Tatsis Evangelos C, Eylert Eva, Maddula Ravi Kumar, Ostrozhenkova Elena, Svatoš Aleš, Eisenreich Wolfgang, Schneider Bernd
Max Planck Institut für chemische Ökologie, Hans Knöll Strasse 8, 07745 Jena (Germany).
Chembiochem. 2014 Jul 21;15(11):1645-50. doi: 10.1002/cbic.201402109. Epub 2014 Jun 11.
Nudicaulins are unique alkaloids responsible for the yellow color of the petals of some papaveraceaous plants. To elucidate the unknown biosynthetic origin of the skeleton, a (13) CO2 -pulse/chase experiment was performed with growing Papaver nudicaule plants. (13) C NMR analysis revealed more than 20 multiple (13) C-enriched isotopologues in nudicaulins from the petals of (13) CO2 -labeled plants. The complex labeling pattern was compared with the isotopologue composition of a kaempferol derivative that was isolated from petals of the same (13) CO2 -labeled plants. The deconvolution of the labeling profiles indicated that the nudicaulin scaffold is assembled from products or intermediates of indole metabolism, the phenylpropanoid pathway, and the polyketide biosynthesis. Naringenin-type compounds and tryptophan/tryptamine are potential substrates for the condensation reaction finally generating the aglycone skeleton of nudicaulins.
裸茎罂粟碱是一类独特的生物碱,它使得某些罂粟科植物花瓣呈现黄色。为了阐明该骨架未知的生物合成起源,对生长中的裸茎罂粟植株进行了¹³CO₂脉冲/追踪实验。¹³C NMR分析显示,来自¹³CO₂标记植株花瓣的裸茎罂粟碱中有20多种多重¹³C富集的同位素异构体。将这种复杂的标记模式与从同一¹³CO₂标记植株花瓣中分离出的山奈酚衍生物的同位素异构体组成进行了比较。标记图谱的反卷积表明,裸茎罂粟碱骨架是由吲哚代谢、苯丙烷途径和聚酮生物合成的产物或中间体组装而成。柚皮素型化合物和色氨酸/色胺是最终生成裸茎罂粟碱苷元骨架的缩合反应的潜在底物。