JPH057973B2 - - Google Patents
Info
- Publication number
- JPH057973B2 JPH057973B2 JP59206155A JP20615584A JPH057973B2 JP H057973 B2 JPH057973 B2 JP H057973B2 JP 59206155 A JP59206155 A JP 59206155A JP 20615584 A JP20615584 A JP 20615584A JP H057973 B2 JPH057973 B2 JP H057973B2
- Authority
- JP
- Japan
- Prior art keywords
- sweetness
- sucrose
- stevia
- sweetener
- sorbose
- 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.)
- Expired - Lifetime
Links
- 235000003599 food sweetener Nutrition 0.000 claims description 37
- 239000003765 sweetening agent Substances 0.000 claims description 37
- 241000544066 Stevia Species 0.000 claims description 22
- 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 description 22
- 239000000203 mixture Substances 0.000 claims description 15
- LKDRXBCSQODPBY-AMVSKUEXSA-N L-(-)-Sorbose Chemical compound OCC1(O)OC[C@H](O)[C@@H](O)[C@@H]1O LKDRXBCSQODPBY-AMVSKUEXSA-N 0.000 claims description 14
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 24
- 229930006000 Sucrose Natural products 0.000 description 24
- 239000005720 sucrose Substances 0.000 description 24
- 229940013618 stevioside Drugs 0.000 description 8
- 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 8
- 235000019202 steviosides Nutrition 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 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 7
- 239000013078 crystal Substances 0.000 description 7
- 235000013305 food Nutrition 0.000 description 6
- 238000011161 development Methods 0.000 description 5
- 230000018109 developmental process Effects 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 230000036541 health Effects 0.000 description 5
- NOESYZHRGYRDHS-UHFFFAOYSA-N insulin Chemical compound N1C(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(NC(=O)CN)C(C)CC)CSSCC(C(NC(CO)C(=O)NC(CC(C)C)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CCC(N)=O)C(=O)NC(CC(C)C)C(=O)NC(CCC(O)=O)C(=O)NC(CC(N)=O)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CSSCC(NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2C=CC(O)=CC=2)NC(=O)C(CC(C)C)NC(=O)C(C)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2NC=NC=2)NC(=O)C(CO)NC(=O)CNC2=O)C(=O)NCC(=O)NC(CCC(O)=O)C(=O)NC(CCCNC(N)=N)C(=O)NCC(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC(O)=CC=3)C(=O)NC(C(C)O)C(=O)N3C(CCC3)C(=O)NC(CCCCN)C(=O)NC(C)C(O)=O)C(=O)NC(CC(N)=O)C(O)=O)=O)NC(=O)C(C(C)CC)NC(=O)C(CO)NC(=O)C(C(C)O)NC(=O)C1CSSCC2NC(=O)C(CC(C)C)NC(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CC(N)=O)NC(=O)C(NC(=O)C(N)CC=1C=CC=CC=1)C(C)C)CC1=CN=CN1 NOESYZHRGYRDHS-UHFFFAOYSA-N 0.000 description 4
- 235000000346 sugar Nutrition 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 3
- 208000002925 dental caries Diseases 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 229930091371 Fructose Natural products 0.000 description 2
- 239000005715 Fructose Substances 0.000 description 2
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 2
