FIELD OF INVENTION

The present invention relates to a process for producing cheese, in which an enzyme preparation comprising a specific protease is added to cheese milk in the course of the process.

BACKGROUND OF THE INVENTION

In traditional cheesemaking, cheese is prepared by adding a starter culture and rennet to warm milk to form a curd (setting) . When the desired consistency and strength of the curd has been obtained, the curd is cut, followed by separa¬ tion of whey from the curd, e.g. by draining after which the curd is salted, pressed and stored (ripened) .

In this process, a considerable loss of milk proteins and - to some extent - fat takes place due to the removal of whey so that the yield of cheese is decreased relative to the total content of proteins and fat in milk. A cheesemaking process has therefore been developed whereby the milk is con¬ centrated, primarily by ultrafiltration, to approximately the fat and protein content desired in the finished product after which a starter culture, rennet and salt are added. No signi¬ ficant whey drainage occurs from the curd, and therefore the whey proteins (notably β-lactoglobulin and ό-lactalbumin) normally lost when the whey is removed are retained in the concentrate resulting (together with retained fat) in an in¬ crease in yield of about 10%.

However, the use of UF-concentrated milk for making cheese has only been commercially successful for a limited number of cheese types. A major cause of this is the effect of whey proteins on the characteristics of the resulting UF cheese. Thus, it has been found that undenaturated whey proteins are resistant to hydrolysis by rennet, starter culture proteases and plasmin (De Boer and Nooy, North European Dairy Journal 46. 1980, pp. 52-61; De Koning et al., Netherlands Milk

and Dairy Journal 35. 1981, pp. 35-46; Quist et al., Beretning fra Statens Me eriforsøα. 1986, p. 268) . The undenaturated whey proteins may act as a filler resulting in cheese with a smoother texture. The change in texture is thought to be ascribable to the fact that the whey proteins do not partici¬ pate in the formation of the casein matrix which is essential for the strength and firmness of many cheeses, in particular cheeses with a low moisture content, or may even negatively affect the matrix if present in an amount of up to 20% of the protein dry matter. It has further been observed that the whey proteins may negatively influence the process of cheese ripening in that they may have a dilution effect by lowering the proportion of casein in the curd (De Koning et al., supra) or that they may limit the accessibility of casein to the enzymes responsible for ripening.

The problem of decreases maturation rate of UF cheese cannot be overcome by denaturing the whey proteins, e.g. by heat treatment of the cheese milk, as it has been found that the presence of denatured whey proteins in certain UF cheeses adversely affect their stretch and melt properties on heating (Covacevich and Kosikowski, Journal of Dairy Science 61. 1978, pp. 704-709; Quist et al., supra; Olson, Dairy Record 85(7) . 1984, p. 85). Furthermore, hydrolysis of denatured whey proteins may give rise to atypical flavours and textures of the ripened cheese (Green et al., Journal of Dairy Research 48, 1981, pp. 333-341; Brown and Ernstrom, Journal of Dairy Science 65. 1982, pp. 2391-2395; Banks and Muir, Journal of the Society of Dairy Technology 38. 1985, pp. 27-32) . Denatured whey proteins may also affect the maturation rate in a similar fashion as undenaturated whey proteins, as discussed above.

SUMMARY OF THE INVENTION

It has surprisingly been found that the adverse effects arising from the retention of whey proteins in concen¬ trated milk used for cheesemaking may be considerably reduced when an enzyme causing a limited specific hydrolysis of whey

proteins without concomitantly causing any clotting of the milk is included in the cheesemaking process.

Accordingly, the present invention relates to a process of producing cheese, wherein: (i) an enzyme preparation which comprises a proteo- lytic enzyme which is capable of effecting a limited specific hydrolysis of whey proteins, but which does not cause any clotting of milk, the enzyme preparation being substantially free from other proteolytic activity, is added to milk so as to effect said limited specific hydrolysis of the whey proteins in the milk;

(ii) a starter culture is added to the milk subse¬ quently to or simultaneously with the enzyme preparation; and (iii) a milk-clotting enzyme is added to the milk subsequently to or simultaneously with the enzyme preparation added in step (i) and subsequently or simultaneously with the starter culture added in step (ii) so as to effect clotting of the milk, after which the resulting curd is processed in a manner known per se for producing cheese.

