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Developmental expression and substrate specificities of alfalfa caffeic acid 3-O-methyltransferase and caffeoyl coenzyme A 3-O-methyltransferase in relation to lignification

Author:
Inoue, K., Sewalt, V.J.H., Ballance, G.M., Ni, W., Sturzer, C., Dixon, R.A.
Source:
Plant physiology 1998 v.117 no.3 pp. 761-770
ISSN:
0032-0889
Subject:
Medicago sativa, leaves, petioles, stems, lignin, biosynthesis, lignification, chemical reactions, caffeic acid, coenzyme A, transferases, enzyme activity, biochemical pathways, chemical structure, amino acid sequences, developmental stages, plant anatomy
Abstract:
The biosynthesis of monolignols can potentially occur via two parallel pathways involving free acids or their coenzyme A (CoA) esters. Caffeic acid 3-O-methyltransferase (COMT) and caffeoyl CoA 3-O-methyltransferase (CCOMT) catalyze functionally identical reactions in these two pathways, resulting in the formation of mono- or dimethoxylated lignin precursors. The activities of the two enzymes increase from the first to the sixth internode in stems of alfalfa (Medicago sativa L.), preceding the deposition of lignin. Alfalfa CCOMT is highly similar at the amino acid sequence level to the CCOMT from parsley, although it contains a six-amino acid insertion near the N terminus. Transcripts encoding both COMT and CCOMT are primarily localized to vascular tissue in alfalfa stems. Alfalfa CCOMT expressed in Escherichia coli catalyzes O-methylation of caffeoyl and 5-hydroxyferuloyl CoA, with preference for caffeoyl CoA. It has low activity against the free acids. COMT expressed in E. coli is active against both caffeic and 5-hydroxyferulic acids, with preference for the latter compound. Surprisingly, very little extractable O-methyltransferase activity versus 5-hydroxyferuloyl CoA is present in alfalfa stem internodes, in which relative O-methyltransferase activity against 5-hydroxyferulic acid increases with increasing maturity, correlating with increased lignin methoxyl content.
Agid:
665677