US20020065410A1 - Branched starches and branched starch hydrolyzates - Google Patents

Branched starches and branched starch hydrolyzates Download PDF

Info

Publication number
US20020065410A1
US20020065410A1 US09/725,990 US72599000A US2002065410A1 US 20020065410 A1 US20020065410 A1 US 20020065410A1 US 72599000 A US72599000 A US 72599000A US 2002065410 A1 US2002065410 A1 US 2002065410A1
Authority
US
United States
Prior art keywords
starch
alpha
glycosidic linkages
amylose
hydrolyzate
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US09/725,990
Inventor
Richard Antrim
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Grain Processing Corp
Original Assignee
Grain Processing Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Grain Processing Corp filed Critical Grain Processing Corp
Priority to US09/725,990 priority Critical patent/US20020065410A1/en
Assigned to GRAIN PROCESSING CORPORATION reassignment GRAIN PROCESSING CORPORATION ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: ANTRIM, RICHARD L.
Publication of US20020065410A1 publication Critical patent/US20020065410A1/en
Priority to US10/226,809 priority patent/US6803459B2/en
Abandoned legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P19/00Preparation of compounds containing saccharide radicals
    • C12P19/18Preparation of compounds containing saccharide radicals produced by the action of a glycosyl transferase, e.g. alpha-, beta- or gamma-cyclodextrins
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L29/00Foods or foodstuffs containing additives; Preparation or treatment thereof
    • A23L29/30Foods or foodstuffs containing additives; Preparation or treatment thereof containing carbohydrate syrups; containing sugars; containing sugar alcohols, e.g. xylitol; containing starch hydrolysates, e.g. dextrin
    • A23L29/35Degradation products of starch, e.g. hydrolysates, dextrins; Enzymatically modified starches
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08BPOLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B30/00Preparation of starch, degraded or non-chemically modified starch, amylose, or amylopectin
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08BPOLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B30/00Preparation of starch, degraded or non-chemically modified starch, amylose, or amylopectin
    • C08B30/12Degraded, destructured or non-chemically modified starch, e.g. mechanically, enzymatically or by irradiation; Bleaching of starch
    • C08B30/18Dextrin, e.g. yellow canari, white dextrin, amylodextrin or maltodextrin; Methods of depolymerisation, e.g. by irradiation or mechanically

