IP Library Granted Patent US 11,408,019
Granted Patent B2
US 11,408,019 · App. 15/780,706 · Granted Aug 9, 2022

Alpha-glucan mixture, its preparation and uses

Inventors: Seiichiro Kishishita (Okayama, JP); Shoko Kanashima (Okayama, JP); Manabu Miyata (Okayama, JP); Takuo Yamamoto (Okayama, JP); Katsuhiko Hino (Okayama, JP); Tomoyuki Nishimoto (Okayama, JP)
Assignee: HAYASHIBARA CO., LTD.
C12P19/04A23L5/00A23L7/109A23L29/00A23L29/20A23L29/269A23L29/35A23P20/105A23P30/10A61K9/20A61K47/36C08B37/0009C08J5/18C12P19/14A23B5/06C08J2305/00C12P19/18C12Y302/01094
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Quick Facts
Patent No.
US 11,408,019
App. No.
15/780,706
Granted
Aug 9, 2022
Kind
B2
Abstract

An object of the present invention is to provide an α-glucan mixture in a preferable molecular weight range, which can be made into a transparent film with advantageous strength and water solubility when an edible film is made by using the α-glucan mixture without adding any plasticizer. The above object is solved by providing an α-glucan mixture, which is obtainable by a process comprising the steps of gelatinizing waxy starch and liquefying the resulting gelatinized waxy starch by allowing an amylase to act on it, having the following characteristics (1) and (2): (1) having the weight average molecular weight (Mw) in a range of 150 kDa to 3,000 kDa; and (2) having the value of dividing weight average molecular weight (Mw) with number average molecular weight (Mn), Mw/Mn, of 35.1 or lower.

Claims (39)

1. An α-glucan mixture, which is obtainable by a process comprising the steps of gelatinizing waxy starch and liquefying the resulting gelatinized waxy starch by allowing an amylase to act on it, having the following characteristics (1) to (3):

(1) having the weight average molecular weight (Mw) in a range of 150 kDa to 3,000 kDa;

(2) having the value of dividing weight average molecular weight (Mw) with number average molecular weight (Mn), Mw/Mn, of 35.1 or lower; and

(3) forming a hydrolyzate with isomaltose content of less than 22% by weight, on a dry solid basis of the hydrolyzate, when digested by isomaltodextranase (EC 3.2.1.94).

2. The α-glucan mixture of claim 1 , which contains a-glucan having an isomaltose structure at the non-reducing end.

3. The α-glucan mixture of claim 2 , wherein said α-glucan mixture forms isomaltose in an amount of over 3% by weight but less than 22% by weight, on a dry solid basis of the hydrolyzate, when digested by isomaltodextranase (EC 3.2.1.94).

4. The α-glucan mixture of claim 3 , wherein said waxy starch is waxy corn starch.

5. The α-glucan mixture of claim 3 , which further has the following characteristic:

a film obtained by steps of molding the α-glucan mixture without plasticizer and drying, with a thickness of 40 to 50 mu.m, exhibits a rupture strength of piercing of 2.0 N/mm 2 or higher when analyzed on a piercing test for rupture strength using an adaptor with a sectional area of 1 mm 2 .

6. The α-glucan mixture of claim 3 , which can be made into a homogeneous solution when dissolved into water by admixing with deionized water to give a solid concentration of 20% by weight and stirring at 30° C. for 15 min.

7. An edible film, which is obtainable by steps of molding the α-glucan mixture of claim 3 , without adding any plasticizer and drying and exhibits a rupture strength of piercing of 2.0 N/mm 2 or higher when analyzed on a piercing test for rupture strength using an adaptor with a sectional area of 1 mm 2 .

8. The α-glucan mixture of claim 2 , wherein said waxy starch is waxy corn starch.

9. The α-glucan mixture of claim 2 , which further has the following characteristic:

a film obtained by steps of molding the α-glucan mixture without plasticizer and drying, with a thickness of 40 to 50 mu.m, exhibits a rupture strength of piercing of 2.0 N/mm 2 or higher when analyzed on a piercing test for rupture strength using an adaptor with a sectional area of 1 mm 2 .

10. The α-glucan mixture of claim 2 , which can be made into a homogeneous solution when dissolved into water by admixing with deionized water to give a solid concentration of 20% by weight and stirring at 30° C. for 15 min.

