HK1194926B

HK1194926B - Methods and compositions for consumables

Info

Publication number: HK1194926B
Application number: HK14108334.2A
Authority: HK
Inventors: Patrick Brown; Monte CASINO; Lynn S. VOCCOLA; Ranjani VARADAN
Original assignee: Impossible Foods Inc.
Priority date: 2011-07-12
Filing date: 2012-07-12
Publication date: 2019-10-18

Description

BACKGROUND OF THE INVENTION

Cheese making has relied on dairy milks as the major ingredient for more than 4000 years. Dairy cheese is made from curds formed from dairy milk. Dairy milks can readily be made to form curds suitable for making cheese by contacting the dairy milk with rennet (an aspartic protease which cleaves kappa-casein) at mildly acidic pH. Some cheeses, e.g., cream cheese, ricotta, cottage cheese and paneer, are made without rennet. In the absence of rennet, dairy cheese may be induced to curdle with acid (e.g., lemon juice, vinegar, etc.) or a combination of heat and acid. Acid coagulation can also occur naturally from starter culture fermentation. The strength of the curds depends on the type of coagulation. Most commercially produced cheeses use some type of rennet (animal, vegetable or microbial-derived) in their production.

The global dairy sector contributes an estimated 4 percent to the total global anthropogenic green house gas emissions. Producing 1 kg of cheddar cheese requires an average of 10,000 Liters of fresh water. Additionally, many individuals cannot digest and metabolize lactose. In these individuals enteric bacteria ferment the lactose, resulting in various abdominal symptoms, which can include abdominal pain, bloating, flatulence, diarrhea, nausea, and acid reflux. Additionally, the presence of lactose and its fermentation products raises the osmotic pressure of the colon contents. 3.4% of children in the U.S.A. are reported to have allergies to dairy milks. Many individuals choose to avoid milk for ethical or religious reasons.

Non-dairy milks, including plant-derived milks avoid many of the environmental, food sensitivity, ethical and religious problems associated with dairy milk and they can be made free of lactose, making the generation of dairy substitutes using the plant derived milks attractive. However, rennet is not an effective agent for inducing non-dairy proteins or emulsions, including plant-derived milks, including almond milk, chestnut milk, pecan milk, hazelnut milk, cashew milk, pine nut milk, and walnut milk, to curdle. Consequently, traditional cheese making techniques have not been successfully used to produce non-dairy cheese replicas.

Flavor and aroma in dairy cheese results in part from the degradation of lactose, proteins and fats, carried out by ripening agents, which include: bacteria and enzymes in the milk, bacterial cultures added during the cheese-making process, rennet, other proteases, lipases, added molds and/or yeasts and bacteria and fungi that opportunistically colonize the cheese during ripening and aging.

Cheese replicas made principally of non-dairy ingredients are commercially available. Most of these cheese replicas include some dairy ingredients, for example, casein. Some commercially available cheese replicas contain no animal products. These include fermented cheese replicas made from nut milks from which insoluble carbohydrates have not been effectively removed, and made without using a protein crosslinking agent and several products in which a starch is a principal ingredient or containing agar, carrageenan and tofu to provide the desired texture. Most tasters consider none of the currently available cheese replicas to adequately replicate the taste, aroma and mouthfeel of dairy cheeses.

Complex carbohydrates in currently available cheese replicas made from nut milks have unfavorable effects on the texture, resulting in a product with a grainy mouthfeel and lacking the creaminess of dairy cheeses.

Starches that comprise the major gelling agent in many currently available cheese replicas lead to a relatively high carbohydrate content, which may be undesirable to consumers, for example those wishing to limit carbohydrate intake.

Because of these deficiencies, there is currently no cheese replica that is acceptable to most consumers as an alternative to traditional dairy cheeses.

Thus, it is clear that there is a great need in the art for an improved method and system for producing non-dairy cheese replicas while avoiding the shortcomings and drawbacks of the cheese replicas that have previously been available to consumers. DE 102007061256 discloses a cheese replica product derived from soy milk, and which is prepared by coagulating an emulsion of soy milk and comminuting nuts. DE 202011002097 discloses a cheese replica product prepared from comminuted seeds and/or nuts and cheese-making microorganisms. GB 2016255 discloses a synthetic cheese-like product produced by forming an emulsion of soybeans. WO 2008/017499 discloses that protein-enriched vegetable or coco milk may be used to obtain visco-elastic cheese-like foodstuff.

SUMMARY OF THE INVENTION

The present invention relates to a cheese replica comprising a gelled emulsion of one or more cross-linked, plant-derived proteins, one or more fats, and a cross-linking enzyme, wherein the emulsion comprises a non-dairy milk having at least 85% of its insoluble solids removed, and wherein said plant-derived proteins are not from soy.

In one embodiment of the invention, the insoluble solids have been removed by centrifugation, straining, filtering, allowing to settle, skimming, or by using coagulants and flocculants.

In another embodiment of the invention, the insoluble solids have been removed by centrifugation.

In another embodiment of the invention, the cheese replica comprises between 10% and 40% proteins from plant sources and between 0% and 65% fats from plant sources.

In one embodiment of the invention, the cheese replica has an insoluble carbohydrate content of less than 5% by mass.

In another embodiment of the invention, the cheese replica further comprises:

(a) cheese-making microbes; and/or
(b) a sugar or other fermentable carbon source.

In another embodiment of the invention, the cross-linking enzyme is a transglutaminase or lysyl oxidase.

In another embodiment of the invention, the plant-derived proteins, and fats are from nuts, legumes, or seeds, optionally wherein the nuts comprise one or more of almonds, cashews, brazil nuts, coconuts, chestnuts, hazelnuts, macadamia nuts, peanuts, pecans, pistachios or walnuts.

In another embodiment of the invention, the plant-derived proteins comprise one or more proteins selected from the group consisting of a ribosomal protein, actin, hexokinase, lactate dehydrogenase, fructose bisphosphate aldolase, phosphofructokinases, a triose phosphate isomerase, a phosphoglycerate kinase, a phosphoglycerate mutase, an enolase, a pyruvate kinase, a glyceraldehyde-3-phosphate dehydrogenase, a pyruvate decarboxylase, an actin, a translation elongation factor, ribulose-1,5-bisphosphate carboxylase oxygenase (rubisco), ribulose-1,5-bisphosphate carboxylase, an oxygenase activase (rubisco activase), an albumin, a glycinin, a conglycinin, a globulin, a vicilin, a conalbumin, a gliadin, a glutelin, a gluten, a glutenin, a hordein, a prolamin, a phaseolin (protein), a proteinoplast, a secalin, an extensin, a zein, a seed storage protein, an oleosin, caloleosin, a steroleosin, vegetative storage protein A, vegetative storage protein B, and moong seed storage SS globulin.

In another embodiment of the invention, the cheese-making microbes are selected from one or more of the following: Penicillium camemberti, Penicillium candidum, Geotrichum candidum, Penicillium roqueforti, Penicillium nalgiovensis, Verticillium lecanii, Kluyveromyces lactis, Saccharomyces cerevisiae, Candida utilis, Debaryomyces hansenii, Rhodosporidum infirmominiatum, Candida jefer, Cornybacteria, Micrococcus sps., Lactobacillus sps., Lactococcus, Staphylococcus, Halomonas, Brevibacterium, Psychrobacter, Leuconostocaceae, Streptococcus thermophilus, Pediococcus sps., or Propionibacteria.

Provided herein are methods and compositions for non-dairy milk and cheese products, including without limitation, plant-derived milk and cheese products, as an alternative to dairy products for human consumption.

Provided herein is a method for producing a non-dairy cheese by preparing an emulsion comprising proteins and fats from plants or other non-animal sources, inducing the emulsion to form a gel by enzymatic cross-linking of the proteins or denaturing the proteins, and producing a cheese- replica from the gel. In one case, the emulsion contains less than 10% animal products. In one case, the emulsion contains less than 8%, 7%, 6%, 5%, or 3% animal products. In one case, the emulsion contains no animal products. In one case, the inducing step of said method comprises adding an enzyme. In one variant of said method the enzyme used is transglutaminase. In one variant the enzyme used is Factor XIII (fibrin-stabilizing factor). In one variant of said method the enzyme used is Keratinocyte transglutaminase (TGMI). In one variant the enzyme used is Tissue transglutaminase (TGM2). In one variant of said method the enzyme used is Epidermal transglutaminase (TGM3). In one variant the enzyme used is Prostate transglutaminase (TGM4). In one variant the enzyme used is TGM X (TGM5). In one variant of said method the enzyme used is TGM Y (TGM6). In one variant of said method the enzyme used is TGM Z (TGM7). In one variant, the enzyme is a transglutaminase from Streptoverticillium mobaraense. In one variant, the enzyme is similar or identical to a transglutaminase from Streptoverticillium mobaraense. In one variant, the enzyme is a lysyl oxidase. In one case the emulsion is non-dairy milk. In one case at least one of the plant sources are nuts. In one case, at least one of the plant sources are legumes. In one case, at least one of the plant sources are seeds. In one case, at least one of the plant sources are leaves. In one case, at least one of the plant sources are fruit from the family Fabaceae. In one case, at least one of the non-animal sources is a species of bacteria. In one case, at least one of the non-animal sources is a species of archaea. In one case, at least one of the non-animal sources is a species of fungus. In one case, at least one of the non-animal sources is a species of algae. In one case, the emulsion is a non-dairy milk. In one case, the nuts are one or more of following: almonds, cashews, brazilnuts, chestnuts, coconuts, hazelnuts, macadamia nuts, peanuts, pecans, pistachios or walnuts. One variant of said method has an additional step of adding a sugar to the emulsion. In one case the sugar added to the emulsion is a monosaccharide. In one case the sugar added to the emulsion is a disaccharide. In one case said method has an additional step of inoculating with lactic acid bacteria. In the case of inoculating with lactic acid bacteria the disclosure provides an addition step of allowing growth of the bacterial cultures. In one case, the method can include an additional step of adding one or more of the following Penicillium camemberti, Geotrichum candidum, Penicilliem roqueforti, Penicillium nalgiovensis, Verticillium lecanii, Kluyveromyces lactis, Saccharomyces cerevisiae, Candida utilis, Debaryomyces hansensil, Rhodosporidum infirmominiatum, Candidajefer, Cornybacteria, Micrococcus sps., Lactobacillus sps.,Lactococcus, Staphylococcus, Halomonas, Brevibacterium, Psychrobacter, Leuconostocaceae, Streptococcus thermophilus, Pediococcus sps., or Propionibacteria. In one case, the method can include an additional step of adding one or more of the following halophilc bacterium or archaea. In one case, the disclosure provides for the use of thermal denaturing and cross-linking. In one case, the disclosure provides thermal denaturing used without the addition of any enzymes. One variantof said method has an additional step of cutting the gel. One variant of said method has an additional step of draining and shaping the cut gel. One variant of said method has an additional step of adding a flavoring component. In one variant the flavoring component is one or more species of bacteria. In one variant the flavoring component is lactic acid bacteria. In one variant the flavoring component is a mold. In one variant the flavoring component is yeast. In one case, the method includes concentrated proteins prior to preparing the emulsion. In one case, the concentrated proteins are each essentially homogeneous proteins. In one case, the method includes the additional step of concentrating proteins and fats from one or more plant sources. In one case, the method includes the additional step of concentrating proteins and fats from one or more non-animal sources. In one case, the method includes the additional step of isolating the proteins and fats from one or more plant sources. In one case, the method includes the additional step of isolating the proteins and fats from one or more non-animal sources. In one case, the method includes the additional step of purifying the proteins and fats from one or more plant sources. In one case, the method includes the additional step of purifying the proteins and fats from one or more non-animal sources. In one case, the disclosure provides for the concentrated proteins to come from the same essentially homogeneous plant-derived protein. In one case, the disclosure provides for the concentrated proteins to come from the same essentially homogeneous non-animal-derived protein. In one case, the disclosure provides for the concentrated proteins to come from separate plant species. In one case, the disclosure provides for the concentrated proteins to come from separate non-animal species.

In addition, provided herein are steps for preparation to undertake methods of producing a non-animal based cheese including (a) obtaining nuts or seeds, and (b) surface sterilizing the nuts or seeds. In one case, the method uses nuts or seeds as the plant sources. In one case, the surface sterilization step is blanching procedure. In one case, the preparation method can also include a step for washing the nuts or seeds. In one case, the method of preparation can also include the step of decompounding the nuts or seeds. In one case, the step of decompounding the nuts or seeds is a blending procedure. In one case, the method of preparation can also include centrifugation. In one case, the method of preparation can also include a centrifugation procedure that results in the removal of at least 85% of the suspended solids. In one case, the method of preparation can also include a centrifugation procedure that results in the removal of at least 75%, 65%, 55%, or 45% of the suspended solids.

