JPH0367560A - Sweetener composition - Google Patents

Sweetener composition

Info

Publication number
JPH0367560A
JPH0367560A JP1205290A JP20529089A JPH0367560A JP H0367560 A JPH0367560 A JP H0367560A JP 1205290 A JP1205290 A JP 1205290A JP 20529089 A JP20529089 A JP 20529089A JP H0367560 A JPH0367560 A JP H0367560A
Authority
JP
Japan
Prior art keywords
dfa
iii
aftertaste
menthol
sweetener composition
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
Application number
JP1205290A
Other languages
Japanese (ja)
Inventor
Tsutomu Kondo
近藤 務
Akio Nishimura
西村 彰夫
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Mitsubishi Chemical Corp
Original Assignee
Mitsubishi Kasei Corp
Mitsubishi Chemical Industries Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Mitsubishi Kasei Corp, Mitsubishi Chemical Industries Ltd filed Critical Mitsubishi Kasei Corp
Priority to JP1205290A priority Critical patent/JPH0367560A/en
Publication of JPH0367560A publication Critical patent/JPH0367560A/en
Pending legal-status Critical Current

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Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明はジ−D−フルクトフラノース1.2’ :2,
3’ジアンハイドライド(以下、r DFA e 11
口と略す)を主成分とするす味料に関するものであり、 詳しくはDFA −IIIの苦み、後味の改良された甘
味料組成物に関する。
Detailed Description of the Invention (Industrial Application Field) The present invention provides di-D-fructofuranose 1.2':2,
3' dianhydride (r DFA e 11
The present invention relates to a sweetener composition containing DFA-III as a main component, and specifically relates to a sweetener composition with improved bitterness and aftertaste of DFA-III.

(従来の技術) 甘味料には糖類、糖アルコール、非糖類甘味料等がある
が、この中でしょ糖が広く普及している。しかしながら
、食生活の向上に伴って栄養の過剰摂取が問題になり、
特にしょ糖は過剰摂取に伴って乳幼児や学童、成人に至
るまで虫歯罹患率の増大等また肥満、糖尿病の促進等の
医学的弊害が指摘されている。
(Prior Art) Sweeteners include sugars, sugar alcohols, non-saccharide sweeteners, etc. Among these sweeteners, sugar is widely used. However, with the improvement of dietary habits, excessive intake of nutrients has become a problem.
In particular, excessive intake of sucrose has been pointed out to have medical adverse effects such as an increased incidence of tooth decay in infants, school children, and even adults, as well as the promotion of obesity and diabetes.

これらの理由からしよ糖が敬遠されつつあり、しよ糖に
代わる非う触性あるいは低カロリーの甘味料が要求され
ている。このようななかでDFA −Hlはほとんど体
内に吸収されず低カロリーであり、さらに抗う触性を持
つ健康上優れた甘味料である。
For these reasons, sucrose is being avoided, and there is a demand for non-carious or low-calorie sweeteners to replace sucrose. Under these circumstances, DFA-Hl is hardly absorbed into the body, has a low calorie content, and has a tactile property that makes it an excellent sweetener for health.

(発明が解決しようとする課題) DFA + IIIは低カロリー、抗う触性のU°味料
で健康に好ましい。しかしながら甘味質に問題がある。
(Problems to be Solved by the Invention) DFA + III is a low-calorie, anti-cariogenic flavoring agent that is good for health. However, there is a problem with sweetness.

しよ糖に比較して苦味がつよく、とくに後味に残る刺激
味は好ましくない。苦味のあると言われているキシリト
ール、マンニトールに比較しても苦味、後味が強い。濃
度5重量%でも苦味を感じ、濃度が高くなると後味に刺
激味を感じる。一般の食品にしよ糖の代替えとしてDF
A−IIIを用いることは嗜好的に問題である。
It has a strong bitterness compared to sucrose, and the pungent taste that remains in the aftertaste is particularly undesirable. It has a strong bitterness and aftertaste compared to xylitol and mannitol, which are said to have a bitter taste. Even at a concentration of 5% by weight, a bitter taste is felt, and as the concentration increases, a pungent aftertaste is felt. DF as a sugar substitute for general foods
Using A-III is a matter of preference.

