Patent Application
20050130279
This invention relates to a process for producing of flavour enhancing esters. More particularly in a preferred embodiment it relates to the use of lipases or enzymes from lactic acid bacteria in catalysing a transesterification reaction to convert a mono-, di-, or triglyceride from a dairy source into desired flavour enhancing esters.
Various flavour enhancing esters are present in cheeses. Ethyl esters of fatty acids (C2 to C1O) are most abundant. Ethyl butanoate and ethyl hexanoate are primarily responsible for causing fruity flavours in raw milk and cheeses (Bills et al, 1965; McGugan et al, 1975; Horwood et al, 1987; Engels et al, 1997; Friedrich and Acree, 1998). Fruity flavours are generally regarded as a defect in Cheddar cheese, but are valued by some consumers (Urbach, 1995; 1997). Fruitiness is characteristic of some Italian-style cheese varieties such as Parmesan and Parmigiano Reggiano in which ethyl esters of C2 to C1O fatty acids are present at significant levels (Dumont et al, 1974; Meinhart and Schreier, 1986; Barbieri et al, 1994).
Esterification of free fatty acids and alcohols by the action of esterases is generally recognised as the mechanism of ester formation in cheeses, where ethanol is the major alcohol (Bills et al, 1965; Morgan, 1976; Fox et al., 2000). Esterases from dairy lactic acid bacteria (LAB) and pseudomonads can esterify ethanol and fatty acids to form esters such as ethyl butanoate and ethyl hexanoate (Hosono and Elliott, 1974; Hosono et al, 1974; Liu et al, 1998), but the esterifying activities are weak in aqueous media.
Thus it is known that it is possible to control at least one aspect of cheese flavour by the substitution of an alkoxy group from an added alcohol for an alkoxy group of naturally occurring glyceryl esters in cheeses. This reaction was thought to occur in two stages (Bills et al, 1965; Morgan, 1976; Fox et al, 2000). Firstly, hydrolysis of the naturally occurring glyceryl ester to form a glyceryl alcohol and also a carboxylic acid. Then secondly, esterification of the resulting carboxylic acid with an alcohol that has a desired alkoxy group (for example, ethanol). It would be advantageous to control this substitution of alkoxy groups with a single reaction (the transesterification reaction) rather than through a two-reaction process of hydrolysis followed by subsequent esterification (the esterification reaction).
For clarity the two stage reaction is illustrated in equations 1 and 2 below. A transesterification reaction is illustrated in equation 3.
Where:
It is an object of this invention to go some way towards achieving the desideratum of a one step process or at least to offer the public a useful choice.
Accordingly the invention may be said broadly to consist of a method for producing flavour enhancing esters which comprises:
In another embodiment the invention may be said broadly to consist in a process for producing flavour enhancing esters which comprises:
In a further embodiment the invention may be said broadly to consist in a process for producing flavour enhancing esters which comprises:
In one embodiment said esterase is a lipase.
In one embodiment said enzyme is added to said glyceride and alcohol in said aqueous medium.
In another embodiment the lactic acid bacteria from which said enzyme is derived is added to said glyceride and alcohol in said aqueous medium to produce said enzyme therein.
Preferably the glyceride from a dairy source is from whole milk cream, milk fat, cheese, enzyme modified cheese (EMC), buttermilk, whey, whey cream, fermented milk or other milk product.
The alcohol is selected so that an ester (or esters) having the desired flavour characteristics is produced. In one alternative, said alcohol is ethanol. In another alternative, said alcohol is 2-phenyl ethanol. However, the invention is not confined to these alcohols and may include a range of straight chain, branched chain and aromatic alcohols including (but not restricted to) those that may occur in natural cheeses.
In another alternative, the method defined above includes a fermentation step to produce alcohol.
Preferably alcohol-producing microorganisms mediate the fermentation step.
In one embodiment the alcohol-producing microorganism is Lactobacillus fermentum.
A number of other alcohol-producing bacteria can be used, (including heterofermentative Lactobacilli and Leuconostocs), and also yeasts.
In one alternative the acyl groups of said mono-, di- or triglyceride each have up to 10 carbon atoms and said alcohol is ethanol.