Provided herein is a method comprising decompounding nuts or seeds in water, removing at least 85% of the suspended solids and adding a transglutaminase to catalyze the formation of crosslinks between proteins from the nuts or seeds.

Provided herein is a method for making a non-dairy cheese replica comprising, obtaining nut milk, centrifugation of the nut milk to remove insoluble matter, and crosslinking proteins within the nut milk with transglutaminase.

In one case, provided herein is a composition comprising centrifuged non-dairy milk wherein at least 85% of the insoluble solids have been removed relative to the non-dairy milk prior to centrifugation.

In one case, provided herein is a composition comprising a non-dairy milk with less than 30% polysaccharides. In one case, the non-dairy milk composition has less than 10% polysaccharides. In one case, the non-dairy milk composition less than 1% polysaccharides. In one case, the non-dairy milk composition is entirely composed of ingredients derived from non-animal sources. In one case, the non-dairy milk composition is at least comprised of 20% protein isolated from a single plant species.

In one case,, provided herein is a composition comprised of non-dairy milk and a cross-linking enzyme. In one case of the non-dairy milk and a cross-linking enzyme composition the cross-linking enzyme is Factor XIII (fibrin-stabilizing factor). In one case of the non-dairy milk and a cross-linking enzyme composition, the enzyme is a transglutaminase from Streptoverticillium mobaraense. In one case of the non-dairy milk and a cross-linking enzyme composition, the enzyme is similar or identical to a transglutaminase from Streptoverticillium mobaraense. In one case of the non-dairy milk and a cross-linking enzyme composition the cross-linking enzyme is Keratinocyte transglutaminase (TGM I). In one case of the non-dairy milk and a cross-linking enzyme composition the cross-linking enzyme is Tissue transglutaminase (TGM2). In one case of the non-dairy milk and a cross-linking enzyme composition the cross-linking enzyme is Epidermal transglutaminase (TGM3). In one case of the non-dairy milk and a cross-linking enzyme composition the cross-linking enzyme is Prostate transglutaminase (TGM4). In one case of the non-dairy milk and a cross-linking enzyme composition the cross-linking enzyme is TGM X (TGM5). In one case of the non-dairy milk and a cross-linking enzyme composition the cross-linking enzyme is TGM Y (TGM6). In one case of the non-dairy milk and a cross-linking enzyme composition the cross-linking enzyme is TGM Z (TGM7). In one case, provided herein is a composition comprised of non-dairy milk and a cross-linking enzyme. In one case of the non-dairy milk and a cross- linking enzyme composition the cross-linking enzyme is lysyl oxidase. In one case of the composition comprising non-dairy milk and a cross-linking enzyme, protein crosslinks are formed between glutamine and lysine side chains of respective protein constituents.

In one case of the non-dairy milk and a cross-linking enzyme composition, at least 85% of the insoluble solids have been removed by centrifugation. In one case of the non-dairy milk and a cross-linking enzyme composition, proteins from non-animal sources comprise at least 50% of the total mass of the composition. In one case of the non-dairy milk and a cross- linking enzyme composition the starch content is less than 1% by mass. In one case of the non-dairy milk and a cross-linking enzyme composition is the starch content is less than 5% by mass. One case of the non-dairy milk and a cross-linking enzyme composition has less than 1% insoluble carbohydrate by mass. One case of the non-dairy milk and a cross-linking enzyme composition has less than 5% insoluble carbohydrate by mass. One case of the non-dairy milk and a cross-linking enzyme composition has less than 5% starch and less than 1% insoluble carbohydrate by mass. One case of the non-dairy milk and a cross-linking enzyme composition has less than 5% starch and less than 5% insoluble carbohydrate by mass. In one case, the non-dairy milk and a cross-linking enzyme composition has a polysaccharide content less than 1% by mass. In one case, the non-dairy milk and a cross-linking enzyme composition has a polysaccharide content less than 5% by mass. In one case, the non-dairy milk and a cross- linking enzyme composition has a carbohydrate content less than 1% by mass. In one case, the non-dairy milk and a cross-linking enzyme composition has a carbohydrate content less than 5% by mass. In one case, the non-dairy milk and a cross-linking enzyme composition has a carbohydrate content less than 10% by mass. In one case of the non-dairy milk and a cross- linking enzyme composition, at least 80% of the protein content comprises a single monomeric or multimeric protein.

In some cases, provided herein is a composition comprising covalently crosslinked non-dairy proteins, a crosslinking enzyme, and cheese microbes. In one case of the composition of covalently crosslinked non-dairy proteins, a crosslinking enzyme, and cheese microbes composition, the proteins are not from soy. In one case of the composition comprising covalently crosslinked non-dairy proteins, a crosslinking enzyme, and cheese microbes, less than 5% of the proteins are from soy. In one case, the composition comprises less than 20% insoluble solids. In one case, the covalently crosslinked non-dairy proteins, a crosslinking enzyme, and cheese microbes composition also contains oils or fats isolated from non- dairy sources. In one case of the composition comprising covalently crosslinked non-dairy proteins, a crosslinking enzyme, and cheese microbes the crosslinking enzyme of the composition is a transglutaminase. In one case of the composition comprising covalently crosslinked non-dairy proteins, a crosslinking enzyme, and cheese microbes the crosslinking enzyme of the composition is a lysyl oxidase. In one case of the composition comprising covalently crosslinked non-dairy proteins, a crosslinking enzyme, and cheese microbes the cross-linking enzyme is Factor XIII (fibrin-stabilizing factor), Keratinocyte transglutaminase (TGM I), Tissue transglutaminase (TGM2), Epidermal transglutaminase (TGM3), Prostate transglutaminase (TGM4), TGM X (TGM5), TGM Y (TGM6), TGM Z (TGM7. In one case of the composition comprising non-dairy milk and a cross-linking enzyme and cheese microbes, the enzyme is a transglutaminase from Streptoverticillium mobaraense. In one case of the composition comprising non-dairy milk and a cross-linking enzyme and cheese microbes, the enzyme is similar or identical to a transglutaminase from Streptoverticillium mobaraense. In one case of the composition comprising non-dairy milk and a cross-linking enzyme and cheese microbes, protein crosslinks are formed between glutamine and lysine side chains of respective protein constituents. In one case of the composition comprising non-dairy milk and a cross-linking enzyme and cheese microbes, protein crosslinks are formed between lysine side chains of respective protein constituents.

In some cases, provided herein is a cheese replica composition comprised of a gelled emulsion of non-dairy proteins and fats. In one case, the cheese replica composition has between 10% and 40% proteins from non-dairy sources and between 0% and 65% fats from non-dairy sources. In one case, the cheese replica composition further comprises a crosslinking enzyme selected from the group consisting of Factor XIII (fibrin-stabilizing factor), Keratinocyte transglutaminase (TGM I), Tissue transglutaminase (TGM2), Epidermal transglutaminase (TGM3), Prostate transglutaminase (TGM4), TGM X (TGM5), TGM Y (TGM6) or TGM Z (TGM7). In one case of the cheese replica composition, the enzyme is a transglutaminase from Streptoverticillium mobaraense. In one case of the cheese replica composition, the enzyme is similar or identical to a transglutaminase from Streptoverticillium mobaraense. In one case of the cheese replica composition, protein crosslinks are formed between glutamine and lysine side chains of respective protein constituents. In one case of the cheese replica composition, protein crosslinks are formed between lysine side chains of respective protein constituents. In some case of the cheese replica composition, formation of protein crosslinks is catalyzed by a lysyl oxidase.

In one case, the cheese replica composition further comprises cheese-making microbes. In one case, the cheese replica composition has one or more cheese-making microbes from the group consisting of Penicillium camemberti, Geotrichum candidum, Penicilliem roqueforti, Penicillium nalgiovensis, Verticillium lecanii, Kluyveromyces lactis, Saccharomyces cerevisiae, Candida utilis, Debaryomyces hansensil, Rhodosporidum infirmominiatum, Candida jefer, Cornybacteria, Micrococcus sps., Lactobacillus sps., Lactococcus, Staphylococcus, Halomonas, Brevibacterium, Psychrobacter, Leuconostocaceae, Streptococcus thermophilus, Pediococcus sps., or Propionibacteria.

In some cases, provided herein is a cheese replica composition, wherein the cheese replica is a cheese equivalent according to a human. In some cases, provided herein is a cheese replica composition, wherein human subjects cannot distinguish the cheese replica from a dairy cheese. In one case of the cheese replica at least 20% of the protein content comprises a single monomeric or multimeric protein. In one case, the cheese replica composition is made without the addition of starches or rennet or any other extrinsic proteases other than those contributed by microbial cultures. In one case, the cheese replica composition has a pH less than 5.5 where the acidification was accomplished solely by microbial fermentation. In one case, the cheese replica composition has a pH less than 5 where the acidification was accomplished solely by microbial fermentation. In one case, the cheese replica composition has a pH less than 6 where the acidification was accomplished solely by microbial In one case, the cheese replica composition is contains no animal products. In one case, the cheese replica has less than 5% by mass insoluble carbohydrates. In one case, the cheese replica composition contains no rennet, vinegar, or lemon juice.

In some cases, provided herein is a cheese replica composition made with the addition of rennet or any aspartic protease or any other type protease (e.g., serine protease) to affect or enhance the flavor and /or aroma and /or texture of the cheese replica.

In some cases, provided herein is a cheese replica composition made with the addition of vinegar, lemon juice or any other type of acid to affect or enhance the flavor and /or aroma and/or texture of the cheese replica.

In some cases, provided herein is a soft fresh cheese replica composition composed of pasteurized almond milk, pasteurized macadamia nut milk, mesophilic starter culture, transglutaminase, water, and salt. In one case, the soft fresh cheese replica composition includes the addition of vinegar. In one case, the soft fresh cheese replica composition includes the addition of microbial coagulant. In one case, the soft fresh cheese replica composition includes the addition of vinegar and microbial coagulant.

In some cases, provided herein is a salted cheese replica composition composed of pasteurized almond milk, pasteurized macadamia nut milk, mesophilic starter culture, transglutaminase, and water. In one case, the salted cheese replica composition includes the addition of vinegar. In one case, the salted cheese replica composition includes a microbial coagulant. In one case, the salted cheese replica composition includes vinegar and a microbial coagulant.

In some cases, provided herein is a soft ripened cheese replica composition composed of pasteurized almond milk, pasteurized macadamia nut milk, mesophilic starter culture, flora danica, Geotrichum candidum, Penicillium candidum, Debaromyces hansenii, transglutaminase, water, and salt. In one case, the soft ripened cheese replica composition includes vinegar. In one case, the soft ripened cheese replica composition includes a microbial coagulant. In one case, the soft ripened cheese replica composition includes vinegar and microbial coagulant.

In some cases, provided herein is a goat cheese replica composition composed of pasteurized almond milk, macadamia nut milk, mesophilic starter culture, transglutaminase, water, and salt. In one case, the goat cheese replica composition includes vinegar. In one case, the goat cheese replica composition includes a microbial coagulant. In one case, the goat cheese replica composition includes vinegar and a microbial coagulant.

In some cases, provided herein is a method for making a cheese replica comprising removing from a non-dairy milk a proportion of insoluble solids. In some cases, provided herein is a method for making a cheese replica comprising removing from a plant- based milk a proportion of insoluble solids. In some cases, provided herein is a method comprising centrifuging a non-dairy milk to sediment a proportion of insoluble solids. In some cases, about 10%, about 20%, about 30%, about 40%, about 50%, about 60%, about 70%, about 80%, about 90%, or about 100% of the insoluble solids are removed.

In some cases, the isolated or enriched proteins of the methods and compositions disclosed herein comprise one or more of: ribosomal proteins, actin, hexokinase, lactate dehydrogenase, fructose bisphosphate aldolase, phosphofructokinases, triose phosphate isomerases, phosphoglycerate kinases, phosphoglycerate mutases, enolases, pyruvate kinases, glyceraldehyde-3- phosphate dehydrogenases, pyruvate decarboxylases, actins, translation elongation factors, ribulose- 1,5-bisphosphate carboxylase oxygenase (rubisco), ribulose-1,5-bisphosphate carboxylase oxygenase activase (rubisco activase), albumins, glycinins, conglycinins, globulins, vicilins, conalbumin, gliadin, glutelin, gluten, glutenin, hordein, prolamin, phaseolin (protein), proteinoplast, secalin, extensins, triticeae gluten, zein, any seed storage protein, oleosins, caloleosins, steroleosins or other oil body proteins, vegetative storage protein A, vegetative storage protein B, moong seed storage 8S globulin.

