Patent Application
20050220966
The invention relates to a process for preparing a spoonable acidified food product suitable for use as an acid cream alternative which cream comprises a fat phase consisting at least partly of vegetable oil or marine oil, said cream further comprising biopolymer, protein and optionally further ingredients. The invention further relates to the cream obtainable by this process.
Spoonable soured low-fat vegetable fat-based cream alternatives have been described in EP-A-540087 and U.S. Pat. No. 5,372,825 which disclose creamy, cultured vegetable fat-based cream alternatives comprising 5-15% fat, up to 3.5% milk protein, the cream alternative having a pH value between 4.0 and 4.8, and the cream alternative having a spoonable texture and good taste.
The products according to EP-A-540087 comprise a thickener system to achieve the desired yield stress. Suitable thickeners are selected from the group consisting of locust bean gum, guar gum, alginate, carrageenan, microcrystalline cellulose and starches. The products are prepared in a process wherein a premix is made of fat, protein components, thickener and water or skimmed milk at 40 to 100° C., which mix is cooled, homogenised, cooled further, cultured to pH 4-4.6 and stored at less than 15° C.
The resulting products were found to have the desired spoonable rheology. However they are still susceptible to syneresis, which is separation of a small volume of water, upon storage at a temperature between 0 and 15° C. Such syneresis reduces the attractiveness of the products for a consumer and is therefore less desired.
It is therefore an object of the current invention to provide a spoonable soured low-fat vegetable fat-based cream alternative, which is stable upon storage.
It has surprisingly been found that a cream with low biopolymer phase volume, which is preferably obtained by specific process measures, fulfils this objective.
Therefore the invention relates to a process for the preparation of a spoonable, soured non-dairy cream comprising from 5 to 35 wt % fat, from 0.05 to 15 wt % protein, 0.01 to 3 wt % biopolymer, said cream product having a pH value between 4.0 and 5.8 said process comprising the steps of
In a further aspect the invention relates to a product obtainable by this process.
In another aspect the invention relates to a spoonable soured non-dairy cream comprising a dispersed oil phase and a continuous aqueous phase said cream comprising from 5 to 35 wt % fat, said fat being either a vegetable oil or marine oil or a combination thereof; from 0.05 to 15 wt % protein in the form of a protein phase, 0.01 to 3 wt % biopolymer, said cream having a pH value between 4.0 and 5.8, wherein the cream comprises a phase separated water phase comprising a biopolymer phase and a protein phase, wherein the phase volume of the biopolymer phase is from 10 to 60 vol % on total product volume.
The invention relates to spoonable creams. Spoonable creams display at 5° C. the following characteristics:
Yield stress and Bingham viscosities are determined utilising the Carrimed Rheometer. Measurements are performed at 5° C. using 4°-cone and plate geometry. The shear stress was increased from zero at a rate of 60 Pa/min and shear rates were measured until values in excess of 600 s−1 were achieved. The measurement was then terminated. A graph of shear stress vs. shear rate was plotted and a straight line fitted to the curve between the shear rates of 100 to 300 s−1. The slope of this line is the Bingham viscosity. The yield stress is determined by extrapolation of this line back to zero shear rate.
Generally the dry matter content of spoonable creams is from 15wt % to 50 wt %, more preferably from 20 to 40 wt %, most preferred from 25 to 35 wt % on total product weight.
Non-dairy creams are emulsions of a water continuous phase and a dispersed fat phase, which is essentially based on vegetable fat. The presence of a small amount of dairy fat is tolerable e.g. when derived from ingredients that are part of the cream such as milk powders.
In the description and claims where weight % is used this is weight % on total product weight unless otherwise is indicated.
In the description and claims the terms “oil” and “fat” are used interchangeably.
Volume fractions are defined on total product volume unless otherwise is indicated.
Syneresis is defined as separation of (part of) the aqueous phase from a cream, in the form of “loose” water. The amount of syneresis is defined as the amount of water (wt % on total cream weight) that can be decanted after storage. The test to determine syneresis levels is described in the examples. Preferred products according to the invention show a syneresis of less than 10 wt %, more preferred less than 5 wt %, even more preferred less than 1 wt %.
