JPH04237463A - Theanderose-containing candy - Google Patents
Theanderose-containing candyInfo
- Publication number
- JPH04237463A JPH04237463A JP3003315A JP331591A JPH04237463A JP H04237463 A JPH04237463 A JP H04237463A JP 3003315 A JP3003315 A JP 3003315A JP 331591 A JP331591 A JP 331591A JP H04237463 A JPH04237463 A JP H04237463A
- Authority
- JP
- Japan
- Prior art keywords
- theanderose
- candy
- sucrose
- cariogenic
- 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.)
- Withdrawn
Links
- 235000009508 confectionery Nutrition 0.000 title claims abstract description 20
- MUPFEKGTMRGPLJ-UHFFFAOYSA-N UNPD196149 Natural products OC1C(O)C(CO)OC1(CO)OC1C(O)C(O)C(O)C(COC2C(C(O)C(O)C(CO)O2)O)O1 MUPFEKGTMRGPLJ-UHFFFAOYSA-N 0.000 title claims abstract description 17
- 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 claims abstract description 16
- 229930006000 Sucrose Natural products 0.000 claims abstract description 16
- 239000005720 sucrose Substances 0.000 claims abstract description 16
- 235000003599 food sweetener Nutrition 0.000 claims abstract description 15
- 239000003765 sweetening agent Substances 0.000 claims abstract description 15
- 150000001720 carbohydrates Chemical class 0.000 claims abstract description 12
- 235000014633 carbohydrates Nutrition 0.000 claims abstract description 12
- 241000235395 Mucor Species 0.000 claims abstract description 5
- 229920001503 Glucan Polymers 0.000 claims abstract description 4
- 102000000340 Glucosyltransferases Human genes 0.000 claims abstract description 4
- 108010055629 Glucosyltransferases Proteins 0.000 claims abstract description 4
- 241000894006 Bacteria Species 0.000 claims description 4
- 230000000675 anti-caries Effects 0.000 claims description 4
- 230000000248 cariostatic effect Effects 0.000 abstract 1
- 244000005700 microbiome Species 0.000 abstract 1
- 229920002472 Starch Polymers 0.000 description 12
- 235000019698 starch Nutrition 0.000 description 12
- 239000008107 starch Substances 0.000 description 12
- 208000002925 dental caries Diseases 0.000 description 10
- 241000700159 Rattus Species 0.000 description 8
- 239000000843 powder Substances 0.000 description 8
- 230000001013 cariogenic effect Effects 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- 235000000346 sugar Nutrition 0.000 description 5
- 239000006188 syrup Substances 0.000 description 5
- 235000020357 syrup Nutrition 0.000 description 5
- 241000194019 Streptococcus mutans Species 0.000 description 4
- 239000008351 acetate buffer Substances 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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 3
- 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 3
- 230000000694 effects Effects 0.000 description 3
- 239000008103 glucose Substances 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 239000000845 maltitol Substances 0.000 description 3
- 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 3
- 235000010449 maltitol Nutrition 0.000 description 3
- 229940035436 maltitol Drugs 0.000 description 3
- 239000012528 membrane Substances 0.000 description 3
- 229940013618 stevioside Drugs 0.000 description 3
- 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 3
- 235000019202 steviosides Nutrition 0.000 description 3
- PVXPPJIGRGXGCY-DJHAAKORSA-N 6-O-alpha-D-glucopyranosyl-alpha-D-fructofuranose Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1OC[C@@H]1[C@@H](O)[C@H](O)[C@](O)(CO)O1 PVXPPJIGRGXGCY-DJHAAKORSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 239000004378 Glycyrrhizin Substances 0.000 description 2
- 241000498617 Mucor javanicus Species 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000001580 bacterial effect Effects 0.000 description 2
- 229920001429 chelating resin Polymers 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 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 2
- 229960004949 glycyrrhizic acid Drugs 0.000 description 2
- 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 2
- 235000019410 glycyrrhizin Nutrition 0.000 description 2
- 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 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 150000008163 sugars Chemical class 0.000 description 2