In some cases, provided herein is a composition comprising (A)covalently crosslinked plant-derived proteins from a set comprising ribosomal proteins, actin, hexokinase, lactate dehydrogenase, fructose bisphosphate aldolase, phosphofructokinases, triose phosphate isomerases, phosphoglycerate kinases, phosphoglycerate mutases, enolases, pyruvate kinases, glyceraldehyde-3-phosphate dehydrogenases, pyruvate decarboxylases, actins, translation elongation factors, ribulose-1,5-bisphosphate carboxylase oxygenase (rubisco), ribulose-1,5-bisphosphate carboxylase oxygenase activase (rubisco activase), albumins, glycinins, conglycinins, globulins, vicilins, conalbumin, gliadin, glutelin, gluten, glutenin, hordein, prolamin, phaseolin (protein), proteinoplast, secalin, extensins, triticeae gluten, zein, any seed storage protein, oleosins, caloleosins, steroleosins or other oil body proteins, vegetative storage protein A, vegetative storage protein B, and moong seed storage 8S globulin; (B) a crosslinking enzyme, and (C) cheese microbes.

In some cases, provided herein is a composition comprising (A)covalently crosslinked plant-derived proteins from a set comprising ribosomal proteins, actin, hexokinase, lactate dehydrogenase, fructose bisphosphate aldolase, phosphofructokinases, triose phosphate isomerases, phosphoglycerate kinases, phosphoglycerate mutases, enolases, pyruvate kinases, glyceraldehyde-3-phosphate dehydrogenases, pyruvate decarboxylases, actins, translation elongation factors, ribulose-1,5-bisphosphate carboxylase oxygenase (rubisco), ribulose-1,5-bisphosphate carboxylase oxygenase activase (rubisco activase), albumins, glycinins, conglycinins, globulins, vicilins, conalbumin, gliadin, glutelin, gluten, glutenin, hordein, prolamin, phaseolin (protein), proteinoplast, secalin, extensins, triticeae gluten, zein, any seed storage protein, oleosins, caloleosins, steroleosins or other oil body proteins, vegetative storage protein A, vegetative storage protein B, and moong seed storage 8S globulin.

BRIEF DESCRIPTION OF THE DRAWINGS

The novel features of the invention are set forth with particularity in the appended claims. A better understanding of the features and advantages of the present invention will be obtained by reference to the following detailed description that sets forth illustrative embodiments, in which the principles of the invention are utilized, and the accompanying drawings of which:

Figure 1 shows freshly cut curds prepared by the method used to produce the soft fresh cheese replicas and salted cheese replicas described in the examples.
Figure 2 shows drained curds prepared by the method used to produce the soft fresh cheese replicas and salted cheese replicas described in the examples.
Figure 3 shows soft fresh cheese replicas made from non-dairy milk.
Figure 4 shows Annatto-colored cheese replicas made from non-dairy milk.
Figure 5 shows salted cheese replica made from non-dairy milk.
Figure 6 shows salted cheese replica with paprika and fennel pollen made from non-dairy milk.
Figure 7 shows waxed cheese replica made from non-dairy milk.
Figure 8 shows soft ripened cheese replica made from non-dairy milk
Figure 9 shows goat cheese replicas made from non-dairy milk (A) with black pepper (B) with chives.
Figure 10 shows cheese replica gels made from partially purified plant proteins and vegetable oil, cultured with mesophilic culture MAI I (Danisco): (A) depicts cultured cheese replicas made from 2% Pea albumin fraction, 3% vegetable oil, heated and crosslinked with transglutaminase; (B) depicts cultured cheese replicas made from 2% Moong bean 8S globulin fraction, 3% vegetable oil, crosslinked with transglutaminase, without prior heating; (C) depicts cultured cheese replicas made from 7.5% Pea globulin fraction, 3% vegetable oil, heated and crosslinked with transglutaminase; (D) depicts cultured cheese replicas made from 7.5% Moong bean 8S globulin fraction, 3% vegetable oil, crosslinked with transglutaminase, without prior heating of proteins.

DETAILED DESCRIPTION OF THE INVENTION

Disclosed herein are methods and compositions based upon the realization that transglutaminase efficiently crosslinks the proteins in many non-dairy milks to produce a soft, moist, elastic gel (a "curdling" of non-dairy milks). This process allows the separation of the crosslinked proteins and associated fats from the "whey." The crosslinked proteins can hold a fat emulsion, and have the essential physical characteristics needed for pressing, culturing and ripening a cheese replica derived from non-dairy milk. In various cases the current disclosure includes cheese replicas principally, entirely or partially composed of ingredients derived from non-animal sources. In additional cases the present disclosure includes methods for making cheese replicas from non-animal sources. In various cases these results are achieved by replicating the curdling process of cheese making in non-dairy milks using enzymes.

The term a cheese "substitute" or "replica" can be any non-dairy product that serves a role as food or in food that is commonly served by traditional dairy cheese. A cheese "substitute" or "replica" can be a product that shares visual, olfactory, textural or taste characteristics of cheese such that an ordinary human observer of the product is induced to think of traditional dairy cheese.

A purified protein can be a preparation in which the cumulative abundance by mass of protein components other than the specified protein, which can be a single monomeric or multimeric protein species, is reduced by a factor of 3 or more, or a factor of 5 or more, or a factor of 10 or more relative to the source material from which the specified protein was said to be purified.

The term "homogeneous" can mean a single protein component comprises more than 90% by mass of the total protein constituents of a preparation.

The term resemble can mean one composition having characteristics recognizably similar to another composition by an ordinary human observer.

The term "indistinguishable" can mean that an ordinary human observer would not be able to differentiate two compositions based on one or more characteristics. It is possible that two compositions are indistinguishable based on one characteristic but not based on another, for example two compositions can have indistinguishable taste while having colors that are different. Indistinguishable can also mean that the product provides an equivalent function as or performs an equivalent role as the product for which it is substituting.

I. Non-dairy milks

Cheese replicas may be made using non-dairy milk prepared from nuts or plant seeds. For example almonds, cashews, brazilnuts, chestnuts, coconuts, hazelnuts, macadamia nuts, peanuts, pecans, pistachios or walnuts can provide non-dairy milk that, in various cases disclosed herein, is used to produce cheese replicas. Nuts can include so called "true nuts" as well as a wide variety of dried seeds from of plants. Any large, oily kernel found within a shell and used in food may be regarded as a nut. Plant seeds can include a wide variety embryonic plants enclosed in a seed coat. Plant seeds can include for example legumes, cereals, and gymnosperms. Non-dairy products or compositions include products or compositions where the constituent proteins, fats and/or small molecules can be isolated from or secreted by plants, bacteria, viruses, archaea, fungi, algae, or they can be made synthetically by chemical synthesis or in vitro. Non-dairy products are generally not derived from cows, goats, buffalo, sheep, horses, camels, or other mammals. In some cases non-dairy products do not contain dairy proteins. In some cases non-dairy products do not contain dairy fats. In some cases non-dairy products do not contain enzymes derived from an animal.

The nuts or seeds of the present disclosure can be raw. In some cases the nuts or seeds used to produce non-dairy milk are all raw. Alternatively some or all of the nuts or seeds used in the production of a non-dairy milk can be processed. The processed nuts or seed can be roasted, dry roasted, toasted, or baked.

Milk, or non-dairy milk, can mean an emulsion comprising proteins and fats or a solution or suspension of proteins, sometimes further comprising other solutes that might include carbohydrates, salts and other small molecules that contribute to flavor, texture, emulsion stability, protein solubility or suspension stability, or its ability to support growth of microbial cultures used in making cheese replicas, yogurt replicas, or other replicas of cultured dairy products.

The non-dairy milk can be made by a method comprising preparing the nuts or plant seeds with processing steps such as sterilizing, blanching, shocking, decompounding, centrifugation, or washing.

The non-dairy milks can be produced by decompounding the nuts or plant seeds, for example by grinding or blending or milling the nuts in a solution comprising water. In various cases alternative methods for decompounding the nuts or dried seeds include crushing, tumbling, crumbling, atomizing, shaving, pulverizing, grinding, milling, water eroding (for example with a water jet), or finely chopping the nuts or plant seeds. In some cases the decompounding step takes place in a blender. In some cases the decompounding is in a continuous flow grinder. In some cases the decompounding is in a continuous flow mill. The decompounding can be followed by a sorting, filtering, screening, or separation step. In some cases the decompounded nuts or seeds can be stored prior to the formation of a non-dairy milk. In some cases an aqueous solution is added before, during, or after the decompounding.

The nuts or seeds used in some cases disclosed herein to make non-dairy milks may have contaminants on the surface which would make a non-dairy milk unsafe or unpalatable. Accordingly the nuts or seeds can be washed prior to use. The nuts or seeds can also be sterilized to remove, reduce, or kill any contaminants on the surface of the nuts or seeds. A sterilization step can be an irradiation step, a heat step (e.g. steam sterilization, flaming, or dry heat), or a chemical sterilization (e.g, exposure to ozone). In some cases the sterilization step kills more than 95% of microbes on the nuts or seeds. In some cases the sterilization step kills more than 99% of microbes on the nuts or seeds. Blanching is a process wherein the food is exposed to hot water (e.g. boiling), removed after a brief timed interval, and finally cooled by exposure to cold water (e.g. iced or cold running water). When nuts, such as almonds or pistachios, are blanched, the skin of the nut (botanically the seed coat surrounding the embryo) softens and can be easily removed later. Accordingly, in some cases, provided herein are non-dairy milk compositions with a reduced percentage of components found in the skin of the nut or seed. For example the composition can have 50%, 40%, 30%, 20%, 10% or less than 5% of the seed coat remaining after the preparation process. In some cases, provided herein are methods for making a non-dairy milk comprising removing the seed coat.

In one case, the blanching procedure is as follows: Place nuts into 212°F heated water and blanch for 30 seconds. Drain nuts. Immediately move drained nuts into cold water. In some cases the temperature of the water is altered by 5%, 10% or 20%. In some cases the cold water temperature is about 0°C, 5°C, 10°C, or 20°C. In some cases the blanching takes about 10, 20, 30, 40, 50 seconds or about 1, 2, or 5 minutes.

In some cases the nuts or seeds can be hydrated, for example by immersion in water for 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, or 24 hours. In some cases the hydration step lasts multiple days. In some cases the water contains other components such as salts or preservatives. In some cases the water is maintained at a constant cool temperature. In some cases the hydration step can occur prior to the decompounding step.

In some cases the nuts or seeds can be dried, for example by exposure to a low humidity and/or heated environment for 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, or 24 hours. In some cases the drying step lasts multiple days. The drying step can occur prior to the decompounding step or the drying step can occur after a decompounding step.

In one case, the decompounding step is a blending procedure as follows: Place nuts in a clean and sanitized blender. Add clean fresh water to the blender. Tum on the blender and gradually increase speed up to maximum, blending for 5 minutes. Accumulate blended slurry in clean and sanitized ice cold container. Immediately begin rapid cooling of slurry by stirring slurry. Once the slurry has cooled to 50°F, move slurry to refrigerator to continue cooling to below 41°F. Allow slurry to rest at 36°F overnight or up to 12 hours at 36°F. In some cases the blending times and speeds are altered by up to 100%. In some cases the temperatures are altered up to 20°.

Insoluble solids may be present in milks prepared by decompounding (e.g. grinding or blending) nuts or seeds. One surprising observation of the present invention is that these insoluble materials can hinder the formation of curds from the non-dairy milks. Insoluble solids can also result in curds or cheese replicas having a texture or mouthfeel perceived as grainy or pasty in comparison to the smoother, creamier texture of dairy cheese. Accordingly provided herein are methods for removing these insoluble materials and compositions of non-dairy milks and cheese replicas with reduced amounts of the insoluble materials. Compositions of the invention can have a mouthfeel or texture indicative of the absence of insoluble solids. For example a cheese replica can have a mouthfeel indicative of the absence of insoluble solids. The insoluble materials can comprise carbohydrates.

In some cases the methods for producing cheese replicas includes a step for the removal of solids from non-dairy milks prior to curdling. For example, in some cases, the non-dairy milks are centrifuged to remove the insoluble solids. In some cases, provided herein is a non-dairy cheese replica with less than 1%, S%, 10%, 20%, 30%, 40% or 50% of insoluble solids found in the non-dairy milk before removal of the insoluble solids. In some cases, provided herein is a non-dairy milk extract with less than 1%, 5 %, 10%, 20%, 30%, 40% or S O% of insoluble solids found in non-dairy milk. In some cases, provided herein is a non-dairy milk with 99%, 95%, 90%, 80%, 70%, 60% or 50% of insoluble solids found in non-dairy milk removed.

