EP0912105A1 - Novel food compositions - Google Patents
Novel food compositionsInfo
- Publication number
- EP0912105A1 EP0912105A1 EP97924968A EP97924968A EP0912105A1 EP 0912105 A1 EP0912105 A1 EP 0912105A1 EP 97924968 A EP97924968 A EP 97924968A EP 97924968 A EP97924968 A EP 97924968A EP 0912105 A1 EP0912105 A1 EP 0912105A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- protein
- potato protein
- undenatured
- fraction
- process according
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 50
- 235000013305 food Nutrition 0.000 title claims abstract description 43
- 235000018102 proteins Nutrition 0.000 claims abstract description 141
- 102000004169 proteins and genes Human genes 0.000 claims abstract description 141
- 108090000623 proteins and genes Proteins 0.000 claims abstract description 141
- 244000061456 Solanum tuberosum Species 0.000 claims abstract description 123
- 235000002595 Solanum tuberosum Nutrition 0.000 claims abstract description 123
- 239000004615 ingredient Substances 0.000 claims abstract description 21
- 239000000416 hydrocolloid Substances 0.000 claims abstract description 10
- 238000000034 method Methods 0.000 claims description 24
- 241000195940 Bryophyta Species 0.000 claims description 18
- 235000011929 mousse Nutrition 0.000 claims description 18
- 238000002360 preparation method Methods 0.000 claims description 14
- 108010000912 Egg Proteins Proteins 0.000 claims description 11
- 102000002322 Egg Proteins Human genes 0.000 claims description 11
- 238000002156 mixing Methods 0.000 claims description 11
- 235000014103 egg white Nutrition 0.000 claims description 9
- 210000000969 egg white Anatomy 0.000 claims description 9
- 238000000108 ultra-filtration Methods 0.000 claims description 8
- 239000005018 casein Substances 0.000 claims description 7
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 claims description 7
- 235000021240 caseins Nutrition 0.000 claims description 7
- 238000005189 flocculation Methods 0.000 claims description 7
- 230000016615 flocculation Effects 0.000 claims description 7
- 235000015203 fruit juice Nutrition 0.000 claims description 7
- QCVGEOXPDFCNHA-UHFFFAOYSA-N 5,5-dimethyl-2,4-dioxo-1,3-oxazolidine-3-carboxamide Chemical compound CC1(C)OC(=O)N(C(N)=O)C1=O QCVGEOXPDFCNHA-UHFFFAOYSA-N 0.000 claims description 6
- 239000012141 concentrate Substances 0.000 claims description 6
- 238000011026 diafiltration Methods 0.000 claims description 5
- 238000001035 drying Methods 0.000 claims description 4
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 3
- 235000015173 baked goods and baking mixes Nutrition 0.000 claims description 3
- 229910052791 calcium Inorganic materials 0.000 claims description 3
- 239000011575 calcium Substances 0.000 claims description 3
- 235000013365 dairy product Nutrition 0.000 claims description 3
- 238000012545 processing Methods 0.000 claims description 3
- 235000013332 fish product Nutrition 0.000 claims description 2
- 235000013372 meat Nutrition 0.000 claims description 2
- 235000014594 pastries Nutrition 0.000 claims description 2
- 238000002203 pretreatment Methods 0.000 claims description 2
- 239000003778 fat substitute Substances 0.000 claims 2
- 235000013341 fat substitute Nutrition 0.000 claims 2
- 239000000654 additive Substances 0.000 claims 1
- 230000000996 additive effect Effects 0.000 claims 1
- 239000000470 constituent Substances 0.000 claims 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 claims 1
- 102000014171 Milk Proteins Human genes 0.000 abstract description 6
- 108010011756 Milk Proteins Proteins 0.000 abstract description 6
- 238000004519 manufacturing process Methods 0.000 abstract description 6
- 235000021239 milk protein Nutrition 0.000 abstract description 6
- 235000021243 milk fat Nutrition 0.000 abstract description 4
- 235000021120 animal protein Nutrition 0.000 abstract description 2
- 239000000047 product Substances 0.000 description 21
- 239000006071 cream Substances 0.000 description 18
- 239000000243 solution Substances 0.000 description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 17
- 108010058846 Ovalbumin Proteins 0.000 description 15
- 239000006260 foam Substances 0.000 description 14
- 235000000346 sugar Nutrition 0.000 description 13
- 235000013618 yogurt Nutrition 0.000 description 11
- 102000011632 Caseins Human genes 0.000 description 10
- 108010076119 Caseins Proteins 0.000 description 10
- 108010073771 Soybean Proteins Proteins 0.000 description 8
- 235000013339 cereals Nutrition 0.000 description 8
- 235000019197 fats Nutrition 0.000 description 8
- 229940001941 soy protein Drugs 0.000 description 8
- 235000019219 chocolate Nutrition 0.000 description 7
- 238000005187 foaming Methods 0.000 description 7
- 235000020183 skimmed milk Nutrition 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 230000001804 emulsifying effect Effects 0.000 description 6
- 239000002245 particle Substances 0.000 description 6
- KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical compound NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 description 5
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 5
- 102000007544 Whey Proteins Human genes 0.000 description 5
- 108010046377 Whey Proteins Proteins 0.000 description 5
- 239000000839 emulsion Substances 0.000 description 5
- 238000001914 filtration Methods 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- 235000004213 low-fat Nutrition 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 229920001592 potato starch Polymers 0.000 description 5
- 229940116317 potato starch Drugs 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 239000006228 supernatant Substances 0.000 description 5
- 235000021119 whey protein Nutrition 0.000 description 5
- 241001465754 Metazoa Species 0.000 description 4
- 229920002472 Starch Polymers 0.000 description 4
- 235000009508 confectionery Nutrition 0.000 description 4
- 210000002969 egg yolk Anatomy 0.000 description 4
- 235000013345 egg yolk Nutrition 0.000 description 4
- 235000019211 fat replacer Nutrition 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 235000013336 milk Nutrition 0.000 description 4
- 239000008267 milk Substances 0.000 description 4
- 210000004080 milk Anatomy 0.000 description 4
- 229940080237 sodium caseinate Drugs 0.000 description 4
- 235000019698 starch Nutrition 0.000 description 4
- 239000008107 starch Substances 0.000 description 4
- 239000013589 supplement Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 3
- 239000004472 Lysine Substances 0.000 description 3
- 150000001413 amino acids Chemical class 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 235000014121 butter Nutrition 0.000 description 3
- 238000005119 centrifugation Methods 0.000 description 3
- 235000008504 concentrate Nutrition 0.000 description 3
- 230000001143 conditioned effect Effects 0.000 description 3
- 230000003750 conditioning effect Effects 0.000 description 3
- 229930008677 glyco alkaloid Natural products 0.000 description 3
- 238000000265 homogenisation Methods 0.000 description 3
- 235000010445 lecithin Nutrition 0.000 description 3
- 239000000787 lecithin Substances 0.000 description 3
- 229940067606 lecithin Drugs 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000012528 membrane Substances 0.000 description 3
- 235000016709 nutrition Nutrition 0.000 description 3
- 235000020374 simple syrup Nutrition 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 description 2
- GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 2
- 244000303965 Cyamopsis psoralioides Species 0.000 description 2
- 108010082495 Dietary Plant Proteins Proteins 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 240000008042 Zea mays Species 0.000 description 2
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 2
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 2
- 238000005273 aeration Methods 0.000 description 2
- 229940072056 alginate Drugs 0.000 description 2
- 235000010443 alginic acid Nutrition 0.000 description 2
- 229920000615 alginic acid Polymers 0.000 description 2
- 238000010009 beating Methods 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 235000021152 breakfast Nutrition 0.000 description 2
- 235000015496 breakfast cereal Nutrition 0.000 description 2
- HOPSCVCBEOCPJZ-UHFFFAOYSA-N carboxymethyl(trimethyl)azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CC(O)=O HOPSCVCBEOCPJZ-UHFFFAOYSA-N 0.000 description 2
- 235000010418 carrageenan Nutrition 0.000 description 2
- 239000000679 carrageenan Substances 0.000 description 2
- 229920001525 carrageenan Polymers 0.000 description 2
- 229940113118 carrageenan Drugs 0.000 description 2
- 229940071162 caseinate Drugs 0.000 description 2
- 238000005345 coagulation Methods 0.000 description 2
- 230000015271 coagulation Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 235000005822 corn Nutrition 0.000 description 2
- 235000013399 edible fruits Nutrition 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000012467 final product Substances 0.000 description 2
- 229920000159 gelatin Polymers 0.000 description 2
- 235000019322 gelatine Nutrition 0.000 description 2
- 235000015110 jellies Nutrition 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 244000005700 microbiome Species 0.000 description 2
- 229920001277 pectin Polymers 0.000 description 2
- 239000001814 pectin Substances 0.000 description 2
- 235000010987 pectin Nutrition 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 239000012460 protein solution Substances 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000008399 tap water Substances 0.000 description 2
- 235000020679 tap water Nutrition 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- 235000011844 whole wheat flour Nutrition 0.000 description 2
- 229920001285 xanthan gum Polymers 0.000 description 2
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 2
- XINQFOMFQFGGCQ-UHFFFAOYSA-L (2-dodecoxy-2-oxoethyl)-[6-[(2-dodecoxy-2-oxoethyl)-dimethylazaniumyl]hexyl]-dimethylazanium;dichloride Chemical compound [Cl-].[Cl-].CCCCCCCCCCCCOC(=O)C[N+](C)(C)CCCCCC[N+](C)(C)CC(=O)OCCCCCCCCCCCC XINQFOMFQFGGCQ-UHFFFAOYSA-L 0.000 description 1