Alternatively, when said glyceride is a diglyceride, the acyl groups thereof have up to 6 carbon atoms and said alcohol is 2-phenylethanol.
In a further alternative when said glyceride is a monoglyceride the acyl groups thereof have up to 8 carbon atoms and said alcohol is 2-phenylethanol.
Preferably said lipase is a 1,3-specific lipase from Rhizomucor miehei.
Alternatively, said enzyme is derived from one or more strains of the following genera: of bacterial cultures, including (but not limited to):
In one embodiment said enzyme is derived from the strain Streptococcus thermophilus ST1.
Alternatively said enzyme is derived from any one of the strains Streptococcus thermophilus NCIMB 700821 (obtained as NCDO 821 and referred to as 821 hereinafter);
Lactobacillus fermentum B4017; Lactococcus lactis subsp. cremoris E8 and Lactococcus lactis subsp. lactis ML3.
In another embodiment the flavour enhancing ester so prepared is added as an ingredient to a food product.
Preferably said food product is a dairy product.
Preferably said dairy product is a cheese or a cheese based product.
The invention may also be said broadly to consist in a flavour enhancing ester prepared by the process defined herein above.
The invention may also be said to consist in a food product containing said flavour enhancing ester.
Preferably said food product is a dairy product.
Preferably said dairy product is a cheese or cheese based product.
This invention may also be said broadly to consist in the parts, elements and features referred to or indicated in the specification of the application, individually or collectively, and any or all combinations of any two or more of said parts, elements or features, and where specific integers are mentioned herein which have known equivalents in the art to which this invention relates, such known equivalents are deemed to be incorporated herein as if individually set forth. The invention consists in the foregoing and also envisages constructions of which the following gives examples.
a, 2b and 2c are plots of the synthesis of ethyl esters by non-growing cells of St. thermophilus ST1 in phosphate buffer against time. (a) ethyl hexanoate from 100 mM ethanol and 35 mM dihexanoin; (b) ethyl octanoate from 500 mM ethanol and 23 mM monooctanoin; and (c) ethyl decanoate from 500 mM ethanol and 10 mM monodecanoin. ●, esters; ◯, fatty acids.
The invention may be more fully understood by reference to the following detailed examples.
As used herein the term “flavour” is intended to mean flavour and/or aroma as appropriate in the context.
As used herein the term “glyceride from a dairy source” is intended to mean a composition comprising one or more of triglycerides, diglycerides and monoglycerides present in or generated from milk fat. This is preferably milk fat of bovine origin, but also includes milk fat of ovine (sheep) or caprine (goat) origin. Triglycerides are the predominant lipid class in milk fat, accounting for 97-98% of total milk fat (Christie, 1995). Small amounts of diglycerides and monoglycerides are also present and levels of these components can be elevated by the hydrolytic action of lipases. The glycerides of milk fat are very diverse in their composition. The huge range of different fatty acids esterified in the glyceride molecules confers this diversity. There are 10 major fatty acids ranging in chain length from four carbons to eighteen carbons. However, in total over 400 different fatty acids have been identified in bovine milk fat (Jensen and Clark, 1988).
In calculating the “transesterification activity” a unit of transesterification activity means the amount of enzyme catalysing the synthesis from tributyrin and ethanol of 1 nmol of ethyl butanoate per minute. A standard assay for determining transesterification activity is set out in example 1.
In calculating the “esterification activity” a unit of esterification activity means the amount of enzyme catalysing the synthesis from butanoic acid and ethanol, of 1 nmol of ethyl butanoate per 24 h. A standard assay for determining esterification activity is set out in example 2.
Microorganisms and Growth Conditions
Streptococcus thermophilus ST1 was from the culture collection of the Fonterra Research Centre, Palmerston North, New Zealand. Cultures were grown at 37° C. in M17-glucose broth (Difco, France). Cultures were innoculated with 1% (v/v) of precultures and were incubated statically for up to 36 h.