- 102000004877 Insulin Human genes 0.000 description 2
- 108090001061 Insulin Proteins 0.000 description 2
- 208000008589 Obesity Diseases 0.000 description 2
- 244000228451 Stevia rebaudiana Species 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 235000009508 confectionery Nutrition 0.000 description 2
- 206010012601 diabetes mellitus Diseases 0.000 description 2
- 229940125396 insulin Drugs 0.000 description 2
- 230000002475 laxative effect Effects 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 235000020824 obesity Nutrition 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 235000019605 sweet taste sensations Nutrition 0.000 description 2
- OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 description 1
- 108010011485 Aspartame Proteins 0.000 description 1
- 241000208838 Asteraceae Species 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- 206010013911 Dysgeusia Diseases 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
- 102000051366 Glycosyltransferases Human genes 0.000 description 1
- 108700023372 Glycosyltransferases Proteins 0.000 description 1
- GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 235000006092 Stevia rebaudiana Nutrition 0.000 description 1
- OMHUCGDTACNQEX-OSHKXICASA-N Steviolbioside Natural products 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]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O OMHUCGDTACNQEX-OSHKXICASA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 238000005904 alkaline hydrolysis reaction Methods 0.000 description 1
- 230000000675 anti-caries Effects 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
- 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
- GUBGYTABKSRVRQ-QUYVBRFLSA-N beta-maltose Chemical compound OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O GUBGYTABKSRVRQ-QUYVBRFLSA-N 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- JLPRGBMUVNVSKP-AHUXISJXSA-M chembl2368336 Chemical compound [Na+].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]1O[C@@H](CO)[C@@H](O)[C@H](O)[C@@H]1O JLPRGBMUVNVSKP-AHUXISJXSA-M 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 235000006694 eating habits Nutrition 0.000 description 1
- 230000000225 effect on diabetes Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 230000007407 health benefit Effects 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 239000000845 maltitol Substances 0.000 description 1
- 235000010449 maltitol Nutrition 0.000 description 1
- VQHSOMBJVWLPSR-WUJBLJFYSA-N maltitol Chemical compound OC[C@H](O)[C@@H](O)[C@@H]([C@H](O)CO)O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O VQHSOMBJVWLPSR-WUJBLJFYSA-N 0.000 description 1
- 229940035436 maltitol Drugs 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000003020 moisturizing effect Effects 0.000 description 1
- 239000001814 pectin Substances 0.000 description 1
- 229920001277 pectin Polymers 0.000 description 1
- 235000010987 pectin Nutrition 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 238000011160 research Methods 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
