WO1991001091A1 - Method for making a reduced fat foodstuff - Google Patents

Method for making a reduced fat foodstuff Download PDF

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Publication number
WO1991001091A1
WO1991001091A1 PCT/US1990/004013 US9004013W WO9101091A1 WO 1991001091 A1 WO1991001091 A1 WO 1991001091A1 US 9004013 W US9004013 W US 9004013W WO 9101091 A1 WO9101091 A1 WO 9101091A1
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WIPO (PCT)
Prior art keywords
starch
foodstuff
fat
high amylose
starch hydrolysate
Prior art date
Application number
PCT/US1990/004013
Other languages
French (fr)
Inventor
Susan L. Furcsik
David J. Mauro
Leonard Kornacki
Eugene J. Ii Faron
Frances L. Turnak
Roger Owen
Original Assignee
American Maize-Products Company
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 American Maize-Products Company filed Critical American Maize-Products Company
Priority to DE69012331T priority Critical patent/DE69012331T2/en
Priority to EP90911792A priority patent/EP0482094B1/en
Publication of WO1991001091A1 publication Critical patent/WO1991001091A1/en

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Classifications

    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23GCOCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
    • A23G9/00Frozen sweets, e.g. ice confectionery, ice-cream; Mixtures therefor
    • A23G9/32Frozen sweets, e.g. ice confectionery, ice-cream; Mixtures therefor characterised by the composition containing organic or inorganic compounds
    • A23G9/34Frozen sweets, e.g. ice confectionery, ice-cream; Mixtures therefor characterised by the composition containing organic or inorganic compounds characterised by carbohydrates used, e.g. polysaccharides
    • AHUMAN NECESSITIES
    • A21BAKING; EDIBLE DOUGHS
    • A21DTREATMENT, e.g. PRESERVATION, OF FLOUR OR DOUGH, e.g. BY ADDITION OF MATERIALS; BAKING; BAKERY PRODUCTS; PRESERVATION THEREOF
    • A21D2/00Treatment of flour or dough by adding materials thereto before or during baking
    • A21D2/08Treatment of flour or dough by adding materials thereto before or during baking by adding organic substances
    • A21D2/14Organic oxygen compounds
    • A21D2/18Carbohydrates
    • A21D2/186Starches; Derivatives thereof
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23GCOCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
    • A23G9/00Frozen sweets, e.g. ice confectionery, ice-cream; Mixtures therefor
    • A23G9/32Frozen sweets, e.g. ice confectionery, ice-cream; Mixtures therefor characterised by the composition containing organic or inorganic compounds
    • A23G9/327Frozen sweets, e.g. ice confectionery, ice-cream; Mixtures therefor characterised by the composition containing organic or inorganic compounds characterised by the fatty product used, e.g. fat, fatty acid, fatty alcohol, their esters, lecithin, glycerides
    • 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

Definitions

  • the '890 patent teaches mixing two different starch hydrolysates to make a product having a DE between 5 to 10.
  • DE dextrose equivalent
  • DE is determined by Lane-Eynon Procedure (E 26, Standard Analytical Methods, revision 5/27/68, CRA Manual) .
  • the gels made from the fat replacer of the present invention must have a gel strength of about 25 grams and above and, preferably, a gel strength of about 100 to about 1200 grams. More preferred is a gel strength between about 500 to about 1100.
  • the gel strengths of the fat replacer of the present invention is determined by preparing an aqueous dispersion of the high amylose starch hydrolysate at 25% solids and cooking the dispersion at about 95°C for about 15 minutes. The paste is then placed in 4 ounce short glass jars, the jars covered and placed into cold storage, 4°C, for 16 hours. After 16 hours at 4°C the jars are allowed to stand at ambient temperature, 25°C, for 1 h hours.
  • a Stevens LFRA Texture Analyser is then used to measure the gel strength. Plunger No. 5 is used at a speed of 0.2 mm/second and a distance of 4 mm. The average of 3 readings is used to determine the gel strength.
  • the cookies were made by creaming the sugar and shortening and then adding the dry ingredients to the creamed mixture. Then the liquid together with the fat replacer was added and mixed in. Finally the chocolate chips were added and the dough was dispersed and baked in a 190°C oven for about 12 minutes,
  • Starch hydrolysates 9 and 10 were made by making a slurry with the starch to a solids level of about 20%; adjusting the pH to about 6; adding bacterial alpha amylase to the slurry; heating the slurry to about 80°C and holding the slurry at this temperature until the desired DE was obtained. The enzyme was then inactivated and the slurry filtered, bleached and dried to form a dried starch hydrolysate.
  • Starch hydrolysates 13 and 14 were commercial products sold by National Starch and Chemical Company under the names N-OIL and INSTANT N-OIL respectively.