Preparation of Cell Suspensions
Unless stated otherwise, cells in 300 mL (24 h-cultures) were harvested by centrifugation at 7000 g for 10 min at 4° C. Cells were washed in 100 mL (2×) of 0.1 M potassium phosphate (pH 7.0), followed by centrifugation. The washed cell pellets were resuspended in 60 mL of the same buffer and dispensed in 10 ml aliquots into universal bottles, and stored at −20° C. before use.
Ester Synthesis by the Transesterification Reaction
A standard assay for determining the transesterification activity consisted of a 5.0 mL reaction mixture containing 80 mM potassium phosphate, pH 7.0, 2.0 mL cell suspension, 500 mM ethanol and 10 to 35 mM glyceride. A tributyrin substrate was prepared as described in Holland & Coolbear (1996) and other glyceride substrates were prepared accordingly. The reaction was started by adding 0.5 mL of 5 M ethanol to the above reaction mixture pre-incubated at 30° C. for 5 min. A 1.0 mL sample was immediately removed and added to a test tube containing diethyl ether and extracted. The remaining reactants were incubated at 30° C. for up to 60 min and samples were taken at intervals and extracted for ester analysis as described below. In some experiments, substrate concentrations were varied according to a particular experiment as indicated. Controls lacking substrates or lacking cells were also included. A unit of enzyme activity (transesterification) was defined as the amount of enzyme catalysing the synthesis from tributyrin and ethanol of 1 nmol of ethyl butanoate per min and specific activity as units per mg protein or cell dry weight (cdw).
Quantitation of Esters by Gas Chromatography (GC)
One mL of sample taken from a reaction mixture or broth culture was added to a 16 mL Kimax screw-capped test tube containing 2 mL of diethyl ether and 1 mL of internal standard (180 mg/L ethyl acetate in water). Extraction was performed by shaking vigorously for about 2.5 min, followed by centrifugation at 1260 g for 5 min in a centrifuge (Heraeus Megafuge 1.0). The top solvent layer was transferred to a vial containing small amounts of oven-dried anhydrous sodium sulphate and analysed for esters by gas chromatography (GC) as described below.
Following sample extraction, esters were analysed by GC. The analysis was performed using a Shimadzu GC-15A gas chromatograph with a fused silica capillary column (liquid phase, DB-1; length, 30m; i.d., 0.25 mm; film thickness, 1.0 μm) (J&W Scientific, CA, USA). The oven was temperature-programmed at 45° C. for 5 min, followed by increasing the temperature to 50° C. at 5° C. min−1, then to 270° C. at 20° C. min−1, and held at 270° C. for 8 min. A split injection was performed at a ratio of 5:1 and 3 μL of sample were injected. The injector and FID (Flame Ionisation Detector) detector temperatures were 250° C. and 275° C., respectively. Other conditions were: carrier gas (He) at 0.9 mL per min−1; H2 and air at 0.6 kg per cm2, respectively; makeup gas (N2 at 2 kg per cm2. The FID output signal was recorded and processed using appropriate software (Shimadzu CLASS-VP™ Chromatography Data System Version 4.2 from Shimadzu, Md., USA). Esters in the samples were identified and quantified by comparison with injections of known amounts of pure standards.
St. thermophilus ST1 was not able to synthesise esters from ethanol and triglycerides of C6 to C14, diglycerides of C10 and C14 and monoglyceride of C14 (data not shown). Tributyrin was the only triglyceride that strain ST1 was active towards. Strain ST1 was also able to synthesise ethyl esters from ethanol and diglyceride of C6 (dihexanoin) and monoglycerides of C8 (monooctanoin) and C10 (monodecanoin) (
Cultures and Growth
Cultures were from the culture collection of Fonterra Research Centre, Palmerston North, New Zealand, and were grown in M17-glucose broth (Difco, France) at 30° C. Lactobacillus fermentum B4017 was grown in MRS broth (Merk, Germany) at 30° C. Cultures were grown in 200 mL of appropriate broths supplemented with 50 mM ethanol and 3.3 mM tributyrin (final concentration). Controls contained either no added culture or no added ethanol or tributyrin. Cultures were incubated as stated above for up to 36 h. Samples were taken at intervals between mid-log to late stationary phases and stored at −20° C. before analysis. Samples were used for determinations of cellular dry weights, ethyl butanoate and other esters.