- JLPULHDHAOZNQI-ZTIMHPMXSA-N 1-hexadecanoyl-2-(9Z,12Z-octadecadienoyl)-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCC\C=C/C\C=C/CCCCC JLPULHDHAOZNQI-ZTIMHPMXSA-N 0.000 description 1
- 240000008886 Ceratonia siliqua Species 0.000 description 1
- 235000013912 Ceratonia siliqua Nutrition 0.000 description 1
- 241001137251 Corvidae Species 0.000 description 1
- 206010012735 Diarrhoea Diseases 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 239000001828 Gelatine Substances 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 235000003332 Ilex aquifolium Nutrition 0.000 description 1
- 241000209027 Ilex aquifolium Species 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 229920000161 Locust bean gum Polymers 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 235000004443 Ricinus communis Nutrition 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- 241000209140 Triticum Species 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- OENHQHLEOONYIE-UKMVMLAPSA-N all-trans beta-carotene Natural products CC=1CCCC(C)(C)C=1/C=C/C(/C)=C/C=C/C(/C)=C/C=C/C=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C OENHQHLEOONYIE-UKMVMLAPSA-N 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 235000013734 beta-carotene Nutrition 0.000 description 1
- TUPZEYHYWIEDIH-WAIFQNFQSA-N beta-carotene Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1=C(C)CCCC1(C)C)C=CC=C(/C)C=CC2=CCCCC2(C)C TUPZEYHYWIEDIH-WAIFQNFQSA-N 0.000 description 1
- 239000011648 beta-carotene Substances 0.000 description 1
- 229960002747 betacarotene Drugs 0.000 description 1
- 235000015895 biscuits Nutrition 0.000 description 1
- 235000008429 bread Nutrition 0.000 description 1
- 235000012970 cakes Nutrition 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 235000020992 canned meat Nutrition 0.000 description 1
- 235000014633 carbohydrates Nutrition 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
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- 239000003795 chemical substances by application Substances 0.000 description 1
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- 238000002425 crystallisation Methods 0.000 description 1
- 235000019543 dairy drink Nutrition 0.000 description 1
- 238000004925 denaturation Methods 0.000 description 1
- 230000036425 denaturation Effects 0.000 description 1
- 235000011850 desserts Nutrition 0.000 description 1
- 235000005911 diet Nutrition 0.000 description 1
- 230000037213 diet Effects 0.000 description 1
- 230000029087 digestion Effects 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 235000013601 eggs Nutrition 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 230000007515 enzymatic degradation Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 206010016766 flatulence Diseases 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 230000005714 functional activity Effects 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 235000013402 health food Nutrition 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 235000019866 hydrogenated palm kernel oil Nutrition 0.000 description 1
- 235000015243 ice cream Nutrition 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 235000010420 locust bean gum Nutrition 0.000 description 1
- 239000000711 locust bean gum Substances 0.000 description 1
- FQXXSQDCDRQNQE-UHFFFAOYSA-N markiertes Thebain Natural products COC1=CC=C2C(N(CC3)C)CC4=CC=C(OC)C5=C4C23C1O5 FQXXSQDCDRQNQE-UHFFFAOYSA-N 0.000 description 1
- 239000008268 mayonnaise Substances 0.000 description 1
- 235000010746 mayonnaise Nutrition 0.000 description 1
- 235000012054 meals Nutrition 0.000 description 1
- 235000013622 meat product Nutrition 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000001471 micro-filtration Methods 0.000 description 1
- QKQQEIVDLRUZRP-UHFFFAOYSA-N northebaine Natural products COC1=CC=C2C(NCC3)CC4=CC=C(OC)C5=C4C23C1O5 QKQQEIVDLRUZRP-UHFFFAOYSA-N 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
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- 235000011837 pasties Nutrition 0.000 description 1
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- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- -1 phosphate compound Chemical class 0.000 description 1
- 235000015108 pies Nutrition 0.000 description 1
- 229920006393 polyether sulfone Polymers 0.000 description 1
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- 235000013824 polyphenols Nutrition 0.000 description 1
- 235000019881 protein-based fat mimetic Nutrition 0.000 description 1
- 235000011962 puddings Nutrition 0.000 description 1
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- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
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- 229940083466 soybean lecithin Drugs 0.000 description 1
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- OENHQHLEOONYIE-JLTXGRSLSA-N β-Carotene Chemical compound CC=1CCCC(C)(C)C=1\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C OENHQHLEOONYIE-JLTXGRSLSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K50/00—Feeding-stuffs specially adapted for particular animals
- A23K50/40—Feeding-stuffs specially adapted for particular animals for carnivorous animals, e.g. cats or dogs
- A23K50/48—Moist feed
-
- A—HUMAN NECESSITIES
- A21—BAKING; EDIBLE DOUGHS
- A21D—TREATMENT OF FLOUR OR DOUGH FOR BAKING, e.g. BY ADDITION OF MATERIALS; BAKING; BAKERY PRODUCTS
- A21D13/00—Finished or partly finished bakery products
- A21D13/50—Solidified foamed products, e.g. meringues
-
- A—HUMAN NECESSITIES
- A21—BAKING; EDIBLE DOUGHS
- A21D—TREATMENT OF FLOUR OR DOUGH FOR BAKING, e.g. BY ADDITION OF MATERIALS; BAKING; BAKERY PRODUCTS
- A21D2/00—Treatment of flour or dough by adding materials thereto before or during baking
- A21D2/08—Treatment of flour or dough by adding materials thereto before or during baking by adding organic substances
- A21D2/24—Organic nitrogen compounds
- A21D2/26—Proteins
- A21D2/264—Vegetable proteins
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23C—DAIRY PRODUCTS, e.g. MILK, BUTTER OR CHEESE; MILK OR CHEESE SUBSTITUTES; MAKING OR TREATMENT THEREOF
- A23C13/00—Cream; Cream preparations; Making thereof
- A23C13/12—Cream preparations
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G1/00—Cocoa; Cocoa products, e.g. chocolate; Substitutes therefor
- A23G1/30—Cocoa products, e.g. chocolate; Substitutes therefor
- A23G1/32—Cocoa products, e.g. chocolate; Substitutes therefor characterised by the composition containing organic or inorganic compounds
- A23G1/44—Cocoa products, e.g. chocolate; Substitutes therefor characterised by the composition containing organic or inorganic compounds containing peptides or proteins
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G1/00—Cocoa; Cocoa products, e.g. chocolate; Substitutes therefor
- A23G1/30—Cocoa products, e.g. chocolate; Substitutes therefor
- A23G1/32—Cocoa products, e.g. chocolate; Substitutes therefor characterised by the composition containing organic or inorganic compounds
- A23G1/48—Cocoa products, e.g. chocolate; Substitutes therefor characterised by the composition containing organic or inorganic compounds containing plants or parts thereof, e.g. fruits, seeds or extracts
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G3/00—Sweetmeats; Confectionery; Marzipan; Coated or filled products
- A23G3/34—Sweetmeats, confectionery or marzipan; Processes for the preparation thereof
- A23G3/36—Sweetmeats, confectionery or marzipan; Processes for the preparation thereof characterised by the composition containing organic or inorganic compounds
- A23G3/44—Sweetmeats, confectionery or marzipan; Processes for the preparation thereof characterised by the composition containing organic or inorganic compounds containing peptides or proteins
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G3/00—Sweetmeats; Confectionery; Marzipan; Coated or filled products
- A23G3/34—Sweetmeats, confectionery or marzipan; Processes for the preparation thereof
- A23G3/36—Sweetmeats, confectionery or marzipan; Processes for the preparation thereof characterised by the composition containing organic or inorganic compounds
- A23G3/48—Sweetmeats, confectionery or marzipan; Processes for the preparation thereof characterised by the composition containing organic or inorganic compounds containing plants or parts thereof, e.g. fruits, seeds, extracts
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23J—PROTEIN COMPOSITIONS FOR FOODSTUFFS; WORKING-UP PROTEINS FOR FOODSTUFFS; PHOSPHATIDE COMPOSITIONS FOR FOODSTUFFS
- A23J1/00—Obtaining protein compositions for foodstuffs; Bulk opening of eggs and separation of yolks from whites
- A23J1/16—Obtaining protein compositions for foodstuffs; Bulk opening of eggs and separation of yolks from whites from waste water of starch-manufacturing plant or like wastes
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K20/00—Accessory food factors for animal feeding-stuffs
- A23K20/10—Organic substances
- A23K20/142—Amino acids; Derivatives thereof
- A23K20/147—Polymeric derivatives, e.g. peptides or proteins
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L13/00—Meat products; Meat meal; Preparation or treatment thereof
- A23L13/40—Meat products; Meat meal; Preparation or treatment thereof containing additives
- A23L13/42—Additives other than enzymes or microorganisms in meat products or meat meals
- A23L13/426—Addition of proteins, carbohydrates or fibrous material from vegetable origin other than sugars or sugar alcohols
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/17—Amino acids, peptides or proteins
- A23L33/185—Vegetable proteins
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23P—SHAPING OR WORKING OF FOODSTUFFS, NOT FULLY COVERED BY A SINGLE OTHER SUBCLASS
- A23P30/00—Shaping or working of foodstuffs characterised by the process or apparatus
- A23P30/40—Foaming or whipping
Definitions
- the present invention relates to the use of potato protein in food compositions.