- 150000003839 salts Chemical class 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- 239000012488 sample solution Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000005846 sugar alcohols Chemical class 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000000892 thaumatin Substances 0.000 description 1
- 235000010436 thaumatin Nutrition 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Landscapes
- Seasonings (AREA)
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は甘味料の一種であるステビア抽出物及
びその誘導体の実用組成に関する。
(従来の技術)
甘味料としては従来天然の糖である蔗糖、麦芽
糖、果糖、ブドウ糖や糖アルコールであるソルビ
トールやマルチトールが用いられている。一方高
度甘味料として天然のグリチルリン、ステビア、
ソーマチンなどが、又合成のサツカリン、アスパ
ルテームが用いられている。この様に天然および
合成の多くの甘味料の内でもとりわけ蔗糖が広く
一般に用いられている。それは蔗糖が食品加工上
多くの有役な機能を持つているに他ならない。例
えば、蔗糖はその優れた甘味の質を有している
他、水に対する溶解度が高い、増量効果がある、
結晶性が良い、保湿性がある、カラメル化する、
腐敗防止能がある、デンプンの老化防止能があ
る、ペクチンのゼリー化作用を有している。しか
しながらこうした有役な機能を持つ反面、健康上
望ましくない点も多く蔗糖に対する批判がある。
例えば、蔗糖は人にとつてカロリー源となる為過
剰摂取により肥満の原因となる。又虫歯を誘発さ
せる原因にもなる他糖尿病患者にとつて望ましく
ないことは衆知の通りである。食生活に於ける健
康への関心が高い近年、蔗糖のこうした欠点を有
しない新規な甘味料開発に対する要望は非常に強
いものがある。最近この様な健康上の理由から注
目されている甘味料として種々の高度甘味料が提
案されている。その中でも、ステビア甘味料は古
くから使用され、すぐれた甘味料である。
この様なステビア甘味料は甘味度が蔗糖の300
〜450倍と高い上、甘味の質が砂糖に近く諸味と
の調和性にも優れている。又熱、酸、塩に対する
安定性にも優れている。例えば食品加工の際PH4
〜10の範囲で100℃まで加熱しても甘味の質に変
化は起らない。健康上に於ても甘味度が高く従つ
て使用量が微量となる為カロリーとして問題にな
らない。非発酵性であり虫歯の原因とならず又糖
尿病に対しても悪影響を与えず非常に望ましい物
性を有している。
しかしながら、こうしたステビア甘味料は呈味
の発現性が蔗糖に比べて遅く現われる為前味に欠
けるという問題がある。又甘味料が300〜450倍と
著しく高い為、食品に所定の甘味度になる様均一
に添加しようとした場合単独で用いるには甘味の
調整が難しくあらかじめ希釈しておく必要があ
る。又甘味度は閾値に於ては上記の通りである
が、蔗糖甘味度分を全量ステビアに置換しようと
すれば極端な甘味倍数の低下をきたすばかりでな
く甘味のクセが発生する為、置換率にはおのずと
限界がある。そこでステビア甘味料の使用時の甘
味度調整すなわち取扱い性の改善と呈味発現の遅
れを改善する為に現在一般には蔗糖、ドウ糖、果
糖など天然糖類甘味料の1種又は2種以上を配合
して希釈するという方法がとられている。しかし
ながらこうした方法ではステビア甘味料の呈味発
現の遅れという甘味を改善し、甘味倍数を落さな
い様にする為には、配合剤であるこれら糖類の配
合比を10〜20倍以上にしなければならず結局ステ
ビア甘味料の持つ低カロリー性、非齲蝕性、非イ
ンシユリン依存性といつた特徴を失つてしまう欠
点を有する結果となる。現在までのところ、健康
指向分野に於けるステビア甘味料の持つこうした
長所を生かしつつ、欠点を改善してくれる様な良
い配合剤がなかつた。
(発明が解決しようとする問題点)
ステビア甘味料は、呈味の発現性が蔗糖に比べ
て遅く甘味が後に曳くという欠点がある。又甘味
度が蔗糖の300〜450倍と高い為単独で食品に用い
る場合甘味の希釈調整が難しい。食品の蔗糖によ
る甘味を全量ステビア甘味料で置換しようとする
と甘味倍数の著しい低下と甘味のクセが強くなる
という問題がある。最后に、レバウデイアナサイ
ドAを除く他のステビア甘味料は一般に水に対す
る溶解度が低く溶解分散に手間と時間がかかると
いう問題を有している。
(問題点を解決する為の手段)
本発明は摂取した場合、肥満、虫歯、糖尿病の
心配がない健康上望ましい性質を有し、秤量、溶
解、保存といつた取扱性が簡便であり、しかも甘
味の質が蔗糖に近似した食品加工及び一般家庭用
甘味料について鋭意研究を行つた結果本発明を完
成するに到つた。
すなわち、ステビア抽出物及びその誘導体にL
−ソルボースを配合してなる甘味料組成物であ
る。
本発明に用いるステビア抽出物及びその誘導体
は菊科多年性植物「ステビア・レバウデイアナ・
ベルトニー」(Stevia rebaudiana Bertoni M.)
に含有される甘味成分の総称であり、成分として
はステビオサイド・レバウデイアナサイドA及び
同じ骨格を有する5種のものがある。又その誘導
体としてアルカリ加水分解生成物であるステビオ
ールバイオサイドや糖転移酵素による合成物であ
るβ−1,4ガラクトシルステビオサイドがあ
る。
本発明の甘味料組成物の製造方法は、市販蔗糖
のグラニユー糖の如き顆粒状の結晶体を得たい場
合、ステビア甘味料とL−ソルボースの混合水溶
液を調整し、これを減圧濃縮し共に結晶として沈
澱させさらに結晶を成長させた後濾過又は遠心分
離后乾燥させて得ることが出来る。そしてこの時
の甘味料組成物の結晶の粒度は結晶成長の条件で
ある温度、減圧度、撹拌の回転数、時間などを調
整することで望みのものを得ることが出来る。ま
た、簡便に微粉末状の複合甘味料を得たい時は、
ステビア甘味料とL−ソルボースの混合水溶液を
調整しこれを減圧濃縮による乾燥または噴霧乾燥
による乾燥をさせた後、粉砕機にて粉砕し、微粉
末状の甘味組成物を得ることが出来る。ステビア
甘味料とL−ソルボースとの配合比はステビア甘
味料の成分及び純度や用途使用目的に応じて定め
