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


Journal

Molecules (Basel, Switzerland)
ISSN: 1420-3049
Titre abrégé: Molecules
Pays: Switzerland
ID NLM: 100964009

Informations de publication

Date de publication:
14 Aug 2022
Historique:
received: 13 07 2022
revised: 05 08 2022
accepted: 11 08 2022
entrez: 26 8 2022
pubmed: 27 8 2022
medline: 30 8 2022
Statut: epublish

Résumé

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.

Identifiants

pubmed: 36014416
pii: molecules27165176
doi: 10.3390/molecules27165176
pmc: PMC9414341
pii:
doi:

Substances chimiques

Alkaloids 0
Antineoplastic Agents 0
Indole Alkaloids 0
Lactams 0
Monoterpenes 0
Vinca Alkaloids 0
strictosamide 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Références

J Ethnopharmacol. 2018 Feb 15;212:106-136
pubmed: 29045823
Phytochemistry. 2017 Nov;143:124-131
pubmed: 28806604
Eur J Biochem. 1993 Apr 1;213(1):305-12
pubmed: 8477701
Nat Prod Rep. 2016 Sep 25;33(9):1034-43
pubmed: 27346294
Nat Prod Commun. 2015 Dec;10(12):2087-90
pubmed: 26882671
ACS Chem Biol. 2017 Dec 15;12(12):3086-3092
pubmed: 29140075
J Biochem. 2001 Sep;130(3):341-9
pubmed: 11530009
Phytochemistry. 2020 May;173:112296
pubmed: 32087436
Phytochemistry. 2022 Feb;194:113029
pubmed: 34844038
Bioorg Med Chem. 2016 Feb 15;24(4):588-95
pubmed: 26749326
Fitoterapia. 2022 Jul;160:105228
pubmed: 35667521
Phytochemistry. 2015 Aug;116:162-169
pubmed: 26043882
Molecules. 2016 Jul 23;21(8):
pubmed: 27455233
Molecules. 2012 Apr 02;17(4):4028-36
pubmed: 22469596
Trends Biotechnol. 2000 May;18(5):197-202
pubmed: 10758514
J Nat Prod. 2001 Aug;64(8):1001-5
pubmed: 11520214
J Chem Soc Perkin 1. 1973;1:13-6
pubmed: 4736241
Behav Neurosci. 1999 Aug;113(4):840-54
pubmed: 10495092
Chem Biodivers. 2005 Oct;2(10):1378-86
pubmed: 17191939
Fitoterapia. 2010 Oct;81(7):830-3
pubmed: 20472039
Planta Med. 1992 Feb;58(1):43-8
pubmed: 1620742
BMC Plant Biol. 2010 Aug 19;10:182
pubmed: 20723215
Chin J Nat Med. 2013 Mar;11(2):188-92
pubmed: 23787188
Nat Prod Res. 2018 Dec;32(24):2922-2927
pubmed: 29072098
Bioorg Chem. 2019 Mar;83:1-5
pubmed: 30339860

Auteurs

Weerasak Songoen (W)

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.

Julia Brunmair (J)

Department of Analytical Chemistry, University of Vienna, Währinger Strasse 38, A-1090 Vienna, Austria.

Florian Traxler (F)

Department of Organic Chemistry, University of Vienna, Währinger Strasse 38, A-1090 Vienna, Austria.

Viktoria Chiara Wieser (VC)

Department of Botany and Biodiversity Research, University of Vienna, Rennweg 14, A-1030 Vienna, Austria.

Witthawat Phanchai (W)

Department of Physics, Faculty of Science, Khon Kaen University, Khon Kaen 40002, Thailand.

Wanchai Pluempanupat (W)

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.

Lothar Brecker (L)

Department of Organic Chemistry, University of Vienna, Währinger Strasse 38, A-1090 Vienna, Austria.

Johann Schinnerl (J)

Department of Botany and Biodiversity Research, University of Vienna, Rennweg 14, A-1030 Vienna, Austria.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs
Humans Male Female Health Knowledge, Attitudes, Practice Middle Aged

Prevalence and implications of fragile X premutation screening in Thailand.

Areerat Hnoonual, Sunita Kaewfai, Chanin Limwongse et al.
1.00
Humans Fragile X Mental Retardation Protein Thailand Male Female
Humans Female Alopecia Breast Neoplasms Middle Aged

Classifications MeSH