Transesterification Assays
Transesterification activities of growing bacterial cultures were assayed by measuring ethyl butanoate accumulation in an assay system similar to that described in Example 1.
Esterification Assays
Bacterial cells cultured in 400 mL of appropriate broth were harvested by centrifugation at 7000 g for 10 min at 4° C. Cells were washed by resuspending cell pellets in 30 mL (2×) of potassium phosphate buffer (100 mM, pH 5.8), followed by centrifugation at 7000 g for 10 min at 4° C. The washed cells were then resuspended in 10 mL of the same buffer, followed by adding 5 mL each of aqueous solutions of 8 mM ethanol and 8 mM butanoic acid to give a final concentration of 2 mM each of ethanol and butanoic acid, and final concentration of 50 mM potassium phosphate in a total volume of approximately 20 mL cell suspension. The final suspension, containing cells, ethanol and butanoic acid, was incubated statically at 22° C. for 24 h and then stored at −20° C. for subsequent analysis of ethyl butanoate by gas liquid chromatography (GLC). In calculating the esterification activity, a unit of esterification activity was the amount of enzyme catalysing the formation of 1 nmol of ethyl butanoate per 24 h. Specific activities were quantified as units per 100 mg dry weight of cells (dwc).
Quantitation of Esters
Esters were quantified by gas chromatography as described in Example 1.
Analysis of Esters by GC-MS
Esters in broth cultures were analysed by solid phase microextraction (SPME) and gas chromatography-mass spectrometry (GC-MS). SPME was performed as described by Liu et al (1998). The gas chromatograph (Shimadzu GC-17A) was equipped with a 30 m×0.25 mm i.d. fused-silica capillary carbowax column (film thickness 0.25 μm; Alltech, Ill., USA) and the injector temperature was 220° C. The carrier gas was helium (column pressure, 54 kPa). The oven temperature was programmed as: 2 min at 50° C., 3° C. min−1 to 80° C., 5° C. min−1 to 120° C., 20° C. min−1 to 220° C. and 6 min at 220° C. The GC column was connected directly to the ion source of a Shimadzu QP-5000 mass spectrometer (interface temperature, 230° C.). The MS was operating in the scanning mode from 40 to 350 M/Z at 2 scan s−1. Structures were assigned by spectrum interpretation and comparison of the spectra with bibliographic data.
A number of lactic acid bacteria were tested for their ability to synthesise ethyl butanoate from tributyrin and ethanol by growth in broths supplemented with the two substrates. Transesterification activities obtained were then compared with the esterification activities (synthesis of esters by reacting free acids with an alcohol). These activities are set out in Table 1. With both esterification activities and transesterification activities, there were some large species and strain differences. While the diversity of transesterification activities is consistent with the diversity of esterification activities, the former activity is higher than the latter by 34-7500-fold. Strains of St. thermophilus produced the highest transesterification activities (by up to 228-fold), compared to other lactic acid bacteria tested. This is consistent with their relatively high esterase activities. Notably, the transesterification activity of Lb. fermentum was comparable to that of St. thermophilus. The transesterification activities of the two lactococcal strains tested were higher, by up to 18-fold, than the activities of the strains of Lactobacillus, Leuconostoc, and Pediococcus that were tested.
aDefined as nmol min−1 mg−1; cdw, cell dry weight.
bDefined as the synthesis of ethyl butanoate from tributyrin and ethanol in broth culture.
cDefined as the esterification of butanoic acid and ethanol to form ethyl butanoate; data are extracted from Liu et al (1998).
dRatio of transesterification activity to esterification activity.
Synthesis of Ethyl Butanoate in Buffer
Ethyl butanoate was synthesised in a 5.0 mL reaction mixture comprising 80 mM potassium phosphate, pH 7.0, 50 mM ethanol and 33 mM tributyrin, unless specified otherwise. The tributyrin substrate was prepared as described elsewhere (Holland & Coolbear, 1996). The reaction was started by adding 0.1 mL of appropriately diluted enzyme preparation (up to 1000-fold dilution) to the above reaction mixture pre-incubated at 30° C. for 5 min. A 1.0 mL sample was immediately removed and added to a test tube containing diethyl ether and extracted (see below). The remaining reactants were incubated at 30° C. for up to 40 min and samples were taken at intervals and extracted for ethyl butanoate analysis as described below.