DETAILED DISCLOSURE OF THE INVENTION

In particular, the proteolytic enzyme is one which has the following characteristics:

(a) it is a serine protease specific for glutamic acid (Glu) and aspartic acid (Asp) residues;

(b) it has a specific activity of at least 25 cpu

(as defined herein) per gram of enzyme protein;

(c) it has a molecular weight of about 23,600;

(d) it is inhibited by diisopropyl phosphofluori- date, but not by phenylmethane sulfonylfluoride;

(e) it exhibits 75% or more of its maximum activity in the pH range of 6.5-10.0;

This proteolytic enzyme has previously been charac¬ terized in US 4,266,031 as a contaminant of subtilisin A produced by Bacillus licheniformis. However, there is no indication of the specific proteolytic activity of the enzyme in this US patent, and its utility in the cheesemaking process of the invention is therefore not anticipated by the disclosure of the enzyme per se in the patent. According to the invention, it has surprisingly been found that the proteolytic enzyme is a protease which is specific for Glu and Asp residues. This property is important for the present purpose since it pro¬ vides for limited and specific hydrolysis of whey proteins at Glu and/or Asp residues. These amino acid residues are hydrophilic, resulting in reduced bitterness of the resulting whey protein hydrolysate which therefore does not have any adverse effect on the flavour of the cheese produced by the process. It has furthermore surprisingly been found that al¬ though the proteolytic enzyme in question is capable of hydrolysing whey proteins, it does not cause any proteolysis of kappa-casein in its native state, presumably because the Glu residues present in casein are not accessible to the enzyme due to the three-dimensional structure of native kappa-casein. This means that, contrary to what might have been expected, the Glu/Asp specific protease used in the process of the invention does not, to the best of our current knowledge, adversely affect the cheesemaking process by changing the properties of the casein coagulum which might be important for the structure and/or texture of the resulting cheese.

Another proteolytic enzyme which is contemplated to be useful for the present purpose is the Staphylococcus aureus V8 protease which is also specific for Glu and Asp residues in proteins. Examples of other proteolytic enzymes contemplated to be of use for the present purpose are a Glu/ sp-specific protease from Streptomyces ther ovul aris (N.V. Khaidarova et al., Biokhimiya 54 (1), 1989, pp. 32 - 38), a Glu/Asp-speci- fie protease from Actinomyces (O.V. Moslova et al., Biokhimiya 52 (3), 1987, pp. 358 - 366) and a Glu/Asp-specific protease from Bacillus subtilis (G.A. Rufo et al., J. Bacteriol. 172 (2), 1990, pp. 1019 - 1023).

By effecting partial hydrolysis of whey proteins by the present process, the subsequent steps in the cheesemaking process, i.e. addition of a starter culture and milk-clotting enzyme, and further salting, pressing and ripening the curd, may be conducted in the traditional way of producing cheese, e.g. as described in R. Scott, Cheesemaking in Practice _r 2nd Ed., Elsevier, London, 1986. It is anticipated that the hydrolysis of the whey proteins by the proteolytic enzyme em¬ ployed in the present process will make the partially hydro- lysed whey proteins accessible to further decomposition by starter culture proteases resulting in an accelerated and more homogeneous cheese ripening (at least compared to that reported for UF cheese) as well as improved melting characteristics. In particular, the graininess of melted UF cheese may be avoided. Any type of milk, in particular milk from ruminants such as cows, sheep or goats, may be used as the starting material in the process of the invention, e.g. reconstituted milk, whole milk, concentrated whole milk or skimmilk. It is, however, believed that the present process is particularly well suited for overcoming the drawbacks previously reported to be connected with the use of concentrated milk.

