IP Library › Granted Patent US 8,557,963
Granted Patent B2
US 8,557,963 · App. 12/451,804 · Granted Oct 15, 2013

Process of aqueous protein extraction from

Inventors: Janitha P. D. Wanasundara (Saskatoon, CA); Tara C. McIntosh (Saskatoon, CA)
Assignee: Her Majesty the Queen in Right of Canada, as Represented by the Minister of Agriculture and Agri-food
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Quick Facts
Patent No.
US 8,557,963
App. No.
12/451,804
Granted
Oct 15, 2013
Kind
B2
Abstract

A process of aqueous protein extraction from Brassicaceae oilseed meal, such as canola, commercial canola meal or yellow mustard, to obtain a napin-rich protein extract, a cruciferin-rich protein extract, and a low-protein residue. The process comprising the steps of performing aqueous extraction of the Brassicaceae oilseed meal at a pH of from about 2.5 to about 5.0 to obtain a soluble napin-rich protein extract and a cruciferin-rich residue followed by performing aqueous extraction of the cruciferin-rich residue to obtain a soluble cruciferin-rich protein extract and a low-protein residue. The cruciferin-rich residue may be treated with cell wall degrading enzymes to obtain a cruciferin-rich fraction The cruciferin-rich protein products may be substantially free of napin protein and may be useful as a non-allergenic food product for human consumption.

Claims (39)

1. A process of aqueous protein extraction from Brassicaceae oilseed meal to obtain a napin-rich protein extract, a cruciferin-rich protein extract, and a low-protein residue, the process comprising the steps of:

(a) performing aqueous extraction of the Brassicaceae oilseed meal at a temperature of from about 18° C. to about 50° C. using an aqueous solvent at a pH of from 2.5 to 3.5 containing a salt at a concentration of from 0.25% to 2.0% w/v of the aqueous solvent, wherein the Brassicaceae oilseed meal is mixed with the aqueous solvent at a meal-to-aqueous solvent ratio of from about 1:10 to about 1:90, to obtain:

(i) a soluble napin-rich protein extract; and

(ii) a cruciferin-rich protein residue; and

(b) performing aqueous extraction of the cruciferin-rich protein residue from step (a) at a temperature of from about 18° C. to about 50° C. using an aqueous alkali solvent at a pH of from about 7.0 to about 13.0, wherein the cruciferin-rich protein residue is mixed with the aqueous alkali solvent at a residue-to-aqueous alkali solvent ratio of from about 1:10 to about 1:90, to obtain:

(i) a soluble cruciferin-rich protein extract; and

(ii) a low-protein residue,

wherein, steps (a) and (b) are performed sequentially.

2. The process of claim 1 , wherein the cruciferin-rich protein extract is substantially free of napin protein.

3. The process of claim 1 , wherein the napin-rich protein extract comprises from about 50% to about 95% total protein content.

4. The process of claim 1 , wherein the cruciferin-rich protein extract comprises from about 60% to about 98% total protein content and is substantially free of napin protein.

5. The process of claim 1 , wherein the low-protein residue comprises from about 1% to about 40% total protein content.

6. The process of claim 1 , wherein the napin-rich protein extract, the cruciferin-rich protein extract and the low-protein residue comprise from about 50% to about 98% of total Brassicaceae oilseed meal protein.

7. The process of claim 1 , wherein the aqueous solvent is alcohol, water or a combination thereof.

8. The process of claim 1 , wherein the aqueous extraction of the Brassicaceae oilseed meal of step (a) is carried out for about 25 minutes to about 360 minutes.

9. The process of claim 1 , wherein the aqueous extraction of the cruciferin-rich protein residue of step (b) is carried out for about 25 minutes to about 360 minutes.

10. The process of claim 1 , wherein the Brassicaceae oilseed meal is commercial canola meal or yellow mustard flour.

11. A process of aqueous protein extraction of Brassicaceae oilseeds to obtain a napin-rich protein extract, a cruciferin-rich protein extract, and a low-protein residue, the process comprising the steps of:

(a) dehulling the Brassicaceae oilseeds to substantially separate Brassicaceae oilseed cotyledons from Brassicaceae oilseed hulls;

(b) defatting the Brassicaceae oilseed cotyledons to obtain Brassicaceae oilseed meal;

(c) performing aqueous extraction of the Brassicaceae oilseed meal at a temperature of from about 18° C. to about 50° C. using an aqueous solvent at a pH of from 2.5 to 3.5 containing a salt at a concentration of from 0.25% to 2.0% w/v of the aqueous solvent, wherein the Brassicaceae oilseed meal is mixed with the aqueous solvent at a meal-to-aqueous solvent ratio of from about 1:10 to about 1:90, to obtain:

(i) a soluble napin-rich protein extract; and

(ii) a cruciferin-rich protein residue; and

(d) performing aqueous extraction of the cruciferin-rich protein residue from step (c) at a temperature of from about 18° C. to about 50° C. using an aqueous alkali solvent at a pH of from about 7.0 to about 13.0, wherein the cruciferin-rich protein residue is mixed with the aqueous alkali solvent at a residue-to-aqueous alkali solvent ratio of from about 1:10 to about 1:90, to obtain:

(i) a soluble cruciferin-rich protein extract; and

(ii) a low-protein residue,

wherein steps (a)-(d) are performed sequentially.

12. A process of aqueous protein extraction from Brassicaceae oilseed meal to obtain a napin-rich protein extract, a cruciferin-rich protein fraction, and a sugar rich fraction comprising:

(a) performing a first aqueous extraction of the Brassicaceae oilseed meal at a temperature of from about 18° C. to about 50° C. using an aqueous solvent at a pH of from 2.5 to 3.5 containing a salt at a concentration of from 0.25% to 2.0% w/v of the aqueous solvent, wherein the Brassicaceae oilseed meal is mixed with the aqueous solvent at a meal-to-aqueous solvent ratio of from about 1:10 to about 1:90, to obtain:

(i) a soluble napin-rich protein extract; and

(ii) a cruciferin-rich protein residue; and

(b) performing a second aqueous extraction of the cruciferin-rich protein residue from step (a) at a temperature of from about 35° C. to about 60° C. and at a pH of from about 3.0 to about 4.5 in the presence of one or more cell wall degrading enzymes to obtain:

(i) a soluble sugar rich extract; and

(ii) a cruciferin-rich protein residue; and

(c) separating the cruciferin-rich protein residue from the soluble sugar rich extract from step (b) to obtain the cruciferin-rich protein fraction and the sugar rich fraction, wherein steps (a)-(c) are performed sequentially.

13. The process of claim 12 , wherein in the step of performing the second aqueous extraction of step (b), the temperature of the second aqueous extraction is from 40° C. to 60° C.

14. The process of claim 13 , wherein the cruciferin-rich protein fraction is substantially free of napin protein.

15. The process of claim 13 , wherein the napin-rich protein extract comprises from about 50% to about 95% total protein content.

16. The process of claim 13 , wherein the cruciferin-rich protein fraction comprises from about 60% to about 98% total protein content and is substantially free of napin protein.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 9, 2009
From: WANASUNDARA, JANITHA P.D.; MCINTOSH, TARA C.
To: HER MAJESTY THE QUEEN IN RIGHT OF CANADA, AS REPRESENTED BY THE MINISTER OF AGRICULTURE AND AGRI-FOOD
Reel/Frame 023626/0626 →
Continuity (2)
Provisional Application 60932654 · Jun 1, 2007
Related Publication 20100249378A1 · Sep 30, 2010