BLENDS OF CHYMOSINS WITH IMPROVED MILK-CLOTTING PROPERTIES

Abstract

Blends of coagulants to control acidification, coagulation and cheese texture.

Claims

1. A composition for clotting milk, comprising two or more coagulants with different clotting activity to proteolytical activity (C/P) ratios.

2. The composition of claim 1, wherein the two or more coagulants include a camel chymosin and a bovine chymosin.

3. The composition according to claim 1, wherein the two or more coagulants include two coagulants having at least a three-fold difference in general proteolytic activity relative to each other.

4. The composition according to claim 1, wherein the two or more coagulants comprises at least one coagulant having a C/P ratio of more than 5 IMCU/mU and at least a second coagulant having a C/P ratio of 0.05 to 1.5 IMCU/mU.

5. The composition according to claim 1, wherein the composition comprises at least 50 w/w % of one coagulant having a C/P ratio of more than 5 IMCU/mU and at least 15 w/w % of a second coagulant having a C/P ratio in the range of 0.05 to 1.51 MCU/mU, relative to the total amount of coagulant.

6. The composition according to claim 1, wherein the composition comprises a blend of two or more coagulants derived from two or more different animal or microbial species or genuses.

7. The composition according to claim 1, wherein the composition comprises at least 70 w/w % of one coagulant having a C/P ratio of more than 5 IMCU/mU and between 15 and 30 w/w % of a second coagulant having a C/P ratio in the range of 0.05 to 1.5 IMCU/mU, relative to the total amount of coagulant.

8. The composition according to claim 1, wherein at least one of the two or more different coagulants is derived from a coagulant derived from cow, buffalo, camel, pig, rat, sheep and/or mucor.

9. A milk composition comprising a composition according to claim 1, wherein the milk composition comprises a milk selected from soya milk, sheep milk, goat milk, buffalo milk, yak milk, lama milk, camel milk and cow milk.

10. The composition according to claim 9, wherein the milk is cow milk.

11. The composition according to claim 9, wherein the milk contain from about 3% to about 5% protein.

12. The composition according to claim 9, wherein the milk comprises from about 1.5% to 5% fat.

13. The composition according to claim 1, wherein the composition is a blend selected from a blend of a bovine coagulant and a non-bovine coagulant and a blend of a camel coagulant and a non-camel coagulant.

14. A food or feed composition comprising a composition according to claim 1.

15. The food or feed composition according to claim 14, wherein the composition is soft-cheese.

16. The food or feed composition according to claim 15, wherein the soft-cheese is a surface ripened soft-cheese.

17. A process for making soft-cheese, comprising adding to milk a composition according to claim 1.

18. The process according to claim 17, wherein the composition is added to the milk no later than 20 minutes after the addition of one or more starter cultures to the milk.

19. A method for making a milk-based product comprising adding to milk an effective amount of a composition according to claim 1.

20. A method for making a fermented milk product comprising: (a) adding a starter culture to milk and incubating the culture at a temperature of 28 to 42 C. for at least five minutes; (b) adding to the culture a composition according to claim 1 in a total concentration between 2000 IMCU/1001 and 3500 IMCU/1001; and (c) further incubating the culture at a temperature of 28 to 42 C. for at least three hours; and (d) optionally, separating whey to obtain a cheese.

21. The method according to claim 20, wherein the composition is added no later than 20 minutes after the addition of one or more starter cultures.

22. The method according to claim 20, wherein the method is for making soft-cheese.

Description

DRAWINGS

[0041] FIG. 1: An alignment of herein relevant different chymosin sequences. The shown Bos_bovis_chymosin B is bovine chymosin of SEQ ID NO: 1 herein and the shown Camelus_dromedarius is camel chymosin of SEQ ID NO: 2 herein. Using bovine chymosin of SEQ ID NO: 1 as reference sequence as described herein is can e.g. be seen that bovine chymosin has V in position 10 and camel chymosin has A in the same position 10. It may e.g. also be seen that bovine/Rat have Q in position 352 and Camel/C._bactrianus have E in the same position 352.

[0042] In relation to the chymosin sequences shown in FIG. 1 sheep has 94.5% sequence identity with bovine SEQ ID NO: 1; C._bactrianus has 83.2% sequence identity with bovine SEQ ID NO: 1; Camelus_dromedarius (camel chymosin of SEQ ID NO: 2) has 84% sequence identity with bovine SEQ ID NO: 1; pig has 80.3% sequence identity with bovine SEQ ID NO: 1 and rat has 71.9% sequence with bovine identity SEQ ID NO: 1.

[0043] As understood by the skilled person in the present contextherein relevant sequence identity percentages of mature polypeptide sequences of e.g. sheep, C._bactrianus, camel, pig or rat chymosin with the mature polypeptide of SEQ ID NO: 1 (bovine chymosini.e. amino acid positions 59 to 381 of SEQ ID NO: 1) are relatively similar to above mentioned sequence identity percentages.

[0044] FIG. 2: Firmness of brie type cheeses made with different coagulant blends.

[0045] FIG. 3: Stickiness of brie type cheeses made with different coagulant blends.

