Steviol glycosides
US-2016213039-A1 · Jul 28, 2016 · US
US11066688B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11066688-B2 |
| Application number | US-201615742561-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 11, 2016 |
| Priority date | Jul 10, 2015 |
| Publication date | Jul 20, 2021 |
| Grant date | Jul 20, 2021 |
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The present invention relates to a composition comprising one or more steviol glycosides which composition comprises nitrogen in an amount of no more than about 1000 ppm. The invention also relates to a method for preparing a steviol glycoside composition, which method comprises: providing a steviol glycoside composition; combining the steviol glycoside composition with water to form a steviol glycoside solution; and crystallizing a steviol glycoside composition from the solution. The invention also relates to a method for reducing the nitrogen content of a steviol glycoside composition, which method comprises: providing a steviol glycoside composition which comprises nitrogen; combining the steviol glycoside composition with water to form a steviol glycoside solution; and crystallizing a steviol glycoside composition from the solution, thereby to reduce the amount of nitrogen in the steviol glycoside composition.
Opening claim text (preview).
The invention claimed is: 1. A method for preparing a steviol glycoside composition, which method comprises: providing a fermentation broth comprising a steviol glycoside; subjecting the fermentation broth to a solid-liquid separation and a crystallization, to yield a first steviol glycoside composition; combining the first steviol glycoside composition with water to form a steviol glycoside solution; and recrystallizing, at pH 7.0 or above, a second steviol glycoside composition from the steviol glycoside solution, wherein: the resulting second steviol glycoside composition comprises less nitrogen than the first steviol glycoside composition; the nitrogen in the resulting second steviol glycoside composition is no more than 800 ppm; and the resulting second steviol glycoside composition comprises at least 80% on a dry weight basis of at least one steviol glycoside selected from the group consisting of rebaudioside A, rebaudioside D, and rebaudioside M. 2. The method according to claim 1 , wherein the first steviol glycoside composition comprises at least 95% on a dry weight basis of at least one steviol glycoside. 3. The method according to claim 2 , wherein the crystallization is carried out at pH 8.0 or above. 4. The method according to claim 3 , wherein the resulting second steviol glycoside composition comprises nitrogen in an amount of no more than about 500 ppm. 5. The method according to claim 4 , wherein the resulting second steviol glycoside composition comprises nitrogen in an amount of no more than about 100 ppm. 6. The method according to claim 5 , wherein the resulting second steviol glycoside composition further comprises one or more of any one of rebaudioside B, rebaudioside C, rebaudioside E, rebaudioside F, stevioside, dulcoside A, rubusoside or steviolbioside. 7. The method according to claim 6 , wherein the resulting second steviol glycoside composition comprises at least 95% on a dry weight basis of at least one steviol glycoside. 8. The method according to claim 7 , wherein the first steviol glycoside composition comprises at least 80% on a dry weight basis of at least one steviol glycoside. 9. The method according to claim 7 , wherein the crystallization is carried out at pH 9.0 or above. 10. The method according to claim 7 , wherein the resulting second steviol glycoside composition comprises nitrogen in an amount of no more than about 200 ppm. 11. The method according to claim 7 , wherein the resulting second steviol glycoside composition comprises nitrogen in an amount of no more than about 50 ppm. 12. The method according to claim 7 , wherein the resulting second steviol glycoside composition comprises at least 97% on a dry weight basis of rebaudioside A. 13. The method according to claim 7 , wherein the resulting second steviol glycoside composition comprises at least 97% on a dry weight basis of rebaudioside D. 14. The method according to claim 7 , wherein the resulting second steviol glycoside composition comprises at least 97% on a dry weight basis of rebaudioside M.
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