Claims
- 1. A process of preparing a protein isolate, which comprises:
(a) continuously extracting an oil seed meal at a temperature of at least about 5° C. to cause solubilization of protein in said oil seed meal and to form an aqueous protein solution having a pH of about 5 to about 6.8, (b) continuously separating said aqueous protein solution from residual oil seed meal, (c) continuously conveying said aqueous protein solution through a selective membrane operation to increase tie protein concentration of said aqueous protein solution to at least about 50 g/L while maintaining the ionic strength substantially constant to provide a concentrated protein solution, (d) continuously mixing said concentrated protein solution with chilled water having a temperature of below about 15° C. to cause the formation of protein micelles in the aqueous phase, (e) continuously flowing the resulting mixture into a settling vessel while permitting supernatant to overflow the vessel, (f) continuously permitting said protein micelles to settle in the settling vessel while continuing to overflow supernatant from the vessel until a desired amount of amorphous, sticky, gelatinous, glutten-like protein micellar mass has accumulated in said settling vessel, and (g) recovering said protein micellar mass from the settling vessel, said protein micellar mass having a protein content, on a dry weight basis, of at least about 90 wt % as determined by Kjeldahl nitrogen×6.25.
- 2. The process of claim 1 wherein said continuous extraction step is effected by:
(i) continuously mixing an oil seed meal with an aqueous salt solution having an ionic strength of at least about 0.10 and a pH of about 5 to about 6.8 at a temperature of about 5° to about 65° C., and (ii) continuously conveying said mixture through a pipe while extracting protein from the oil seed meal to form an aqueous protein solution having a protein content of about 5 to about 40 g/L in a period of time up to about 10 minutes.
- 3. The process of claim 2 wherein said salt solution has an ionic strength of about 0.15 to about 0.8.
- 4. The process of claim 2 wherein the salt solution has a pH of about 5.3 to about 6.2.
- 5. The process of claim 2 wherein the concentration of oil seed meal in said aqueous salt solution in said mixing step is about 5 to about 15% w/v.
- 6. The process of claim 2 wherein said temperature is at least about 35° C.
- 7. The process of claim 2 wherein said aqueous protein solution has a protein content of about 10 to about 30 g/L.
- 8. The process of claim 1 wherein said extraction step is effected using an aqueous salt solution having an ionic strength of at least about 0.10 and a pH of about 3 to about 5 or about 6.8 to about 9.9 and, following said separation of the aqueous protein solution from residual oil seed meal, the pH of the aqueous protein solution is adjusted to a pH of about 5 to about 6.8.
- 9. The process of claim 8 wherein said salt solution has an ionic strength of about 0.15 to about 0.6.
- 10. The process of claim 8 wherein the pH of the aqueous protein solution is adjusted to a pH of about 5.3 to about 6.2.
- 11. The process of claim 1 wherein said oil seed meal is canola oil seed meal and, following said separation of the aqueous protein solution from the residual canola seed meal, the aqueous protein solution is subjected continuously to a pigment removal step.
- 12. The process of claim 11 wherein said pigment removal step is effected by diafiltration of the aqueous protein solution.
- 13. The process of claim 11 wherein said pigment removal step is effected by continuously mixing a pigment adsorbing agent with the aqueous protein solution and subsequently continuously removing the pigment adsorbing agent from the aqueous protein isolation.
- 14. The process of claim 13 wherein the pigment adsorbing agent is powdered activated carbon.
- 15. The process of claim 1 wherein said oil seed meal is continuously extracted by water and, subsequent thereto, salt is continuously added to the resulting aqueous protein solution to provide an aqueous protein solution having an ionic strength of at least about 0.10.
- 16. The process of claim 1 wherein said concentration step is effected by ultrafiltration to produce a concentrated protein solution having a protein content of at least about 200 g/L.
- 17. The process of claim 16 wherein said concentration step is effected to produce a concentrated protein solution having a protein content of at least about 250 g/L.
- 18. The process of claim 16 wherein said concentrated protein solution is warmed to a temperature of at least about 20° C. to decrease the viscosity of the concentrated protein solution but not beyond a temperature above which the temperature of the concentrated protein solution does not permit micelle formation.
- 19. The process of claim 18 wherein said concentrated protein solution is warmed to a temperature of about 25° C. to about 40° C.
- 20. The process of claim 1 wherein said concentrated protein solution is continuously mixed with said chilled water to provide a dilution of the concentrated protein solution by about 15 fold or less
- 21. Thc process of claim 20 wherein said chilled water has a temperature of less than about 10° C.
- 22. The process of claim 21 wherein said dilution is by about 10 fold or less.
- 23. The process of claim 1 wherein said recovered protein micellar mass is dried to a proteinaceous powder.
- 24. The process of claim 1 wherein said recovered protein micellar mass has a protein content of at least about 100 wt % (N×6.25).
- 25. The process of claim 1 wherein said supernatant is processed, on a batch, semi-continuous or continuous basis, to recover additional qualities of protein isolate therefrom.
- 26. The process of claim 25 wherein said additional quantities of protein solution are recovered from the overflowing supernatant by concentrating the supernatant to a protein concentration of about 100 to about 400 g/L, preferably about 200 to about 300 g/L, and drying the concentrated supernatant to produce a protein isolate having a protein content of at least about 90 wt % (N×6.25), preferably at least about 100 wt %, and which is substantially undenatured (as determined by differential scanning calorimetry).
- 27. The process of claim 25 wherein said additional quantities of protein isolate was recovered from tie overflowing supernatant by concentrating The supernatant to a protein concentration of about 100 to about 400 g/L, preferably about 200 to about 300 g/L, mixing the concentrated supernatant with the recovered protein micellar mass, and drying the mixture to obtain a protein while having a protein content of at least about 90 wt % (N×6.25), preferably at least about 100 wt %, and which is substantially indenatured (as determined by differential scanning calorimetry).
- 28. The process of claim 25 wherein said additional quantities of protein isolate are recovered from the supernatant by concentrating the overflowing supernatant to a protein concentration of about 100 to about 400 g/L, preferably about 200 to about 300 g/L, mixing a portion of the concentrated supernatant with at least a portion of the recovered protein micellar mass, and drying the resulting mixture, and optionally drying the remainder of the concentrated supernatant and the remainder of the recovered protein micellar mass.
- 29. The process of claim 1 wherein said oil seed meal is canola oil seed meal.
- 30. The process of claim 29 wherein said canola oil seed meal is cold pressed canola oil seed meal.
- 31. The process of claim 29 wherein said canola oil seed meal is white flake.
- 32. The process of claim 29 wherein said canola oil seed meal is derived from a non-genetically modified canola oil seed.
- 33. The process of claim 29 wherein said canola oil seed meal is low temperature desolventized canola oil seed meal
- 34. The process of claim 1 wherein said oil seed meal is rapeseed meal.
- 35. The process of claim 1 wherein said oil seed meat is mustard seed meal.
REFERENCE TO RELATED APPLICATIONS
[0001] This application claim priority under 35 USC 119(e) from U.S. Provisional Patent Applications Nos. 60/331,646 filed Nov. 20, 2001 and 60/383,809 filed May 30, 2002.
Provisional Applications (2)
|
Number |
Date |
Country |
|
60331646 |
Nov 2001 |
US |
|
60383809 |
May 2002 |
US |