In one case the centrifugation procedure is as follows: Pour decompounded nut or seed slurry into container. Using a centrifuge with the JS-S.O rotor, spin at about 5000 RPM for 30 mins. In some cases the spin is at about 500, 1000, 1500, 2000, 2500, 3000, 3500, 4000, 4500, 5000, 5500, 6000, 6500, 7000, 7500, 8000, 8500, 9000, 9500, or 10,000 RPM for about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, or 60 minutes. In some cases the centrifugation speed or time is altered, for example by 20%.

In one case the centrifugation procedure is as follows: Pour decompounded nut or seed slurry at a flow rate of 15.1-75.7 liters per minute (4-20 gallons per minute), for example, at a flow rate of 30.3 liters (8 gallons) per minute, into decanter centrifuge (such as the Flottweg S4 sedicanter), spinning at a bowl speed of between 3000 and 5000 RPM. Collect the liquid outflow for further use as a non-dairy milk, and set aside the ejected solids.

Other methods for removal of solids from non-dairy milks include, but are not limited to, straining, filtering, allowing to settle, skimming, or using coagulants and flocculants (including cations, polymer flocculants, or polyelectrolytes such as pectin, carrageenan, alginates, or carboxymethyl cellulose) to agglomerate particles for removal.

Centrifugation step can result in a "cream layer" and a "skim layer". The cream layer is an emulsion comprising fats, proteins and water. The skim layer is a solution comprising proteins in water. In some cases, the cream layer and skim layer are separated by centrifugal separation. In some cases, the cream layer and skim layer are separated by centrifugal separation in a Flotwegg ac 1500 or GEA ME55. In some cases the cream layer and the skim layer are incompletely separated. The skim layer and the cream layer can be separated from the insoluble solids in a separation process. In some cases the skim layer and the cream layer are stored separately. The non-dairy milk can comprise the skim layer. The non-dairy milk can comprise the cream layer. Typically the skim layer and the cream layer are combined to form the non-dairy milk. The non-dairy milk can be up to 100% cream layer. In some cases the ratio of cream layer to skim layer in the non-dairy milk is about 100:1, 90: 1, 80:1, 70: 1, 60: 1,50: 1,40: 1, 30:1, 20:1, 10:1, 9:1, 8:1, 7:1, 6:1, S:1, 4:1, 3:1, 2:1, 1:1, 1:2, 1:3, 1:4,1 :S, 1:6, 1:7, 1:8, 1:9, 1:10, 1:20, 1:30, 1:40, 1:50, or 1:60. In some cases the methods described herein comprise measuring the amount of skim layer and cream layer being added to a non-dairy milk.

In one case, the separation procedure is as follows: Remove cream layer from centrifuged bucket and place in new container that is buried in an ice bath. Move the liquid layer (skim layer) from the bucket into a container that is ice cold. Keep skim and cream ice cold at all times.

In another case, the separation procedure is as follows: Flow the non-dairy milk, from which insoluble solids have been substantially removed by passage through a decanter centrifuge, into a separator centrifuge, for example, a Flotwegg acl500 or GEA ME55. In some cases, the cream layer and skim layer are separated by centrifugal separation in the separator centrifuge. In some cases the separated skim and cream layers are kept refrigerated.

In some cases the non-dairy milk is pasteurized or sterilized. The pasteurization can be high-temperature, short-time (HTST), "extended shelflife" (ESL) treatment, or ultra-high temperature (UHT or ultra-heat-treated). In some cases the pasteurization procedure is as follows: Pasteurize blended non-dairy milk at 73.3°C-75°C (164°F-167°F) for 16 seconds. Using controlled chilling system, bring non-dairy milk temperature down rapidly and store in a refrigerator at 2.2°C (36°F).

Cheese replicas may also be made using non-dairy milk prepared using proteins isolated, enriched, or purified from a plant, or microbial source or synthesized in vitro. For example ribulose-1,5-bisphosphate carboxylase oxygenase (rubisco) can isolated from a plant source and included in a non-dairy milk for the production of a cheese replica. For example 8S globulins can isolated from a Moong beans and included in a non-dairy milk for the production of a cheese replica. For example Pea globulins can isolated from Pea seeds and included in a non-dairy milk for the production of a cheese replica. For example Pea albumins can isolated from peas and included in a non-dairy milk for the production of a cheese replica. Isolated, enriched, or purified plant proteins can be combined with one or more oils or fats also isolated from plant sources, in a colloidial suspension, solution or emulsion to form the non-dairy milk for making a cheese replica. In some cases the isolated non-dairy proteins are combined with non-non-dairy oils or fats to form a non-dairy milk. In some cases multiple isolated, enriched or purified plant proteins are used to make a non-dairy milk. Without being bound by theory the non-dairy milks derived from isolated, enriched, or purified proteins may reduce the problems which can be caused by insoluble solids obtained in a slurry derived from a nut or seed. Without being bound by theory the non-dairy milks derived from isolated, enriched, or purified proteins may reduce the problems which can be caused by proteins with undesirable properties, such as lipoxygenases or proteases. Additional non-limiting examples of proteins that may be isolated, enriched, or purified from a plant source for the production of a non-dairy milk for cheese replica production include: seed-storage proteins from any seed, ribosomal proteins, actin, hexokinase, lactate dehydrogenase, fructose bisphosphate aldolase, phosphofructokinases, triose phosphate isomerases, phosphoglycerate kinases, phosphoglycerate mutases, enolases, pyruvate kinases, glyceraldehyde-3-phosphate dehydrogenases, pyruvate decarboxylases, actins, translation elongation factors, ribulose-1,5-bisphosphate carboxylase oxygenase (rubisco), ribulose-1,5-bisphosphate carboxylase oxygenase activase (rubisco activase), albumins, glycinins, conglycinins, globulins, vicilins, conalbumin, gliadin, glutelin, gluten, glutenin, hordein, prolamin, phaseolin (protein), proteinoplast, secalin, extensins, triticeae gluten, zein, oleosins, caloleosins, steroleosins or other oil body proteins, vegetative storage protein A, vegetative storage protein B, moong seed storage 8S globulin. Non-limiting examples of oils that may be incorporated in a non-dairy milk include: com oil, olive oil, soy oil, peanut oil, walnut oil, almond oil, sesame oil, cottonseed oil, rapeseed oil, canola oil, safflower oil, sunflower oil, flax seed oil, algal oil, palm oil, palm kernel oil, coconut oil, babassu oil, shea butter, mango butter, cocoa butter, wheat germ oil, rice bran oil, oils produced by bacteria, algae, archaea or fungi or genetically engineered bacteria, algae, archaea or fungi, triglycerides, monoglycerides, diglycerides, sphingosides, glycolipids, lecithin, lysolecithin, phophatidic acids, lysophosphatidic acids, oleic acid, palmitoleic acid, palmitic acid, myristic acid, lauric acid, myristoleic acid, caproic acid, capric acid, caprylic acid, pelargonic acid, undecanoic acid, linoleic acid, 20: 1 eicosanoic acid, arachidonic acid, eicosapentanoic acid, docosohexanoic acid, 18:2 conjugated linoleic acid, conjugated oleic acid, or esters of: oleic acid, palmitoleic acid, palmitic acid, myristic acid, lauric acid, myristoleic acid, caproic acid, capric acid, caprylic acid, pelargonic acid, undecanoic acid, linoleic acid, 20: 1 eicosanoic acid, arachidonic acid, eicosapentanoic acid, docosohexanoic acid, 18:2 conjugated linoleic acid, or conjugated oleic acid, or glycerol esters of oleic acid, palmitoleic acid, palmitic acid, myristic acid, lauric acid, myristoleic acid, caproic acid, capric acid, caprylic acid, pelargonic acid, undecanoic acid, linoleic acid, 20: 1 eicosanoic acid, arachidonic acid, eicosapentanoic acid, docosohexanoic acid, 18:2 conjugated linoleic acid, or conjugated oleic acid, or triglyceride derivatives of oleic acid, palmitoleic acid, palmitic acid, myristic acid, lauric acid, myristoleic acid, caproic acid, capric acid, caprylic acid, pelargonic acid, undecanoic acid, linoleic acid, 20: 1 eicosanoic acid, arachidonic acid, eicosapentanoic acid, docosohexanoic acid, 18:2 conjugated linoleic acid, or conjugated oleic acid.

In some instances the proteins used to make the non-dairy milk may be purified proteins. Accordingly, in some cases the total protein content of the cheese replica can, in some cases, consist of greater than 25%, 50%,75%, or 90%, of a purified protein, for example any single monomeric or multimeric protein.

Non-dairy milk compositions can also contain sugars or other fermentable carbon sources and other nutrients. Without being bound by theory these sugars or nutrients can favor growth of the cheese culture microbes or serve as substrates for production of lactic acid or other organic acids by the cheese culture microbes. For example, in some cases, the non-dairy milk comprises glucose. In other cases, the non-dairy milk comprises fructose. In other cases, the non-dairy milk comprises sucrose. In other cases, the non-dairy milk comprises high-fructose com syrup. In other cases, the non-dairy milk comprises sugar-cane extract. In other cases, the non-dairy milk comprises a fruit juice. In other cases, the non-dairy milk comprises sugar-cane extract. In other cases, the non-dairy milk comprises agave syrup. In other cases, the non-dairy milk comprises molasses. Molasses can be cane molasses or beet molasses or made from other non-dairy sources. In other cases the non-dairy milk can comprises treacle, honey, refined sugars, or syrup (e.g high fructose com syrup). In some cases fuel for glycolosis, or a component (or intermediate) of the glycolysis pathway, can be included in the compositions. Oligosaccharides can be a part of the non-dairy milk. Disaccharides (eg., maltose, sucrose) can be part of a non-dairy milk. Monosaccharides (e.g. fructose, glucose, or galactose) can be a part of the non-dairy milk. In some cases the sugars are added as an addition step. In some cases the sugars are not derived from the same organism as the proteins and fats in the composition.

In some cases a sugar in the composition disclosed herein is not treacle, honey, refined sugars, or syrup (e.g high fructose com syrup). In some cases a sugar in the composition disclosed herein is not a monosaccharide (e.g. fructose, glucose, or galactose). In some cases a sugar in the composition disclosed herein is not a disaccharide. In some cases a sugar in the composition disclosed herein is not an oligosaccharide.

Non-dairy milk can, in some cases, contain one or more organic acids, such as lactic acid, or acetic acid, for example to adjust the pH and/or produce the characteristic sour taste of cheese. These organic acids may be used in addition to or as an alternative to microbial cultures. Accordingly, in some cases the non-dairy milk comprises an organic acid. The organic acid can be one or more of: lactic acid, acetic acid, citric acid, malonic acid, malic acid, propionic acid.

In some instances the compositions disclosed herein do not contain any animal products. In some cases the compositions disclosed herein use no components that are derived from animals. In some cases the compositions disclosed herein contain no fats from animals. In some cases the compositions disclosed herein contain no proteins from animals. In some cases the compositions disclosed herein contain no enzymes from animals. In some cases the compositions disclosed herein contain no dairy products.

In one case, provided herein is a composition free of or substantially free of one or more of the following: dairy products, animal products, agar, carrageenan, or tofu.

In some cases the compositions have less than 20%, less than 15%, less than 10%, less than 5%, less than 1% or less than 0.5% starch content. In some cases no refined starch (e.g. cornstarch, tapioca, wheat, or potato starch) is added to the compositions disclosed herein.

In some cases the non-dairy milk contains no artificial flavoring or coloring.

In some instances the non-dairy milk does contain some animal products. For example, in some cases, non-dairy milk comprises enzymes obtained from animals. In some cases, the non-dairy milk contains dairy products. In some cases animal fats are included in the non-dairy milk. In some cases the non-dairy milk can comprise enzymes (e.g. proteases and lipases), and/or microbes (e.g. flactic bacteria, yeast and mold). Without being bound by theory these enzymes and or microbes can be added to non-dairy milk formulations to produce desirable flavor and aroma compounds.

Enzymes, including proteases and lipases, and microbes, including lactic bacteria, yeast and mold, can be added to non-dairy milk formulations to produce desirable flavor and aroma compounds.