The spoonable creams according to the invention comprise from 5 to 35 wt % fat, from 0.05 to 15 wt % protein and from 0.01 to 3 wt % of a biopolymer.
In the context of the invention protein phase is defined as the phase separated protein rich part of the water phase. In the context of the invention the products may comprise more than one protein enriched phase, which can be separated due to physical barrier or may differ in type of protein. In the below the combination of protein phases is referred to as “the” protein phase.
In the context of the invention the biopolymer phase is defined as the protein depleted part of the phase separated water phase. Depending on the composition of the water phase more than one biopolymer phase may form. For the purpose of the invention the combination of biopolymer phases is referred to as “the” biopolymer phase. In the context of the invention, the terms biopolymer and thickener are used interchangeably.
The invention relates to water continuous cream alternatives containing a dispersed oil phase.
Consistency of these products is defined in terms of the yield value and Bingham viscosity as described above.
It is well known that some aqueous compositions comprising both proteins and other biopolymers such as polysaccharides may form an inhomogeneous mixture. Gelation/network formation of the protein phase, e.g. by acidification, followed by mixing in of a biopolymer phase, results in inhomogeneous phase. For the present invention we will refer to such an inhomogeneously mixed system as a phase separated system.
It was surprisingly found that the moment, at which a biopolymer is added in the process during preparation of a cream, determines the level of syneresis and storage stability of the cream to a large extent. Therefore in the process of the invention, the biopolymer is added after network formation of the protein due to acidification of the product (step d).
Without wishing to be bound by any theory applicants believe that the above described order of addition will lead to creams wherein the biopolymer phase occupies a smaller volume, leading to a higher viscosity of the biopolymer phase and therefore to reduced syneresis compared to products prepared according to another process such as that described in EP-A-540087. It is believed that the biopolymer is able to bind this water such that syneresis is reduced. The underlying reason for this is believed to be found in the presence of a separate protein phase and a separate biopolymer phase and especially in the relative volumes of the separate protein phase and the separate biopolymer phase in the products according to the invention.
The mixing in of the biopolymer in step (d) is preferably at a temperature above the gelation temperature of the polymer.
The products according to the invention comprise a phase separated water phase comprising a biopolymer phase and a protein phase. Without wishing to be bound by any theory it is believed that the protein is present in the form of an acidified protein network containing protein coated fat droplets, which are the dispersed phase. The biopolymer phase is separately present and preferably forms the remainder of the aqueous phase.
In a preferred embodiment, the biopolymer is selected from the group comprising carrageenan, gellan, alginate, tara gum, guar gum, locust bean gum, methylcellulose, pectin, xanthan gum or a combination thereof.
In the context of the invention, ungelatinised, crosslinked starch is not included in the definition of biopolymer. These compounds may be added at any stage of the process.
Furthermore proteins (other than impurities contained in the biopolymer sources) are not included in the definition of biopolymer.
The fat is preferably added in step (a) as part of the premix.
To obtain a cream with the desired dispersed fat phase properties such as particle size, it is preferred that one or more homogenisation steps are included in the process. In a preferred process after step (a) or (b) the obtained mixture is homogenised at a pressure of between 100 and 400 bar, preferably at a temperature above the melting point of the fat.
A further preferred process includes homogenisation of the mixture of step (e) before step (f), preferably at a pressure of between 100 and 400 bar, and preferably at a temperature above the melting point of the fat. Optionally the mixture of step (e) is homogenised before heating, which takes place in step (e).
Most preferably both homogenisation steps are included in the process. This means that homogenisation preferably takes place before and after the mixing in of biopolymer.
Although the addition of the biopolymer(s) has been assigned to step (d) in the process above, biopolymer addition as described in step (d) could also take place after step (e) or (f).
Heating as in step (b) and (e) may take place in order to ensure pasteurisation or sterilisation of the product, or to achieve protein denaturation. The heating conditions need not be the same in step (b) and (e). The heating steps (b) and (e) can be combined into one heat treatment which is either carried out before or after acidification. More complicated temperature profiles involving more heating and cooling steps throughout the process are possible as well.
