EP0871374A1 - Procede de production d'extrait de levure s'utilisant dans des produits alimentaires, les aromatisants indesirables presents dans ledit extrait ayant ete elimines - Google Patents
Procede de production d'extrait de levure s'utilisant dans des produits alimentaires, les aromatisants indesirables presents dans ledit extrait ayant ete eliminesInfo
- Publication number
- EP0871374A1 EP0871374A1 EP96919846A EP96919846A EP0871374A1 EP 0871374 A1 EP0871374 A1 EP 0871374A1 EP 96919846 A EP96919846 A EP 96919846A EP 96919846 A EP96919846 A EP 96919846A EP 0871374 A1 EP0871374 A1 EP 0871374A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- adsorbent
- yeast extract
- yeast
- flavouring
- extract
- 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- Withdrawn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
- 239000012138 yeast extract Substances 0.000 title claims abstract description 97
- 229940041514 candida albicans extract Drugs 0.000 title claims abstract description 91
- 238000000034 method Methods 0.000 title claims abstract description 50
- 239000000796 flavoring agent Substances 0.000 title claims abstract description 20
- 235000013355 food flavoring agent Nutrition 0.000 title claims abstract description 9
- 239000000284 extract Substances 0.000 title description 12
- 239000003463 adsorbent Substances 0.000 claims abstract description 90
- 240000004808 Saccharomyces cerevisiae Species 0.000 claims abstract description 64
- 235000014680 Saccharomyces cerevisiae Nutrition 0.000 claims abstract description 64
- 239000000126 substance Substances 0.000 claims abstract description 31
- 102000004190 Enzymes Human genes 0.000 claims abstract description 17
- 108090000790 Enzymes Proteins 0.000 claims abstract description 16
- 239000003623 enhancer Substances 0.000 claims abstract description 12
- 229920001429 chelating resin Polymers 0.000 claims description 42
- 238000011282 treatment Methods 0.000 claims description 33
- 239000002773 nucleotide Substances 0.000 claims description 23
- 125000003729 nucleotide group Chemical group 0.000 claims description 22
- 235000013372 meat Nutrition 0.000 claims description 20
- 239000003513 alkali Substances 0.000 claims description 17
- 235000013305 food Nutrition 0.000 claims description 13
- 150000001413 amino acids Chemical class 0.000 claims description 11
- 239000004793 Polystyrene Substances 0.000 claims description 10
- 229920002223 polystyrene Polymers 0.000 claims description 10
- 230000003301 hydrolyzing effect Effects 0.000 claims description 9
- 108091005804 Peptidases Proteins 0.000 claims description 8
- 239000004365 Protease Substances 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 8
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 claims description 7
- 230000015556 catabolic process Effects 0.000 claims description 6
- 238000006731 degradation reaction Methods 0.000 claims description 6
- 102000004196 processed proteins & peptides Human genes 0.000 claims description 6
- 108090000765 processed proteins & peptides Proteins 0.000 claims description 6
- MYRTYDVEIRVNKP-UHFFFAOYSA-N divinylbenzene Substances C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 claims description 5
- 235000013599 spices Nutrition 0.000 claims description 5
- 102000006382 Ribonucleases Human genes 0.000 claims description 4
- 108010083644 Ribonucleases Proteins 0.000 claims description 4
- -1 acryl skeleton Chemical group 0.000 claims description 4
- 229920000642 polymer Polymers 0.000 claims description 4
- 235000020991 processed meat Nutrition 0.000 claims description 4
- 235000011888 snacks Nutrition 0.000 claims description 4
- 229920001577 copolymer Polymers 0.000 claims description 3
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 claims description 3
- 238000000746 purification Methods 0.000 claims description 3
- 238000011084 recovery Methods 0.000 claims description 3
- 241000251468 Actinopterygii Species 0.000 claims description 2
- 241000238424 Crustacea Species 0.000 claims description 2
- 241000287828 Gallus gallus Species 0.000 claims description 2
- 235000013351 cheese Nutrition 0.000 claims description 2
- 238000001035 drying Methods 0.000 claims description 2
- 229920001568 phenolic resin Polymers 0.000 claims description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 1
- 230000000593 degrading effect Effects 0.000 abstract description 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 26
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 24
- 235000019640 taste Nutrition 0.000 description 24
- 235000019658 bitter taste Nutrition 0.000 description 18
- 238000012360 testing method Methods 0.000 description 16
- 239000000725 suspension Substances 0.000 description 14
