IP Library Granted Patent US 8,647,844
Granted Patent B2
US 8,647,844 · App. 13/567,707 · Granted Feb 11, 2014

Glucosyl stevia composition

Inventor: Avetik Markosyan (Yerevan, AM)
Assignee: PureCircle USA Inc.
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Quick Facts
Patent No.
US 8,647,844
App. No.
13/567,707
Granted
Feb 11, 2014
Kind
B2
Abstract

Glucosyl stevia compositions are prepared from steviol glycosides of Stevia rebaudiana Bertoni. The glucosylation was performed by cyclodextrin glucanotransferase using the starch as source of glucose residues. The short-chain glucosyl stevia compositions were purified to >95% content of total steviol glycosides. The compositions can be used as sweetness enhancers, flavor enhancers and sweeteners in foods, beverages, cosmetics and pharmaceuticals.

Claims (63)

1. A sweetener composition comprising a highly purified glucosyl stevia composition made by a process comprising the steps of:

(a) adding starch into water to form a starch suspension;

(b) adding a mixture of α-amylase and CGTase into the starch suspension and incubating for about 0.5 to 2 hours at about 75-80° C., resulting in a liquefied starch suspension;

(c) inactivating the α-amylase by low pH heat treatment; cooling the liquefied starch suspension and adjusting the pH to about 5.5 to 7.0;

(d) adding steviol glycosides into the liquefied starch suspension, resulting in a reaction mixture;

(e) adding a second batch of CGTase into the reaction mixture and incubating for about 12 to 48 hours at about 55-75° C.;

(f) adding β-amylase to reaction mixture and incubating for about 12-24 hours at about 35-55° C.;

(g) inactivating the enzymes in the reaction mixture by heat treatment;

(h) decolorizing the reaction mixture;

(i) removing non-diterpene compounds by contacting the decolorized reaction mixture with macroporous adsorbent resin and subsequently eluting adsorbed diterpene glycosides with aqueous ethanol to result in a glycoside-containing aqueous ethanol eluate;

(j) desalting the glycoside-containing aqueous ethanol eluate with ion-exchange resins;

(k) removing ethanol from the aqueous ethanol eluate, resulting in an aqueous eluate;

(l) concentrating and drying the aqueous eluate to obtain the highly purified glucosyl stevia composition; and

(m) adding an additional sweetening agent,

wherein the highly purified glucosyl stevia composition comprises greater than about 34% by weight di-, tri- and tetraglucosyl steviol glycosides, and unmodified steviol glycosides, and the additional sweetening agent is selected from the group consisting of: stevia extract, steviol glycosides, stevioside, Rebaudioside A, Rebaudioside B, Rebaudioside C, Rebaudioside D, Rebaudioside E, Rebaudioside F, dulcoside A, steviolbioside, rubusoside, other steviol glycosides found in Stevia rebaudiana Bertoni plant and mixtures thereof, Luo Han Guo extract, mogrosides, high-fructose corn syrup, corn syrup, invert sugar, fructooligosaccharides, inulin, inulooligosaccharides, coupling sugar, maltooligosaccharides, maltodextins, corn syrup solids, glucose, maltose, sucrose, lactose, aspartame, saccharin, sucralose, sugar alcohols, and a combination thereof.

2. The sweetener composition of claim 1 , wherein the highly purified glucosyl stevia composition comprises greater than about 25% by weight di-, tri- and tetraglucosyl Rebaudioside A and greater than about 9% tri- and tetraglucosyl steviosides.

3. A flavor composition comprising a highly purified glucosyl stevia composition made by a process comprising the steps of:

(a) adding starch into water to form a starch suspension;

(b) adding a mixture of α-amylase and CGTase into the starch suspension and incubating for about 0.5 to 2 hours at about 75-80° C., resulting in a liquefied starch suspension;

(c) inactivating the α-amylase by low pH heat treatment; cooling the liquefied starch suspension and adjusting the pH to about 5.5 to 7.0;

(d) adding steviol glycosides into the liquefied starch suspension, resulting in a reaction mixture;

(e) adding a second batch of CGTase into the reaction mixture and incubating for about 12 to 48 hours at about 55-75° C.;

(f) adding β-amylase to reaction mixture and incubating for about 12-24 hours at about 35-55° C.;

(g) inactivating the enzymes in the reaction mixture by heat treatment;

(h) decolorizing the reaction mixture;

(i) removing non-diterpene compounds by contacting the decolorized reaction mixture with macroporous adsorbent resin and subsequently eluting adsorbed diterpene glycosides with aqueous ethanol to result in a glycoside-containing aqueous ethanol eluate;

(j) desalting the glycoside-containing aqueous ethanol eluate with ion-exchange resins;

(k) removing ethanol from the aqueous ethanol eluate, resulting in an aqueous eluate;

(l) concentrating and drying the aqueous eluate to obtain the highly purified glucosyl stevia composition; and

(m) adding an additional flavoring agent,

wherein the highly purified glucosyl stevia composition comprises greater than about 34% by weight di-, tri- and tetraglucosyl steviol glycosides, and unmodified steviol glycosides, and the additional flavoring agent is selected from the group consisting of: lemon, orange, fruity, banana, grape, pear, pineapple, mango, bitter almond, cola, cinnamon, sugar, cotton candy, vanilla, and a combination thereof.