[0046] FIG. 4: The pH at the demolding step for brie type cheeses made with the different coagulant blends.

[0047] FIG. 5: Dry matter (DM) at the demolding step for brie type cheeses made with the different coagulant blends.

[0048] FIG. 6: Relative proteolysis specificity of a selection of coagulants of particular interest in present invention.

[0049] FIG. 7: Coagulation speed and firmness development of three different coagulant solutions: Camel chymosin (Chymax M1000) marked in red full line, bovine chymosin (Chymax +) marked in green broken lines and a camel/bovine chymosin blend in a 80/20 ratio (Chymax soft) marked in blue dotted line.

DETAILED DESCRIPTION OF THE INVENTION

[0050] As exemplified in detail herein, the present invention relates to compositions comprising two or more different coagulants.

[0051] In a related aspect, the present invention relates to compositions for clotting milk, the composition comprising a blend of two or more coagulants having different origins.

[0052] In a related aspect, the present invention relates to a composition as disclosed herein, wherein the two or more coagulants have different C/P ratios and/or clotting activities, such as e.g. at least a three-fold difference.

[0053] In a related aspect, milk clotting activity is determined from the time needed for a visible flocculation of a standard milk substrate prepared from a low-heat, low fat milk powder with a calcium chloride solution of 0.5 g per liter (pH 6.5). The clotting time of a rennet sample is compared to that of a reference standard having known milk-clotting activity and having the same enzyme composition by IDF Standard 110B as the sample. Samples and reference standards are measured under identical chemical and physical conditions. Variant samples are adjusted to approximately 3 IMCU/ml using an 84 mM acetic acid pH 5.5 buffer. Hereafter, 200 l enzyme is added to 10 ml preheated milk (32 C.) in a glass test tube placed in a water bath, capable of maintaining a constant temperature of 32 C.1 C. under constant stirring.

[0054] The total milk-clotting activity (strength) of a rennet is calculated in International Milk-Clotting Units (IMCU) per ml relative to a standard having the same enzyme composition as the sample according to the formula:

Strength in IMCU/ml=SstandardTstandardDsample DstandardTsample [0055] Sstandard: The milk-clotting activity of the international reference standard for rennet. [0056] Tstandard: Clotting time in seconds obtained for the standard dilution. [0057] Dsample: Dilution factor for the sample [0058] Dstandard: Dilution factor for the standard [0059] Tsample: Clotting time in seconds obtained for the diluted rennet sample from addition of enzyme to time of flocculation

Determination of Total Protein Content

[0060] Total protein content was determined using the Pierce BCA Protein Assay Kit from Thermo Scientific following the instructions of the providers.

Calculation of Specific Clotting Activity

[0061] Specific clotting activity (IMCU/mg total protein) was determined by dividing the clotting activity (IMCU/ml) by the total protein content (mg total protein per ml).

[0062] In working Example 3 herein is provided an Example of a standard method to determine proteolytical activity.

[0063] As an example, general proteolytic activity may be measured using fluoresecently labelled Bodipy-FL casein as a substrate (EnzChek; Molecular Bioprobes, E6638). Casein derivatives heavily labeled with pH-insensitive green-fluorescent Bodipy-FL result in almost complete quenching of the conjugate's fluorescence. Protease catalyzed hydrolysis releases fluorescent Bodipy-FL. This method is very sensitive which is essential for this experiment as high C/P coagulants often have low general proteolytical activity compared to low C/P coagulants.

[0064] The assay was conducted in a 0.2 M phosphate buffer adjusted to the desired pH at a final substrate concentration of 0.04 mg/ml. Prior to mixing 1 part of substrate with 1 part of enzyme, both prepared in the phosphate buffer, all enzyme variants where normalized to 50 IMCU/ml (according to example 2). The substrate and enzyme were mixed in a 96-well Nunc Fluoro microtitter plates, sealed and incubated at 32 C. for 60 min. After incubation the sealing was removed and the fluorescence recorded in a fluorimeter.

[0065] As known in the art the herein relevant so-called C/P ratio is determined by dividing the specific clotting activity (C)(IMCU/ml) with the proteolytical activity (P)(mU/ml.

[0066] As known in the arta higher C/P ratio implies generally that the loss of protein during e.g. cheese manufacturing due to non-specific protein degradation is reduced, i.e. the yield of cheese is improved, and that the development of bitter taste in the cheese during maturation is reduced.

[0067] Another aspect of the invention relates to compositions comprising two or more different chymosins, wherein the compositions entail beneficial properties on the curd firmness and coagulation speed.

[0068] On way of measuring this is to use the CHYMOgraph. The CHYMOgraph allows for an estimation of the milk flocculation time as well as the curd firmness evolution in cheese production.

[0069] The software measures the organization speed of the protein network in the curd. The variation in milk density and curd visco-elasticity is tranformed in user-friendly graphical data, which can be used for the coagulant characterization or to define the optimal curd cut time.

[0070] The CHYMOgraph measures the milk flocculation time, the curd firmness and its evolution and the organisation speed of the protein network.

