AU2002228475A1 - Food coating - Google Patents

Food coating

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Publication number
AU2002228475A1
AU2002228475A1 AU2002228475A AU2002228475A AU2002228475A1 AU 2002228475 A1 AU2002228475 A1 AU 2002228475A1 AU 2002228475 A AU2002228475 A AU 2002228475A AU 2002228475 A AU2002228475 A AU 2002228475A AU 2002228475 A1 AU2002228475 A1 AU 2002228475A1
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AU
Australia
Prior art keywords
starch
food
cross
coating
degraded
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Granted
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AU2002228475A
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AU2002228475B2 (en
Inventor
Pieter Lykle Buwalda
Heine Roelf Meima
Jantje Van Gijssel
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Cooperative Avebe UA
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Cooperative Avebe UA
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Priority claimed from EP01200313A external-priority patent/EP1228700A1/en
Application filed by Cooperative Avebe UA filed Critical Cooperative Avebe UA
Publication of AU2002228475A1 publication Critical patent/AU2002228475A1/en
Application granted granted Critical
Publication of AU2002228475B2 publication Critical patent/AU2002228475B2/en
Assigned to COOPERATIE AVEBE U.A. reassignment COOPERATIE AVEBE U.A. Request for Assignment Assignors: COOPERATIVE VERKOOP-EN PRODUCTIEVERENIGING VAN AARDAPPELMEEL EN DERIVATEN AVEBE B.A.
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Description