- Potato protein has traditionally been regarded as a waste product of starch manufacture. However, its nutritional qualities (i.e. protein efficiency ratio and biological value) has been shown to be greater than that of casein and comparable to that of whole egg (Kapoor et al.1975; Stegemann, 1977); Knorr, 1978) . Potato protein is rich in lysine and theoretically an excellent supplement for lysine-poor proteins such as those of cereals. Despite its unique nutritional qualities, potato protein is currently only used as animal feed, because the product exhibits a number of serious drawbacks.
- potato protein becomes denatured and as a consequence becomes devoid of functional properties, i.e. emulsifying capacity, foaming capacity, thermogelling capacity, water binding capacity. Even the most essential requirement for its application in the food industry, i.e. solubility in water, cannot be met.
- the present invention relates to a food composition which comprises undenatured potato protein as an ingredient and to a method for preparing such undenatured potato protein.
- this invention relates to the use of undenatured potato protein as a substitute for protein, fat or hydrocolloids in food compositions.
- This allows for a diet based on vegetable proteins, with high nutritional value. Consequently, in contrast to known food compositions which contain protein, fat or hydrocolloid substitutes which are animal or milk proteins, food compositions according to the invention may be used by people who prefer not to use such proteins .
- 'food composition refers to any substance containing nutrients, whether for human or animal consumption, whether comprised of a single ingredient or a mixture of ingredients, whether liquid, liquid containing or solid, whether primarily carbohydrate, fat, protein or any mixture thereof, whether edible per se or requiring processing like cooking, mixing, cooling, mechanical treatment and the like.
- the undenatured potato protein used in the food composition is preferably isolated from potato fruit juice, a waste product of the starch manufacturing industry. Both diluted and undiluted potato fruit juice may be used.
- Other suitable sources of undenatured potato protein include for example potato peel extracts and effluent streams from potato processing industries other than the potato-starch industry.
- undenatured potato protein refers to potato protein which has retained most of its intrinsic functional properties, such as emulsifying capacity, solubility, foaming capacity, water binding capacity and thermogellmg capacity, on isolation. As a consequence, its functional properties will be better than those of denatured potato protein and at least as good as those of soy protein.
- undenatured potato protein is prepared by a low-temperature process comprising conditioning (pre-treatment) , ultrafiltration, diafiltration and, optionally, drying.
- the undenatured potato protein of the invention is recovered from a potato protein containing fraction, such as potato fruit juice, after the latter has been conditioned.
- conditioning should be carried out at a temperature which does not exceed 40°C.
- the potato protein containing fraction is conditioned by means of flocculation, which encapsulates the contaminations, and centrifugation.
- Flocculation may be carried out at a pH from about 7.0 to 8.0, preferably at pH 7.5, and at a temperature of from about 10°C to about 40°C, preferably at a temperature of from about 20°C to about 30°C.
- the flocculant is preferably food-grade.
- flocculation is carried out at room temperature using CaHPO, which is formed by the addition of a calcium salt and a phosphate compound to the potato protein containing fraction.
- CaHPO is formed by the addition of a calcium salt and a phosphate compound to the potato protein containing fraction.
- a suitable calcium:phosphate ratio is about 0.3:0.18.
- Preferably, from about 0.1 to about 1.0% w/v calcium is used.
- the flocculent may be removed from the liquid phase by e.g. filtration, centrifugation, decanting or any other suitable means. If CaHP0 4 is used for flocculation, the two phases are preferably separated by centrifugation, which will result in a clear supernatant .
- the potato protein containing supernatant is concentrated and washed, e.g. by filtration, evaporation, adsorption-elution, or a combination of these methods. Preferably, it is concentrated and washed by filtration. Any ultrafiltration, hyperfiltration or microfiltration membrane which is convenient for the concentration of protein may be used, as long as they retain the undenatured potato protein. Membranes with a cut-off value of from about 3 kDa to 100 kDa are preferably used. Any type of filtration unit can be used. Preferred units are continuous systems, such as a continuous multistage filtration unit or a feed and bleed unit. The temperature during ultrafiltration should not exceed 40°C and is preferably from about 15°C to about 25°C.
- the supernatant is concentrated by ultrafiltration and washed by diafiltration to reduce the concentration of salts, metals, etc.
- the concentrate is washed with water, preferably in the presence of bisulphite to prevent undesired colour changes of the protein.
- the amount of washing required depends on the application specification of the final product to be met.
- the concentrate may be dried. If freeze- dried, freezing should be done in as short a time as possible and preferably the drying temperature should not exceed 35°C.
- the inlet temperature may be from about 100°C to about 140°C, the product outlet temperature should preferably not exceed 75°C, because higher temperatures will lead to a product with inferior foaming capacities. Preferred temperatures are lower than about 120°C (inlet) and from about
- glycoalkaloid compound levels may be reduced, preferably by enzymatic degradation, e.g. by an enzyme preparation as described in WO 97/04107, since the majority of acid and solvent extraction methods used to remove glycoalkaloids result in the denaturation of the protein and hence in loss of functional properties.
- Undenatured potato protein according to the invention is particularly suitable for the preparation of essentially non- potato food compositions.
- Non-limiting examples of such food compositions are bakery products, such as bread, cake, biscuits, pies and pastries; dairy products, such as dairy drinks, desserts, ice, yogurt, cheese, spreads, pudding and ice cream; meat products, both for human and animal consumption, whether fresh, cooked or cured; and fish products, whether processed or unprocessed.
- Other food compositions which may contain undenatured potato protein as an ingredient are mayonnaise, soups, sauces, non-dairy spreads, dressings, frozen confectionery, jellified confectionery, such as fruit jellies, jams and jellies and restructured foods, such as reformed fruits and food analogues.
- the examples illustrate that the use of undenatured potato protein is especially advantageous in whipped products .
- Undenatured potato protein may replace all or a portion of the protein (such as egg albumin, casein or soy protein) , fat or hydrocolloids (such as pectin, alginate, gelatine, carrageenan, xanthan, guar, locust bean gum) in food compositions.
- egg white, milk proteins, fat and hydrocolloids are replaced for about 100% by undenatured potato protein.
- Undenatured protein may also be used as a supplement in lysin-poor food compositions.
- undenatured potato protein is used to supplement cereal-based meals.
- Potato fruit juice obtained from a potato starch manufacturer was used within one or two days of reception for the preparation of potato protein.
- To 700 1 of potato fruit juice 0.3% w/v CaCl 2 .2H 2 0 and 0.18% w/v Na 2 HP0 4 .2H 2 0 were added.
- the mixture was stirred for 5 minutes at room temperature.
- the pH was raised to 7.5 using a 20% w/v NaOH solution.
- the conditioned potato fruit juice was centrifuged in a disc stack centrifuge for removal of the flocculation, including solids and microorganisms.
- the supernatant was concentrated about 12 times by ultrafiltration using a continuous ultrafiltration unit equipped with polyethersulfon membranes, cut-off value 5 kDa.