- 238000000108 ultra-filtration Methods 0.000 description 2
- 108010011485 Aspartame Proteins 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
- 239000004278 EU approved seasoning Substances 0.000 description 1
- 229930091371 Fructose Natural products 0.000 description 1
- 239000005715 Fructose Substances 0.000 description 1
- 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 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000008122 artificial sweetener Substances 0.000 description 1
- 235000021311 artificial sweeteners Nutrition 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
- 239000004202 carbamide Substances 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 238000004042 decolorization Methods 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 235000013373 food additive Nutrition 0.000 description 1
- 239000002778 food additive Substances 0.000 description 1
- 235000011194 food seasoning agent Nutrition 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 125000002791 glucosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 239000003456 ion exchange resin Substances 0.000 description 1
- 229920003303 ion-exchange polymer Polymers 0.000 description 1
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 235000021096 natural sweeteners Nutrition 0.000 description 1
- 230000001151 other effect Effects 0.000 description 1
- 235000019449 other food additives Nutrition 0.000 description 1
- 229940093429 polyethylene glycol 6000 Drugs 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- -1 sorbitol and xylitol Chemical class 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
- 235000019605 sweet taste sensations Nutrition 0.000 description 1
- 238000006276 transfer reaction Methods 0.000 description 1
- 150000004043 trisaccharides Chemical class 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000000811 xylitol Substances 0.000 description 1
- 235000010447 xylitol Nutrition 0.000 description 1
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 1
- 229960002675 xylitol Drugs 0.000 description 1
Landscapes
- Confectionery (AREA)
- Seasonings (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は、テアンデロースを含有
する抗う蝕キャンディに関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an anti-caries candy containing theanderose.
【0002】0002
【従来の技術】近年、口腔衛生の立場から、う蝕性(虫
歯)の原因となる蔗糖を大量に含む飴を、幼児、児童に
与えることを嫌う傾向が強まっている。それにともない
、蔗糖に代わる低う蝕性の甘味料に対する関心が高まっ
ている。この種の甘味料としては、合成甘味料もあるが
、安全性の点で問題があったり、それほど問題がなくて
も消費者が心理的に嫌う傾向が強くなってきたこともあ
って、グリチルリチン、ステビオサイドなど、天然由来
の高度甘味料が注目されてきている。BACKGROUND OF THE INVENTION In recent years, from the standpoint of oral hygiene, there has been a growing tendency to dislike giving candies containing large amounts of sucrose, which causes caries (tooth decay), to infants and children. Accordingly, interest in low-cariogenic sweeteners that can replace sucrose is increasing. Synthetic sweeteners are also available as this type of sweetener, but they have safety issues, and even if there is no problem, consumers have a strong tendency to dislike them psychologically, so glycyrrhizin Naturally derived advanced sweeteners such as stevioside and stevioside are attracting attention.
【0003】しかしながら、これらの甘味料は、砂糖と
比較すると、味質などの点において砂糖と比較して劣る
ものとなっている。たとえば、グリチルリチンは、蔗糖
と比較して50〜100倍、純品においては250倍の
甘味度を有しながら、甘味が遅効性であり、しかも不快
な後味を残すという欠点がある。また、味質の点で比較
的良質なマルチトールやパラチノースなどの糖質系の低
う蝕性甘味料を用いたキャンディも開発されている。However, these sweeteners are inferior to sugar in terms of taste quality and the like. For example, glycyrrhizin has a sweetness level 50 to 100 times higher than that of sucrose, and 250 times higher in pure form, but has the disadvantage that its sweetness is slow-acting and leaves an unpleasant aftertaste. In addition, candies using carbohydrate-based low-cariogenic sweeteners such as maltitol and palatinose, which are relatively good in taste, have been developed.
【0004】しかしながら、マルチトール、パラチノー
スは、低う蝕性とは言いつつも、積極的にう蝕を抑制す
る効果が無いばかりか、デンプンと同程度もしくはこれ
より高いう蝕性を有し、これを用いたキャンディは真の
意味でう蝕性が無いとは言えない。[0004] However, although maltitol and palatinose are said to have low cariogenicity, they not only do not have the effect of actively inhibiting caries, but also have a cariogenicity comparable to or higher than that of starch. Candies made with this cannot be said to be cariogenic in the true sense.