- 239000000047 product Substances 0.000 description 12
- 239000007787 solid Substances 0.000 description 12
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 10
- RQFCJASXJCIDSX-UUOKFMHZSA-N guanosine 5'-monophosphate Chemical compound C1=2NC(N)=NC(=O)C=2N=CN1[C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]1O RQFCJASXJCIDSX-UUOKFMHZSA-N 0.000 description 10
- 235000013928 guanylic acid Nutrition 0.000 description 10
- 235000013902 inosinic acid Nutrition 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 235000019634 flavors Nutrition 0.000 description 8
- 239000011148 porous material Substances 0.000 description 7
- 239000003456 ion exchange resin Substances 0.000 description 6
- 229920003303 ion-exchange polymer Polymers 0.000 description 6
- 229920005989 resin Polymers 0.000 description 6
- 239000011347 resin Substances 0.000 description 6
- DJJCXFVJDGTHFX-XVFCMESISA-N uridine 5'-monophosphate Chemical compound O[C@@H]1[C@H](O)[C@@H](COP(O)(O)=O)O[C@H]1N1C(=O)NC(=O)C=C1 DJJCXFVJDGTHFX-XVFCMESISA-N 0.000 description 6
- 210000005253 yeast cell Anatomy 0.000 description 6
- 239000011780 sodium chloride Substances 0.000 description 5
- 150000003512 tertiary amines Chemical class 0.000 description 5
- 208000035404 Autolysis Diseases 0.000 description 4
- 206010057248 Cell death Diseases 0.000 description 4
- 150000001450 anions Chemical class 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N formaldehyde Natural products O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 4
- 102000004169 proteins and genes Human genes 0.000 description 4
- 108090000623 proteins and genes Proteins 0.000 description 4
- 230000028043 self proteolysis Effects 0.000 description 4
- 229930010555 Inosine Natural products 0.000 description 3
- UGQMRVRMYYASKQ-KQYNXXCUSA-N Inosine Chemical compound O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C2=NC=NC(O)=C2N=C1 UGQMRVRMYYASKQ-KQYNXXCUSA-N 0.000 description 3
- UDMBCSSLTHHNCD-KQYNXXCUSA-N adenosine 5'-monophosphate Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]1O UDMBCSSLTHHNCD-KQYNXXCUSA-N 0.000 description 3
- 235000019568 aromas Nutrition 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229960003786 inosine Drugs 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 230000008929 regeneration Effects 0.000 description 3
- 238000011069 regeneration method Methods 0.000 description 3
- UDMBCSSLTHHNCD-UHFFFAOYSA-N Coenzym Q(11) Natural products C1=NC=2C(N)=NC=NC=2N1C1OC(COP(O)(O)=O)C(O)C1O UDMBCSSLTHHNCD-UHFFFAOYSA-N 0.000 description 2
- NYHBQMYGNKIUIF-UUOKFMHZSA-N Guanosine Chemical group C1=NC=2C(=O)NC(N)=NC=2N1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O NYHBQMYGNKIUIF-UUOKFMHZSA-N 0.000 description 2
- 229930193815 Isohumulone Natural products 0.000 description 2
- 229920002774 Maltodextrin Polymers 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- OIRDTQYFTABQOQ-KQYNXXCUSA-N adenosine Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O OIRDTQYFTABQOQ-KQYNXXCUSA-N 0.000 description 2
- 229950006790 adenosine phosphate Drugs 0.000 description 2
- 239000003957 anion exchange resin Substances 0.000 description 2
- 239000011324 bead Substances 0.000 description 2
- 238000005119 centrifugation Methods 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000012467 final product Substances 0.000 description 2
- 239000002655 kraft paper Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000000194 supercritical-fluid extraction Methods 0.000 description 2
- 125000001302 tertiary amino group Chemical group 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 1
- MEUAVGJWGDPTLF-UHFFFAOYSA-N 4-(5-benzenesulfonylamino-1-methyl-1h-benzoimidazol-2-ylmethyl)-benzamidine Chemical compound N=1C2=CC(NS(=O)(=O)C=3C=CC=CC=3)=CC=C2N(C)C=1CC1=CC=C(C(N)=N)C=C1 MEUAVGJWGDPTLF-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 239000002126 C01EB10 - Adenosine Substances 0.000 description 1
- MIKUYHXYGGJMLM-GIMIYPNGSA-N Crotonoside Natural products C1=NC2=C(N)NC(=O)N=C2N1[C@H]1O[C@@H](CO)[C@H](O)[C@@H]1O MIKUYHXYGGJMLM-GIMIYPNGSA-N 0.000 description 1
- NYHBQMYGNKIUIF-UHFFFAOYSA-N D-guanosine Natural products C1=2NC(N)=NC(=O)C=2N=CN1C1OC(CO)C(O)C1O NYHBQMYGNKIUIF-UHFFFAOYSA-N 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- GRSZFWQUAKGDAV-KQYNXXCUSA-N IMP Chemical compound O[C@@H]1[C@H](O)[C@@H](COP(O)(O)=O)O[C@H]1N1C(NC=NC2=O)=C2N=C1 GRSZFWQUAKGDAV-KQYNXXCUSA-N 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 102000035195 Peptidases Human genes 0.000 description 1
- 102000004167 Ribonuclease P Human genes 0.000 description 1
- 108090000621 Ribonuclease P Proteins 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 241000006364 Torula Species 0.000 description 1
