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Biosynthesis of caffeine underlying the diversity of motif B' methyltransferase.
- Source :
-
Natural product communications [Nat Prod Commun] 2015 May; Vol. 10 (5), pp. 799-801. - Publication Year :
- 2015
-
Abstract
- Caffeine (1,3,7-trimethylxanthine) and theobromine (3,7-dimethylxanthine) are well-known purine alkaloids in Camellia, Coffea, Cola, Paullinia, Ilex, and Theobroma spp. The caffeine biosynthetic pathway depends on the substrate specificity of N-methyltransferases, which are members of the motif B' methyl-transferase family. The caffeine biosynthetic pathways in purine alkaloid-containing plants might have evolved in parallel with one another, consistent with different catalytic properties of the enzymes involved in these pathways.
- Subjects :
- Amino Acid Motifs
Genetic Variation
Methyltransferases chemistry
Methyltransferases genetics
Phylogeny
Plant Proteins chemistry
Plant Proteins genetics
Plants classification
Plants genetics
Plants metabolism
Caffeine biosynthesis
Methyltransferases metabolism
Plant Proteins metabolism
Plants enzymology
Subjects
Details
- Language :
- English
- ISSN :
- 1934-578X
- Volume :
- 10
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Natural product communications
- Publication Type :
- Academic Journal
- Accession number :
- 26058161