(課題を解決するための手段) 本発明の要旨はDFA −IIIに対してメントールを
0.02重量%以上含有してなる甘味料組成物である。
(Means for Solving the Problems) The gist of the present invention is a sweetener composition containing 0.02% by weight or more of menthol based on DFA-III.

本発明において用いるDFA−IIIは外銭は白色結晶
粉宋で水によく溶は甘味度はしよ糖の約半分の物質であ
る。
DFA-III used in the present invention is a white crystalline powder that is well soluble in water and has a sweetness about half that of sucrose.

DFA −IIIは通常イヌリン等のp2−17ラクタ
ン構造を持つ化合物よりDFA + IIII成酵素を
用いてつくられる。この酵素の生産菌としては、例えば
アルスロ゛くフタ・グロビフ1ルミスC11−1、アル
スロバクタ、ウレアファシェンス7116、アルスロバ
クタ・アウレッセンスIFO12136、シュードモナ
ス・フルオレッセンス949、アルスロバクタ・イリシ
スMCl−2297などが知られている。これらの生産
菌より得られる酵素あるいは菌体自身を用いて、イヌリ
ン等よりDFA −IIIを製造することが可能である
。しかし上記生産菌を用いて製造したDFA −III
はどれも苦味、後味があり問題である。
DFA-III is usually produced from a compound having a p2-17 lactan structure, such as inulin, using DFA + III synthase. Bacteria producing this enzyme include, for example, Arthrobacter globiflorumis C11-1, Arthrobacter ureafaciens 7116, Arthrobacter aurescens IFO 12136, Pseudomonas fluorescens 949, Arthrobacter iris MCl-2297, etc. It is being DFA-III can be produced from inulin or the like using enzymes obtained from these producing bacteria or the bacterial cells themselves. However, DFA-III produced using the above-mentioned producing bacteria
All of them have a bitter taste and aftertaste, which is problematic.

本発明者はこれらの課題をDFA −IIIにメントー
ルを0.02重量%以上加えることで解決した。
The present inventor solved these problems by adding 0.02% by weight or more of menthol to DFA-III.

本発明で用いるメントールはdiまたはe−メントール
どちらを用いてもよいが、eの方が一般的である。
The menthol used in the present invention may be either di or e-menthol, but e is more common.

メントールは単品で用いてもよいし、メントールを含有
するもの、例えばペパーミント油を用いてもよい。さら
にユーカリ油、スペアミント油などを併用すれば風味は
好ましいものになる。メントールで苦味、後味をマスキ
ングしさらにフレーバを加えれば色々なタイプの香りが
可能である。
Menthol may be used alone, or a product containing menthol, such as peppermint oil, may be used. Furthermore, if eucalyptus oil, spearmint oil, etc. are used in combination, the flavor becomes more desirable. By masking the bitterness and aftertaste with menthol and adding flavor, you can create a variety of aromas.

フレバーとしてはオレンジ、ストロベリー、パイナツプ
ル、グレーグ、ラズベリー、ピーチ、レモン、バニラ、
コーヒー、チョコレート、ココア、紅茶、ミルク、ハー
ブ、又これらの混合物等が挙げられる。
Flavors include orange, strawberry, pineapple, gray, raspberry, peach, lemon, vanilla,
Examples include coffee, chocolate, cocoa, tea, milk, herbs, and mixtures thereof.

本発明品は菓子類からはキャンデー、チューインガム、
チョコレート、打錠菓子等が挙げられる。口腔剤として
は、練歯磨、含そう剤、口中清涼剤、口中清潔剤等、口
腔内に適用される薬剤であればすべてに用いられる。
The products of this invention can be used in confectionery such as candy, chewing gum,
Examples include chocolate, compressed confectionery, and the like. As oral medicines, it can be used for all medicines that can be applied in the oral cavity, such as toothpaste, mouthwash, mouth fresheners, and mouth cleansers.

(友施例) 次に実施例により本発明をさらに詳細に説明するが、本
発明はかかる実施例に限定されるもので!1.シい。
(Friendly Examples) Next, the present invention will be explained in more detail with reference to Examples, but the present invention is not limited to these Examples. 1. Yes.