The milk may be concentrated in various ways such as by evaporation or spray-drying, but is preferably concentrated by membrane filtration, i.e. ultrafiltration in which molecules with a molecular weight of up to 20,000 are allowed to pass the membrane, optionally with diafiltration before or after ultrafiltration, or possibly hyperfiltration in which mole¬ cules of a molecular weight of up to 500 are allowed to pass the membrane. Filtration implies that a larger amount of dry matter is retained in the curd, and consequently a higher yield of cheese is obtained. Ultrafiltration may be performed by cycling milk across a membrane such as a membrane of a suitable organic polymer or an inorganic ceramic material at an elevated pressure whereby the milk may be concentrated up to about 8 times. In this process, water and low molecular weight compo¬ nents are passed through the membrane, while proteins (includ¬ ing casein, lactoglobulin and lactalbumin) and fats are

retained. For a more detailed description of the ultrafiltra¬ tion process, see for instance Quist et al., supra.

When the milk used in the process of the invention is concentrated milk, it may, for practical reasons, be more convenient to add the proteolytic enzyme after the milk has been concentrated.

The amount of the proteolytic enzyme added according to the present process will vary according to the degree of concentration of the milk (which determines the amount of whey proteins in the concentrate) , but will usually be added in an amount of 0.005-0.25 cpu/1 of milk, preferably 0.01-0.1 cpu/1 of milk, such as 0.05 cpu/1 of milk.

According to the invention, hydrolysis of the whey proteins may be carried out for 0.5-4 hours, typically about 2 hours, to ensure a satisfactory degree of hydrolysis (cleavage at a sufficient number of accessible Glu and Asp residues in the whey protein molecule) . The pH is suitably in the range of 6.4-7.0, typically about 6.7. The temperature is suitably be¬ tween 30 and 37°C, typically about 34°C. The proteolytic enzyme employed in the present process may be one producible by a microorganism, in particular a bacterium. Such a bacterium may be a strain of Bacillus licheniformis. e.g. a strain known to produce subtilisin A as well as another protease corresponding to the proteolytic enzyme defined above. In this case, the proteolytic enzyme may be prepared by culturing the bacterial strain under conditions conducive to the production of alkaline protease which may then be isolated, after which the protease activities may be separated by methods known per se, e.g. by the process de- scribed in the above-mentioned US 4,266,031.

The strain of Bacillus licheniformis may also be a mutant strain, such as a mutant in which the gene encoding subtilisin A has been inactivated, for instance by conventional mutagenesis procedures involving the use of a mutagen such as nitrosoguanidine, e.g. substantially by the procedure dis¬ closed in the above-mentioned US 4,266,031 (disclosing the inactivation of the gene encoding the proteolytic enzyme of current interest) . Alternatively, the inactivation of the

subtilisin A gene may also take place by recombinant DNA techniques, e.g. by inserting one or more nucleotides into the subtilisin A gene so as to disrupt the sequence. This may, for instance, be done by homologous recombination, e.g. as de-

5 scribed in F.A. Ferrari et al., J. Bacteriol. 154 (3), 1983, pp. 1513 - 1515. The proteolytic enzyme may also be produced by isolating the DNA sequence from a cDNA or genomic library of microorganism producing the enzyme, e.g. a strain of Bacillus licheniformis. inserting the DNA sequence into a suitable

10 expression vector, transforming a suitable host microorganism with the vector, growing the host under conditions which are conducive to the production of the enzyme and recovering the enzyme from the culture. These steps may be carried out by standard procedures, cf. T. Maniatis et al., Molecular Cloning:

15 A Laboratory Manual. Cold Spring Harbor, 1982.

In a particular embodiment of the present process, the proteolytic enzyme is one which has the amino acid sequence shown in the appended Fig. 4, or a derivative thereof.

In the present context, the term "derivative" is

20 understood to indicate a proteolytic enzyme which is derived from the native enzyme by addition of one or more amino acids to either or both the C- and N-terminal end of the native protein, substitution of one or more amino acids at one or a number of different sites in the native amino acid sequence,

25 deletion of one or more amino acids at either or both ends of the native protein or at one or more sites in the amino acid sequence, or insertion of one or more amino acids at one or more sites in the native amino acid sequence, provided that the proteolytic activity of the enzyme is not thereby impaired.

