US4384898A
Expired / Lapsed
US
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Process for producing cyclodextrins
Assignee: Nihon Shokuhin Kako Co Ltd
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Filing: 1981-07-20
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Granted: 1983-05-24
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Expires: 2001-07-20
Abstract
Abstract This invention relates to a process for producing cyclodextrins, which comprises passing a solution containing cyclodextrins and reducing sugars as primary ingredients through a column packed with alkali or alkali earth metal salts of strongly acidic cation exchange resin to separate and collect cyclodextrins from the sugar solution.
Inventors
- 👤 Minoru Okada
- 👤 Masamitsu Matsuzawa
- 👤 Osamu Uezima
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-28 19:22
CPC Classifications
C; C08; C08B; C08B37/00; C08B37/0006; C08B37/0009; C08B37/0012; Y; Y10; Y10S; Y10S435/00; Y10S435/803
Claims Analysis
Total Claims: 10
Claim 1
Independent Claim
122 words
A process for the production and recovery of cyclodextrins which consists of the steps of: (a) reacting gelatinized or liquefied starch with cyclodextrin glycosyltransferase to prepare a mixture containing cyclodextrins and acyclic dextrins; (b) reacting said mixture from step (a) with a saccharogenic enzyme capable of hydrolyzing said acyclic dextrins and having substantially no hydrolytic action on said cyclodextrins, to convert said acyclic dextrins into reducing sugars, whereby a sugar solution containing cyclodextrins and reducing sugars as primary components is obtained; (c) passing said sugar solution from step (b) through a column packed with an alkali or an alkaline earth metal salt of a strongly acidic cation exchange resin; and (d) eluting the cyclodextrins from the column with water to recover them.
Claim 2
Dependent Claim
122 words
A process for the production and recovery of cyclodextrins which consists of the steps of: (a) reacting gelatinized or liquefied starch with cyclodextrin glycosyltransferase to prepare a mixture containing cyclodextrins and acyclic dextrins; (b) reacting said mixture from step (a) with a saccharogenic enzyme capable of hydrolyzing said acyclic dextrins and having substantially no hydrolytic action on said cyclodextrins, to convert said acyclic dextrins into reducing sugars, whereby a sugar solution containing cyclodextrins and reducing sugars as primary components is obtained; (c) passing said sugar solution from step (b) through a column packed with an alkali or an alkaline earth metal salt of a strongly acidic cation exchange resin; and (d) eluting the cyclodextrins from the column with water to recover them.
Claim 3
Dependent Claim
32 words
The process according to claim 1, wherein said saccharogenic enzyme is selected from the group consisting of glucoamylase, β-amylase, a mixture of α-1,6-glucosidase with glucoamylase, and a mixture of α-1,6-glucosidase with β-amylase.
Claim 4
Dependent Claim
21 words
The process according to claim 1, wherein said strongly acidic cation exchange resin is a cross-linked styrene-divinylbenzene copolymer having sulfonyl groups.
Claim 5
Dependent Claim
133 words
A process for the production and recovery of α-cyclodextrin which consists of the steps of: (a) reacting gelatinized or liquefied starch with cyclodextrin glycosyltransferase to prepare a mixture containing α, β and γ-cyclodextrins and acyclic dextrins; (b) reacting the mixture from step (a) with a saccharogenic enzyme capable of hydrolyzing said acyclic dextrins, γ-cyclodextrin and β-cyclodextrin, said enzyme having substantially no hydrolytic action on α-cyclodextrin, whereby said γ-cyclodextrin and β-cyclodextrin and said acyclic dextrins are converted into reducing sugars, and a sugar solution is obtained containing α-cyclodextrin and reducing sugars as primary ingredients; (c) passing the sugar solution from step (b) through a column packed with an alkali or an alkaline earth metal salt of a strongly acidic cation exchange resin; and (d) eluting α-cyclodextrin with water from the column to recover it.
Claim 6
Dependent Claim
133 words
A process for the production and recovery of α-cyclodextrin which consists of the steps of: (a) reacting gelatinized or liquefied starch with cyclodextrin glycosyltransferase to prepare a mixture containing α, β and γ-cyclodextrins and acyclic dextrins; (b) reacting the mixture from step (a) with a saccharogenic enzyme capable of hydrolyzing said acyclic dextrins, γ-cyclodextrin and β-cyclodextrin, said enzyme having substantially no hydrolytic action on α-cyclodextrin, whereby said γ-cyclodextrin and β-cyclodextrin and said acyclic dextrins are converted into reducing sugars, and a sugar solution is obtained containing α-cyclodextrin and reducing sugars as primary ingredients; (c) passing the sugar solution from step (b) through a column packed with an alkali or an alkaline earth metal salt of a strongly acidic cation exchange resin; and (d) eluting α-cyclodextrin with water from the column to recover it.
Claim 7
Dependent Claim
38 words
The process according to claim 4, wherein said saccharogenic enzyme is selected from the group consisting of bacterial saccharogenic α-amylase, fungal α-amylase, a mixture of bacterial saccharogenic α-amylase with glucoamylase, and a mixture of fungal α-amylase with glucoamylase.
Claim 8
Dependent Claim
21 words
The process according to claim 4, wherein said strongly acidic cation exchange resin is a cross-linked styrene-divinylbenzene copolymer having sulfonyl groups.
Claim 9
Dependent Claim
33 words
The process according to claim 1, wherein the particle size of the resin is 20-200 mesh and said step (c) is carried out at a temperature of 50°-80° C., and pH of 3-6.
Claim 10
Dependent Claim
33 words
The process according to claim 4, wherein the particle size of the resin is 20-200 mesh and said step (c) is carried out at a temperature of 50°-80° C., and pH of 3-6.
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USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1986-05-23 | 1986-11-22 | 1987-05-24 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1990-05-23 | 1990-11-22 | 1991-05-24 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1994-05-23 | 1994-11-22 | 1995-05-24 | $7700.00 | Window Closed / Lapsed |