られるもので特に限定はし難いが例えば、純度90
%のステビオサイドの場合重量比で500〜0.1倍、
好ましくは200〜0.5倍のL−ソルボースを用いる
のが良い。純度90%のレバウデイアナサイドAの
場合は700〜0.1倍、好ましくは300〜0.5倍のL−
ソルボースを用いるのが良い。また本発明の甘味
料組成物に他の甘味料あるいは分散剤、賦形剤、
場合によつて香料、着色料など添加することによ
つて本発明の効果をより高めることが出来る。
(発明の効果)
本発明の甘味料組成物は、ステビアの甘味発現
性が蔗糖に比し遅く後味を曳くという欠点をL−
ソルボースの呈味発現性の早いという性質がうま
く補つて相乗効果を示し蔗糖に非常に近似した呈
味発現性が得られる。次に蔗糖の300〜450倍もの
甘味を持ち、水に対する溶解性の低いステビア甘
味料がL−ソルボースと配合することでその甘味
倍数を大きく低下させることなく、水にすみやか
に分散、溶解させ、蔗糖甘味を100%置換するこ
とが出来る様になる。逆にL−ソルボースは甘味
度が蔗糖の0.7倍と低い為これのみで甘味が十分
になる様に摂取すると必然的に使用量が多くなり
緩下作用を示すという欠点があるステビア甘味料
の高甘味度を利用することで、摂取量を大きく減
じることが出来、緩下作用を無くすことが出来
る。しかも本発明の甘味料組成物は、低カロリー
性、抗齲蝕性、インシユリン非依存性と云つた健
康上のメリツトを兼ねそなえた甘味料組成物であ
る。更にL−ソルボースが水に対して易溶性であ
るにもかかわらず結晶性にすぐれ、吸湿性が低い
為、粉末状で取扱う場合保存中に吸湿しベタツキ
を生じることがない大変優れた甘味料組成物であ
る。
(実施例)
実施例 1
L−ソルボース100g、ステビオサイド(純度
98%)1.0gを100mlの水に溶解した後、50〜60℃
で減圧下濃縮し水の半量である50mlを溜去した時
点で0℃一夜放置し析出した結晶を濾別した。こ
の結晶を室温で減圧下一夜乾燥した所、75gであ
つた。そこでこの中のステビオサイドの含量を高
速液体クロマトグラフイーで分析して見た所、
0.3%であり甘味度は蔗糖に対して約1.5倍であつ
た。
実施例 2
L−ソルボース100g、ステビオサイド(純度
98%)100mgを100mlの水に溶解した後、50〜60で
減圧下濃縮乾固したものをミキサーで微粉砕し、
粉末状の甘味料組成物を得た。このものの甘味度
は蔗糖とほぼ同等であつた。
実施例 3
ステビオサイドの甘味の呈味発現性の改善効果
を見る為、実施例1のサンプルを用いて、98%ス
テビオサイドとの二者の比較を行つた。比較テス
トは、10名のパネル員により2点比較法で、温度
20℃の水溶液を用いた。又試料溶液の甘味度はほ
ぼ蔗糖の5%濃度となる様に調整した。その結果
を下表に示す。
【表】DETAILED DESCRIPTION OF THE INVENTION (Industrial Application Field) The present invention relates to a practical composition of stevia extract, which is a kind of sweetener, and its derivatives. (Prior Art) Conventionally, natural sugars such as sucrose, maltose, fructose, and glucose, and sugar alcohols such as sorbitol and maltitol have been used as sweeteners. On the other hand, natural glycyrrhin, stevia, and
Thaumatin, etc., as well as synthetic saccharin and aspartame are used. As described above, among many natural and synthetic sweeteners, sucrose is particularly widely used. This is because sucrose has many useful functions in food processing. For example, sucrose has excellent sweetness, has high solubility in water, and has a bulking effect.
Good crystallinity, moisturizing properties, caramelization,
It has the ability to prevent spoilage, the ability to prevent starch from aging, and the jelly-forming effect of pectin. However, despite having these useful functions, sucrose has been criticized for its many undesirable health issues.
For example, sucrose is a source of calories for humans, and excessive intake can cause obesity. It is also well known that it can induce tooth decay and is undesirable for diabetic patients. In recent years, there has been a strong interest in the health of dietary habits, and there has been a strong demand for the development of new sweeteners that do not have the drawbacks of sucrose. Various advanced sweeteners have been proposed as sweeteners that have recently attracted attention for such health reasons. Among them, stevia sweetener has been used for a long time and is an excellent sweetener. This kind of stevia sweetener has a sweetness level of 300% compared to sucrose.