30 The starter culture added in step (ii) of the process of the present invention, is a culture of lactic acid bacteria used, in conventional cheesemaking, to ferment the lactose present in the milk and to cause further decomposition of the clotted casein into smaller peptides and free amino acids as a

35 result of their production of proteases and peptidases. The starter culture may be added in amounts which are conventional for the present purpose, i.e. typically amounts of about 1x10 - lxlO ⁵ bacteria/g of cheese milk, and may be added in the form

of freeze-dried, frozen or liquid cultures. When the milk em¬ ployed in the process of the invention is concentrated milk, it is preferred to add the starter culture after concentrating the milk, although this is not an absolute requirement as the starter bacteria will be retained during filtration.

In the process of the present invention, the milk- clotting enzyme may be any enzyme which is capable of effecting casein coagulation under cheesemaking conditions. Thus, the enzyme may be of animal or microbial origin. An example of a suitable milJ-clotting enzyme of animal origin is chymosin (also known as rennet) which may be obtained from the lining of the fourth stomach of the calf, or which may be produced by re- combinant DNA techniques, e.g. as described in GB 2,100,737. Examples of suitable milk-clotting enzymes of microbial origin are fungal proteases such as Mucor miehei acid protease (commercially available from Novo Nordisk A/S under the trademark Rennilase; cf. also GB 1108287) , Mucor pusillus (K. Arima et al., Methods in Enzvmolocry. vol. 19, 1970, pp. 446- 459) or Endothia parasitica (J.R. Whitaker, Method in En- zvmology. vol. 19, 1970, pp. 436-445). The Mucor proteases may furthermore be chemically modified to improve their prop¬ erties, e.g. as described in US 4,255,454 or US 4,357,357.

The amount of milk-clotting enzyme added in the present process will vary according to the type of enzyme used and the degree of concentration of the milk, but the enzyme will usually be added in an amount of 18-25 ml of a commercial enzyme preparation (single-strength = 1:14,000 Soxhlet units) per 100 1 of milk.

It is at present contemplated that most types of cheese may advantageously be prepared by the process of the invention. There is, however, some indication that hard or semi-hard cheeses (with a dry matter content of about 50-70%) similar to Edam, Mozzarella, Danbo, Havarti or Cheddar are particularly advantageous to produce by the present process. Problems connected with the production of cheese from UF milk have primarily been encountered in the production of hard or semi-hard cheese. For instance, it has been reported that UF Mozzarella has significantly impaired melting characteristics

compared to traditionally produced Mozzarella (Covacevich, 2nd Biennial Marschall International Cheese Conference. 1981, Madison WI Marschall Products, pp. 237-244) . It has also been reported that UF Mozzarella is difficult to grind and that the ground product becomes soft and releases serum on storage (Hansen, North European Dairy Journal 53. 1987, pp. 21-23). Impaired melting characteristics have also been reported for UF Havarti (Quist et al., supra) and cheese base (Ernstrom et al, Journal of Dairy Science 63. 1980, pp. 228-234) . The reason for the impaired characteristics of hard and semi-hard UF cheeses in particular is believed to be the greater dependence of these cheeses on casein-casein interactions for obtaining a firm texture. Whey proteins which may interfere with such interactions, e.g. by dilution effects (De Koning et al., supra) , are therefore expected to exert a greater influence on the texture of these cheese types. It has surprisingly been found that when a proteolytic enzyme as defined above which is capable of hydrolysing whey proteins into smaller (poly)pepti- des is added to the cheese milk according to the invention, the drawbacks associated with the use of concentrated milk for cheesemaking may be overcome or at least substantially reduced, in particular with respect to hard or semi-hard UF cheese or UF cheese which stretches and melts on heating.

In another aspect, the present invention relates to an enzyme preparation in liquid, stabilized, spray-dried, vacuum-dried, freeze-dried or granulated form, the preparation comprising a proteolytic enzyme with the following characteris¬ tics:

(a) it is a serine protease specific for glutamic acid (Glu) and aspartic acid (Asp) residues;

(b) it has a specific activity of at least 25 cpu (as defined herein) per gram of enzyme protein;

(c) it has a molecular weight of about 23,600;

(d) it is inhibited by diisopropyl phosphofluori- date, but not by phenylmethane sulfonylfluoride;

(e) it exhibits 75% or more of its maximum activity in the pH range of 6.5-10.0;

the enzyme preparation being substantially free from other proteolytic activity, for use in a process of producing cheese. The various ways in which the enzyme preparation may be formulated are well known in the enzyme art, cf. for instance K. Aunstrup et al., "Production of Microbial Enzymes", in Miβrobial Technology (H.J. Peppier and D. Perlman, Eds.), 2nd Ed., Vol I, Academic Press 1979, pp. 295-297.

