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Caffeine biosynthesis in young leaves of Camellia sinensis: In vitro studies on N-methyltransferase activity involved in the conversion of xanthosine to caffeine
Authors:Misako Kato  Tomomi Kanehara  Hisayo Shimizu  Takeo Suzuki  Fiona M Gillies  Alan Crozier  Hiroshi Ashihara
Institution:Dept of Biology, Ochanomizu Univ., Tokyo, 112, Japan;Dept of Applied Biology, Kyoto Inst. of Technology, Matsugasaki, Kyoto, 606, Japan;Bower Building, Division of Biochemistry and Molecular Biology, Institute of Biomedical and Life Sciences, Univ. of Glasgow, Glasgow G12 8QQ, Scotland, UK.
Abstract:The aim of this study was to investigate the S -adenosylmethionine dependent N -methyltransferase(s) (NMT) associated with the three methylation steps in the caffeine biosynthesis pathway in tea ( Camellia sinensis L.). NMT activity in cell-free preparations from young leaves was purified by anion-exchange and gel-filtration column chromatography. In both systems, a single zone of NMT activity, with broad substrate specificity was detected. The N-3 position of dimethylxanthine and monomethylxanthines was methylated more readily than N-1 while comparatively little substitution occurred at the N-7 locus. When xanthosine was used as a substrate only the N-7 position was methylated. These results indicate that a single NMT may participate in the conversion of xanthosine to caffeine. The apparent Mr of the NMT, estimated by gel filtration chromatography, was 61 000. The substrate specificity of the NMT is compatible with the operation of a xanthosine → 7-methylxanthosine → 7-methylxanthine → theobromine → caffeine pathway as the main biosynthetic route to caffeine in young tea leaves. The data also indicate that the conversion of 7-methylxanthine → paraxanthine → caffeine may function as one of a number of minor pathways that also contribute to the production of caffeine.
Keywords:Caffeine biosynthesis              Camellia sinensis                        N-methyltransferase  purine alkaloids  substrate specificity  tea leaves
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