Definitions

  • This invention relates to novel branched starch and starch hydrolyzates, solutions thereof, and methods of making and using them.
  • amylose is a linear polymer of glucose linked by alpha 1-4 glycosidic bonds.
  • Amylopectin is a branched polymer of glucose containing up to 4% alpha 1-6 glycosidic bonds and about 96% alpha 1-4 glycosidic bonds. It is the 1-6 bonds which create the branches in an otherwise linear polymer.
  • Starch normally is found in nature as a mixture of about 25% amylose and 75% amylopectin. So called waxy varieties of plants exist which contain up to 100% amylopectin.
  • Corn processed by the corn processing industry is, for the most part, dent corn, although small amounts of waxy or a high amylose variety are also processed into specialty products.
  • Amylose molecules or partial hydrolyzates thereof because they are linear tend to associate through hydrogen bonding with themselves and with other amylose molecules to form essentially water-insoluble aggregates.
  • the process of insolubilization is usually termed retrogradation. This phenomenon is problematic in the starch processing industry in that it causes processing difficulties in the production of carbohydrate products from starch. Perhaps more importantly, retrogradation phenomena cause defects in product quality, such as hazing, precipitation and clouding in solutions of the carbohydrates. Stable solutions of carbohydrates are deemed desirable in the industry.
  • the present invention provides a starch that includes at least one glucose polymer having greater than 4% alpha 1-6 glycosidic linkages.
  • the present invention further provides a starch hydrolyzate that includes at least one glucose oligomer having greater than 4% alpha 1-6 glycosidic linkages.
  • the starch and starch hydrolyzate of the present invention provide stable aqueous solutions that would not be attainable with unbranched linear poly- or oligo-saccharides.
  • the present invention provides a stable aqueous starch solution that includes one or more amylose molecules that are branched by one or more alpha 1-6 glycosidic linkages.
  • the present invention also provides a stable aqueous starch hydrolyzate solution that includes one or more amylose hydrolyzate molecules that are branched by one or more alpha 1-6 glycosidic linkages.
  • the present invention further provides a method of improving the aqueous solution stability of a starch that contains amylose molecules, which method includes introducing one or more alpha 1-6 glycosidic linkages so as to branch one or more of the amylose molecules in the starch.
  • the method of the present invention also can be applied to starch hydrolyzates, preferably those that contain amylose hydrolyzates.
  • the present invention provides a method of improving the aqueous solution stability of a starch hydrolyzate, which method includes introducing one or more alpha 1-6 glycosidic linkages so as to branch one or more of the amylose hydrolyzate molecules in the starch hydrolyzate.
  • the method of the present invention similarly applies to amylose and amylose hydrolyzates.
  • the present invention provides a method of improving the aqueous solution stability of amylose by introducing one or more alpha 1-6 glycosidic linkages so as to branch one or more of the amylose molecules.
  • the present invention also provides a method of improving the aqueous solution stability of an amylose hydrolyzate by introducing one or more alpha 1-6 glycosidic linkages so as to branch one or more amylose hydrolyzate molecules.
  • the present invention is predicated on the discovery that starch branching enzymes derived from, for example, corn, rice or potato, or produced from microbes as a result of a cloned plant gene, when used to treat starches or starch hydrolyzates such as malto-oligosaccharides can significantly improve the properties of starches or starch hydrolyzates such as malto-oligosaccharides.
  • starch branching enzymes derived from, for example, corn, rice or potato, or produced from microbes as a result of a cloned plant gene
  • starches or starch hydrolyzates such as malto-oligosaccharides
  • a 1-6 branch points are introduced. Up to 10% or even higher of the glycosidic bonds can be provided as ⁇ 1-6 bonds (i.e., alpha 1-6 bonds).
  • starches or starch hydrolyzates so treated can be derived for any number of sources, such as corn, wheat, barley, rice, and the like.
  • Starch hydrolyzates are described, for example, in U.S. patent application Ser. Nos. 09/366,065, 09/378,673 and 60/139,184, and in International Patent Application No. PCT/US99/10198, all of which are incorporated herein by reference.
  • the branched species are more stable in solution resulting in reduced tendency to haze or precipitate.
  • the branched species exhibit novel and useful function properties such as viscosity, higher achievable solution concentrations, flowability, coating behavior, solution thickening behavior and film-forming properties.
  • Physiological properties such as rate of caloric release or glycemic response are improved, opening opportunities for use in nutraceutical products.
  • Enzymes known as starch branching enzymes exist in all plants that contain amylopectin starch, and function in nature to create ⁇ 1-6 branches during synthesis of starch in the plant. These enzymes, although known to starch scientists for years, have not been seriously considered for commercial use because they occurred in minute amounts in plants and were not produced commercially. Although the branching enzymes are still not produced commercially today, the potential exists for commercial and inexpensive production as a result of modern methods of DNA cloning whereby a gene from a plant such as corn, rice or potato coding for synthesis of starch branching enzyme can be cloned into microbes. Most enzymes used for commercial conversion of starch today are produced by large-scale microbial fermentation.
  • the present invention provides a starch that includes at least one glucose polymer having greater than 4% alpha 1-6 glycosidic linkages.
