IP Library › Granted Patent US 9,556,401
Granted Patent B2
US 9,556,401 · App. 12/669,803 · Granted Jan 31, 2017

Method for producing EPA-enriched oil and DHA-enriched oil

Inventors: Kiyomi Furihata (Hachioji, JP); Hiroyuki Kawahara (Hachioji, JP); Hideaki Yamaguchi (Hachioji, JP); Hideo Ikemoto (Hachioji, JP); Nobushige Doisaki (Hachioji, JP)
Assignee: NIPPON SUISAN KAISHA, LTD.
C11C1/045C11C3/10C12P7/6472
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Quick Facts
Patent No.
US 9,556,401
App. No.
12/669,803
Granted
Jan 31, 2017
Kind
B2
Abstract

Alcoholysis of oils and fats containing EPA and DHA is performed by a lipase having substrate specificity for fatty acids having 18 carbons or less and in the presence of a reaction additive such as magnesium oxide; then the glyceride fraction is separated; alcoholysis of the glyceride fraction is performed by a lipase having substrate specificity for fatty acids having 20 carbons or less and in the presence of a reaction additive such as magnesium oxide; and EPA-enriched oil and DHA-enriched oil are simultaneously obtained.

Claims (13)

1. A method for producing eicosapentaenoic acid-enriched oil and docosahexaenoic acid-enriched oil from oils and fats containing eicosapentaenoic acid and docosahexaenoic acid as constituent fatty acids, said method comprising:

a) a step wherein said oils and fats are subjected to alcoholysis accompanied by hydrolysis, by a lipase having substrate specificity for fatty acids having 18 carbons or less and in the presence of an aqueous alcohol and magnesium oxide as a reaction additive, and an eicosapentaenoic acid and docosahexaenoic acid-enriched glyceride fraction is obtained from the resulting reaction mixture,

wherein water is added in the amount of 5% (v/v) to 20% (v/v) in terms of amount of the aqueous alcohol, and

b) a step wherein said glyceride fraction is subjected to alcoholysis accompanied by hydrolysis, by a lipase having substrate specificity for fatty acids having 20 carbons or less and in the presence of an aqueous alcohol and magnesium oxide as a reaction additive, and the eicosapentaenoic acid-enriched ester fraction and docosahexaenoic acid-enriched glyceride fraction are separated from the resulting reaction mixture,

wherein water is added in the amount of 5% (v/v) to 20% (v/v) in terms of amount of the aqueous alcohol;

wherein the lipase used in step a) is a lipase obtained from a microorganism belonging to Alcaligenes sp. and the lipase used in step b) is a lipase obtained from a microorganism belonging to Thermomyces lanuginosus;

and wherein the oils and fats used in step a) are fish oil.

2. The method according to claim 1 , wherein the lipase used in step a) is Lipase QLM®.

3. The method according to claim 1 , wherein the lipase used in step b) is Lipozyme TL IM®.

4. The method according to claim 1 , wherein the amount of reaction additive added in step a) and/or step b) is 0.01 to 30% (w/w) in terms of oils and fats.

5. The method according to claim 1 , wherein the alcohol is a lower alcohol selected from the group consisting of ethanol, methanol, 2-propanol, and butanol.

6. The method according to claim 1 , wherein in step (a) water is added in the amount of 10% (v/v) to 20% (v/v) in terms of amount of the aqueous alcohol.

7. The method according to claim 1 , wherein in step (b) water is added in the amount of 5.78% (v/v) to 20% (v/v) in terms of amount of the aqueous alcohol.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 20, 2010
From: FURIHATA, KIYOMI; KAWAHARA, HIROYUKI; YAMAGUCHI, HIDEAKI; IKEMOTO, HIDEO; DOISAKI, NOBUSHIGE
To: NIPPON SUISAN KAISHA, LTD.
Reel/Frame 023815/0341 →
Priority Claims (1)
JP 2007-197253 · Jul 30, 2007 · national
Continuity (1)
Related Publication 20100190220A1 · Jul 29, 2010