【0005】[0005]
【発明が解決しようとする課題】本発明は、う蝕性のな
いキャンディを提供することを目的とする。なお、本発
明で言うテアンデロースとは下記化1の構造を有する三
糖類である。SUMMARY OF THE INVENTION An object of the present invention is to provide a cariogenic candy. The theanderose referred to in the present invention is a trisaccharide having the structure shown below.
【0006】[0006]
【化1】[Chemical formula 1]
【0007】[0007]
【課題を解決するための手段】本発明者らは、上記の問
題点の解決につき鋭意研究を重ねた結果、それ自体甘味
を有し、かつう蝕を抑制する効果があるテアンデロース
を添加すると、う蝕性の無いキャンディが得られるとの
知見を得、本発明を完成したものである。すなわち、本
発明は、甘味料として各種炭水化物を含むキャンディに
おいて、ムコール属菌由来のグルコシルトランスフェラ
ーゼを用いてグルカンと蔗糖より生成したテアンデロー
スを含むことを特徴とする抗う蝕性キャンディである。[Means for Solving the Problems] As a result of extensive research into solving the above-mentioned problems, the present inventors found that the addition of theanderose, which itself has a sweet taste and has the effect of suppressing dental caries. The present invention was completed based on the knowledge that a cariogenic-free candy can be obtained. That is, the present invention is an anti-caries candy containing various carbohydrates as a sweetener, which is characterized by containing theanderose produced from glucan and sucrose using glucosyltransferase derived from Mucor bacteria.
【0008】本発明に用いられる各種炭水化物は、甘味
料の全部または一部を構成する。その例としては、蔗糖
、ぶどう糖、果糖、異性化糖、その他糖、ソルビトール
、キシリトールなどの糖アルコール、水飴等そのほかの
糖類が上げられ、他の甘味料と併用する場合、組み合わ
せる甘味料は、サッカリン、ステビオサイド、アスパル
テームなどの天然もしくは人工の甘味料のいずれも使用
できるが、う蝕防止を目的としたキャンディの製造には
、できる限りう蝕性の無いものを用いることが望ましい
。[0008] The various carbohydrates used in the present invention constitute all or part of the sweetener. Examples include sucrose, glucose, fructose, isomerized sugar, other sugars, sugar alcohols such as sorbitol and xylitol, and other sugars such as starch syrup. Natural or artificial sweeteners such as , stevioside, and aspartame can be used; however, in the production of candy for the purpose of preventing caries, it is desirable to use sweeteners that are as carious-free as possible.
【0009】本発明におけるテアンデロースは、う蝕防
止の目的で加えられる食品添加物の一部または全部を構
成する。他の食品添加物と併用する場合には、相互の効
果を妨げない限りに於いて、如何なる物質との組合せも
可能である。また、各種炭水化物甘味料との混合率につ
いては、製品の形状、目的、保存状況、他の添加物の存
在に応じて適宜設定すれば良い。また、その製造方法と
しては、ムコール(Mucor)属菌由来のグルコシル
トランスフェラーゼを用いてグルカンと蔗糖より生成し
、特にムコール(Mucor)属菌がMucor j
avanicusである時に効率的に生成することがで
きる。[0009] Theanderose in the present invention constitutes part or all of the food additive added for the purpose of preventing dental caries. When used in combination with other food additives, any combination is possible as long as they do not interfere with each other's effects. Further, the mixing ratio with various carbohydrate sweeteners may be appropriately set depending on the shape of the product, its purpose, storage conditions, and the presence of other additives. In addition, as for its production method, it is produced from glucan and sucrose using glucosyltransferase derived from Mucor genus bacteria.
avanicus can be efficiently generated.
【0010】さらに、上記成分以外に、着色料、香料、
酸味料、調味料、そのほか添加物などを本発明の目的を
逸脱しない範囲で添加することは、当然可能である。[0010] In addition to the above ingredients, colorants, fragrances,
It is of course possible to add acidulants, seasonings, and other additives within the scope of the purpose of the present invention.
