship between degradation of wood and production of H2O2-producing or one-electron oxidases by brown-rot fungi. Wood Sci Technol, 1989, 23: 1–12

    Article  CAS  Google Scholar 

  4. Rimko T H, Pauline J M. Oxidative mechanisms involved in lignin degradation by white-rot fungi. Chem Rev 2001, 101: 3397–3413

    Article  CAS  Google Scholar 

  5. Hammel K E, Kapich A N, Jensen K A, et al. Reactive oxygen species as agents of wood decay by fungi. Enzyme Microb Technol, 2002, 30(4): 445–453

    Article  CAS  Google Scholar 

  6. Srebotnik E, Messner K, Foisner R. Penetrability of white rot-degraded pine wood by the lignin peroxidase of Phanerochaete chrysosporium. Appl Environ Microbiol, 1988, 54(11): 2608–2614

    PubMed  CAS  Google Scholar 

  7. Goodell B, Jellison J, Liu J, et al. Low molecular weight chelators and phenolic compounds isolated from wood decay fungi and their role in the fungal biodegradation of wood. J Biotechnol, 1997, 53: 133–162

    Article  CAS  Google Scholar 

  8. Tanaka H, Itakura S, Enoki A. Hydroxyl radical generation by an extracellular low-molecular-weight substance and phenol oxidase activity during wood degradation by the white-rot basidiomycete Trametes versicolor. J Biotechnol, 1999, 75(1): 57–70

    Article  PubMed  CAS  Google Scholar 

  9. Tanaka H, Itakura S, Enoki A. Phenol oxidase activity and one-electron oxidation activity in wood degradation by soft-rot deuteromycetes. Holzforschung, 2000, 54(5): 463–468

    Article  CAS  Google Scholar 

  10. Hirano T, Tanaka H, Enoki A. Relationship between hydroxyl radicals and degradation of wood by the brown-rot fungus, Tyromyces palustris. Holzforschung, 1996, 50: 541–548

    Article  Google Scholar 

  11. Liu J, Shen X Y, Gao P J. Short fibre formation during cellulose degradation by celluloytic fungi. Biotechnol Lett, 1996, 18(11): 1235–1240

    Article  CAS  Google Scholar 

  12. Yang W H, Liu J, Gao P J, et al. Function of a low molecular peptide generated by cellulolytic fungi for the degradation of native cellulose. Biotechnol Lett, 2004, 26: 1799–1802

    Article  PubMed  CAS  Google Scholar 

  13. Wang W, Gao P J. A peptide-mediated and hydroxyl radical HO·-involved oxidative degradation of cellulose by brown-rot fungi. Biodegradation, 2002, 13: 383–394

    Article  PubMed  CAS  Google Scholar 

  14. Wang W, Huang F, Gao P J. Lignin degradation by a novel peptide, Gt factor, from brown rot fungus Gloeophyllum trabeum. Biotechnol J, 2006, 1: 447–453

    Article  PubMed  CAS  Google Scholar 

  15. Hu M, Zhang W C, Gao P J, et al. Purification and characteristics of a low-molecular-weight peptide possessing oxidative capacity for phenol from Phanerochaete chrysosporium. Sci China Ser C-Life Sci, 2006, 49(3): 243–250

    Article  CAS  Google Scholar 

  16. Huang F, Gao P J. Using cyclic liquid-liquid extraction method for isolation and identification of relative compounds during lignin biodegradation. Sci China Ser E-Tech Sci, 1999, 42: 644–651

    CAS  Google Scholar 

  17. Schwyn B, Neilands J B. Universal chemical assay for the detection and determination siderophores. Anal Biochem, 1987, 160: 47–56

    Article  PubMed  CAS  Google Scholar 

  18. Gibbs C R. Characterization and application of ferrozine iron reagent as a ferrous iron indicator. Anal Chem, 1976, 48: 1197–1201

    Article  CAS  Google Scholar 

  19. Chen C L. Methods in Lignin Chemistry. Heidelberg: Springer Series in Wood Sciences, 1992. 215–319

    Google Scholar 

  20. Arantes V, Milagres A M. 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 effluent of an ECF kraft pulp mill. J Hazard Mater, 2007, 141(1): 273–279

    Article  PubMed  CAS  Google Scholar 

  21. Huang F, Fang J, Gao P J, et al. Synergistic effects of cellubiose dehydrogenase and manganese-dependent peroxidases during lignin degradation. Chin Sci Bull, 2001, 46(23): 1956–1962

    Article  CAS  Google Scholar 

  22. Kenneth A, Carl J, Kenneth E. Pathways for extracellular fenton chemistry in the brown rot basidiomycete Gloeophyllum trabeum. Appl Environ Microbiol 2001, 67: 2705–2711

    Article  Google Scholar 

  23. Fang J, Huang F, Gao P J. Optimization of cellobiose dehydrogenase production by Schizophyllum commune and effect of the enzyme on kraft pulp bleaching by ligninases. Process Biochem, 1999, 34(9): 957–961

    Article  CAS  Google Scholar 

  24. Eggert C, Temp U, Dean J F D, et al. Laccase-mediated formation of the phenoxazinone derivative, cinnabarinic acid. FEMS Lett, 1995, 376(3): 202–206

    CAS  Google Scholar 

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Correspondence to Huang Feng or Gao PeiJi.

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Supported by the National Natural Science Foundation of China (Grant Nos. 30170027 and 30371136)

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Wang, L., Yan, W., Chen, J. et al. Function of the iron-binding chelator produced by Coriolus versicolor in lignin biodegradation. Sci. China Ser. C-Life Sci. 51, 214–221 (2008). https://doi.org/10.1007/s11427-008-0033-9

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  • DOI: https://doi.org/10.1007/s11427-008-0033-9

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