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  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Food Science & Technology (AREA)
  • Molecular Biology (AREA)
  • Polymers & Plastics (AREA)
  • Inorganic Chemistry (AREA)
  • Nutrition Science (AREA)
  • Grain Derivatives (AREA)
  • Confectionery (AREA)
  • Bakery Products And Manufacturing Methods Therefor (AREA)
  • General Preparation And Processing Of Foods (AREA)
  • Edible Oils And Fats (AREA)

Abstract

The method for making a reduced fat foodstuff entails replacing at least a portion of the fat and/or oil in the foodstuff with a high amylose starch hydrolysate having an apparent amylose content above about 40% and a DE greater than 5 and less than 15.0. A high amylose corn starch is the preferred starch base.

Description

METHOD FOR MAKING A REDUCED FAT FOODSTUFF
This invention relates to foodstuffs and more particularly to a method for making a reduced fat foodstuff by replacing a portion of the fats and/or oils in the foodstuff with a high amylose starch hydrolysate.
Consumer awareness of the caloric content of foods has increased dramatically over the past few years and has brought about a demand for foods having a reduced fat content. This demand has created a need in the food industry to replace at least a portion of the fat and/or oil in prepared foodstuffs with a component that does not detract from the taste, appearance, smell and mouthfeel of the foodstuffs and which has reduced caloric content.
It has been suggested that certain starch hydrolysates may be used as fat and/or oil replacers in foods, see U.S. Patent No. 4,510,166 issued April 9, 1985,
U.S. Patent No. 3,962,465 issued June 8, 1976 and U.S. Patent No. 3,986,890 issued October 19, 1976. The '166 patent teaches using starch hydrolysate having a DE less than 5 as a fat and/or oil replacer. A problem with these less than 5 DE starch hydrolysates is that they have poor taste and impart an undesirable starchy or roasted taste to the foodstuff. Additionally, it has been found that these less than 5 DE starches produce a gel that has a gray or tan color which is also undesirable.
The '465 patent teaches a detailed stepwise process for converting starch to a starch hydrolysate having a DE between 5 to 25. This process is extremely long and tedious and is not deemed acceptable for a large commercial operation.
The '890 patent teaches mixing two different starch hydrolysates to make a product having a DE between 5 to 10.
It has now been discovered that a foodstuff with reduced fat content may be made by replacing at least a portion of the fat and/or oil in the foodstuff with water and an effective amount of a high amylose starch hydrolysate having a DE between about 5 to about 15 and having a peak average molecular weight less than about 10,000, said starch hydrolysate being made from a base starch having an apparent amylose content greater than about 40%.
It has been found that an aqueous dispersion of the high amylose starch hydrolysate of the present invention possesses good gel strength, an important attribute in a fat replacer. The gels produced by the fat replacer of the present invention are smooth, creamy and white and do not have a sticky-pasty consistency.
It has also been found that the gels of the fat replacer of the present invention do not have a starchy or roasted flavor. This makes the fat replacer of the present invention a suitable substitute for natural fats and oils which generally have a non-distinct flavor.
Suitable forms of the fat replacer of the present invention are an aqueous dispersion of the hydrolysate and a paste.
The aqueous dispersion is formed by mixing the dried starch hydrolysate with water. The paste is formed by cooking the aqueous dispersion. Cooking entails raising the temperature of the dispersion to above about 90°C and holding the dispersion at that temperature for about 5 minutes while subjecting the dispersion to agitation. More preferably the temperature of ttie dispersion is raised to about 100°C. Stirring is done in a conventional manner such as by an impeller. Gels are formed by cooling the paste.
In situ formation of the aqueous dispersion and paste can be performed. If the foodstuff contains water, then the high amylose starch hydrolysate of the present invention can be added directly to the foodstuff and mixed in. The aqueous dispersion will form therein. If the foodstuff containing the high amylose starch hydrolysate is then cooked, a paste will form. The paste, whether made in situ or prior to addition to the foodstuff is the preferred form of the fat replacer of the present invention.
An effective amount of the high amylose starch hydrolysate of the present invention is dispersed in water to form the fat replacer of the present invention. Preferably, the dispersion has a solids content of about 5% to about 50% and more preferred is a dispersion with a solids content of about 15% to about 30%. Starch obtained from corn, potato, wheat, rice, sago, tapioca, or sorghum are acceptable base starches so long as they have an apparent amylose content greater than about 40%. Suitable sources for such high amylose starch include high amylose corn starch and high amylose barley starch. Preferably, high amylose corn starch is used.
The apparent amylose content must be above about 40% and more preferably about
