Literature DB >> 22329755

Improved isolation procedure for azaspiracids from shellfish, structural elucidation of azaspiracid-6, and stability studies.

Jane Kilcoyne1, Adela Keogh, Ger Clancy, Patricia LeBlanc, Ian Burton, Michael A Quilliam, Philipp Hess, Christopher O Miles.   

Abstract

Azaspiracids are a group of lipophilic polyether toxins produced by the small dinoflagellate Azadinium spinosum. They may accumulate in shellfish and can result in illnesses when consumed by humans. Research into analytical methods, chemistry, metabolism, and toxicology of azaspiracids has been severely constrained by the scarcity of high-purity azaspiracids. Consequently, since their discovery in 1995, considerable efforts have been made to develop methods for the isolation of azaspiracids in sufficient amounts and purities for toxicological studies, in addition to the preparation of standard reference materials. A seven-step procedure was improved for the isolation of azaspiracids-1-3 (1, 2, and 3) increasing recoveries 2-fold as compared to previous methods and leading to isolation of sufficiently purified azaspiracid-6 (6) for structural determination by NMR spectroscopy. The procedure, which involved a series of partitioning and column chromatography steps, was performed on 500 g of Mytilus edulis hepatopancreas tissue containing ~14 mg of 1. Overall yields of 1 (52%), 2 (43%), 3 (43%), and 6 (38%) were good, and purities were confirmed by NMR spectroscopy. The structure of 6 was determined by one- and two-dimensional NMR spectroscopy and mass spectrometry. The stability of 6 relative to 1 was also assessed in three solvents in a short-term study that demonstrated the greatest stability in aqueous acetonitrile.

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Year:  2012        PMID: 22329755     DOI: 10.1021/jf2048788

Source DB:  PubMed          Journal:  J Agric Food Chem        ISSN: 0021-8561            Impact factor:   5.279


  5 in total

1.  Marine harmful algal blooms, human health and wellbeing: challenges and opportunities in the 21st century.

Authors:  Elisa Berdalet; Lora E Fleming; Richard Gowen; Keith Davidson; Philipp Hess; Lorraine C Backer; Stephanie K Moore; Porter Hoagland; Henrik Enevoldsen
Journal:  J Mar Biol Assoc U K       Date:  2015-11-20       Impact factor: 1.394

2.  Marine algal toxin azaspiracid is an open-state blocker of hERG potassium channels.

Authors:  Michael J Twiner; Gregory J Doucette; Andrew Rasky; Xi-Ping Huang; Bryan L Roth; Michael C Sanguinetti
Journal:  Chem Res Toxicol       Date:  2012-08-10       Impact factor: 3.739

3.  Production and isolation of azaspiracid-1 and -2 from Azadinium spinosum culture in pilot scale photobioreactors.

Authors:  Thierry Jauffrais; Jane Kilcoyne; Véronique Séchet; Christine Herrenknecht; Philippe Truquet; Fabienne Hervé; Jean Baptiste Bérard; Cíara Nulty; Sarah Taylor; Urban Tillmann; Christopher O Miles; Philipp Hess
Journal:  Mar Drugs       Date:  2012-06-13       Impact factor: 6.085

4.  Effects of Temperature, Growth Media, and Photoperiod on Growth and Toxin Production of Azadinium spinosum.

Authors:  Jane Kilcoyne; Amy McCoy; Stephen Burrell; Bernd Krock; Urban Tillmann
Journal:  Mar Drugs       Date:  2019-08-22       Impact factor: 5.118

5.  Structure Elucidation and in Vitro Toxicity of New Azaspiracids Isolated from the Marine Dinoflagellate Azadinium poporum.

Authors:  Bernd Krock; Urban Tillmann; Éric Potvin; Hae Jin Jeong; Wolfgang Drebing; Jane Kilcoyne; Ahmed Al-Jorani; Michael J Twiner; Qun Göthel; Matthias Köck
Journal:  Mar Drugs       Date:  2015-10-30       Impact factor: 5.118

  5 in total

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