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Improving derivatization efficiency of BMAA utilizing AccQ-Tag ia a complex cyanobacterial matrix
Stockholm University, Faculty of Science, Department of Botany.
Stockholm University, Faculty of Science, Department of Botany.
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2009 (English)In: Amino Acids, ISSN 0939-4451, E-ISSN 1438-2199, no 36, 43-48 p.Article in journal (Refereed) Published
Abstract [en]

Two different assays have been developed and used in order to investigate the optimal conditions for derivatization and detection of acid β-N-methyl-amino-l-alanine (BMAA) in a cyanobacterial sample. BMAA was extracted from cyanobacterial cultures both from the cytosolic (“free”) fraction and in the precipitated (“protein”) fraction using a newly developed extraction scheme and the sample matrix was standardized according to protein concentration to ensure the highest possible derivative yield. A rapid and sensitive HPLC method for fluorescence detection of the non-protein amino acid BMAA in cyanobacteria, utilizing the Waters AccQ-Tag® chemistry and Chromolith® Performance RP-18e columns was developed. Using this new method and utilizing a different buffer system and column than that recommended by Waters, we decreased the time between injections by 75%. The limit of quantification was determined to be 12 nmol and limit of detection as 120 fmol. The linear range was in the range of 8.5 nmol–84 pmol. Accuracy and precision were well within FDA guidelines for bioanalysis.

Place, publisher, year, edition, pages
wien: Springer , 2009. no 36, 43-48 p.
Keyword [en]
β-N-methyl-amino-l-alanine (BMAA) - Cyanobacteria - Carbamate 6-aminoquinolyl-N-hydrosuccinimidyl (AQC) - Derivatization - High-performance liquid chromatography (HPLC)
National Category
Botany
Research subject
Plant Physiology
Identifiers
URN: urn:nbn:se:su:diva-36243DOI: 10.1007/s00726-007-0023-4ISI: 000262231400006OAI: oai:DiVA.org:su-36243DiVA: diva2:289059
Available from: 2010-01-22 Created: 2010-01-22 Last updated: 2017-12-12Bibliographically approved

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