CA2035472C - Oat soluble dietary fiber compositions - Google Patents

Abstract

Water-soluble dietary fiber compositions can be prepared by treatment of oat-milled products with .alpha.-amylase. The dietary fiber compositions are colorless and devoid of inherent undesirable flavors and are, therefore, uniquely suitable for use in a variety of foods.

Description

~'.'091/00027 PCT/US90/03~5 --1-- 2 ~3 3 ~ L~ 7 ~

OAT SOLUBLE DIETARY FIBER COMPOSITIONS

Backqround of the Invention Field of the Invention Dietary fiber is considered to be the soluble and insoluble components of food that are not digested by enzymes in the human gastrointestinal tract. The primary sources of dietary fiber include such cell wall materials as cellulose, hemicelluloses, lignin, and pectins, along with gums and mucilages. Dietary fiber has been considered an important food component since early times. Recently, Burkitt et al. ~Lancet 2:1408-1411 (1972)~ concluded that dietary fiber has a role in the prevention of certain large-intestine diseases, including cancer of the colon and diverticulitis. Diets containing large amounts of dietary fiber lead to stools that are softer and larger, and bowel movements are generally more frequent. Burkitt also mentioned that the serum cholesterol rises when dietary fiber is removed from the diet, and that eating a fiber-rich diet lowers serum cholesterol. Trowell [Am. J.
Clin. Nutr. 25:464-465 (1972)] reached a similar conclusion regarding the relationship between fiber and health benefits.
It is now known that all dietary fiber is not the same and that different fibers provide different heath benefits. For example, wheat bran is very rich in insoluble dietary fiber (mainly cellulose and SUBSTITUTE SHET

PCT/US90/03~5 "091/00027 ~0 3 3 ~ 7 r~
_ -2 hemicelluloses) and is excellent for decreasing the transit time of food through the digestive tract ~Anderson et al., Am. J. Clin. Nutr. 32:346-363 (1979)]. Some fibers are reported to reduce total plasma cholesterol [Munox et al., Am. J. Clin. Nutri. 32:580-592 (1979)~. This invention relates to a novel food composition from oats that provides soluble dietary fiber useful as a functionally and nutritionally advantageous ingredient for a variety of food products.

Description of the Prior Art The first indication of serum cholesterol lowering by rolled oats was observed in rats by Degroot et al.
[Lancet 2:303-304 (1963)]. Fisher et al. [Pro. Soc. Exp.
Biol. Med. 126:108-111 (1967)~ report that the fiber fraction of oats is responsible for its unique effect on cholesterol. Over the years, numerous experiments with animals have shown that oat fiber has a strong hypocholesterolemic effect. Anderson et al. [Am. J. Clin.
Nutr. 34:824-829 (1981); 40:1146-1155 (1984)] have confir~ed hypocholesterolemic effects of oats in humans.
It is the soluble fiber that is effective in lowering cholesterol levels. Oatmeal, or rolled oats, and especially oat bran are the best sources of this soluble fiber. Moreover, oat fiber reduces the amount of low density lipoprotein (LDL) without lowering the beneficial high density lipoprotein (HDL). In fact, Anderson et al.
[66th Annual Meeting, Am. Assoc. Cer. Chemists, Abstract No. 112 (1981)] teach that oat bran fed to humans can reduce LDL 58% while increasing HDL 82%. Other water-soluble fibers, such as pectin and guar gum, can lower serum cholesterol, but they are frequently accompanied by undersirable side effects such ~s nausea and ~IIRSTITUTE SHET

~091/00027 PCT/US90/03645 3 2û~72 vomiting. The results of another study by Anderson et al.
(supra, 1984) indicate that oat bran diets decrease total serum cholesterol 19% and LDL 23% and that oat bran increases bile acid excretion 65%. These studies clearly document the hypocholesterolemic effects in humans of oat products which are rich in soluble fiber.
In the art of starch hydrolysis, it is known that starch can be hydrolyzed by acids or enzymes to give a variety of products with properties depending on the degree of conversion. Acid conversions are known to give uniform distribution of hydrolysate fraqments because of the random cleavages of the starch molecule, whereas enzymes result in variations in amounts of the different oligomer fraqments [Inglett, J. Food Biochem. 11:249-258 (1987)]. Various amylolytic enzymes are used in the thinning or liquefaction of starch and in the production of low conversion starch hydrolysates which are known in the trade as maltodextrins or corn syrup solids, depending upon the degree of hydrolysis (Morehouse, U.S. Patent No. 3,663,369). It is also recognized that specific maltodextrins can be prepared at a D.E. within the range of 10-13 (Coker, U.S. Patent No.
4,447,532). The starches used to prepare maltodextrins are obtained primarily from the wet milling of corn. Other sources of starch for commercial products are tapioca, potato and rice.
Whole cereal flours have also been subjected to starch-hydrolyzing conditions and have yielded, for example, a whole-grain hydrolyzed product (Conrad, U.S.
Patent No. 4,377,602) and a ready-to-eat, enzyme-saccharified cereal (Fulger et al., U.S. Patent No.
4,710,386). Ronai (U.S. Patent No. 3,640,729) arrives at a similar product by addinq prehydrolyzed starch to oat flour to yield an instant oat cereal product.

