Subscribe to RSS
DOI: 10.1055/s-2005-864154
© Georg Thieme Verlag KG Stuttgart · New York
13C-Labelling of Xanthohumol in Hop Cones (Humulus lupulus)
This paper is dedicated to Prof. Dr. A. Nahrstedt on the occasion of his retirement and leaving his position as long-standing editor of Planta MedicaPublication History
Received: August 18, 2004
Accepted: February 11, 2005
Publication Date:
21 June 2005 (online)

Abstract
Biolabelling conditions in hop cones of xanthohumol (Xn) were studied by feeding [U-13C]glucose, [1-13C]glucose, [ring-13C6]phenylalanine, [2-13C]sodium acetate or [2-13C]malonic acid as biosynthetic precursors to hop sprouts. Quantitative 13C-NMR spectroscopic analysis of the resulting labelled Xn showed different labelling patterns and ratios depending on precursor and feeding concentrations. The highest incorporation rate was achieved with [U-13C]glucose (9.41 ± 1.22 %). With [ring-13C6]phenylalanine only ring B was labelled (3.51 ± 0.08 % enrichment). [2-13C]sodium acetate and [2-13C]malonic acid allowed labelling of the A-ring (1.82 ± 0.02 % and 1.74 ± 0.03 % enrichment). The specific labelling pattern of the prenyl side chain with [1-13C]glucose (2.36 ± 0.27 % enrichment) confirmed the biosynthetic origin to be MEP pathway-derived. On the basis of these results radiolabelling of Xn will be performed for in vivo bioavailability studies.
Key words
Xanthohumol - hops - Humulus lupulus - Cannabinaceae - biolabelling - biosynthesis
References
- 1 Stevens J F, Taylor A W, Deinzer M L. Quantitative analysis of xanthohumol and related prenylflavonoids in hops and beer by liquid chromatography-tandem mass spectrometry. J Chromatogr A. 1999; 832 97-107
- 2 Miranda C L, Stevens J F, Ivanov V, McCall M, Frei B, Deinzer M L. et al . Antoxidant and prooxidant actions of prenylated and nonprenylated chalcones and flavanones in vitro . J Agric Food Chem. 2000; 48 3876-84
- 3 Miranda C L, Stevens J F, Helmrich A, Henderson M C, Rodriguez R J, Yang Y H. et al . Antiproliferative and cytotoxic effects of prenylated flavonoids from hops (Humulus lupulus) in human cancer cell lines. Food Chem Toxicol. 1999; 37 271-85
- 4 Gerhäuser C, Alt A, Heiss E, Gamal-Elden A, Klimo K, Knauft J. et al . Cancer chemopreventive activity of xanthohumol, a natural product derived from hop. Mol Cancer Ther. 2002; 1 959-69
- 5 Bertl E, Klenke F, Sckell A, Becker H, Bartsch H, Gerhäuser C. Xanthohumol, a potential chemopreventive agent derived from hop (Humulus lupulus L.) inhibits angiogenesis and tumor growth in vivo. Proc Am Asssoc Cancer Res. 2004; 45 (suppl.) #LB327
- 6 Yilmazer M, Stevens J F, Deinzer M L, Buhler D R. In vitro biotransformation of xanthohumol, a flavonoid from hops (Humulus lupulus), by rat liver microsomes. Drug Metab Dispos. 2001; 29 223-31
- 7 Nookandeh A, Frank N, Steiner F, Ellinger R, Schneider B, Gerhäuser C. et al . Xanthohumol metabolites in faeces of rats. Phytochemistry. 2004; 65 561-70
- 8 Déprez S, Mila I, Scalbert A. Carbon-14C biolabeling of (+)-catechin and proanthocyanidin oligomers in willow tree cuttings. J Agric Food Chem. 1999; 47 4219-30
- 9 Solon E G, Balani S K, Lee F W. Whole-body autoradiography in drug discovery. Curr Drug Metab. 2002; 3 451-62
- 10 Goese M, Kammhuber K, Bacher A, Zenk M H, Eisenreich W. Biosynthesis of bitter acids in hops. A 13C-NMR and 2H-NMR study on the building blocks of humulone. Eur J Biochem. 1999; 263 447-54
- 11 Heller W, Forkmann G. Biosynthesis of flavonoids. In: The flavonoids, Advances in research since 1986. Harborne, JB editor Chapmann & Hall London; 1994: pp 499-508
- 12 Braun S, Kalinowski H O, Berger S. In: 100 and more basic NMR experiments. VHC-Wiley Weinheim; 1996: pp 228-36
- 13 Gamborg O L, Miller R A, Ojiama K. Plant cell cultures. 1. Nutrient requirements of suspension cultures of soybean root cells. Exp Cell Res. 1968; 50 151-8
- 14 Gardner D SJ, Purification of hop e xtracts. United States Patent 3,794,744. 1972
- 15 Kloostermann H, Hessels G I, Vrijbloed J W, Euverink G J, Dijkhuizen L. (De)regulation of key enzyme steps in the shikimate pathway and phenylalanine-specific pathway of the actinomycete Amycolatopsis methanolica . Microbiology. 2003; 149 3321-30
- 16 Adam K P, Thiel R, Zapp J, Becker H. Involvement of the mevalonic acid pathway and the glyceraldehyde-pyruvate pathway in terpenoid biosynthesis of the liverworts Ricciocarpos natans and Conocephalum conicum . Arch Biochem Biophys. 1998; 354 181-7
- 17 Thiel R. Biosynthese der Isopren-Einheiten pflanzlicher Terpene. Arbeitsteilung von Mevalonat- und Methylerythritolphosphat-Weg. Dissertation Saarbrücken; 1999
- 18 Liebermann B, Nussbaum R P, Günther W, Tuscher J M. Biosynthesis of the bicycloalternarenes, mixed terpenoids of Alternaria alternata . Phytochemistry. 2001; 56 551-7
Prof. Hans Becker
Pharmakognosie und Analytische Phytochemie
Universität des Saarlandes
Im Stadtwald
66041 Saarbrücken
Germany
Fax: +49-681-302-2476
Email: hans.becker@mx.uni-saarland.de