In some cases, provided herein is a method comprising isolating or purifying a single non-dairy protein, mixing the isolated non-dairy protein with a non-dairy fat source, and adding a microorganism selected from the group consisting of Penicillium camemberti, Geotrichum candidum, Penicilliem roqueforti, Penicillium nalgiovensis, Verticillium lecanii, Kluyveromyces lactis, Saccharomyces cerevisiae, Candida utilis, Debaryomyces hansensil, Rhodosporidum infirmominiatum, Candidajefer, Cornybacteria, Micrococcus sps., Lactobacillus sps.,Lactococcus, Staphylococcus, Halomonas, Brevibacterium, Psychrobacter, Leuconostocaceae, Streptococcus thermophilus, Pediococcus sps., or Propionibacteria. In some cases at least 1 kg of the plant protein is isolated or purified from a single non-dairy source. In some cases the fat is isolated from another non-dairy source.

In some cases, provided herein is a composition comprising an isolated or purified non-dairy protein and a polynucleotide identifiable as derived from one or more of Penicillium camemberti, Geotrichum candidum, Penicilliem roqueforti, Penicillium nalgiovensis, Verticillium lecanii, Kluyveromyces lactis, Saccharomyces cerevisiae, Candida utilis, Debaryomyces hansensil, Rhodosporidum infirmominiatum, Candidajefer, Cornybacteria, Micrococcus sps., Lactobacillus sps.,Lactococcus, Staphylococcus, Halomonas, Brevibacterium, Psychrobacter, Leuconostocaceae, Streptococcus thermophilus, Pediococcus sps., or Propionibacteria. In some cases the cheese replicas comprise Penicillium camemberti, Geotrichum candidum, Penicilliem roqueforti, Penicillium nalgiovensis, Verticillium lecanii, Kluyveromyces lactis, Saccharomyces cerevisiae, Candida utilis, Debaryomyces hansensil, Rhodosporidum infirmominiatum, Candidajefer, Cornybacteria, Micrococcus sps., Lactobacillus sps., Lactococcus, Staphylococcus, Halomonas, Brevibacterium, Psychrobacter, Leuconostocaceae, Streptococcus thermophilus, Pediococcus sps., or Propionibacteria. In some cases compositions disclosed herein comprise Penicillium, Geotrichum, Saccharomyces, Kluyveromyces, or Debaryomyces.

II. "Curdling" the non-dairy milk

Generally the cheese-replicas are made by causing cross linking or denaturation of proteins in non-dairy milks. These processes replicate the curdling process of traditional dairy cheese making.

Crosslinking is typically induced using an enzyme that creates covalent crosslinks between polypeptide chains. In some cases cross-linking enzymes are used in a cross-linking step to curdle the non-dairy milk. In various cases, transglutaminase is the cross-linking enzyme used to induce the curdling of non-dairy milk replicas. In some cases the crosslinking enzyme used to induce curdling in non-dairy milk replicas is a lysyl oxidase. In one case, provided herein is a method of inducing the curdling of a non-dairy milk comprising obtaining a non-dairy milk and adding a cross-linking enzyme to the non-dairy milk. In some cases the cross-linking enzyme is transglutaminase. In some cases the cross-linking enzyme is not derived from an animal source. In some cases the curdling process does not use rennet.

In some cases between 0.1 and 20 units (U) of transglutaminase is added per 1 mL of non-dairy milk. In some cases about 0.1, 0.5, 1, 1.5, 2, 2.5, 3, 5, 7, 10, 15, or 20 U transglutaminase is added per 1 mL of non-dairy milk. In some embodiments the transglutaminase is followed by heated incubation, for example in a 100°F water bath. The heated incubation can be at a temperature optimized for the enzyme function. In some cases the temperature is about 18.3, 21.1, 23.9, 26.7, 29.4, 32.2, 35, 37.8, 40.6, 43.3, 46.1, 48.9, or 51.7 °C (about 65, 70, 75, 80, 85, 90, 95, 100, 105, 110, 115, 120 or 125 °F).

Transglutaminases are a family of enzymes that catalyze the formation of a covalent bond between a free amine and the gamma-carboxyl group of glutamine thereby linking proteins together. For example, transgluaminases catalyze crosslinking of e.g., lysine in a protein or peptide and the gamma-carboxamide group of a protein- or peptide- glutamine residue. The covalent bonds formed by transglutaminase exhibit high resistance to proteolytic degradation.

Many types of transglutaminase can be used in various cases disclosed herein. Acceptable transglutaminases include, but are not limited to, Streptoverticillium mobaraense transglutaminase, an enzyme is similar or identical to a transglutaminase from Streptoverticillium mobaraense, other microbial transglutaminases, transglutaminases produced by genetically engineered bacteria, fungi or algae, Factor XIII (fibrin-stabilizing factor), Keratinocyte transglutaminase (TGM I), Tissue transglutaminase (TGM2), Epidermal transglutaminase (TGM3), Prostate transglutaminase (TGM4), TGM X (TGM5), TGM Y (TGM6), TGM Z (TGM7), or lysyl oxidase. Accordingly, in some cases an enzyme selected from the group consisting of a transglutaminase is used to crosslink a non-dairy milk protein. In some cases the transglutaminase is Streptoverticillium mobaraense transglutaminase, other microbial transglutaminases, transglutaminases produced by genetically engineered bacteria, fungi or algae, Factor XIII (fibrin-stabilizing factor), Keratinocyte transglutaminase (TGMI), Tissue transglutaminase (TGM2), Epidermal transglutaminase (TGM3), Prostate transglutaminase (TGM4), TGM X (TGM5), TGM Y (TGM6), TGM Z (TGM7), or lysyl oxidase In some cases, provided herein is a composition comprising a non-dairy milk and Streptoverticillium mobaraense transglutaminase, an enzyme is similar or identical to a transglutaminase from Streptoverticillium mobaraense, other microbial transglutaminases, transglutaminases produced by genetically engineered bacteria, fungi or algae, Factor XIII (fibrin-stabilizing factor), Keratinocyte transglutaminase (TGM I), Tissue transglutaminase (TGM2), Epidermal transglutaminase (TGM3), Prostate transglutaminase (TGM4), TGM X (TGM5), TGM Y (TGM6) and/or TGM Z (TGM7). In some cases the enzyme used for cross-linking is not Factor XIII (fibrin-stabilizing factor), Keratinocyte transglutaminase (TGMI), Tissue transglutaminase (TGM2), Epidermal transglutaminase (TGM3), Prostate transglutaminase (TGM4), TGM X (TGM5), TGM Y (TGM6), TGM Z (TGM7), or lysyl oxidase.

In some cases, provided herein is a composition comprising a non-dairy milk, wherein the composition is free of Factor XIII (fibrin-stabilizing factor), Keratinocyte transglutaminase (TGM I), Tissue transglutaminase (TGM2), Epidermal transglutaminase (TGM3), Prostate transglutaminase (TGM4), TGM X (TGM5), TGM Y (TGM6) and/or TGM Z (TGM7).

Transglutaminases can be produced by Streptoverticillium mobaraense fermentation in commercial quantities or extracted from animal tissues. Additionally, the transglutaminase (TGM) of the present disclosure may be isolated from bacteria or fungi, expressed in bacteria or fungi from a synthetic or cloned gene, Factor XIII, keratinocyte transglutaminase, tissue transglutaminase, epidermal transglutaminase, prostate transglutaminase, TGM X, TGM Y, TGM Z, or another member of the transglutaminase family. In some particular cases transglutaminase is obtained from commercial sources, for example in the form of Activa™ from Ajinmoto Food Ingredients LLC.

In some cases the compositions disclosed herein have a detectable amount of a nucleic acid from the genome of a cell that encoded and produced an enzyme, for example a transglutaminase. For example a cheese replica can have a detectable amount of Streptoverticillium mobaraense DNA. This detectable amount can, for example, be a small amount of DNA that has carried over to the cheese replica from the production of transglutaminase by Streptoverticillium mobaraense.

In some cases the cross-linking of proteins in non-dairy milk is induced by transglutaminase. In some cases the cross-linking of proteins in non-dairy milk is induced by a lysyl oxidase. Various non-dairy milks have been crosslinked with transglutaminase. In some cases, provided herein is a composition comprising a non-dairy milk and transglutaminase. In some cases, provided herein is a composition comprising a curdled non-dairy milk and transglutaminase. In some cases, provided herein is a cheese replica containing transglutaminase. In some case, provided herein is a cheese replica with a detectable amount of degraded transglutaminase. In some case, provided herein is a cheese replica with a detectable amount of improperly folded transglutaminase. In some case, provided herein is a cheese replica with a detectable amount of transglutaminase by-product. In some case, provided herein is a cheese replica with a detectable peptide which is identifiable as portion of a transglutaminase used in the manufacturing process for making the cheese replica. In some case, provided herein is a cheese replica with one or more detectable peptides containing a crosslink between a lysine and glutamine residue. For example the crosslinked glutamine and lysine residues may be detectable by mass spectroscopy. In some case, provided herein is a cheese replica with one or more detectable peptides containing a crosslink between two lysine residues. For example the crosslinked lysine residues may be detectable by mass spectroscopy.

Denaturation can be used instead of, or in addition to, the cross-linking enzyme for curdling the non-dairy milk. For example, heat denaturation of a non-dairy milk followed by cooling of the mixture can result in a curd-like gel as, for example, described in example 7. Accordingly, provided herein are non-dairy milk curds comprising denatured non-dairy proteins. Provided herein are also methods for making a non-dairy milk curd by heating a non-dairy milk to a temperature of about between 30-35, 35-40, 40-45, 45-50, 50-55, 55-60, 60-65, 65-70, 70-75, 75-80, 80-85, 90-95, 95-100 °C for about 10, 20, 30, 40, 50, 60 seconds or about 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 minutes followed by cooling. In some cases non-dairy milks are curdled using both enzymatic cross-linking with transglutaminase and heat denaturation.

Additional denaturization procedures are possible in additional cases disclosed herein. Acids, solvents, chaotropic agents, or disulfide bond reducers can be used to denature the proteins in the non-dairy milk. In one case urea is added to the non-dairy milk to form curds.

III. Cheese replica production from the curdled non-dairy milk

Cheese replicas can be produced from the curdled non-dairy milk. Accordingly, provided herein are methods for producing cheese replicas from curdled non-dairy milk, as well as cheese replica compositions.

To create the cheese replicas one might use elements of the traditional cheese making process. Cheese replicas can be produced using one or more steps including cutting, draining, forming, pressing, waxing, aging, scalding, smoking, salting or ripening.

The curd and whey may be separated in a traditional way. For example, the cheese may be scalded to create a replica of traditional cheddar or other hard cheese, or, the whey and curd might be separated through a cloth drain.

The cheese replicas may be ripened in a way similar to traditional cheese. For example, surface mould may be allowed to grow to create a rind. In order to create a rind or color, the process may introduce certain bacteria to the cheese replicas in the ripening process. By way of example only, Brevibacterium linens can be introduced to produce an orange color and pungent aroma to the cheese replica.

In some cases, the cheese replica can be a salted or salt-washed cheese replica. The salting process can preserve the cheese replica and/or add flavor. In some cases the salt is chosen based on the geographic location of where the salt is originally obtained. In some cases salt is added to the cut curds. In some cases salt is contacted with the outside surface of the cheese replica, for example by rubbing. In some cases the cheese replica is contacted with or soaked in brine.

In some cases, the cheese replica can be a soft fresh cheese produced by procedures exemplified by example 3.

In some cases, the cheese replica can be a salted or salt-washed cheese produced by procedures exemplified by example 4.

In some cases, the cheese replica can be a soft ripened or molded-rind cheese produced by procedures exemplified by example 5.

In some cases, the cheese replica can be a goat cheese replica produced by procedures exemplified by example 6.

In some cases, the cheese replica can have edible materials added (e.g. herbs, pepper, spices) on its surface to enhance flavor or add to the visual appeal of the product, as exemplified by examples 4 and 6. In some cases the edible materials are embedded in the cheese replica.

In some case the cheese replica can be shaped. For example the cheese replica can be shaped in a basket or a mold. In some cases the cheese replica is pressed, for example with a weight. The pressing can help expel any additional liquid from the cheese replica.

In some cases the production of the cheese replica includes a waxing step. In one case the waxing procedure is as follows: Cut food-grade paraffin wax into 1.3 cm (½-inch) pieces. Place in double boiler and heat wax to 98.9°C (210°F). Place cheese replicas in standard freezer for fifteen minutes to reduce temperature of cheese replicas to 0.5°C (33°F). Using 3-grams of melted wax per piece, brush wax onto cheese replicas one side at a time. Placed waxed cheese replicas onto clean waxed paper on aging racks. Age waxed cheese replicas in aging room at 2.2°C (36°F) with 75% humidity, for example for six months. In some cases the aging room is between 0.5-21.2°C (33-70°F). In some cases the humidity of the aging room is altered to aid in rind formation. In some cases the waxed cheese is stored for years, for example for 2 years or more.