SllESTITUTE SH~ET

PCT/~S90/03645 ~091/00027 ~35~7~

~ummarY of the Invention I have now discovered that water-soluble dietary fiber compositions can be recovered from milled products of oats such as oat bran and oat flour after enzymatic hydrolysis of these substrates with ~-amylases. The resulting soluble dietary fiber compositions separated with the soluble hydrolyzate fractions are colorless and devoid of inherent undesi~ab~e flavors. The soluble fiber compositions are, therefore, uniquely suitable for use in a variety of foods such as dairy products, dairy product substitutes, high-soluble fiber bakery products, frozen foods, yogurt, snacks, confectioneries, coatings, dietary-fiber beverages, and breakfast foods.
In accordance with this discovery, it is an object of the invention to provide a novel source of water-soluble dietary fiber compositions for incorporation into ingestible formulations.
Another object of the invention is to provide a novel protein-rich ingredient for food or animal feed compositions.
Other objects and advantages of this invention will become readily apparent from the ensuing description.
Detailed Descri~tion of the Invention Suitable substrates contemplated for use in the invention include milled products of oats such as oat bran and oat flour. The substrate is slurried in a sufficient amount of water to give a concentration is in the range of about 10-40% by weight. The water should contain a suitable calcium salt in an amount sufficient to stabilize the subsequently added ~-amylase [preferably about 25-50 parts per million (ppm) of calcium~. The slurried substrate may be gelatinized prior to enzymatic treatment, using any method known in the art. The pH of the SUBSTITUTE SHEET

._ ungelatinized slurry or the gelatinized dispersion is adjusted to about 5.6-7.5, preferably about 6.0, with sodium hydroxide or other alkali, and the ~-amylase is added.
It is advantageous to use thermostable a-amylase referred to as l,4-~-D-glucan glucanohydrolases and having the essential enzymatic characteristics of those produced by the Bacillus stearothermophilus strains ATTC Nos. 31,195; 31,196; 31,197; 31,198; 31,199; and 31,783. These strains are described in U.S. Patent No. 4,284,722. Other sources of this enzyme include organisms such as B. Subtills which have been genetically modified to express the thermostable ~-amylase of B.
stearothermophilus as described in U.S. Patent No.
4,493,893. These enzymes are available commercially under the trademark "Enzeco Thermolase" (Enzyme Development, Div., Biddle Sawyer Corp., New York, NY).
Other suitable ~-amylases are those having the essential enzymatic characteristics of those produced by B. licheniformis var. as described in U.S. Patent Nos. 4,171,662 and 4,724,208. These enzymes are available commercially under the trademark "Takalite"
(Miles Laboratories, Inc., Biotech Products Division, Elkhart, IN). Of course, any ~-amylase which is useful in the thinning of the oat starch is contemplated for use herein.
The conditions of enzyme treatment, including the enzyme concentration and the time and temperature of reaction, are selected to achieve liquefaction of the starch in the substrate to the extent that the soluble fiber bound by the cellular matrix is substantially ~':

PCI'/US90/03645 ~5~72 completely liberated into solution. When using a thermostable ~-amylase, a preferred treatment temperature is in the range of 70--lOO-C, preferably about 95-C. At these temperatures, gelatinization of the starch in the substrate occurs concurrently with the hydrolysis. The duration of the treatment at the desired conversion temperature depends on the desired product properties and will generally range from about 10-60 min.
After completion of the enzymatic hydrolysis, the enzyme is inactivated, such as by passing the mixture through a steam injection pressure cooker at a temperature of about 140-C. Alternatively, the enzyme may be inactivated by acidification (pH 3.5-4.0) at 95-C for about 10 min. Optional neutralization with alkali increases the salt concentration of the product. After the enzyme has been inactivated, the soluble fraction comprising the soluble oat fiber and maltooligosaccharides is separated from the insoluble residue by centrifugation. Water is then removed from the soluble fraction in the centrifugate by any of a variety of conventional techniques, and the soluble oat fiber product of the invention is recovered.
It was surprising to find that the products of this invention are readily obtainable in a colorless, white, and smooth-textured form, devoid of inherent undesirable color, flavor, and grittiness associated with the starting materials. They are remarkably adapted for use as functional and nutritional components of many foods including dairy products, in which consumer preference dictates the virtual absence of the flavor, color, and grittiness inherent to the starting substrate and to most dietary fibers currently marketed.

