JPH01171454A - Mixed sweetener - Google Patents
Mixed sweetenerInfo
- Publication number
- JPH01171454A JPH01171454A JP62328439A JP32843987A JPH01171454A JP H01171454 A JPH01171454 A JP H01171454A JP 62328439 A JP62328439 A JP 62328439A JP 32843987 A JP32843987 A JP 32843987A JP H01171454 A JPH01171454 A JP H01171454A
- Authority
- JP
- Japan
- Prior art keywords
- product
- taste
- stevia
- glycosylglycyrrhizin
- sweetener
- 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.)
- Pending
Links
- 235000003599 food sweetener Nutrition 0.000 title claims abstract description 36
- 239000003765 sweetening agent Substances 0.000 title claims abstract description 36
- HELXLJCILKEWJH-NCGAPWICSA-N rebaudioside A Chemical compound O([C@H]1[C@H](O)[C@@H](CO)O[C@H]([C@@H]1O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)O[C@]12C(=C)C[C@@]3(C1)CC[C@@H]1[C@@](C)(CCC[C@]1([C@@H]3CC2)C)C(=O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O HELXLJCILKEWJH-NCGAPWICSA-N 0.000 claims abstract description 24
- 241000544066 Stevia Species 0.000 claims abstract description 23
- 241000202807 Glycyrrhiza Species 0.000 claims description 19
- 235000001453 Glycyrrhiza echinata Nutrition 0.000 claims description 18
- 235000006200 Glycyrrhiza glabra Nutrition 0.000 claims description 18
- 235000017382 Glycyrrhiza lepidota Nutrition 0.000 claims description 18
- 229940010454 licorice Drugs 0.000 claims description 18
- 239000000284 extract Substances 0.000 claims description 14
- 239000008123 high-intensity sweetener Substances 0.000 claims description 13
- 235000013615 non-nutritive sweetener Nutrition 0.000 claims description 13
- 239000012043 crude product Substances 0.000 claims description 4
- 239000000047 product Substances 0.000 abstract description 42
- 235000019640 taste Nutrition 0.000 abstract description 38
- 235000009508 confectionery Nutrition 0.000 abstract description 9
- 239000012264 purified product Substances 0.000 abstract description 5
- 239000000126 substance Substances 0.000 abstract description 3
- 235000019605 sweet taste sensations Nutrition 0.000 abstract description 3
- 239000003814 drug Substances 0.000 abstract 1
- 229940079593 drug Drugs 0.000 abstract 1
- 239000004378 Glycyrrhizin Substances 0.000 description 17
- 229960004949 glycyrrhizic acid Drugs 0.000 description 17
- LPLVUJXQOOQHMX-UHFFFAOYSA-N glycyrrhetinic acid glycoside Natural products C1CC(C2C(C3(CCC4(C)CCC(C)(CC4C3=CC2=O)C(O)=O)C)(C)CC2)(C)C2C(C)(C)C1OC1OC(C(O)=O)C(O)C(O)C1OC1OC(C(O)=O)C(O)C(O)C1O LPLVUJXQOOQHMX-UHFFFAOYSA-N 0.000 description 16
- UYRUBYNTXSDKQT-UHFFFAOYSA-N glycyrrhizic acid Natural products CC1(C)C(CCC2(C)C1CCC3(C)C2C(=O)C=C4C5CC(C)(CCC5(C)CCC34C)C(=O)O)OC6OC(C(O)C(O)C6OC7OC(O)C(O)C(O)C7C(=O)O)C(=O)O UYRUBYNTXSDKQT-UHFFFAOYSA-N 0.000 description 16
- 235000019410 glycyrrhizin Nutrition 0.000 description 16
- LPLVUJXQOOQHMX-QWBHMCJMSA-N glycyrrhizinic acid Chemical compound O([C@@H]1[C@@H](O)[C@H](O)[C@H](O[C@@H]1O[C@@H]1C([C@H]2[C@]([C@@H]3[C@@]([C@@]4(CC[C@@]5(C)CC[C@@](C)(C[C@H]5C4=CC3=O)C(O)=O)C)(C)CC2)(C)CC1)(C)C)C(O)=O)[C@@H]1O[C@H](C(O)=O)[C@@H](O)[C@H](O)[C@H]1O LPLVUJXQOOQHMX-QWBHMCJMSA-N 0.000 description 16
- 230000000694 effects Effects 0.000 description 15
- 238000000034 method Methods 0.000 description 14
- 239000000203 mixture Substances 0.000 description 9
- 235000002639 sodium chloride Nutrition 0.000 description 9
- 239000007864 aqueous solution Substances 0.000 description 7
- 235000019658 bitter taste Nutrition 0.000 description 7
- 235000019606 astringent taste Nutrition 0.000 description 6
- 239000004615 ingredient Substances 0.000 description 6
- 229940069445 licorice extract Drugs 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 206010013911 Dysgeusia Diseases 0.000 description 5
- -1 Organic acid salts Chemical class 0.000 description 5
- 239000000796 flavoring agent Substances 0.000 description 5
- 235000019634 flavors Nutrition 0.000 description 5
- 235000013305 food Nutrition 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- 239000008187 granular material Substances 0.000 description 5
- 239000001509 sodium citrate Substances 0.000 description 5
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 5
- 241000251468 Actinopterygii Species 0.000 description 4
- 229920001353 Dextrin Polymers 0.000 description 4
- 239000004375 Dextrin Substances 0.000 description 4
- 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 4
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 4
- 229920002472 Starch Polymers 0.000 description 4
- 229940024606 amino acid Drugs 0.000 description 4
- 235000001014 amino acid Nutrition 0.000 description 4
- 150000001413 amino acids Chemical class 0.000 description 4
- 235000019425 dextrin Nutrition 0.000 description 4
- 239000008103 glucose Substances 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 238000000746 purification Methods 0.000 description 4
- 239000008107 starch Substances 0.000 description 4
- 235000019698 starch Nutrition 0.000 description 4
- 230000002195 synergetic effect Effects 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 108090000790 Enzymes Proteins 0.000 description 3
- 102000004190 Enzymes Human genes 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 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 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 239000008101 lactose Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 150000007524 organic acids Chemical class 0.000 description 3
- 235000021110 pickles Nutrition 0.000 description 3
- 235000021067 refined food Nutrition 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 235000013311 vegetables Nutrition 0.000 description 3
- QNAYBMKLOCPYGJ-UHFFFAOYSA-N Alanine Chemical compound CC([NH3+])C([O-])=O QNAYBMKLOCPYGJ-UHFFFAOYSA-N 0.000 description 2
