JPS60188035A - Taste improvement in stevioside - Google Patents
Taste improvement in steviosideInfo
- Publication number
- JPS60188035A JPS60188035A JP59044537A JP4453784A JPS60188035A JP S60188035 A JPS60188035 A JP S60188035A JP 59044537 A JP59044537 A JP 59044537A JP 4453784 A JP4453784 A JP 4453784A JP S60188035 A JPS60188035 A JP S60188035A
- Authority
- JP
- Japan
- Prior art keywords
- stevioside
- cyclodextrin
- taste
- bitterness
- organic acid
- 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.)
- Granted
Links
Abstract
Description
【発明の詳細な説明】
本発明はステビオサイド(レバウディオサイドを含む)
を含む甘味料の呈味を改善する方法に関するものである
。[Detailed Description of the Invention] The present invention provides stevioside (including rebaudioside)
The present invention relates to a method for improving the taste of a sweetener containing.
その目的とするところは、酒石酸ナトリウム、クエン酸
ナトリウム、リンゴ酸ナトリウム等の有8N酸塩とサイ
クロデキストリンとを併用添加することにより、ステビ
オサイド及びそれらを含むステビア抽出物の呈味上の苦
味、嫌味等の欠点を除去し、経済的に良質の甘味を得る
ことである。The purpose is to reduce the bitterness and unpleasant taste of stevioside and stevia extract containing them by adding 8N salts such as sodium tartrate, sodium citrate, and sodium malate together with cyclodextrin. The purpose is to eliminate the disadvantages such as, and economically obtain high-quality sweetness.
ステビオリ”イドは、砂糖の300倍の甘味度をもつ天
然甘味物質であり、最近の合成甘味料の安全性の問題、
または納置が社会問題となりつつある今日、これを解決
し得るl味淵として急激に注目されてきた。Stevioli"ide is a natural sweetening substance that is 300 times sweeter than sugar, and has recently become a subject of concern regarding the safety of synthetic sweeteners.
Nowadays, when storage is becoming a social problem, it has suddenly attracted attention as a potential solution.
しかしステビオサイド及びステビア抽出物は砂糖に比較
しU味の発現性が遅く且つ苦味、嫌味等の不快味の欠点
を右しており、ステビオサイドの実用上の大きな障害と
なっている。However, compared to sugar, stevioside and stevia extracts develop the U taste more slowly and suffer from unpleasant tastes such as bitterness and sarcastic taste, which is a major obstacle in the practical use of stevioside.
従って、ステビオライド及びステビア抽出物の呈味性の
改良については、種々の提案かなされているにもかかわ
らず、未だ解決されCいない。Therefore, although various proposals have been made to improve the taste of steviolide and stevia extracts, the problem remains unsolved.
一方、特公昭57−18779号で、ステビオサイドと
例えばマルトース、マルトオリゴ糖等のα−グルコシル
糖化合物を共存させ、このα−グルコシル塁をステビオ
サイドに転移しうるα−グルコシル転移酵素を作用させ
てα−グリコジルステビオサイドを作る方法が提案され
U味質の良好な甘味料が市場へ提供させているが価格が
高く実用上に問題がある。On the other hand, in Japanese Patent Publication No. 57-18779, stevioside and an α-glucosyl sugar compound such as maltose or maltooligosaccharide are made to coexist, and an α-glucosyltransferase capable of transferring this α-glucosyl base to stevioside is activated to produce an α- A method for producing glycodyl stevioside has been proposed, and a sweetener with good taste has been provided on the market, but it is expensive and has problems in practical use.
本発明者らは、上述した事情に鑑み、ステビオサイド及
びステビア抽出物の苦味、嫌味を除去する方法につい−
(鋭意検問した結果、サイクロデキストリンを有機酸塩
類と併用添加することにより不快味を早する物質をマス
キング出来る事実を発見し、本発明を完成した。In view of the above-mentioned circumstances, the present inventors have developed a method for removing the bitterness and unpleasant taste of stevioside and stevia extracts.