[0071] For preparation of the milk, a container 500 g of milk according to the target of milk composition was prepared and heated to renneting temperature at 38 C. in water bath 1 hour before adding rennet. Before use of milk, pH was controlled and register. An example of a preferred milk composition is:

[0072] Fortified milk with 3.8% of protein, high heat treated at 90 C. for 30 s, pH at renneting: 6.18 at 38 C. and 6.28 at (4 C.).

[0073] Renneting temperature: 38 C. This milk type corresponds to the milk composition used when producing soft cheese milk type.

[0074] Preferred coagulant are prepared as: 3 coagulant solutions are tested: Camel chymosin (ChyMax M1000), Bovine Chymosin (ChyMax+) and ChyMaxM soft (a blend of 80% Camel chymosin (ChyMax M1000) and 20% bovine chymosin (ChyMax +)). Each coagulant solution may be prepared with a strength of 20 IMCU/mL dilution with warm water. This dilution aims to bring enough coagulant in the milk sample to facilitate its dispersion.

[0075] Each coagulant solution may be added to the milk (1 mL for 500 g of milk, so 40 IMCU/1 L). After coagulant addition the sample was mixed 30 seconds by turning. After turning, 10 mL of each coagulant solution was added to the Chymograph.

[0076] As known in the artdifferent natural wildtype chymosin polypeptide sequences obtained from different mammalian species (such as e.g. bovines, camels, sheep, pigs, or rats) are having a relatively high sequence similarity/identity.

[0077] In FIG. 1 herein this is exemplified by an alignment of herein relevant different chymosin sequences.

[0078] In the present context a naturally obtained wildtype chymosin (such as bovine chymosin or camel chymosin) as shown in FIG. 1 may herein be an example of a parent polypeptide i.e. a parent polypeptide to which an alteration is made to produce a variant chymosin polypeptide of the present invention.

[0079] In a further related aspect, the present invention relates to a composition as disclosed herein, wherein the two or more coagulants form S1 and/or -casein at different rates.

[0080] In yet a related aspect, the present invention relates to a composition as disclosed herein, wherein the two or more coagulants have different general proteolytic activity, such as e.g. at least a three-fold difference.

[0081] Hence in an aspect, the present invention provides compositions as described above, wherein the composition comprises at least one coagulant having a C/P ratio of more than 5 IMCU/mU and at least a second coagulant having a C/P ratio in the range of 0.05 to 1.5 IMCU/mU.

[0082] For example, the composition may comprise at least 50 w/w % of one coagulant having a C/P ratio of more than 5 IMCU/mU and at least 15 w/w % of a second coagulant having a C/P ratio in the range of 0.05 to 1.5 IMCU/mU, wherein the w/w % indicates the concentration of one coagulant relative to the total amount of coagulant. In a further aspect, the invention provides a composition comprising at least 70 w/w % of one coagulant having a C/P ratio of more than 5 IMCU/mU and between 15 and 30 w/w % of a second coagulant having a C/P ratio in the range of 0.05 to 1.5 IMCU/mU, wherein the w/w % indicates the concentration of one coagulant relative to the total amount of coagulant.

[0083] In yet a related aspect, the present invention relates to a composition as disclosed herein, wherein the composition comprising a blend of two or more coagulants derived from two or more different animal or microbial species or genuses.

[0084] In yet a related aspect, the present invention relates to a composition as disclosed herein, wherein the composition comprises a blend of two or more coagulants that are variants of the same parent coagulant.

[0085] In yet a related aspect, the present invention relates to a composition as disclosed herein, wherein the two or more different genuses or species is selected from the list consisting of: cow, buffalo, camel, pig, rat, sheep or mucor.

[0086] In yet a related aspect, the present invention relates to a composition as disclosed herein, wherein at least one of the two or more different coagulants is derived from a coagulant derived from cow, buffalo, camel, pig, rat, sheep and/or mucor.

[0087] In yet a related aspect, the present invention relates to a composition as disclosed herein, wherein the composition comprises milk such as e.g. soya milk, sheep milk, goat milk, buffalo milk, yak milk, lama milk, camel milk or cow milk; and

[0088] In yet a related aspect, the present invention relates to a composition as disclosed herein, wherein the composition is a blend of a bovine coagulant and a non-bovine coagulant or is a blend of a camel coagulant and a non-camel coagulant.

[0089] In yet a related aspect, the present invention relates to a composition as disclosed herein, wherein the composition comprise from 10-50%, such as e.g. 20% of a non-bovine or a non-camel coagulant, relative to the total amount of coagulant.

[0090] In yet a related aspect, the present invention relates to a composition as disclosed herein, wherein the composition comprise a high C/P ratio coagulant and a low C/P ratio coagulant. In yet a related aspect, the present invention relates to a composition as disclosed herein, wherein the composition comprise from 10-50%, such as e.g. 20% of a low C/P ratio coagulant relative to the total amount of coagulant.

[0091] In a further embodiment the present invention provides a food or feed composition comprising a blend of two or more coagulants as described above.

[0092] The food or feed composition can be a soft-cheese, such as e.g. brie or camembert.

[0093] In yet a related aspect, the present invention relates to a composition as disclosed herein, wherein the composition is for making soft-cheese, such as e.g. brie or camembert, optionally, the soft-cheese is a surface ripened soft-cheese.