- 108010025880 Cyclomaltodextrin glucanotransferase Proteins 0.000 description 2
- 239000004471 Glycine Substances 0.000 description 2
- 244000294411 Mirabilis expansa Species 0.000 description 2
- 235000015429 Mirabilis expansa Nutrition 0.000 description 2
- YBHQCJILTOVLHD-YVMONPNESA-N Mirin Chemical compound S1C(N)=NC(=O)\C1=C\C1=CC=C(O)C=C1 YBHQCJILTOVLHD-YVMONPNESA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 235000011194 food seasoning agent Nutrition 0.000 description 2
- 238000004128 high performance liquid chromatography Methods 0.000 description 2
- 238000005342 ion exchange Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 230000000873 masking effect Effects 0.000 description 2
- 235000013372 meat Nutrition 0.000 description 2
- 235000013536 miso Nutrition 0.000 description 2
- LPUQAYUQRXPFSQ-DFWYDOINSA-M monosodium L-glutamate Chemical compound [Na+].[O-]C(=O)[C@@H](N)CCC(O)=O LPUQAYUQRXPFSQ-DFWYDOINSA-M 0.000 description 2
- 235000013923 monosodium glutamate Nutrition 0.000 description 2
- 235000019645 odor Nutrition 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 235000021148 salty food Nutrition 0.000 description 2
- 235000013580 sausages Nutrition 0.000 description 2
- HELHAJAZNSDZJO-OLXYHTOASA-L sodium L-tartrate Chemical compound [Na+].[Na+].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O HELHAJAZNSDZJO-OLXYHTOASA-L 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 239000001433 sodium tartrate Substances 0.000 description 2
- 229960002167 sodium tartrate Drugs 0.000 description 2
- 235000011004 sodium tartrates Nutrition 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 235000013555 soy sauce Nutrition 0.000 description 2
- 230000002747 voluntary effect Effects 0.000 description 2
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- CHHHXKFHOYLYRE-UHFFFAOYSA-M 2,4-Hexadienoic acid, potassium salt (1:1), (2E,4E)- Chemical compound [K+].CC=CC=CC([O-])=O CHHHXKFHOYLYRE-UHFFFAOYSA-M 0.000 description 1
- KZMAWJRXKGLWGS-UHFFFAOYSA-N 2-chloro-n-[4-(4-methoxyphenyl)-1,3-thiazol-2-yl]-n-(3-methoxypropyl)acetamide Chemical compound S1C(N(C(=O)CCl)CCCOC)=NC(C=2C=CC(OC)=CC=2)=C1 KZMAWJRXKGLWGS-UHFFFAOYSA-N 0.000 description 1
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 1
- 239000004475 Arginine Substances 0.000 description 1
- 108010011485 Aspartame Proteins 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 229920000858 Cyclodextrin Polymers 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- 239000004278 EU approved seasoning Substances 0.000 description 1
- 239000001512 FEMA 4601 Substances 0.000 description 1
- 239000005715 Fructose Substances 0.000 description 1
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 description 1
- ODKSFYDXXFIFQN-BYPYZUCNSA-P L-argininium(2+) Chemical compound NC(=[NH2+])NCCC[C@H]([NH3+])C(O)=O ODKSFYDXXFIFQN-BYPYZUCNSA-P 0.000 description 1
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 description 1
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- HELXLJCILKEWJH-SEAGSNCFSA-N Rebaudioside A Natural products O=C(O[C@H]1[C@@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1)[C@@]1(C)[C@@H]2[C@](C)([C@H]3[C@@]4(CC(=C)[C@@](O[C@H]5[C@H](O[C@H]6[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O6)[C@@H](O[C@H]6[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O6)[C@H](O)[C@@H](CO)O5)(C4)CC3)CC2)CCC1 HELXLJCILKEWJH-SEAGSNCFSA-N 0.000 description 1
- 241000785681 Sander vitreus Species 0.000 description 1
- 239000001744 Sodium fumarate Substances 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- UEDUENGHJMELGK-HYDKPPNVSA-N Stevioside Chemical compound O([C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1O[C@]12C(=C)C[C@@]3(C1)CC[C@@H]1[C@@](C)(CCC[C@]1([C@@H]3CC2)C)C(=O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O UEDUENGHJMELGK-HYDKPPNVSA-N 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229960003767 alanine Drugs 0.000 description 1
- 235000004279 alanine Nutrition 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 description 1
- 239000000605 aspartame Substances 0.000 description 1
- 235000010357 aspartame Nutrition 0.000 description 1
- IAOZJIPTCAWIRG-QWRGUYRKSA-N aspartame Chemical compound OC(=O)C[C@H](N)C(=O)N[C@H](C(=O)OC)CC1=CC=CC=C1 IAOZJIPTCAWIRG-QWRGUYRKSA-N 0.000 description 1
- 229960003438 aspartame Drugs 0.000 description 1
- 235000003704 aspartic acid 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
- OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 235000013365 dairy product Nutrition 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 235000011850 desserts Nutrition 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- WPUMTJGUQUYPIV-JIZZDEOASA-L disodium (S)-malate Chemical compound [Na+].[Na+].[O-]C(=O)[C@@H](O)CC([O-])=O WPUMTJGUQUYPIV-JIZZDEOASA-L 0.000 description 1
- MSJMDZAOKORVFC-SEPHDYHBSA-L disodium fumarate Chemical compound [Na+].[Na+].[O-]C(=O)\C=C\C([O-])=O MSJMDZAOKORVFC-SEPHDYHBSA-L 0.000 description 1
- 229950010030 dl-alanine Drugs 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- HELXLJCILKEWJH-UHFFFAOYSA-N entered according to Sigma 01432 Natural products C1CC2C3(C)CCCC(C)(C(=O)OC4C(C(O)C(O)C(CO)O4)O)C3CCC2(C2)CC(=C)C21OC(C1OC2C(C(O)C(O)C(CO)O2)O)OC(CO)C(O)C1OC1OC(CO)C(O)C(O)C1O HELXLJCILKEWJH-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 229940049906 glutamate Drugs 0.000 description 1
- 229930195712 glutamate Natural products 0.000 description 1
- 238000006206 glycosylation reaction Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 235000015243 ice cream Nutrition 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- LTINPJMVDKPJJI-UHFFFAOYSA-N iodinated glycerol Chemical compound CC(I)C1OCC(CO)O1 LTINPJMVDKPJJI-UHFFFAOYSA-N 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- 229940099690 malic acid Drugs 0.000 description 1