【0011】[0011]
【0012】0012
【参考例1】本参考例はMucor javanic
us IFO 4570の細胞抽出液を利用して、
可溶性デンプンからショ糖にグルコシル基を転移させ、
膜分離技術を利用してテアンデロースを含む甘味料を取
得した例である。
(1)Mucor javanicus IFO
4570からの細胞抽出液の調製
Mucor javanicus IFO 45
70を、100mlの天然培地〔可溶性デンプン4g、
コーンスチープリカー(pH5.5〜5.8)3g、N
aNO3 0.5g、KH2 PO4 0.1g、Mg
SO4 ・7H2 O0.05g、KCl0.05gを
蒸留水に溶解して1リットルとする〕の500mlフラ
スコ中で、30℃で2日間振盪培養した。同培養液5m
lを、100mlの前記天然培地を入れた500mlフ
ラスコに移植して、30℃で2日間振盪培養した。同方
法で培養したフラスコ300本から濾過により集菌し、
脱イオン水で洗浄後、−20℃で保存した。同菌体を尿
素4Mを含んだ1M酢酸緩衝液(pH5.3)5.1リ
ットルに懸濁し、30℃で48時間抽出した。同抽出液
より濾過により菌体残渣を除去した後、同濾過液を0℃
に冷却した。
次に、同濾過液に、−20℃に冷却したアセトンを50
%(v/v)になるまで攪拌しながら添加した。同液か
ら遠心分離により沈澱を除去した後、1M CaCl
2 水溶液を1.45ml添加した。同抽出液にポリエ
チレングリコール6000を20%(v/w)まで添加
した後、4℃で1時間放置し、生じた沈澱を遠心分離し
、0.05M酢酸緩衝液(pH5.3)50mlに溶解
し、同液を細胞抽出液として以後の操作に用いた。
(2)テアンデロースの調製
可溶性デンプン3%(w/v)、ショ糖17%を含む0
.05M酢酸緩衝液(pH5)3リットルに、Muco
r javanicus IFO 4570由来
の細胞抽出液0.3ml(前記(1)で取得した細胞抽
出液)を加えて、50℃で6時間反応させた。得られた
反応液を、100℃で15分間加熱した後、3gの活性
炭(武田薬品工業株式会社製 白鷺A)を添加し、5
0℃で1時間加熱して脱色を行った。活性炭を除去した
後、アンバーライトIR・120およびアンバーライト
IRA・400のイオン交換樹脂で処理した。次に、分
子量分画500の限外濾過膜(アドバンテック東洋株式
会社製 ウルトラフィルター)により、濃縮と水によ
る希釈を繰り返し、テアンデロース36%、ショ糖36
%、グルコース2%、可溶性デンプン27%の糖組成を
有する非う蝕性または低う蝕性混合液を調製した後、7
0%(w/w)濃度に濃縮して非う蝕性または低う蝕性
の固形物214gを得た。[Reference example 1] This reference example is Mucor javanic
Using the cell extract of US IFO 4570,
Transfers glucosyl groups from soluble starch to sucrose,
This is an example of obtaining a sweetener containing theanderose using membrane separation technology. (1) Mucor javanicus IFO
Preparation of cell extract from 4570 Mucor javanicus IFO 45
70 in 100 ml of natural medium [4 g of soluble starch,
Corn steep liquor (pH 5.5-5.8) 3g, N
aNO3 0.5g, KH2 PO4 0.1g, Mg
Shaking culture was carried out at 30° C. for 2 days in a 500 ml flask containing 0.05 g of SO4 .7H2 O and 0.05 g of KCl dissolved in distilled water to make 1 liter. Same culture solution 5m
1 was transplanted into a 500 ml flask containing 100 ml of the above natural medium, and cultured with shaking at 30° C. for 2 days. Bacteria were collected by filtration from 300 flasks cultured using the same method,
After washing with deionized water, it was stored at -20°C. The same bacterial cells were suspended in 5.1 liters of 1M acetate buffer (pH 5.3) containing 4M urea and extracted at 30°C for 48 hours. After removing bacterial cell residue from the same extract by filtration, the filtrate was heated to 0°C.
It was cooled to Next, 50% of acetone cooled to -20°C was added to the same filtrate.
