Abstract
A crude cell-free extract from Forsythia intermedia catalyses the formation of (-)secoisolariciresinol, and not its (+) enantiomer, when incubated with coniferyl alcohol in the presence of NAD(P)H and H2O2. This is the first report of an enzyme reaction specifically involved in the coupling reaction between two phenylpropanoid monomers to afford an optically pure lignan.
Publication types
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Research Support, U.S. Gov't, Non-P.H.S.
MeSH terms
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Butylene Glycols / chemistry
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Butylene Glycols / isolation & purification
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Butylene Glycols / metabolism*
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Cell-Free System
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Lignans*
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Lignin / chemistry
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Lignin / isolation & purification
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Lignin / metabolism*
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Mass Spectrometry
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Molecular Structure
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Plants / metabolism*
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Spectrophotometry, Ultraviolet
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Stereoisomerism
Substances
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Butylene Glycols
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Lignans
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Lignin
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secoisolariciresinol