| Literature DB >> 24919663 |
Evangelos C Tatsis1, Eva Eylert, Ravi Kumar Maddula, Elena Ostrozhenkova, Aleš Svatoš, Wolfgang Eisenreich, Bernd Schneider.
Abstract
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.Entities:
Keywords: Papaver nudicaule; biosynthesis; indole alkaloids; isotopic labeling; nudicaulin
Mesh:
Substances:
Year: 2014 PMID: 24919663 DOI: 10.1002/cbic.201402109
Source DB: PubMed Journal: Chembiochem ISSN: 1439-4227 Impact factor: 3.164