Process for making flavor and fragrant compounds
AssigneeFirmenich SA
InventorsFredi Bruhlmann, Rebecca Buller
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Abstract
Described herein are methods of producing hexenols including: a) contacting a hydroperoxide of a polyunsaturated fatty acid with a modified hydroperoxide lyase to form a hexenal; and b) reducing the hexenal to a hexenol in the presence of a hydride donor, a ketoreductase, and a co-factor, where the contacting and reducing steps are carried out at essentially the same time in the substantial absence of baker's yeast.
Claims5
A composition comprising (Z,Z)-3,6-nonadienol, wherein the composition is produced by a method comprising:
- a) contacting a 9-hydroperoxide of a polyunsaturated fatty acid selected from the group consisting of linoleic acid and alpha linolenic acid with a 9-hydroperoxide lyase to form an aldehyde selected from the group consisting of a nonenal and nonadienal;
- and
- b) reducing the aldehyde in the presence of a hydride donor, a ketoreductase, and a co-factor;
- wherein the contacting and reducing steps are carried out concomitantly;
- wherein
- the hydride donor is selected from the group consisting of a secondary alcohol, a primary alcohol, an alkandiol and a hydroxy acid or one of its esters;
- the cofactor is selected from the group consisting of NADH and NADPH;
- the hydroperoxide lyase is stable in the presence of the hydride donor, thus allowing for the concomitant hydroperoxide cleavage and aldehyde reduction;
- and
- the method is performed in the absence of intact cells;
- wherein the composition comprises (Z,Z)-3,6-nonadienol in an amount greater than or equal to 0.74 g/l, and wherein the composition may comprise less than or equal to 1 g/l (Z)-3-nonenol.
A composition comprising an alcohol, wherein the composition is produced by a method comprising:
- a) contacting a 9- or 13-hydroperoxide of a polyunsaturated fatty acid selected from the group consisting of linoleic acid and alpha linolenic acid with the respective hydroperoxide lyase to form an aldehyde;
- and
- b) reducing the aldehyde to form the alcohol in the presence of a hydride donor, a ketoreductase, and a co-factor wherein the contacting and reducing steps are carried out concomitantly;
- wherein
- the hydride donor is selected from the group consisting of a secondary alcohol, a primary alcohol, an alkandiol and a hydroxy acid or one of its esters;
- the cofactor is selected from the group consisting of NADH and NADPH;
- the hydroperoxide lyase is stable in the presence of the hydride donor, thus allowing for the concomitant hydroperoxide cleavage and aldehyde reduction;
- and
- the method is performed in the absence of intact cells.
Dependencies are inferred from the claim text.