Title: Food coating
The present invention relates to a food coating or a batter based on starch and to a method for the preparation thereof. The invention also relates to the use of said starch hased food coating in improving textural characteristics of the coated food product. A wide variety of food products are on the market that have a coating or batter applied to them. They include poultry, meat, seafood, vegetables, cheese and snacks. In the past the composition of coatings and batters of ready-to -prep are food items has gained much attention. A high . demand for convenience combined with a need for traditional bite, crispiness and other textural attributes has led to a wide variety of inventions relating to frozen French fries, frozen fish, meat and poultry, and frozen vegetables. Upon frying, baking or cooking, these products should regain a fresh appearance and tender crispy taste. Another reason for coating or battering foods is that it makes products larger and less expensive, because the batter is usually cheaper than the product itself.
A further demand on coated food derives from the fast food area. In the fast food area products are prepared in advance and kept warm using an infrared lamp or an oven. If the product is not sold within a certain time frame the product or the coating becomes soggy and unattractive and must be discarded. The application of a coating can prolong the holding time and therefor save costs for the fast food caterer.
Applying a coating or batter to a certain food item has previously been disclosed. US patent 5,141,759 describes a method of applying a starch based coating to frozen French fries. The coating consists of ungelatinized potato starch, ungelatinized modified corn starch, rice flour, and other minor ingredients (salt, baking soda, etc.). US patent 5,760,168 describes a coating consisting of cross-linked tapioca, rice flour, minor ingredients and/or tapioca dextrin, high amylose corn starch, cross-linked potato starch, acid converted corn starch. In order to keep the non-gelatinized starches from settling sometimes xanthan, guar or other gums are added. US patent 3,751,268 describes a batter, that essentially consists of water and an unmodified, ungelatinized high amylose corn starch. US 4,504,509 describes a liquid batter of cross-linked high amylose starch. In general the high amylose starch in these patents is applied in order to further enhance the textural characteristics as compared to a batter in which it is omitted. Although many high amylose starches are known, only the varieties on corn are commercially available. One such a commercially available high amylose starch (Su2) is described in US 5,476,674 and is essentially used as a thickener. The application of high amylose corn starches has certain distinct disadvantages: the pricing is high, it has a distinct grainy off-taste which is a particular draw back when applied on a potato product and the availability is rather limited. It is a surprising benefit of the present invention that enhanced textural characteristics of batters can be attained on the basis of conventional starches that are also more accessible. Using high amylose type starch is not necessary according to the invention.
US 5,997,918 describes a method for the preparation of coatings on food products based on cross-linked corn starches that are not degraded.
It is a goal of the present invention to provide for a starch based food coating or a batter that does not have the above described disadvantages. It is a further goal of the invention to provide a method for the preparation of a starch based coating for food that is independent of the source of starch. It is a further goal of the invention to provide for food products having improved textural characteristics. Other goals of the invention will become clear from the following description of the invention and a number of its specific embodiments.
It has presently been found that when a specifically treated starch-is used that is cross-linked, degraded and non-gelatinized, a food coating can be prepared that meets the above defined criteria and provides for the desired texture of the resulting coating.
In one aspect the invention pertains to a food coating or batter " composition comprising degraded, cross-linked non-gelatinized starch. These food coatings are capable of sustaining a crispy texture and prevent the product coated with the food coating according to the invention from becoming soggy. Furthermore a food coating according to the invention exerts an essentially neutral taste on the product to which the coating is applied. This is especially advantageous on products of which the taste is significantly different from the origin of the starch such as is the case with for example fish with a coating based on corn starch or on potatoes with a coating based on corn. The degraded, cross-linked non-gelatinized starch according to the invention is also advantageously used in the (partial) replacement of conventional high amylose starches which have previously been used in this type of food coating. A combination of degradation and cross-linking of starch in relation to food products is known. The application of pre-gelatinized degraded cross- linked starches in gelled food-stuffs has been disclosed in for instance in US Patent 4,228,199. For the coating of foodstuffs, however, this type of product has never been described or contemplated. For instance EP 0 901 756 discloses starch-based dust coatings that are preferably gelatinized to obtain the desired properties and that comprise either hydrolyzed or cross-linked starches, but not starches that have both been degraded and cross-linked.
In another aspect the invention pertains to a method for the production of a preparation for a starch-based food coating or batter composition comprising the steps of degrading the starch and cross-linking the starch.
