IP Library Granted Patent US 11,241,031
Granted Patent B2
US 11,241,031 · App. 16/594,313 · Granted Feb 8, 2022

Rebaudioside A and stevioside with improved solubilities

Inventors: Mel Clinton Jackson (Waikoloa, HI); Samuel Mel Jackson (Honolulu, HI); Dean Edward Francis (Bellingham, WA)
Assignee: SWEET GREEN FIELDS USA, LLC
A23L33/125A23C9/1307A23L2/02A23L2/60A23L5/00A23L27/30A23L27/34A23L27/36A23L29/30C07H1/08C07H15/24C07H15/256A23L7/00A23L21/00A23V2002/00A23V2200/00A23V2200/132A23V2250/262A23V2250/61
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Quick Facts
Patent No.
US 11,241,031
App. No.
16/594,313
Granted
Feb 8, 2022
Kind
B2
Abstract

The invention describes sweetening compositions and methods to prepare sweetening compositions containing steviol glycosides, salts, and other natural or synthetic sweeteners with improved solubilities and sensory profiles.

Claims (35)

1. A method for improving sensory profile of a steviol glycoside (SG) composition comprising rebaudioside A (RA), comprising:

introducing one or more salts and one or more non-SG sweeteners into the SG composition to produce a final product comprising:

RA in an amount between 70-85 wt % of the final product,

RB in an amount between 10-25 wt % of the final product,

the one or more salts in an amount between 0.1-5% wt. % of the final product, and

one or more non-SG sweeteners in an amount between 1-10 wt. % of the final product,

wherein the one or more salts are selected from the group consisting of a metal or metal alkali halide, a metal or metal alkali carbonate or bicarbonate, a metal or metal alkali sulfate or metabisulfate, and any combination thereof, and

wherein the one or more non-SG sweeteners are selected from the group consisting of sucrose, fructose, maltose, lactose, xylitol, sorbitol, dextrose, glucose, mannitol, aspartame, inulin, sucralose, acesulfame-K, sodium cyclamate, erythritol, thaumatin, arabinose, galactose, mannose, rhamnose, xylose, trehalose, raffinose, cellobiose, tagatose, allulose, mogroside, and any combination thereof.

2. The method of claim 1 , wherein the one or more salts are selected from the group consisting of sodium chloride, potassium chloride, magnesium chloride, sodium sulfate, magnesium sulfate, potassium sulfate, sodium carbonate, potassium carbonate, magnesium carbonate, sodium bicarbonate, potassium bicarbonate, calcium chloride and any combination thereof.

3. The method of claim 1 , wherein the one or more salts are selected from the group consisting of sodium chloride, potassium chloride, sodium carbonate, and any combination thereof.

4. The method of claim 1 , wherein the one or more non-SG sweeteners are selected from the group consisting of fructose, glucose and sucralose.

5. The method of claim 1 , wherein the final product comprises an additional SG in an amount less than about 2 wt %.

6. The method of claim 5 , wherein the additional SG is rebaudioside C, stevioside, or steviolbioside.

7. The method of claim 1 , wherein the final product has increased solubility compared to the SG composition.

8. The method of claim 1 , wherein the final product has an improved sensory profile compared to the SG composition.

9. The method of claim 1 , wherein the final product comprises one or more non-SG sweeteners in an amount between 1-5 wt. % of the final product.

10. The method of claim 1 , wherein the final product comprises one or more non-SG sweeteners in an amount between 5-10 wt. % of the final product.

11. The method of claim 1 , wherein the final product comprises:

RA in an amount between 70-80 wt % of the final product,

RB in an amount between 10-20 wt % of the final product,

the one or more salts in an amount between 0.1-5% wt. % of the final product, and

one or more non-SG sweeteners in an amount between 1-10 wt. % of the final product.

12. A method for improving sensory profile of a steviol glycoside (SG) composition comprising rebaudioside A (RA), comprising:

(a) adding rebaudioside B (RB) to the SG composition, hydrolyzing at least some of the RA in the SG composition to form RB, or both; and

(b) adding one or more salts and one or more non-SG sweeteners into the SG composition,

wherein the one or more salts are selected from the group consisting of a metal or metal alkali halide, a metal or metal alkali carbonate or bicarbonate, a metal or metal alkali sulfate or metabisulfate, and any combination thereof, and

wherein the one or more non-SG sweeteners are selected from the group consisting of sucrose, fructose, maltose, lactose, xylitol, sorbitol, dextrose, glucose, mannitol, aspartame, inulin, sucralose, acesulfame-K, sodium cyclamate, erythritol, thaumatin, arabinose, galactose, mannose, rhamnose, xylose, trehalose, raffinose, cellobiose, tagatose, allulose, mogroside, and any combination thereof,

wherein steps (a) and (b) are carried out so that a modified composition resulting thereof comprises:

RA in an amount between 70-85 wt % of the modified SG composition,

RB in an amount between 10-25 wt % of the modified SG composition,

the one or more salts in an amount between 0.1-5% wt. % of modified SG composition, and

the one or more non-SG sweeteners in an amount between 1-10 wt. % of the modified SG composition.

13. The method of claim 12 , wherein RB is added to the SG composition.

14. The method of claim 12 , wherein at least some of the RA in the SG composition is hydrolyzed to form RB by adding an alkali to the SG composition.

15. The method of claim 14 , wherein the alkali is sodium hydroxide.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 1, 2025
From: SWEET GREEN FIELDS USA LLC
To: TATE & LYLE TECHNOLOGY LIMITED
Reel/Frame 072431/0286 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 18, 2020
From: JACKSON, MEL CLINTON; JACKSON, SAMUEL MEL; FRANCIS, DEAN EDWARD
To: SWEET GREEN FIELDS USA, LLC
Reel/Frame 051847/0282 →
Continuity (4)
Continuation 16103787 · Aug 14, 2018
Continuation In Part 14739887 · Jun 15, 2015
Provisional Application 62012936 · Jun 16, 2014
Related Publication 20200029612A1 · Jan 30, 2020