[0094] Further, the invention relates to the use of a composition according as described in any of the aspects herein, in a process for making soft-cheese. The composition as described in the aspects herein, may be added no later than 20 minutes, such as e.g. no later than 15 minutes, such as e.g. no later than 10 minutes, such as e.g. no later than 5 minutes after the addition of one or more starter cultures

[0095] If applicable, further manufacturing steps to obtain the milk based product any be added.

[0096] For example, the present invention provides a method for making a fermented milk product comprising the following steps: [0097] (a) adding a starter culture to milk and incubating the culture at a temperature of 28 to 42 C. for at least five minutes; [0098] (b) adding a composition comprising two or more different coagulants in a total concentration between 2000 IMCU/1001 and 3500 IMCU/1001; [0099] (c) further incubating the culture at a temperature of 28 to 42 C. for at least three hours; [0100] (d) separating the whey to obtain a cheese.

[0101] The method can advantageously be used to make soft-cheese, such as e.g. brie or camembert.

[0102] Again, the composition as described in any of the aspects herein may as a related embodiment be added no later than 20 minutes, such as e.g. no later than 15 minutes, such as e.g. no later than 10 minutes, such as e.g. no later than 5 minutes after the addition of one or more starter cultures.

Determining the Amino Acid Position of a Chymosin of Interest

[0103] As discussed aboveas a reference sequence for determining the amino acid position of a herein relevant chymosin polypeptide of interest (e.g. camel, sheep, bovine etc.) is herein used the public known bovine chymosin sequence disclosed as SEQ ID NO: 1 herein.

[0104] By using well-known computer programs as mentioned above it is routine work for the skilled person to determine the amino acid position of a herein relevant chymosin polypeptide of interest (e.g. camel, sheep, bovine etc.) in a corresponding chymosin.

A Method for Making an Isolated Chymosin Polypeptide Variant

[0105] As discussed aboveas known in the art, the skilled person may, based on his common general knowledge, routinely produce and purify chymosin and chymosin variants. Said in other words, once the skilled person is in possession of a herein relevant parent polypeptide having chymosin activity of interest (e.g. from bovines, camels, sheep, pigs, or rats) it is routine work for the skilled person to make a variant of such a parent chymosin of interest.

[0106] An example of a suitable method to produce and isolate a chymosin (variant or parent) may be by well-known e.g. fungal recombinant expression/production based technology as e.g. described in WO02/36752A2 (Chr. Hansen).

[0107] As known in the artchymosin activity may be determined by the so-called C/P ratio, which is determined by dividing the specific clotting activity (C) with the proteolytical activity (P).

[0108] In working Example 2 herein is described a suitable method to determine the specific clotting activity (C) and in working Example 3 herein is described a suitable method to determine proteolytical activity (P).

[0109] As discussed aboveas a reference sequence for determining the amino acid position of a herein relevant chymosin polypeptide of interest (e.g. camel, sheep, bovine etc.) is herein used the public known bovine chymosin sequence disclosed as SEQ ID NO: 1 herein.

[0110] As discussed abovebased on e.g. the computer sequence alignment programs discussed hereinit is routine work for the skilled person to determine the herein relevant amino acid position of a herein relevant chymosin polypeptide of interest (e.g. camel, sheep, bovine etc.).

[0111] As understood by the skilled person in the present contexta herein relevant parent polypeptide having chymosin activity may already e.g. be a variant of e.g. a corresponding wildtype chymosin. For instance, a camel chymosin variant with e.g. 5-10 alterations (e.g. substitutions) as compared to wildtype camel chymosin polypeptide of SEQ ID NO: 2 will still be a parent polypeptide that has at least 65% sequence identity with the mature polypeptide of SEQ ID NO: 1 (Bovine) as required in e.g. first aspect herein.

[0112] Said in other words, a herein relevant isolated chymosin polypeptide variant may comprise alterations (e.g. substitutions) in other position than the positions of e.g. the first aspect herein.

[0113] An embodiment relates to an isolated chymosin polypeptide variant, wherein the alteration comprises a substitution, a deletion or an insertion in at least one amino acid position corresponding to any of positions of e.g. the first aspect herein.

[0114] It may be preferred that the difference in chymosins exist in at least one alteration of the peptide is a substitutioni.e. a herein relevant coagulant relates to an isolated bovine chymosin polypeptide variant, such as e.g. a variant wherein the alteration is comprising a substitution in at least one amino acid position corresponding to any of positions 51 and/or 221, preferably A51V and K221M in a mature bovine chymosin parent sequence.

[0115] Preferably, the parent polypeptide has at least 70% sequence identity with the mature polypeptide of SEQ ID NO: 1 (bovine chymosin), more preferably the parent polypeptide has at least 75% sequence identity with the mature polypeptide of SEQ ID NO: 1 (bovine chymosin).

[0116] As an examplea herein suitable relevant parent polypeptide could e.g. be bovine chymosin Aas known in the art bovine chymosin A may only have one amino acid difference as compared to bovine chymosin B of SEQ ID NO: 1 herein.