  • the number of alpha 1-6 glycosidic linkages in the starch of the present invention exceeds that of even pure amylopectin.
  • the starch of the present invention preferably includes a glucose polymer having greater than about 5% alpha 1-6 glycosidic linkages, but more preferably includes a glucose polymer having greater than about 6% alpha 1-6 glycosidic linkages.
  • the starch of the present invention includes a glucose polymer having greater than about 7% alpha 1-6 glycosidic linkages, for example, from about 8% to about 10% alpha 1-6 glycosidic linkages, or even greater than 10% alpha 1-6 glycosidic linkages.
  • the present invention further provides a starch hydrolyzate that includes at least one glucose oligomer having greater than 4% alpha 1-6 glycosidic linkages.
  • the branched starch hydrolyzates of the present invention include branched partial starch hydrolyzates.
  • the number of alpha 1-6 glycosidic linkages in the starch of the present invention exceeds the number of such linkages that can be obtained even from hydrolyzates of pure amylopectin.
  • the starch hydrolyzate of the present invention preferably includes a glucose oligomer having greater than about 5% alpha 1-6 glycosidic linkages, but more preferably includes a glucose oligomer having greater than about 6% alpha 1-6 glycosidic linkages. Most preferably, the starch hydrolyzate of the present invention preferably includes a glucose oligomer having greater than about 7% alpha 1-6 glycosidic linkages, for example, from about 8% to about 10% alpha 1-6 glycosidic linkages, or even greater than 10% alpha 1-6 glycosidic linkages.
  • the starch of the present invention provides a stable aqueous solution that overcomes retrogradation problems typically associated with linear unbranched starch molecules.
  • the present invention provides a stable aqueous starch solution that includes one or more amylose molecules that are branched via one or more alpha 1-6 glycosidic linkages.
  • the amylose in the starch solution of the present invention contains at least about 4% alpha 1-6 glycosidic linkages, but more preferably contains at least about 5% alpha 1-6 glycosidic linkages, and still more preferably contains at least about 6% alpha 1-6 glycosidic linkages.
  • amylose in the starch solution of the present invention contains at least about 7% alpha 1-6 glycosidic linkages, for example, from about 8% to about 10% alpha 1-6 glycosidic linkages, or even greater than 10% alpha 1-6 glycosidic linkages.
  • the starch hydrolyzate of the present invention also provides a stable aqueous solution that overcomes retrogradation problems that can be associated with certain unbranched linear starch hydrolyzate molecules.
  • the present invention provides a stable aqueous starch hydrolyzate solution that includes one or more amylose hydrolyzate molecules that are branched via one or more alpha 1-6 glycosidic linkages.
  • the amylose hydrolyzate in the starch hydrolyzate solution of the present invention contains at least about 4% alpha 1-6 glycosidic linkages, but more preferably contains at least about 5% alpha 1-6 glycosidic linkages, and still more preferably contains at least about 6% alpha 1-6 glycosidic linkages.
  • amylose hydrolyzate in the starch hydrolyzate solution of the present invention contains at least about 7% alpha 1-6 glycosidic linkages, for example, from about 8% to about 10% alpha 1-6 glycosidic linkages, or even greater than 10% alpha 1-6 glycosidic linkages.
  • the present invention further provides methods of improving the aqueous solution stability of starch and hydrolyzates thereof.
  • the present invention provides a method of improving the aqueous solution stability of a starch that contains amylose molecules, which method includes introducing one or more alpha 1-6 glycosidic linkages so as to branch one or more of the amylose molecules in the starch.
  • the present invention also provide a method of improving the aqueous solution stability of a starch hydrolyzate that contains amylose hydrolyzate molecules, which method includes introducing one or more alpha 1-6 glycosidic linkages so as to branch one or more of the amylose hydrolyzate molecules in the starch hydrolyzate.
  • the method of the present invention likewise can be applied to a method of improving the solution stability of amylose.
  • the present invention provides a method of improving the aqueous solution stability of amylose, which method includes introducing one or more alpha 1-6 glycosidic linkages so as to branch one or more of the amylose molecules.
  • the method of the present invention applies to hydrolyzates of amylose.
  • the present invention provides a method of improving the aqueous solution stability of an amylose hydrolyzate, which method includes introducing one or more alpha 1-6 glycosidic linkages so as to branch one or more molecules of the amylose hydrolyzate.
  • a slurry of dent corn starch in water at about 30% solids is partially hydrolyzed with alpha amylase to form a solution of malto-oligosaccharides.
  • the DE of the solution is about 10.
  • about 50 IU of branching enzyme is added to the starch mixture and held for 4 hours at pH 6, and a temperature of 40° C.
  • a portion of the treated starch is concentrated to a syrup, and another portion is spray dried.
  • the alpha amylase is obtained from Genencor International, Inc.
  • the branching enzyme is obtained from sweet corn endosperm by water extraction of the ground endosperm and isolation of active fractions resulting from chromatography on a column of DEAE-cellulose.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Biochemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Polymers & Plastics (AREA)
  • Zoology (AREA)
  • Medicinal Chemistry (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nutrition Science (AREA)
  • Biotechnology (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Microbiology (AREA)
  • Food Science & Technology (AREA)
  • Molecular Biology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Polysaccharides And Polysaccharide Derivatives (AREA)