- 238000001471 micro-filtration Methods 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 239000004223 monosodium glutamate Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 230000008092 positive effect Effects 0.000 description 1
- 239000004302 potassium sorbate Substances 0.000 description 1
- 229940069338 potassium sorbate Drugs 0.000 description 1
- 235000010241 potassium sorbate Nutrition 0.000 description 1
- 235000020991 processed meat Nutrition 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 235000019633 pungent taste Nutrition 0.000 description 1
- 235000019203 rebaudioside A Nutrition 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 235000019204 saccharin Nutrition 0.000 description 1
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
- 229940081974 saccharin Drugs 0.000 description 1
- 239000000901 saccharin and its Na,K and Ca salt Substances 0.000 description 1
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 1
- 235000014102 seafood Nutrition 0.000 description 1
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 1
- 230000035807 sensation Effects 0.000 description 1
- 235000019615 sensations Nutrition 0.000 description 1
- 235000019265 sodium DL-malate Nutrition 0.000 description 1
- 229960001790 sodium citrate Drugs 0.000 description 1
- 229940005573 sodium fumarate Drugs 0.000 description 1
- 235000019294 sodium fumarate Nutrition 0.000 description 1
- 229940073490 sodium glutamate Drugs 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 239000001394 sodium malate Substances 0.000 description 1
- 229940074404 sodium succinate Drugs 0.000 description 1
- ZDQYSKICYIVCPN-UHFFFAOYSA-L sodium succinate (anhydrous) Chemical compound [Na+].[Na+].[O-]C(=O)CCC([O-])=O ZDQYSKICYIVCPN-UHFFFAOYSA-L 0.000 description 1
- WTWSHHITWMVLBX-DKWTVANSSA-M sodium;(2s)-2-aminobutanedioate;hydron Chemical compound [Na+].[O-]C(=O)[C@@H](N)CC(O)=O WTWSHHITWMVLBX-DKWTVANSSA-M 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 229940013618 stevioside Drugs 0.000 description 1
- OHHNJQXIOPOJSC-UHFFFAOYSA-N stevioside Natural products CC1(CCCC2(C)C3(C)CCC4(CC3(CCC12C)CC4=C)OC5OC(CO)C(O)C(O)C5OC6OC(CO)C(O)C(O)C6O)C(=O)OC7OC(CO)C(O)C(O)C7O OHHNJQXIOPOJSC-UHFFFAOYSA-N 0.000 description 1
- 235000019202 steviosides Nutrition 0.000 description 1
- 235000019465 surimi Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 229960001367 tartaric acid Drugs 0.000 description 1
- 235000021419 vinegar Nutrition 0.000 description 1
- 239000000052 vinegar Substances 0.000 description 1
Landscapes
- Seasonings (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は高甘味度甘味料を用いた混合甘味料に於いて、
α−グリコシルグリチルリチン(以下、α−GGと略記
する)を規定量の範囲で共存せしめることにより、従来
解決し得なかった味質上、物性上の問題点を大幅に改善
する方法に関するものである。[Detailed description of the invention] [Industrial application field] The present invention relates to a mixed sweetener using a high-intensity sweetener,
This invention relates to a method for significantly improving taste and physical property problems that could not be solved in the past by allowing α-glycosylglycyrrhizin (hereinafter abbreviated as α-GG) to coexist within a specified amount. .
高甘味度甘味料の1種類または2種類に味質や物性の改
善目的で有機酸塩類、アミノ酸類などを加え、更にay
mなどで倍散して粉体状若しくは顆粒状に成型して供用
されている。Organic acid salts, amino acids, etc. are added to one or two types of high-intensity sweeteners for the purpose of improving taste quality and physical properties.
It is used after being triturated with m, etc. and molded into powder or granules.
(発明が解決しようとする問題点〕
高甘味度甘味料を混合甘味料として用いる理由は数拾倍
から数百倍と云う高い甘味を倍数材により適度な倍率に
迄希釈することにより作業性の向上を図る他に次の様な
目的を持っている。(Problem to be solved by the invention) The reason why a high-intensity sweetener is used as a mixed sweetener is that the high sweetness, which is several tens to hundreds of times sweeter, is diluted to an appropriate ratio with a multiplier, thereby improving workability. In addition to improving performance, the following objectives are also in place:
第1に高甘味度甘味料が本来持っている甘味質の改善で
ある。例えば甘草抽出物に就いて言えば、独特の臭気、
苦味、渋味、夫れに砂糖に比べて味の立ち上がりが遅く
、後味がいつ迄も継続する欠点がある点である。Firstly, it improves the inherent sweetness of high-intensity sweeteners. For example, licorice extract has a unique odor,
It has the disadvantages of bitterness and astringency, both of which are slow to develop compared to sugar, and the aftertaste that lasts for a long time.
そこでDL−アラニン、グリシンなどのアミノ酸類やク
エン酸ナトリウム、酒石酸ナトリウムなどの有機酸塩類
を配合することにより、之等の味質上の欠点を矯正し様
という試みが行なわれ(特公昭49−7227) 、こ
の方法が現在でも主流を占めている。しかもこの方法も
欠点の一部の改善にしか過ぎず、2等添加物が独自の味
質を持っている点からも添加量には自ずから制限があり
、本来の目的を達成するには未だ不充分な状況である。Therefore, an attempt was made to correct these taste defects by adding amino acids such as DL-alanine and glycine, and organic acid salts such as sodium citrate and sodium tartrate (Special Publications Publication No. 1973- 7227), and this method still occupies the mainstream. Moreover, this method only improves a part of the drawbacks, and since secondary additives have their own taste qualities, there is a natural limit to the amount of additives added, and it is still insufficient to achieve the original purpose. The situation is sufficient.
第2に甘草抽出物は水に対する溶解度が低く、高濃度や
PHの低い状態では、ゲル状になったり不溶解物として
沈殿を生じる。之に対して有機酸塩の添加が溶解性の改
善に有効であるとして、味質改善に要する量以上に大量
の有機酸塩が配合される例がある。しかしこの方法も食
品に使用される段階では必ずしも満足の行く結果が得ら
れていない。本発明は之等従来の混合甘味料の持つ問題
点を解決せんとするものである。Second, licorice extract has low solubility in water, and at high concentrations or low pH conditions, it becomes gel-like or precipitates as an insoluble substance. However, since the addition of organic acid salts is effective in improving solubility, there are examples in which a large amount of organic acid salts is added in an amount greater than the amount required to improve taste quality. However, this method does not always give satisfactory results when used in food products. The present invention aims to solve these problems with conventional mixed sweeteners.
