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J Microbiol Biotechnol ; 34(6): 1356-1364, 2024 Jun 28.
Article in English | MEDLINE | ID: mdl-38754998

ABSTRACT

Isoamyl fatty acid esters (IAFEs) are widely used as fruity flavor compounds in the food industry. In this study, various IAFEs were synthesized from isoamyl alcohol and various fatty acids using a cutinase enzyme (Rcut) derived from Rhodococcus bacteria. Rcut was immobilized on methacrylate divinylbenzene beads and used to synthesize isoamyl acetate, butyrate, hexanoate, octanoate, and decanoate. Among them, Rcut synthesized isoamyl butyrate (IAB) most efficiently. Docking model studies showed that butyric acid was the most suitable substrate in terms of binding energy and distance from the active site serine (Ser114) γ-oxygen. Up to 250 mM of IAB was synthesized by adjusting reaction conditions such as substrate concentration, reaction temperature, and reaction time. When the enzyme reaction was performed by reusing the immobilized enzyme, the enzyme activity was maintained at least six times. These results demonstrate that the immobilized Rcut enzyme can be used in the food industry to synthesize a variety of fruity flavor compounds, including IAB.


Subject(s)
Carboxylic Ester Hydrolases , Enzymes, Immobilized , Flavoring Agents , Molecular Docking Simulation , Rhodococcus , Enzymes, Immobilized/metabolism , Enzymes, Immobilized/chemistry , Rhodococcus/enzymology , Rhodococcus/metabolism , Flavoring Agents/metabolism , Flavoring Agents/chemistry , Carboxylic Ester Hydrolases/metabolism , Carboxylic Ester Hydrolases/chemistry , Esters/metabolism , Esters/chemistry , Pentanols/metabolism , Pentanols/chemistry , Fatty Acids/metabolism , Fatty Acids/chemistry , Bacterial Proteins/metabolism , Bacterial Proteins/genetics , Bacterial Proteins/chemistry , Temperature , Substrate Specificity , Butyric Acid/metabolism , Butyric Acid/chemistry , Catalytic Domain
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