Related Experiment Video
Updated: May 23, 2025

HKUST-1 as a Heterogeneous Catalyst for the Synthesis of Vanillin
Published on: July 23, 2016
Hazelnut: Explorations toward the Biocatalytic Synthesis of its Aroma Precursor
Mireia Salvadó-Pau1, Wolf-Dieter Fessner2, Zvjezdana Findrik Blažević3
1Department of White Biotechnology Research - Biocatalysis, BASF SE, RGR/DB, Carl-Bosch-Strasse 38, 67056, Ludwigshafen am Rhein, Germany.
Abstract:
Biocatalysis gains significant industrial interest due to its controlled stereoselectivity and use of mild process conditions. Here, a biosynthetic route is proposed for the synthesis of filbertone (5-methyl-2-hepten-4-one, 1), which is the principal flavor compound of hazelnut. The enantiomeric purity of the industrially synthesized compound is defined, contrary to the natural aroma, which varies according to the source of the nut, extraction conditions, and treatments. The novel synthetic pathway for a hazelnut aroma precursor proposed here consists of a multienzyme cascade, which starts from the two amino acids D-Ile and L-Thr that are individually converted by enzyme catalysts, i.e., D-amino acid oxidase and threonine deaminase, followed by CC ligation of the obtained products, allowing a potentially sustainable production of the natural aroma. The most critical step is CC ligation, which uses two carbonyl compounds as starting material. This step is catalyzed by a regioselective transketolase (TK) that originates from Geobacillus stearothermophilus. The approach holds promise for the industrial production of natural hazelnut aroma precursors, addressing the growing demand in the aroma industry for synthesis methods that sustain the regulatory claims for natural compounds.
More Related Videos
06:31Highly Stereoselective Synthesis of 1,6-Ketoesters Mediated by Ionic Liquids: A Three-component Reaction Enabling Rapid Access to a New Class of Low Molecular Weight Gelators
Published on: November 27, 2015
11:01Preparation and In Vivo Use of an Activity-based Probe for N-acylethanolamine Acid Amidase
Published on: November 23, 2016
Related Concept Videos
Benzene to Phenol via Cumene: Hock Process
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
Alkylation of β-Ketoester Enolates: Acetoacetic Ester Synthesis
Ketones with Nonenolizable Aromatic Aldehydes: Claisen–Schmidt Condensation
As the self-condensation of ketones is generally not favored in basic conditions, the self-condensed products do not form in the reaction between ketones and benzaldehyde. The general reaction of Claisen–Schmidt...
Benzene to 1,4-Cyclohexadiene: Birch Reduction Mechanism
Reactions of Aldehydes and Ketones: Baeyer–Villiger Oxidation
The carbonyl center is...