Mass Spectrometric Analysis of Cucurbitacins and Dihydrocucurbitacins from the Tuber of Citrullus naudinianus

Author:

Benka Moritz123ORCID,Görlitz Kristof1,Schöttgen Michael C.14,Lagies Simon15ORCID,Mohl Daniel A.123ORCID,Kather Michel1,Du Preez-Bruwer Iwanette6,Mumbengegwi Davis6,Teufel Robin7ORCID,Kowarschik Stefanie4,Huber Roman4,Plattner Dietmar A.2,Kammerer Bernd128

Affiliation:

1. Core Competence Metabolomics, Hilde-Mangold-Haus, University of Freiburg, 79104 Freiburg, Germany

2. Institute of Organic Chemistry, University of Freiburg, 79104 Freiburg, Germany

3. Hermann Staudinger Graduate School, University of Freiburg, 79104 Freiburg, Germany

4. Center for Complementary Medicine, Department of Internal Medicine II, University Hospital, Faculty of Medicine, University of Freiburg, 79106 Freiburg, Germany

5. Institute of Medical Microbiology and Hygiene, Faculty of Medicine, Medical Center—University of Freiburg, 79104 Freiburg, Germany

6. Centre for Research Services, University of Namibia, Private Bag, Mandume, Ndemufayo Avenue, Pioneers Park, Windhoek 13301, Namibia

7. Department of Pharmaceutical Sciences, University of Basel, 4056 Basel, Switzerland

8. BIOSS Centre for Biological Signalling Studies, University of Freiburg, 79104 Freiburg, Germany

Abstract

The vast pool of structurally and functionally distinct secondary metabolites (i.e., natural products (NPs)) is constantly being expanded, a process also driven by the rapid progress in the development of analytical techniques. Such NPs often show potent biological activities and are therefore prime candidates for drug development and medical applications. The ethyl acetate extract of the tuber of Citrullus naudinianus (C. naudinianus), an African melon with edible fruits and seeds, shows in vitro immunomodulatory activity presumably elicited by cucurbitacins that are known major constituents of this plant. Further potentially immunomodulatory cucurbitacins or cucurbitacin derivatives were assumed to be in the tuber. Given the typically high content of cucurbitacins with similar physicochemical features but often distinct bioactivities, an efficient and reliable separation process is a prerequisite for their detailed characterization and assessment in terms of bioactivity. We therefore developed a detection method to screen and differentiate cucurbitacins via high-performance liquid chromatography/quadrupole-time-of-flight tandem mass spectrometry (HPLC-QTOF-MS/MS). In order to confirm the identification, the fragmentation patterns of two cucurbitacins and one 23,24-dihydrocucurbitacin were also investigated. Six characteristic fragments were identified and three of them were employed for the identification of cucurbitacins and 23,24-dihydrocucurbitacins in the extract. As a result, in addition to eight previously reported cucurbitacins from this plant four distinct 23,24-dihydrocucurbitacins (B, D, E, and I) were putatively identified and newly found in the ethyl acetate extract of the tuber of C. naudinianus. The established methodology enables rapid and efficient LC-MS-based analysis and identification of cucurbitacins and 23,24-dihydrocucurbitacins in plant extracts.

Publisher

MDPI AG

Subject

Molecular Biology,Biochemistry

Reference13 articles.

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