Abstract

The present invention provides a starch that includes at least one glucose polymer having greater than 4% alpha 1-6 glycosidic linkages. The present invention further provides a starch hydrolyzate that includes at least one glucose oligomer having greater than 4% alpha 1-6 glycosidic linkages. The starch and starch hydrolyzate present invention have improved aqueous solution stability and are less likely to retrograde than are solutions of unbranched linear starches or starch hydrolyzates.
The present invention further provides a method of improving the aqueous solution stability of a starch or a hydrolyzate thereof, which method includes introducing one or more alpha 1-6 glycosidic linkages so as to branch one or more of the linear polysaccharides or hydrolyzates thereof. The method of the present invention also includes a method of improving the aqueous solution stability of amylose and amylose hydrolyzates by introducing one or more alpha 1-6 glycosidic linkages so as to branch one or more molecules of amylose or hydrolyzate thereof.

Description

    CROSS-REFERENCE TO RELATED PATENT APPLICATIONS
  • This patent application claims priority to provisional U.S. Patent Application No. 60/168,785, filed on Dec. 2, 1999.[0001]
  • TECHNICAL FIELD OF THE INVENTION
  • This invention relates to novel branched starch and starch hydrolyzates, solutions thereof, and methods of making and using them. [0002]
  • BACKGROUND OF THE INVENTION
  • The molecular structure and origins of starch are well documented in the literature. Starch from plant sources typically exists in two forms, amylose and amylopectin. Amylose is a linear polymer of glucose linked by alpha 1-4 glycosidic bonds. Amylopectin is a branched polymer of glucose containing up to 4% alpha 1-6 glycosidic bonds and about 96% alpha 1-4 glycosidic bonds. It is the 1-6 bonds which create the branches in an otherwise linear polymer. Starch normally is found in nature as a mixture of about 25% amylose and 75% amylopectin. So called waxy varieties of plants exist which contain up to 100% amylopectin. Corn processed by the corn processing industry is, for the most part, dent corn, although small amounts of waxy or a high amylose variety are also processed into specialty products. [0003]
  • Amylose molecules or partial hydrolyzates thereof, because they are linear tend to associate through hydrogen bonding with themselves and with other amylose molecules to form essentially water-insoluble aggregates. The process of insolubilization is usually termed retrogradation. This phenomenon is problematic in the starch processing industry in that it causes processing difficulties in the production of carbohydrate products from starch. Perhaps more importantly, retrogradation phenomena cause defects in product quality, such as hazing, precipitation and clouding in solutions of the carbohydrates. Stable solutions of carbohydrates are deemed desirable in the industry. [0004]
  • As such, there is a need for new carbohydrates that form stable aqueous solutions as well as a need for a method of treating linear carbohydrates so as to overcome the retrogradation problems associated therewith. The present invention provides such carbohydrates and methods. These and other advantages of the present invention, as well as additional inventive features, will be apparent from the description of the invention provided herein. [0005]
  • THE INVENTION
  • The present invention provides a starch that includes at least one glucose polymer having greater than 4% alpha 1-6 glycosidic linkages. The present invention further provides a starch hydrolyzate that includes at least one glucose oligomer having greater than 4% alpha 1-6 glycosidic linkages. The starch and starch hydrolyzate of the present invention provide stable aqueous solutions that would not be attainable with unbranched linear poly- or oligo-saccharides. In this regard, the present invention provides a stable aqueous starch solution that includes one or more amylose molecules that are branched by one or more alpha 1-6 glycosidic linkages. The present invention also provides a stable aqueous starch hydrolyzate solution that includes one or more amylose hydrolyzate molecules that are branched by one or more alpha 1-6 glycosidic linkages. [0006]
  • The present invention further provides a method of improving the aqueous solution stability of a starch that contains amylose molecules, which method includes introducing one or more alpha 1-6 glycosidic linkages so as to branch one or more of the amylose molecules in the starch. The method of the present invention also can be applied to starch hydrolyzates, preferably those that contain amylose hydrolyzates. In this regard, the present invention provides a method of improving the aqueous solution stability of a starch hydrolyzate, which method includes introducing one or more alpha 1-6 glycosidic linkages so as to branch one or more of the amylose hydrolyzate molecules in the starch hydrolyzate. [0007]
  • The method of the present invention similarly applies to amylose and amylose hydrolyzates. In this respect, the present invention provides a method of improving the aqueous solution stability of amylose by introducing one or more alpha 1-6 glycosidic linkages so as to branch one or more of the amylose molecules. The present invention also provides a method of improving the aqueous solution stability of an amylose hydrolyzate by introducing one or more alpha 1-6 glycosidic linkages so as to branch one or more amylose hydrolyzate molecules. [0008]
  • DESCRIPTION OF THE INVENTION
  • The present invention is predicated on the discovery that starch branching enzymes derived from, for example, corn, rice or potato, or produced from microbes as a result of a cloned plant gene, when used to treat starches or starch hydrolyzates such as malto-oligosaccharides can significantly improve the properties of starches or starch hydrolyzates such as malto-oligosaccharides. By treatment of the starches or starch hydrolyzates, a 1-6 branch points are introduced. Up to 10% or even higher of the glycosidic bonds can be provided as α 1-6 bonds (i.e., alpha 1-6 bonds). The starches or starch hydrolyzates so treated can be derived for any number of sources, such as corn, wheat, barley, rice, and the like. Starch hydrolyzates are described, for example, in U.S. patent application Ser. Nos. 09/366,065, 09/378,673 and 60/139,184, and in International Patent Application No. PCT/US99/10198, all of which are incorporated herein by reference. [0009]
  • By introduction of additional branch points in starches or starch hydrolyzates over those naturally occurring in the amylopectin fraction of starch, a number of functional properties of commercial importance are greatly improved. Also, new useful functional properties are provided. For example, the branched species are more stable in solution resulting in reduced tendency to haze or precipitate. The branched species exhibit novel and useful function properties such as viscosity, higher achievable solution concentrations, flowability, coating behavior, solution thickening behavior and film-forming properties. Physiological properties such as rate of caloric release or glycemic response are improved, opening opportunities for use in nutraceutical products. Although applicant does not wish to be bound by any one particular theory, it is believed that the branches introduced to the starch or starch hydrolyzate of the present invention interfere with the inter- or intra-molecular association of molecules that would otherwise promote retrogradation. [0010]