- 241000222354 Trametes Species 0.000 description 1
- DJJCXFVJDGTHFX-UHFFFAOYSA-N Uridinemonophosphate Natural products OC1C(O)C(COP(O)(O)=O)OC1N1C(=O)NC(=O)C=C1 DJJCXFVJDGTHFX-UHFFFAOYSA-N 0.000 description 1
- 238000005903 acid hydrolysis reaction Methods 0.000 description 1
- 229960005305 adenosine Drugs 0.000 description 1
- LNQVTSROQXJCDD-UHFFFAOYSA-N adenosine monophosphate Natural products C1=NC=2C(N)=NC=NC=2N1C1OC(CO)C(OP(O)(O)=O)C1O LNQVTSROQXJCDD-UHFFFAOYSA-N 0.000 description 1
- 235000013405 beer Nutrition 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 210000002421 cell wall Anatomy 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- IERHLVCPSMICTF-XVFCMESISA-N cytidine 5'-monophosphate Chemical compound O=C1N=C(N)C=CN1[C@H]1[C@H](O)[C@H](O)[C@@H](COP(O)(O)=O)O1 IERHLVCPSMICTF-XVFCMESISA-N 0.000 description 1
- IERHLVCPSMICTF-UHFFFAOYSA-N cytidine monophosphate Natural products O=C1N=C(N)C=CN1C1C(O)C(O)C(COP(O)(O)=O)O1 IERHLVCPSMICTF-UHFFFAOYSA-N 0.000 description 1
- 239000008121 dextrose Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 229940116441 divinylbenzene Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 230000002255 enzymatic effect 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
- 238000000855 fermentation Methods 0.000 description 1
- 230000004151 fermentation Effects 0.000 description 1
- 229960005191 ferric oxide Drugs 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000001963 growth medium Substances 0.000 description 1
- 229940029575 guanosine Drugs 0.000 description 1
- 239000002198 insoluble material Substances 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 125000003010 ionic group Chemical group 0.000 description 1
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
- QARXXMMQVDCYGZ-UHFFFAOYSA-N isohumulone Chemical compound CC(C)CC(=O)C1=C(O)C(O)(C(=O)CC=C(C)C)C(CC=C(C)C)C1=O QARXXMMQVDCYGZ-UHFFFAOYSA-N 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 238000009629 microbiological culture Methods 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 230000001172 regenerating effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000002798 spectrophotometry method Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N1/00—Microorganisms, e.g. protozoa; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor
- C12N1/005—Microorganisms, e.g. protozoa; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor after treatment of microbial biomass not covered by C12N1/02 - C12N1/08
-
- 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
- A23J1/18—Obtaining protein compositions for foodstuffs; Bulk opening of eggs and separation of yolks from whites from yeasts
-
- 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
- A23J3/00—Working-up of proteins for foodstuffs
- A23J3/20—Proteins from microorganisms or unicellular algae
-
- 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
- A23J3/00—Working-up of proteins for foodstuffs
- A23J3/30—Working-up of proteins for foodstuffs by hydrolysis
- A23J3/32—Working-up of proteins for foodstuffs by hydrolysis using chemical agents
- A23J3/34—Working-up of proteins for foodstuffs by hydrolysis using chemical agents using enzymes
- A23J3/347—Working-up of proteins for foodstuffs by hydrolysis using chemical agents using enzymes of proteins from microorganisms or unicellular algae
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
- A23L27/20—Synthetic spices, flavouring agents or condiments
- A23L27/23—Synthetic spices, flavouring agents or condiments containing nucleotides
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
- A23L27/20—Synthetic spices, flavouring agents or condiments
- A23L27/24—Synthetic spices, flavouring agents or condiments prepared by fermentation
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- 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
- A23L33/14—Yeasts or derivatives thereof
- A23L33/145—Extracts
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L5/00—Preparation or treatment of foods or foodstuffs, in general; Food or foodstuffs obtained thereby; Materials therefor
- A23L5/20—Removal of unwanted matter, e.g. deodorisation or detoxification
- A23L5/27—Removal of unwanted matter, e.g. deodorisation or detoxification by chemical treatment, by adsorption or by absorption
- A23L5/273—Removal of unwanted matter, e.g. deodorisation or detoxification by chemical treatment, by adsorption or by absorption using adsorption or absorption agents, resins, synthetic polymers, or ion exchangers
Definitions
- the invention relates to a method of producing and treating a yeast extract to remove unpleasant odour and flavouring components from the yeast extract while maintaining the desirable flavouring agents in the yeast extract.
