Cell-Wall-Associated Oxidases from the Lignifying Xylem of Angiosperms and Gymnosperms: Monolignol Oxidation
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Nigel Deighton
Summary
Cell-wall-associated oxidases extracted from the lignifying xylem of Sitka spruce and ash oxidise sinapyl alcohol at a greater rate than coniferyl alcohol and p-coumaryl alcohol (SA > CA > pCA). The enzyme from ash shows a marked preference, on a specific activity basis, for the oxidation of SA over CA and pCA (SA ≫ CA ≥ pCA) and has a particularly low affinity for the oxidation of coniferyl alcohol compared to the enzyme from spruce (SA > CA > pCA). This difference in monolignol preference between the spruce and ash enzymes may relate to their required functions during lignification, in that the hardwood enzyme would be supplied mainly SA and the softwood enzyme would be supplied mainly CA. The spruce enzyme also displayed a marked preference for the oxidation of sinapyl alcohol over sinapyl aldehyde even when the two compounds were presented in a mixture.
Purified cell walls from the lignifying xylem of spruce could oxidise CA by the action of bound oxidase activity and dissolved oxygen (~ 240 μM) but CA oxidation was increased many fold by the action of the bound peroxidase activity and 240 μM H2O2. However, the initial dimeric and trimeric products of the peroxidase- and oxidase-catalysed reactions detected by liquid chromatography-mass spectrometry were the same and present in similar proportions. This indicates that the oxidation of CA by oxidase or by peroxidase proceeds via the same intermediates and occurs by a similar mechanism.
Insoluble dehydrogenation polymers (DHPs) of CA were formed in similar yields by spruce extracts in the absence (oxidase activity) or presence (peroxidase activity) of H2O2. The peroxidase-catalysed DHPs and the oxidase-catalysed DHPs gave Fourier transform infra-red spectra with maxima that were characteristic of DHPs of CA. However, differences in the comparative intensities of some maxima suggest that the oxidase-catalysed DHPs were less condensed than the peroxidase-catalysed polymers. These findings are discussed with respect to the possible contribution of oxidases to lignin structure in developing wood.
Copyright © 1999 by Walter de Gruyter GmbH & Co. KG
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Artikel in diesem Heft
- The Significance of Accelerated Laboratory Testing Methods Determining the Natural Durability of Wood
- The Thermomechanical Behaviour of Wood Subject to Fungal Decay
- Fixation of Chromium in Wood from Trivalent Chromium Salt Solutions
- Spatial Distribution of Metal Ions in Spruce Wood by Synchrotron Radiation Microbeam X-Ray Fluorescence Analysis
- Chemical Composition of Lipophilic Extractives from Eucalyptus globulus Labill. Wood
- Antifungal Compounds in the Ethyl Acetate Soluble Fraction of the Extractives of Taiwania (Taiwania cryptomerioides Hayata) Heartwood
- Efficacy of Pinosylvins against White-Rot and Brown-Rot Fungi
- Investigations into Laccase-Mediator Delignification of Kraft Pulps
- Cell-Wall-Associated Oxidases from the Lignifying Xylem of Angiosperms and Gymnosperms: Monolignol Oxidation
- Atmospheric Acetic Acid Pulping of Rice Straw IV: Physico-Chemical Characterization of Acetic Acid Lignins from Rice Straw and Woods. Part 1. Physical Characteristics
- Lignin-Polyphenol Interaction in Azobe (Lophira alata) Heartwood. A Study on Milled Wood Lignin (MWL) and Klason Residues
- Electrospray Ionization Mass Spectrometry as a Tool for Lignins Molecular Weight and Structural Characterisation
- Determination of Phenolic Hydroxyl Groups in Lignin by Combined Use of 1H NMR and UV Spectroscopy
- The Effective Diffusion Coefficient and Mass Transfer Coefficient of Nordic Softwoods as Calculated from Direct Drying Experiments
- Stress Relaxation of Sugi (Cryptomeria japonica D.Don) Wood in Radial Compression under High Temperature Steam
- Structural Performance of Fire-Retardant Treated Plywood: Effect of Elevated Temperature
- Sorption Behaviour and Dimensional Changes of Wood-Coating Composites
- Literature Reports