11. An edible film, which is obtainable by steps of molding the α-glucan mixture of claim 2 , without adding any plasticizer and drying and exhibits a rupture strength of piercing of 2.0 N/mm 2 or higher when analyzed on a piercing test for rupture strength using an adaptor with a sectional area of 1 mm 2 .

12. The α-glucan mixture of claim 1 , wherein said waxy starch is waxy corn starch.

13. The α-glucan mixture of claim 1 , which further has the following characteristic:

a film obtained by steps of molding the a-glucan mixture without plasticizer and drying, with a thickness of 40 to 50 mu.m, exhibits a rupture strength of piercing of 2.0 N/mm 2 or higher when analyzed on a piercing test for rupture strength using an adaptor with a sectional area of 1 mm 2 .

14. The α-glucan mixture of claim 1 , which can be made into a homogeneous solution when dissolved into water by admixing with deionized water to give a solid concentration of 20% by weight and stirring at 30° C. for 15 min.

15. A process for producing the α-glucan mixture of claim 1 , comprising the steps of:

gelatinizing waxy starch by heating a waxy starch suspension with a solid concentration of 20% by weight; and

forming α-glucan mixture having the weight average molecular weight (Mw) in a range of 150 kDa to 3,000 kDa by allowing an amylase to act on the resulting gelatinized waxy starch.

16. The process of claim 15 , further comprising a step of allowing an α-glucosyltransferase, which acts on starch hydrolyzate and catalyzes α-1,6 transglucosylation reaction to the non-reducing end of the starch hydrolyzate, to act on the formed α-glucan mixture.

17. The process of claim 16 , wherein said α-glucosyltransferase is derived from a microorganism of the genus Bacillus or Arthrobacter and has the following characteristics (A) to (F):

(A) Action

Acting on maltose and/or α-1,4 glucan having a glucose polymerization degree of 3 or higher, catalyzing mainly α-1,4 transglucosylation reaction and α-1,6 transglucosylation reaction, and transferring glucose to the C-4 or C-6 hydroxyl group of the glucose residue at the non-reducing end;

(B) Molecular weight

90,000±10,000 daltons on SDS-polyacrylamide gel electrophoresis;

(C) Optimum temperature

About 50° C. when reacted at pH 6.0 for 30 min;

(D) Optimum pH

About pH 6.0 when reacted at 40° C. for 30 min;

(E) Thermal stability

Stable up to the temperature of 40° C. when incubated at pH 6.0 for 60 min;

and

(F) pH stability

Stable in the range of pH 4.0 to 8.0 when incubated at 4° C. for 24 hours.

18. An edible film, which is obtainable by the steps of molding the α-glucan mixture of claim 1 , without adding any plasticizer and drying and exhibits a rupture strength of piercing of 2.0 N/mm 2 or higher when analyzed on a piercing test for rupture strength using an adaptor with a sectional area of 1 mm 2 .

Assignments (3)
CHANGE OF NAME Recorded Mar 18, 2025
From: HAYASHIBARA CO., LTD.
To: NAGASE VIITA CO., LTD.
Reel/Frame 070538/0828 →
CORRECTIVE ASSIGNMENT TO CORRECT THE THE LAST NAME OF THE FIRST INVENTOR PREVIOUSLY RECORDED AT REEL: 046186 FRAME: 0937. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Jun 2, 2022
From: HINO, KATSUHIKO; KISHISHITA, SEIICHIRO; MIYATA, MANABU; KANASHIMA, SHOKO; YAMAMOTO, TAKUO; NISHIMOTO, TOMOYUKI
To: HAYASHIBARA CO., LTD.
Reel/Frame 060255/0318 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 25, 2018
From: KINISHITA, SEIICHIRO; HINO, KATSUHIKO; MIYATA, MANABU; KANASHIMA, SHOKO; YAMAMOTO, TAKUO; NISHIMOTO, TOMOYUKI
To: HAYASHIBARA CO., LTD.
Reel/Frame 046186/0937 →
Priority Claims (1)
JP JP2015-237947 · Dec 4, 2015 · national
Continuity (1)
Related Publication 20180346949A1 · Dec 6, 2018