4. The flavor composition of claim 3 , wherein the highly purified glucosyl stevia composition comprises greater than about 25% by weight di-, tri- and tetraglucosyl Rebaudioside A and greater than about 9% tri- and tetraglucosyl steviosides.

5. A food ingredient comprising a highly purified glucosyl stevia composition made by a process comprising the steps of:

(a) adding starch into water to form a starch suspension;

(b) adding a mixture of α-amylase and CGTase into the starch suspension and incubating for about 0.5 to 2 hours at about 75-80° C., resulting in a liquefied starch suspension;

(c) inactivating the α-amylase by low pH heat treatment; cooling the liquefied starch suspension and adjusting the pH to about 5.5 to 7.0;

(d) adding steviol glycosides into the liquefied starch suspension, resulting in a reaction mixture;

(e) adding a second batch of CGTase into the reaction mixture and incubating for about 12 to 48 hours at about 55-75° C.;

(f) adding β-amylase to reaction mixture and incubating for about 12-24 hours at about 35-55° C.;

(g) inactivating the enzymes in the reaction mixture by heat treatment;

(h) decolorizing the reaction mixture;

(i) removing non-diterpene compounds by contacting the decolorized reaction mixture with macroporous adsorbent resin and subsequently eluting adsorbed diterpene glycosides with aqueous ethanol to result in a glycoside-containing aqueous ethanol eluate;

(j) desalting the glycoside-containing aqueous ethanol eluate with ion-exchange resins;

(k) removing ethanol from the aqueous ethanol eluate, resulting in an aqueous eluate;

(l) concentrating and drying the aqueous eluate to obtain the highly purified glucosyl stevia composition; and

(m) adding an additional food agent,

wherein the highly purified glucosyl stevia composition comprises greater than about 34% by weight di-, tri- and tetraglucosyl steviol glycosides, and unmodified steviol glycosides, and the additional food ingredient is selected from the group consisting of: acidulants, organic and amino acids, coloring agents, bulking agents, modified starches, gums, texturizers, preservatives, antioxidants, emulsifiers, stabilisers, thickeners, gelling agents, and a combination thereof.

6. The food ingredient of claim 5 , wherein the highly purified glucosyl stevia composition comprises greater than about 25% by weight di-, tri- and tetraglucosyl Rebaudioside A and greater than about 9% tri- and tetraglucosyl steviosides.

7. A food, beverage, cosmetic or pharmaceutical product comprising a highly purified glucosyl stevia composition made by a process comprising the steps of:

(a) adding starch into water to form a starch suspension;

(b) adding a mixture of α-amylase and CGTase into the starch suspension and incubating for about 0.5 to 2 hours at about 75-80° C., resulting in a liquefied starch suspension;

(c) inactivating the α-amylase by low pH heat treatment; cooling the liquefied starch suspension and adjusting the pH to about 5.5 to 7.0;

(d) adding steviol glycosides into the liquefied starch suspension, resulting in a reaction mixture;

(e) adding a second batch of CGTase into the reaction mixture and incubating for about 12 to 48 hours at about 55-75° C.;

(f) adding β-amylase to reaction mixture and incubating for about 12-24 hours at about 35-55° C.;

(g) inactivating the enzymes in the reaction mixture by heat treatment;

(h) decolorizing the reaction mixture;

(i) removing non-diterpene compounds by contacting the decolorized reaction mixture with macroporous adsorbent resin and subsequently eluting adsorbed diterpene glycosides with aqueous ethanol to result in a glycoside-containing aqueous ethanol eluate;

(j) desalting the glycoside-containing aqueous ethanol eluate with ion-exchange resins;

(k) removing ethanol from the aqueous ethanol eluate, resulting in an aqueous eluate; and

(l) concentrating and drying the aqueous eluate to obtain the highly purified glucosyl stevia composition;

wherein the highly purified glucosyl stevia composition comprises greater than about 34% by weight di-, tri- and tetraglucosyl steviol glycosides, and unmodified steviol glycosides.

8. The food, beverage, cosmetic or pharmaceutical product of claim 7 , wherein the highly purified glucosyl stevia composition comprises greater than about 25% by weight di-, tri- and tetraglucosyl Rebaudioside A and greater than about 9% tri- and tetraglucosyl steviosides.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 18, 2017
From: MARKOSYAN, AVETIK
To: PURECIRCLE USA
Reel/Frame 041008/0212 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 18, 2017
From: PURECIRCLE USA/PURECIRCLE USA, INC.
To: PURECIRCLE SDN BHD
Reel/Frame 041008/0316 →
Continuity (2)
Division 13029263 · Feb 17, 2011
Related Publication 20120301589A1 · Nov 29, 2012