グリチルリチンは甘草(Glycyrrhiza gl
abraLINNE’ war)の根及びストロンに含
まれる甘味成分で1通常は水で抽出後、pH2前後の酸
性下で沈殿させて得られる粗製品と、之を更にアルコー
ルに溶解して晶析やイオン交換などの精製工程を経て得
られる精製品とがある。之等は独特の甘味を有しており
、日中に入れてからの甘味の発現が遅く、また可成り長
時間に渉って甘味が持続する上□に、渋味や甘草具と言
われる臭気が存在するので、単品で砂糖や異性化糖の代
替として使われることは少ない。一方、この呈味曲線が
食塩のそれに類似していて1食塩の辛味、刺激性をマス
キングする所謂塩馴れ効果が強いので漬物、味噌、醤油
。Glycyrrhizin is found in licorice (Glycyrrhiza GL)
AbraLINNE' war) is a sweet ingredient contained in the root and stolone.1 It is usually extracted with water and then precipitated under acidic conditions around pH 2 to obtain a crude product, which is further dissolved in alcohol and subjected to crystallization or ion exchange. There are purified products obtained through purification processes such as These have a unique sweet taste, and the onset of sweetness is slow after being eaten during the day, and the sweetness lasts for quite a long time. Due to its odor, it is rarely used alone as a substitute for sugar or high-fructose sugar. On the other hand, this taste curve is similar to that of table salt, and it has a strong so-called salt-acclimating effect that masks the spiciness and irritation of single table salt, so it is used in pickles, miso, and soy sauce.
佃煮、水産練製品、珍味の用途には広く使われている。It is widely used in tsukudani, seafood paste products, and delicacies.
その際、味質上の欠点を改善する目的で前述の様に他成
分を混合する方法以外にグリチルリチンそのものに酵素
を用いてグルコースを付加する方法が提案されている(
特開昭62−259594) 、之によればα−GGの
製造法は概路次の通りである。In this case, in addition to the method of mixing other ingredients as mentioned above, a method of adding glucose to glycyrrhizin itself using an enzyme has been proposed in order to improve the taste defects (
According to Japanese Unexamined Patent Publication No. 62-259594), the outline of the method for producing α-GG is as follows.
即ち上記文献の特許請求の範囲第1項によればrグリチ
ルリチンと澱粉質とを含有する水溶液に、シクロデキス
トリングルカノトランスフェラーゼを作用させてα−グ
リコジル残基がグリチルリチンに等モル以上結合したα
−グリコシルグリチルリチンを生成せしめ、之を採取す
ることを特徴とするα−グリコシルグリチルリチンの製
造方法。」とあり、その結果として「α−GGが従来の
グリチルリチン製品とは全く違って、
(1)嫌味、薬品臭が無く、円やかな甘味を呈する。That is, according to claim 1 of the above-mentioned document, cyclodextrin glucanotransferase is applied to an aqueous solution containing r-glycyrrhizin and starch to form an α-glycodyl residue bound to glycyrrhizin in equal mole or more.
- A method for producing α-glycosylglycyrrhizin, which comprises producing glycosylglycyrrhizin and collecting the same. As a result, ``α-GG is completely different from conventional glycyrrhizin products in that: (1) It has no unpleasant taste or chemical odor, and has a mild sweet taste.
(2)甘味が速く現われ、後味として長く尾を引かない
。(2) Sweetness appears quickly and does not linger as an aftertaste.
(3)酸性下においても沈殿形成、ゲル形成が極度に抑
えられる。(3) Precipitate formation and gel formation are extremely suppressed even under acidic conditions.
(4)泡立ちが抑制され、取り扱いが容易となる。(4) Foaming is suppressed and handling becomes easy.
など甘味料として極めて優れた性質を有していることを
見い出した。」と述べられている。本発明者等は上記混
合甘味料の抱えている問題点解決のため特開昭62−2
59594による上記製品を利用すべく種々検討を重ね
た結果、本発明に到達した。It was discovered that it has extremely excellent properties as a sweetener. ” is stated. In order to solve the problems faced by the above-mentioned mixed sweeteners, the inventors of the present invention have proposed
As a result of various studies to utilize the above-mentioned product manufactured by No. 59594, we have arrived at the present invention.
ここで本発明に用いるα−GGはグリチルリチン分子1
モルにグルコース分子が1モル以上付加したものであれ
ばよく、不純分の比率や反応に供した澱粉質残存の有無
或いはその量は問わない。Here, α-GG used in the present invention is glycyrrhizin molecule 1
It is sufficient that one mole or more of glucose molecules is added to each mole, and the ratio of impurities and the presence or absence of starch remaining in the reaction and its amount do not matter.
即ちα−グリコジル化に供する甘草抽出物には、粗製品
から純品に近い高純度の製品迄あり、何れの場合でも酵
素を付加することによって大幅に味質の向上することが
確認されているからである。In other words, licorice extracts that can be subjected to α-glycosylation range from crude products to highly purified products, and in all cases, it has been confirmed that the addition of enzymes significantly improves the taste quality. It is from.
また例えばグルコースの供与体として用いられたデキト
スリンの一部が残っていても最終製品の味質には殆んど
影響を与えないからである。Furthermore, even if a portion of dextothrin used as a glucose donor remains, it will hardly affect the taste of the final product.
ここに用いられる高甘味度甘味料としては我国で流通し
ている一般的な製品を対象とするが、本発明では混合甘
味料を可能な限り天然の製品で構成したいという意図が
あるので、天然の高甘味度甘味料として甘草精製物、甘
草粗製物、ステビア抽出物それに糖付加ステビアが適当
である。The high-intensity sweetener used here is a general product distributed in Japan, but since the intention of the present invention is to make the mixed sweetener as natural as possible, Suitable high-intensity sweeteners include purified licorice, crude licorice, stevia extract, and sugar-added stevia.
之等の高甘味度甘味料は夫々単独では、欠点を持ってい
るが、α−GGの併用により、之等欠点が矯正されたり
、従来認められなかった特性が得られるからである。These high-intensity sweeteners each have drawbacks when used alone, but when used in combination with α-GG, these drawbacks can be corrected or properties not previously recognized can be obtained.
一般に混合甘味料に添加するアミノ酸類はアラニン、グ
リシン、グルタミン酸ナトリウム、アスパラギン酸ナト
リウム、アスパラギン酸、アルギニン・グルタミン酸塩
などが用いられるが何れも高甘味度甘味料の味質矯正が
主目的であり、一部甘味度の向上を期待出来るものもあ
る。Generally, the amino acids added to mixed sweeteners include alanine, glycine, monosodium glutamate, sodium aspartate, aspartic acid, and arginine/glutamate, but the main purpose of all of these is to correct the taste of high-intensity sweeteners. There are some products that can be expected to improve their sweetness.
しかし混合甘味料の使用対象である加工食品類には2等
アミノ酸類を含んだ物が多いので、対象になる食品によ
ってはアミノ酸添加は必須条件ではない。However, since many of the processed foods for which mixed sweeteners are used contain secondary amino acids, addition of amino acids is not an essential condition for some foods.
一般に用いられる有機酸類としては、クエン酸。Citric acid is a commonly used organic acid.
クエン酸ナトリウム、コハク酸ナトリウム、酒石酸、酒
石酸ナトリウム、フマル酸ナトリウム、リンゴ酸、リン
ゴ酸ナトリウムなどが用いられる。Sodium citrate, sodium succinate, tartaric acid, sodium tartrate, sodium fumarate, malic acid, sodium malate, etc. are used.
