Detection and characterization of twenty-eight isomers of fumonisin B1 (FB1) mycotoxin in a solid rice culture infected with Fusarium verticillioides by reversed-phase high-performance liquid chromatography/electrospray ionization time-of-flight and ion trap mass spectrometry

被引:52
作者
Bartok, Tibor [1 ,3 ]
Tolgyesi, Laszlo [2 ,4 ]
Szekeres, Andras [3 ]
Varga, Monika [1 ]
Bartha, Richard [4 ]
Szecsi, Arpad [5 ]
Bartok, Mihaly [6 ]
Mesterhazy, Akos [1 ]
机构
[1] Cereal Res Nonprofit Ltd Co, H-6701 Szeged, Hungary
[2] Eotvos Lorand Univ, Joint Res & Training Lab Separat Techn, H-1117 Budapest, Hungary
[3] FumoPrep Ltd Co, H-6782 Morahalom, Hungary
[4] Kromat Ltd Co, H-1124 Budapest, Hungary
[5] Hungarian Acad Sci, Dept Plant Pathol, Inst Plant Protect, H-1525 Budapest, Hungary
[6] Univ Szeged, Dept Organ Chem, H-6720 Szeged, Hungary
关键词
TOXIN T-A; ABSOLUTE-CONFIGURATION; RELATIVE CONFIGURATION; MONILIFORME; STEREOCHEMISTRY; SPHINGOSINE; ASPERGILLUS; BACKBONE; FRAGMENT; CANCER;
D O I
10.1002/rcm.4353
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Fumonisin rnycotoxins which are hazardous to humans and animals were produced in a Fusarium verticillioides-infected solid rice culture. To decrease the possibility of the formation of artifacts, the fumonisins were analysed by reversed-phase high-performance liquid chromatography/electrospray ionization time-of-flight (RP-HPLC/ESI-TOFMS) and ion trap mass spectrometry (RP-HPLC/ESI-ITMS) immediately after the extraction of the culture material, without any further sample clean-up. The fumonisin isomers were separated by using a flat gradient on a special, high-coverage C-18, narrow-bore HPLC column (YMC-Pack J'sphere ODS H80) suggested for the separation of structural isomers by the manufacturer. Exact mass measurements (TOFMS) of the protonated molecules and extraction of the ion chromatogram corresponding to the empirical formula (C34H59NO15) of FB1 toxins led to the identification of 29 peaks and shoulders, including those of FBI. The FBI toxin and 28 of its isomers were also detected by ITMS after separation with RP-HPLC. The characteristic m/z values of the product ions, including the backbones obtained by ITMS2, undoubtedly indicated the structures of the FB1 isomers for 28 peaks and shoulders. In the MS2 spectra of the protonated molecules of the FB1 isomers, with some exceptions, 15 characteristic product ions including the hydrocarbon backbone at m/z 299 were observed. The abundance ratio of the cation at m/z 299 ranged up to 5.8%. The relative quantities of the isomers found in the sample extract were expressed as percentages of the FB1 content (0.001-0.579%). The total amount of the 28 FB1 isomers was 2.803% of the quantity of FB1 that is important from the aspect of food and feed safety. Copyright (C) 2009 John Wiley & Sons, Ltd.
引用
收藏
页码:35 / 42
页数:8
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