SUBSTITUTE SHEET

~'091/00027 PCT/~S90/03645 2 13 3 5 Ll 7 2 _ -7-Characterization of the insoluble residue from the conversion mixture (supra) reveals a high proportion of protein. The protein is believed to complex with the lipid and to become insolubilized by heat denaturation. The residue also contains the insoluble fiber and the majority of the flavor and color components. This byproduct, therefore, has potential as an ingredient in foods or animal feeds and is considered an ancillary asset to the inventive process.
The following examples are presented only to further illustrate the invention and are not intended to limit the scope of the invention which is defined by the claims.
All percentages herein disclosed are by weight unless otherwise specified.

Examples 1-4 Effect of Process PH. For each preparation, 100 g (dry basis) of oat flour (The Quaker Oats Company, Cedar Rapids, IA) was slurried in 500 ml of water containing 25 ppm of calcium (O.O9 g/l CaC12.2H2O) and gelatinized by passage through a steam injection cooker at 138'-143'C
(30-40 psi of steam pressure). The gelatinized mixture was collected in a container, and the pH was adjusted with 1.0 N sodium hydroxide as desired (Table I). " Enzeco Thermolase" (supra) was added to the mixture at 95-C in an amount sufficient to provide 24 units per gram of oat required to hydrolyze lO mg. of starch per minute under specified conditions [Enzyme Development Div., Biddle Sawyer Corp., New York, NY, Technical Bulletin No. 20 (Revised 7/86)]. After 20 min. of stirring at 95-C, the starch was liquefied, and the enzyme was inactivated by passing the mixture though a steam injection cooker SUBS~I~UTE SHEE~

~-091/00027 PCT/US90/03~5 2035~72 (supra). The mixture was then allowed to cool to about 70-C, and it was centrifuged 30 min. at 5000 rpm. The water-soluble fiber product in the supernatant solution was recovered by decanting the solution and freeze-drying. The insoluble reside obtained from centrifuging was removed and air-dried. The results in Table I show that the higher ph"s (9 and 11) are accompanied by undesirably high levels of protein in the soluble products and decreased protein amounts in the insoluble residues.

Examples 5-7 ~ ffect of Enzyme Level. Compositions were prepared as described in Examples 1-4 except that the starting oat flour was obtained from National Oats Company (Cedar Rapids, IA), the process pH was 6.0 for all preparations, and enzyme was added in varying amounts as reported in Table II. The DP distribution of starch oligomers in the products was determined by high-pressure liquid chromatography (Inglett, supra). The data in Table II show that lower enzyme amounts results in higher DP
starch oligomers.

Exam~le 8 T.nw Temperature Treatment. Two hundred grams (dry basis) of oat flour (National Oats Company, supra)] were slurried in 800 ml of water containing 50 ppm of calcium (0.185 g/l CaC12.2H2O). The pH of the slurry was adjusted to 6.0 with 1.0 N sodium hydroxide, and "Enzeco Thermolase" (supra) was added to the stirred slurry in an amount sufficient to provide 48 units (supra) per gram of oat flour. The temperature was increased to 80'C, and stirring was continued until the starch was liquefied.
After 20 min., the pH was adjusted to 4.0 with 1 N sulfuric acid, and the mixture was heated at 95 C for 10 min. to SU~S~ lt SHEET

PCI'/US90/0364s ~'0 91tO0027 9 2~)?.. ~472 Table I

Product- Protein ~%) residue Soluble Inso~u~le Example pHratio product resldue 1 6 2.79 3.3 66.1 2 7 2.47 3.1 44.1 3 9 5.43 13.9 35.5 4 11 15.3 17.7 16.6 Table II
Enzyme conce~tration DP >9 (unlts/g (% of total Example substrate) oligomers) 6 93.0 6 12 47.7 7 24 36.5 SUBSTITUTE SHEE~

''091/00027 -lo- ~ O ~ fl 72 inactivate the enzyme. The pH was ten adjusted to 6.2 with 1 N sodium hydroxide, and the soluble product was separated ~rom the insoluble residue following the procedure described in Examples 1-4. The total dietary fiber ~Prosky et al., J. Assoc. Off. Anal. Chem. 67:1044 (1984); 68:399 (1985)] amounted to 4.8% of the product, compared to 7-8 normally obtained in the products of this invention.
Becaus~ of the acid inactivation of the enzyme and subsequent neutralization with sodium hydroxide, the sodium content of this soluble product was 5215 microg/g, in contrast to the range of 200-900 g/g for products having the enzyme inactivated by steam injection cooking.