- the method of the invention improves the quality of the final yeast extract product such that it can be used e.g. as a flavouring enhancer or a flavouring in food industry.
- the invention also relates to a yeast extract produced by the method and to use of the yeast extract as a flavouring enhancer or flavouring or a component of the same in food industry.
- the method of the invention is based on the use of polymeric adsorbents.
- the method is particularly well-suited for brewer's yeast extracts, and it can also be applied to yeast extracts of other origin, such as baker's yeast extracts.
- a yeast extract produced from brewer's yeast also comprises unpleasant flavouring components that impart a bitter and yeasty flavour. These unpleasant flavouring components are primarily derived from a hop extract used in brewing, the extract containing bitter substances that adsorb to the surface of the yeast.
- the bitter substances the most significant of which is isohumulone (structurally an ⁇ -resin acid) , restrict the use of a brewer's yeast extract as a foodstuff, so they must be removed to produce a passable final product.
- the use of a baker's yeast extract is in some cases hindered by its too distinctive yeasty flavour and odour and by its bitterness.
- the polymeric adsorbent treatment according to the invention reduces the yeasty odour and flavour and the bitterness.
- bitter substances are conventionally removed by treating the brewer's yeast with alkali, whereby the isohumulones are dissolved and can be washed off.
- Alkali wash of yeast is described e.g. in Process Biochemistry (1966) no. 9, p. 316, and it is also mentioned in U.S. Patent 4,097,614 (West, S.M., Kraft Foods Ltd.) .
- alkali wash however, some of the valuable proteins of yeast are lost in the soluble phase.
- Bitter substances can also be removed from the yeast cell tissue by supercritical extraction. The use of supercritical extraction is described in EP Bl 0,041,723 (Eisenbach, W.
- Brewer's yeast is thereby treated with C0 2 , ethane, ethylene and/or propane under hypercritical conditions of pressure and temperature, and the gas loaded with bitter substances is passed through an adsorbent (activated carbon) to purify the gas.
- adsorbent activated carbon
- U.S. Patent 2,149,306 (Millar, J.H. , Arthur Guinness Son and Company) teaches the use of autolysis for producing a soluble food extract from brewer's yeast. After the autolysis, the yeast extract is purified by treating it with activated carbon. Activated carbon is known to effectively remove bitter substances from a yeast extract, but it has the clear disadvantage that it also adsorbs some of the desirable nucleotides and proteins and that it is difficult to filter. It should also be noted that powdery activated carbon can be used, in principle, only once, whereas granulated activated carbon can be regenerated, although the regeneration must be performed outside the process.
- brewer's yeast should be treated with porous material produced e.g. from an activated carbon-PVA-iron-oxide mixture (U.S. Patent 4,097,614, West, S.M., Kraft Foods Ltd.) .
- the adsorbent used can be regenerated e.g. with lye.
- U.S. Patent 3,443,969 (Nakajima, N. et al . ,
- a yeast extract can be produced by hydrolysing yeast cell tissue with acid or enzymes.
- the enzymes may be derived from the yeast cell tissue itself or they may be specific enzymes, proteases, ribonucleases and deaminases that have been added. Enzymatic production of yeast extracts is described e.g. in U.S. patents 3,914,450 (Robbins, E.A. et al . , Anheuser-Busch Inc.) , 3,443,969 (Nakajima, N. , Takeda Chemical Industries Ltd.) and 5,288,509 (Potman, R.P., Lever Brothers Company) , in EP Al 299,078 (Harada, S. et al .
- 'yeast extract' is a solution obtained by degrading a yeast cell tissue with enzymes present in the yeast itself (autolysis) , with added enzymes or acid under specific conditions, and by separating the components extracted from the degraded yeast cell mass to water.
- a brewer's yeast extract is a product obtained in the above manner using as a starting material a residual yeast obtained in a beer fermentation process and separated therefrom.
- a baker's yeast extract is a product produced in the above manner using, baker's yeast, e.g. Saccharomyces cerevisiae, as yeast.
- the invention relates to a method of producing a yeast extract suitable for use in foodstuffs, the method comprising the following steps :
- the hydrolytic degradation (a) can be performed enzymatically either by the action of the enzymes of the yeast itself (autolysis) , or with specifically added enzymes, or by acid hydrolysis.
