
Phytochemistry p. 1701 - 1706 (1986)
Update date:2022-08-04
Topics:
Morelli, Elisa
Rej, Rabinda N.
Lewis, Norman G.
Just, George
Towers, G. H. Neil
Lignification in all plant species is assumed to occur exclusively via the dehydrogenative polymerization of the trans (E) monolignols, p-coumaryl, coniferyl and sinapyl alcohols.This assumption may have to be revised somewhat due to the presence of both E (trans) and Z (cis) isomers of p-hydroxy substituted cinnamic acids in grasses, and cis-coniferyl and cis-sinapyl alcohols in beech bark (Fagus grandifolia).This suggests that lignification of these tissues may use either cis- or trans-monolignols.By means of H2O2/peroxidase induction, we have prepared synthetic dehydrogenative polymerized (DHP) lignin from both cis- and trans-coniferyl alcohols.Under the tests employed, the degradation products from both DHPs were identical suggesting that either cis- or trans-monolignols are suitable substrates for this enzyme and, therefore, lignification.An alternative hypothesis is that the cis-monolignols accumulate in beech bark because they are not suitable substrates.Therefore, it would follow that the enzymes involved in lignification in vivo are highly specific. Key Word Index - Fagus grandifolia; Fagaceae; American beech; biosynthesis; cis/trans-monolignols; lignin; p-hydroxycinnamyl alcohols; dehydrogenative polymerized lignin.
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