Synthesis of Esters in Cheese Based Medium
Ethyl butanoate was also synthesised in a cheese-based medium using 1,3-specific lipase from Rhizomucor miehei (sold by Novo Nordisk, Denmark as “Palatase 20000L”). This was carried out in a 9 mL reaction mixture consisting of 4 g young Cheddar cheese slurry and 10 mM ethanol. A slurry was prepared using proteolytic enzymes, emulsifying salts (tri- and disodium citrate) and water. The reaction was initiated with the addition of 40 μL of lipase and the mixture was incubated at 30° C. for 4 h. A control containing no added ethanol was also included.
Extraction and Analysis of Ethyl Butanoate
One mL of sample taken from a reaction mixture was immediately added to a 16-mL Kimax screw-capped test tube containing 2 mL of diethyl ether and 1 mL of internal standard (180 mg/L ethyl acetate in water). Extraction was performed by shaking vigorously for approximately 2.5 min, followed by centrifugation at 1260×g for 5 min (Heraeus Megaflige 1.0). The top solvent layer was transferred to a GLC vial containing small amounts of oven-dried anhydrous sodium sulphate and analysed for ethyl butanoate by gas liquid chromatography (GLC).
Fresh milk was separated and recombined to give a protein to fat ratio of 1:0.82. The recombined mix was pasteurised in a continuous system which held the milk at 72° C. for 15 seconds. The milk was cooled to 32° C. and 375 L placed in each of three temperature-controlled cheese-making vats (vats 3A, 3B and 4).
A culture mix of mesophilic starter strains, 1.8% of vat volume, 100 mL of propionibactena starter adjunct (to produce cheese flavour) and 10 mL of adjunct culture containing Lactobacillus rhamnosus HN001 (as described in W099/10476) was added to each vat except that in vat 4 the mesophilic starter culture was replaced by a Streptococcus thermophilus strain. A further 1875 mL of a culture (LF2) of Lactobacillus fermentum was added to vat 4 to produce ethanol in situ. Three grams of Hansen Kid lamb lipase powder (80 LFU) was mixed into each vat and then rennet added at a rate of 10 mL per 100 L of milk. The mix was then held for 40 minutes and then the curd was cut with a curd knife with blades spaced at 12 mm intervals.
The temperature was raised to 38° C. and the whey drained after a total treatment time of 130 minutes at which time the pH was 6.2. When 30% of the vat volume had been removed, the whey was replaced with 20% of the vat volume of water. When the curd had reached pH 5.2, it was completely drained, allowed to stand for 60 minutes and then milled. Salt (NaC1) was added at a rate of 17g/kg. Two 20 kg blocks, A and B of cheese were produced from each vat. To the curd for block B of vat 3, 118 mL of ethanol mixed with 118 mL of water were added.
The curd was pressed and then the blocks placed in porous bags, to allow CO2 to escape. The blocks were stored at 20° C. for one month and then at 5° C. for a further month before being tasted and samples taken for chemical analysis.
The results of the chemical analysis are shown in the table below.
These results demonstrate that when ethanol is added the transesterification reaction leads to production of esters, particularly ethyl butanoate. Ethanol produced in situ also leads to production of esters, particularly ethyl butanoate.
Tasting of Fruity Flavour in Cheese
Cheeses manufactured as described above were assessed for flavour attributes by an expert sensory assessment panel. Panellists were asked to taste the cheeses and to record fruity and bitter notes and descriptors of other flavour notes present. The results, shown in the table below confirm that addition of ethanol was effective in creating the fruity flavour notes and masking bitter flavour. The fruit flavours achieved correlate well with the higher levels of ethyl butanoate noted.
Ethanol was added to cream which was incubated with lipase from Rhizomucor miehei as described in Example 3.
