Functionalized beta-sheet peptide stabilized membrane proteins, constructs comprising same, and methods of forming and using same
US-2017259217-A1 · Sep 14, 2017 · US
US12268227B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12268227-B2 |
| Application number | US-201716762887-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 9, 2017 |
| Priority date | Nov 9, 2017 |
| Publication date | Apr 8, 2025 |
| Grant date | Apr 8, 2025 |
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The present invention relates to a process for preparing of a food concentrate in which an aqueous starting solution from a foodstuff is concentrated by osmosis with a semi-permeable biomimetic membrane. In addition, the present invention relates to a food concentrate which can be produced by the process according to the invention, a food concentrate which is free of disturbing aroma components with an OAV (odour activity value) ≥1 and which does not contain any solvent additives. Furthermore, the present invention relates to the use of the food concentrates and products comprising the food concentrate according to the invention.
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The invention claimed is: 1. A process for preparing a food concentrate comprising: preparing an aqueous starting solution from a food, wherein the aqueous starting solution is a vapor condensate obtained from a fruit or a vegetable, concentrating the aqueous starting solution by forward osmosis with a semi-permeable biomimetic membrane, and thereby forming a food concentrate as a retentate; wherein the semipermeable biomimetic membrane comprises: vesicles of liposomes comprising at least one aquaporin protein incorporated therein or vesicles of polymersomes comprising at least one aquaporin protein incorporated therein; a thin film composite matrix in which the vesicles are embedded; and a carrier layer; wherein the osmosis is carried out at a temperature in a range of 10° C. to 40° C.; and wherein the aqueous starting solution is concentrated by a factor of 20 to 1000. 2. A process according to claim 1 , wherein the liposome comprises lipids selected from DPhPC, DOPC, mixed soybean lipids, asolectin, mixed lipids of E. coli , or combinations thereof; and wherein the polymersome comprises: triblock copolymers of the hydrophilic-hydrophobic-hydrophilic-type (A-B-A, A-B-C, C-B-A, wherein A is PMOXA, B is PDMS and C is PEO), diblock copolymers of the hydrophilic-hydrophobic type (A-B, wherein A is PB and B is PEO), or combinations thereof. 3. A process according to claim 1 , wherein the aquaporin protein comprises at least one selected from the group consisting of AQP0, AqpZ, SoPIP2, AQP10, and their isoforms. 4. A process according to claim 1 , wherein the thin film composite matrix is prepared by polymerizing an aqueous solution of an amine with a solution of an acid chloride in an organic solvent. 5. A process according to claim 1 , comprising recovering in the retentate aroma substances having an OAV (odour activity value) ≥1 in the aqueous starting solution wherein a recovery rate of the aroma substances having an OAV ≥1 in the aqueous starting solution is >90% in the retentate, by weight relative to the aroma substances having an OAV ≥1 in the aqueous starting solution. 6. A process according to claim 1 , comprising recovering in the retentate aroma substances having a log-sensory recovery coefficient W>3 in the aqueous starting solution wherein the recovery rate of aroma substances having log-sensory recovery coefficient W of the aroma substances with W>−3, is ≥50%; by weight relative to the aroma substances having a log-sensory recovery coefficient W>−3 in the aqueous starting solution. 7. A process according to claim 1 , wherein the aqueous starting solution comprises ethanol, and wherein any remaining ethanol content in the retentate is reduced by at least 50%, by weight relative to the ethanol content in the aqueous starting solution.
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