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- W2023343774 endingPage "367" @default.
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- W2023343774 abstract "The regio- and stereospecificity of bimolecular phenoxy radical coupling reactions, of especial importance in lignin and lignan biosynthesis, are clearly controlled in some manner in vivo; yet in vitro coupling by oxidases, such as laccases, only produce racemic products. In other words, laccases, peroxidases, and comparable oxidases are unable to control regio- or stereospecificity by themselves and thus some other agent must exist. A 78-kilodalton protein has been isolated that, in the presence of an oxidase or one electron oxidant, effects stereoselective bimolecular phenoxy radical coupling in vitro. Itself lacking a catalytically active (oxidative) center, its mechanism of action is presumed to involve capture of E -coniferyl alcohol-derived free-radical intermediates, with consequent stereoselective coupling to give (+)-pinoresinol." @default.
- W2023343774 created "2016-06-24" @default.
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- W2023343774 date "1997-01-17" @default.
- W2023343774 modified "2023-10-11" @default.
- W2023343774 title "Stereoselective Bimolecular Phenoxy Radical Coupling by an Auxiliary (Dirigent) Protein Without an Active Center" @default.
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- W2023343774 doi "https://doi.org/10.1126/science.275.5298.362" @default.
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