In some cases the production of the cheese replica includes a smoking step. In some caess the cheese replica is cold smoked. In some cases the cheese replica is smoked at the curd stage or prior to the curd stage. In some cases the cheese replica is smoked after the cheese replica is formed. In some cases the smoking procedure is as follows: Soak wood chips for six hours. Drain chips of all water and place in smoking unit. Ignite smoker and as soon as chips have fully ignited, snuff out flames to create smoke-filled unit. Place cheese replicas on racks in smoker for five minutes per side. Remove from smoker and place on cooling racks. Place cheese replicas in cooling room for 24 hours, at 2.2°C (36°F). In various cases smoking times and cooling times and temperatures will be adjusted according to the particular cheese replica and particular desired taste profile.

In some instances the cheese replica is exposed to or injected with mold or yeast. In some cases the cheese replica is exposed to a particular bacterial strain or strains.

When the cheese replica is made without any dairy ingredients, the production process requires no dairy farming. Accordingly, the process for making cheese replicates is suitable for locations where keeping animals or storing milk is difficult or costly. In some cases the cheese replicas are made in non-dairy producing regions. This will reduce the need for shipping the products. So in some cases the cheese replica is a product that is made in the same locality as its eventual consumption. For example the cheese replica is made within 16.1, 32.2, 80.5, or 161 km (10, 20, 50, or 100 miles) of its point of sale. The cheese replica production process may also be useful in remote areas where dairy farming is difficult or impossible. For example the cheese replica production process could occur on an island, aboard an oil platform, or aboard a space station.

The cheese replicas may further contain microbes useful for cheese making. So in some cases the cheese replicas may be made by a process involving culturing with any microbes used for cheese making. The cheese replicates may be made by a process involving fermentation. In any process, the proteins may be crosslinked by treatment with an enzyme, which may be from the family of transglutaminase. The cheese replicas may be created from curds formed by a treatment of a protein-containing liquid with a transglutaminase, or other enzymes that promote gelling, or they may be prepared by a process involving heat denaturation of one or more of the protein components in the solution, suspension or emulsion to induce formation of a gel.

In some cases the cheese replicas comprise Penicillium, Geotrichum, Saccharomyces, Kluyveromyces, or Debaryomyces.

IV. Non-dairy cheese replicas

The cheese replicas can be made for consumption by either humans or other animals or both. In some instances the cheese replicas are used to feed domesticated animals. For example, a cheese replica of the present disclosure can be fed to a dog. In one particular case, the cheese replica contains a veterinary medication In another case the cheese replica comprises a treat for a domestic animal. In some cases the domestic animal treat is shaped like traditional a wedge of cheese. In some cases the animal treat is artificially colored to resemble dairy cheese, e.g. cheddar cheese.

The cheese replicas include products similar to conventional cheese, yogurt and other dairy products. Cheese replica can be made from a liquid extract of nuts or other fruits or seeds. The current disclosure also includes cheese replicas made from proteins and fats isolated and enriched or purified from one or more plant. The current disclosure also includes cheese replicas made from proteins and fats isolated and enriched or purified from one or more non-dairy source.

In some cases the cheese replica has less than 1%, 5%, 10%, 20%, 25% or 30% polysaccharides.

In some cases the cheese replica has less than 1%, 5%, 10%, 20%, 25% or 30% polysaccharides because of centrifugal separation.

In some cases the cheese replica has less than 1%, 5%, 10%, 20%, 25% or 30% polysaccharides because of the use of purified proteins.

The cheese replicas may be suitable for consumption by humans or animals who are unable to eat certain animal products, such as a person who is lactose-intolerant or allergic to dairy. Accordingly, in some cases the cheese-replica does not contain lactose. The cheese replicas might contain enough protein or other nutrients to be nutritionally equivalent to traditional cheese or other animal products.

The cheese replicas may contain less fat, less saturated fat or less cholesterol than traditional cheese or animal products, and may be suitable for a healthier diet. So in some cases provided herein is a method for distributing cheese replicas comprising the steps of informing a lactose intolerant person of the cheese replica, receiving an order for a cheese replica, and making the cheese replica available to the lactose intolerant person.

In some cases the lactose intolerant person is informed through advertising. In some cases the lactose intolerant person is informed by their personal physician. In some cases the order for the cheese replica is sent by the lactose intolerant person. In some cases the lactose intolerant person receives the cheese replica via a distributor that places the order. In some cases the informing and receiving steps take place on a network, for instance a computer network and are enacted with specialized computer software stored on a computer readable media. In some cases the method further comprises producing a cheese replica of the present disclosure and supplying it to lactose intolerant person.

The cheese replicas are, in some cases, designed to replicate the experience of eating cheese. The look, texture, and taste of the cheese replicas can be such that it is similar or indistinguishable from cheese. Provided herein are methods for determining whether an animal or human can distinguish the cheese replicas from cheese. In some cases a property of the compositions disclosed herein is that an animal, for example a human, will identify the composition as cheese. In some cases the human identifies the composition disclosed herein as equivalent to cheese. In some cases one or more properties of cheese are equivalent according to an ordinary human's perception. Such properties include the properties that can be tested listed below. In some cases an ordinary human identifies a cheese replica of the present disclosure as more cheese like than cheese substitutes found in the art.

One method to determine whether the cheese replica is comparable to cheese is to a) define the properties of cheese and b) determine whether the cheese replicas has similar properties. Properties of cheese that can be tested include mechanical properties such as hardness, cohesiveness, brittleness, chewiness, gumminess, viscosity, elasticity, and adhesiveness. Properties of cheese or a cheese replica that can be tested also include geometric properties such as particle size and shape, and particle shape and orientation. Additional properties can include moisture content and fat content. The properties of the cheese replica can be described using terms such as "soft," "firm" or "hard" describe hardness; "crumbly," "crunchy," "brittle," "chewy," "tender," "tough," "short," "mealy," "pasty," or "gummy," to describe cohesiveness; "thin" or "viscous" or "spreadable" to describe viscosity; "plastic" or "elastic" to describe elasticity; "sticky," "tacky" or "gooey" to describe adhesiveness; "gritty," "grainy" or "coarse" or "heterogeneous" to describe particle shape and size; "fibrous," "cellular" or "crystalline" to describe particle shape and orientation, "dry," "moist," "wet," or "watery" to describe moisture content; or "oily" or "greasy" to describe fat content. In one case a group of people can be asked to rate a certain cheese, for instance cheddar, according to properties which describe the cheese. These ratings can be used as an indication of the properties of the cheese. The cheese replicas of the present disclosure can then be compared to the properties of traditional dairy cheese to determine how similar the cheese replica is to the dairy cheese. In some instances the properties of the cheese replicas are then altered to make the cheese replica more similar to the cheese. In some cases, the cheese replica has a property or properties that are rated similar to cheese according to human evaluation. In some cases the cheese replica is indistinguishable from real cheese to a human. In some cases the cheese replica is distinguishable by some properties from real cheese to a human.

In some cases the cheese replica is compared to real cheese based upon olfactometer readings. In various cases the olfactometer can be used to assess odor concentration and odor thresholds, odor suprathresholds with comparison to a reference gas, hedonic scale scores to determine the degree of appreciation, or relative intensity of odors. In some cases the olfactometer allows the training and automatic evaluation of expert panels. In some cases the cheese replica is a product that causes similar olfactometer readings to those of a particular target cheese. In some cases the cheese replica is a product that causes nearly similar, but slightly different olfactometer readings to those of a particular target cheese.

Gas chromatography-mass spectrometry (GCMS) is a method that combines the features of gas-liquid chromatography and mass spectrometry to identify different substances within a test sample. GCMS can, in some cases, be used to evaluate the properties of a cheese replica. For example volatile chemicals can be isolated from the head space around cheese. These chemicals can be identified using GCMS. A profile of the volatile chemicals in the headspace around cheese is thereby created. In some instances each peak of the GCMS can be further evaluated. For instance, a human could rate the experience of smelling the chemical responsible for a certain peak. This information could be used to further refine the profile. GCMS could then be used to evaluate the properties of the cheese replicas. The GCMS could be used to refine the cheese replica. In some cases the cheese replica has a GCMS profile similar to that of cheese. In some cases the cheese replica has a GCMS profile identical to that of cheese.

The cheese replicas may be modified to fit into traditional cheese-types, including: fresh, bloomy, semi-soft, washed, firm, hard and blue. There may be additional processes to modify the cheese replicas and fit them into any cheese-type category. These categories also include different presentations of the cheese replicas, for example: sliced, shredded, block, with rind, without rind, wet or dry. The cheese replicas may be aged, or a method may be created to mimic the taste of traditionally-aged dairy cheese. The cheese replicas may be classified in taste the same way traditional cheese is. For example, they may be tart, tangy, smooth, creamy, buttery, fluffy, rich, earthy, pungent, aromatic, eggy, fruited, sharp, dry, caramelly, grainy, punchy or complex, among other descriptions. The disclosure includes methods to modify the cheese replicas to fit into any category or taste description.

The cheese replicas may be modified to have or not have a rind, may be coated in wax, and may have craters or veins typical to blue cheese. The cheese replicas may be spreadable, such as cream cheese. The cheese replicas can contain flavor additives, for example: truffle, mushrooms, nuts, herbs, chives, and other flavors.

The cheese replicas may be meltable, and have other properties of conventional cheese.

The cheese replicas may also be similar in consistency and taste to traditional yogurt or cottage cheese. The cheese replicas might be flavored with fruits, sweeteners, or other flavor additives. The cheese replicas might contain bacteria to aid with digestion or other health additives. The cheese replicas may be modified to have an appropriate or appealing consistency.

In various cases the cheese replicas may be used in all cooking and recipes as a substitute for traditional cheese. In some cases the cheese replicas may be used in cooking and recipes as a flavor substitute for traditional cheese. In some cases the cheese replicas may be used in cooking and recipes as a functional substitute for traditional cheese.

EXAMPLES EXAMPLE 1

THE EFFECTIVENESS OF TRANSGLUTAMINASE IN CURDLING VARIOUS NUT MILKS WAS COMPARED.

Cashews, almonds, macadamia nuts, brazilnuts were used to produce a slurry, by adding fresh water in a 3:1 weight ratio to the nuts, then blending in a Vitamix 4500 blender at high speed for 2 minutes. Because we found in preliminary experiments that the insoluble solids in the milks at this stage (slurry) inhibited formation of optimal creamy curds and produced a cheese replica with grainy mouth feel the slurry was subjected to centrifugation at 10,000 G for 15 minutes at 4°C to remove insoluble solids. The liquid supernatant, consisted of two layers, a lighter, creamy, opaque layer and a slightly denser clear to translucent aqueous layer. Liquid supernatant layers were recovered and blended together and the pelleted solids were discarded. The blended supernatants are referred to as "nut milks" (a non-dairy milk). Each of the 4 resulting nut milks and each pair-wise combination at a 1:1 blend, were evaluated for curdling in the presence of transglutaminase (TG): 30 U TG was added to 15 mls of each nut milk or blend in a 20 ml glass vial, followed by incubation in a 37.8°C (100°F) water bath. After 5 hours all but the pure cashew nut milk had formed sturdy curds, sufficient to retain their form when the glass vial was inverted. The cashew milk and cashew brazilnut milks formed soft curds. The macadamia and almond milks formed the most solid curds. Control samples without added transglutaminase remained liquid under these conditions.

EXAMPLE 2 PREPARATION OF ALMOND AND MACADAMIA NUT MILKS Blanching (surface sterilization of the nuts):

Note: Almonds and macadamia nuts were blanched separately.

A 113.6 liter (30 gallon) tilt skillet filled to ½-capacity with fresh water was heated to 100°C (212°F). 25 pounds of either almonds or macadamia nuts were dumped into the boiling water bath and left for 30 seconds. The nuts were recovered by draining into a colander then immediately immersed in fresh ice-cold water in a second tilt skillet to rapidly cool them. After rapid cooling the nuts were recovered by draining in a colander and spread on sheet trays to dry.

Macadamia nuts proceeded directly to the blending process. Almonds were first hydrated as described below before blending.

Hydration of Almonds:

The blanched almonds were transferred to Cambro buckets and fresh water was added to a level 5.1 cm (two inches) above the level of the nuts. The buckets were then placed at 2.2°C (36°F) for up to 16 hours. After hydration, the nuts were recovered by draining into a colander, rinsed with fresh water, then proceeded to the blending step.

Blending of nuts:

Note: Almonds and macadamia nuts were blended separately.

