IP Library Granted Patent US 11,324,237
Granted Patent B2
US 11,324,237 · App. 16/402,413 · Granted May 10, 2022

Tasteful natural sweetener and flavor

Inventors: Jingang Shi (Beijing, CN); Hansheng Wang (Beijing, CN); Xin Shi (Beijing, CN); Yi Wang (Beijing, CN); Wei Lv (Beijing, CN); Yingxiang Xin (Beijing, CN); Thomas Eidenberger (Beijing, CN); Weiyao Shi (Bethlehem, PA)
Assignee: EPC Natural Products Co., Ltd.
A23L2/60A21D2/181A21D2/245A21D2/26A23C9/1307A23C9/156A23C9/1526A23F5/465A23L2/02A23L2/38A23L2/54A23L2/56A23L2/66A23L27/11A23L27/215A23L27/31A23L27/33A23L27/34A23L27/36A23L27/88A23L33/105A23L33/125A23L33/145A23L33/175A23L33/18A23F3/405A23G3/36A23L2/58A23V2002/00A23V2250/262A23V2250/266A23V2250/54A23V2250/60
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Quick Facts
Patent No.
US 11,324,237
App. No.
16/402,413
Granted
May 10, 2022
Kind
B2
Abstract

The invention describes products, uses thereof, compositions thereof, and methods to prepare products formed from Maillard reaction products from a sugar donor and/or sweet tea extracts, stevia extracts, swingle (mogroside) extracts, one or more sweet tea extract components, one or more steviol glycosides, one or more mogrosides, one or more glycosylated sweet tea glycosides, one or more glycosylated steviol glycosides or one or more glycosylated mogrosides and an amine donor/reactant.

Claims (19)

1. A sweetener or flavoring agent composition, comprising: one or more Maillard reaction product(s) (MRPs) formed from a Maillard reaction mixture comprising: (a) a glycosylated steviol glycoside; and (b) one or more amine donor(s) having a free amino group, wherein (a) and (b) undergo Maillard reaction, at a temperature between 50-250° C. wherein either: (1) the reaction mixture further includes one or more non-nutritive sweeteners or one or more sweetener enhancer(s), or (2) the one or more non-nutritive sweeteners or one or more sweetener enhancer(s) are added to the MRPs following completion of the Maillard reaction, and wherein the one or more MRPs improve the taste of the sweetener or flavoring agent composition; wherein the taste improvement is determined by a consesus of a sensory panel of four trained human tasters; wherein the taste improvement is in terms of bitternes, sweetness onset, aftertaste, and/or sweetness linger.

2. The sweetener or flavoring agent composition of claim 1 , wherein the one or more amine donor(s) comprise one or more of a primary amine compound, a secondary amine compound, an amino acid, a protein, a peptide, a yeast extract or a mixture thereof.

3. The sweetener or flavoring agent composition of claim 2 , wherein the one or more amino donor(s) comprise one or more amino acids selected from the group consisting of alanine, arginine, asparagine, aspartic acid, cysteine, glutamine, glutamic acid, glycine, histidine, isoleucine, leucine, lysine, methionine, phenylalanine, proline, serine, threonine, tryptophan, tyrosine, and valine.

4. The sweetener or flavoring agent composition of claim 1 , wherein the one or more non-nutritive sweetener(s) or the one or more sweetener enhancer(s) are selected from the group consisting of sorbitol, xylitol, mannitol, sucralose, aspartame, acesulfame-K, neotame, erythritol, trehalose, raffinose, cellobiose, tagatose, allulose, inulin, [N-[3-(3-hydroxy-4-methoxyphenyl)propyl]-alpha-aspartyl]-L-phenylalanine 1-methyl ester, glycyrrhizin, sodium cyclamate, brazzein, miraculin, curculin, pentadin, mabinlin, thaumatin, neohesperidin dihydrochalcone (NHDC), maltol and advantame.

5. The sweetener or flavoring agent composition of claim 1 , wherein (a) and (b) undergo Maillard reaction at a temperature between 90-120° C.

6. The sweetener or flavoring agent composition of claim 1 , further comprising a sweetening agent selected from the group consisting of sweet tea extracts, swingle extracts, sweet tea glycosides, mogrosides, glycosylated sweet tea glycosides, glycosylated mogrosides and mixtures thereof.

7. A method for preparing a sweetener or flavoring agent composition, comprising the steps of: preparing a Maillard reaction mixture comprising (a) a glycosylated steviol glycoside and (b) one or more amine donor(s) comprising a free amino group; heating the reaction mixture at a temperature between 50-250° C., wherein (a) and (b) undergo Maillard reaction to form a Maillard reaction product (RP) composition that comprise one or more MRP 5 ; and mixing the MRP composition with a non-nutritive sweetener or sweetener enhancer to form the sweetener or flavoring agent composition, wherein the MRP composition improves the taste of the beverage; wherein the taste improvement is determined by a consensus of a sensory panel of four trained human tasters; wherein the taste improvement is in terms of bitterness, sweetness onset, aftertaste, and/or sweetness linger.

8. The method of claim 7 , wherein the one or more amine donor(s) comprise one or more of a primary amine compound, a secondary amine compound, an amino acid, a protein, a peptide, a yeast extract or a mixture thereof.

