論文

査読有り 国際誌
2020年6月12日

Characterization of maitotoxin-4 (MTX4) using electrospray positive mode ionization high-resolution mass spectrometry and UV spectroscopy.

Rapid communications in mass spectrometry : RCM
  • Francesco Pisapia
  • ,
  • Manoëlla Sibat
  • ,
  • Ryuichi Watanabe
  • ,
  • Catherine Roullier
  • ,
  • Toshiyuki Suzuki
  • ,
  • Philipp Hess
  • ,
  • Christine Herrenknecht

開始ページ
e8859
終了ページ
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1002/rcm.8859

RATIONALE: The dinoflagellate genera Gambierdiscus and Fukuyoa are producers of toxins responsible for Ciguatera Poisoning (CP). Although having very low oral potency, maitotoxins (MTXs) are very toxic following intraperitoneal injection and feeding studies have shown they may accumulate in fish muscle. To date, six MTX congeners have been described but two congeners (MTX2 and MTX4) have not yet been structurally elucidated. The aim of the present study was to further characterize MTX4. METHODS: Chemical analysis was performed using Liquid Chromatography coupled to a Diode Array Detector (DAD) and positive ionization mode High Resolution Mass Spectrometry (LC/HRMS) on partially purified extracts of G. excentricus (strain VGO792). HRMS/MS studies were also carried out to tentatively explain the fragmentation pathways of MTX and MTX4. RESULTS: The comparison of UV and HRMS (ESI+ ) spectra between MTX and MTX4 led us to propose the elemental formula of MTX4 (C157 H241 NO68 S2 , as unsalted molecule). The comparison of the theoretical and measured m/z values of the doubly charged ions of the isotopic profile in ESI+ were coherent with the proposed elemental formula of MTX4. The study of HRMS/MS spectra on the tri-ammoniated adduct ([M-H+3NH4 ]2+ ) of both molecules gave additional information about structural features. The cleavage observed, probably located at C99 -C100 in both MTX and MTX4, highlighted the same A-side product ion shared by the two molecules. CONCLUSION: All these investigations on the characterization of MTX4 contribute to highlighting that MTX4 belongs to the same structural family of MTXs. However to accomplish a complete structural elucidation of MTX4, NMR-based study and LC/HRMSn investigation will have to be carried out.

リンク情報
DOI
https://doi.org/10.1002/rcm.8859
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/32530533
ID情報
  • DOI : 10.1002/rcm.8859
  • PubMed ID : 32530533

エクスポート
BibTeX RIS