一般に高甘味度甘味料は砂糖に比して甘味の発現が遅く
、また後に長く持続すると云う欠点を持っているが、有
機酸類の添加により成る程度矯正出来ると云われている
。In general, high-intensity sweeteners have the disadvantage that the onset of sweetness is slower than that of sugar, and the sweetness persists for a long time, but it is said that this can be corrected to some extent by adding organic acids.
また甘草製品の場合には有機酸塩の添加が水溶液中の溶
解性の向上に役立つことが認められている。It has also been recognized that in the case of licorice products, the addition of organic acid salts helps improve solubility in aqueous solutions.
倍散剤としては乳糖、ブドウ糖、澱粉またはその部分分
解物などが用いられる。As the dispersing agent, lactose, glucose, starch or a partially decomposed product thereof, etc. are used.
之は単に高甘味度甘味料の甘味倍率を適当なレベルに迄
希釈すると云う目的のみでなく、成型する場合には成形
助剤としての役目を有している。This not only serves the purpose of diluting the sweetness ratio of a high-intensity sweetener to an appropriate level, but also serves as a molding aid when molded.
即ちステビア抽出物などはその侭で顆粒にするのは極め
て困望であるが、上記倍散剤を添加することにより作業
性の容易な形状にすることが出来る。That is, it is extremely difficult to form stevia extract into granules, but by adding the above-mentioned dispersing agent, it can be made into a shape that is easy to work with.
混合甘味料の形態は顆粒などの成型品でも、粉体の侭混
合したものでもよく、また場合によっては水溶液でもよ
い。The mixed sweetener may be in the form of a molded product such as granules, a mixture of powders, or an aqueous solution depending on the case.
α−GGは特開昭62−259594に示された方法に
よって生産されるが、前述の様にこのものによる製品は
発成になる甘草抽出物中のグリチルリチン含量に差があ
るから正確に添加率を決めるためにはα−GGの純品を
ベースにしたものでなくてはならない。従って本発明の
範囲、記述に用いられる数量は明示したちの以外は総べ
て純品基準である。α-GG is produced by the method shown in Japanese Patent Application Laid-Open No. 62-259594, but as mentioned above, products made using this method differ in the glycyrrhizin content in the licorice extract, so the addition rate must be determined accurately. In order to determine this, it must be based on a pure α-GG product. Accordingly, all quantities used in the scope and description of the present invention are based on pure products, unless otherwise specified.
本発明に用いられる甘草精製物とは甘草工業懇話会が定
めた甘草抽出物の自主規格の中で定義されたもので、高
速液体クロマトグラフィーによる定量でグリチルリチン
を15%以上含む製品で黄褐色から白色の範囲にある製
品である。このものに対してはα−GGを重量比で0.
02〜1.0共存せしめるのが適当である。The purified licorice used in the present invention is defined in the voluntary standards for licorice extract established by the Licorice Industry Association, and is a product containing 15% or more glycyrrhizin as determined by high-performance liquid chromatography. The product is in the white range. For this product, α-GG was added at a weight ratio of 0.
It is appropriate that 02 to 1.0 coexist.
甘草抽出物は一般に甘味成分であるグリチルリチン以外
にも加工食品中で調味、矯正効果の有る成分が多数存在
していることが知られており、グリチルリチン含量の低
い製品もその他成分をそれなりに評価して取引きされる
ケースが多い、従って本発明に於いてもα−GGがその
他成分に対する作用も含めて考える必要が出て来る。我
々はこの点に就いても種々検討した結果、之等の成分が
通常プラスの効果とは別に渋味、苦味、臭気など、味質
上好ましくない面も有しているのに対して、之等をマス
キングしプラス面を強調する効果も見出した。従って高
純度品に比して低純度品に対してはα−GGをグリチル
リチン含量相当分より多口に添加するのが好ましい。添
加量が0.02より少ない場合は雑味マスキングやグリ
チルリチンの味の切れの改善には不充分であり、また水
溶液の溶解性の改善にも殆んど効果が無い。1.0を超
す場合は甘草抽出物の本来の味質上の特性が活かせなく
なるので、本発明の目的から外れることになる。In addition to glycyrrhizin, which is generally a sweetening ingredient, licorice extract is known to contain many other ingredients that have seasoning and corrective effects in processed foods, and products with low glycyrrhizin content are also evaluated for other ingredients. Therefore, in the present invention, it is necessary to consider the effect of α-GG on other components as well. As a result of various studies on this point, we found that apart from the usual positive effects, these ingredients also have unfavorable taste aspects such as astringency, bitterness, and odor. We also found the effect of masking the negative aspects and emphasizing the positive aspects. Therefore, it is preferable to add α-GG in an amount corresponding to the glycyrrhizin content in a larger amount to a low-purity product than to a high-purity product. If the amount added is less than 0.02, it is insufficient for masking the unpleasant taste and improving the sharpness of the taste of glycyrrhizin, and it is also hardly effective for improving the solubility of an aqueous solution. If it exceeds 1.0, the original taste characteristics of the licorice extract will not be utilized, which will defeat the purpose of the present invention.
甘草粗製物は前記自主規格の定義で高速液体クロマトグ
ラフィーによる定量値が15%未満の製品であって製造
工程で酸祈以外殆んど精製を行なわない黒褐色から黄褐
色の物である。このものは甘草由来の非グリチルリチン
成分の比率が高く、強い独特の雑味を有している。Licorice crude product is defined by the above-mentioned voluntary standards as a product with a quantitative value of less than 15% by high performance liquid chromatography, and is a dark brown to yellowish brown product that undergoes almost no purification other than acid removal during the manufacturing process. This product has a high proportion of non-glycyrrhizin components derived from licorice, and has a strong and unique taste.
従ってこのものにはグリチルリチン含量に対して相対的
に高目に添加するのが好ましく、重量比で0.04〜1
.2の範囲が適当である。 0.04未満では雑味に消
されて効果が発現し壁く、1.2を超すと効果がそれ以
上増加しないから不利である。Therefore, it is preferable to add a relatively high amount of glycyrrhizin to this product, with a weight ratio of 0.04 to 1.
.. A range of 2 is appropriate. If it is less than 0.04, the effect will be lost due to the unpleasant taste, and if it exceeds 1.2, the effect will not increase any further, which is disadvantageous.