- the retentate was washed by means of diafiltration in the presence of bisulphite to minimise polyphenol oxidation. Diafiltration was continued until salts and metal concentrations had reached acceptable levels. The concentrate was freeze-dried until a dry solid content of 92% was reached. The freeze-dried powder contained 70% protein and no detectable levels of glycoalkaloids (HPLC analysis as described by R. Houben & K. Brunt, J. Chromatography 661, 169-174) .
- Example 2 Solubility of undenatured potato protein compared to denatured potato protein, whey protein and soy protein.
- Undenatured potato protein was prepared essentially as described in Example 1.
- Whey protein (Espiron 580; 78% protein) was obtained from DMV-
- Soy protein (Supro 500E; 90% protein) was obtained from Protein
- a 10% (w/w) solution in demineralised water was prepared. After solubilisation (as far as possible) , the pH of the solution was adjusted to the desired value by the drop-wise addition of either NaOH or HCI. Subsequently the solution with the adjusted pH value was centrifuged for 10 minutes at 14.000 rpm in an Eppendorf centrifuge after which the dry weights of both starting material and supernatant were determined.
- Example 3 Emulsifying properties of undenatured potato compared to lecithin, whey protein, soy protein and casein.
- Lecithin (Bolec I 55) was obtained from Quest International.
- Soy protein (Supro 500E, 90% protein) was obtained from Protein
- Casein (EM7, 90% protein) was obtained from DMV-International (Holland) .
- Example 4 Artisanal chocolate mousse made with egg albumin Ingredients 0 1 part of fresh egg white (egg albumin) 0.4 part of Castor Sugar 1 part of chocolate 0.5 part of fresh egg yolk
- the egg albumin was mixed with the aid of an Hobart mixer and an whire whip, starting with speed 1 and after formation of a foam with speed 3. While beating the sugar was added. The addition of the sugar was finished before the foam was beaten stiff. The 0 chocolate was melted au bain-marie and mixed with the egg yolk. This chocolate mixture was added to the beaten egg white during mixing with the Hobart mixer and an whire whip at speed 1. The final mixture, the mousse, was cooled down and stored for checking the stability of the mousse the next two days. The mousse showed some drainage and volume loss The fresh egg yolk s may be replaced by soybean lecithin.
- This mousse was equal to the one prepared with egg-albumin.
- the specific volume of this mousse 0 (ml mousse per gram of material) was in the same order or greater than the mousse prepared with egg-albumin.
- Example 3 illustrates how the outstanding emulsification properties of potato protein demonstrated in Example 3 can be advantageously applied in a food product.
- the industrially elaborated mousse has the composition given in Table 2.
- the product is based on cream (typically 38% fat), milk
- the ingredients are mixed for rehydration of the ingredients, followed by a heat treatment to pasteurize, homogenization and aeration, giving a typical overrun of around 60-100% and packaged.
- the stability was in the order of one week.
- the industrially elaborated mousse has the composition given in Table 3.
- the product is based on cream (typically 38% fat) , milk protein, sugar, emulsifier/stabiliser blends, flavouring.
- the ingredients are mixed for rehydration of the ingredients, followed by a heat treatment to pasteurize, homogenization and aeration, giving a typical overrun of around 80-150% and packaged.
- the stability was also in the order of one week.
- undenatured potato protein can be used in whipped food products m such a way that it retains its foaming and emulsifying properties. Therefore, it can replace egg albumin as well as casein.
- the egg albumin was mixed with the aid of an Hobart mixer and a whire whip, starting with speed 1 and after formation of a foam with speed 3 While beating the sugar was added. The addition of the sugar was finished before the foam was beaten stiff. The foam was piped with the aid of notched pipe.
- the meringue was baked with an ceiling (upper) oven temperature of 145°C and a (bottom) lower oven temperature of 115°C for one hour The meringue was further dried m an oven with an ceiling temperature of 95°C and a bottom temperature of 80°C for half an hour
- Powdery samples of the undenatured potato protein product of the invention were obtained as mentioned in Example 1. From these samples a solution was made by gently mixing with tap water The solution contained approximately 10 % of potato protein This is in the same order as the concentration of egg albumin in fresh egg whites. This solution was beaten in the same way as the egg albumin in Example 8 While mixing, the sugar was added. The stiff foam was piped and baked in the same way as the egg white meringue of Example 8. In contrast to meringues made with egg albumin, one does not observe the flow of foam while baking (the sharp edges formed by piping remained) .
- Example 8 showed a fast setting of the foam, resulting in cracks in the meringue due to a small further increase in volume
- the meringue from potato protein showed a gradual increase in volume giving rise to a non- cracked meringue with a much larger volume per gram of original foam.
- This example illustrates how undenatured potato protein can be used in a bakery product without losing its foaming properties, aerating capacity and foam stability while heated.
- Example 10 Potato protein as lysine-rich fat replacer
- Oil droplets in a well homogenised emulsion typically exhibit droplet diameters between 1 to 10 micron diameter.
- the scientific literature claims that the fatty mouthfeel of such emulsions is almost entirely based on the mere presence of such droplets or particles in the solution.
- fat replacer products exist that are based on this principle. Ingredients for such fat replacers include starch, cellulose, pectin and proteins. For nutritionally optimised products, a potato protein based fat replacer could be desirable.
- undenatured potato protein of the invention was processed to obtain hollow particles with an average diameter between 2 and 10, micron.
- different techniques are known for the production of such particles, for the purpose of this example we have used a technique described in WO 94/08627 (incorporated herein be reference) .
- 20 grams of undenatured potato protein was dissolved in 150 ml of water containing 0.75 grams of sodium chloride and subsequently atomised at a temperature of 220 "C inlet temperature (92 * C outlet temperature) .
- C inlet temperature 92 * C outlet temperature
- Example 11 Breakfast cereals made with potato protein
- Potato protein is rich in lysine and as such an excellent supplement for lysin-poor proteins such as those of cereals.
- This complementary relationship has not only been historically proven but has also been shown in several scientific publications (e.g. Kofranyi, E. and Jekat, F. Die biologi Wertmaschine von toysproteinen. West Germanr Verlag, K ⁇ ln (1965) . Therefore, in the health food sector, the combination of potato protein and, for example, breakfast cereals is desirable.
- the following example illustrates one route to provide such a combination.
- Typical starting materials for cereal breakfast foods include corn, wheat and rice. Because of the relatively low protein content of these products, it would be desirable to optimise this protein in terms of amino acid composition.
- Example 12 Pet food made with potato protein Another example illustrating the wide applicability of undenatured potato protein is in pet food manufacturing.
- the unique thermogelling properties of the protein can be used in waterbinding to replace hydrocolloids like carrageenan, xanthan, guar or locust bean.
- disadvantage of the latter compounds is that digestion in the gut is not without difficulties so that phenomena like diarrhoea and flatulence can occur.
- the following recipe specifies a canned meat product from which hydrocolloids have been removed and replaced by potato protein.
- Potato protein was evaluated in a low fat yogurt formulation which was cultured with the protein present.
- the reference yielded a yogurt with a thin, smooth and continuous texture, typical of low-fat yogurt.
- the potato protein yogurt had thicker texture than the reference, which can be attributed to its outstanding gelling properties.
- potato protein can form a stable foam at long whisking. It also shows that potato protein can be used to form a stable foam in the presence of high fat (48% milk fat) . These observations are unusual for protein foaming agents, which tend to form a butter at long whisking.
- Imitation whipping cream formulations normally contain sodium caseinate. This example shows the impact of replacing the caseinate with undenatured potato protein or water.
- Undenatured potato protein was used in a confectionery formulation using the following recipe.
- a foamed product was formed. This shows that undenatured potato protein of the invention also retains its foaming capacity in the presence of high sugar syrup.
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Abstract
The present invention relates to food compositions which comprise undenatured potato protein as an ingredient, more specifically to food compositions in which all or a portion of the animal protein, milk protein, fat or hydrocolloids is replaced by undenatured potato protein and to a process for preparing such undenatured protein.
Description
NOVEL FOOD COMPOSITIONS
FIELD OF THE INVENTION
The present invention relates to the use of potato protein in food compositions.
BACKGROUND OF THE INVENTION
Potato protein has traditionally been regarded as a waste product of starch manufacture. However, its nutritional qualities (i.e. protein efficiency ratio and biological value) has been shown to be greater than that of casein and comparable to that of whole egg (Kapoor et al.1975; Stegemann, 1977); Knorr, 1978) . Potato protein is rich in lysine and theoretically an excellent supplement for lysine-poor proteins such as those of cereals. Despite its unique nutritional qualities, potato protein is currently only used as animal feed, because the product exhibits a number of serious drawbacks.
