Incorporation of whey into process cheese

Details Incorporation of whey into process cheese Incorporation of whey into process cheese

1999-06-03

2001-08-07

Wong, Leslie (Department: 1761)

Food or edible material: processes, compositions, and products

Fermentation processes

Of milk or milk product

C426S034000, C426S038000, C426S040000, C426S583000

Reexamination Certificate

active

06270814

ABSTRACT:

FIELD OF THE INVENTION
This invention relates to a method that increases the incorporation of whey proteins and lactose into process cheese. The method applies transglutaminase crosslinking of whey and milk proteins prior to blending with cheese to provide a process cheese. The resulting process cheese includes a significant proportion of whey protein and supersaturated lactose in the moisture phase.
BACKGROUND OF THE INVENTION
Cheese compositions are generally prepared from dairy liquids by processes that include treating the liquid with a coagulating or clotting agent. The coagulating agent may be a curding enzyme, an acid, or a suitable bacterial culture or it may include such a culture. The coagulum or curd that results generally incorporates transformed casein, fats including natural butter fat, and flavorings that arise especially when a bacterial culture is used. The curd is usually separated from the whey. The resulting liquid whey generally contains soluble proteins not affected by the coagulation; such proteins are, of course, not incorporated into the coagulum. Whey also includes low molecular weight components, such as lactose and salts. The inability of whey proteins to be retained in the coagulum is an important factor contributing to a lack of efficiency in production of cheese curds, and to a reduction in overall yield relating to the incorporation of all the protein solids that are present in the starting dairy liquids into resulting cheese curds. Furthermore, lactose is incorporated with difficulty into cheese products because, under the conditions prevalent in cheese during storage, lactose crystallizes from the aqueous phase, thereby producing a graininess that detracts from the overall organoleptic quality of the cheese product. Nevertheless, increased incorporation of lactose into cheese products would increase the efficiency of use of all the nutritive components present in the starting dairy liquids. These problems have been recognized for many years.
Several methods were proposed early with the objective of recovering whey proteins in cheese products. For example, whey proteins have been concentrated or dried from whey, and then recombined with cheese (see, e.g., Kosikowski, Cheese and Fermented Foods, 2nd ed., Edwards Brothers, Inc., Ann Arbor, Mich., 1977, pp. 451-458). Unfortunately the whey recovered from such procedures does not have the appropriate physical and chemical properties conducive to making good quality natural cheeses or process cheeses. An alternative approach has been to coprecipitate whey proteins with casein, as disclosed, for example, in U.S. Pat. No. 3,535,304. Again, however, the final product of this process lacks the proper attributes for making processed and imitation cheeses.
A further attempt to incorporate whey proteins into cheese products has employed ultrafiltration of milk to concentrate the components, such as casein, whey protein, and butterfat, that do not permeate the ultrafiltration membrane. When such a composition is coagulated by contact with an acid or rennet, a curd forms. This curd, however, loses considerable quantities of the whey protein during compaction. An example of such a process is provided in U.S. Pat. No. 4,205,090 wherein the milk is concentrated to about one-fifth of its original volume. The resulting curd could only be used to provide soft cheeses such as Camembert or Roblechon. Hard cheeses, such as cheddar, Colby, and the like, could not be prepared using this method.
Ernstrom et al. (J. Dairy Science 63:2298-234 (1980)) described a process in which milk is concentrated to about 20% of the original volume by ultrafiltration, diafiltration, and evaporation. The resulting composition is then inoculated with a cheese starter to ferment the lactose and form a cheese base. The cheese base can be used to replace natural cheese components of process cheese. This process does not employ any renneting step to prepare a cheese curd.
Food processing methods employing transglutaminases have also been disclosed in recent years. For example, Japanese Patent 59059151 discloses treating an emulsion containing proteins, oils or fats, and water with transglutaminase to produce a gelatinous, crosslinked gel. Japanese Patent 02276541 discloses a heat-resistant food protein having a fiber texture. The fiberlexture is developed by treatment of a protein hydrogel with a transglutaminase in the presence of calcium ion to induce crosslinking of the surface of a fiber bundle.
U.S. Pat. No. 5,156,956 discloses a transglutaminase purified from strains of the genus Streptoverticillium, as well as its chemical, physical, and enzymatic properties. This transglutaminase catalyzes formation of protein gelation products from protein solutions to produce conventional gel foodstuffs such as yoghurt, jelly, cheese, gel cosmetics, and the like. This method did not use transglutaminase and enzymatic clotting agents to produce cheese.
U.S. Pat. No. 5,356,639 discloses a process for the production of a fermented concentrate from milk, including whole milk, skim milk, and milk with added milk components. The concentrate could be used to make cheese. The process includes the steps of (1) selectively concentrating milk; (2) increasing the ionic strength of the concentrate to maintain the milk in the liquid phase (coagulum formation is prevented both during and after fermentation); (3) fermenting the concentrate with lactic acid producing bacteria; and (4) removing water from the fermented liquid concentrate. The final product includes substantially all of the whey proteins originally present in the milk.
U.S. Pat. No. 5,681,598 describes a process for producing cheese with a transglutaminase. The process includes (1) adding a transglutaminase to a milk or milk protein solution, (2) heat-treating the mixture, (3) adding a milk clotting enzyme for a fixed time, and (4) recovering a cheese. This process provides a large amount of cheese curd compared to conventional methods. Additionally, processes in which conventional cheese fermentation occurs first and transglutaminase treatment occurs subsequently, as well as simultaneous treatments, are disclosed. The milk clotting enzyme is preferably an animal rennet. Increases in total weight, but not in dry weight, of the curd when using transglutaminase were observed.
U.S. Pat. No. 5,731,183 discloses a transglutaminase purified from strains of
Bacillus subtilis
, having particular physical and enzymatic characteristics, and a method for producing protein, peptide, or non-protein amino acid polymers that are crosslinked via their glutamine and lysine residues to form intermolecular or intramolecular conjugates. The transglutaminase may be used to produce crosslinked protein polymers that can be used in a variety of food substances, including cheese.
Banks et al. (
Milchwissenschaft
42:212-215 (1987)) disclose that heating milk at temperatures from 95° C. to 140° C. and then acidifying permits a modest increase in protein content in the cheese upon Cheddar production. Unfortunately, the resulting cheese developed a bitter off-flavor. Law et al. (
Milchwissenschaft
49:63-37 (1994)) report that heat treatment of milk prior to cheddaring results in reduction of proteins in whey and/or in acid filtrates of the milk.
Han et al. (
J. Agri. Food Chem
. 44:1211-1217 (1996)) examined the activity of transglutaminase in forming heterologous dimers and trimers. It was found that &bgr;-casein forms homopolymers whereas &bgr;-lactoglobulin does not. In heterologous mixtures, transglutaminase was shown to catalyze dimer formation between &agr;-lactalbumin and &bgr;-casein but not between &bgr;-casein and &bgr;-lactoglobulin. Cheese production is not discussed.
U.S. Pat. No. 5,523,237 discloses a plastein material which is defined as one made by reversing the activity of a protease enzyme (e.g., a serine protease) acting on proteinaceous material. The proteinaceous substrate is present at a concentration of 5-50%, and is preferably whey, casein, or soy protein. The enzyme preparation is substantially free

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