Preferably in both cases heating is carried out to a temperature above 60° C., preferably from 70 to 100° C.
Acidification may take place by microbiological or chemical acidification or a combination of both. In case the products are acidified microbiologically it is preferred that the cultures are made inactive after the acidification. Furthermore in case of microbiological acidification it is preferred that after step (c) the composition is set to a temperature of from 5 to 50° C.
After step (e) the products may be filled in containers either before or after including a cooling step (f) e.g. to a temperature of from 5 to 10° C.
In the process, heating as indicated in step (b) and (e) and the above-described homogenization can be carried out in any order. It is preferred to homogenize at a temperature above 60° C.
The homogenisation described above can be combined into one homogenisation step, which is either carried out before or after acidification. The separation in two homogenisation steps is preferred.
The creams produced by the process according to the invention are storage stable in that they show reduced syneresis compared to products obtained by a prior art process such as that disclosed in EP-A-540087 wherein biopolymer is added in step (a). These products show syneresis.
Therefore in a further aspect the invention relates to a spoonable soured non-dairy cream obtainable by the process according to the invention.
In another embodiment the invention regards a spoonable soured non-dairy cream comprising a dispersed oil phase and a continuous aqueous phase said cream comprising from 5 to 35 wt % fat, said fat being either a vegetable oil or marine oil or a combination thereof; from 0.05 to 15 wt % protein in the form of a protein phase, 0.01 to 3 wt % biopolymer, said cream having a pH value between 4.0 and 5.8, wherein the cream comprises a phase separated water phase comprising a biopolymer phase and a protein phase, wherein the phase volume of the biopolymer phase is from 10 to 60 vol % on total product volume.
In the products according to the invention the biopolymer is present in the form of a biopolymer phase. Preferably the volume fraction of the biopolymer phase is from 10 to 50 vol %, more preferred 10 to 40 vol %, even more preferred 20 to 40 vol %.
The concentration of biopolymer in the non-dairy cream according to the invention is from 0.01 to 3 wt %, preferably from 0.1 to 1.5 wt %. It will be appreciated that each individual biopolymer will have its own optimal concentration, which may depend on other characteristics of the food product such as the protein source, pH and salt content.
Preferably the composition of the biopolymer phase is such that the viscosity of the biopolymer phase is from 10 to 20 mPa.s at a shear rate of 100 s−1 determined at 40° C. It was found that an increased viscosity of the biopolymer phase generally was linked to an increased ability to reduce syneresis.
The protein is preferably selected from the group comprising milk protein, soy protein, pea protein or combinations thereof. The use of milk protein as at least part of the protein is highly preferred because of the positive effect of milk protein on the taste and flavour of the final product.
Suitable sources of milk protein are for example selected from the group comprising milk, skimmed milk or skim milk powder, butter milk or butter milk powder, butter serum powder, whey or whey powder, whey protein concentrate, whey protein isolate, caseinate or a combination thereof. The most preferred protein is protein originating from buttermilk because of its superb taste and flavour contribution.
The amount of protein is from 0.05 to 15 wt %, preferably from 2 to 10 wt %, more preferred from 2 to 6 wt %. In general the lowest possible protein concentration is most advantageous because of cost reasons.
The products according to the invention comprise from 5 to 35 wt % fat. Preferred products comprise 15 to 35 wt %, more preferred from 18 to 25 wt % fat.
The fat is either a vegetable oil or marine oil or a combination thereof. The fat is essentially free of dairy fat which implies that the level of dairy fat on total fat is preferably below 10 wt %, more preferred below 5 wt %, even more preferred below 1 wt %. This regards added dairy fat and does not include dairy fat derived from the other ingredients such as dairy fat included in milk powders.
The fat is preferably selected from the group comprising coconut oil, palm oil, olive oil, palm kernel oil, soybean oil, rapeseed oil, sunflower oil, safflower oil, or fully or partially hardened fractions thereof.
