stilbenes and 4-6-dinitro-o-cresol

stilbenes has been researched along with 4-6-dinitro-o-cresol* in 2 studies

Other Studies

2 other study(ies) available for stilbenes and 4-6-dinitro-o-cresol

ArticleYear
Production of Bioactive 3'-Hydroxystilbene Compounds Using the Flavin-Dependent Monooxygenase Sam5.
    Journal of microbiology and biotechnology, 2018, Jul-28, Volume: 28, Issue:7

    The flavin-dependent monooxygenase Sam5 was previously reported to be a bifunctional hydroxylase with a coumarte 3-hydroxylase and a resveratrol 3'-hydroxylase activity. In this article, we showed the Sam5 enzyme has 3'-hydroxylation activities for methylated resveratrol (pinostilbene and pterostilbene), hydroxylated resveratrol (oxyresveratrol) and glycosylated resveratrol (piceid) as substrates. However, the use of piceid, a glycone type stilbene, as a substrate for bioconversion experiments with the Sam5 enzyme expressed in,

    Topics: Dinitrocresols; Escherichia coli; Flavins; Glucosides; Hydroxylation; Mixed Function Oxygenases; Plant Extracts; Resveratrol; Stilbenes

2018
The two common polymorphic forms of human NRH-quinone oxidoreductase 2 (NQO2) have different biochemical properties.
    FEBS letters, 2014, May-02, Volume: 588, Issue:9

    There are two common forms of NRH-quinone oxidoreductase 2 (NQO2) in the human population resulting from SNP rs1143684. One has phenylalanine at position 47 (NQO2-F47) and the other leucine (NQO2-L47). Using recombinant proteins, we show that these variants have similar steady state kinetic parameters, although NQO2-L47 has a slightly lower specificity constant. NQO2-L47 is less stable towards proteolytic digestion and thermal denaturation than NQO2-F47. Both forms are inhibited by resveratrol, but NQO2-F47 shows negative cooperativity with this inhibitor. Thus these data demonstrate, for the first time, clear biochemical differences between the variants which help explain previous biomedical and epidemiological findings.

    Topics: 2,6-Dichloroindophenol; Amino Acid Substitution; Dinitrocresols; Enzyme Inhibitors; Enzyme Stability; Humans; Isoenzymes; Kinetics; Niacinamide; Oxidation-Reduction; Polymorphism, Single Nucleotide; Proteolysis; Quinone Reductases; Resveratrol; Stilbenes

2014