One pound batches of nuts were placed in a Vitamix blender (model Vitaprep 3), with one liter of fresh water and blended for 5 minutes, gradually increasing the blender speed to high. The blended slurries from each batch were collected in a stainless steel bain-marie sitting in a large container of ice and stirred with a frozen cooling stick to cool. Once the accumulated slurry cooled to 50°F, the bain-marie was placed in a refrigerator at 2.2°C (36°F) for up to 12 hours.

Separation of skim and cream:

Sets of four 1800 ml aliquots of the blended slurry RPM I 7480 G at 4°C for 30 minutes in a Beckman-Coulter Avanti J-HC Centrifuge with a JS-5.0 rotor, resulting in separation of the blend into 3 layers, a dense pellet of insoluble solids, a clear to translucent aqueous layer (which we refer to as the "skim"), and a lighter, creamy, opaque layer (which we refer to as the "cream"). The cream layer was carefully collected from each bucket using a spoon, and placed in a pan sitting in a container of ice. The viscous aqueous layer (skim) from each bucket was carefully poured into a 1h-Cambro sitting in a container of ice. The accumulated cream and skim layers were kept at 2.2°C (36°F) until the pasteurization step. Typical yields were about 0.35 kg (0.77 lbs) of cream and 0.43 kg (0.95 lbs) of skim per 0.45 kg (lb) of macadamia nuts and about 0.13 kg (0.29 lbs) of cream and 0.73 kg (1.62 lbs) of skim per 0.45 kg (lb) of almonds.

Blending

Almond skim and cream were combined in a ratio specified by the recipe for the specific cheese replica being produced (Table 1), and blended with an immersion blender. Macadamia skim and cream were combined in a ratio specified by the recipe for the specific cheese replica being produced (Table 1), and blended with an immersion blender. We hereafter refer to each blended mixture of skim and cream as "non-dairy milk." The two non-dairy milks were then blended in a ratio specified by the recipe for the specific cheese replica being produced (Table 1).

Pasteurization:

The non-dairy milk blend was pasteurized at 167°F for 16 seconds after which the non- dairy milk temperature was rapidly reduced to 50°C in 12 seconds by a controlled chilling system. The non-dairy milk temperature was then further reduced by placing containers in an ice bath at 2.2°C (36°F). Pasteurized non-dairy milks were stored at 2.2°C (36°F). Non-dairy milks were discarded if the pH of the non-dairy milk dropped below pH 6.0 during storage, indicating spoilage.

EXAMPLE 3 PRODUCTION OF A SOFT FRESH CHEESE REPLICA.

The ingredients and amounts needed for one batch (about one and a half pieces) of soft fresh cheese replica are listed in Table 2. The recipe can be scaled up or down proportionately.

Soft fresh cheese replica was prepared by the following procedure: Bring pasteurized non-dairy milk formula (see Table 2) to 26.7°C (80°F) in a water bath.

Sprinkle the mesophilic starter culture (see Table 2) onto the non-dairy milk formula and allow the culture to hydrate for five minutes without stirring. Gently stir in the starter culture with a spatula for two minutes. Hold at 26.7°C (80°F) for one hour.

Increase the water bath temperature to begin to bring the non-dairy milk temperature to 37.8°C (100°F).

Optional step: Add microbial "rennet" and/or distilled vinegar (see Table 2), folding gently with a spatula. Hold for 15 minutes.

Dilute the hydrated transglutaminase (see Table 2) with a small amount of warm nondairy milk formula and then add it to the non-dairy milk formula, folding gently with a spatula for two minutes. Allow formula to reach 37.7°C (100°F).

Remove the container of non-dairy milk formula from the water bath and cover with plastic wrap and aluminum foil. Allow the non-dairy milk formula to coagulate for twelve hours at room temperature.

Cut curd into 1.3 cm (½ inch) dice pieces. ( Figure 1 ). Allow curd to re-mat for 10 minutes. Pour the coagulated formula (curd and whey) into a draining bag and measure its weight. Hang bag and allow curd to drip for a minimum of20 minutes until proper viscosity and density of curd is achieved. The drained curd should weigh about 60% of original formula weight.

Place curd in a mixing bowl. Add cheese salt (see Table 2). Gently whisk the curd for ten minutes, or blend for five minutes with a Hobart mixer on low to medium speed.

Place 390 g (13.75 ounces) of curd (enough to yield 227 g (eight ounces) after completion of draining and brining) into a micro-perforated mold ( Figure 2 ). Drain at room temperature for one hour without the follower in place. Then place the follower in the mold and add 600 grams of weight to the follower. Refrigerate at 2.2°C (36°F) for 24 hours.

Preheat saturated brine to 10°C (50°F). Fully immerse the cheese replica, still in its mold, into the preheated brine for 1/2 hour. After brining, place mold on draining rack and return it to 2.2°C (36°F) for 24 hours.

Remove cheese replica from the mold. Place on draining mat and return it to 2.2°C (36°F) for 24 hours.

The soft fresh cheese replica ( Figure 3 ) is now ready for packaging and shipment. Packaging process includes nitrogen flush and airtight heat-sealing.

EXAMPLE 4 PRODUCTION OF A SALTED CHEESE REPLICA

The ingredients and amounts needed for one batch (about one and a half pieces) of salted cheese replica are listed in Table 2. The recipe can be scaled up or down proportionately.

Bring pasteurized non-dairy milk formula (see Table 2) to 26.7°C (80°F) in a water bath.

Sprinkle the mesophilic starter culture (see Table 2) onto the non-dairy milk formula and allow the culture to hydrate for five minutes without stirring. Gently stir in starter culture with a spatula for full two minutes. Hold at 26.7°C (80°F) for one hour.

Increase water bath temperature to begin to bring non-dairy milk temperature to 37.7°C (100°F).

Optional: Add microbial "rennet" and/or distilled vinegar (see Table 2), folding gently with a spatula. Hold for 15 minutes.

Dilute the hydrated transglutaminase (see Table 2) with a small amount of warm non- dairy milk formula and then add it to the non-dairy milk formula, folding gently with a spatula for two minutes. Allow formula to reach 37.7°C (100°F).

Remove container of non-dairy milk formula from the water bath and cover. Allow the non-dairy milk formula to coagulate for twelve hours at room temperature.

Cut curd into 1.3 cm (½ inch) dice pieces. Allow curd to re-mat for 10 minutes. Pour the coagulated formula (curd and whey) into a draining bag and measure its weight. Hang bag and allow curd to drip for a minimum of 20 minutes until proper viscosity and density of curd is achieved. The drained curd should weigh about 60% of original formula weight.

Place curd in mixing bowl. Optional: For the classic presentation of a cheddar cheese replica ( Figure 3 ), annatto- a natural vegetable dye, is added to create the yellow cheddar color. The percentage of annatto evenly distributed throughout the curd is 0.08%. Gently whisk curd for ten minutes, or blend for five minutes with a Hobart mixer on low to medium speed.

Place 462 g (16.3 ounces) of curd (enough to yield 227 g (eight ounces) after completion of draining and brining) into a micro-perforated mold (see Figure 1 ). Drain at room temperature for one hour without the follower in place. Then place the follower in the mold and add 600 grams of weight to the follower. Refrigerate at 2.2°C (36°F) for 24 hours.

Preheat saturated brine to 10°C (50°F). Fully immerse the cheese replica, still in its mold, into the preheated brine for ½ hour. After brining, place mold on draining rack and return it to 2.2°C (36°F) for 24 hours.

Remove the cheese replica from the mold. Place the cheese replica on a draining mat and return it to 2.2°C (36°F) for 24 hours.

Move the cheese replica into a drying room for seven days at 12.8°C (55°F), with 55% humidity, and minimal airflow. Tum the cheese replica and place on a fresh draining mat daily.

After the seven-day drying period, remove the draining mats and place the salted cheese replica ( Figures 4 and 5 ) directly on an aging rack.

If the cheese replica is to be waxed or smoked, return the cheese replica to the drying room for two additional weeks at 12.8°C (55°F), with 55% humidity and minimal airflow. Then follow the procedure for waxing or smoking.

If the cheese replica is to be rolled in paprika and fennel pollen mixture, follow the steps for the paprika & fennel pollen process.

Paprika and fennel pollen process:

Brush the salted cheese replica with cold water using a pastry brush. Roll the cheese replica in 1.5 grams of a mixture of 10-parts organic paprika and 1-part fennel pollen. Place the coated cheese replica on an aging rack and return it to the drying room for two weeks at 12.8°C (55°F), with 55% humidity and minimal airflow, turning daily.

Following the drying period, move the cheese replica to 2.2°C (36°F) for 24-hours. The paprika-fennel pollen cheese replica ( Figure 6 ) is now ready for packaging and shipment.

Waxing Process:

Cut food-grade paraffin wax into 1.3 cm (½-inch) pieces and heat to 98.9°C (210°F) in a double boiler.

Place the cheese replica in a freezer to reduce its temperature to 0.6°C (33°F). Using three grams of melted wax per piece of cheese replica, brush wax onto cheese replica one side at a time. Place waxed-side down onto waxed paper and then continue brushing remainder of the cheese replica including sides and top. Placed waxed cheese replica ( Figure 7) onto clean waxed paper on an aging rack.

Age the waxed cheese replica in aging room at 2.2°C (36°F) with 75% humidity for up to six months. The waxed cheese replica is now ready for packaging and shipment.

Smoking Process:

Soak equal parts apple and cherry wood chips for six hours. Drain chips of all water and place in a smoking unit. Ignite smoker and as soon as chips have fully ignited, snuff out flames to create a smoke-filled unit. Place salted cheese on rack into smoker for five minutes per side. Remove cheese from smoker and place on cooling rack.

Place the cheese at 2.2°C (36°F) for 24 hours. Smoked cheese is now ready for vacuum aging or packaging and shipment.

EXAMPLE 5 PRODUCTION OF A SOFT RIPENED CHEESE REPLICA.

The ingredients and amounts needed for one batch (about one and a half pieces) of soft ripened cheese replica are listed in Table 2. The recipe can be scaled up or down proportionately.

Bring pasteurized non-dairy milk formula (see Table 2) to 32.2°C (90°F) in a water bath.

Sprinkle lactose-free preparations of Florica Danica, Mesophilic Starter, Geotrichum Candidum, Penicillium Candidum, and Debaromyces hansenii (see Table 2) onto the milk formula. Optional: Add microbial "rennet." (see Table 2). Let milk sit for 5 minutes. Gently fold in and top stir with a spatula for two minutes. Hold at 32.2°C (90°F) for 90 minutes.

Increase water bath temperature to start to bring non-dairy milk temperature up to 37.8°C (100°F).

Optional: Add in distilled vinegar (see Table 2), folding gently with spatula. Hold 15 minutes.

Dilute the hydrated transglutaminase (see Table 2) with a small amount of warm non-dairy milk formula and then add it to the non-dairy milk formula, folding gently with a spatula for two minutes. Allow formula to reach 37.8°C (100°F).

Remove container of non-dairy milk formula from the water bath and cover with plastic wrap and aluminum foil. Allow the non-dairy milk formula to coagulate for twelve hours at room temperature.

Cut curd into 1.3 cm (½-inch) dice pieces. Allow curd to re-mat for 10 minutes. Pour the coagulated formula (curd and whey) into a draining bag and measure its weight. Hang bag and allow curd to drip for a minimum of 20 minutes until proper viscosity and density of curd is achieved. The drained curd should weigh about 60% of original formula weight.

Place curd in mixing bowl. Add cheese salt. Gently whisk curd for ten minutes, or blend for five minutes with a Hobart mixer on low to medium speed.

Place 17.64 ounces (500 grams) of curd (enough to yield 227 g (eight ounces) after completion of draining and brining) into a micro-perforated mold ( Figure 8 ) on a draining mat. Drain at room temperature for one hour without the follower in place. Then place the follower in the mold just touching the cheese replica. Do not add any additional weight to the follower. Refrigerate at 2.2°C (36°F) for 24 hours.

Remove the cheese replica from the mold. Place on draining mat and return it to 2.2°C (36°F) for 24 hours.

Transfer the cheese from 2.2°C (36°F) to dry yeasting room for three days at 15.6°C (60°F), with 75% humidity.

After three days, transfer cheese from a draining mat to an aging mat. Place the mat on an aging rack, and move to ripening room at 10°C (50°F), with 90% humidity and continuous airflow. Tum the cheese replica and replace mat daily.

After seven days, transfer the cheese replica directly onto an aging rack, allowing maximum aeration for seven more days, or until mold coverage is complete.

After the cheese replica has thoroughly molded ( Figure 8 ), move it to 2.2°C 36°F) for sixteen hours. Wrap cheese in perforated paper and place in a wooden box for shipment.

EXAMPLE 6 PRODUCTION OF A GOAT CHEESE REPLICA.

