TY - JOUR
T1 - Initial Steps of Ferulic Acid Polymerization by Lignin Peroxidase
AU - Ward, Gary
AU - Hadar, Yitzhak
AU - Bilkis, Itzhak
AU - Konstantinovsky, Leonid
AU - Dosoretz, Carlos G.
PY - 2001/6/1
Y1 - 2001/6/1
N2 - The major products of the initial steps of ferulic acid polymerization by lignin peroxidase included three dehydrodimers resulting from β-5′ and β-β′coupling and two trimers resulting from the addition of ferulic acid moieties to decarboxylated derivatives of β-O-4′- and β-5′-coupled dehydrodimers. This is the first time that trimers have been identified from peroxidase-catalyzed oxidation of ferulic acid, and their formation appears to be favored by decarboxylation of dehydrodimer intermediates. After initial oxidation, the coupling reactions appear to be determined by the chemistry of ferulic acid phenoxy radicals, regardless of the enzyme and of whether the reaction is performed in vitro or in vivo. This claim is supported by our finding that horseradish peroxidase provides a similar product profile. Furthermore, two of the dehydrodimers were the two products obtained from laccase-catalyzed oxidation (Tatsumi, K. S., Freyer, A., Minard, R. D., and Bollag, J.-M. (1994) Environ. Sci. Technol. 28, 210-215), and the most abundant dehydrodimer is the most prominent in grass cell walls (Ralph, J., Quideau, S., Grabber, J. H., and Hatfield, R. D. (1994) J. Chem. Soc. Perkin Trans. 1, 3485-3498). Our results also indicate that the dehydrodimers and trimers are further oxidized by lignin peroxidase, suggesting that they are only intermediates in the polymerization of ferulic acid. The extent of polymerization appears to be dependent on the ionization potential of formed intermediates, H2O2 concentration, and, probably, enzyme stability.
AB - The major products of the initial steps of ferulic acid polymerization by lignin peroxidase included three dehydrodimers resulting from β-5′ and β-β′coupling and two trimers resulting from the addition of ferulic acid moieties to decarboxylated derivatives of β-O-4′- and β-5′-coupled dehydrodimers. This is the first time that trimers have been identified from peroxidase-catalyzed oxidation of ferulic acid, and their formation appears to be favored by decarboxylation of dehydrodimer intermediates. After initial oxidation, the coupling reactions appear to be determined by the chemistry of ferulic acid phenoxy radicals, regardless of the enzyme and of whether the reaction is performed in vitro or in vivo. This claim is supported by our finding that horseradish peroxidase provides a similar product profile. Furthermore, two of the dehydrodimers were the two products obtained from laccase-catalyzed oxidation (Tatsumi, K. S., Freyer, A., Minard, R. D., and Bollag, J.-M. (1994) Environ. Sci. Technol. 28, 210-215), and the most abundant dehydrodimer is the most prominent in grass cell walls (Ralph, J., Quideau, S., Grabber, J. H., and Hatfield, R. D. (1994) J. Chem. Soc. Perkin Trans. 1, 3485-3498). Our results also indicate that the dehydrodimers and trimers are further oxidized by lignin peroxidase, suggesting that they are only intermediates in the polymerization of ferulic acid. The extent of polymerization appears to be dependent on the ionization potential of formed intermediates, H2O2 concentration, and, probably, enzyme stability.
UR - http://www.scopus.com/inward/record.url?scp=0035378662&partnerID=8YFLogxK
U2 - 10.1074/jbc.M009785200
DO - 10.1074/jbc.M009785200
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C2 - 11278569
AN - SCOPUS:0035378662
SN - 0021-9258
VL - 276
SP - 18734
EP - 18741
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 22
ER -