IP Library Granted Patent US 12,297,477
Granted Patent B2
US 12,297,477 · App. 17/165,922 · Granted May 13, 2025

Process for making flavor and fragrant compounds

Inventors: Fredi Bruhlmann (Geneva, CH); Rebecca Buller (Wadenswil, CH)
Assignee: FIRMENICH SA
C12P7/04C07B31/00C11B9/0015C12N9/004C12N9/88C12P7/24
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Quick Facts
Patent No.
US 12,297,477
App. No.
17/165,922
Granted
May 13, 2025
Kind
B2
Abstract

The present invention relates to the production of aromatic hexanols and compositions containing them. In particular provided herein are methods of producing hexenols comprising: 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 wherein the contacting and reducing steps are carried out at essentially the same time in the substantial absence of baker's yeast.

Claims (12)

1. A composition comprising (Z)-3-hexenol produced by a method of producing an alcohol comprising:

a) contacting a 13-hydroperoxide of a polyunsaturated fatty acid selected from the group consisting of linoleic acid and alpha linolenic acid with a 13-hydroperoxide lyase to form a hexenal; and

b) reducing the hexenal 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 hexanal reduction; and

the method does not require intact cells;

wherein the composition comprises (Z)-3-hexenol in an amount of greater than or equal to 12000 mg/L and less than or equal to 400 mg/L of the total amount of n-hexanal, (Z)-3-hexenal, (E)-2-hexenal, (E)-2-hexenol, and n-hexanol, and wherein no n-hexanal, (Z)-3-hexenal, (E)-2-hexenal, (E)-2-hexenol or n-hexanol have been removed after processing.

2. The composition as recited in claim 1 wherein the ratio of (Z)-3-hexenol to the total amount of n-hexanal, (Z)-3-hexenal, (E)-2-hexenal, (E)-2-hexenol, and n-hexanol ranges, by weight, from 30:1 to 71:1.

3. The composition as recited in claim 1 comprising (Z)-3-hexenol wherein the composition comprises (Z)-3-hexenol in an amount of greater than or equal to 12000 mg/L and less than or equal to 400 mg/L of the total amount of n-hexanal, (Z)-3-hexenal, (E)-2-hexenal, (E)-2-hexenol, and n-hexanol produced in the reaction, and wherein no n-hexanal, (Z)-3-hexenal, (E)-2-hexenal, (E)-2-hexenol, or n-hexanol have been removed after processing.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 27, 2023
From: BRUHLMANN, FREDI; BULLER, REBECCA
To: FIRMENICH SA
Reel/Frame 065961/0116 →
Priority Claims (1)
WO PCT/EP2015/052174 · Feb 3, 2015 · international
Continuity (2)
Division 15547563
Related Publication 20210163994A1 · Jun 3, 2021
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