It is ~450 times more expensive, and its sweetness is close to that of sugar and blends well with moromi. It also has excellent stability against heat, acids, and salts. For example, during food processing, PH4
There is no change in the quality of sweetness even when heated up to 100℃ in the range of ~10. From a health standpoint, it has a high degree of sweetness, so the amount used is very small, so the calorie content is not a problem. It is non-fermentable, does not cause dental caries, does not have an adverse effect on diabetes, and has very desirable physical properties. However, these stevia sweeteners have a problem in that they lack foretaste because their taste develops later than that of sucrose. Also, since the sweetener is extremely high at 300 to 450 times higher, if you want to add it uniformly to foods to achieve a predetermined sweetness level, it is difficult to adjust the sweetness if you use it alone, and you need to dilute it in advance. In addition, the sweetness threshold is as described above, but if you try to replace the entire amount of sucrose sweetness with stevia, it will not only cause an extreme decrease in the sweetness multiple but also create a sweet taste, so the replacement rate naturally has its limits. Therefore, in order to adjust the sweetness level when using Stevia sweetener, i.e. to improve handling properties and to improve the delay in taste onset, one or more natural sugar sweeteners such as sucrose, dow sugar, and fructose are currently added. The method used is to dilute it. However, with these methods, in order to improve the sweetness caused by the delayed taste onset of the Stevia sweetener and to prevent the sweetness factor from decreasing, the blending ratio of these saccharides as compounding agents must be increased by 10 to 20 times or more. As a result, it loses the characteristics of the stevia sweetener, such as low calorie, non-cariogenicity, and non-insulin dependence. To date, there has been no good formulation that can take advantage of the advantages of stevia sweeteners in the health-oriented field while improving its disadvantages. (Problems to be Solved by the Invention) Stevia sweeteners have the disadvantage that their taste development is slower than that of sucrose, and the sweetness lingers later. Also, since its sweetness is 300 to 450 times higher than sucrose, it is difficult to dilute and adjust the sweetness when used alone in foods. When attempting to replace the entire sweetness of sucrose in foods with a stevia sweetener, there are problems in that the sweetness multiple drops significantly and the sweetness becomes more addictive. Finally, stevia sweeteners other than rebaudieanaside A generally have a problem of low solubility in water and require time and effort to dissolve and disperse. (Means for Solving the Problems) The present invention has desirable properties for health without the risk of obesity, tooth decay, or diabetes when ingested, and is easy to handle such as weighing, dissolving, and storing. The present invention was completed as a result of intensive research into sweeteners for food processing and general household use whose sweetness quality is similar to that of sucrose. That is, L is added to Stevia extract and its derivatives.
- A sweetener composition containing sorbose. The stevia extract and its derivatives used in the present invention are derived from the perennial plant "Stevia rebaudiana" of the Asteraceae family.
Bertoni” (Stevia rebaudiana Bertoni M.)
It is a general term for the sweet ingredients contained in ``stevioside'', and the ingredients include stevioside, rebaudianaside A, and five other substances that have the same skeleton. Further, its derivatives include steviol bioside, which is an alkaline hydrolysis product, and β-1,4-galactosyl stevioside, which is a synthetic product using glycosyltransferase. In the method for producing the sweetener composition of the present invention, when it is desired to obtain granular crystals such as commercially available granulated sucrose, a mixed aqueous solution of a stevia sweetener and L-sorbose is prepared, and this is concentrated under reduced pressure to crystallize both. It can be obtained by precipitating as a crystal, growing crystals, filtering or centrifuging, and drying. The desired grain size of the crystals of the sweetener composition can be obtained by adjusting the crystal growth conditions such as temperature, degree of vacuum, stirring rotation speed, and time. Also, if you want to easily obtain a fine powder complex sweetener,
A mixed aqueous solution of stevia sweetener and L-sorbose is prepared, dried by vacuum concentration or spray drying, and then pulverized in a pulverizer to obtain a finely powdered sweet composition. The blending ratio of the stevia sweetener and L-sorbose is determined depending on the ingredients and purity of the stevia sweetener and the intended use, and is difficult to limit, but for example, purity 90.