The ingredients and amounts needed for one batch (about one and a half pieces) of goat cheese replica are listed in Table 2. The recipe can be scaled up or down proportionately.

Bring pasteurized milk formula (see Table 2) to 26.7°C (80°F) in a water bath.

Increase water bath temperature to begin to bring non-dairy milk temperature to 37.8°C (100°F).

Dilute the hydrated transglutaminase (see Table 2) with a small amount of warm non- dairy milk formula and then add it to the non-dairy milk formula, folding gently with a spatula for two minutes. Allow formula to reach 37.8°C (100°F).

Cut curd into 1.3 cm (½ inch) dice pieces. Allow curd to re-mat for 10 minutes. Pour the coagulated formula (curd and whey) into a draining bag and measure its weight. Hang bag and allow curd to drip for a maximum of 24 hours until proper viscosity and density of curd is achieved. The drained curd should weigh about 50% of original formula weight.

Place curd in mixing bowl. Add cheese salt (see Table 2). Using Hobart mixer on high speed, mix and aerate completely.

Place 454 g (sixteen ounces) of curd (enough to yield 227 g (eight ounces) after completion of draining and brining) into a cylindrical goat cheese mold ( Figure 9) and stand the mold upright on a draining mat. Refrigerate at 2.2°C (36°F) for 24 hours allowing the cheese replica to drain.

Preheat saturated brine to 10°C (50°F). Fully immerse the cheese replica, still in its mold, horizontally into the preheated brine for ½ hour.

After brining, stand mold on draining mat placed at 2.2°C (36°F) for 24 hours. Tum mold and change mat every twelve hours for two days.

Slide shaped goat cheese replica out of mold directly onto a bed of three grams of coarse ground pepper. Gently roll the cheese replica in pepper, covering evenly and completely. Place the cheese replica on waxed paper and return to 2.2°C (36°F) for 48 hours.

The goat cheese replica ( Figure 10 ) is now ready for packaging and shipment. Packaging includes Cryovac sealing process.

EXAMPLE 7 CULTURED GELS MADE WITH EMULSIONS OF PURIFIED PLANT PROTEINS AND FATS. Procedure

Mixtures of purified or partially purified protein + glucose + oil were assembled and mixed with a vortex mixer to create an emulsion. Emulsions were either treated with transglutaminase (Ajinomoto Activa TI at a final concentration of 2% or 4%, as noted) or first heated to 85°C, rapidly cooled on ice and then treated with transglutaminase. Mesophilic starter culture (Danisco Choozit MA11) was added to a concentration of 0.01% (wt/vol) concomitantly with transglutaminase to allow cultures to ferment, acidify and impart flavors and aroma to the gels. Reactions were incubated overnight at 30°C before evaluating for gel formation and aroma.

Protein purification methods:

All steps were carried out at 4°C whenever possible. Centrifugation steps were at 8000 g for 20mins, 4°C. Once fractionated, all ammonium sulfate precipitate fractions of interest were stored at -20C until further use. Prior to their use in experiments, the precipitates were resuspended in 50mM KPhosphate buffer pH 7.4 + 0.5M NaCl and dialyzed overnight against the same buffer to remove ammonium sulfate. The dialyzed solution was then centrifuged at 12000 g for 20min to remove precipitate and then used in experiments. Protein composition at individual fractionation steps was monitored by SDS-PAGE and protein concentrations were measured by standard UV-Vis methods.

(i) Pea-albumins: Dry flour of green peas was used as a source of pea albumins. The flour was resuspended in 10 volumes of 50mM sodium acetate buffer pH 5 and stirred for 1 hr. The slurry was centrifuged at 8000 g for 20 minutes and the supernatant was collected. To this crude protein extract, solid ammonium sulfate was added to 50% saturation. The solution was stirred for 1 hour and then centrifuged. To the supernatant from this step, ammonium sulfate was added to bring to 90% saturation. After stirring for 1 hour, the solution was stirred and then centrifuged to collect the pea albumin proteins in the pellet. The pellet was stored at -20°C until further use.
(ii) Pea-globulins: Dry green pea flour was used to extract pea globulin proteins. The flour was resuspended in 10 volumes of 50mM KPhosphate buffer pH 8 + 0.4M NaCl and stirred for 1 hr. After centrifugation, the supernatant was subjected to ammonium sulfate fractionation in two steps at 50% and 80% saturation. The 80% pellet containing globulins of interest was stored at -20°C until further use.
(iii) Moong bean 8S globulins: Moong bean flour was used to extract 8S globulins by first resuspending the flour in 4 volumes of 50mM KPhosphate buffer pH 7 (+ 0.5M NaCl for lab scale purifications). After centrifugation, proteins in the supernatant were fractionated by addition of ammonium sulfate in 2 steps at 50% and 90% saturation respectively. The precipitate from the 90% fraction contained the 8S globulins and was saved at -20°C until further use.

Gel formation was tested with the following protein fractions:

(i) Pea-albumins (90% ammonium sulfate fraction from green pea dry seed flour)
(ii) Pea-globulins (80% ammonium sulfate fraction from green pea dry seed flour)
(iii) Moong bean 8S globulin (90% ammonium sulfate fraction from moong flour)

The protein solutions were dialyzed into 50mM KPhosphate buffer pH 7-7.4 + 0.5M NaCl and used at concentrations between 8mg/ml and 75mg/ml (0.8-7.5%) as described below.

Canola oil was used to make emulsions. Stock solutions of transglutaminase (Ajinomoto) were prepared at 40% in 50mM KPhosphate pH 7. Mesophilic starter culture (MAO l 1 from Danisco) was used as the cheese bacterial culture; the freeze-dried culture was resuspended at a 10% in 50mM KPhosphate buffer and used immediately in the experiments. Glucose (1%) was used as sugar source for growth of mesophilic cultures; stock solution was prepared at 40% in water.

Two conditions were used to form gels:

(i) 'Set 1': 2% protein + 3% oil + 4% transglutaminase; the rest water. Emulsify by vortex mixing.

'Set 2': 7.5% protein + 3% oil + 2% transglutaminase; the rest water. Emulsify by vortex mixing.

Both gel compositions listed above were tested for gel formation catalyzed by transglutaminase, with and without heat denaturation of the protein component. All reactions (total volume of each, 1 ml) were first assembled in 1.5 ml micro-centrifuge tubes with protein + oil + sugar components. Emulsions were made by vortexing the samples for 30sec. Samples to be heat denatured were immediately placed in a water bath and heated at 85°C for 30minutes. These samples were subsequently rapidly cooled on ice for 20 minutes. Transglutaminase and starter culture were added to all samples and mixed. Samples that formed gels upon heat/cool step were vortexed to mix the enzyme and cultures in. All samples were removed from the reaction tubes and evaluated for gel consistency and aroma after overnight incubation at 30°C.

Aroma evaluation:

The following gels were tested for aroma (smell by 4 individuals):

Set 1: pea-albumin (heat/cool), moong (heat/cool), moong (no heat/cool),
Set 2: pea globulin (heat/cool), moong (no heat/cool)

All four individuals reported yogurt-like/fermented/sour aroma in the moong (set 1, no heat/cool) gels. They reported similar smells but to a lower degree in the moong (set 2, no heat/cool) and pea globulin (set 2, heated) gel samples. For pea-albumins (set 1, heated) and moong (set 1, heated), very faint or no aroma was reported. One of the four testers reported the aroma from moong (set 2, no heat/cool) - to be unpleasant.

Gel firmness evaluation: (Figure 10)

'Set 1': all samples formed gels. In general these gels were weak and disintegrated easily. Pea albumins (heat/cooled) were slightly firmer in this regard.

'Set 2': All samples with exception of pea-globulins (no heat/cool) formed gels. Gels were stronger compared to Set 1 and held their shape even after removal from the tubes. Gels formed without heat/cool.

Table 1: MILK FORMULAS FOR SOFT FRESH, SALTED, SOFT RIPENED AND GOAT CHEESE REPLICAS


Soft fresh, salted or goat
Almond skim	725.0
Almond Fat	75.0
Macadamia nut skim	328.5
Macadamia nut fat	337 .5

Soft ripened

	Almond skim	725.0
	Almond Fat	75.0


	Macadamia nut skim	291.0
	Macadamia nut fat	375.0

Table 2: INGREDIENTS FOR ONE BATCH OF CHEESE REPLICA



Pasteurized almond milk	800.0
Pasteurized macadamia nut milk	666.0
Mesophilic starter culture (MA011 direct set)	0.5
Transglutaminase (900 units in 15 mls of water)	15.0
Cheese salt (internal)	2.5

Table 2: INGREDIENTS FOR ONE BATCH OF CHEESE REPLICA


Pasteurized almond milk	800.0
Pasteurized macadamia nut milk	666.0
Mesophilic starter culture (MA011 direct set)	0.5
Transglutaminase (900 units in 15 mls of water)	15.0

Table 2: INGREDIENTS FOR ONE BATCH OF CHEESE REPLICA


Pasteurized almond milk	800.0
Pasteurized macadamia nut milk	666.0
Mesophilic starter culture (MA011 direct set)	0.3
Flora Danica	0.2
Geotrichum candidum	0.1
Penicillium candidum	0.1
Debaromyces hansenii	0.1
Transglutaminase (733 units in 15 mls of water)	15.0
Cheese salt (internal)	4.2

Table 2: INGREDIENTS FOR ONE BATCH OF CHEESE REPLICA


Distilled white vinegar	5.3
Microbial "rennet:"	0.2

Table 2: INGREDIENTS FOR ONE BATCH OF CHEESE REPLICA

Claims

A cheese replica comprising a gelled emulsion of one or more cross-linked, plant-derived proteins, one or more fats, and a cross-linking enzyme, wherein the emulsion comprises a non-dairy milk having at least 85% of its insoluble solids removed, and wherein said plant-derived proteins are not from soy.
The cheese replica of claim 1, wherein the insoluble solids have been removed by centrifugation, straining, filtering, allowing to settle, skimming, or by using coagulants and flocculants.
The cheese replica of claim 1, wherein the insoluble solids have been removed by centrifugation.
The cheese replica of any one of claims 1 to 3, comprising between 10% and 40% proteins from plant sources and between 0% and 65% fats from plant sources.
The cheese replica of any one of claims 1 to 3, wherein the cheese replica has an insoluble carbohydrate content of less than 5% by mass.
The cheese replica of any one of claims 1 to 3, further comprising:
(a) cheese-making microbes; and/or

(b) a sugar or other fermentable carbon source.
The cheese replica of any one of claims 1 to 3, wherein the cross-linking enzyme is a transglutaminase or lysyl oxidase.
The cheese replica of any one of claims 1 to 3, wherein the plant-derived proteins, and fats are from nuts, legumes, or seeds, optionally wherein the nuts comprise one or more of almonds, cashews, brazil nuts, coconuts, chestnuts, hazelnuts, macadamia nuts, peanuts, pecans, pistachios or walnuts.
The cheese replica of any one of claims 1 to 3, wherein the plant-derived proteins comprise one or more proteins selected from the group consisting of a ribosomal protein, actin, hexokinase, lactate dehydrogenase, fructose bisphosphate aldolase, phosphofructokinases, a triose phosphate isomerase, a phosphoglycerate kinase, a phosphoglycerate mutase, an enolase, a pyruvate kinase, a glyceraldehyde-3-phosphate dehydrogenase, a pyruvate decarboxylase, an actin, a translation elongation factor, ribulose-1,5-bisphosphate carboxylase oxygenase (rubisco), ribulose-1,5-bisphosphate carboxylase, an oxygenase activase (rubisco activase), an albumin, a glycinin, a conglycinin, a globulin, a vicilin, a conalbumin, a gliadin, a glutelin, a gluten, a glutenin, a hordein, a prolamin, a phaseolin (protein), a proteinoplast, a secalin, an extensin, a zein, a seed storage protein, an oleosin, caloleosin, a steroleosin, vegetative storage protein A, vegetative storage protein B, and moong seed storage SS globulin.
The cheese replica of claim 6, wherein the cheese-making microbes are selected from one or more of the following: Penicillium camemberti, Penicillium candidum, Geotrichum candidum, Penicillium roqueforti, Penicillium nalgiovensis, Verticillium lecanii, Kluyveromyces lactis, Saccharomyces cerevisiae, Candida utilis, Debaryomyces hansenii, Rhodosporidum infirmominiatum, Candida jefer, Cornybacteria, Micrococcus sps., Lactobacillus sps., Lactococcus, Staphylococcus, Halomonas, Brevibacterium, Psychrobacter, Leuconostocaceae, Streptococcus thermophilus, Pediococcus sps., or Propionibacteria.