Example g Pilot Scale Treatment of Oat Bran. Four kilograms of oat bran [National Oats Company (supra)] was slurried in 8 1 of water containing 25 ppm of calcium (supra). The pH
of the slurry was adjusted to 6.0 with 1.0 N sodium hydroxide, and "Takalite L-340" (supra) was added to the slurry in a large Sigma mixer in an amount sufficient to provide 1632 Modified Wohlgemuth Units (MWU) per gram of substrate, where a MWU is that activity which will dextrinize 1 mg of soluble starch to a defined size dextrin in 30 min. under specified conditions (Biotech Products Div., Miles Laboratories, Inc., Elkhart, IN). During a period of about 10-15 min., the temperature was increased to about 95-C with steam heat. After 20 min., the enzyme was inactivated by passing the mixture through a stem injection cooker. The warm slurry was centrifuged at 15,000 rpm by a large "Sharples" centrifuge to separate the soluble components from the insoluble components. The percent oligomer composition of the solubles was: DP >9, 32.3; DP 9, 0; DP 8, 0; DP 7, 1.0; DP 6, 13.0; DP 5, 13.9;
DP 4 6.4; DP 3, 13.0; DP 2, 12.1; DP 1, 5.6.

SU~S~ITIJT~ SHEET

w09l/00027 - ~3~72 Example 10 Pilot-Scale Treatment of Oat Flour. Six kilogram of oat flour ~National Oats Company (supra)~ was slurried in 18 l of water containing 25 ppm of calcium (supra). The pH of the slurry was 5.75. After gelatinization by passage of the mixture through a steam injection cooker, the slurry was collected in a 30-gal steam-heated kettle. "Enzeco Thermolase" (supra) was added to the slurry in an amount sufficient to provide 1 unit per gram of oat flour. After 5 min. of stirring at 80 -90-, the enzyme was inactivated by passing the slurry through a steam injection cooker (supra). The warm slurry was centrifuged at 15,000 rpm by a large "Sharples" centrifuge to separate the soluble and insoluble components. The products were dried separately on hot rolls. The oligomer composition indicated 98% DP g and larger.

Example 11 Sensory Evaluation of Oat Fiber-Containinq Ice Milks. The soluble oat fiber product of Example 7 and the starting oat flour from which it was obtain (supra), were evaluated as ingredients in ice milks. For each preparation, 484 g of 0.5%-fat milk, 100 g of sugar, 1.9 g of vanilla extract, and 0.4 g of uniodized salt were mixed for 1 min. in a blender with the oat products and in the amounts reported in Table III. Each mixture was treated in a 2-qt. ice cream mixer (Oster) for 30 min.
An 18-member trained panel experienced in testing cereal products evaluated the ice milk samples for flavor, texture, and overall quality by a modification of the method of Warner et al. ~Cereal Chem. 60:102-106 (1983)], herein incorporated by reference. At each panel session, the testers received a control sample of SIJBSIIT'~TE SHEET

~09l/00027 PCT/US90/03645 ,~ 0 3 ~ 4 7 ~

laboratory-prepared ice cream and two randomized, unidentified ice milk samples. The panelists were instructed to rate the three samples for intensity of the descriptors listed in Table III, using the scales in the Table footnotes. Scores were statistically analyzed for significant differences at the 95% confidence level <0.05) The results in Table III show that the sweetness of the oat-containing samples did not vary significantly from that of the plain ice milk, and two of the oat samples (llD and llG) did not vary significantly from the ice cream control. The vanilla flavor intensity was highest in the ice cream control, and two of the oat samples (llD and llF) were not significantly different; all the oat-containing samples ranged between 4.9 and 5.5 except llG and llH, which were significantly lower than the others. The creamy flavor intensity also was highest in the ice cream control;
next in creamy flavor were the highest in the ice cream control; next in creamy flavor were the three ice milk samples containing the invention product. Cereal flavor intensity was significantly lower in the three samples containing the invention product than in the three samples containing the starting oat flour, and two of the invention samples were not significantly different from the ice cream control and the ice milk that contained no oat product.
The creamiest texture among the ice milks was exhibited by llE; all the other ice milks did not vary significantly from sample to sample. Graininess was significantly lower in the three invention samples than in the other three oat-containing samples. Cohesiveness of llE did not vary significantly from that of the ice cream control; all the other ice milks ranged from 2.9-4.0 Density values ranged from a low of 2.2 for the plain ice SUBSIiTUIE SHET

