Starch-derived clathrate-forming compositions
US-11959114-B2 · Apr 16, 2024 · US
US11408019B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11408019-B2 |
| Application number | US-201615780706-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 2, 2016 |
| Priority date | Dec 4, 2015 |
| Publication date | Aug 9, 2022 |
| Grant date | Aug 9, 2022 |
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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.
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The invention claimed is: 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 .
Coating with compositions containing vegetable or microbial fermentation gums, e.g. cellulose or derivatives; Coating with edible polymers, e.g. polyvinyalcohol · CPC title
Preparation or treatment of foods or foodstuffs, in general; Food or foodstuffs obtained thereby; Materials therefor · CPC title
produced by the action of a carbohydrase {(EC 3.2.x)}, e.g. by alpha-amylase {, e.g. by cellulase, hemicellulase} · CPC title
alpha-D-Glucans, e.g. polydextrose, alternan, glycogen; (alpha-1,4)(alpha-1,6)-D-Glucans; (alpha-1,3)(alpha-1,4)-D-Glucans, e.g. isolichenan or nigeran; (alpha-1,4)-D-Glucans; (alpha-1,3)-D-Glucans, e.g. pseudonigeran; Derivatives thereof · CPC title
containing gelling or thickening agents (marmalades, jams, jellies or other similar fruit or vegetable compositions A23L21/10) · CPC title
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