50% and above. Good results have been obtained with a corn starch having an apparent amylose content of about 50-65%. Such a high amylose corn starch is available from American Maize- Products Company under the trademark AMAIZO® 5. The term "amylose content" or "apparent amylose content" of the base starch as used in the specification and claims means the amylose content of the base starch as determined by conventional spectrophotometric iodine absorption, Sowbhagya and Bhattacharya, Die Starke 23 Jan. 1971 Nr. 2, p. 53-56. The high amylose starch hydrolysate has a DE greater than about 5 and less than about 15. Good results have been obtained when the DE is about 5 to about 9.
The dextrose equivalent, DE, is a conventional term used to describe the degree of conversion of starch to starch hydrolysate. There -5-
are a number of methods of determining DE. For the purposes of this specification and the claims herein, the DE is determined by Lane-Eynon Procedure (E 26, Standard Analytical Methods, revision 5/27/68, CRA Manual) .
The high amylose starch hydrolysate of the present invention has a peak average molecular weight of less than about 10,000 when measured by Gel Permeation Chromatography. More preferably, the high amylose starch hydrolysate of the present invention has a peak average molecular weight less than about 7500 and even more preferably about 6000 and below.
Peak average molecular weight is determined by the Gel Permeation Chromatograph using two ULTRAHYDROGELtιn linear columns in series, each measuring 11.81 inches (30 cm) in height and .31 inches (.78 cm) in diameter. 100 microliters of a 0.1% wt./vol. sample was eluted with 0.1M aNOβ containing 0.02% NaN3 (40°C) at a flow rate of 0.8 cc/minute. A Refractive Index detector maintained at 40°C is used. The peak average molecular weight is the value of the molecular weight at the highest point of the chromatogram generated by the chromatograph.
The gels made from the fat replacer of the present invention must have a gel strength of about 25 grams and above and, preferably, a gel strength of about 100 to about 1200 grams. More preferred is a gel strength between about 500 to about 1100. The gel strengths of the fat replacer of the present invention is determined by preparing an aqueous dispersion of the high amylose starch hydrolysate at 25% solids and cooking the dispersion at about 95°C for about 15 minutes. The paste is then placed in 4 ounce short glass jars, the jars covered and placed into cold storage, 4°C, for 16 hours. After 16 hours at 4°C the jars are allowed to stand at ambient temperature, 25°C, for 1 h hours. A Stevens LFRA Texture Analyser is then used to measure the gel strength. Plunger No. 5 is used at a speed of 0.2 mm/second and a distance of 4 mm. The average of 3 readings is used to determine the gel strength.
The term "foodstuffs" as used in the specification and claims means foods that have been formulated from more than one component. Examples of such foodstuffs are spoonable and pourable salad dressings, frozen novelties, ice cream, whipping toppings, icings, and sauces.
Replacing the fat and/or oil in order to make a reduced fat foodstuff in accordance with the present invention is accomplished by replacing at least a portion of the fat and/or oil used in formulating the foodstuff with water and an effective amount of a starch hydrolysate of the present invention. Suitably the fat replacer of the present invention is substituted for the fat and/or oil on about a 1 to 1 weight basis, i.e. about 1 gram of fat replacer for about 1 gram of fat and/or oil. -7-
Since the caloric content of fat and/or oil is about 9 calories''per gram and the caloric content of the fat replacer of the present invention in a 25% solids dispersion is about 1 calorie per gram, a caloric decrease of more than about 90% is obtained by replacing all of the fat and/or oil.
Typically, formulated foodstuffs contain up to about 80% by weight fat- and/or oil. Preferably, in any foodstuffs formulated with a fat and/or oil, up to about 50% by weight of the fat and/or oil is replaced with the water and an effective amount of the starch hydrolysate of the present invention and more preferably up to about 90% of the fat and/or oil is replaced.
The high amylose starch hydrolysate of the present invention is preferably- made by treating a slurry of high amylose starch with bacterial alpha amylase to the desired
DE. More specifically, a high amylose starch is slurried with water to about 20% solids and the pH is adjusted to about 6. To this slurry is added about 0.4% by weight bacterial alpha amylase based on dry starch weight.
This slurry is then subjected to a prepaster at a temperature of about 104°C to gelatinize the starch. The starch slurry is then held at about 80°C long enough to convert the starch to a hydrolysate having a DE greater than 5 and less than 15, typically about 30 to about 45 minutes. The enzyme is then inactivated by adjusting the pH to about 2.5. After inactivating the enzyme the pH is adjusted to about 4.5 and the slurry is filtered and carbon bleached at about 90°C. The slurry is then dried by evaporation followed by spray drying in a conventional manner. Preferably the high amylose starch hydrolysate is dried to a moisture of less than about 12% and more preferably, about 4% and below.
These and other aspects of the present invention may be more fully understood by reference to the following examples.
Example 1 This example illustrates making a frozen novelty in accordance with the present invention. Two formulations were made. Each formulation was found to have comparable taste, appearance and mouthfeel. Table I below illustrates these formulations.