One of the major drawbacks is that the recovery of potato protein from the effluent of potato starch mills is commonly carried out on an industrial scale by heat coagulation (Oosten
(1976); De Boer & Hiddink, 1977; Knorr et al , 1977) . Due to the heat coagulation, potato protein becomes denatured and as a consequence becomes devoid of functional properties, i.e. emulsifying capacity, foaming capacity, thermogelling capacity, water binding capacity. Even the most essential requirement for its application in the food industry, i.e. solubility in water, cannot be met.
Although there are a handful of publications about the recovery of undenatured potato protein, see for example Jackman & Yada {J. Food Science (1988) 53:1427), Holm & Eriksen (J. Food Technol. (1980) 15:71) and GB 1,520,738, it is not clear whether or how such undenatured potato protein can be used in food compositions.
DETAILED DESCRIPTION
The present invention relates to a food composition which comprises undenatured potato protein as an ingredient and to a method for preparing such undenatured potato protein.
In particular, this invention relates to the use of undenatured potato protein as a substitute for protein, fat or hydrocolloids in food compositions. This allows for a diet based on vegetable proteins, with high nutritional value. Consequently, in contrast to known food compositions which contain protein, fat or hydrocolloid substitutes which are animal or milk proteins, food compositions according to the invention may be used by people who prefer not to use such proteins .
In this context 'food composition' refers to any substance containing nutrients, whether for human or animal consumption, whether comprised of a single ingredient or a mixture of ingredients, whether liquid, liquid containing or solid, whether primarily carbohydrate, fat, protein or any mixture thereof, whether edible per se or requiring processing like cooking, mixing, cooling, mechanical treatment and the like.
The undenatured potato protein used in the food composition is preferably isolated from potato fruit juice, a waste product of the starch manufacturing industry. Both diluted and undiluted potato fruit juice may be used. Other suitable sources of undenatured potato protein include for example potato peel extracts and effluent streams from potato processing industries other than the potato-starch industry.
In this context, 'undenatured potato protein' refers to potato protein which has retained most of its intrinsic functional properties, such as emulsifying capacity, solubility, foaming capacity, water binding capacity and thermogellmg capacity, on isolation. As a consequence, its functional properties will be better than those of denatured potato protein and at least as good as those of soy protein. In the method of the invention, undenatured potato protein is prepared by a low-temperature process comprising conditioning (pre-treatment) , ultrafiltration, diafiltration and, optionally, drying. The undenatured potato protein of the invention is recovered from a potato protein containing fraction, such as potato fruit juice, after the latter has been conditioned. During conditioning undesired particles and microorganisms are removed,
which allows for high initial fluxes. In order to retain functional activities, in particular foaming capacity, conditioning should be carried out at a temperature which does not exceed 40°C. Preferably, the potato protein containing fraction is conditioned by means of flocculation, which encapsulates the contaminations, and centrifugation. Flocculation may be carried out at a pH from about 7.0 to 8.0, preferably at pH 7.5, and at a temperature of from about 10°C to about 40°C, preferably at a temperature of from about 20°C to about 30°C. The flocculant is preferably food-grade. In one preferred embodiment, flocculation is carried out at room temperature using CaHPO,, which is formed by the addition of a calcium salt and a phosphate compound to the potato protein containing fraction. A suitable calcium:phosphate ratio is about 0.3:0.18. Preferably, from about 0.1 to about 1.0% w/v calcium is used.
The flocculent may be removed from the liquid phase by e.g. filtration, centrifugation, decanting or any other suitable means. If CaHP04 is used for flocculation, the two phases are preferably separated by centrifugation, which will result in a clear supernatant .
The potato protein containing supernatant is concentrated and washed, e.g. by filtration, evaporation, adsorption-elution, or a combination of these methods. Preferably, it is concentrated and washed by filtration. Any ultrafiltration, hyperfiltration or microfiltration membrane which is convenient for the concentration of protein may be used, as long as they retain the undenatured potato protein. Membranes with a cut-off value of from about 3 kDa to 100 kDa are preferably used. Any type of filtration unit can be used. Preferred units are continuous systems, such as a continuous multistage filtration unit or a feed and bleed unit. The temperature during ultrafiltration should not exceed 40°C and is preferably from about 15°C to about 25°C.
In a preferred embodiment, the supernatant is concentrated by ultrafiltration and washed by diafiltration to reduce the concentration of salts, metals, etc. The concentrate is washed with water, preferably in the presence of bisulphite to prevent undesired colour changes of the protein. The amount of washing required depends on the application specification of the final product to be met.
After washing, the concentrate may be dried. If freeze- dried, freezing should be done in as short a time as possible and preferably the drying temperature should not exceed 35°C. If the preparation is spray-dried the inlet temperature may be from about 100°C to about 140°C, the product outlet temperature should preferably not exceed 75°C, because higher temperatures will lead to a product with inferior foaming capacities. Preferred temperatures are lower than about 120°C (inlet) and from about
50°C to about 70°C (outlet) . If necessary, glycoalkaloid compound levels may be reduced, preferably by enzymatic degradation, e.g. by an enzyme preparation as described in WO 97/04107, since the majority of acid and solvent extraction methods used to remove glycoalkaloids result in the denaturation of the protein and hence in loss of functional properties.
Undenatured potato protein according to the invention is particularly suitable for the preparation of essentially non- potato food compositions. Non-limiting examples of such food compositions are bakery products, such as bread, cake, biscuits, pies and pastries; dairy products, such as dairy drinks, desserts, ice, yogurt, cheese, spreads, pudding and ice cream; meat products, both for human and animal consumption, whether fresh, cooked or cured; and fish products, whether processed or unprocessed. Other food compositions which may contain undenatured potato protein as an ingredient are mayonnaise, soups, sauces, non-dairy spreads, dressings, frozen confectionery, jellified confectionery, such as fruit jellies, jams and jellies and restructured foods, such as reformed fruits and food analogues. The examples illustrate that the use of undenatured potato protein is especially advantageous in whipped products .
Undenatured potato protein may replace all or a portion of the protein (such as egg albumin, casein or soy protein) , fat or hydrocolloids (such as pectin, alginate, gelatine, carrageenan, xanthan, guar, locust bean gum) in food compositions. In one preferred embodiment of the invention, egg white, milk proteins, fat and hydrocolloids are replaced for about 100% by undenatured potato protein.
Undenatured protein may also be used as a supplement in lysin-poor food compositions. In another preferred embodiment of
the invention, undenatured potato protein is used to supplement cereal-based meals.
The following examples illustrate how undenatured potato protein can be used for preparing food products .
EXAMPLES
Example 1 Production of undenatured potato protein (large scale)
Potato fruit juice obtained from a potato starch manufacturer was used within one or two days of reception for the preparation of potato protein. To 700 1 of potato fruit juice 0.3% w/v CaCl2.2H20 and 0.18% w/v Na2HP04.2H20 were added. The mixture was stirred for 5 minutes at room temperature. The pH was raised to 7.5 using a 20% w/v NaOH solution. The conditioned potato fruit juice was centrifuged in a disc stack centrifuge for removal of the flocculation, including solids and microorganisms. The supernatant was concentrated about 12 times by ultrafiltration using a continuous ultrafiltration unit equipped with polyethersulfon membranes, cut-off value 5 kDa. The retentate was washed by means of diafiltration in the presence of bisulphite to minimise polyphenol oxidation. Diafiltration was continued until salts and metal concentrations had reached acceptable levels. The concentrate was freeze-dried until a dry solid content of 92% was reached. The freeze-dried powder contained 70% protein and no detectable levels of glycoalkaloids (HPLC analysis as described by R. Houben & K. Brunt, J. Chromatography 661, 169-174) .
Example 2 Solubility of undenatured potato protein compared to denatured potato protein, whey protein and soy protein.
Materials
Undenatured potato protein was prepared essentially as described in Example 1.
Denatured potato protein was obtained from Emsland-Starke
(Germany) .
Whey protein (Espiron 580; 78% protein) was obtained from DMV-
International (Holland) . Soy protein (Supro 500E; 90% protein) was obtained from Protein
Technologies International (Belgium) .
Method
Of each one of the above-mentioned protein products a 10% (w/w) solution in demineralised water was prepared. After solubilisation (as far as possible) , the pH of the solution was adjusted to the desired value by the drop-wise addition of either NaOH or HCI. Subsequently the solution with the adjusted pH value was centrifuged for 10 minutes at 14.000 rpm in an Eppendorf centrifuge after which the dry weights of both starting material and supernatant were determined.
The data obtained are provided in Table 1. These data show clearly that the water solubility of undenatured potato protein is far better than denatured potato protein or soy protein.
Table 1 Solubility of undenatured potato protein
Example 3 Emulsifying properties of undenatured potato compared to lecithin, whey protein, soy protein and casein.
