A liquid chromatography-electrospray ionization-mass spectrometry method for quantification of cyclotides in plants avoiding sorption during sample preparation

Rikke Gleerup Ovesen, Ulf Göransson, Steen Honore' Hansen, John Nielsen, Hans Chr. Bruun Hansen

    11 Citationer (Scopus)

    Abstract

    Cyclotides are plant-produced, bioactive, cyclic mini-proteins with interesting pharmaceutical and agricultural applications. A reverse phase liquid chromatography electrospray ionization mass spectrometry (RP-LC-ESI-MS) method for analysis of cyclotides in plant materials with a minimum of sample pre-treatment is presented. Three exemplary cyclotides (kalata B1, kalata B2 and cycloviolacin O2) were used as reference substances for the method development. Linearity (r 2>0.99) was achieved in the concentration range 0.05-10mg/L and the limit of detection was 1.7-4.0μg/L. The present study is the first to demonstrate that cyclotides dissolved in water sorb to glass vials, but the addition of 15% of acetonitrile or 40mg/L of bovine serum albumin is sufficient to keep the cyclotides in solution. Cyclotides were extracted from candied violets, violet tea, and the plants Oldenlandia affinis and Viola odorata using 70% methanol containing 0.1% formic acid (v/v). The plant content was determined to be 23.5-14,200μg/g (dry weight). The highest content of cyclotide was found in wild Danish V. odorata, and it is the highest content of cyclotide in a plant reported hitherto. Candied violets contained 0.00-8.66μg/g (dry weight), while no cyclotides were detected in commercial violet tea.

    OriginalsprogEngelsk
    TidsskriftJournal of Chromatography A
    Vol/bind1218
    Udgave nummer44
    Sider (fra-til)7964-7970
    Antal sider7
    ISSN0021-9673
    DOI
    StatusUdgivet - 4 nov. 2011

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