Table I
Figure imgf000010_0001
-9-
The numbers in Table I are based on percent by weight of formulation. The fat replacer was a paste made from a high amylose starch hydrolysate wherein the DE was 8.6* and the apparent amylose content of the base starch was about 60%. The paste was made by forming an aqueous dispersion at a solids content of 25% by weight, heating the dispersion to about 100°C and holding the dispersion at that temperature for about
5 minutes. The dispersion was stirred constantly during heating.
The gel strength of the fat replacer was about 695 grams and the hydrolysate had a peak average molecular weight of about 2874. Both gel strength and peak average molecular weight were determined as outlined above.
Both formulations were prepared by adding the preblended dry components to the butter, milk, water and corn syrup. The mix was then pasteurized, homogenized, cooled to 4°C and aged for 24 hours. The mix was then processed in an ice cream maker. The fat replacer paste was combined with the butter, milk, water and corn syrup initially.
Example 2 This example illustrates making a chocolate chip cookie with the fat replacer of the present invention. The cookies made by this formulation were found to have good taste, appearance and mouthfeel. Control was a chewy cookie while the test was a cake-like cookie. Table II
Figure imgf000012_0001
Chocolate chips , 2000 ct. 16.00 16.00
The numbers in Table II are based on the percent by weight formulation. The fat replacer used in this formulation is the same as in Example 1 above.
The cookies were made by creaming the sugar and shortening and then adding the dry ingredients to the creamed mixture. Then the liquid together with the fat replacer was added and mixed in. Finally the chocolate chips were added and the dough was dispersed and baked in a 190°C oven for about 12 minutes,
EXAMPLE 3 This example compares the gel strength of the fat replacer of the present invention to other starch hydrolysates.
Figure imgf000013_0001
The gel strength measurements were made in the manner as outlined above and the dextrose equivalents were likewise measured in the manner outlined above. Starch hydrolysates 1-3, 6 and 7 were made in a continuous process where a slurry of starch and water was made to about 20% solids. The pH of the slurry was adjusted to about 6 and bacterial alpha amylase was added to the slurry. The slurry was then subjected to a prepaster which raised the temperature of the slurry to about 104°C and the slurry was subsequently held at about 106°C in plug flow converters until the indicated DE was obtained. Then the enzyme was deactivated by adjusting the pH and the slurry was subsequently filtered, carbon bleached and spray dried to produce a dry starch hydrolysate. The base starch used for 1-3 was a high amylose corn starch while 6-7 was a waxy corn starch. Starch hydrolysates 4 and 5 were made in accordance with Example 1 of U.S. Patent No. 3,962,465 except different DE's were obtained. It is readily evident that the 6.4 DE and 10 DE material made in accordance with the teachings of the '465 patent did not have the gel strength of the fat replacer of the present invention.
Starch hydrolysate 8 was a commercial product sold by National Starch and Chemical Company under the trade name N-OIL. This is thought to be made from a tapioca starch and the apparent amylose content listed in Table III above for N-OIL is that of a typical tapioca starch, see 10. Starch hydrolysate 9 is a conventional common corn starch hydrolysate converted by enzyme to the desired DE while starch hydrolysate 10 is a conventional tapioca starch hydrolysate also made by an enzymatic process to the desired DE. Starch hydrolysates 9 and 10 were made by making a slurry with the starch to a solids level of about 20%; adjusting the pH to about 6; adding bacterial alpha amylase to the slurry; heating the slurry to about 80°C and holding the slurry at this temperature until the desired DE was obtained. The enzyme was then inactivated and the slurry filtered, bleached and dried to form a dried starch hydrolysate.
Starch hydrolysate 11 was a commercial product sold by Avebe under the name PASELLI SA-2. Such material is thought to be made from a potato starch base. The apparent amylose content listed in Table III is that of a typical potato starch, see 4 and 5. It is apparent from Table III above that the fat replacer of the present invention has both a higher amylose content and gel strength than starch hydrolysates of comparable DE's.
EXAMPLE 4 This example compares the peak average molecular weights of the fat replacer of the present invention with other starch hydrolysates. Table IV
Figure imgf000016_0001
Starch hydrolysate 12 was a commercial product sold by Avebe under the name PASELLI SA-2. It was thought that this material was made from potato starch and the amylose content as reported above is typical for potato starches.
Starch hydrolysates 13 and 14 were commercial products sold by National Starch and Chemical Company under the names N-OIL and INSTANT N-OIL respectively.
Starch hydrolysates 15 and 16 were made in accordance with the present invention.
Starch hydrolysate 17 was made in accordance with Example 1 of U.S. Patent No. 3,962,465. It will be understood that the claims are intended to cover all modifications and changes of the preferred embodiment of the invention herein chosen for illustration which do not constitute a departure from the spirit and scope of the invention.