  • Enzymes known as starch branching enzymes exist in all plants that contain amylopectin starch, and function in nature to create α 1-6 branches during synthesis of starch in the plant. These enzymes, although known to starch scientists for years, have not been seriously considered for commercial use because they occurred in minute amounts in plants and were not produced commercially. Although the branching enzymes are still not produced commercially today, the potential exists for commercial and inexpensive production as a result of modern methods of DNA cloning whereby a gene from a plant such as corn, rice or potato coding for synthesis of starch branching enzyme can be cloned into microbes. Most enzymes used for commercial conversion of starch today are produced by large-scale microbial fermentation. [0011]
  • Accordingly, the present invention provides a starch that includes at least one glucose polymer having greater than 4% alpha 1-6 glycosidic linkages. The number of alpha 1-6 glycosidic linkages in the starch of the present invention exceeds that of even pure amylopectin. The starch of the present invention preferably includes a glucose polymer having greater than about 5% alpha 1-6 glycosidic linkages, but more preferably includes a glucose polymer having greater than about 6% alpha 1-6 glycosidic linkages. Most preferably, the starch of the present invention includes a glucose polymer having greater than about 7% alpha 1-6 glycosidic linkages, for example, from about 8% to about 10% alpha 1-6 glycosidic linkages, or even greater than 10% alpha 1-6 glycosidic linkages. [0012]
  • The present invention further provides a starch hydrolyzate that includes at least one glucose oligomer having greater than 4% alpha 1-6 glycosidic linkages. It will be appreciated that the branched starch hydrolyzates of the present invention include branched partial starch hydrolyzates. The number of alpha 1-6 glycosidic linkages in the starch of the present invention exceeds the number of such linkages that can be obtained even from hydrolyzates of pure amylopectin. [0013]
  • The starch hydrolyzate of the present invention preferably includes a glucose oligomer having greater than about 5% alpha 1-6 glycosidic linkages, but more preferably includes a glucose oligomer having greater than about 6% alpha 1-6 glycosidic linkages. Most preferably, the starch hydrolyzate of the present invention preferably includes a glucose oligomer having greater than about 7% alpha 1-6 glycosidic linkages, for example, from about 8% to about 10% alpha 1-6 glycosidic linkages, or even greater than 10% alpha 1-6 glycosidic linkages. [0014]
  • The starch of the present invention provides a stable aqueous solution that overcomes retrogradation problems typically associated with linear unbranched starch molecules. In this regard, the present invention provides a stable aqueous starch solution that includes one or more amylose molecules that are branched via one or more alpha 1-6 glycosidic linkages. Preferably, the amylose in the starch solution of the present invention contains at least about 4% alpha 1-6 glycosidic linkages, but more preferably contains at least about 5% alpha 1-6 glycosidic linkages, and still more preferably contains at least about 6% alpha 1-6 glycosidic linkages. Most preferably, the amylose in the starch solution of the present invention contains at least about 7% alpha 1-6 glycosidic linkages, for example, from about 8% to about 10% alpha 1-6 glycosidic linkages, or even greater than 10% alpha 1-6 glycosidic linkages. [0015]
  • The starch hydrolyzate of the present invention also provides a stable aqueous solution that overcomes retrogradation problems that can be associated with certain unbranched linear starch hydrolyzate molecules. In this regard, the present invention provides a stable aqueous starch hydrolyzate solution that includes one or more amylose hydrolyzate molecules that are branched via one or more alpha 1-6 glycosidic linkages. Preferably, the amylose hydrolyzate in the starch hydrolyzate solution of the present invention contains at least about 4% alpha 1-6 glycosidic linkages, but more preferably contains at least about 5% alpha 1-6 glycosidic linkages, and still more preferably contains at least about 6% alpha 1-6 glycosidic linkages. Most preferably, the amylose hydrolyzate in the starch hydrolyzate solution of the present invention contains at least about 7% alpha 1-6 glycosidic linkages, for example, from about 8% to about 10% alpha 1-6 glycosidic linkages, or even greater than 10% alpha 1-6 glycosidic linkages. [0016]
  • The present invention further provides methods of improving the aqueous solution stability of starch and hydrolyzates thereof. In particular, the present invention provides a method of improving the aqueous solution stability of a starch that contains amylose molecules, which method includes introducing one or more alpha 1-6 glycosidic linkages so as to branch one or more of the amylose molecules in the starch. The present invention also provide a method of improving the aqueous solution stability of a starch hydrolyzate that contains amylose hydrolyzate molecules, which method includes introducing one or more alpha 1-6 glycosidic linkages so as to branch one or more of the amylose hydrolyzate molecules in the starch hydrolyzate. [0017]
  • The method of the present invention likewise can be applied to a method of improving the solution stability of amylose. Thus, in another embodiment the present invention provides a method of improving the aqueous solution stability of amylose, which method includes introducing one or more alpha 1-6 glycosidic linkages so as to branch one or more of the amylose molecules. The method of the present invention applies to hydrolyzates of amylose. In this respect, the present invention provides a method of improving the aqueous solution stability of an amylose hydrolyzate, which method includes introducing one or more alpha 1-6 glycosidic linkages so as to branch one or more molecules of the amylose hydrolyzate. [0018]
  • The following examples further illustrate the present invention but, of course, should not be construed as in any way limiting its scope.[0019]
  • EXAMPLE
  • This example illustrates the preparation of a branched starch hydrolyzate of the present invention. [0020]
  • A slurry of dent corn starch in water at about 30% solids is partially hydrolyzed with alpha amylase to form a solution of malto-oligosaccharides. The DE of the solution is about 10. Either during the alpha amylase hydrolysis or subsequent to the hydrolysis about 50 IU of branching enzyme is added to the starch mixture and held for 4 hours at pH 6, and a temperature of 40° C. A portion of the treated starch is concentrated to a syrup, and another portion is spray dried. The alpha amylase is obtained from Genencor International, Inc. The branching enzyme is obtained from sweet corn endosperm by water extraction of the ground endosperm and isolation of active fractions resulting from chromatography on a column of DEAE-cellulose. Compared to control solutions of malto-oligosaccharides, which are not treated with branching enzyme, the solutions resulting from treatment are stable against hazing upon storage. Spray dried malto-oligosaccharides which are treated with branching enzyme, when dissolved in water, form solutions which are clear and stable against hazing compared to non-treated controls. [0021]
  • While particular embodiments of the invention have been shown, it will be understood that the invention is not limited thereto since modifications may be made by those skilled in the art, particularly in light of the foregoing teachings. It is, therefore, contemplated by the appended claims to cover any such modifications as incorporate those features which constitute the essential features of these improvements within the true spirit and scope of the invention. [0022]