Materials
Undenatured potato protein: see Example 1.
Denatured potato protein: see Example 2.
Whey protein: see Example 2.
Lecithin (Bolec I 55) was obtained from Quest International.
Soy protein (Supro 500E, 90% protein) was obtained from Protein
Technologies International (Belgium) .
Casein (EM7, 90% protein) was obtained from DMV-International (Holland) .
Method s Of each of the above mentioned material a 10% (w/w) solution in demineralised water was prepared. Of each one of these solutions 10 grams was poured into a measuring cylinder after which to each of these samples 70 grams of demineralised water and 20 grams of soy oil was added. Emulsions were prepared by mixing for either 2 o or 4 minutes at either 8000, 9500 or 13.500 rpm with an Ultra- Turrax T25. The quality of each emulsion was established by taking photographs using a Sony CCD camera linked to a UP3030P videoprinter (magnification: 337.5 x) . The formation of many small and homogeneously formed oil droplets was the major s criterium for establishing emulsifying properties.
.Results
In order of efficacy, the following emulsifier ranking was obtained: 0 1. lecithin 2. undenatured potato protein 3. whey protein 4. soy protein 5. casein 6. denatured potato protein.
These data underline the potential of undenatured potato protein relative to commercially available protein products in terms of emulsifying power. 5
Example 4 Artisanal chocolate mousse made with egg albumin Ingredients 0 1 part of fresh egg white (egg albumin) 0.4 part of Castor Sugar 1 part of chocolate 0.5 part of fresh egg yolk
5 Preparation
The egg albumin was mixed with the aid of an Hobart mixer and an whire whip, starting with speed 1 and after formation of a foam with speed 3. While beating the sugar was added. The addition of the sugar was finished before the foam was beaten stiff. The 0 chocolate was melted au bain-marie and mixed with the egg yolk. This chocolate mixture was added to the beaten egg white during
mixing with the Hobart mixer and an whire whip at speed 1. The final mixture, the mousse, was cooled down and stored for checking the stability of the mousse the next two days. The mousse showed some drainage and volume loss The fresh egg yolk s may be replaced by soybean lecithin.
Example 5 Artisanal chocolate mousse made with potato protein
Ingredients
1 part of potato protein solution (for preparation see below) o 0.4 part of Castor Sugar 1 part of chocolate 0.5 part of fresh egg yolk
Preparation s Powdery samples of the potato protein product of the invention were prepared essentially as described m Example 1 From these samples a solution was made by gently mixing with tap water The solution contained approximately 10% w/v of potato protein. This is m the same order as the concentration of egg albumin in fresh 0 egg whites. This solution was beaten in the same way as the egg albumin in Example 4 While mixing, the sugar was added. The addition of the sugar was finished before the foam was beaten stiff. After beaten stiff the chocolate mixture (see Example 4) was added to the beaten potato protein while mixing with the 5 Hobart mixer and an whire whip at speed 1. The final mixture, the mousse, was cooled down and stored for checking the stability of the mousse the next two days.
The storage stability of this mousse was equal to the one prepared with egg-albumin. The specific volume of this mousse 0 (ml mousse per gram of material) was in the same order or greater than the mousse prepared with egg-albumin.
This example illustrates how the outstanding emulsification properties of potato protein demonstrated in Example 3 can be advantageously applied in a food product.
35
Example 6 Industrial Manufactured Mousse with Milk Proteins
The industrially elaborated mousse has the composition given in Table 2. The product is based on cream (typically 38% fat), milk
40 protein, sugar, emulsifler/stabiliser blends, flavouring.
The ingredients are mixed for rehydration of the ingredients, followed by a heat treatment to pasteurize, homogenization and aeration, giving a typical overrun of around 60-100% and packaged. The stability was in the order of one week.
Table 2 Mousse comprising milk proteins
Table 3 Mousse containing undenatured potato protein
Example 7 Industrial manufactured mousse with potato proteins
The industrially elaborated mousse has the composition given in Table 3. The product is based on cream (typically 38% fat) , milk protein, sugar, emulsifier/stabiliser blends, flavouring. The
ingredients are mixed for rehydration of the ingredients, followed by a heat treatment to pasteurize, homogenization and aeration, giving a typical overrun of around 80-150% and packaged. The stability was also in the order of one week.
This example shows that undenatured potato protein can be used in whipped food products m such a way that it retains its foaming and emulsifying properties. Therefore, it can replace egg albumin as well as casein.
Example 8 Meringue containing egg albumin
Ingredients
1 part of fresh egg whites (egg albumin) l part of Castor Sugar
Preparation
The egg albumin was mixed with the aid of an Hobart mixer and a whire whip, starting with speed 1 and after formation of a foam with speed 3 While beating the sugar was added. The addition of the sugar was finished before the foam was beaten stiff. The foam was piped with the aid of notched pipe. The meringue was baked with an ceiling (upper) oven temperature of 145°C and a (bottom) lower oven temperature of 115°C for one hour The meringue was further dried m an oven with an ceiling temperature of 95°C and a bottom temperature of 80°C for half an hour
Example 9 Meringue containing potato protein Ingredients
1 part of potato protein solution (for preparation see below) 1 part of castor sugar
Powdery samples of the undenatured potato protein product of the invention were obtained as mentioned in Example 1. From these samples a solution was made by gently mixing with tap water The solution contained approximately 10 % of potato protein This is in the same order as the concentration of egg albumin in fresh egg whites. This solution was beaten in the same way as the egg albumin in Example 8 While mixing, the sugar was added. The stiff foam was piped and baked in the same way as the egg white meringue of Example 8.
In contrast to meringues made with egg albumin, one does not observe the flow of foam while baking (the sharp edges formed by piping remained) . Furthermore a clear difference was seen in the expansion in the oven, Whereas the meringue in Example 8 showed a fast setting of the foam, resulting in cracks in the meringue due to a small further increase in volume, the meringue from potato protein showed a gradual increase in volume giving rise to a non- cracked meringue with a much larger volume per gram of original foam. This example illustrates how undenatured potato protein can be used in a bakery product without losing its foaming properties, aerating capacity and foam stability while heated.
Example 10 Potato protein as lysine-rich fat replacer
A typical example to illustrate how the unique properties of undenatured potato protein can be advantageously employed in the food segment is presented underneath. In this example the extreme thermogelling properties and the very specific amino acid com¬ position of undenatured potato protein are combined to make a lysin-rich fat replacer. Obviously such a product combines ideally with lysin-poor cereal-based food products.
Oil droplets in a well homogenised emulsion typically exhibit droplet diameters between 1 to 10 micron diameter. The scientific literature claims that the fatty mouthfeel of such emulsions is almost entirely based on the mere presence of such droplets or particles in the solution. Nowadays many fat replacer products exist that are based on this principle. Ingredients for such fat replacers include starch, cellulose, pectin and proteins. For nutritionally optimised products, a potato protein based fat replacer could be desirable.
To test the latter concept, undenatured potato protein of the invention was processed to obtain hollow particles with an average diameter between 2 and 10, micron. Although different techniques are known for the production of such particles, for the purpose of this example we have used a technique described in WO 94/08627 (incorporated herein be reference) . In this approach 20 grams of undenatured potato protein was dissolved in 150 ml of water containing 0.75 grams of sodium chloride and subsequently atomised at a temperature of 220 "C inlet temperature (92*C outlet
temperature) . To render the hollow protein vesicles formed less water-soluble, after atomising the vesicles were subjected to an¬ other heat treatment for 30 minutes at 175"C. Finally, size distribution of the vesicles formed was tested in a Coulter LS particle analyser. According to the data obtained the average particle diameter in this experiment was 7 microns. The resulting powdered vesicles were then added in a concentration of 10% to a pre-gelatinised solution of 6% potato starch (Paselli BC from AVEBE, Holland) . After complete homogenisation of the dry potato vesicles in the starch, solution, the sample was tasted. For reference 10% homogenates of respectively egg-protein (Omegalux PI9, Henningsen and Van der Burg, Holland) and 10% undenatured potato protein material of the invention in 6% potato starch, were included in the test. The following data summarise the results obtained.
Table 4 Mouthfeel experiment
poor; (±) moderate; (+) good; (++) excellent
Example 11 Breakfast cereals made with potato protein Potato protein is rich in lysine and as such an excellent supplement for lysin-poor proteins such as those of cereals. This complementary relationship has not only been historically proven but has also been shown in several scientific publications (e.g. Kofranyi, E. and Jekat, F. Die biologische Wertigkeit von Kartoffelproteinen. Westdeutscher Verlag, Kόln (1965) . Therefore, in the health food sector, the combination of potato protein and, for example, breakfast cereals is desirable. The following example illustrates one route to provide such a combination.