Optionally the fat is an interesterified fat blend. In a further preferred embodiment, the total amount of saturated fatty acid components in the fat is less than 45 wt %, based on the total amount of fatty acid components, and further preferred less than about 30 wt %.
Most preferably the solids content of the fat or fat blend that forms the dispersed fat phase is from 5 to 95% at 10° C., from 1 to 50% at 20° C. and from 0 to 10% at 35° C. More preferred the solids content is from 25 to 75% at 10° C., from 7.5 to 35% at 20° C. and from 0 to 5% at 35° C. Most preferred the solids content is from 60 to 75% at 10° C., from 10 to 35% at 20° C. and from 0 to 5% at 35° C.
Without wishing to be bound by any theory, it is believed that in products according to the invention, the fat droplets are coated by protein and hence may mimic protein particles in many characteristics. When studied under a microscope, the products according to the invention preferably show a continuous aqueous phase in which fat droplets are dispersed in the form of fine droplets that are preferably at least partly coated with protein. Preferably at least 75 vol %, more preferred 90vol % of the fat droplets is in the protein phase. Optionally a small part of the fat droplets (preferably less than 10 vol %) is located at the interface between the protein phase and the biopolymer phase or in the biopolymer phase.
Optionally the products according to the invention comprise emulsifier. For the purpose of the invention the term emulsifier does not encompass protein. However very high amount of emulsifier are preferably avoided as this could lead to a change in texture in terms of the contribution of the fat droplets to consistency of the product, especially over the protein phase and the biopolymer phase. Preferably the amount of emulsifier is below 1 wt %, more preferred below 0.5 wt %. Suitable emulsifiers are for example monoglycerides (saturated or unsaturated), diglycerides, phospholipids such as lecithin.
Optionally, usual additives for emulsions such as salt, herbs, spices, flavours, colouring matter, preservatives, sweetener and the like may be added.
Normally, for use as a cream alternative at least some salt may optionally be present. The amount of salt may vary depending on the consumer preference in a specific country, but amounts up to 1.5 wt % are generally recommended. The preferred salt is sodium chloride.
The products have a pH of about 4.0 to 5.8, preferably between 4.2 and 5.2, and most preferred between 4.2 and 4.6. Acidification of the starting ingredients to this pH can be obtained by any suitable method such as microbial acidification or chemical acidification for example using lactic acid, glucono deltalactone or another acidifying agent. The pH can be further adjusted by the use of a base such as sodium hydroxide.
For obtaining further improved mouthfeel, in one embodiment of this invention preferably some gelatin will be present. The product preferably comprises at least 0.5 wt % gelatin (based on. total weight of the product), and further preferred at least 0.6 wt %.
The invention is illustrated in the following non-limiting example.
General
Method to Determine Syneresis
A sample of 200 g in tub was taken. Half of the product was taken out with a spoon. The product is put to a temperature of 25° C. for 4 hours and then for 20 hours at 5° C. The water is removed and by weighing the sample both before and after water removal, the amount of syneresis is determined.
Determination of Phase Separation
The product was poured in tubes that were centrifuged at 50° C. for 2 h using a Gerber centrifuge at a speed, which corresponds to about 100 g force. Phase volumes for upper biopolymer-rich and lower protein-rich phase were quantified for each tube.
Products were prepared according to table 1
The fat type was sunflower oil.
Process
Water phase and fat phase ingredients except for guar gum and acids were mixed at about 60° C. After mixing the composition was pasteurized at 85° C. for 10 minutes, and cooled down to 44° C., after which homogenisation at 200 bar took place. To the homogenized composition acid was added, until a pH of about 4.8 was reached. Subsequently guar gum was added, followed by heating the mixture to 85° C. The obtained product was homogenized at 300 bar, and subsequently heated to a temperature of 75° C. for filling small containers. The product was cooled down to below 10° C. and stored at chill temperature.
Result
The phase volume of the biopolymer phase was about 40%.
The obtained product showed little to no syneresis under the storage conditions described above.
| Number | Date | Country | Kind |
|---|---|---|---|
| 02252704.8 | Apr 2002 | EP | regional |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/EP03/02750 | 3/17/2003 | WO | 10/15/2004 |