[0117] As discussed abovein working examples herein were made variants using the polypeptide of SEQ ID NO: 1 (Bovine) as parent polypeptidesuch variant may herein be termed bovine chymosin variants.

[0118] Accordingly, in a preferred embodimentthe parent polypeptide has at least 90% sequence identity with the mature polypeptide of SEQ ID NO: 1 (bovine chymosin), more preferably the parent polypeptide has at least 95% sequence identity with the mature polypeptide of SEQ ID NO: 1 (bovine chymosin) and even more preferably the parent polypeptide has at least 97% sequence identity with the mature polypeptide of SEQ ID NO: 1 (bovine chymosin). It may be preferred that the parent polypeptide is the mature polypeptide of SEQ ID NO: 1 (bovine chymosin).

[0119] As understood by the skilled person in the present contexta herein relevant parent polypeptide having chymosin activity may already e.g. be a variant of e.g. a corresponding wildtype chymosin.

A Method for Making a Milk Based Product

[0120] As discussed abovean composition comprising two or more different coagulants as described herein may be used according to the arte.g. to make a milk based product of interest (such as e.g. a cheese product).

[0121] As discussed abovean aspect of the invention relates to a method for making a food or feed product comprising adding an effective amount of the coagulant blends as described herein to the food or feed ingredient(s) and carrying our further manufacturing steps to obtain the food or feed product.

[0122] Preferably, the food or feed product is a milk based product and wherein the method comprises adding an effective amount of the coagulant blend as described herein to milk and carrying our further manufacturing steps to obtain the milk based product.

[0123] The milk may e.g. be soy milk, sheep milk, goat milk, buffalo milk, yak milk, lama milk, camel milk or cow milk.

[0124] The milk based product may e.g. be a fermented milk product, a quark or a cheese.

[0125] The invention further relates to the following related summarizing aspects:

[0126] Aspect 1. A composition for clotting milk, the composition comprising a blend of two or more coagulants with different C/P ratios.

[0127] Aspect 2. A composition for clotting milk, the composition comprising a blend of two or more coagulants with different origins, such as e.g. a camel chymosin and a bovine chymosin.

[0128] Aspect 3. A composition according to aspect 1 or 2, wherein the two or more coagulants have different general proteolytic activity, such as e.g. at least a three-fold difference.

[0129] Aspect 4. A composition according to any of the preceding aspects wherein the composition comprises at least one coagulant having a C/P ratio of more than 5 IMCU/mU and at least a second coagulant having a C/P ratio of 0.05 to 1.5 IMCU/mU.

[0130] Aspect 5. A composition according to any of the preceding aspects, wherein the composition comprises at least 50 w/w % of one coagulant having a C/P ratio of more than 5 IMCU/mU and at least 15 w/w % of a second coagulant having a C/P ratio in the range of 0.05 to 1.5 IMCU/mU, wherein the w/w % indicates the concentration of one coagulant relative to the total amount of coagulant.

[0131] Aspect 6. A composition according to any of the preceding aspects wherein the composition comprises a blend of two or more coagulants derived from two or more different animal or microbial species or genuses.

[0132] Aspect 7. A composition according to any one of the preceding aspects, wherein the composition comprises at least 70 w/w % of one coagulant having a C/P ratio of more than 5 IMCU/mU and between 15 and 30 w/w % of a second coagulant having a C/P ratio in the range of 0.05 to 1.5 IMCU/mU, wherein the w/w % indicates the concentration of one coagulant relative to the total amount of coagulant.

[0133] Aspect 8. A composition according to any one of aspects 1 to 7, wherein at least one of the two or more different coagulants is derived from a coagulant derived from cow, buffalo, camel, pig, rat, sheep and/or mucor.

[0134] Aspect 9. A composition according to any of the preceding aspects, wherein the composition comprises milk such as e.g. soya milk, sheep milk, goat milk, buffalo milk, yak milk, lama milk, camel milk or cow milk.

[0135] Aspect 10. A composition according to aspect 9, wherein the milk is cows milk.

[0136] Aspect 11. A composition according to aspect 9 or 10, wherein the milk contain from about 3% to about 5% protein, such as from 3.5% to 4.5% protein, such as 3.8% protein.

[0137] Aspect 12. A composition according to any of aspects 9 to 11, wherein the milk comprises from about 1.5% to 5% fat, such as from 2.5% to 4% fat, such as 3.5% fat.

[0138] Aspect 13. A composition according to any of aspects 1 to 12, wherein the composition is a blend of a bovine coagulant and a non-bovine coagulant or is a blend of a camel coagulant and a non-camel coagulant, such as e.g. a blend of camel and bovine chymosin.

[0139] Aspect 14. Food or feed composition comprising a blend of two or more coagulants according to any of the preceding aspects.

[0140] Aspect 15. Food or feed composition according to aspect 14, wherein the composition is soft-cheese, such as e.g. brie or camembert.

[0141] Aspect 16. Food or feed composition according to aspect 15, wherein the soft-cheese is a surface ripened soft-cheese.

[0142] Aspect 17. Use of a composition according to any one of aspects 1 to 13 in a process for making soft-cheese.