Claims (22)

What is claimed is:
1. A starch comprising at least one glucose polymer having greater than 4% alpha 1-6 glycosidic linkages.
2. The starch of claim 1, comprising a glucose polymer having greater than about 5% alpha 1-6 glycosidic linkages.
3. The starch of claim 1, comprising a glucose polymer having greater than about 6% alpha 1-6 glycosidic linkages.
4. The starch of claim 1, comprising a glucose polymer having greater than about 7% alpha 1-6 glycosidic linkages.
5. A starch hydrolyzate comprising at least one glucose oligomer having greater than 4% alpha 1-6 glycosidic linkages.
6. The starch hydrolyzate of claim 5, comprising a glucose oligomer having greater than about 5% alpha 1-6 glycosidic linkages.
7. The starch hydrolyzate of claim 5, comprising a glucose oligomer having greater than about 6% alpha 1-6 glycosidic linkages.
8. The starch hydrolyzate of claim 5, comprising a glucose oligomer having greater than about 7% alpha 1-6 glycosidic linkages.
9. A stable aqueous solution comprising the starch of claim 1, wherein said starch comprises one or more amylose molecules that are branched by one or more alpha 1-6 glycosidic linkages.
10. The solution of claim 9, wherein said amylose in said solution contains at least about 4% alpha 1-6 glycosidic linkages.
11. The solution of claim 9, wherein said amylose in said solution contains at least about 5% alpha 1-6 glycosidic linkages.
12. The solution of claim 9, wherein said amylose in said solution contains at least about 6% alpha 1-6 glycosidic linkages.
13. The solution of claim 9, wherein said amylose in said solution contains at least about 7% alpha 1-6 glycosidic linkages.
14. A stable aqueous solution comprising the starch hydrolyzate of claim 5, wherein said starch hydrolyzate comprises one or more amylose hydrolyzate molecules that are branched by one or more alpha 1-6 glycosidic linkages.
15. The solution of claim 14, wherein said amylose hydrolyzate in said solution contains at least about 4% alpha 1-6 glycosidic linkages.
16. The solution of claim 14, wherein said amylose hydrolyzate in said solution contains at least about 5% alpha 1-6 glycosidic linkages.
17. The solution of claim 14, wherein said amylose hydrolyzate in said solution contains at least about 6% alpha 1-6 glycosidic linkages.
18. The solution of claim 14, wherein said amylose hydrolyzate in said solution contains at least about 7% alpha 1-6 glycosidic linkages.
19. A method of improving the aqueous solution stability of a starch that contains amylose molecules, said method comprising introducing one or more alpha 1-6 glycosidic linkages so as to branch one or more of said amylose molecules in said starch.
20. A method of improving the aqueous solution stability of a starch hydrolyzate that contains amylose hydrolyzate molecules, said method comprising introducing one or more alpha 1-6 glycosidic linkages so as to branch one or more of said amylose hydrolyzate molecules in said starch hydrolyzate.
21. A method of improving the aqueous solution stability of amylose, said method comprising introducing one or more alpha 1-6 glycosidic linkages so as to branch one or more molecules of said amylose.
22. A method of improving the aqueous solution stability of an amylose hydrolyzate, said method comprising introducing one or more alpha 1-6 glycosidic linkages so as to branch one or more molecules of said amylose hydrolyzate.
US09/725,990 1999-12-02 2000-11-29 Branched starches and branched starch hydrolyzates Abandoned US20020065410A1 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
US09/725,990 US20020065410A1 (en) 1999-12-02 2000-11-29 Branched starches and branched starch hydrolyzates
US10/226,809 US6803459B2 (en) 1999-12-02 2002-08-23 Branched starches and branched starch hydrolyzates

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US16878599P 1999-12-02 1999-12-02
US09/725,990 US20020065410A1 (en) 1999-12-02 2000-11-29 Branched starches and branched starch hydrolyzates

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US10/226,809 Continuation US6803459B2 (en) 1999-12-02 2002-08-23 Branched starches and branched starch hydrolyzates

Publications (1)

Publication Number Publication Date
US20020065410A1 true US20020065410A1 (en) 2002-05-30

Family

ID=26864452

Family Applications (2)

Application Number Title Priority Date Filing Date
US09/725,990 Abandoned US20020065410A1 (en) 1999-12-02 2000-11-29 Branched starches and branched starch hydrolyzates
US10/226,809 Expired - Lifetime US6803459B2 (en) 1999-12-02 2002-08-23 Branched starches and branched starch hydrolyzates

Family Applications After (1)

Application Number Title Priority Date Filing Date
US10/226,809 Expired - Lifetime US6803459B2 (en) 1999-12-02 2002-08-23 Branched starches and branched starch hydrolyzates

Country Status (1)

Country Link
US (2) US20020065410A1 (en)

Cited By (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003106502A1 (en) * 2002-06-17 2003-12-24 Novozymes A/S Methods for producing dextrins using enzymes
WO2004022602A1 (en) * 2002-08-16 2004-03-18 Fresenius Kabi Deutschland Gmbh Highly branched, unsubstituted or low-substituted starch products, dialysis solution and plasma expander containing the same, and the use thereof
US20060019877A1 (en) * 2002-09-11 2006-01-26 Conradt Harald S Hasylated polypeptides
US20060217293A1 (en) * 2002-03-06 2006-09-28 Michele Orlando Coupling low-molecular substances to a modified polysaccharide
US20070134197A1 (en) * 2004-03-11 2007-06-14 Wolfram Eichner Conjugates of hydroxyalkyl starch and a protein, prepared by reductive amination
WO2008082298A2 (en) * 2006-12-29 2008-07-10 Nederlandse Organisatie Voor Toegepast Natuurwetenschappelijk Onderzoek Tno Novel slowly digestible storage carbohydrate
US20080274948A1 (en) * 2003-08-08 2008-11-06 Fresenius Kabi Deutschland Gmbh Conjugates of Hydroxyalkyl Starch and G-Csf
US20090047251A1 (en) * 2004-03-11 2009-02-19 Wolfram Eichner Conjugates of hydroxyalkyl starch and a protein
EP2070951A1 (en) 2007-12-14 2009-06-17 Fresenius Kabi Deutschland GmbH Method for producing a hydroxyalkyl starch derivatives with two linkers
EP2070950A1 (en) 2007-12-14 2009-06-17 Fresenius Kabi Deutschland GmbH Hydroxyalkyl starch derivatives and process for their preparation
US20100062973A1 (en) * 2005-03-11 2010-03-11 Fresenius Kabi Deutschland Gmbh Production of bioactive glycoproteins from inactive starting material
US20100311670A1 (en) * 2004-03-11 2010-12-09 Nobert Zander Conjugates of hydroxyalkyl starch and a protein, prepared by native chemical ligation
FR2955861A1 (en) * 2010-02-02 2011-08-05 Roquette Freres SOLUBLE GLUCOSE BRANCHES POLYMERS FOR PERITONEAL DIALYSIS
WO2012004004A1 (en) 2010-07-09 2012-01-12 Fresenius Kabi Deutschland Gmbh Nitric oxide delivering hydroxyalkyl starch derivatives
US8916518B2 (en) 2002-03-06 2014-12-23 Fresenius Kabi Deutschland Gmbh Coupling proteins to a modified polysaccharide
EP1369432B2 (en) 2002-06-06 2015-10-07 Roquette Frères Soluble highly branched glucose polymers and process for their preparation
FR3055898A1 (en) * 2016-09-15 2018-03-16 Roquette Freres NOVEL GLUCOSE POLYMERS FOR PERITONEAL DIALYSIS

