Biosynthesis of Liriodendrin by Liriodendron tulipifera
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概要
- 論文の詳細を見る
この論文は国立情報学研究所の学術雑誌公開支援事業により電子化されました。^<14>C-Labeled lignin precursors (L-phenylalanine-U-^<14>C, ferulic acid-2-^<14>C, coniferyl alcohol-2-^<14>C, sinapic acid-2-^<14>C and sinapyl alcohol-2-^<14>C) were administered to young twigs of a yellow poplar (Liriodendron tulipifera). Sinapyl alcohol was most effectively incorporated into liriodendrin (dilution value, 6.5～13.5) and syringaresinol (dilution value, 1.1), and followed by L-phenylalanine. However, the incorporation of sinapic acid was rather low and coniferyl alcohol was scarcely incorporated. Liriodendrin isolated as its octaacetate and syringaresinol were all levorotatory. Biogenetic relationship between liriodendrin and syringyl lignin was discussed.
- 京都大学の論文
- 1977-02-28
著者
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Fujimoto Hideto
Division Of Lignin Chemistry Wood Research Institute Kyoto University
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Higuchi Takayoshi
Division Of Lignin Chemistry Wood Research Institute Kyoto University
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Fujimoto Hideo
Division of Lignin Chemistry, WOOD RESEARCH INSTITUTE, KYOTO UNIVERSITY
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