尚、甘草製品とα−GGの混合系に於いては各々を単味
系で測定した値よりは常に高い甘味が得られる。一般に
甘味料の混合系に於いては同系の味質の場合、相乗効果
が発現し難いが、上記の混合系で相乗効果の有る事実は
グリチルリチンへの糖の付加前後で甘味の質が変化して
いることを示唆していて大変興味深い。In addition, in a mixed system of a licorice product and α-GG, a sweetness that is always higher than the value measured with a single taste system of each can be obtained. Generally, in a sweetener mixture system, it is difficult to develop a synergistic effect if the taste quality is similar, but the fact that there is a synergistic effect in the above mixture system is that the sweetness quality changes before and after adding sugar to glycyrrhizin. This is very interesting as it suggests that
ステビア抽出物とはステビア蒸葉を通常の方法で抽出、
精製したステビア甘味成分を80〜95%含んだものを
云う0通常の方法とは例えば比較的多量の水で抽出し、
抽出液中の甘味成分を非極性の多孔性樹脂に選択吸着さ
せた後、アルコール溶媒で脱着後に、イオン交換法など
で精製する方法である。しかし本発明に於いては抽出、
精製の方法。What is stevia extract? Stevia steamed leaves are extracted in the usual way.
It refers to a product containing 80 to 95% of purified stevia sweetness components.The usual method is, for example, extraction with a relatively large amount of water,
In this method, sweet components in the extract are selectively adsorbed onto a non-polar porous resin, desorbed with an alcohol solvent, and then purified using an ion exchange method or the like. However, in the present invention, extraction,
Method of purification.
更には得られた製品の甘味成分比、また精製後に添加さ
れた他成分には拘束されるものではない。Furthermore, there are no restrictions on the sweet component ratio of the obtained product or on other components added after purification.
ステビア抽出物の甘味成分は、ステビオサイドを主とし
、他にレバウデイオサイド−A、レバウデイオサイド−
Cなどが存在する。この物の甘味′質は甘草精製物と比
較しても可成り砂糖に近いと云われているが、尚僅かの
苦味と甘味の切れの悪さが用途を制限する傾向にある。The sweet component of stevia extract is mainly stevioside, and also rebaudioside-A and rebaudioside-
There are C, etc. The sweetness of this product is said to be quite close to that of sugar, even compared to refined licorice, but its slightly bitter taste and lack of sweetness tend to limit its uses.
このステビア抽出物にα−GGを共存せしめる場合、重
量比で0゜02〜0.5の範囲が好ましい、この範囲内
ではステビア抽出物の僅かの苦味や渋味のマスキングは
もとより混合甘味料に求められる味のパンチないしは加
工食品中での味の伸びが期待出来る。 0.02未満で
は効果が認められず、0.5を超えると本来の甘味質が
大きく変わるので好ましくない。When α-GG is allowed to coexist with this stevia extract, the weight ratio is preferably in the range of 0°02 to 0.5. Within this range, it can be used not only to mask the slight bitterness and astringency of the stevia extract, but also to be used as a mixed sweetener. It can be expected to provide the desired flavor punch or enhance the taste in processed foods. If it is less than 0.02, no effect will be observed, and if it exceeds 0.5, the original sweetness will change significantly, which is not preferable.
ステビア抽出物とα−GGとの味の調和性は極めて高く
、適度の配合により大変優れた甘味料が得られる。この
傾向は有機酸の共存下でより強調される。The taste harmony between stevia extract and α-GG is extremely high, and an excellent sweetener can be obtained by appropriately blending them. This tendency is more accentuated in the coexistence of organic acids.
糖付加ステビアとは特許第1169566号に示される
方法で生産されるステビア抽出物の味質改良品であって
、このもの自体は苦味、渋味が殆んど無く、後味も幾分
改良されている。しかし砂糖と比較した場合、未だ味の
発現の遅れと後引き、それに味の淡白さが使用上の欠点
とされ、この欠点の改良が大きな課題となっている。Sugar-added stevia is a taste-improved product of stevia extract produced by the method shown in Patent No. 1169566, and this product itself has almost no bitterness or astringency, and the aftertaste has been improved to some extent. There is. However, when compared with sugar, it is still considered to have disadvantages in its use, such as delayed onset of flavor, aftertaste, and bland taste, and improvement of these disadvantages is a major challenge.
本発明者等の検討結果によれば、この物にα−GGを重
量比で0.01〜0.2の範囲で添加することにより上
記欠点が可成り改善出来る。この範囲の添加では味に幅
が出ると共にパンチか加わることにより口中に含んだ際
に前味に感じられる。According to the study results of the present inventors, the above-mentioned drawbacks can be considerably improved by adding α-GG to this product in a weight ratio of 0.01 to 0.2. When added in this range, the taste becomes wider and the punch is added, making it feel like a foretaste when you put it in your mouth.
甘味の後引きは本発明に於いても未だ充分に改善されな
いが、甘味発現のピークが強く感じられることにより相
対的に後引きが弱く感じられる。Although the lingering sweetness has not been sufficiently improved even in the present invention, the lingering sensation is felt to be relatively weak due to the strong peak of sweetness development.
味質に就いては上記の改善以外に、味にコクが付与され
ることにより、より砂糖に近く感じられる様になる。ス
テビア甘味料に就いても混合による甘味度の相乗効果は
認められる。In terms of taste quality, in addition to the above-mentioned improvements, the taste is given a richer taste, making it feel more like sugar. A synergistic effect on sweetness by mixing Stevia sweeteners is also observed.
以上4種類の高甘味度甘味料に対する添加効果を纏めて
列挙すると次の様になる。The effects of addition to the above four types of high-intensity sweeteners are summarized as follows.
即ち各単品で使用する場合に比して、 (1)甘味の立ち上がりが速く感じられる。In other words, compared to when each item is used individually, (1) The onset of sweetness is felt to be rapid.
(2)甘味の後引きが適度に感じられる。(2) A moderate aftertaste of sweetness can be felt.
(3)甘味質にコクと厚みが出る。(3) Adds richness and thickness to the sweetness.
(4)苦味、渋味、臭気などの嫌味がマスキングされる
。(4) Unpleasant tastes such as bitterness, astringency, and odor are masked.
(5)甘味の相乗効果が期待出来る。(5) A synergistic effect of sweetness can be expected.
(6)溶解性が改善され、従来使われていた溶解性改善
剤の使用量の減少、省略が可能である。(6) Solubility is improved, and it is possible to reduce or omit the amount of solubility improvers conventionally used.
以上の効果は上記高甘味度甘味料が複数で存在する場合
でもほぼ同様に発現されることが確認されている。例え
ば甘草精製物としてステビア抽出物の共用などは塩性食
品を対象にした混合甘味料に於いては常識的である。It has been confirmed that the above effects are expressed in substantially the same way even when a plurality of the above-mentioned high-intensity sweeteners are present. For example, it is common sense to use stevia extract as a purified licorice product in mixed sweeteners for salty foods.
またサッカリン、アスパルテームなどの合成甘味料との
共存に於いても類似の効果が期待される。Similar effects are also expected when coexisting with synthetic sweeteners such as saccharin and aspartame.
