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Biotransformation of (1S)-2-Carene and (1S)-3-Carene by Picea abies Suspension Culture

  1. 1.
    SYSNO ASEP0369831
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleBiotransformation of (1S)-2-Carene and (1S)-3-Carene by Picea abies Suspension Culture
    Author(s) Dvořáková, Marcela (UEB-Q) RID, ORCID
    Valterová, Irena (UOCHB-X) RID, ORCID
    Šaman, David (UOCHB-X) RID, ORCID
    Vaněk, Tomáš (UEB-Q) RID, ORCID
    Source TitleMolecules. - : MDPI
    Roč. 16, č. 12 (2011), s. 10541-10555
    Number of pages15 s.
    Languageeng - English
    CountryCH - Switzerland
    Keywordsbiotransformation ; carene ; oxidation
    Subject RIVED - Physiology
    R&D ProjectsME08070 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    2B08058 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    CEZAV0Z50380511 - UEB-Q (2005-2011)
    AV0Z40550506 - UOCHB-X (2005-2011)
    UT WOS000298411200054
    DOI10.3390/molecules161210541
    AnnotationBiotransformation of (1S)-2-carene and (1S)-3-carene by Picea abies suspension culture led to the formation of oxygenated products. (1S)-2-Carene was transformed slowly and the final product was identified as (1S)-2-caren-4-one. On the other hand, the transformation of (1S)-3-carene was rapid and finally led to the formation of (1S)-3-caren-5-one and (1S)-2-caren-4-one as equally abundant major products. The time-course of the reaction indicates that some products abundant at the beginning of the reaction (e.g. (1S,3S,4R)-3,4-epoxycarane and (1R)-p-mentha-1(7),2-dien-8-ol) were consumed by a subsequent transformations. Thus, a precise selection of the biotransformation time may be used for a production of specific compounds.
    WorkplaceInstitute of Experimental Botany
    ContactDavid Klier, knihovna@ueb.cas.cz, Tel.: 220 390 469
    Year of Publishing2012
Number of the records: 1  

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