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106572677A (en) 2014-05-08 2017-04-19 艾维贝合作公司 Chewy candy comprising a highly branched starch (HBS) and method for providing the same

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3974032A (en) * 1973-03-05 1976-08-10 Cpc International Inc. Low D.E. starch hydrolysates of improved stability prepared by enzymatic hydrolysis of dextrins
US4454161A (en) * 1981-02-07 1984-06-12 Kabushiki Kaisha Hayashibara Seibutsu Kagaku Kenkyujo Process for the production of branching enzyme, and a method for improving the qualities of food products therewith
US5904941A (en) * 1997-08-21 1999-05-18 National Starch And Chemical Investment Holding Corporation Use of enzymatically-treated starches as viscosifiers and their use in food products

Cited By (39)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060217293A1 (en) * 2002-03-06 2006-09-28 Michele Orlando Coupling low-molecular substances to a modified polysaccharide
US8466277B2 (en) 2002-03-06 2013-06-18 Fresenius Kabi Deutschland Gmbh Coupling low-molecular substances to a modified polysaccharide
US8916518B2 (en) 2002-03-06 2014-12-23 Fresenius Kabi Deutschland Gmbh Coupling proteins to a modified polysaccharide
EP1369432B2 (en) 2002-06-06 2015-10-07 Roquette Frères Soluble highly branched glucose polymers and process for their preparation
WO2003106502A1 (en) * 2002-06-17 2003-12-24 Novozymes A/S Methods for producing dextrins using enzymes
US7550446B2 (en) 2002-08-16 2009-06-23 Fresenius Kabi Deutschland Gmbh Highly branched, unsubstituted or low-substituted starch products, dialysis solution and plasma expander containing the same, and the use thereof
WO2004022602A1 (en) * 2002-08-16 2004-03-18 Fresenius Kabi Deutschland Gmbh Highly branched, unsubstituted or low-substituted starch products, dialysis solution and plasma expander containing the same, and the use thereof
US20060032400A1 (en) * 2002-08-16 2006-02-16 Fresenius Kabi Deutschland Gmbh Highly branched, unsubstituted or low-substituted starch products, dialysis solution and plasma expander containing the same, and the use thereof
US8475765B2 (en) 2002-09-11 2013-07-02 Fresenius Kabi Deutschland Gmbh Hydroxyalkyl starch derivatives
US8618266B2 (en) 2002-09-11 2013-12-31 Fresenius Kabi Deutschland Gmbh Hasylated polypeptides
US20110054152A1 (en) * 2002-09-11 2011-03-03 Fresenius Kabi Deutschland Gmbh Hydroxyalkyl Starch Derivatives
US20060019877A1 (en) * 2002-09-11 2006-01-26 Conradt Harald S Hasylated polypeptides
US20080274948A1 (en) * 2003-08-08 2008-11-06 Fresenius Kabi Deutschland Gmbh Conjugates of Hydroxyalkyl Starch and G-Csf
US20090047251A1 (en) * 2004-03-11 2009-02-19 Wolfram Eichner Conjugates of hydroxyalkyl starch and a protein
US8840879B2 (en) 2004-03-11 2014-09-23 Fresenius Kabi Deutschland Gmbh Conjugates of hydroxyalkyl starch and a protein
US8287850B2 (en) 2004-03-11 2012-10-16 Fresenius Kabi Deutschland Gmbh Conjugates of hydroxyalkyl starch and a protein, prepared by reductive amination
US20100311670A1 (en) * 2004-03-11 2010-12-09 Nobert Zander Conjugates of hydroxyalkyl starch and a protein, prepared by native chemical ligation
US20070134197A1 (en) * 2004-03-11 2007-06-14 Wolfram Eichner Conjugates of hydroxyalkyl starch and a protein, prepared by reductive amination
US20110200555A1 (en) * 2004-03-11 2011-08-18 Fresenius Kabi Deutschland Gmbh Conjugates of hydroxyalkyl starch and a protein
US8017739B2 (en) 2004-03-11 2011-09-13 Fresenius Kabi Deutschland Gmbh Conjugates of hydroxyalkyl starch and a protein
US20100062973A1 (en) * 2005-03-11 2010-03-11 Fresenius Kabi Deutschland Gmbh Production of bioactive glycoproteins from inactive starting material
US20100099864A1 (en) * 2006-12-29 2010-04-22 Van Der Maarel Marc Jos Elise Novel slowly digestible storage carbohydrate
JP2010514443A (en) * 2006-12-29 2010-05-06 ネーデルランドセ オルガニサティエ フォール トエゲパストナトールヴェテンシャッペリク オンデルゾエク ティエヌオー Newly stored carbohydrates that can be slowly digested
WO2008082298A3 (en) * 2006-12-29 2008-08-21 Tno Novel slowly digestible storage carbohydrate
EP1943908A1 (en) * 2006-12-29 2008-07-16 Nederlandse Organisatie voor toegepast-natuurwetenschappelijk Onderzoek TNO Novel slowly digestible storage carbohydrate
WO2008082298A2 (en) * 2006-12-29 2008-07-10 Nederlandse Organisatie Voor Toegepast Natuurwetenschappelijk Onderzoek Tno Novel slowly digestible storage carbohydrate
US20100305033A1 (en) * 2007-12-14 2010-12-02 Fresenius Kabi Deutschland Gmbh Hydroxyalkyl starch derivatives and process for their preparation
US8404834B2 (en) 2007-12-14 2013-03-26 Fresenius Kabi Deutschland Gmbh Hydroxyalkyl starch derivatives and process for their preparation
US20100297078A1 (en) * 2007-12-14 2010-11-25 Fresenius Kabi Deutschland Gmbh Method for producing a hydroxyalkyl starch derivative with two linkers
EP2070950A1 (en) 2007-12-14 2009-06-17 Fresenius Kabi Deutschland GmbH Hydroxyalkyl starch derivatives and process for their preparation
EP2070951A1 (en) 2007-12-14 2009-06-17 Fresenius Kabi Deutschland GmbH Method for producing a hydroxyalkyl starch derivatives with two linkers
CN102741296A (en) * 2010-02-02 2012-10-17 罗盖特公司 Branched soluble glucose polymers for peritoneal dialysis
JP2013518562A (en) * 2010-02-02 2013-05-23 ロケット・フルーレ Branched soluble glucose polymer for peritoneal dialysis
WO2011095736A1 (en) * 2010-02-02 2011-08-11 Roquette Freres Branched soluble glucose polymers for peritoneal dialysis
FR2955861A1 (en) * 2010-02-02 2011-08-05 Roquette Freres SOLUBLE GLUCOSE BRANCHES POLYMERS FOR PERITONEAL DIALYSIS
US9200087B2 (en) 2010-02-02 2015-12-01 Roquette Freres Branched soluble glucose polymers for peritoneal dialysis
WO2012004004A1 (en) 2010-07-09 2012-01-12 Fresenius Kabi Deutschland Gmbh Nitric oxide delivering hydroxyalkyl starch derivatives
FR3055898A1 (en) * 2016-09-15 2018-03-16 Roquette Freres NOVEL GLUCOSE POLYMERS FOR PERITONEAL DIALYSIS
WO2018051020A1 (en) * 2016-09-15 2018-03-22 Roquette Freres Novel glucose polymers for peritoneal dialysis