BRIEF DESCRIPTION OF THE DRAWINGS

The present invention is further illustrated in the following examples with reference to the appended drawings wherein:

Fig. 1 is a graph showing the pH activity of the SP 446 pro¬ tease;

Fig. 2 is a graph showing the temperature activity of the SP 446 protease in the presence (white squares) and absence (black squares) of sodium tripolyphosphate (STPP) ;

Fig. 3 shows the cleavage of insulin by the SP 446 protease; and

Fig. 4 shows the amino acid sequence of the SP446 protease, wherein the amino acids are indicated in the established one- letter code.

The invention is further illustrated in the following examples which are not intended to be in any way limiting to the scope of the invention as claimed.

EXAMPLE 1

Characterization of Bacillus 1icheniformis SP 446 protease

Yield of SP 446 protease

Alcalase™ PPA 1618 was purified as described in US 4,266,031. The yield of purified SP 446 protease was deter¬ mined by measuring the enzymatic activity of the starting and purified SP 446 protease using CBZ-Phe-Leu-Glu-pNA (Boehringer Mannheim) as substrate. It was necessary to add phenylmethane sulfonylfluoride (1:10 vol) in order to inactivate subtilisin A present in the enzyme preparation, as subtilisin A is able to degrade the substrate, apparently by cleaving after Phe or Leu. The enzymatic activity of the starting material (40 ml) was measured in a Perkin-Elmer, Lambda reader as the ab- sorbance at 405 nm/ in./ml and was determined to be 166,920. The enzymatic activity of the purified material (31 ml) was similarly measured and determined to be 158,720. Thus, the yield of SP 446 protease was 95%.

Proteolytic activity

The proteolytic activity of the SP 446 protease was determined to be 27 cpu/g using casein as substrate. 1 casein protease unit (cpu) is defined as the amount of enzyme liberat¬ ing 1 millimole of primary amino groups (determined by compari¬ son with a serine standard) per minute under standard condi¬ tions as described below: A 2% (w/v) solution of casein (Hammarsten, supplied by Merck AG, Darmstadt, FRG) is prepared with the Universal Buffer described by Britton and Robinson, J. Chem. Soc.. 1931, p. 1451), adjusted to a pH of 9.5. 2 ml of the substrate so¬ lution are pre-incubated in a water bath for 10 in. at 25"C. 1 ml of an enzyme solution containing b g/ml of the enzyme preparation, corresponding to about 0.2-0.3 cpu/ l of the Universal Buffer (pH 9.5) is added. After 30 min. of incuba¬ tion at 25 "C, the reaction is terminated by the addition of a quenching agent (5 ml of a solution containing 17.9 g of trichloroacetic acid, 29.9 g of sodium acetate and 19.8 g of

acetic acid made up to 500 ml with deionized water) . A blank is prepared in the same way as the test solution with the ex¬ ception that the quenching agent is added prior to the enzyme solution. The reaction mixtures are kept for 20 min. in a wa- ter bath after which they are filtered through Whatman 42 paper filters. A folder AF 228/1 describing this analytical method is available upon request from Novo Nordisk A/S, Denmark.

Primary amino groups are determined by their colour development with o-phthaldialdehyde (OPA) , as follows: 7.62 g of disodium tetraborate decahydrate and 2.0 g of sodium dodecylsulfate are dissolved in 150 ml of water. 160 g of OPA dissolved in 4 ml of methanol were then added to¬ gether with 400 μl of β-mercaptoethanol after which the solu¬ tion is made up to 200 ml with water. To 3 ml of the OPA rea- gent are added 400 μl of the filtrates obtained above, with mixing. The optical density (OD) at 340 nm is measured after about 5 min. The OPA test is also performed with a serine standard containing 10 mg of serine in 100 ml of Universal Buffer (pH 9.5). The buffer alone is used as a blank. The protease activity is calculated from the OD measurements by means of the following formula:

(OD _t - 0D _b ) x C _ser x Q cpu/ l enzyme solution: ser ^b ser "

cpu/g of enzyme preparation = cpu/ml: b

wherein 0D _t , OD _b , OD and OD _B is the optical density of the test solution, blank, serine standard and buffer, respective¬ ly, C is the concentration of serine (mg/ml) in the stand- ard (in this case 0.1 mg/ml) , and M Sex is the molecular weight of serine (105.09). Q is the dilution factor for the enzyme solution (in this case 8) and _? is the incubation time in minutes (in this case 30 minutes) .

pH activity

The pH dependence of the activity of the SP 446 protease was determined by the OPA casein method described above with the modification that the Universal Buffer was 5 adjusted to different pH values, i.e. pH 6, 7, 8, 9, 10 and 11. The results are shown in Fig. 1 from which it appears that the SP 446 protease has a pH optimum in the range of pH 8-10.

Temperature activity

The temperature dependence of the activity of the SP

10446 protease was determined by the OPA casein method described above with the modifications that the enzyme reaction was carried out at different temperatures, i.e. 15"C, 30°C, 40°C, 50°C, 60 " C and 70°C, and that the enzyme reaction was conducted in the presence and absence of 0.1% sodium tripolyphosphate

15 (STPP) which is a common ingredient in many commercial deter¬ gents. The results are shown in Fig. 2 from which it appears that the SP 446 protease has a temperature optimum of about 50 ^β C whether STPP is present or not.

Glu specificity

20 The Glu specificity of the SP 446 protease was determined as follows:

0.5 ml of 1 mg/ml human insulin in Universal Buffer, pH 9.5 (vide supra) . and 75 μl SP 446 protease (0.6 cpu/1) in the same buffer were incubated for 120 min. at 37°C. The

25 reaction was terminated by adding 50 μl IN hydrochloric acid.

The insulin molecule was cleaved into a number of peptide fragments. These were separated and isolated by reverse phase HPLC using a suitable C-18 column (Hibar LiChrosorb RP-

18, 5 μ particles provided by Merck AG, Darmstadt, FRG) . The

30 fragments were eluted with the following solvents:

A. 0.2 M sodium sulfate and 0.1 M phosphoric acid, pH 2.5;

B. Acetonitrile/water, 50%;

on a linear gradient of from 90% A/10% B to 80% A/20% B for 0- 5 min. and subsequently for 50 min. with 80% A/20% B. The isolated fragments were subjected to amino acid sequencing by automated Edman degradation, using an Applied Biosystems, Inc., (Foster City, CA, USA) Model 470A gas-phase sequencer and the phenylthiohydantoin (PTH-) amino acids were analyzed by high performance liquid chromatography as described by L. Thi et al., "Secretion of human insulin by a transformed yeast cell", FEBS Letters 212(2) . 1987, p.307, whereby the cleavage sites in the insulin molecule were identified as shown in Fig. 3.

N-terminal amino acid sequence

The N-terminal amino acid sequence of the purified SP 446 protease was determined as described above. The N- terminal sequence was determined to be

1 5 10 15 20

S V I G S D D R T R V T N T T A Y M T -

Complete amino acid sequence

The complete amino acid sequence was determined from the DNA sequence. The DNA sequence was determined by standard techniques as described in the section entitled "Detailed

Disclosure Of The Invention". The complete amino acid sequence is shown in the appended Fig. 4.

Based on this amino acid sequence, the molecular weight of the SP 446 protease was determined to be 23,600.

Inactivation of the SP 446 protease with DFP

Incubation of the enzyme with PMSF (1% in isopro- panol) in a ratio of 1 to 10 (by volume) did not result in any inactivation of the SP 446 protease. However, incubation of 10 μl (1 mg/ml) of the enzyme with 80 μl 10 mM MOPS, pH 7.2, + 10 μl 0.1 M diisopropyl phosphofluoridate (DFP) for 60 min. re¬ sulted in complete inactivation of the enzyme as measured by its activity on the substrate CBZ-Phe-Leu-Glu-pNA.