Claims

What is claimed is:
1. A method for preparing a foodstuff with reduced fat comprising the step of replacing at least a portion of the fat and/or oil in the foodstuff with water and an effective amount of a high amylose starch hydrolysate having a DE between about 5 to about 15 and a peak average molecular weight less than 10,000, said starch hydrolysate being made from a base starch having an apparent amylose content greater than 40%.
2. The method of claim 1 wherein the starch has an apparent amylose content of about 60%. *
3. The method of claim 1 wherein the high amylose starch hydrolysate is in the form of an aqueous dispersion.
4. The method of claim 3 wherein the aqueous dispersion is a paste.
5. The method of claim 3 or 4 wherein the aqueous dispersion has a solids content of about 5 to about 50% by weight.
6. The method of claim 1 wherein the foodstuff is selected from the group consisting of spoonable and pourable salad dressings, frozen novelties, ice cream, whipping toppings, icings, cookies and sauces.
7. The method of claim.1 wherein the starch hydrolysate is obtained from corn.
8. The method of claim 1 wherein up to about 90% of the fat and/or oil is replaced with the high amylose starch hydrolysate.
9. A method for preparing a foodstuff with reduced fat comprising the following sequential steps:
(a) forming a slurry of high amylose corn starch;
(b) mixing about 0.4% by weight bacteria alpha amylase based on dry starch weight;
(c) gelatinizing said corn starch at a temperature of about 105°C;
(d) holding said gelatinized corn starch at about 80°C until the DE reaches about 5 to about 9;
(e) recovering a high amylose corn starch hydrolysate having a DE between about 5 to about 9; and
(f) replacing up to about 90% of the fat and/or oil in the foodstuff with said water and high amylose corn starch hydrolysate.
10. The method of claim 9 wherein the high amylose corn starch hydrolysate is in the form of a paste with a solids content between about 5 to about 50% when added to said foodstuff.
11. A foodstuff made by the process of claim 1.
12. A foodstuff made by the process of claim 9.
13. A foodstuff made by the process of claim 10.
PCT/US1990/004013 1989-07-19 1990-07-17 Method for making a reduced fat foodstuff WO1991001091A1 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
DE69012331T DE69012331T2 (en) 1989-07-19 1990-07-17 PRODUCTION PROCESS OF FOODSTUFFS WITH REDUCED FAT CONTENT.
EP90911792A EP0482094B1 (en) 1989-07-19 1990-07-17 Method for making a reduced fat foodstuff

