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Literature summary for 1.1.1.331 extracted from

  • Okunishi, T.; Sakakibara, N.; Suzuki, S.; Umezawa, T.; Shimada, M.
    Stereochemistry of matairesinol formation by Daphne secoisolariciresinol dehydrogenase (2004), J. Wood Sci., 50, 77-81.
No PubMed abstract available

Organism

Organism UniProt Comment Textmining
Daphne genkwa
-
-
-
Daphne odora
-
-
-

Source Tissue

Source Tissue Comment Organism Textmining
callus
-
Daphne odora
-
shoot
-
Daphne genkwa
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
(-)-secoisolariciresinol + 2 NAD+
-
Daphne genkwa (-)-matairesinol + 2 NADH + 2 H+ product is optically pure, more than 99% enantiomeric excess. (-)-Matairesinol is formed preferentially in the in vitro reactions with enzyme preparations. The opposite (+)-enantiomer is isolated from Daphne genkwa shoot ?
(-)-secoisolariciresinol + 2 NAD+
-
Daphne odora (-)-matairesinol + 2 NADH + 2 H+ product is optically pure, more than 99% enantiomeric excess. (-)-Matairesinol is formed preferentially in the in vitro reactions with enzyme preparations. The opposite (+)-enantiomer is isolated from Daphne odora callus ?