Also Published As

Publication number Publication date
US6803459B2 (en) 2004-10-12
US20030005922A1 (en) 2003-01-09

Similar Documents

Publication Publication Date Title
US6803459B2 (en) Branched starches and branched starch hydrolyzates
EP0710674B1 (en) Method for producing a glucan having cyclic structure
JP2589941B2 (en) Glucoamylase enzyme fractionation
EP0688872B1 (en) Process for preparing starchy products
US6436678B2 (en) High purity maltose process and products
Wang et al. Sago starch as a biomass source: raw sago starch hydrolysis by commercial enzymes
Govindasamy et al. Characterization of changes of sago starch components during hydrolysis by a thermostable alpha-amylase
US10526627B2 (en) Method for producing high molecular weight reduced viscosity starch pastes
WO2012077322A1 (en) Method for industrially producing cyclic-structure-containing branched glucan
US6248566B1 (en) Glucan having cyclic structure and method for producing the same
US5686132A (en) Glucans having a cycle structure, and processes for preparing the same
US6235505B1 (en) Process for the production of cyclodextrin
JPS6318480B2 (en)
JP6906346B2 (en) Aroma component retention agent and aroma component retention method for food and drink
US5827697A (en) Process for preparing glucans having a cyclic structure
EP0907662B1 (en) Galactosylated hydroxyalkyl polysaccharides and their derivatives
EP4086288A1 (en) Method for preparing branched dextrin having improved white turbidity
JP2024502807A (en) Dextrin with improved cloudiness and method for producing the same
Slomińska Studies on modification of enzymatic saccharification process
KR20230089914A (en) Branched dextrin with improved turbidity
KR0136363B1 (en) Preparation process of cyclodextrin
KR970008130B1 (en) Isomaltodextrin and the preparation process thereof
WO2020069396A1 (en) Dietary fiber production using a glycosyl-transferase
Raju et al. Characterization of Edta-Soluble Polysaccharides from the Scape of
JPH04293493A (en) Produciton of dextran

Legal Events

Date Code Title Description
AS Assignment

Owner name: GRAIN PROCESSING CORPORATION, IOWA

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:ANTRIM, RICHARD L.;REEL/FRAME:011452/0050

Effective date: 20010105

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION