Quantification of the Emetic Toxin Cereulide in Food Products by Liquid Chromatography-Mass Spectrometry Using Synthetic Cereulide as a Standard

Author:

Biesta-Peters Elisabeth G.1,Reij Martine W.1,Blaauw Richard H.2,in ′t Veld Paul H.3,Rajkovic Andreja4,Ehling-Schulz Monika56,Abee Tjakko1

Affiliation:

1. Wageningen University and Research Centre, Laboratory of Food Microbiology, P.O. Box 8129, 6700 EV Wageningen, Netherlands

2. Chiralix B.V., P.O. Box 31070, 6503 CB Nijmegen, Netherlands

3. Food and Consumer Product Safety Authority, Region South, P.O. Box 2168, 5600 CD Eindhoven, Netherlands

4. Laboratory for Food Microbiology and Food Preservation, Department for Food Safety and Food Quality, Faculty of Bioscience Engineering, Ghent University, Coupure Links 653, B-9000 Ghent, Belgium

5. Abteilung Mikrobiologie, Zentralinstitut für Ernährungs-und Lebensmittelforschung, Technische Universität München, Weihenstephaner Berg 3, D-85354 Freising, Germany

6. Food Microbiology Unit, Clinic for Ruminants, Department for Farm Animals and Veterinary Public Health, University of Veterinary Medicine, Veterinaerplatz 1, 1210 Vienna, Austria

Abstract

ABSTRACT Bacillus cereus produces the emetic toxin cereulide, a cyclic dodecadepsipeptide that can act as a K + ionophore, dissipating the transmembrane potential in mitochondria of eukaryotic cells. Because pure cereulide has not been commercially available, cereulide content in food samples has been expressed in valinomycin equivalents, a highly similar cyclic potassium ionophore that is commercially available. This research tested the biological activity of synthetic cereulide and validated its use as a standard in the quantification of cereulide contents in food samples. The synthesis route consists of 10 steps that result in a high yield of synthetic cereulide that showed biological activity in the HEp-2 cell assay and the boar sperm motility assay. The activity is different in both methods, which may be attributed to differences in K + content of the test media used. Using cereulide or valinomycin as a standard to quantify cereulide based on liquid chromatography-mass spectrometry (LC-MS), the concentration determined with cereulide as a standard was on average 89.9% of the concentration determined using valinomycin as a standard. The recovery experiments using cereulide-spiked food products and acetonitrile as extraction solute showed that the LC-MS method with cereulide as a standard is a reliable and accurate method to quantify cereulide in food, because the recovery rate was close to 100% over a wide concentration range.

Publisher

American Society for Microbiology

Subject

Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology

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