The materials used were: full cream (40% fat), lipase from Rhizomucor miehei, and ethanol (10M solution). These ingredients were combined in screw-capped bottles. Each bottle contained 50 mL of cream, 40 mL of water and 10 mL of ethanol. One bottle was retained as a control. Lipase from Rhizomucor miehei (0.15 mL of enzyme solution) was added to a second bottle—the test sample. The bottles containing these combinations were held in a water bath at 30° C. Samples (5 mL) were removed at intervals of 1, 3, 5 and 24 hours after enzyme addition to the test bottle, and stored in a freezer. The samples were later extracted using standard methods for analysis of ethyl ester content by Gas Liquid Chromatography (as described in example 1).
The analysis results are shown in
Forty litres of water was held in a tank at 43° C. Disodium phosphate (1.2 kg dissolved in 5 L of hot water) and 30 kg of grated young Cheddar cheese curd were added. After twenty minutes of stirring, 120 g of protease dissolved in 5 L of water at 43° C. was added. The mixture was stirred for a further five minutes after which time a further 20 kg of grated curd was added over a period of ten minutes. The temperature of the stirred reaction mixture was held at 43° C. for four hours and the mixture was controlled at pH 5.6 by addition of 4M NaOH added in 100 mL aliquots. The enzyme was then inactivated by heating the mixture to 93° C. and holding at that temperature for 15 minutes. After cooling, the mixture was held at 32° C. and pH 5.4-5.6. The mixture was then inoculated with 4 L of a culture of Enterococcus faecalis, strain EF2 and 2 L of a culture of Lb plantarum to provide a balanced mature cheese flavour.
The mixture was held at 32° C. and pH controlled in the range 5.4-5.6 for 45 hours. Samples were taken from the mixture (sample T4) for chemical analysis. Next, 440 mL of 100% ethanol and 75 mL of lipase from Rhizomucor miehei were added to the mixture. After 5 hours a further sample was taken (T5). The next day, after 20 hours reaction, sample 16 was taken. A fruity and cheesy odour was evident in the mixture. The mixture was then further processed to meet commercial requirements.
Results of the chemical analysis shown in table 4 confirm the formation of volatile esters in the reaction mixture following the addition of lipase and ethanol.
A solution of 90 mL sheep's milk and 10 mL of 10 M ethanol was heated to 37° C. Palatase 20000 L (0.03%) was added and the mixture incubated for 5 h. Samples (10 ml) were acidified with 1 mL of 2.5 M H2SO4 and stored at −20° C. before analysing for esters. Esters were determined by gas chromatography (GC) in a modification of the method described in Example 1. One mL of thawed, acidified sample was added to a 16 mL Kimax screw-capped test tube containing 5 mL of diethyl ether. Extraction was performed by shaking vigorously for about 2.5 min, followed by centrifugation at 1260 g for 5 min in a centrifuge (Heraeus Megafuge 1.0). One mL of the solvent layer was then transferred to a 16 mL Kimax tube containing 1 mL of internal standard (180 mg/L ethyl acetate in water). The total solvent extract containing internal standard was then run through a 500 mg amino-propyl solid phase extraction (SPE) cartridge to remove triglycerides. Ester compounds which pass straight through were then collected in a GC vial containing a small amount of oven-dried anhydrous sodium sulphate. This sample was analysed for esters by GC as described below.
Following sample extraction, esters were analysed by GC. The analysis was performed using a Shimadzu GC-15A gas chromatograph with a fused silica capillary column (liquid phase, DB-1; length, 30 m; i.d., 0.25 mm; film thickness, 1.0 μm) (J&W Scientific, CA, USA). The oven was temperature-programmed at 45° C. for 5 min, followed by increasing the temperature to 50° C. at 5° C. min−1, then to 270° C. at 20° C. min−1, and held at 270° C. for 8 min. A split injection was performed at a ratio of 5:1 and 3 μL of sample were injected. The injector and FID (Flame Ionisation Detector) detector temperatures were 250° C. and 275° C., respectively. Other conditions were: carrier gas (He) at 0.9 mL per min−1; H2 and air at 0.6 kg per cm2, respectively; makeup gas (N2 at 2 kg per cm2. The FID output signal was recorded and processed using appropriate software (Shimadzu CLASS-VP™ Chromatography Data System Version 4.2 from Shimadzu, Md., USA). Esters in the samples were identified and quantified by comparison with injections of known amounts of pure standards.
