Methods involving whey protein isolates
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IPC분류정보
국가/구분 |
United States(US) Patent
등록
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국제특허분류(IPC7판) |
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출원번호 |
US-0123960
(2005-05-06)
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등록번호 |
US-7378123
(2008-05-27)
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발명자
/ 주소 |
- Etzel,Mark R.
- Helm,Thomas R.
- Vyas,Harit K.
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출원인 / 주소 |
- Wisconsin Alumni Research
- Grande Cheese Company
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대리인 / 주소 |
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인용정보 |
피인용 횟수 :
2 인용 특허 :
5 |
초록
▼
The present invention concerns methods and compositions that involve whey protein isolates. Methods of the invention include purification processes for preparing whey proteins that are substantially nondenatured across a range of pH, including their isoelectric points. As such, they have low turbidi
The present invention concerns methods and compositions that involve whey protein isolates. Methods of the invention include purification processes for preparing whey proteins that are substantially nondenatured across a range of pH, including their isoelectric points. As such, they have low turbidity in solution across a wide range of pH values. Whey protein isolates can be integrated into compositions and solutions that have nutritional, pharmaceutical, and other applications.
대표청구항
▼
What is claimed is: 1. A method for preparing nondenatured whey proteins comprising: a) contacting whey proteins to a cation exchange support under conditions to allow whey proteins to be adsorbed to the support; b) flowing a buffered desorption solution having a pH of about 10.5 or more across the
What is claimed is: 1. A method for preparing nondenatured whey proteins comprising: a) contacting whey proteins to a cation exchange support under conditions to allow whey proteins to be adsorbed to the support; b) flowing a buffered desorption solution having a pH of about 10.5 or more across the support, wherein the desorbed whey proteins are nondenatured; and c) collecting the desorbed nondenatured whey proteins, wherein each buffered desorption solution that contacts the support is about pH 10.5 or higher. 2. The method of claim 1, wherein the buffered desorption solution has a pH between about 10.5 and about 13. 3. The method of claim 2, wherein the buffered desorption solution has a pH of about 11.5. 4. The method of claim 1, wherein the support is on a bead, membrane, or paddle. 5. The method of claim 4, wherein the support is on a bead. 6. The method of claim 5, wherein the bead is in a resin or gel. 7. The method of claim 6, wherein the resin or gel is in a non-reacting structure. 8. The method of claim 7, wherein the non-reacting structure is a column. 9. The method of claim 5, wherein the beads have a diameter between about 30 μm and about 500 μm. 10. The method of claim 9, wherein the beads have a diameter between about 100 μm and about 300 μm. 11. The method of claim 1, wherein the buffer is selected from the group consisting of phosphate and citrate. 12. The method of claim 11, wherein the buffer is phosphate. 13. The method of claim 1, wherein the concentration of buffer in the buffered desorption solution is between about 0.5 mM and about 100 mM. 14. The method of claim 13, wherein the concentration of buffer in the buffered desorption solution is less than about 20 mM. 15. The method of claim 1, wherein the buffered desorption solution comprises salt. 16. The method of claim 9, wherein the salt is a sodium salt. 17. The method of claim 16, wherein the sodium salt is sodium phosphate. 18. The method of claim 16, wherein the buffered desorption solution further comprises sodium chloride. 19. The method of claim 1, wherein the buffered desorption solution flows across the support at a flow rate between about 10 support volumes per hour and about 200 support volumes per hour. 20. The method of claim 19, wherein the flow rate is between about 50 support volumes per hour and about 150 support volumes per hour. 21. The method of claim 1, wherein whey proteins are in a solution having a pH between about 1 and about 7 when contacted with the support. 22. The method of claim 21, wherein whey proteins are in a solution having a pH between about 4 and 7 when contacted with the support. 23. The method of claim 1, further comprising subjecting the desorbed whey proteins to ultrafiltration. 24. The method of claim 1, further comprising drying the desorbed whey proteins. 25. The method of claim 1, wherein desorbed whey proteins is spray dried. 26. The method of claim 1, wherein the desorbed whey proteins have a turbidity below about 400 NTU across a pH range between about 2 and about 8 when in a solution comprising 25 mg/ml of desorbed whey proteins. 27. The method of claim 26, wherein the desorbed whey proteins have a turbidity below about 200 NTU across a pH range between about 2 and about 8 when in a solution comprising 25 mg/ml of desorbed whey proteins. 28. The method of claim 27, wherein the desorbed whey proteins have a turbidity below about 100 NTU across a pH range between about 2 and about 8 when in a solution comprising 25 mg/ml of desorbed whey proteins.
이 특허에 인용된 특허 (5)
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Gandhi Amita, Clear or translucent liquid beverage with souluble fiber and nutrients.
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Etzel Mark R., Isolating .beta.-lactoglobulin and .alpha.-lactalbumin by eluting from a cation exchanger without sodium chloride.
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Kuwata Tamotsu (Saitama JPX) Ohtomo Hideo (Tokyo JPX), Method for removing
b
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