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Conversion of (3S,4R)-Tetrahydrodaidzein to (3S)-Equol by THD Reductase: Proposed Mechanism Involving a Radical Intermediate

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Absolute configuration determination of isoflavan-4-ol stereoisomers

(2010) Mihyang Kim et al.   BIOORGANIC & MEDICINAL CHEMISTRY LETTERS

Time-dependent density functional theory-assisted absolute configuration determination of cis-dihydrodiol metabolite produced from isoflavone by biphenyl dioxygenase

(2009) Jiyoung Seo et al.   ANALYTICAL BIOCHEMISTRY

Stereospecific Biotransformation of Dihydrodaidzein into (3S)-Equol by the Human Intestinal Bacterium Eggerthella Strain Julong 732

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Location of flavone B-ring controls regioselectivity and stereoselectivity of naphthalene dioxygenase from Pseudomonas sp. strain NCIB 9816-4

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Interactions of gut microbiota with functional food components and nutraceuticals

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Bioconversion of soy isoflavones daidzin and daidzein by Bifidobacterium strains

(2008) Stefano Raimondi et al.   APPLIED MICROBIOLOGY AND BIOTECHNOLOGY

Conversion of puerarin into its 7-O-glycoside derivatives by Microbacterium oxydans (CGMCC 1788) to improve its water solubility and pharmacokinetic properties

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