Product ion filtering with rapid polarity switching for the detection of all fumonisins and AAL‐toxins. (14th October 2015)
- Record Type:
- Journal Article
- Title:
- Product ion filtering with rapid polarity switching for the detection of all fumonisins and AAL‐toxins. (14th October 2015)
- Main Title:
- Product ion filtering with rapid polarity switching for the detection of all fumonisins and AAL‐toxins
- Authors:
- Renaud, Justin B.
Kelman, Megan J.
Qi, Tianyu F.
Seifert, Keith A.
Sumarah, Mark W. - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="rcm7374-sec-0001" sec-type="section"> <title>Rationale</title> <p>Fumonisins and AAL‐toxins are structurally similar mycotoxins that contaminate agricultural crops and foodstuffs. Traditional analytical screening methods are designed to target the known compounds for which standards are available but there is clear evidence that many other derivatives exist and could be toxic. A fast, semi‐targeted method for the detection of all known fumonisins, AAL‐toxins and related emerging toxins is required.</p> </sec> <sec id="rcm7374-sec-0002" sec-type="section"> <title>Methods</title> <p>Strains of <italic>Fusarium verticillioides</italic>, <italic>Alternaria arborescens</italic> and <italic>Aspergillus welwitschiae</italic> were grown on their associated crops (maize, tomatoes, and grapes, respectively). Extracts were first analyzed in negative mode using product ion filtering to detect the tricarballylic ester product ion that is common to fumonisins and AAL‐toxins (<italic>m/z</italic> 157.0142). During the same liquid chromatography (LC) run, rapid polarity switching was then used to collect positive mode tandem mass spectrometric (MS<sup>2</sup>) data for characterization of the detected compounds.</p> </sec> <sec id="rcm7374-sec-0003" sec-type="section"> <title>Results</title> <p>Fumonisin B<sub>1</sub>, B<sub>2</sub>, B<sub>3</sub> and B<sub>4</sub> were detected on<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="rcm7374-sec-0001" sec-type="section"> <title>Rationale</title> <p>Fumonisins and AAL‐toxins are structurally similar mycotoxins that contaminate agricultural crops and foodstuffs. Traditional analytical screening methods are designed to target the known compounds for which standards are available but there is clear evidence that many other derivatives exist and could be toxic. A fast, semi‐targeted method for the detection of all known fumonisins, AAL‐toxins and related emerging toxins is required.</p> </sec> <sec id="rcm7374-sec-0002" sec-type="section"> <title>Methods</title> <p>Strains of <italic>Fusarium verticillioides</italic>, <italic>Alternaria arborescens</italic> and <italic>Aspergillus welwitschiae</italic> were grown on their associated crops (maize, tomatoes, and grapes, respectively). Extracts were first analyzed in negative mode using product ion filtering to detect the tricarballylic ester product ion that is common to fumonisins and AAL‐toxins (<italic>m/z</italic> 157.0142). During the same liquid chromatography (LC) run, rapid polarity switching was then used to collect positive mode tandem mass spectrometric (MS<sup>2</sup>) data for characterization of the detected compounds.</p> </sec> <sec id="rcm7374-sec-0003" sec-type="section"> <title>Results</title> <p>Fumonisin B<sub>1</sub>, B<sub>2</sub>, B<sub>3</sub> and B<sub>4</sub> were detected on <italic>Fusarium</italic> contaminated maize, AAL‐toxins TA, TB, TD, TE were detected on <italic>Alternaria</italic> inoculated tomatoes and fumonisin B<sub>2</sub>, B<sub>4</sub> and B<sub>6</sub> on <italic>Aspergillus</italic> contaminated grapes. Additionally, over 100 structurally related compounds possessing a tricarballylic ester were detected from the mould inoculated plant material. These included a hydroxyl‐FB<sub>1</sub> from <italic>F. verticillioides</italic> inoculated maize, keto derivatives of AAL‐toxins from <italic>A. arborescens</italic> inoculated tomatoes, and two previously unreported classes of non‐aminated fumonisins from <italic>Asp. welwitschiae</italic> contaminated grapes.</p> </sec> <sec id="rcm7374-sec-0004" sec-type="section"> <title>Conclusions</title> <p>A semi‐targeted method for the detection of all fumonisins and AAL‐toxins in foodstuffs was developed. The use of the distinctive tricarballylic ester product anion for detection combined with rapid polarity switching and positive mode MS<sup>2</sup> is an effective strategy for differentiating between known isomers such as FB<sub>1</sub> and FB<sub>6</sub>. This analytical tool is also effective for the identification of new compounds as evident from the discoveries of the previously unreported hydroxyl‐FB<sub>1</sub>, keto‐AAL‐toxins, and the two new families of non‐aminated fumonisins. © 2015 Her Majesty the Queen in Right of Canada Rapid Communications in Mass Spectrometry © 2015 John Wiley &amp; Sons Ltd. Reproduced with the permission of the Ministers of Agriculture and Agri‐Food Canada.</p> </sec> </abstract> … (more)
- Is Part Of:
- Rapid communications in mass spectrometry. Volume 29:Number 22(2015)
- Journal:
- Rapid communications in mass spectrometry
- Issue:
- Volume 29:Number 22(2015)
- Issue Display:
- Volume 29, Issue 22 (2015)
- Year:
- 2015
- Volume:
- 29
- Issue:
- 22
- Issue Sort Value:
- 2015-0029-0022-0000
- Page Start:
- 2131
- Page End:
- 2139
- Publication Date:
- 2015-10-14
- Subjects:
- Mass spectrometry -- Periodicals
543.65 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/rcm.7374 ↗
- Languages:
- English
- ISSNs:
- 0951-4198
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 7254.440000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3106.xml