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Lignin demethylation and polysaccharide decomposition in spruce sapwood degraded by brown rot fungi

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ORGANIC GEOCHEMISTRY
卷 33, 期 2, 页码 111-124

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PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/S0146-6380(01)00144-9

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The organic residues produced in the brown-rot (BR) of wood by many basidiomycetes fungi Lire ubiquitous on most coniferous forest floors. This degraded wood tissue is characterized by low levels of polysaccharides and a high proportion of demethylated lignin with minor glycerol side chain oxidation. Because of the selective enrichment in an aromatic dihydroxy-rich lignin residue. the chemical and biological reactivity of BR degraded wood will be distinctly different from white rot. the other primary class of fungal wood decal. which typically produces oxidized. lignin-depleted residues. The biochemical mechanism by which BR fungi perform this distinctive degradative chemistry is only starting to become known. and Molecular studies which examine the chemical changes imparted to lignin over the long-term decay process are lacking. Using C-13-labeled tetramethylammonium hydroxide thermochemolysis (C-13-TMAH) and solid state C-13 NMR, we investigated the relationship between lignin oxidation demethylation and polysaccharide metabolism in a 32-week time series study Of Spruce sapwood inoculated with either of two BR fungi (Postia placenta and Gloeophyllum trabeum). Our findings demonstrate a close relationship between lignin demethylation and polysaccharide loss and suggest demethylation may play a mechanistic role in poly-saccharide loss. possibly by assisting in Fenton reactions where catechol quinone oxidation and cycling aids in iron reduction. The residue remaining after 16 cheeks of decay is devoid of polysaccharides. in contrast to the 68% polysaccharide carbon present in the Initial spruce. and exhibits an increased aromatic dihydroxy content (resulting from demethylation of the 3-methoxyl carbon) of up to 22% of the lignin. as determined by C-13-TMAH thermochemolysis. In a typical soil or porewater environment these chemical changes would make BR residues highly reactive toward redox sensitive polyvalent metals (e.g. ferric iron) and likely to adsorb to metal hydroxide surfaces. (C) 2002 Published by Elsevier Science Ltd.

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