1. Polymerization of monolignols by redox shuttle-mediated enzymatic oxidation: a new model in lignin biosynthesis I.
- Author
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Onnerud H, Zhang L, Gellerstedt G, and Henriksson G
- Subjects
- Acrolein chemistry, Acrolein metabolism, Biopolymers chemistry, Catalysis, Cell Wall metabolism, Chromatography methods, Lignin chemical synthesis, Magnetic Resonance Spectroscopy, Manganese metabolism, Manganese Compounds metabolism, Models, Chemical, Oxidation-Reduction, Oxygen metabolism, Peroxidases metabolism, Phenols chemistry, Phenols metabolism, Wood, Acrolein analogs & derivatives, Biopolymers metabolism, Enzymes metabolism, Lignin biosynthesis
- Abstract
Lignin is one of the most abundant biopolymers, and it has a complex racemic structure. It may be formed by a radical polymerization initiated by redox enzymes, but much remains unknown about the process, such as how molecules as large as enzymes can generate the compact structure of the lignified plant cell wall. We have synthesized lignin oligomers according to a new concept, in which peroxidase is never in direct contact with the lignin monomers coniferaldehyde and coniferyl alcohol. Instead, manganese oxalate worked as a diffusible redox shuttle, first being oxidized from Mn(II) to Mn(III) by a peroxidase and then being reduced to Mn(II) by a simultaneous oxidation of the lignin monomers to radicals that formed covalent linkages of the lignin type. Furthermore, a high molecular mass polymer was generated by oxidation of coniferyl alcohol by Mn(III) acetate in a dioxane and water mixture. This polymer was very similar to natural spruce wood lignin, according to its NMR spectrum. The possible involvement of a redox shuttle/peroxidase system in lignin biosynthesis is discussed.
- Published
- 2002
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