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Chemoenzymatic Synthesis and Radical Scavenging of Sulfated Hydroxytyrosol, Tyrosol, and Acetylated Derivatives

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    SYSNO ASEP0507895
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleChemoenzymatic Synthesis and Radical Scavenging of Sulfated Hydroxytyrosol, Tyrosol, and Acetylated Derivatives
    Author(s) Begines, P. (ES)
    Biedermann, David (MBU-M) RID, ORCID
    Valentová, Kateřina (MBU-M) RID, ORCID
    Petrásková, Lucie (MBU-M) ORCID
    Pelantová, Helena (MBU-M) ORCID, RID
    Maya, I. (ES)
    Fernandez-Bolanos, J.G. (ES)
    Křen, Vladimír (MBU-M) RID, ORCID
    Source TitleJournal of Agricultural and Food Chemistry. - : American Chemical Society - ISSN 0021-8561
    Roč. 67, č. 26 (2019), s. 7281-7288
    Number of pages8 s.
    Languageeng - English
    CountryUS - United States
    Keywordsolive phenols ; arylsulfotransferase ; hydroxytyrosol
    Subject RIVCE - Biochemistry
    OECD categoryBiochemistry and molecular biology
    R&D ProjectsGA18-00121S GA ČR - Czech Science Foundation (CSF)
    GA19-00043S GA ČR - Czech Science Foundation (CSF)
    Method of publishingLimited access
    Institutional supportMBU-M - RVO:61388971
    UT WOS000474669600009
    EID SCOPUS85069265451
    DOI10.1021/acs.jafc.9b01065
    AnnotationPotential metabolites of bioactive compounds are important for their biological activities and as authentic standards for metabolic studies. The phenolic compounds contained in olive oil are an important part of the human diet, and therefore their potential metabolites are of utmost interest. We developed a convenient, scalable, one-pot chemoenzymatic method using the arylsulfotransferase from Desulfitobacterium hafniense for the sulfation of the natural olive oil phenols tyrosol, hydroxytyrosol, and of their monoacetylated derivatives. Respective monosulfated (tentative) metabolites were fully structurally characterized using LC-MS, NMR, and HRMS. In addition, Folin-Ciocalteu reduction, 1,1-diphenyl-2-picrylhydrazyl radical scavenging, and antilipoperoxidant activity in rat liver microsomes damaged by tert-butylhydroperoxide were measured and compared to the parent compounds. As expected, the sulfation diminished the radical scavenging properties of the prepared compounds. These compounds will serve as authentic standards of phase II metabolites.
    WorkplaceInstitute of Microbiology
    ContactEliška Spurná, eliska.spurna@biomed.cas.cz, Tel.: 241 062 231
    Year of Publishing2020
    Electronic addresshttps://pubs.acs.org/doi/10.1021/acs.jafc.9b01065
Number of the records: 1  

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