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Biosynthesis of caffeine underlying the diversity of motif B' methyltransferase.

Authors :
Nakayama F
Mizuno K
Kato M
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.

Details

Language :
English
ISSN :
1934-578X
Volume :
10
Issue :
5
Database :
MEDLINE
Journal :
Natural product communications
Publication Type :
Academic Journal
Accession number :
26058161