% (v/v) while stirring. After removing the precipitate from the same solution by centrifugation, 1M CaCl
2 1.45 ml of aqueous solution was added. After adding polyethylene glycol 6000 to 20% (v/w) to the same extract, it was left at 4°C for 1 hour, and the resulting precipitate was centrifuged and dissolved in 50 ml of 0.05 M acetate buffer (pH 5.3). The same solution was used as a cell extract for subsequent operations. (2) Preparation of theanderose 0 containing 3% (w/v) soluble starch and 17% sucrose
.. Add Muco to 3 liters of 05M acetate buffer (pH 5)
0.3 ml of cell extract derived from r. After heating the obtained reaction solution at 100°C for 15 minutes, 3 g of activated carbon (Shirasagi A, manufactured by Takeda Pharmaceutical Company Limited) was added, and 5
Decolorization was performed by heating at 0° C. for 1 hour. After removing the activated carbon, it was treated with Amberlite IR-120 and Amberlite IRA-400 ion exchange resins. Next, concentration and dilution with water were repeated using an ultrafiltration membrane with a molecular weight fraction of 500 (Ultrafilter, manufactured by Advantech Toyo Co., Ltd.), resulting in 36% theanderose and 36% sucrose.
%, glucose 2%, soluble starch 27% after preparing a non-cariogenic or hypocariogenic mixture with a sugar composition of 7%.
Concentration to 0% (w/w) concentration yielded 214 g of non-cariogenic or less cariogenic solid.
【0013】さらに、限外濾過膜を通過した液を用いて
、次のグルコース転移反応液〔可溶性デンプン3%、蔗
糖17%を含む酢酸緩衝液(pH5.0)〕を調製し、
同様の操作を繰り返すことにより、本法に於ける蔗糖の
利用効率を70%以上にすることができた。また、上記
非う蝕性または低う蝕性の固形物を蒸留水に溶解し、活
性炭カラム(50×900mm)により数回に分けて分
画することによりテアンデロース67gを得ることがで
きた。Furthermore, the following glucose transfer reaction solution [acetate buffer containing 3% soluble starch and 17% sucrose (pH 5.0)] was prepared using the solution that had passed through the ultrafiltration membrane.
By repeating the same operation, it was possible to increase the utilization efficiency of sucrose in this method to 70% or more. In addition, 67 g of theanderose could be obtained by dissolving the above-mentioned non-cariogenic or low-cariogenic solid in distilled water and fractionating the solution in several batches using an activated carbon column (50 x 900 mm).
【0014】[0014]
【実施例1】蔗糖
67gテアンデロース
67g水飴
66g上記成分を加熱溶融し、十
分均一に溶融した。冷却固化後、細かく粉砕し、この粉
末を重量比56%で含み、唯一の炭水化物源とする飼料
を調製した。この飼料を、S.mutans PS−
14株を経口感染させたラット10匹に与え、58日間
飼育した。この結果、ラットの平均う蝕スコアは3.1
±1.8であった。[Example 1] Sucrose
67g Theanderose
67g starch syrup
66g of the above components were heated and melted to be sufficiently uniform. After cooling and solidifying, the powder was finely ground to prepare a feed containing this powder at a weight ratio of 56% as the sole carbohydrate source. This feed was used for S. mutans PS-
The 14 strains were given to 10 rats that were orally infected and kept for 58 days. As a result, the average caries score for rats was 3.1.
It was ±1.8.
【0015】[0015]
【比較例1】蔗糖
134g水飴
66g上記成分を加熱溶融し、十
分均一に溶融した。冷却固化後、細かく粉砕し、この粉
末を重量比56%で含み、唯一の炭水化物源とする飼料
を調製した。この飼料を、S.mutans PS−
14株を経口感染させたラット10匹に与え、58日間
飼育した。この結果、ラットの平均う蝕スコアは83.
2±5.6であった。[Comparative Example 1] Sucrose
134g starch syrup
66g of the above components were heated and melted to be sufficiently uniform. After cooling and solidifying, the powder was finely ground to prepare a feed containing this powder at a weight ratio of 56% as the sole carbohydrate source. This feed was used for S. mutans PS-
The 14 strains were given to 10 rats that were orally infected and kept for 58 days. As a result, the average caries score of rats was 83.
