Veratrylchitosan, a polysaccharide-supported lignin model compound, has been synthesised by covalently attaching 3-(3,4-dimethoxybenzyloxy)propionic acid to the polysaccharide chitosan through an amide linkage. When this polymer was used as a substrate in the oxidation promoted by lignin peroxidase (LiP), significant decomposition of the lignin model resulted in the formation of veratraldehyde. The oxidation mechanism involves an initial transfer of one electron from chitosan to the active species of UP (LiP I) followed by C-alpha-H deprotonation of an aromatic cation radical. A benzylic radical is then formed which is further oxidised to a benzyl cation. Reaction with water and hydrolysis of the hemiacetal then lead to veratraldehyde formation. An increase in the yields of the oxidation product is observed in the presence of the mediator 2-chloro-1,4-dimethoxybenzene, thus indicating that a more efficient degradation results from the transfer of an electron from the polymer to the radical cation of the mediator. (C) 2003 Elsevier Inc. All rights reserved.

First synthesis of a polysaccharide-supported lignin model compound and study of its oxidation promoted by lignin peroxidase / D'Acunzo, Francesca; Lanzalunga, Osvaldo. - In: BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS. - ISSN 0006-291X. - 313:1(2004), pp. 17-21. [10.1016/j.bbrc.2003.11.083]

First synthesis of a polysaccharide-supported lignin model compound and study of its oxidation promoted by lignin peroxidase

D'ACUNZO, Francesca;LANZALUNGA, Osvaldo
2004

Abstract

Veratrylchitosan, a polysaccharide-supported lignin model compound, has been synthesised by covalently attaching 3-(3,4-dimethoxybenzyloxy)propionic acid to the polysaccharide chitosan through an amide linkage. When this polymer was used as a substrate in the oxidation promoted by lignin peroxidase (LiP), significant decomposition of the lignin model resulted in the formation of veratraldehyde. The oxidation mechanism involves an initial transfer of one electron from chitosan to the active species of UP (LiP I) followed by C-alpha-H deprotonation of an aromatic cation radical. A benzylic radical is then formed which is further oxidised to a benzyl cation. Reaction with water and hydrolysis of the hemiacetal then lead to veratraldehyde formation. An increase in the yields of the oxidation product is observed in the presence of the mediator 2-chloro-1,4-dimethoxybenzene, thus indicating that a more efficient degradation results from the transfer of an electron from the polymer to the radical cation of the mediator. (C) 2003 Elsevier Inc. All rights reserved.
2004
chitosan; electron transfer; lignin model; lignin model compound; lignin peroxidase; mediation
01 Pubblicazione su rivista::01a Articolo in rivista
First synthesis of a polysaccharide-supported lignin model compound and study of its oxidation promoted by lignin peroxidase / D'Acunzo, Francesca; Lanzalunga, Osvaldo. - In: BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS. - ISSN 0006-291X. - 313:1(2004), pp. 17-21. [10.1016/j.bbrc.2003.11.083]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/46363
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