The amounts of the ethyl esters formed in this reaction is set out below in table 5.
A solution of 90 mL goat's milk and 10 mL of 10 M ethanol was heated to 37° C. Palatase 20000 L (0.03%) was added and the mixture incubated for 7 h. Samples (10 mL) were acidified with 1 mL of 0.5 M H2SO4 and stored at −20° C. before analysing for esters. Esters were determined by gas chromatography (GC) as described in Example 7.
The amounts of the ethyl esters formed in this reaction is set out below in table 6.
25 kilograms of cream (40% fat)[please specify % of milk fat] were mixed with 0.075 kg Palatase 20000 L, 2.31 kg of ethanol (99.8% food grade from whey fermentation) and 22.63 kg of water in a stirred tank with circulating pump and heating. After the enzyme was added the mixture was stirred and pumped for 48 hours at 37° C. The pH at the end of three hours was 5.5. The pH at the end of 48 hours was 4.6. The reaction can be heat treated at this stage to make a stable flavour ingredient. However, in this example, 50 kg of grated cheddar cheese was added to the ester flavoured ingredient and this mixture was heated to 85 degrees for 15 minutes. The bulk of the esters/cream/cheese was put in 20 L plastic pails. The blending of the ester and the cream with the cheese stopped phase separation. The heat step inactivated the Palatase and made the product aseptic.
A second batch flavour ingredient was prepared from cream as outlined above, but it was made from an initial mixture of 70 kg of cream, with Palatase 20000 L, ethanol (99.8% food grade from whey fermentation) and water added in the same ratio as described above for the first batch prepared. Sixty kg of the resulting product was mixed with 60 kg of cheddar cheese and heat treated to 85 degrees for 15 minutes to inactivate the Palatase and make the product aseptic.
The ester analysis of the resulting product from the second batch is set out below in table 7.
a) White Sauce
A sample of ester flavoured ingredient prepared in accordance with the second batch in example 9 was mixed at 1% in a white sauce formulation. The white sauce was made from mixing and heating 125 g of sauce powder (5 g salt, 120 g standard white flour and 500 g cream powder), and blending with 450 g of water.
The resulting taste was determined by the expert sensory panel (see example 4) to be fruity, sweet (pineapple lump) flavour with soapy notes.
b) Cheddar Cheese
A cheddar formulation was prepared as follows. 0.5% of an ester flavoured ingredient prepared according to the second batch in example 9 was mixed with 58.8% cheddar cheese, 1.75% trisodium citrate and 39.4% water, the percentages being on a weight/weight basis.
The resulting product had a balanced, fruity flavour which came through late.
c) Parmesan-Style Cheese
A parmesan style cheese mixture was prepared as followed. 0.5% of an ester flavoured ingredient prepared according to the second batch in example 9 was mixed with 56.2% parmesan cheese, 1.75% try sodium citrate and 42% water.
This was described by the expert panel to have a pleasant sweet, fruity flavour which provided a good balance to the savoury flavour notes of parnesan style cheese.
d) Gouda Cheese
A gouda cheese formulation was made by mixing 0.5% of ester flavoured ingredients prepared as described for the second batch in example 9 with 63.7% gouda cheese, 1.75% trisodium citrate and 34.5% water.
This was described by the expert panel as having a fruity flavour with no chemical after taste.
e) Fondue Cheese
A fondue recipe was prepared using 14% cheddar cheese, 23% cream, 47% milk, 9% butter, 4% flour, 1% other flavours and 2% of the ester flavoured ingredient prepared in accordance with the method described in example 6.
The expert panel stated that the resulting fondue formulation had improved savoury/fruity and cheesy taste.
References
| Number | Date | Country | Kind |
|---|---|---|---|
| 517358 | Feb 2002 | NZ | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/NZ03/00029 | 2/20/2003 | WO |
