Fellermeier M, Eisenreich W, Bacher A, Zenk M H
Biozentrum-Pharmazie, Universität Halle, Halle/Saale, Germany.
Eur J Biochem. 2001 Mar;268(6):1596-604. doi: 10.1046/j.1432-1033.2001.02030.x.
The biosynthesis of cannabinoids was studied in cut sprouts of Cannabis sativa by incorporation experiments using mixtures of unlabeled glucose and [1-(13)C]glucose or [U-(13)C(6)]glucose. (13)C-labeling patterns of cannabichromenic acid and tetrahydrocannabinolic acid were analyzed by quantitative NMR spectroscopy. (13)C enrichments and coupling patterns show that the C(10)-terpenoid moiety is biosynthesized entirely or predominantly (> 98%) via the recently discovered deoxyxylulose phosphate pathway. The phenolic moiety is generated by a polyketide-type reaction sequence. The data support geranyl diphosphate and the polyketide, olivetolic acid, as specific intermediates in the biosynthesis of cannabinoids.
通过使用未标记葡萄糖与[1-(13)C]葡萄糖或[U-(13)C(6)]葡萄糖的混合物进行掺入实验,研究了大麻切割芽中大麻素的生物合成。通过定量核磁共振光谱分析了大麻色烯酸和四氢大麻酚酸的(13)C标记模式。(13)C富集和偶合模式表明,C(10)-萜类部分完全或主要(>98%)通过最近发现的磷酸脱氧木酮糖途径生物合成。酚类部分由聚酮类反应序列产生。这些数据支持香叶基二磷酸和聚酮类化合物橄榄酸作为大麻素生物合成中的特定中间体。