[0143] Aspect 18. Use according to aspect 17, wherein the composition according to any of aspects 1 to 13 is added to milk no later than 20 minutes, such as e.g. no later than 15 minutes, such as e.g. no later than 10 minutes, such as e.g. no later than 5 minutes after the addition of one or more starter cultures.

[0144] Aspect 19. A method for making a milk-based product comprising adding an effective amount of the composition according to any of aspects 1 to 13 and carrying out further manufacturing steps to obtain the milk based product.

[0145] Aspect 20. A method for making a fermented milk product comprising the following steps: [0146] (a) adding a starter culture to milk and incubating the culture at a temperature of 28 to 42 C. for at least five minutes; [0147] (b) adding a composition according to any one of aspects 1 to 13 in a total concentration between 2000 IMCU/1001 and 3500 IMCU/1001; [0148] (c) further incubating the culture at a temperature of 28 to 42 C. for at least three hours; [0149] (d) separating the whey to obtain a cheese.

[0150] Aspect 21. The method according to aspect 20, wherein the composition according to any of aspects 1 to 13 is added no later than 20 minutes, such as e.g. no later than 15 minutes, such as e.g. no later than 10 minutes after the addition of one or more starter cultures.

[0151] Aspect 22. The method according to aspect 20 or 21, wherein the method is used to make soft-cheese, such as e.g. brie or camembert.

EXAMPLES

Example 1: Alignment and Numbering of Chymosin Protein Sequences and Variant Sequences

[0152] Chymosin protein sequences were aligned using the ClustalW algorithm as provided by the EBI (EBI, tools, multiple sequence alignment, CLUSTALW, http://www.ebi.ac.uk/Tools/msa/clustalw2/) and as described in Larkin M A, Blackshields G, Brown N P, Chenna R, McGettigan P A, McWilliam H, Valentin F, Wallace I M, Wilm A, Lopez R, Thompson J D, Gibson T J, Higgins D G (2007). Bioinformatics 23(21), 2947-2948.

[0153] ClustalW2 settings for multiple sequence alignments were Protein weight Matrix=BLOSUM, GAP open=10, GAP EXTENSION=0.05, GAP DISTANCES=8, No End Gaps, ITERATION=none, NUMITER=1, CLUSTERING=NJ

[0154] As a reference sequence the bovine chymosin B preprochymosin was used (Genbank accession number P00794 disclosed herein as SEQ ID NO: 1), where the N-terminal Methionin has number 1 (MRCL) and the C-terminal Isoleucin (in the protein sequence . . . LAKAI) has number 381. Variants were aligned against the bovine B pre-pro-chymosin and residues were numbered according to the corresponding bovine chymosin residue.

Example 2: Determination of Specific Chymosin Activity

2.1 Determination of Clotting Activity

[0155] Milk clotting activity was determined using the REMCAT method, which is the standard method developed by the International Dairy Federation (IDF method) Milk clotting activity is determined from the time needed for a visible flocculation of a standard milk substrate prepared from a low-heat, low fat milk powder with a calcium chloride solution of 0.5 g per liter (pH 6.5). The clotting time of a rennet sample is compared to that of a reference standard having known milk-clotting activity and having the same enzyme composition by IDF Standard 110B as the sample. Samples and reference standards were measured under identical chemical and physical conditions. Variant samples were adjusted to approximately 3 IMCU/ml using an 84 mM acetic acid pH 5.5 buffer. Hereafter, 200 l enzyme was added to 10 ml preheated milk (32 C.) in a glass test tube placed in a water bath, capable of maintaining a constant temperature of 32 C.1 C. under constant stirring.

[0156] The total milk-clotting activity (strength) of a rennet was calculated in International Milk-Clotting Units (IMCU) per ml relative to a standard having the same enzyme composition as the sample according to the formula:

[00001]$\mathrm{Strength}.Math..Math.\mathrm{in}.Math..Math.\mathrm{IMCU}.Math.\text{/}.Math.\mathrm{ml}=\frac{\mathrm{Sstandard}\mathrm{Tstandard}\mathrm{Dsample}}{\mathrm{Dstandard}\mathrm{Tsample}}$ [0157] Sstandard: The milk-clotting activity of the international reference standard for rennet. [0158] Tstandard: Clotting time in seconds obtained for the standard dilution. [0159] Dsample: Dilution factor for the sample [0160] Dstandard: Dilution factor for the standard [0161] Tsample: Clotting time in seconds obtained for the diluted rennet sample from addition of enzyme to time of flocculation

2.2 Determination of Total Protein Content

[0162] Total protein content was determined using the Pierce BCA Protein Assay Kit from Thermo Scientific following the instructions of the providers.

2.3 Calculation of Specific Clotting Activity

[0163] Specific clotting activity (IMCU/mg total protein) was determined by dividing the clotting activity (IMCU/ml) by the total protein content (mg total protein per ml).