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US38225389A 1989-07-19 1989-07-19
US382,253 1989-07-19

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WO1992011769A2 (en) * 1990-12-31 1992-07-23 The Haagen-Dazs Company, Inc. Frozen dessert compositions and products
EP0529892A1 (en) * 1991-08-16 1993-03-03 A.E. Staley Manufacturing Company Fragmented, alpha amylase hydrolysed amylose precipitate as fat replacer
EP0529893A1 (en) * 1991-08-16 1993-03-03 A.E. Staley Manufacturing Company Debranched amylopectin-starch as fat replacer
EP0529891A1 (en) * 1991-08-16 1993-03-03 A.E. Staley Manufacturing Company Method of preparing reduced fat foods
EP0529894A1 (en) * 1991-08-16 1993-03-03 A.E. Staley Manufacturing Company Fragmented, debranched amylopectin starch precipitate as fat replacer
WO1993003630A1 (en) * 1991-08-16 1993-03-04 A.E. Staley Manufacturing Company Fragmented, debranched amylopectin starch precipitate as fat replacer
WO1993010675A1 (en) * 1991-11-26 1993-06-10 A.E. Staley Manufacturing Company Fragmented alpha amylase hydrolyzed amylose precipitate as fat replacer
EP0588556A2 (en) * 1992-09-16 1994-03-23 Unilever Plc Processing of maltodextrins
WO1994021128A1 (en) * 1993-03-25 1994-09-29 Unilever N.V. Fat-reduced laminated doughs
WO1995010627A1 (en) * 1993-10-14 1995-04-20 Novo Nordisk A/S Method for production of maltose and a limit dextrin, the limit dextrin, and use of the limit dextrin
AU661869B2 (en) * 1992-11-02 1995-08-10 National Starch And Chemical Investment Holding Corporation Extruded foods containing high amylose starch
WO1996003057A1 (en) * 1994-07-22 1996-02-08 Societe Des Produits Nestle S.A. Food grade texture agent comprising particles of high-amylose starch and process for its preparation.
EP0848908A1 (en) * 1996-11-21 1998-06-24 Societe Des Produits Nestle S.A. Bread products
US5912031A (en) * 1994-04-11 1999-06-15 Fitchett; Colin Stanley Process for preparing a fat replacer by enzymatic digestion of a ground cereal with alpha-amylase
US6379736B1 (en) 1999-10-05 2002-04-30 The Pillsbury Company Gelato composition
WO2018123254A1 (en) * 2016-12-27 2018-07-05 株式会社J-オイルミルズ Whipped cream improving agent
WO2020004052A1 (en) * 2018-06-27 2020-01-02 株式会社J-オイルミルズ Whipped cream
CN112806557A (en) * 2021-02-05 2021-05-18 瑞泰高直生物科技(武汉)有限公司 Fat substitute with high resistant starch content and preparation method and application thereof
CN112806558A (en) * 2021-02-05 2021-05-18 瑞泰高直生物科技(武汉)有限公司 Preparation method of fat substitute