9. The method of claim 7 , wherein the one or more amino donor(s) comprise one or more amino acids selected from the group consisting of alanine, arginine, asparagine, aspartic acid, cysteine, glutamine, glutamic acid, glycine, histidine, isoleucine, leucine, lysine, methionine, phenylalanine, proline, serine, threonine, tryptophan, tyrosine, and valine.

10. The method of claim 7 , wherein the one or more non-nutritive sweetener(s) or the one or more sweetener enhancer(s) are selected from the group consisting of sorbitol, xylitol, mannitol, sucralose, aspartame, acesulfame-K, neotame, erythritol, trehalose, raffinose, cellobiose, tagatose, allulose, inulin, N—[N-[3-(3-hydroxy-4-methoxyphenyl)propyl]-alpha-aspartyl]-L-phenylalanine 1-methyl ester, glycyrrhizin, sodium cyclamate, brazzein, miraculin, curculin, pentadin, mabinlin, thaumatin, neohesperidin dihydrochalcone (NHDC), maltol and advantame.

11. The method of claim 7 , wherein (a) and (b) undergo Maillard reaction at a temperature between 90-120° C.

12. The method of claim 7 , further comprising the step of adding to the sweetener or flavoring composition a sweetening agent selected from the group consisting of sweet tea extracts, swingle extracts, sweet tea glycosides, mogrosides, glycosylated sweet tea glycosides, glycosylated mogrosides and mixtures thereof.

13. A method for improving a taste and/or mouthfeel profile of a food or beverage, comprising the steps of: preparing a Maillard reaction mixture comprising (a) a glycosylated steviol glycoside and (b) and one or more amine donor(s) comprising a free amino group; heating the reaction mixture at atemperature between 50-250° C., wherein (a) and (b) undergo Maillard reaction to form a Maillard reaction product (MRP) composition comprising one or more MRP 5 ; and adding the MRP composition to a food or beverage, wherein either: ( 1 ) the reaction mixture further includes a non-nutritive sweetener or a sweetener enhancer, or ( 2 ) a non-nutritive sweetener or sweetener enhancer is added to the MRP composition, and wherein the taste and/or mouthfeel profile of the food or beverage is improved after adding the MRP composition thereto; wherein the taste improvement is determined by a consensus of a sensory panel of four trained human tasters; wherein the taste improvement is in terms of bitterness, sweetness onset, aftertaste, and/or sweetness linger.

14. The method of claim 13 , wherein the one or more amine donor(s) comprise a primary amine compound, a secondary amine compound, an amino acid, a protein, a peptide, or a mixture thereof.

15. The method of claim 13 , wherein the one or more amino donor(s) comprise one or more amino acids selected from the group consisting of alanine, arginine, asparagine, aspartic acid, cysteine, glutamine, glutamic acid, glycine, histidine, isoleucine, leucine, lysine, methionine, phenylalanine, proline, serine, threonine, tryptophan, tyrosine, and valine.

16. The method of claim 13 , wherein the one or more non-nutritive sweetener(s) or the one or more sweetener enhancer(s) are selected from the group consisting of sorbitol, xylitol, mannitol, sucralose, aspartame, acesulfame-K, neotame, erythritol, trehalose, raffinose, cellobiose, tagatose, allulose, inulin, N—[N-[3-(3-hydroxy-4-methoxyphenyl)propyl]-alpha-aspartyl]L-phenylalanine 1-methyl ester, glycyrrhizin, sodium cyclamate, brazzein, miraculin, curculin, pentadin, mabinlin, thaumatin, neohesperidin dihydrochalcone (NHDC), maltol and advantame.

17. The method of claim 13 , wherein (a) and (b) undergo Maillard reaction at a temperature between 90-120° C.

18. The method of claim 13 , further comprising the step of adding to the sweetener or flavoring composition a sweetening agent selected from the group consisting of sweet tea extracts, swingle extracts, sweet tea glycosides, mogrosides, glycosylated sweet tea glycosides, glycosylated mogrosides and mixtures thereof.

19. A food or beverage having an improved taste and/or mouthfeel, wherein the food or beverage comprises the sweetener or flavoring agent composition of claim 1 , and wherein the sweetener or flavoring agent composition improves the taste of the food or beverage; wherein the taste improvement is determined by a consensus of a sensory panel of four trained human tasters; wherein the taste improvement is in terms of bitterness, sweetness onset, aftertaste, and/or sweetness linger.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 20, 2026
From: EPC NATURAL PRODUCTS CO., LTD.
To: EPC NEXTASTE PTE. LTD.
Reel/Frame 075717/0201 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 15, 2019
From: SHI, JINGANG; WANG, HANSHENG; SHI, XIN; WANG, YI; LV, WEI; XIN, YINGXIANG; EIDENBERGER, THOMAS; SHI, WEIYAO
To: EPC NATURAL PRODUCTS CO., LTD.
Reel/Frame 050718/0378 →
Continuity (8)
Provisional Application 62841858 · May 2, 2019
Provisional Application 62819980 · Mar 18, 2019
Provisional Application 62775983 · Dec 6, 2018
Provisional Application 62771485 · Nov 26, 2018
Provisional Application 62744755 · Oct 12, 2018
Provisional Application 62696481 · Jul 11, 2018
Provisional Application 62668580 · May 8, 2018
Related Publication 20200107567A1 · Apr 9, 2020
Cited By (2)
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