Example 3: Determination of Proteolytic Activity

[0164] General proteolytic activity was measured using fluoresecently labelled Bodipy-FL casein as a substrate (EnzChek; Molecular Bioprobes, E6638). Casein derivatives heavily labeled with pH-insensitive green-fluorescent Bodipy-FL result in almost complete quenching of the conjugate's fluorescence. Protease catalyzed hydrolysis releases fluorescent Bodipy-FL. This method is very sensitive which was essential for this experiment as CHYMAX M has the lowest general proteolytical activity of all coagulants known to date.

[0165] The assay was conducted in a 0.2 M phosphate buffer adjusted to the desired pH at a final substrate concentration of 0.04 mg/ml. Prior to mixing 1 part of substrate with 1 part of enzyme, both prepared in the phosphate buffer, all enzyme variants where normalized to 50 IMCU/ml (according to example 2). The substrate and enzyme were mixed in a 96-well Nunc Fluoro microtitter plates, sealed and incubated at 32 C. for 60 min. After incubation the sealing was removed and the fluorescence recorded in a fluorimeter.

Example 4: Evaluation of Two Types of Coagulant Blends: CamelBovine Chymosin Blend and CamelMucor miehei Coagulant

[0166] In soft cheese technology, using a high C/P ratio coagulant such as ChyMaxM has several interests. Some of the more important are: increased shelf life, reduced bitterness, increased fat recovery due to higher firmness at cutting, reduced post-acidification especially in the case of use of fast strains. However, a general modification which can in some case be considered as a default is higher cheese firmness.

[0167] In order to keep the interests of High C/P ratio such as ChyMaxM and reduce firmness of the cheese, a blend of ChyMaxM and other coagulants with lower C/P ratio have been defined.

[0168] Brie type stabilized soft cheeses have been produced with different coagulant ratios. Cheeses have been analyzed at demolding and during shelf life.

Milk: (Same for all Trials)

[0169] Proteins: 36.2 g/L (no whey protein where added) [0170] Fat: 61.7 g/L [0171] Fat/Protein ratio: 1.7 [0172] Pasteurization: 72 C./205 [0173] Total volume/trial: 500 L (5 vats of 100 L) [0174] CaCl2 added: 15 g/100 L [0175] Temperature at coagulant addition: 40 C. [0176] pH at coagulant addition: 6.3 [0177] Coagulant dose: 3000 IMCU/100 L of milk (corresponding to 8287 IMCU/g of proteins).

Coagulant Blends:

[0178] A first type of blends have been tested: ChyMaxM with 20%, 30% or 50% of ChyMax (bovine coagulant with low C/P), indicated with red lines with square markers in FIGS. 2-5. [0179] A second type of blends have been tested: ChyMaxM with 20% or 30% of Hannilase (Mucor miehei coagulant with a low C/P ratio), indicated with blue lines with diamond shaped markers in FIGS. 2-5. [0180] A Pure ChyMaxM test with the same dosages and parameters has been made as a reference. This Reference is used for both types of blends being a blend with 0% of the non-ChyMaxM component, indicated in the first column of the tables included in FIGS. 2-5.

Results:

[0181] (Values are Average of 5 Vats) [0182] pH at demolding (FIG. 4): a slight tendency to get a lower pH at demolding when increasing the low C/P ratio component is observed for both types of low C/P ratio coagulant used: from pH 5.06 for the pure ChyMaxM test, the pH was 5.03 for blend with 20% Hannilase and still 5.06 with 20% of ChyMax. Being close to pH meter precision, this variability is still significant as it is an average of 5 vats. Then at 30%, pH is 5.03 for blends with Hannilasesimilar to 20% blendand 5.02 for blends with ChyMaxsimilar to results with Hannilase 20% and 30% blends. Then with the 50% ChyMax blend, the pH is similar to 30% blend. This shows that using a blend of high C/P ratio coagulant such as ChyMaxM and lower C/P ratio such as ChyMax or Hannilase has a tendency to reduce pH value at demolding in a brie type soft cheese. This tendency is already effective with 20% of Hannilase when for ChyMax this tendency is seen only with more than 30%. [0183] Texture: Texture measurements have been performed on cheeses after 25 days of shelf life using TAXT2 penetrometer with a guillotine tool. [0184] Firmness (FIG. 2): Firmness was clearly decreased with increasing percentage of low C/P coagulant in the blends and then stabilized for higher percentages. For ChyMax blends, firmness is decreasing from 1325 g for the pure ChyMaxM test to 1180 g for the 20% blend then to 1022 g for the 30% blend. For Hannilase blends, firmness is already decreased to 1050 with 20% and then keeps approximately the same value 1053 g with 30% blend. [0185] Stickiness (FIG. 3): Stickiness clearly increasing when blending ChyMaxM with a lower C/P ratio coagulant. For 20% both types of low C/P ratio coagulants where slightly increasing stickiness: from a value of 50 g/s for the pure ChyMaxM the test with 20% ChyMax reached 72 g/s and the test with 20% Hannilase blend reached 59 g/s. These values corresponded to still acceptable stickiness of the cheeses. Then with 30% both types of blends are reaching values close to 95 (96 for ChyMax and 92 for Hannilase). These values where clearly linked with not acceptable cheeses in term of stickiness. [0186] Texture optimum: The objective of this experiment was to decrease firmness; however the stickiness is not a desired characteristic. Therefore the optimum blends for texture improvement was 20% for both types of low C/P ratio coagulants. [0187] Dry matter (DM) at demolding (FIG. 5): Dry matter is increased with blends compared with the pure ChyMaxM test. For both types of blends the dry mater at demolding is increased at 20% and at 30%from 48.2% for the pure ChyMaxM test, with 20% blends the dry mater was 49% for ChyMax blend and 50.5% for Hannilase blend and for 30% test, dry matter was 52% for ChyMax blend and 52.5% for Hannilase blend. [0188] Dry matter versus firmness: Comparing these dry mater results with texture measurement we can see that even if the cheeses are dryer at demolding with blends compared with pure ChyMaxM trials, the texture is still softer. This shows that blending ChyMaxM with lower C/P coagulants is strongly effective to reduce firmness even with an increased dry matter. [0189] Optimum results: Using these different results we can see that for a blend of ChyMaxM and ChyMax as well as for a blend of ChyMaxM and Hannilase, the optimum ratio is close to 20% to keep the advantages of high C/P ratio coagulant and reduce firmness when this is not wanted.