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US4981709A (en) * 1989-07-19 1991-01-01 American Maize-Products Company Method for making a reduced fat foodstuff
AU652743B2 (en) * 1990-02-20 1994-09-08 A.E. Staley Manufacturing Company Hydrolysed starch as a substitute for fat in food
US5294453A (en) * 1990-09-04 1994-03-15 Penwest, Ltd. Method of removing off-flavor components from hydroxypropyl starch hydrolyzate products
AU657443B2 (en) 1992-12-24 1995-03-09 Corn Products Development, Inc. Food compositions including resistant starch

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WO1992011769A3 (en) * 1990-12-31 1992-09-03 Pillsbury Corp Frozen dessert compositions and products
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EP0529893A1 (en) * 1991-08-16 1993-03-03 A.E. Staley Manufacturing Company Debranched amylopectin-starch as fat replacer
EP0529891A1 (en) * 1991-08-16 1993-03-03 A.E. Staley Manufacturing Company Method of preparing reduced fat foods
EP0529894A1 (en) * 1991-08-16 1993-03-03 A.E. Staley Manufacturing Company Fragmented, debranched amylopectin starch precipitate as fat replacer
WO1993003628A1 (en) * 1991-08-16 1993-03-04 A.E. Staley Manufacturing Company Method of preparing reduced fat foods
WO1993003629A1 (en) * 1991-08-16 1993-03-04 A. E. Staley Manufacturing Company Debranched amylopectin starch as a fat replacer
EP0529892A1 (en) * 1991-08-16 1993-03-03 A.E. Staley Manufacturing Company Fragmented, alpha amylase hydrolysed amylose precipitate as fat replacer
WO1993010675A1 (en) * 1991-11-26 1993-06-10 A.E. Staley Manufacturing Company Fragmented alpha amylase hydrolyzed amylose precipitate as fat replacer
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EP0588556A3 (en) * 1992-09-16 1995-01-18 Unilever Plc Processing of maltodextrins.
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USRE39005E1 (en) * 1993-10-14 2006-03-07 Novozymes A/S Method for production of maltose and a limit dextrin, the limit dextrin, and use of the limit dextrin
US5912031A (en) * 1994-04-11 1999-06-15 Fitchett; Colin Stanley Process for preparing a fat replacer by enzymatic digestion of a ground cereal with alpha-amylase
WO1996003057A1 (en) * 1994-07-22 1996-02-08 Societe Des Produits Nestle S.A. Food grade texture agent comprising particles of high-amylose starch and process for its preparation.
US5759581A (en) * 1994-07-22 1998-06-02 Nestec Sa Food texture agent comprising particles of high-amylose starch and method of making same
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WO2018123254A1 (en) * 2016-12-27 2018-07-05 株式会社J-オイルミルズ Whipped cream improving agent
JPWO2018123254A1 (en) * 2016-12-27 2019-10-31 株式会社J−オイルミルズ Whipping cream improver
TWI746729B (en) * 2016-12-27 2021-11-21 日商J 制油股份有限公司 Whip cream improver, whip cream and manufacturing method thereof, foods and beverages containing the whip cream, method for enhancing the fatty or bubbly feeling of whip cream, and cream for whip cream
WO2020004052A1 (en) * 2018-06-27 2020-01-02 株式会社J-オイルミルズ Whipped cream
CN112334008A (en) * 2018-06-27 2021-02-05 J-制油株式会社 Whipped cream
CN112806557A (en) * 2021-02-05 2021-05-18 瑞泰高直生物科技(武汉)有限公司 Fat substitute with high resistant starch content and preparation method and application thereof
CN112806558A (en) * 2021-02-05 2021-05-18 瑞泰高直生物科技(武汉)有限公司 Preparation method of fat substitute

Also Published As

Publication number Publication date
AU628206B2 (en) 1992-09-10
DK0482094T3 (en) 1994-11-21
EP0482094A4 (en) 1992-05-13
DE69012331T2 (en) 1995-03-23
AU6063090A (en) 1991-02-22
DE69012331D1 (en) 1994-10-13
EP0482094A1 (en) 1992-04-29
EP0482094B1 (en) 1994-09-07

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