4.6 Article

Yellow Twig (Nauclea orientalis) from Thailand: Strictosamide as the Key Alkaloid of This Plant Species

期刊

MOLECULES
卷 27, 期 16, 页码 -

出版社

MDPI
DOI: 10.3390/molecules27165176

关键词

Nauclea orientalis; Rubiaceae; monoterpene indole alkaloid; enzymatic deglucosylation; strictosamide

资金

  1. Science Achievement Scholarship of Thailand (SAST)
  2. postdoctoral Fellowship from Kasetsart University, Center of Excellence for Innovation in Chemistry (PERCH-CIC), Ministry of Higher Education, Science, Research, and Innovation
  3. Kasetsart University Research and Development Institute (KURDI)
  4. Department of Chemistry, Faculty of Science, Kasetsart University
  5. Mass Spectrometry Centre
  6. NMR Spectroscopy Centre of the Faculty of Chemistry, University of Vienna

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This study conducted a comprehensive phytochemical examination of the yellow twig Nauclea orientalis, identifying 13 tryptamine-derived alkaloids. The analysis showed that strictosamide is the key compound in the overall alkaloid composition, and it may contribute significantly to the yellow color of the wood. The study also analyzed the metabolomics of alkaloids and investigated the enzymatic deglucosylation of strictosamide. Furthermore, anti-feedant assays revealed the potential role of strictosamide in plant defense.
Comprehensive phytochemical examination from different perspectives using preparative and analytical chromatographic techniques combined with spectroscopic/spectrometric methods of the so-called yellow twig Nauclea orientalis (L.) L. (Rubiaceae) led to the identification of 13 tryptamine-derived (=monoterpene-indole) alkaloids. The identified alkaloids comprise strictosamide and four of its glucosidic derivatives, three oxindole derivatives, and five yellow-colored angustine-type aglycones. Qualitative and quantitative HPLC analyses showed the enrichment of strictosamide in all studied organs. Based on these results, we performed metabolomic analyses of monoterpene-indole alkaloids and made a H-1 NMR in vitro monitoring of enzymatic deglucosylation of strictosamide. A comparison of the stability of strictosamide and its enantiomer vincoside lactam by theoretical calculations was also performed revealing a slightly higher stability of vincoside lactam. Additionally, we conducted two different anti-feedant assays of strictosamide using larvae of the polyphageous moth Spodoptera littoralis Boisduval. The obtained results indicate that generally two different biosynthetic pathways are most likely responsible for the overall alkaloid composition in this plant. Strictosamide is the key compound in the broader pathway and most likely the source of the identified angustine-type aglycones, which may contribute significantly to the yellow color of the wood. Its cross-organ accumulation makes it likely that strictosamide is not only important as a reservoir for the further biosynthesis, but also acts in the plants' defense strategy.

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