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Sulfated Metabolites of Luteolin, Myricetin, and Ampelopsin: Chemoenzymatic Preparation and Biophysical Properties

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61988987%3A17310%2F20%3AA2102808" target="_blank" >RIV/61988987:17310/20:A2102808 - isvavai.cz</a>

  • Alternative codes found

    RIV/61388971:_____/20:00534618 RIV/61388963:_____/20:00534618

  • Result on the web

    <a href="https://dx.doi.org/10.1021/acs.jafc.0c03997" target="_blank" >https://dx.doi.org/10.1021/acs.jafc.0c03997</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1021/acs.jafc.0c03997" target="_blank" >10.1021/acs.jafc.0c03997</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Sulfated Metabolites of Luteolin, Myricetin, and Ampelopsin: Chemoenzymatic Preparation and Biophysical Properties

  • Original language description

    Authentic standards of food flavonoids are important for human metabolic studies. Their isolation from biological materials is impracticable; however, they can be prepared in vitro. Twelve sulfated metabolites of luteolin, myricetin, and ampelopsin were obtained with arylsulfotransferase from Desulfitobacterium hafniense and fully characterized by high-performance liquid chromatography, MS, and NMR. The compounds were tested for their ability to scavenge 1,1-diphenyl-2-picrylhydrazyl, 2,2'- azinobis(3-ethylbenzothiazoline-6-sulphonic acid), and N,N-dimethyl-p-phenylenediamine radicals, to reduce ferric ions and Folin-Ciocalteu reagent, and to inhibit tert-butyl hydroperoxide-induced lipid peroxidation of rat liver microsomes. The activity differed considerably even between monosulfate isomers. The parent compounds and myricetin-3'-O-sulfate were the most active while other compounds displayed significantly lower activity, particularly luteolin sulfates. No mutagenic activity of the parent compounds and their main metabolites was observed; only myricetin showed minor pro-mutagenicity. The prepared sulfated metabolites are now available as authentic standards for future in vitro and in vivo metabolic studies.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    40401 - Agricultural biotechnology and food biotechnology

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    O - Projekt operacniho programu

Others

  • Publication year

    2020

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    J. Agric. Food Chem.

  • ISSN

    0021-8561

  • e-ISSN

    1520-5118

  • Volume of the periodical

    40

  • Issue of the periodical within the volume

    68

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    10

  • Pages from-to

    11197-11206

  • UT code for WoS article

    000580512000016

  • EID of the result in the Scopus database

    2-s2.0-85092681503