Department of Chemistry and Center of Excellence for Innovation in Chemistry, Special Research Unit for Advanced Magnetic Resonance, Faculty of Science, Kasetsart University, Bangkok 10900, Thailand.
Department of Organic Chemistry, University of Vienna, Währinger Strasse 38, A-1090 Vienna, Austria.
Molecules. 2022 Aug 14;27(16):5176. doi: 10.3390/molecules27165176.
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 1H 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.
采用制备和分析色谱技术结合光谱/光谱方法,从不同角度对所谓的“黄枝”鸡骨常山(L.)L.(茜草科)进行全面的植物化学研究,鉴定出 13 种色胺衍生的(单萜吲哚)生物碱。鉴定出的生物碱包括斯特罗卡酰胺和其 4 种糖苷衍生物、3 种吲哚衍生物和 5 种黄色的安古斯汀型苷元。定性和定量 HPLC 分析表明,所有研究的器官中都含有丰富的斯特罗卡酰胺。基于这些结果,我们对单萜吲哚生物碱进行了代谢组学分析,并进行了体外监测酶去葡萄糖化斯特罗卡酰胺的 1H NMR。还通过理论计算比较了斯特罗卡酰胺及其对映异构体长春苷内酰胺的稳定性,结果表明长春苷内酰胺的稳定性略高。此外,我们使用多鳞蛾幼虫 Spodoptera littoralis Boisduval 进行了两种不同的抗饲料实验,检测了斯特罗卡酰胺的活性。得到的结果表明,通常有两种不同的生物合成途径可能是该植物中总生物碱组成的主要原因。斯特罗卡酰胺是更广泛途径中的关键化合物,很可能是鉴定出的安古斯汀型苷元的来源,这些苷元可能对木材的黄色有重要贡献。其跨器官积累表明,斯特罗卡酰胺不仅作为进一步生物合成的储备库很重要,而且还可能在植物的防御策略中发挥作用。