It was 2±5.6.
【0016】[0016]
【比較例2】澱粉
134g水飴
66g上記成分を加熱し、十分均
一になるよう混和した。冷却固化後、細かく粉砕し、こ
の粉末を重量比56%で含み、唯一の炭水化物源とする
飼料を調製した。この飼料を、S.mutans P
S−14株を経口感染させたラット10匹に与え、58
日間飼育した。この結果、ラットの平均う蝕スコアは8
.5±3.1であった。[Comparative Example 2] Starch
134g starch syrup
66g of the above ingredients were heated and mixed until thoroughly homogeneous. After cooling and solidifying, the powder was finely ground to prepare a feed containing this powder at a weight ratio of 56% as the sole carbohydrate source. This feed was used for S. mutans P
S-14 strain was given to 10 rats orally infected, and 58
It was kept for days. As a result, the average caries score for rats was 8.
.. It was 5±3.1.
【0017】[0017]
【比較例3】蔗糖
67gマルチトール
67g水飴
66g上記成分を加熱溶融し、
十分均一に溶融した。冷却固化後、細かく粉砕し、この
粉末を重量比56%で含み、唯一の炭水化物源とする飼
料を調製した。この飼料を、S.mutans PS
−14株を経口感染させたラット10匹に与え、58日
間飼育した。この結果、ラットの平均う蝕スコアは13
.5±2.8であった。[Comparative Example 3] Sucrose
67g maltitol
67g starch syrup
Heat and melt 66g of the above ingredients,
It melted sufficiently uniformly. After cooling and solidifying, the powder was finely ground to prepare a feed containing this powder at a weight ratio of 56% as the sole carbohydrate source. This feed was used for S. mutans PS
-14 strain was given to 10 rats orally infected and kept for 58 days. As a result, the average caries score for rats was 13.
.. It was 5±2.8.
【0018】これらの結果からテアンデロースを含むキ
ャンディは抗う蝕性のあることが分かる。また、粉砕す
る前の本発明のキャンディおよび比較例1〜3で作成し
たキャンディを12名のパネラーにより味質のさわやか
さに付いて官能試験を実施したところ、本発明のキャン
ディは比較例のものよりも良好な結果を得た。この結果
を表1に示す。These results show that the candy containing theanderose has anti-caries properties. In addition, when the candies of the present invention before being crushed and the candies prepared in Comparative Examples 1 to 3 were subjected to a sensory test by 12 panelists regarding the refreshing taste, it was found that the candies of the present invention were better than those of the comparative examples. also obtained good results. The results are shown in Table 1.
【0019】[0019]
【表1】[Table 1]
【0020】[0020]
【発明の効果】本発明は、各種炭水化物を主たる甘味料
とするキャンディの成分として、テアンデロースを含む
ことによって、う蝕性のない味質のさわやかなキャンデ
ィが得られる。Effects of the Invention According to the present invention, by including theanderose as a component of a candy containing various carbohydrates as a main sweetener, a refreshing candy with a non-cariogenic taste can be obtained.
Claims (1)
ンディにおいて、ムコール属菌由来のグルコシルトラン
スフェラーゼを用いてグルカンと蔗糖より生成したテア
ンデロースを含むことを特徴とする抗う蝕性キャンディ
。1. An anti-caries candy containing various carbohydrates as a sweetener, characterized in that it contains theanderose produced from glucan and sucrose using glucosyltransferase derived from Mucor bacteria.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3003315A JPH04237463A (en) | 1991-01-16 | 1991-01-16 | Theanderose-containing candy |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3003315A JPH04237463A (en) | 1991-01-16 | 1991-01-16 | Theanderose-containing candy |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH04237463A true JPH04237463A (en) | 1992-08-25 |
Family
ID=11553926
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP3003315A Withdrawn JPH04237463A (en) | 1991-01-16 | 1991-01-16 | Theanderose-containing candy |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH04237463A (en) |
-
1991
- 1991-01-16 JP JP3003315A patent/JPH04237463A/en not_active Withdrawn
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