- the method can also comprise an alkali wash prior to the hydrolytic treatment (a) .
- the product purified with an adsorbent is also usually dried, using e.g. spray drying.
- the hydrolytic degradation (a) is advantageously performed enzymatically.
- prior art can be applied (see e.g. above- mentioned U.S. Patents 3,914,450, 3,443,969 and 5,288,509, EP Al 299,078, and Japanese Patent Application JP 57-219695) .
- the degradation usually comprises one or more enzyme treatments. It is possible to conduct e.g. only a protease treatment or e.g. a three-step enzyme treatment comprising a protease treatment, ribonuclease treatment and deaminase treatment (see e.g. EP Al 299,078) .
- the protease treatment breaks the cell walls of yeast, whereby RNA and amino acids are released.
- the ribonuclease treatment splits the RNA of yeast cells into different nucleotides, and the deaminase treatment converts adenosine mononucleotide (AMP, adenosine monophosphate) into inosine mononucleotide (IMP, inosine mono ⁇ phosphate) , which is a desirable nucleotide component with respect to flavour.
- AMP adenosine mononucleotide
- IMP inosine mono ⁇ phosphate
- GMP guanosine mononucleotide
- a specific example for an enzyme treatment is a treatment with protease, 5' -phosphodiesterase and 5'- adenylic acid deaminase (Japanese patent application JP 57-219695) .
- step (b) of the method according to the invention i.e. recovery of soluble substances obtained from the hydrolytic treatment, it is also possible to apply the technique known per se.
- a soluble fraction that comprises the desirable components but also comprises non-desirable bitter substances can be separated from an insoluble fraction e.g. by separation.
- alkali treatment of the method according to the invention
- An alkali wash can be performed e.g. with a NaOH solution. It removes some of the bitter substances but also some of the desirable proteins. If an alkali wash is used in combination with an adsorbent treatment according to the invention, a product containing but few bitter substances is obtained. When the alkali wash is left out, i.e. replaced with an adsorbent treatment, a corresponding product is obtained but the adsorbent capacity is naturally lower, since the amount of removable bitter substances per dry solids is greater.
- Step (c) of the method according to the invention i.e. purification of the resultant yeast extract, is performed with polymeric adsorbents.
- the invention also relates to a method of treating a yeast extract useable in foodstuffs by contacting it with a polymeric adsorbent.
- the invention relates to a method of removing bitter substances, yeastiness and other undesirable flavouring agents from a yeast extract by contacting the yeast extract with a polymeric adsorbent that binds bitter substances and other undesirable flavouring agents but does not bind peptides, amino acids or nucleotides to a significant extent .
- polymeric adsorbents any polymer based adsorbents that bind undesirable bitter substances to a significant extent but do not bind essential quantities of desirable peptides, amino acids and nucleotides that provide the taste profile.
- important parameters are its pore size and specific surface. Essential characteristics are also its water retention capacity, porosity and controlled pore size distribution.
- non-ionic macroporous polymeric adsorbents or slightly basic macroporous polymeric adsorbents.
- the purpose of the ionic groups, if present, is to improve the hydrophilic properties of the adsorbent.
- the pore size of the polymeric adsorbents is in the range of 25 to 1000 A (2.5 to 100 nm) and preferably 200 to 500 A (20 to 50 nm) and the specific surface thereof is in the range of 150 to 1500 m 2 /g.
- the polymeric adsorbent is preferably an adsorbent having a polystyrene skeleton and optionally comprising weakly basic groups, e.g. a styrene/divinyl- benzene copolymer based adsorbent.
- adsorbent is Amberlite XAD-16 (by Rohm & Haas) .
- Amberlite XAD-7 by Rohm & Haas
- Amberlite XAD-7 by Rohm & Haas
- Amberlite XAD 765 (by Rohm & Haas) .
- Amberlite XAD-16 is a non-ionic macroporous crosslinked polystyrene that is commercially available as 0.3 to 1.2 mm beads, has a water retention capacity of 64 to 68%, pore size of 200 to 250 A (20 to 25 nm) , specific surface of at least 750 m 2 /g and porosity of 0.58 to 0.63 ml pores/ml of beads.
- the adsorbent treatment is usually carried out in conventional columns. It can be carried out at a temperature of 5 to 100°C, preferably at 10 to 25°C.
- the pH may vary from 1 to 14, preferably it is from 4 to 6.
- the dry solids content of the yeast extract used may be 0.1 to 70%, preferably 2 to 6%.
