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Two types of alcohol dehydrogenase from Perilla can form citral and perillaldehyde.

Phytochemistry (2014-05-28)
Naoko Sato-Masumoto, Michiho Ito
RÉSUMÉ

Studies on the biosynthesis of oil compounds in Perilla will help in understanding regulatory systems of secondary metabolites and in elucidating reaction mechanisms for natural product synthesis. In this study, two types of alcohol dehydrogenases, an aldo-keto reductase (AKR) and a geraniol dehydrogenase (GeDH), which are thought to participate in the biosynthesis of perilla essential oil components, such as citral and perillaldehyde, were isolated from three pure lines of perilla. These enzymes shared high amino acid sequence identity within the genus Perilla, and were expressed regardless of oil type. The overall reaction from geranyl diphosphate to citral was performed in vitro using geraniol synthase and GeDH to form a large proportion of citral and relatively little geraniol as reaction products. The biosynthetic pathway from geranyl diphosphate to citral, the main compound of citral-type perilla essential oil, was established in this study.

MATÉRIAUX
Référence du produit
Marque
Description du produit

Sigma-Aldrich
Géraniol, 98%
Sigma-Aldrich
Citral, 95%
Sigma-Aldrich
Poly(dimethylsiloxane), viscosity 1.0 cSt (25 °C)
Sigma-Aldrich
Citral, natural, ≥96%, FCC, FG
Sigma-Aldrich
Géraniol, ≥97%, FCC, FG
Sigma-Aldrich
Géraniol, natural, ≥97%, FG
Sigma-Aldrich
Citral, mixture of cis and trans, ≥96%, FG
Sigma-Aldrich
Hexaméthyldisiloxane, viscosity 0.65 cSt (25 °C)
Supelco
Géraniol, analytical standard
Supelco
Citral, analytical standard