この様にして調整された混合甘味料は通常、甘草精製物
、甘草粗製物、ステビア抽出物、糖付加ステビアが混合
甘味料若しくは単独で用いられている食品には総べて用
いることが出来るが、その際にも前記の混合甘味料にし
た場合の効果を有効に活かせる様な使い方が好ましい。The mixed sweetener prepared in this way can be used in all foods in which purified licorice, crude licorice, stevia extract, and sugar-added stevia are used as a mixed sweetener or alone. In this case, it is also preferable to use the sweetener in a manner that can effectively utilize the effects of the mixed sweetener described above.
より詳しく述べると、塩性食品類、例えば味噌、醤油、
漬物。To be more specific, salty foods such as miso, soy sauce,
Pickles.
佃煮などやカマボコ、チクワ、魚肉ソーセージ。Tsukudani, kamaboko, chikuwa, and fish sausage.
魚肉ハム、魚肉の揚物類などの水産練製品、ハム。Fish meat ham, fish paste products such as fried fish meat, and ham.
ソーセージなどの畜肉加工製品、塩辛、みりん干しなど
の珍味類などは本来の混合甘味料の用途としては最も適
した物であって効果も発揮し易い。Processed meat products such as sausages, delicacies such as salted fish and dried mirin, etc. are the most suitable mixed sweeteners for which they are most likely to be effective.
更には複合調味料、アイスクリーム、シャーベットなど
の冷菓類、煮豆、天ぷらなどの惣菜類、野菜、果実、山
菜などの缶詰、ビン語順や、乳製品関係に於いても効果
が発揮出来る。Furthermore, it can be effective in complex seasonings, frozen desserts such as ice cream and sherbet, prepared foods such as boiled beans and tempura, canned vegetables, fruits, and wild vegetables, bottle order, and dairy products.
本発明により混合甘味料の食品加工への利用度が高まり
、更に新しい用途の開発も期待出来る。The present invention increases the degree of utilization of mixed sweeteners in food processing, and can also be expected to develop new applications.
実験1
特開昭62−259594の方法に準じ耐熱性のサイク
ロデキストリングリコジルトランスフェラーゼ(特公昭
53−27791)を用いてα−GGを次の条件で生産
した。Experiment 1 α-GG was produced under the following conditions using heat-stable cyclodextrin lycosyltransferase (Japanese Patent Publication No. 53-27791) according to the method of JP-A No. 62-259594.
デキストリン(商品名サンデック70. DE8)
300g苛性ソーダ
6g塩化カルシウム
0.15 g水
1.2QCGTas
e以外の上記成分を60℃で混合、95℃で20分間殺
菌した後、70℃に冷却してCGTaseを添加した後
、24時間反応を行なわせた。反応終了後、95℃で3
0分間加熱して酵素を失活後、精密濾過して固形分を除
いた。この炉液の約172を減圧乾固後、粉砕して試料
1とした。Dextrin (product name Sandek 70. DE8)
300g caustic soda
6g calcium chloride
0.15 g water
1.2QCGTas
The above components other than e were mixed at 60°C, sterilized at 95°C for 20 minutes, cooled to 70°C, CGTase was added, and the mixture was allowed to react for 24 hours. After the reaction is complete, heat at 95°C for 3
After heating for 0 minutes to inactivate the enzyme, microfiltration was performed to remove solids. Approximately 172 ml of this furnace liquid was dried under reduced pressure and then ground to give Sample 1.
残りを非極性吸着接脂(商品名デュオライトS−861
)に吸着させた後、アルコール溶媒で脱着して、反応残
デキストリンを分離した。このものも同様に濃縮乾固し
て後、粉砕し試料2とした。Apply the rest with non-polar adsorption greasing (product name: Duolite S-861)
) and then desorbed with an alcohol solvent to separate the reaction residual dextrin. This product was similarly concentrated to dryness and then ground to give Sample 2.
之等の甘味成分を分析した結果は次の通りである。The results of analyzing the sweetness components are as follows.
試料1 α−G G 17.3%未反応
グリチルリチン 2.9
計 20.2試料2 α−G
G 46.1%未反応グリチルリチン
7.7
計 53.8%実施例1
次の処方により混合甘味料(粉体)を調製した。Sample 1 α-G G 17.3% unreacted glycyrrhizin 2.9 Total 20.2 Sample 2 α-G
G 46.1% Unreacted glycyrrhizin 7.7 Total 53.8% Example 1 A mixed sweetener (powder) was prepared according to the following formulation.
デキストリン 76.0 84.1計
100.0 10
0.OA、Bの各混合甘味料を20%水溶液として8人
のパネラ−による味覚試験を行なった。その結果、Aに
於いてはBの有している苦味、渋味などの雑味が減少し
ており、全体が円やかで且つコクが強化されていた。8
人のパネラ−の全員がAの方が好ましい味であると判定
した。また単味での甘味度で同じレベルになる様に配合
したにも拘わらず、8人中6人がAの甘味の方が強いと
判定した。Dextrin 76.0 84.1 total 100.0 10
0. A taste test was conducted by eight panelists using a 20% aqueous solution of each of the mixed sweeteners OA and B. As a result, in A, the bitterness, astringency, and other unpleasant tastes that B had were reduced, and the overall taste was rounder and richer. 8
All human panelists judged that A had a more preferable taste. In addition, even though they were mixed to have the same level of sweetness as a single flavor, 6 out of 8 people judged that the sweetness of A was stronger.
実施例2 次の処方により混合甘味料(顆粒)を調製した。Example 2 A mixed sweetener (granules) was prepared according to the following formulation.
クエン酸ナトリウム −15,0デキストリ
ン 64,6 62.2計
100.0 100.OA、
Bを夫々酢酸で調整しつつ、固形分15%。Sodium citrate -15,0 Dextrin 64,6 62.2 total
100.0 100. OA,
While adjusting B with acetic acid, the solid content was 15%.
pH2,0の水溶液を造った。この溶状を観察した処、
ノ
Bに於いて僅かにゲル状の塊が見られたが、Aに於いて
は全く見られず、試料2がクエン酸ナトリウムと同等か
、それ以上の溶解性の改善効果の有することが認められ
た。An aqueous solution with a pH of 2.0 was prepared. When I observed this solution,
A slight gel-like mass was observed in No. B, but no gel-like lumps were observed in No. A, indicating that Sample 2 had a solubility improvement effect equal to or greater than that of sodium citrate. It was done.
実施例3 次の処方で混合甘味料(液状)を調製した。Example 3 A mixed sweetener (liquid) was prepared using the following formulation.
A、Bを夫々4 g / 100 gになる様にコーヒ
ー(ミルクは使用せず)に添加して8人のパネラ−によ
り味質比較した処、全員がAの方がより砂糖に近い、好
ましい味と判定した。When A and B were added to coffee (without milk) at 4g/100g each and the taste was compared by 8 panelists, all of them agreed that A was more similar to sugar and was preferable. I judged it to be tasteful.