- the flow rate at which the yeast extract is passed through the adsorbent column may vary from 0.1 to 70 resin volume/h (RV/h) , preferably it is from 5 to 40 RV/h, most preferably from 10 to 20 RV/h.
- the adsorbent column may be regenerated with NaOH and subsequently neutralized with HCl, but a good result is also obtained by using only NaOH regeneration.
- the following advantages are achieved with the polymer adsorbent treatment according to the invention: losses of desirable flavouring agents are negligible, it is easy to use in continuous processes and can be regenerated in position as part of the process, bitter substances are removed effectively, and the meat taste of the yeast product is intensified. If the alkali wash is left out altogether and the debittering is conducted entirely by the adsorbent treatment, the yield of flavouring components of the yeast extract is higher, since dissolving of proteins caused by the alkali wash is hereby avoided.
- the invention also relates to a yeast extract product produced by the above methods.
- the yeast extract product may be a brewer's yeast extract or a baker's yeast extract.
- a yeast extract produced in accordance with the invention can be used as a flavouring enhancer or a flavouring in different foodstuff applications, optionally in combination with other flavouring enhancers and flavourings. It can be used as such or mixed e.g. with salt, dextrose or maltodextrine to provide a flavouring enhancer for finished and semifinished food products, processed meat, spice mixtures and snacks.
- the yeast extract according to the invention can also be used as a flavouring together with e.g. baking aromas in corresponding food products. It can also be used as an intermediate when different flavourings and baking aromas are prepared, the yeast extract usually undergoing Maillard reactions during the preparation.
- the invention thus also relates to the use of a yeast extract as a flavouring enhancer or flavouring or a component of the same in foodstuffs, such as finished and semifinished food products, processed meat, spice mixtures and snacks.
- a yeast extract as a flavouring enhancer or flavouring or a component of the same in foodstuffs, such as finished and semifinished food products, processed meat, spice mixtures and snacks.
- Example 1A The starting yeast extract (brewer's yeast extract) can be produced as follows:
- a brewer's yeast suspension (20% d.s., pH 6.3) obtained as a side fraction of brewer's yeast is heated (300 g based on dry solids) to a temperature of 80 to 100°C about 30 minutes and subsequently cooled to 50°C.
- Example IB (Daiwa Kasei K.K.) is added to the yeast suspension, and the enzyme is allowed to effect for 10 hours, while the suspension is stirred. After the reaction, the temperature of the suspension is raised to 80°C for 30 minutes, after which the suspension is cooled to 65°C. After this, 0.2 g of enzyme Ribonuclease P (Amano Pharmaceutical Ltd.) is added to the suspension, and the suspension is stirred slowly for three hours. The suspension is cooled to 45°C, and 0.2 g of enzyme Deamizyme (Amano Pharmaceuticals Ltd.) is added to it, after which stirring is continued at this temperature for two hours . The insoluble material is removed from the suspension e.g. by centrifugation to produce a brewer's yeast extract for an adsorbent treatment.
- Example IB Example IB
- the produced brewer's yeast extract that contained 2.7% of dry solids was treated with different adsorbents and ion exchange resins by passing 3000 ml of the yeast extract solution (pH 5.7, temperature 20 to 25°C) at a flow rate of 600 ml/h through a column (500 ml, diameter 2.5 cm) packed with 200 ml of test materials mentioned in table 1, i.e. regenerated adsorbent (Optipore, Amberlite XAD-16) , ion exchange resin (Amberlite IRA 68, Amberlite IRA 958) or granulated activated carbon (Chemviron SA) .
- GMP guanosine monophosphate
- IMP inosine monophosphate
- Optipore weakly basic adsorbent with polystyrene skeleton
- Amberlite XAD-16 non-ionic adsorbent with polystyrene skeleton
- Amberlite IRA 68 weakly basic anion exchanger with polyacrylic skeleton containing tertiary amino groups
- Amberlite IRA 958 strongly basic anion exchanger having a polyacrylic skeleton and containing quaternary ammonium groups
- Table 2 shows the results of a test in which the treatment was performed otherwise in the same way as above but the pH of the yeast extract solution supplied to the column was 4.5 and Optipore and XAD-16 were neutralized after NaOH regeneration with HCl.
- the table shows that polymeric adsorbents removed bitterness more effectively than e.g. powdery activated carbon or ion exchange resins.
- the reduction of bitterness intensified the meat taste evidently because the components concealing the taste were removed.
- the losses of dry solids and nucleotides were clearly smaller when polymeric adsorbents were used.
- the losses of those nucleotide components that are the most valuable with respect to flavour, i.e. GMP and IMP were negligible when adsorbent Amberlite XAD-16 was used.