Example 5: Determination of the Coagulation Behavior of Bovine, Camel and Blended Chymosins

[0190] To follow the coagulation behavior, we have used the CHYMOgraph (patented Chr. Hansen tool). The CHYMOgraph allows for an estimation of the milk flocculation time as well as the curd firmness evolution in cheese production.

[0191] The software measures the organization speed of the protein network in the curd. The variation in milk density and curd visco-elasticity is tranformed in user-friendly graphical data, which can be used for the coagulant characterization or to define the optimal curd cut time.

[0192] The CHYMOgraph measures the milk flocculation time, the curd firmness and its evolution and the organisation speed of the protein network.

Milk Preparation

[0193] A container 500 g of milk according to the target of milk composition was prepared and heated to renneting temperature at 38 C. in water bath 1 hour before adding rennet. Before use of milk, pH was controlled and register.

Milk Composition

[0194] Fortified milk with 3.8% of protein, high heat treatment: 90 C. for 30 s, pH at renneting: 6.18 at 38 C. and 6.28 at (4 C.).

[0195] Renneting temperature: 38 C. This milk type corresponds to the milk composition used when producing soft cheese milk type.

Coagulant Preparation

[0196] 3 coagulant solutions were tested: Camel chymosin (ChyMax M1000), Bovine Chymosin (ChyMax+) and ChyMaxM soft (a blend of 80% Camel chymosin (ChyMax M1000) and 20% bovine chymosin (ChyMax +)). Each coagulant solution was prepared with a strength of 20 IMCU/mL dilution with warm water. This dilution aims to bring enough coagulant in the milk sample to facilitate its dispersion.

[0197] Each coagulant solution was added to the milk (1 mL for 500 g of milk, so 40 IMCU/1 L). After coagulant addition the sample was mixed 30 seconds by turning. After turning, 10 mL of each coagulant solution was added to the Chymograph.

Results

[0198] As depicted in FIG. 7, the speed of coagulation when using a blend of bovine and camel chymosin (ChyMax soft) exceeds the speed of coagulation when using camel chymosin (ChyMax M1000) or bovine chymosin (ChyMax+) alone. This is highly surprising as the skilled scientist would expect a performance of the blend corresponding to the weighted average of the two components included in the blend.

REFERENCES

[0199] 1: WO02/36752A2 (Chr. Hansen) [0200] 2: Suzuki et al: Site directed mutagenesis reveals functional contribution of Thr218, Lys220 and Asp304 in chymosin, Protein Engineering, vol. 4, January 1990, pages 69-71 [0201] 3: Suzuki et al: Alteration of catalytic properties of chymosin by site-directed mutagenesis, Protein Engineering, vol. 2, May 1989, pages 563-569 [0202] 4: van den Brink et al: Increased production of chymosin by glycosylation, Journal of biotechnology, vol. 125, September 2006, pages 304-310. [0203] 5: Pitts et al: Expression and characterisation of chymosin pH optima mutants produced in Tricoderma reesei, Journal of biotechnology, vol. 28, March 1993, pages 69-83 [0204] 6: M. G. Williams et al: Mutagenesis, biochemical characterization and X-ray structural analysis of point mutants of bovine chymosin, Protein engineering design and selection, vol. 10, September 1997, pages 991-997 [0205] 7: Strop et al: Engineering enzyme subsite specificity: preparation, kinetic characterization, and x-ray analysis at 2.0 ANG resolution of Val111phe site mutated calf chymosin, Biochemistry, vol. 29, October 1990, pages 9863-9871 [0206] 8: Supannee et al: Site-specific mutations of calf chymosin B which influence milk-clotting activity, Food Chemistry, vol. 62, June 1998, pages 133-139 [0207] 9: Zhang et al: Functional implications of disulfide bond, Cys45-Cys50, in recombinant prochymosin, Biochimica et biophysica acta, vol. 1343, December 1997, pages 278-286. [0208] 10: WO2013/174840A1 (Chr. Hansen). [0209] 11: WO2013/164479A2 (DSM).