Typical starting materials for cereal breakfast foods include corn, wheat and rice. Because of the relatively low protein content of these products, it would be desirable to optimise this protein in terms of amino acid composition. Because of the 'poor- in-lysin' nature of cereal proteins, these products would certainly benefit from a combination with a lysin-rich vegetable protein. Although the preparation of granular-type breakfast products is rather complicated, the incorporation of other ingre¬ dients in such a product during dough mixing is easy. Depending upon the desired amino acid balance, the ratio between whole wheat flour and potato protein added can be chosen. Adding up to 300 g potato protein per kg of whole wheat flour, yielded no unfavourable textural changes in the final crumb structure. Apart from granular-type cereals, reasonable amounts of potato protein could be incorporated in other ready-to-serve cereals as long as dosage of the dissolved potato protein is followed by adequate heating to gel the protein completely.
Example 12 Pet food made with potato protein Another example illustrating the wide applicability of undenatured potato protein is in pet food manufacturing. In this field the unique thermogelling properties of the protein can be used in waterbinding to replace hydrocolloids like carrageenan, xanthan, guar or locust bean. Although quite effective in waterbinding, disadvantage of the latter compounds is that digestion in the gut is not without difficulties so that phenomena like diarrhoea and flatulence can occur. The following recipe specifies a canned meat product from which hydrocolloids have been removed and replaced by potato protein.
w/w
Meat (chunks) 50%
Water 37.5%
Undenatured potato protein 4% Plasma 0.5%,
Gelatin 3%
Flour 5%
After preliminary mixing of the ingredients, water is added. The wet mix is then filled into cans and sterilised. Gelling occurs during sterilisation.
Example 13 Low Fat Yogurt
Potato protein was evaluated in a low fat yogurt formulation which was cultured with the protein present.
Ingredients % w/w
1. Skimmed Milk Powder 3.5
2. Skimmed Milk 96.5
Preparation Method: 1. Switch on the proving oven and start boiling the water in the bain marie 2. Weigh milk into bain marie
3. Disperse blended dry ingredients into milk using whisk
4. Place wooden spoon in bain marie and tare balance 5. Heat and hold the milk for 7 minutes at 90°C, stirring continuously 6. Remove from heat and add back lost water
7. Cool samples to 44°C in the cold store
8. Make up the culture - 10 grams of culture to 100 grams of skimmed milk
9. To each 1 kg batch add 4 grams of culture mix. Culture all batches at the same time
10. Pour 800 grams into labelled Hamilton beakers
11. Incubate in the proving oven until the pH is between 4.6 - 4.7
12. Remove from the proving oven and Braun (shear) each yogurt in the Hamilton beakers. 10 short bursts - any viscosity lost will recur once cooled
13. Cool to 20°C in a sink with the coll packs and water 14. Parafilm the beakers and place in cold store overnight
The following day:
15. Measure the pH (approximately pH 4.2) , mix the yogurts well with a hand whisk and transfer,into pots
16. Silversoning grainy yogurts (fine head, 3000rpm for 2 minutes) at this stage gives a smooth final product
The samples which were evaluated were (i) low fat yogurt (reference) and (ii) low fat yogurt + 1% potato protein
The results were as follows:
The reference yielded a yogurt with a thin, smooth and continuous texture, typical of low-fat yogurt. The potato protein yogurt had thicker texture than the reference, which can be attributed to its outstanding gelling properties.
Example 14 Whipped Cream
An assessment of whipping capability was made through addition of 1% potato protein to double cream (48% milk fat) and whisking the resulting mixture for 3 minutes. The samples evaluated in this way were as follows:
(i) Double cream (reference) (ii) Double cream + 1% potato protein (iii) Double cream + 1% sodium caseinate
The results were as follows:
(i) Double cream: after 3 minutes, the cream had formed a texture like butter.
(ii) Double cream + 1% potato protein: after 3 minutes, the foam successfully held air, it was softer than the double cream and almost cuttable and pasty.
(iii) Double cream + 1% sodium caseinate: after 3 minutes, the cream plus caseinate had formed butter similar to the cream alone.
This shows that potato protein can form a stable foam at long whisking. It also shows that potato protein can be used to form a stable foam in the presence of high fat (48% milk fat) . These observations are unusual for protein foaming agents, which tend to form a butter at long whisking.
Example 15 Imitation Whipping Cream,
Imitation whipping cream formulations normally contain sodium caseinate. This example shows the impact of replacing the caseinate with undenatured potato protein or water.
Ingredients Reference Test 1 Test 2
% w/w %w/w % w/w
1 Skimmed Milk Powder Sol. (9%) 61.903 61.903 61.903
2 Hydrogenated Palm Kernal Oil 29.000 29.000 29.000
3 Sucrose 5.000 5.000 5.000
4 Sodium Caseinate-Alanate 180 3.000
5 Acidin N12 Veg 0.800 0.800 0.800
6 Panodan-165 0.100 0.100 0.100
7 Alginate-FD155 0.070 0.070 0.070
8 Cream Flavour-LC 24049 WA 0.125 0.125 0.125
9 Beta-Carotene-5% Emulsion 0.002 0.002 0.002
10 Water - 3.000
11 Potato Protein - - 3.000
Preparation Method
1. Shear in the skimmed milk powder and potato protein when added. Allow to hydrate overnight.
2. Melt the HPKO and Acidin N12 Veg in the microwave until liquid.
3. Add the panodan, sodium caseinate, betacarotene and flavour to the skimmed milk powder solution. Heat to 70°C. Dry blend the alginate with sugar and disperse into the heated skimmed milk powder solution, mix in well. 4. Add the fat phase and heat to 85°C, hold for 15 seconds and cool to 75°C.
5. Shear using the ultratorrex on a medium speed for 2 minutes.
6. Cool rapidly, stirring at regular intervals.
7. Age for 24 hrs before whipping. 8. Whisk in a Hobart bowl for 4 minutes on speed 3. 9. Transfer to suitable container.
After preparation, the imitation cream formulations were aged at 4°C for 24 hours prior to evaluation by whipping on a Hobart mixer at speed 3 for 4 minutes. The potato protein imitation whipping cream could be stored for 48 hrs at 4°C without syneresis (phase separation) , which was observed in the other two samples.
Example 16 Confectionery formulation
Undenatured potato protein was used in a confectionery formulation using the following recipe.
Ingredients:
157 ml light corn syrup 72 ml light brown sugar 30 ml hot water 30 g (10%) native potato protein
1. Make a hot sugar syrup, by boiling to 100°C (special procedure for specific sugar crystallisation)
2. Whip whipping agent until stiff point 3. Add hot sugar syrup while whipping
4. Pour in container (store: 7°C, 20°C)
A foamed product was formed. This shows that undenatured potato protein of the invention also retains its foaming capacity in the presence of high sugar syrup.
Claims
1. A process for the preparation of undenatured potato protein in which a fraction comprising undenatured potato protein is s subjected to concentration and, optionally, drying which process is characterised in that the temperatures in the steps preceding the drying of the fraction do not exceed 40°C.
0 2. A process according to claim l which is characterised in that the fraction comprising the undenatured potato protein is subjected to a pre-treatment at a temperature in the range of 10 to 40°C before the fraction is concentrated.
s 3. A process according to claim 1 or 2 which is characterised m that the fraction comprising the undenatured potato protein is concentrated at a temperature in the range of 15 to 25°C, and, optionally, dried at a product temperature which does not exceed 75°C. 0
4. A process according to claim 2 or 3, which is characterised in that the fraction comprising the undenatured protein is pre-treated by flocculation.
5. A process according to claim 4, which is characterised in that the flocculation is carried out by mixing the fraction comprising the undenatured potato protein with calcium and phosphate compounds.
6. A process according to claim 1-5, which is characterised in that the fraction comprising the undenatured potato protein is concentrated by ultrafiltration.
7. A process according to claim 1-6, which is characterised in
35 that the concentrate is dried by freeze-drymg at a temperature lower than 35°C.
8. A process according to claim 6, which is characterised in that the concentrate after ultrafiltration is subjected to diafiltration before the concentrate is dried.
9. A process according to claim 1-8, which is characterised in that the fraction comprising the undenatured potato protein is potato fruit juice.
10. A food composition comprising undenatured potato protein as obtainable by a process according to claims 1-9 as an additive or an ingredient.
11. A food composition according to claim 10 which is essentially a non-potato food product.
12. A food composition according to claim 11 in which all or a portion of the fat, protein or hydrocolloids is replaced by undenatured potato protein.