なお、官能評価を行うパネラ−は三菱化成(株)総合研
究所において食品開発研究に長く従事している5名で行
った。
The panel that conducted the sensory evaluation was five people who have long been engaged in food development research at Mitsubishi Kasei Research Institute.

(DFA −IIIの甘味質の官能評価)15重量%D
FA −IIII溶液と、甘味料の標準としての7重量
%しよ糖水溶液との比較官能評価を行った。各試料温度
は20℃で行った。
(Sensory evaluation of sweetness quality of DFA-III) 15% by weight D
A comparative sensory evaluation was conducted between the FA-III solution and a 7% by weight aqueous sucrose solution as a sweetener standard. The temperature of each sample was 20°C.

しよ糖の評価値を0として、次の評価尺度によって評価
した。
The evaluation was made using the following evaluation scale, with the evaluation value of sucrose as 0.

評価尺度 2 非常に  かなり ・あっさりしている 0 やや  普通 1 やや 2 かなり ・しつこい 3 非常に ・好まない 評価結果を第1表に示す。rating scale 2 very, very much ・It's light 0 Somewhat normal 1 somewhat 2 pretty ·Insistent 3 very ·I do not like The evaluation results are shown in Table 1.

・好む 第1表 比較例I DFA −IIIに次に示す糖、非糖類甘味料、食塩、
酸を混合して、DFA + IIIの苦味、後味のマス
キング効果を調べた。混合溶液の甘味度はしょ糖7%水
溶液に相当する甘味に調整した。
・Table 1 Comparative Example I DFA-III contains the following sugars, non-saccharide sweeteners, salt,
The bitterness and aftertaste masking effect of DFA + III was investigated by mixing acids. The sweetness of the mixed solution was adjusted to be equivalent to a 7% sucrose aqueous solution.

である。It is.

評価結果は次の通り 評価値説明  千生  苦味、後味かなりあり+  苦
味、後味あり 苦味、後味なし このように、DFA −111の苦味後味を改良するた
め糖、非糖類甘味料、塩、酸等を混合しても、どれも苦
味後味を改良することは出来ながった。
The evaluation results are explained as follows: Chio: Quite bitter, aftertaste + Bitter, aftertaste Bitter, no aftertaste In this way, to improve the bitter aftertaste of DFA-111, sugar, non-saccharide sweeteners, salt, acid, etc. Even when mixed, none of them could improve the bitter aftertaste.

実施例I DFA−■I 50gにe−メントール0.005〜1
.0gノ範囲で加えたものに各々水を加え100gに調
整し官能評価をした。結果は次の通りである。
Example I DFA-■I 50g and e-menthol 0.005-1
.. Each sample was added in a range of 0 g, water was added to each sample to adjust the total amount to 100 g, and sensory evaluation was performed. The results are as follows.

このように、メントールをDFA−IIIに対して0.
02重量%以上含有させると、DFA −IIIの苦味
、後味が改良されることがわかる。
In this way, menthol was added to DFA-III at 0.0%.
It can be seen that when DFA-III is contained in an amount of 0.2% by weight or more, the bitterness and aftertaste of DFA-III are improved.

実施例2 キャンデー DFA −III 90g、粉飴10g及び水Logの
混合物を120℃まで煮つめた。さらに真空下(110
℃、720mmHg)で煮つめた。煮つめた後、80℃
に冷却しメントール0.03g及びペパーミント?Il
] 0.5gを加えよく混合し成型器に入れ成型した。
Example 2 A mixture of 90 g of candy DFA-III, 10 g of powdered candy, and Log of water was boiled down to 120°C. Further under vacuum (110
℃, 720 mmHg). After boiling, 80℃
Cool to 0.03g of menthol and peppermint? Il
] 0.5 g was added, mixed well, and then placed in a molding machine and molded.

比較品としてメントール無添加のものを同様に調整した
。盲姥訂″コをおこなった結果は次の通りである。
As a comparative product, a product without menthol was prepared in the same manner. The results of the blind revision are as follows.