The degradation of starch generally encompasses the reduction of both molecular weight and viscosity of the starch. A number of ways and reagents are known to reduce molecular weight and viscosity. These methods involve dry roasting, dextrinization, phosphorylation at elevated temperature, enzymatic conversion, acid hydrolysis or oxidation in solution, etc. For granular products in general acid degradation, enzymatic hydrolysis or oxidation are preferred. For acid degradation hydrogen chloride and sulphuric acid are the acids of choice, although other acids can be used. The oxidation of starch can be accomplished with a large number of agents such as ozone, potassium permanganate, hydrogen peroxide (with or without a catalyst) and sodium hypochlorite. The sodium hypochlorite oxidation of starch is preferred. For enzymatic degradation α-amylase, β-amylase, isoamylase, pullulanase, or glycosyltransferases may be employed. (For a review see Modified starches: properties and uses; O.B. Wurzburg, CRC Press, Boca Raton 1987, Chapter 2). A preferred degradation method comprises oxidation using a hypochlorite, preferably an alkali metal hypochlorite such as sodium hypochlorite. Typically, this method involves 1 to 45 grams of active chlorine per kilogram of starch. It is preferred that between 5 and 30 grams of active chlorine per kilogram starch is used. In another preferred embodiment, the degradation is carried out using a strong acid, preferably a mineral acid such as hydrochloric acid or sulfuric acid. Both acids give essentially the same results, with minor differences in process conditions. The type of acid, the concentration of the acid, the temperature, the concentration of the starch, and the reaction time will vary depending on the desired properties of the product (see Modified starches: properties and uses; O.B. Wurzburg, CRC Press, Boca Raton 1987, page 19 et seq). The acid is preferably used in an amount to obtain a reaction mixture having a pH of three or lower. The conditions during the reaction will typically comprise a temperature of 0-65°C, preferably 35-55°C, more preferably 30-50°C.
Cross-linking of starch is also considered as a well known reaction. A wide variety of reagents are known that can render the starch polymer into a network. In general these bi-, tri-, or multifunctional reagents are capable of reacting with the hydroxylic functions of the starch. The cross-linking can be achieved by esterification or etherification. Among the reagents are adipic anhydride, acrolein, epichlorohydrin, phosphorous oxychloride, sodium trimetaphosphate, cyanuric acid chloride, formaldehyde, dimethylol urea, and divinyl sulphone. For the food market, the mixed acetic adipic anhydride, phosphorous oxychloride and sodium trimetaphosphate are significant. A special way of cross-linking is physical modification. This can be accomplished by heating at higher moisture contents or by heating at elevated pH and temperature and low moisture content which is described in for instance WO 96/04135. It is also possible to cross-link the starch by means of applying certain physical means, such as heating the starch under humid conditions (annealing), and the like. Preferred is to carry out the cross-linking using agents that yield distarch phosphates, such as a methaphosphate salt (e.g. sodium trimetaphosphate (STMP)) and phosphorous oxy trichloride. The extent of cross-linking will be based on regulations of food legislation in the specific countries that the product is intended for. The phosphate content of the product should not exceed 0.4 wt.%, based on the weight of the product.
In a method according to the present invention the order of the reactions, degradation/cross-linking or cross-linking/degradation, is of minor importance. In the present invention the degraded cross-linked starch may be derived from maize, barley, wheat, rice, triticale, millet, tapioca, arrow root, banana, potato, sweet potato, etc. or from high amylose starches like amylomaize, mung bean starch pea starches, high amylose potato starch, etc. These high amylose starches may be derived from plants that preferentially produce amylose through natural processes or by genetically modifying plants. It is to be noted that, although it is in principal possible to use a high amylose starch to base a food coating or batter composition therefor in accordance with the invention on, it is preferred to use a starch having a normal amylose content, i.e. of 60 wt.% or less, based on the weight of the dry starch. In a more preferred aspect of the invention a starch having an amylose content of 45 wt.% or less, based on the weight of the dry starch is used.
It will be appreciated that it is possible to use a slightly modified starch to prepare the degraded cross-linked starch from (e.g. esterified or etherified to a DS <0.02). It is well known to the artesian that a slight modification has little or no effect on the properties of starch. Suitable derivatives include esters such as acetates, succinates, adipates, and octenylsuccinates, prepared by reaction with corresponding anhydrides or vinyl esters. Other esters are phosphates prepared by reaction with orthophosphates or polyp hosp hates. Ethers include hydroxypropylethers prepared by the reaction of starch with propylene oxide. In another aspect the invention pertains to the use of degraded, cross-linked non-gelatinized starch for improving textural characteristics of coatings for food. It has been found that particularly the crispiness of a food coating based on a degraded, cross-linked non- gelatinized starch is very good and also stays of good quality over a prolonged period of time. The regularly holding time for fried or oven treated coated food of five minutes can be extended to over fifteen minutes.
In food services, different types of prepared hot food stuffs are placed under a heating lamp in order to keep them warm. The use of a coating or batter composition according to the invention in combination with the heating lamp can significantly extend the crispiness, and thus the holding time (thirty minutes or even longer), of the food stuffs. Another way of obtaining food with a longer holding time, in particular with respect to French fries, is the traditional way of increasing the dry substance content. In that way, a thicker dry surface is created which avoids food (French fries) from becoming tough after frying or oven treatment. However, products treated in this manner are not really crispy.