13. A food composition according to claim 12, wherein the food composition is a bakery product, preferably a pastry.
14. A whipped food composition comprising undenatured potato protein as an ingredient.
15. A meringue in which all or a portion of the egg white is replaced by undenatured potato protein.
16. A mousse in which all or a portion of the egg white or casein is replaced by undenatured potato protein.
17. A food composition according to claim 12, wherein the food composition is a dairy, meat, pet food or fish product.
18. A process for the preparation of a fat substitute comprising processing undenatured potato protein.
19. A fat substitute obtainable by a process according to claim 18.
20. A method for changing a food composition comprising the addition of undenatured potato protein to said food composition, optionally replacing all or a part of a constituent selected from the group consisting of fat, protein and hydrocolloids.
21. The use of undenatured potato protein to minimise syneresis in a whipped food product.
22. The use of undenatured potato protein to completely or partially replace fat, protein or hydrocolloids.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP97924968A EP0912105A1 (en) | 1996-05-13 | 1997-05-12 | Novel food compositions |
Applications Claiming Priority (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP96201300 | 1996-05-13 | ||
| EP96201299 | 1996-05-13 | ||
| EP96201299 | 1996-05-13 | ||
| EP96201300 | 1996-05-13 | ||
| EP97924968A EP0912105A1 (en) | 1996-05-13 | 1997-05-12 | Novel food compositions |
| PCT/EP1997/002596 WO1997042834A1 (en) | 1996-05-13 | 1997-05-12 | Novel food compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP0912105A1 true EP0912105A1 (en) | 1999-05-06 |
Family
ID=26142792
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP97924968A Withdrawn EP0912105A1 (en) | 1996-05-13 | 1997-05-12 | Novel food compositions |
Country Status (6)
| Country | Link |
|---|---|
| EP (1) | EP0912105A1 (en) |
| CN (1) | CN1218371A (en) |
| AU (1) | AU3028197A (en) |
| CA (1) | CA2253553A1 (en) |
| PL (1) | PL329883A1 (en) |
| WO (1) | WO1997042834A1 (en) |
Families Citing this family (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6280779B1 (en) | 1999-12-28 | 2001-08-28 | Colgate-Palmolive Company | Pet food for maintaining normal bowel health |
| EP1264545A1 (en) * | 2001-06-08 | 2002-12-11 | Coöperatieve Verkoop- en Productievereniging van Aardappelmeel en Derivaten 'AVEBE' B.A. | A method for improving a protein product |
| EP2705849B1 (en) | 2004-07-19 | 2018-04-04 | N.V. Nutricia | A preparation for use of aspartate for regulating glucose levels in blood |
| EP1920662A1 (en) | 2006-11-10 | 2008-05-14 | Coöperatie Avebe U.A. | Native potato protein isolates |
| PL2083636T3 (en) * | 2006-11-10 | 2014-02-28 | Cooperatie Avebe U A | Glycoalkaloid removal |
| CA2669152C (en) * | 2006-11-10 | 2015-04-14 | Cooperatie Avebe U.A. | Glycoalkaloid removal |
| WO2008069649A1 (en) * | 2006-11-10 | 2008-06-12 | Coöperatie Avebe U.A. | Protein gel formation |
| US9480277B2 (en) * | 2007-11-07 | 2016-11-01 | Cooperatic Avebe U.A. | Method for preparing food product |
| FR2944949B1 (en) * | 2009-04-29 | 2011-06-03 | Sas Genialis | PASTRY PASTRY |
| DE102009023740A1 (en) | 2009-06-03 | 2011-07-21 | Süd-Chemie AG, 80333 | Process for separating plant proteins |
| WO2013067453A1 (en) * | 2011-11-02 | 2013-05-10 | Beyond Eggs, Inc. | Plant-based egg substitute and method of manufacture |
| JP2013243990A (en) * | 2012-05-29 | 2013-12-09 | Tsukishima Foods Industry Co Ltd | Foaming composition not containing egg white, meringue-like foamed product, and food |
| CN103875754B (en) * | 2014-03-06 | 2016-03-23 | 天津科技大学 | A deep reddish-brown and high-gloss baked food skin coating liquid and a method for processing baked food using the skin coating liquid |
| CA2956687C (en) * | 2014-09-03 | 2021-02-16 | Cooperatie Avebe U.A. | Flocculation |
| ES2871528T3 (en) * | 2016-02-22 | 2021-10-29 | Cooeperatie Koninklijke Avebe U A | Concentration by freezing of root or tuber juice |
| EP3213638A1 (en) * | 2016-03-01 | 2017-09-06 | Coöperatie Avebe U.A. | Vegan cheese analogue |
| WO2018050708A1 (en) * | 2016-09-13 | 2018-03-22 | Nestec S.A. | Spoonable nutritional composition |
| AU2017327600B2 (en) | 2016-09-13 | 2022-05-19 | Société des Produits Nestlé S.A. | Fermented nutritional composition for cow's milk protein allergic subjects |
| DK3599879T3 (en) * | 2017-03-21 | 2021-02-22 | Cooeperatie Koninklijke Avebe U A | GELATINE-FREE AIR-MIXED CONFECTIONERY PRODUCTS, FOAM STRUCTURING COMPOSITIONS AND MANUFACTURING METHODS |
| CN110461166A (en) * | 2017-03-21 | 2019-11-15 | 艾维贝合作公司 | Gelatin-free aerated confectionery products, foam structure compositions and methods of making them |
| CA3055986C (en) * | 2017-03-31 | 2025-09-16 | J.R. Simplot Company | Potato protein powders |
| MX2022003478A (en) | 2019-09-23 | 2022-04-25 | Unilever Ip Holdings B V | EMULSION OF OIL IN WATER WITH VEGETABLE PROTEINS. |
| EP4167754A2 (en) * | 2020-06-23 | 2023-04-26 | Duynie Holding B.V. | Method for separation of potato proteins with reduced enzymatic activity from potato fruit juice |
| EP4167755A1 (en) * | 2020-06-23 | 2023-04-26 | Duynie Holding B.V. | Method for separation of potato proteins from phenolic and/or glycoalkaloid compounds |
| US20230232860A1 (en) * | 2020-06-23 | 2023-07-27 | Duynie Holding B.V. | Method for separation of potato proteins and insoluble fibers from phenolic and/or glycoalkaloid compounds |
| WO2021260038A1 (en) | 2020-06-23 | 2021-12-30 | Duynie Holding B.V. | Method for separation of potato proteins from phenolic and/or glycoalkaloid compounds |
| EP3944769B1 (en) | 2020-07-30 | 2025-09-03 | Coöperatie Koninklijke Avebe U.A. | Patatin as binder in meat substitutes |
| EP4238425A1 (en) * | 2022-03-04 | 2023-09-06 | Silvan Leibacher | Egg substitute product, method for producing such an egg substitute product and use of such an egg substitute product |
| DE202022105549U1 (en) | 2022-09-30 | 2024-01-03 | Emsland-Stärke Gesellschaft mit beschränkter Haftung | Native functional potato protein |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE688659C (en) * | 1937-01-30 | 1940-02-27 | Norddeutsche Kartoffelmehl Fab | Process for the production of seasonings, nutrients and animal feed from potato fruit water |
| NL6501845A (en) * | 1965-02-15 | 1966-08-16 | ||
| GB1520738A (en) * | 1974-09-23 | 1978-08-09 | Scholten Honig Nv | Production of porotein from non-diluted or diluted potato corm water |
| FR2439791A1 (en) * | 1978-10-27 | 1980-05-23 | Rhone Poulenc Ind | Pure non-denatured plant protein prepn. - e.g. for human nutrition, comprises aq. extract contact with ion exchanger resin, silica or alumina (BE 28.4.80) |
| DE3266590D1 (en) * | 1981-01-21 | 1985-11-07 | Unilever Plc | Lipid and protein containing material in particulate form and process therefor |
-
1997
- 1997-05-12 CN CN97194578A patent/CN1218371A/en active Pending
- 1997-05-12 PL PL97329883A patent/PL329883A1/en unknown
- 1997-05-12 WO PCT/EP1997/002596 patent/WO1997042834A1/en not_active Ceased
- 1997-05-12 AU AU30281/97A patent/AU3028197A/en not_active Abandoned
- 1997-05-12 EP EP97924968A patent/EP0912105A1/en not_active Withdrawn
- 1997-05-12 CA CA002253553A patent/CA2253553A1/en not_active Abandoned
Non-Patent Citations (1)
| Title |
|---|
| See references of WO9742834A1 * |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1218371A (en) | 1999-06-02 |
| PL329883A1 (en) | 1999-04-12 |
| WO1997042834A1 (en) | 1997-11-20 |
| AU3028197A (en) | 1997-12-05 |
| CA2253553A1 (en) | 1997-11-20 |
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