練歯磨 実施例3 キシンデー DFA−11160g、 Lよ糖30g1粉飴10g1
及び水Logの混合物を120℃まで煮つめた。さらに
真空下(ILO℃、720mmHg)で煮つめた。煮つ
めた後80℃に冷却しメントール0.02g及びオレン
ジ油0.1gを加え、よく混合し成型器に入れ底型した
Toothpaste Example 3 Kisinday DFA-11 160g, L-yoko sugar 30g1 powdered candy 10g1
A mixture of water and water was boiled down to 120°C. It was further boiled down under vacuum (ILO°C, 720 mmHg). After boiling, the mixture was cooled to 80° C., 0.02 g of menthol and 0.1 g of orange oil were added, mixed well, and placed in a mold to form a bottom mold.

出来たDFA + IIIのオレンジキャンデーは苦味
、後味−ノくなく嗜好性良好であった。
The resulting DFA + III orange candy had no bitterness or aftertaste and had good palatability.

害施例4 練歯磨 以下の材料をよく混練りした後、チューブに詰め/−ル
して練歯磨を試作した。比較品としてメントールなしの
ものを同様に試作した。
Example 4 Toothpaste A prototype toothpaste was prepared by thoroughly kneading the following ingredients and filling them into tubes. As a comparison product, a sample without menthol was similarly produced.

燐酸水素カルシウム DFA−III 水添オリゴ糖 ラウリル硫酸ナトリウム L−メントール カルボキシメチルセルロースNa 水 50(重量%) 4 0 0.05 23.95 官能評価結果は次の通りであった。calcium hydrogen phosphate DFA-III hydrogenated oligosaccharide sodium lauryl sulfate L-menthol Carboxymethyl cellulose Na water 50 (weight%) 4 0 0.05 23.95 The sensory evaluation results were as follows.

(発明の効果) 本発明の甘味料組成物は低カロリー、抗う触性で健康上
優れたものであり、かつDFA −III特有の苦味、
後味が感じられず嗜好上からも好ましいものである。
(Effects of the Invention) The sweetener composition of the present invention is low in calories, resistant to caries, and has excellent health benefits, and has the bitter taste characteristic of DFA-III.
It has no aftertaste and is preferable from a taste standpoint.

Claims (1)

【特許請求の範囲】[Claims] (1)ジ−D−フルクトフラノース1,2′:2,3′
ジアンハイドライドに対してメントールを0.02重量
%以上含有してなる甘味料組成物。
(1) Di-D-fructofuranose 1,2':2,3'
A sweetener composition containing 0.02% by weight or more of menthol based on dianhydride.
JP1205290A 1989-08-08 1989-08-08 Sweetener composition Pending JPH0367560A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1205290A JPH0367560A (en) 1989-08-08 1989-08-08 Sweetener composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1205290A JPH0367560A (en) 1989-08-08 1989-08-08 Sweetener composition

Publications (1)

Publication Number Publication Date
JPH0367560A true JPH0367560A (en) 1991-03-22

Family

ID=16504525

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1205290A Pending JPH0367560A (en) 1989-08-08 1989-08-08 Sweetener composition

Country Status (1)

Country Link
JP (1) JPH0367560A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5695746A (en) * 1995-07-28 1997-12-09 Chesebrough-Pond's Usa Co., Division Of Conopco, Inc. Liquid dentifrice with mouthwash fresh taste
JP2005170855A (en) * 2003-12-11 2005-06-30 Nippon Beet Sugar Mfg Co Ltd Crystalline or crystal grain end difructose anhydride III
US8017168B2 (en) 2006-11-02 2011-09-13 The Coca-Cola Company High-potency sweetener composition with rubisco protein, rubiscolin, rubiscolin derivatives, ace inhibitory peptides, and combinations thereof, and compositions sweetened therewith

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5695746A (en) * 1995-07-28 1997-12-09 Chesebrough-Pond's Usa Co., Division Of Conopco, Inc. Liquid dentifrice with mouthwash fresh taste
JP2005170855A (en) * 2003-12-11 2005-06-30 Nippon Beet Sugar Mfg Co Ltd Crystalline or crystal grain end difructose anhydride III
US8017168B2 (en) 2006-11-02 2011-09-13 The Coca-Cola Company High-potency sweetener composition with rubisco protein, rubiscolin, rubiscolin derivatives, ace inhibitory peptides, and combinations thereof, and compositions sweetened therewith

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