A food coating according to the present invention can be used in and/or on a wide variety of foods. Preferred foods are meat, fish, potato products, such as French fries, snacks and vegetables but also vegetarian products such as soy-based products as tofu or tempeh can be coated with the batter according to the invention. A food coating according to the invention may be prepared from any conventional batter composition to which degraded, cross-linked non- gelatinized starch is added. A typical batter composition of which a coating for the above foods may be prepared comprises water, flour (wheat flour, rice flour), modified starch (e.g. pre-gelatinized starch, cross-linked acetylated starch and the like), phosphates, baking powder, spices, proteins, various salts and other minor additives. Examples of such additives include gums, such as xanthan gum, guar gum, and locust bean gum. The amounts in which these ingredients are used, will depend on the specific application and the food product to be coated. The chosen combination of ingredients determines the properties of the coating. Examples of such properties include adherence to the surface of the food product, binding to the food stuff, texture properties, appearance (visibility / invisibility).
The above described batter composition may be applied to a food product to be provided with a food coating according to the invention in any conventional way, such as applying the batter composition to the food product by dipping, spraying, encapsulating and the like.
After provision with the batter composition, the products to be provided with a coating according to the invention can be prepared in any conventional way such as deep frying, steaming or baking (e.g. in a pan or an oven) but also more convenience based cooking techniques can be employed such as those involving microwave or infrared ovens.
It will be understood that the invention also pertains to a food product coated with a food coating or batter according to the invention and to a method for the manufacture of a food product of increased crispiness comprising a step wherein a coating comprising a degraded, cross-linked non- gelatinized starch is applied to the food product.
Examples Experimental part
- Sensory evaluation: The coated foods were tested by an expert panel in sensory attributes. The products were evaluated and ranked. The attributes are expressed as the sum of the ranking on the total of the panel.
- Viscosity: The viscosity was measured using a Postumus flow cup - Pick up: The pick-up of a coating is determined by weighing a sample of French fries after and before coating. The pick-up is expressed as the percentage weight increase.
Example I The preparation of acid degraded cross-linked potato starch:
A 39% starch slurry is prepared of 1 kg of potato starch and water. To this slurry 50 mL of 10 N sulfuric acid are added. The temperature was raised to 45°C. The reaction is allowed to proceed for 17 hours. The slurry is neutralized with sodium hydroxide to pH 5-6 and washed. The resulting starch is resuspended in water to a 39% suspension.
To this slurry 25 g of sodium chloride and 170.5 g of a 4.4% (w/w) sodium hydroxide solution are added. The temperature is set to 35°C and 1.5 g of sodium trimetaphosphate are added. The reaction is allowed to proceed for 6 hours. The slurry is neutralized with sulfuric acid to pH 5-6 and washed and dried using conventional methods known to the art. Preparation of coated oven French fries
10 kg of potatoes were peeled in a carbon peeler. The potatoes were cut in pieces of similar length and a height and breadth of 10 mm in a snit of 10x10 mm. The resulting pieces were blanched for 8 minutes at 80°C. Pieces were selected with similar size. They were dried in a cabinet at 70°C at 20% RH until a drying loss of 24% was attained. The dried strips were divided into portions of 200 g and coated (see below). The coated strips were parfried for 2 minutes at 180°C. The products were frozen at -25°C packaged and stored at - 25°C for 1 day or longer.
The coating of French fries
A mixture was prepared of 173 g of Perfectamyl FFC (cross-linked starch of AVEBE), 67 g of AVEDEX W-90 (white dextrin of AVEBE), Rice flour BL100 (Silvo, Papendrecht), 67 g of degraded cross-linked potato starch, 12 g of salt and 14 g of Paselli P (pre-gelatinized cross-linked starch of AVEBE) in a mixing bowl. Trough this mixture 600 g of water was mixed with moderate stirring. After 1.5 hr this mixture was stirred for 10 minutes. The coating is poured over 200 g of French fry strips as previously prepared. The excess coating is discarded by dripping and venting air.
Oven preparation of French fries
Frozen samples are taken and placed in a small pre-heated kitchen oven at 225°C. The products are baked for 12 minutes. After cooling for 5 min. at room temperature the products are judged.
Comparative Example I Coating without degraded cross-linked starch
A second coating was prepared with 67 g of Perfectamyl FFC instead of 67 g of degraded, cross-linked non- gelatinized starch. The coating was applied to French fries, which were processed as previously described.
The results are summarized in table 1. It can be concluded that the addition of degraded cross-linked potato improves the crispiness of the French fry.
Table 1
Example I Comparative Example I
Coating composition:
AVEDEX W90 67 g 67 g
Rice flour 67 g 67 g
Salt 12 g 12 g
Perfectamyl FFC 173 g 240 g
Degraded cross-linked product 67 g
Viscosity: 36.5 sec 34 sec
Pick up: 28.4% 32.2%
Crispiness: 26 7
Example II
The coating of fsh
40 g of degraded cross-linked potato starch is mixed with a battermix (consisting of wheat flour, baking soda, spices and salt) and water until a viscous batter is obtained. A deep frozen piece of fish is dipped into the batter ensuring complete cover of the fish with batter. Any excess batter is removed. The fish is covered with breadcrumb. Subsequently the fish is parfried for 1 min at 180°C. The fish is left to cool and transferred to a bag and sealed. The bag is stored for 1 day at 20°C. The fish is cooked in an oven for 45-50 min at 180°C. After cooking the fish is evaluated
The fish had a very crispy texture in conjunction with a nice coloration of the batter. The adhesion of the batter was somewhat uneven.
Example III
Coating with adhesive properties
Example II was repeated with a mixture of 30 g of degraded cross- linked starch and 10 g of Perfectabind M20 (acetylated distarch phosphate of AVEBE) instead of the degraded cross-linked starch alone.
The batter had an excellent adherence to the surface of the fish. The crispiness was good.