- Example 2 A brewer's yeast suspension (10% d.s.) obtained as a by-product in brewing was treated with alkali by adjusting its pH to 9 and was stirred for 30 minutes at 25°C. The suspension was subjected to centrifugation to produce an alkali washed brewer's yeast suspension (23% d.s.) , which was washed three times with water to remove the alkali. A brewer's yeast extract that contained 3.3% of dry solids was produced from the suspension and used in the tests that followed.
- the extract was treated with adsorbents Amberlite XAD-16 and Amberlite XAD 765 by passing 23 1 of the yeast extract solution (pH 5.7, temperature 20 to 25°C) at a flow rate of 5 1/h through a column packed with 500 ml of a regenerated adsorbent.
- the adsorbents were regenerated for removal of bitter substances by regenerating with 4% NaOH (2.5 RV) , washing with water (10 RV) , neutralizing with 5% HCl (0.5 RV) and washing with water (8 RV) .
- Cycle length 1500 g d.s./l litre of resin.
- Amberlite XAD 765 a slightly basic adsorbent with phenolformaldehyde skeleton containing few tertiary amino groups
- An alkali washed brewer's yeast extract was produced in the same way as in example 2.
- the extract contained 3.5% of dry solids.
- Removal of bitter substances and other undesirable components was carried out by passing 88 1 of the yeast extract solution (pH 5.7, temperature 20 to 25°C) at a flow rate of 10 1/h through a column packed with 700 ml of adsorbent Amberlite XAD-16.
- the adsorbent had been regenerated with 4% NaOH (1.7 1) , washed with water (6 1) , neutralized with 5% HCl (0.35 1) , and washed with water (7 1) .
- 10 1 fractions were collected and subjected to an organoleptic test to evaluate their bitterness.
- a baker's yeast extract was produced from a commercially available baker's yeast suspension (23% d.s.) by the use of enzymes in the same way as in example 1A.
- the extract contained 5.8% of dry solids. Removal of bitter substances and other undesirable components was carried out by passing 50 1 of the yeast extract solution at a flow rate of 10 1/h (pH 5.7, temperature 12°C) through a column packed with 700 ml of adsorbent Amberlite XAD-16.
- the adsorbent had been regenerated with 4% NaOH (1.7 1) , washed with water (5 1) , neutralized with 5% HCl (0.35 1) and washed with water (7 1) .
- the 50 1 fraction of a baker's yeast extract passed through the column was analyzed for the dry solids content, amino acids, nucleotides and bitterness. Organoleptic estimation of bitterness was conducted on a 2% solution with a pH of 5.5. The effect of the adsorbent treatment in the light of the results measured is presented in table 5. The number of components imparting an unpleasant flavour ('yeasty flavour') and odour for a baker's yeast extract was reduced and the meat taste was intensified when the extract was treated with adsorbent Amberlite XAD-16. Further, no significant losses of nucleotides or amino acids seemed to result from the treatment .
- Table 6 presents a summary of the properties of the adsorbents of the invention and the ion exchange resins (comparison) used in the above examples for debittering a yeast extract .
- Table 7 presents a summary of the test results of debittering a yeast extract .
- a yeast extract produced in accordance with the above examples can be used for the preparation of flavouring enhancers and flavourings.
- Flavouring enhancer compositions comprising 45 to 100%, preferably 70 to 90%, of a yeast extract according to the invention, 0 to 30%, preferably 10 to 20%, of NaCl, and 0 to 20% of other components, such as sugar, were produced.
- Flavouring compositions comprising 1 to 80%, preferably 10 to 50%, of a yeast extract according to the invention, 5 to 60%, preferably 20 to 40%, of baking aromas, 0 to 20% of NaCl, and 0 to 40% of other components, such as sugar, maltodextrine, lactose and mixed spices, were also produced.
- flavouring enhancer and flavouring compositions were used in the production of finished and semifinished food products, processed meat, spice mixtures and snacks.
- organoleptic tests conducted the taste of the food products containing a yeast extract according to the invention was found excellent.