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milk to a high of 7.6 for the ice cream control. Both the invention samples and the other oat samples yielded increasing density with increasing concentration of additive.
The ice milks were significantly lower in overall quality than the ice cream control, and the highest levels of oat flour staring material (llG and llH) resulted in significantly lower overall quality than that of the other ice milks. The ice milks containing the invention product had the highest score among the ice milks.
In summary, the soluble oat fiber product of the invention increased the creamy flavor, creamy texture, cohesiveness, and density of ice milks without imparting the inherent cereal flavor and grainy texture of the starting oat flour.

ExamPle 12 SensorY Evaluation of Oat Fiber-Containin~ Milks.
The oat materials listed in Table IV were blended into milk and evaluated for flavor characteristics as in Example 11.
For each preparation, 300 g of 0.5%-fat milk and 30 g of oat product were mixed for 1 min. in a blender, poured into a flask, and swirled before serving to the test panel.
Each panelist received a control of 0.5%-fat milk identified as having a milky flavor intensity score of 8, plus two randomized, unidentified test samples. The panelists were instructed to score the three samples for intensity of the descriptors listed in Table IV. Scoring was based on a O-lO scale (lO = strong; O = none). Scores were statistically analyzed as in Example 11. Values that were not significantly different are followed by the same letter in Table IV. The results reported in the Table show that the soluble oat fiber products of the invention (12E
and SUeSllTUlE SHEET

~'0 91tO0027 PCr/US90/03645 ~ Q .~ l 7 2 12F) had significantly lower cereal flavor intensity scores than the other oat materials.

ExamPle 13 Preparation of Yogurt. A yogurt was prepared from retail 2% milk, instant nonfat dry milk, sugar (sucrose), water, potassium sorbate, and the soluble oat fiber obtain in Example 10. A control yogurt without the fiber was also prepared. Compositions of the starting mixtures are set forth in Table V below. The ingredients were blended together with a wire whip. The resulting mixture were heated to 185-F in stainless steel beakers, held at temperature for 30 min., cooled to llO-F, and then inoculated with 2% bulk starter (Hansen's CH3 propagated once in 11% nonfat milk). The inoculated mixtures were cultured to a pH of 4.35-4.40 (270 min. for the control;
165 min. for the test sample). The yogurt was then stirred, poured into containers, and cooled overnight, achieving a final pH of 4.0-4.2. The samples were evaluated in a Brookfield viscometer Model RVT equipped with a No. 2 spindle at 0.5 rpm and at 50-F. They were also evaluated for sensory properties.
The control was characterized by a viscosity of 48,000 cp and a good yogurt flavor with smooth texture.
The test sample with the oat fiber of Example 10 had a viscosity of 22,400 cp, a slight cereal flavor, and a smooth texture.

SUeSTlTUTE SHEET

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~ ~9l/00027 2~3~ -~ 72 Table V

Control Example 13 Composition (~

Butterfat 1.00 1.00 MsNFa 12.00 7.00 Sucrose 6.00 6.00 K-Sorbate 0.04 0.04 Soluble Fiber... 5.00 a Mll~ sollds, non~at.

It is understood that the foregoing detailed description is given merely by way of illustration and that modification and variations may be made therein without departing from the spirit and scope of the invention.

SU~STIT~E SHEET

Claims (10)

THE EMBODIMENTS OF THE INVENTION IN WHICH AN EXCLUSIVE
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:

1. A method for producing a water-soluble dietary fiber composition comprising treating an aqueous dispersion of a gelatinized, milled, oat substrate with an .alpha.-amylase under conditions which will hydrolyze the substrate and yield a soluble fraction and an insoluble fraction, and recovering from said soluble fraction said water-soluble dietary fiber substantially free of water-insoluble fiber.

2. The method as described in claim 1 wherein the solids content of said oat substrate dispersion is in the range of about 10-40%.

3. The method as described in claim 1 wherein said oat substrate is selected from the group consisting of oat flour and oat bran.

4. The method as described in claim 1 wherein said treatment is performed at a temperature in the range of about 70°-100°C.

5. The method as described in claim 1 wherein said .alpha.-amylase is thermostable and wherein the starch is gelatinized concurrently with said hydrolysis.

6. A dietary fiber product produced by the method of claim 1.

7. A dietary fiber product produced by the method of claim 2.

8. A dietary fiber product produced by the method of claim 3.

9. A dietary fiber product produced by the method of claim 4.

10. A dietary fiber product produced by the method of claim 5.