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. 1975 Oct;30(4):650–656. doi: 10.1128/am.30.4.650-656.1975

Enzymatic Transformation of Morphine by Hydroxysteroid Dehydrogenase from Pseudomonas testosteroni

Paloma Liras 1,1, Stephen S Kasparian 1,2, Wayne W Umbreit 1
PMCID: PMC187243  PMID: 172013

Abstract

Enzyme preparations from Pseudomonas testosteroni containing α- and β-hydroxysteroid dehydrogenases catalyzed the oxidation of morphine and codeine by nicotinamide adenine dinucleotide. Morphine was converted in relatively low yield into 14-hydroxymorphinone probably via morphinone as an intermediate. Codeine was converted to codeinone and 14-hydroxycodeinone. Only the conversions at the 6-position were carried out by the hydroxysteroid dehydrogenase. Hydroxylation at the 14-position did occur spontaneously (or enzymatically with a contaminating enzyme) after oxidation at the 6-position.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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