Claims (17)

Claims
1. Food coating or batter composition comprising degraded, cross-linked non-gelatinized starch.
2. Food coating according to claim 1, wherein the starch is degraded using hypochlorite or a strong acid.
3. Food coating according to claim 1 or 2, wherein the starch is cross-linked to yield a distarch phosphate.
4. Food coating according to claims 1-3, wherein the starch has an amylose content of 60 wt.% or less, based on the weight of the dry starch.
5. Food coating according to any of the preceding claims, wherein the starch has an amylose content of 45 wt.% or less, based on the weight of the dry starch.
6. Food coating according to any of the preceding claims, wherein starch is derived from potato, tapioca, wheat, corn or a mixture thereof.
7. Food coating or batter composition according to any of the preceding claims, further comprising one or more of wheat flour, rice flour, salt, a phosphate, baking powder, a spice, a protein, a modified starch.
8. Method for the preparation of a starch-based food coating or batter composition comprising the steps of degrading the starch and cross-linking the starch.
9. Method according to claim 8, wherein the starch is degraded using a strong acid or a hypochlorite.
10. Method according- to claim 8 or 9, wherein the cross-linking of starch is achieved with a metaphosphate salt or phosphorous oxychloride or by physical means.
11. Method according to any of the claims 8-10, wherein the starch is esterified or etherified.
12. Use of degraded, cross-linked non- elatinized starch for improving textural characteristics of coatings for food.
13. Use according to claim 12 wherein one of the textural characteristics is an increased crispiness.
14. Use of degraded, cross-linked non- gelatinized starch as a substitute for high amylose starch in coatings for food.
15. Food product coated with a food coating or batter composition according to claim 1.
16. Method for the manufacture of a food product of increased crispiness comprising a step wherein a coating comprising a degraded, cross-linked non- gelatinized starch is applied to the food product.
17. Method according to claim 16, wherein the food product is prepared by deep-frying, baking or heating.
AU2002228475A 2001-01-29 2002-01-22 Food coating Ceased AU2002228475B2 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP01200313A EP1228700A1 (en) 2001-01-29 2001-01-29 Food coating
EP01200313.3 2001-01-29
PCT/NL2002/000048 WO2002060277A1 (en) 2001-01-29 2002-01-22 Food coating

Publications (2)

Publication Number Publication Date
AU2002228475A1 true AU2002228475A1 (en) 2003-02-20
AU2002228475B2 AU2002228475B2 (en) 2006-08-10

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AU2002228475A Ceased AU2002228475B2 (en) 2001-01-29 2002-01-22 Food coating

Country Status (9)

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US (1) US20040062837A1 (en)
EP (2) EP1228700A1 (en)
JP (1) JP4503233B2 (en)
CN (1) CN100396203C (en)
AU (1) AU2002228475B2 (en)
BR (1) BR0206781A (en)
CA (1) CA2435746C (en)
MX (1) MXPA03006698A (en)
WO (1) WO2002060277A1 (en)

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