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Abstract
L'invention concerne un procédé de production d'un extrait de levure s'utilisant dans des produits alimentaires, obtenu par décomposition de la levure par voie hydrolytique, de préférence avec des enzymes, par récupération des substances solubles et par purification de la solution qui en résulte avec un adsorbant polymère. L'invention concerne en outre un procédé permettant d'éliminer les substances amères, le goût de levure et/ou d'autres aromatisants indésirables contenus dans l'extrait de levure, par traitement de l'extrait de levure avec un adsorbant polymère. L'extrait de levure peut être un extrait de levure de bière ou de levure de boulanger. L'invention concerne en outre un extrait de levure obtenu à l'aide dudit procédé et son utilisation comme aromatisant, activateur d'aromatisants ou de constituant de ceux-ci, dans des produits alimentaires.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FI952726 | 1995-06-02 | ||
FI952726A FI952726A (fi) | 1995-06-02 | 1995-06-02 | Menetelmä ruokatuotteen valmistamiseksi |
PCT/FI1996/000326 WO1996038057A1 (fr) | 1995-06-02 | 1996-05-31 | Procede de production d'extrait de levure s'utilisant dans des produits alimentaires, les aromatisants indesirables presents dans ledit extrait ayant ete elimines |
Publications (1)
Publication Number | Publication Date |
---|---|
EP0871374A1 true EP0871374A1 (fr) | 1998-10-21 |
Family
ID=8543529
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP96919846A Withdrawn EP0871374A1 (fr) | 1995-06-02 | 1996-05-31 | Procede de production d'extrait de levure s'utilisant dans des produits alimentaires, les aromatisants indesirables presents dans ledit extrait ayant ete elimines |
Country Status (4)
Country | Link |
---|---|
EP (1) | EP0871374A1 (fr) |
AU (1) | AU5823596A (fr) |
FI (1) | FI952726A (fr) |
WO (1) | WO1996038057A1 (fr) |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FI109759B (fi) | 1996-12-23 | 2002-10-15 | Suomen Rehu Oy | Ravinnon lisäaineen käyttö |
US6387420B1 (en) * | 1996-12-23 | 2002-05-14 | Juhani Vuorenmaa | Procedure for preparing a food additive, and an additive and its use |
EP0920812B1 (fr) * | 1997-04-16 | 2003-07-09 | Sapporo Breweries Ltd. | Procede permettant de preparer de l'extrait de levure |
AU4292000A (en) * | 1999-03-30 | 2000-10-23 | Hans Drexel | Method of seasoning food |
DE19922362A1 (de) * | 1999-03-30 | 2000-10-05 | Hans Drexel | Verfahren zum Würzen von Nahrungsmitteln |
US6974597B2 (en) * | 1999-11-29 | 2005-12-13 | Kyowa Hakko Kogyo Co., Ltd. | Method of enhancing salty taste, salty taste enhancer, salty taste seasoning agent and salty taste-enhanced foods |
FI114895B (fi) * | 2001-05-14 | 2005-01-31 | Suomen Rehu Oy | Ravinnon lisäaine |
FR2825004B1 (fr) * | 2001-05-22 | 2005-02-11 | Bio Springer | Produit dietetique satiant |
EP1662893B9 (fr) * | 2003-08-15 | 2008-10-15 | Grain Processing Corporation | Procede de dissociation cellulaire |
EP2532232A1 (fr) | 2011-06-10 | 2012-12-12 | InterMed Discovery GmbH | Glycolipides à longue chaîne utiles pour éviter l'altération ou la contamination microbienne de matériaux |
EP2737808A1 (fr) * | 2012-11-30 | 2014-06-04 | Symrise AG | Additifs alimentaires |
CN116406758A (zh) * | 2021-12-30 | 2023-07-11 | 安琪酵母(德宏)有限公司 | 一种浅色酵母抽提物的制备方法 |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB933828A (en) * | 1959-07-20 | 1963-08-14 | Takeda Pharmaceutical | A process for preparing condiments |
US4097614A (en) * | 1975-12-24 | 1978-06-27 | Kraft Foods Limited | Method of removing bitter substances from brewers yeast and brewers yeast autolysates |
CH635491A5 (fr) * | 1979-01-26 | 1983-04-15 | Nestle Sa | Procede de desamerisation d'un hydrolysat de proteines et hydrolysat desamerise obtenu. |
-
1995
- 1995-06-02 FI FI952726A patent/FI952726A/fi not_active Application Discontinuation
-
1996
- 1996-05-31 EP EP96919846A patent/EP0871374A1/fr not_active Withdrawn
- 1996-05-31 AU AU58235/96A patent/AU5823596A/en not_active Abandoned
- 1996-05-31 WO PCT/FI1996/000326 patent/WO1996038057A1/fr not_active Application Discontinuation
Non-Patent Citations (1)
Title |
---|
KIRK-OTHMER: "Encyclopedia of Chemical Technology,Vol.14", 1995, J.WILEY&SONS INC., USA * |
Also Published As
Publication number | Publication date |
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AU5823596A (en) | 1996-12-18 |
FI952726A (fi) | 1996-12-03 |
FI952726A0 (fi) | 1995-06-02 |
WO1996038057A1 (fr) | 1996-12-05 |
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