Počet záznamů: 1  

Analysis of cytokinin nucleotides by capillary zone electrophoresis with diode array and mass spectrometric detection in a recombinant enzyme in vitro reaction

  1. 1.
    SYSNO ASEP0385991
    Druh ASEPJ - Článek v odborném periodiku
    Zařazení RIVJ - Článek v odborném periodiku
    Poddruh JČlánek ve WOS
    NázevAnalysis of cytokinin nucleotides by capillary zone electrophoresis with diode array and mass spectrometric detection in a recombinant enzyme in vitro reaction
    Tvůrce(i) Béres, Tibor (UEB-Q) RID
    Gemrotová, Markéta (UEB-Q)
    Tarkowski, P. (CZ)
    Ganzera, M. (AT)
    Maier, V. (CZ)
    Fridecký, D. (CZ)
    Dessoy, M. A. (DE)
    Wessjohann, L. A. (DE)
    Spíchal, Lukáš (UEB-Q) RID, ORCID
    Strnad, Miroslav (UEB-Q) RID, ORCID
    Doležal, Karel (UEB-Q) RID, ORCID
    Zdroj.dok.Analytica Chimica Acta. - : Elsevier - ISSN 0003-2670
    Roč. 751, Feb (2012), s. 176-181
    Poč.str.6 s.
    Jazyk dok.eng - angličtina
    Země vyd.NL - Nizozemsko
    Klíč. slovaCytokinin nucleotides ; Capillary electrophoresis ; Isopentenyltransferase
    Vědní obor RIVED - Fyziologie
    CEPLC06034 GA MŠMT - Ministerstvo školství, mládeže a tělovýchovy
    CEZAV0Z50380511 - UEB-Q (2005-2011)
    UT WOS000311013100021
    DOI10.1016/j.aca.2012.08.049
    AnotaceA capillary zone electrophoresis (CZE) method for separation of adenosine and N-6-isopentenyladenosine (cytokinin) nucleotides was developed, optimized and validated. Aqueous solutions of several amino acids were evaluated as the background electrolyte constituents. Separation of six nucleotides in less than 20 min with high theoretical plate number (up to 400 000 for isopentenyladenosine triphosphate) was achieved using a 100 mM sarcosine/ammonia buffer at pH 10.0. The detection limits of the CZE-UV method are in the low micromolar range (0.69-1.27 mu mol L-1). Good repeatability of migration times (within 1.3%), peak areas (within 1.8%) and linearity (R-2 >0.999) was achieved over the concentration range 5-1000 mu mol L-1. The method was used to assay the activity of the recombinant Arabidopsis thaliana isopentenyltransferase 1 (AtIPT1). Baseline separation of isopentenylated nucleotides by CE-ESI-MS using a volatile buffer (30 mM ammonium formate; pH 10.0) was accomplished. The identities of the reaction products - isopentenyladenosine di- and triphosphate were confirmed by HPLC-QqTOE-MS. Dephosphorylation of ATP was observed as a parallel reaction.
    PracovištěÚstav experimentální botaniky
    KontaktDavid Klier, knihovna@ueb.cas.cz, Tel.: 220 390 469
    Rok sběru2013
Počet záznamů: 1  

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