% stevioside by weight ratio of 500 to 0.1 times,
It is preferable to use 200 to 0.5 times as much L-sorbose. In the case of rebaudianaside A with a purity of 90%, the L-
It is better to use sorbose. In addition, the sweetener composition of the present invention may contain other sweeteners, dispersants, excipients,
The effects of the present invention can be further enhanced by adding fragrances, coloring agents, etc., depending on the case. (Effects of the Invention) The sweetener composition of the present invention overcomes the drawback that stevia has a slower sweetness development than sucrose and leaves an aftertaste.
The property of sorbose, which has a quick taste development, is well complemented by the synergistic effect, resulting in a taste development very similar to that of sucrose. Next, the stevia sweetener, which is 300 to 450 times sweeter than sucrose and has low solubility in water, is blended with L-sorbose to quickly disperse and dissolve in water without significantly reducing its sweetness multiple. It becomes possible to replace 100% of the sweetness of sucrose. On the other hand, L-sorbose has a sweetness level that is 0.7 times lower than that of sucrose, so if you take it to get enough sweetness with just L-sorbose, you will inevitably need to use a large amount of it and it will have a laxative effect. By utilizing the sweetness level, the intake amount can be greatly reduced and the laxative effect can be eliminated. Furthermore, the sweetener composition of the present invention is a sweetener composition that has health benefits such as low calorie, anti-caries, and insulin independence. Furthermore, although L-sorbose is easily soluble in water, it has excellent crystallinity and low hygroscopicity, so when handled in powder form, it does not absorb moisture and become sticky during storage, making it an excellent sweetener composition. It is a thing. (Example) Example 1 100g of L-sorbose, stevioside (purity
98%) 1.0g dissolved in 100ml water, 50~60℃
The mixture was concentrated under reduced pressure, and when half of the water (50 ml) had been distilled off, it was left to stand overnight at 0°C, and the precipitated crystals were filtered off. The crystals weighed 75 g after being dried overnight under reduced pressure at room temperature. Therefore, the content of stevioside in this was analyzed using high performance liquid chromatography, and it was found that
It was 0.3%, and the sweetness was about 1.5 times that of sucrose. Example 2 L-sorbose 100g, stevioside (purity
After dissolving 100mg of 98%) in 100ml of water, it was concentrated to dryness under reduced pressure at 50 to 60℃, and then finely ground with a mixer.
A powdered sweetener composition was obtained. The sweetness level of this product was almost equivalent to that of sucrose. Example 3 In order to see the effect of stevioside on improving the sweet taste expression, the sample of Example 1 was used to compare the two with 98% stevioside. The comparison test was conducted by 10 panel members using the two-point comparison method.
An aqueous solution at 20°C was used. The sweetness of the sample solution was adjusted to approximately 5% sucrose concentration. The results are shown in the table below. 【table】
Claims (1)
L−ソルボースを配合してなる甘味料組成物。1. A sweetener composition containing L-sorbose and a Stevia extract and its derivatives.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59206155A JPS6185164A (en) | 1984-10-03 | 1984-10-03 | Stevia sweetener composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59206155A JPS6185164A (en) | 1984-10-03 | 1984-10-03 | Stevia sweetener composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6185164A JPS6185164A (en) | 1986-04-30 |
| JPH057973B2 true JPH057973B2 (en) | 1993-01-29 |
Family
ID=16518707
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP59206155A Granted JPS6185164A (en) | 1984-10-03 | 1984-10-03 | Stevia sweetener composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6185164A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5283173B2 (en) * | 2006-11-10 | 2013-09-04 | 松谷化学工業株式会社 | Non-cariogenic materials and anti-cariogenic agents containing rare sugars |
| JP5876205B2 (en) * | 2009-02-06 | 2016-03-02 | 松谷化学工業株式会社 | Method for improving deficiency of sweetness of D-sorbose in sweetener comprising D-sorbose and improving sweetness persistence |
-
1984
- 1984-10-03 JP JP59206155A patent/JPS6185164A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6185164A (en) | 1986-04-30 |
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