実施例4 次の処方で混合甘味料(顆粒)を調製した。Example 4 A mixed sweetener (granules) was prepared according to the following formulation.
クエン酸ソーダ −20,0乳糖
88,2 71.5計
100.0 100.OA
、Bを夫々1%水溶液として8人のパネラ−で味質評価
を行なった結果、実施例1とほぼ同様の改善効果が認め
られた。Sodium citrate -20,0 lactose
88.2 71.5 total
100.0 100. OA
, B were used as 1% aqueous solutions, and as a result of the taste evaluation performed by eight panelists, almost the same improvement effect as in Example 1 was observed.
実施例5 次の処方により混合甘味料(粉体)を調製した。Example 5 A mixed sweetener (powder) was prepared according to the following formulation.
乳糖 71,2 77.3計
100.0 10
0.0上記混合甘味料を用いて、下記の様ならつきょう
漬を作成した。Lactose 71.2 77.3 total 100.0 10
0.0 Using the above mixed sweetener, the following pickled vegetables were prepared.
■ ■
塩漬らつきよう 500 g 500 g
砂糖 5555混合甘味料
、 A 4.OB 4.0食酢
333 333みりん
7777
ソルビン酸カリウム 1.0 1.0水
70g 7
0g計 1040 g
1040 gこのものを、11人のパネラ−により
、味質比較テストを行なった。■ ■ Let's pickle salt 500 g 500 g
Sugar 5555 mixed sweetener
, A4. OB 4.0 vinegar
333 333 Mirin
7777 Potassium sorbate 1.0 1.0 Water
70g 7
0g total 1040g
A taste comparison test was conducted on 1040 g of this product by 11 panelists.
総合評価として■の方が、■より優れているとする者が
8人であり、他の3人は差が認められないとした。As for the overall evaluation, 8 people said that ``■'' is better than ``■'', and the other 3 people said that there was no difference.
■の方が優れているとした理由は味の切れが良くなると
云うもの7人、バランスが良くなる5人、コクが出ると
した者2人(複数回答)であった。The reasons why item (■) was better were: 7 people said it had a sharper flavor, 5 people said it had a better balance, and 2 people said it had a richer flavor (multiple answers allowed).
実施例6
実施例5の混合甘味料を用いて次の様ながまぼこを試作
した。Example 6 Using the mixed sweetener of Example 5, the following Gamaboko was made as an experimental product.
■ ■
すけそうすり身 10kg 10kg
砂糖 0.5 0.5食塩
0,3 0.3グルタミ
ン酸ソーダ 0.1 0.1澱粉
0.1 0.1混合甘味料
Ao、02g Bo、02水
1.0 1.0計
約 12kg 12kg
このものを10人のパネラ−により、味質比較テストを
行なった処、総合評価で7人が■の方を優れているとし
、2人が有意差なし、1名が■の方を良とした。■ ■ Walleye Surimi 10kg 10kg
Sugar 0.5 0.5 Salt 0.3 0.3 Sodium glutamate 0.1 0.1 Starch
0.1 0.1 mixed sweetener
Ao, 02g Bo, 02 water
1.0 1.0 total
Approx. 12kg 12kg
A taste comparison test was conducted on this product by 10 panelists, and in the overall evaluation, 7 people said that ■ was better, 2 people said that there was no significant difference, and 1 person said that ■ was better. did.
■を良とした理由は、味のバランスが良いとした者が7
人全員であり、その他に味の切れがよいとした者2人、
甘味が強いからとした者2人があ東京食材株式会社
代理人 弁理士 野 間 忠 夫The reason why ■ was rated good was that those who said the taste was well balanced were rated 7.
All of them, and two others who said they had good taste.
The two people who argued that it was because of its strong sweetness were Tadao Noma, patent attorney and agent for Tokyo Shokuryo Co., Ltd.
Claims (1)
草粗製物、ステビア抽出物、糖付加ステビアの群から選
ばれた1種又は2種以上の高甘味度甘味料とを、ともに
共存させることを特徴とする混合甘味料であつて、その
共存比(重量比)が 1、α−グリコシルグリチルリチンと甘草精製物とは0
.02〜1.0:1、 2、α−グリコシルグリチルリチンと甘草粗製物とは0
.04〜1.2:1、 3、α−グリコシルグリチルリチンとステビア抽出物と
は0.02〜0.5:1、 4、α−グリコシルグリチルリチンと糖付加ステビアと
は0.01〜0.2:1、 である、混合甘味料。[Scope of Claims] 1. α-glycosylglycyrrhizin and one or more high-intensity sweeteners selected from the group of purified licorice, crude licorice, stevia extract, and sugar-added stevia. It is a mixed sweetener characterized in that the coexistence ratio (weight ratio) of α-glycosylglycyrrhizin and purified licorice is 0.
.. 02-1.0: 1, 2, α-glycosylglycyrrhizin and licorice crude product are 0
.. 04-1.2:1, 3, α-glycosylglycyrrhizin and stevia extract: 0.02-0.5:1, 4, α-glycosylglycyrrhizin and sugar-added stevia: 0.01-0.2: 1. A mixed sweetener that is.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62328439A JPH01171454A (en) | 1987-12-26 | 1987-12-26 | Mixed sweetener |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62328439A JPH01171454A (en) | 1987-12-26 | 1987-12-26 | Mixed sweetener |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01171454A true JPH01171454A (en) | 1989-07-06 |
Family
ID=18210281
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62328439A Pending JPH01171454A (en) | 1987-12-26 | 1987-12-26 | Mixed sweetener |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01171454A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101445521B1 (en) * | 2011-08-31 | 2014-09-29 | 다이니폰 인사츠 가부시키가이샤 | Method for producing pattern phase difference film |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS588700A (en) * | 1981-07-08 | 1983-01-18 | 株式会社リコー | Pen-written recorder |
JPS62259594A (en) * | 1987-04-04 | 1987-11-11 | Hayashibara Biochem Lab Inc | Production of alpha-glycosylglycyrrhizin |
-
1987
- 1987-12-26 JP JP62328439A patent/JPH01171454A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS588700A (en) * | 1981-07-08 | 1983-01-18 | 株式会社リコー | Pen-written recorder |
JPS62259594A (en) * | 1987-04-04 | 1987-11-11 | Hayashibara Biochem Lab Inc | Production of alpha-glycosylglycyrrhizin |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101445521B1 (en) * | 2011-08-31 | 2014-09-29 | 다이니폰 인사츠 가부시키가이샤 | Method for producing pattern phase difference film |
US8871410B2 (en) | 2011-08-31 | 2014-10-28 | Dai Nippon Printing Co., Ltd. | Method for producing pattern phase difference film |
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