EXAMPLE 2

Hydrolysis of whey protein

To 75 g of spray-dried whey protein (Lacprodan-80, available from Danmark Protein A/S, Nr. Vium, 6920 Videbaek, 5 Denmark) dissolved in 800 ml of deionized water were added 14.7 cpu per 100 g of protein of the SP 446 protease and commercial trypsin (Pancreas Trypsin Novo 6.0 S, available from Novo Nordisk A/S, used as reference) , respectively. The proteases were incubated with the whey protein for 4 hours at 65°C and pH

108.0 by the so-called pH-stat method described in Information Sheet No. B 163f, November 1984, entitled "Use of Food Grade Alcalase ^R or Neutrase ^R for Controlled Enzymatic Hydrolysis of Proteins", available from Novo Nordisk A/S on request. The degree of hydrolysis measured for the whey protein was 12.1%

15 obtained with SP 446 and 10.4 obtained with trypsin (the percentage is calculated from the total number of peptide bonds in the protein) .

The degree of hydrolysis may be calculated by means of the following formula:

20 Number of peptide bonds cleaved

DH = x 100

Total number of peptide bonds

The total number of peptide bonds in a protein may be calculated from its amino acid composition. The number of

25 peptide bonds cleaved may be determined from an assay of the free ό-amino groups in the hydrolysate by the following method using trinitrobenzene sulphonic acid (TNBS) :

0.25 ml of a sample containing between 0.25xl0 ^"3 and 2.5X10 ^"3 amino equivalents/1 is mixed in a test tube with 2.00

30 ml phosphate buffer at pH 8.2. 2 ml of a 0.1 % TNBS solution is added and the test tube is shaken and placed in a water bath at 50 +/- l ^β C for 60 min. During incubation, the test tube and water bath are covered with aluminium foil because the blank reaction is accelerated by exposure to light. After 60 min. ,

354.00 ml HCl is added to terminate the reaction, and the test

tube is allowed to stand at room temperature for 30 min. before reading the absorbance spectrophotometrically against water at 340 nm. For further details, see J. Adler-Nissen, J. Agric. Food Chem. 27. 1979, p. 1256-1262.

5 EXAMPLE 3

To determine the ability of the SP 446 protease to hydrolyse whey proteins in milk without concomitantly clotting the milk, 0.2 cpu/1 of subtilisin A and the SP 446 protease, respectively, were each added to 15 ml of whole milk at a pH of

106.8 and a temperature of 35°C. The reaction mixtures were allowed to stand for 3-4 hours. The milk containing subtili¬ sin A clotted after a few minutes ¹ incubation, whereas no clotting was observed in the milk containing the SP 446 pro¬ tease after 3-4 hours' incubation with the enzyme. To the re-

15 action mixture containing the SP 446 protease was then added Rennilase (registered trademark of Novo Nordisk A/S) to a concentration of 17.5 KRU/1 (KRU = kilorenneting units, vide Information Sheet No. B250f, 1989, entitled "Cheesemaking with Rennilase" available from Novo Nordisk A/S on request) re-

20 suiting in clotting of the milk after a few minutes' incuba¬ tion.

EXAMPLE 4

0.1 cpu of the SP 446 protease was added to 1 1 of pasteurized cow's milk standardized at 3.5 % of fat at 34°C and

25 incubated for 3 hours followed by addition of 10 ml of a com¬ mercial starter culture in an amount of Ixl0 ⁶ -lxl0 ⁷ bacteria/g of milk. After standing for 10 minutes a stock solution of Ca was added, corresponding to 0.2 g of CaCl ₂ . 0.2 g of Rennilase 14 L (trademark of Novo Nordisk A/S for a commercial Mucor

30 miehei protease) Batch PRN 1382 was then added with stirring and was then allowed to stand, resulting in the formation of a sufficiently firm curd after about 20 minutes. The curd was cut and salted in a manner known per se for the production of Feta cheese.

The remaining whey was subjected to SDS-PAGE in a manner known per se. from which it appeared that the high- molecular weight proteins (>30,000) had been decomposed to peptides with a molecular weight of less than 10,000.