(As a result of extensive investigation, we discovered that by adding cyclodextrin in combination with organic acid salts, it is possible to mask substances that cause unpleasant taste, and thus completed the present invention.
こ)でいう有機酸塩とはクエン酸プトリウム、リンゴ酸
ナトリウム、酒石酸ナトリウム等で、ステビオサイド1
重間部に対して有機酸塩の一種又は二押以上を0.2〜
50重量部の範囲で添加すれば良く、好ましくは0.5
〜4重量部が良好である。The organic acid salts referred to in this) include putrium citrate, sodium malate, sodium tartrate, etc. Stevioside 1
Apply 0.2 to 0.2 or more of one or more organic acid salts to the interheavy area.
It may be added in an amount of 50 parts by weight, preferably 0.5 parts by weight.
~4 parts by weight is good.
また、ここでいうサイクロデキストリンとは6〜12個
のグルコースがα−1,4グルコシド結合で環状に連な
った非還元性のマルトオリゴ糖で、3acillυSF
Aのある種の微生物から得られるサイクロデキストリン
生成酵素を沢粉に作用させて得られる。サイクロデキス
トリンには3種類あり、グルコースが6個のα−17個
のβ−18個のγ−サイクロデキストリンがある。市場
では主としてβ−サイクロデキストリンの粉末かα、β
、γの混合物でサイクロデキストリン含量20%の水あ
め状のものが多く使用されている。In addition, the cyclodextrin referred to here is a non-reducing maltooligosaccharide in which 6 to 12 glucose units are linked in a ring through α-1,4 glucoside bonds, and 3acillυSF
It is obtained by allowing a cyclodextrin-producing enzyme obtained from a certain type of microorganism (A) to act on sawdust. There are three types of cyclodextrins: α-cyclodextrin, which has 6 glucose units, β-17 units, and γ-cyclodextrin, which has 18 β units. The market mainly consists of β-cyclodextrin powder, α, β
, γ in the form of starch syrup with a cyclodextrin content of 20% is often used.
本発明では、β−サイクロデキストリンに効果が認めら
れたが、勿論β−サイク[1デギストリンを含むもので
あれば良い。ステビオサイドに対するサイクロデキスト
リンの添加量はステビオサイドの1重量部に対して0.
5〜100匝量部であれば良い。サイクロデキストリン
の最適添加量はステビア抽出物中の不純物の量によって
変動ηるために特定は出来ないが、ステビオサイドの純
度が80〜98%の場合、ステビオサイドの100%純
疫換韓1重最部に対して3〜10重量添加すれば良い。In the present invention, β-cyclodextrin was found to be effective, but of course any substance containing β-cyclodextrin may be used. The amount of cyclodextrin added to stevioside is 0.00% per part by weight of stevioside.
It may be 5 to 100 parts by weight. The optimal amount of cyclodextrin to be added cannot be determined because it varies depending on the amount of impurities in the stevia extract, but when the purity of stevioside is 80 to 98%, 100% pure stevioside is added. What is necessary is to add 3 to 10 weights to the total amount.
ステビオサイドの純度が40〜80%の場合は、ステビ
オサイドの100%純度換11tuff)部あたり10
〜30重量部添加すれば良い。If the purity of stevioside is 40-80%, use 10 parts per 100% pure (11 tuff) part of stevioside.
It is sufficient to add up to 30 parts by weight.
次に実施例によって本発明をさらに説明り−る。Next, the present invention will be further explained by examples.
実施1シ1j−1
及テビア抽出物(ステビオサイド含量86.3%)の0
.5%水溶液(、ニクエン酸ナトリウム、酒6 酸ナト
リウム、α、β、γ−ザイクロデキストリンを組合わせ
て、ステビア抽出物の苦味、嫌味の改善度合を官能検査
IZ J、って比較した。Example 1 1j-1 and Tevia extract (stevioside content 86.3%)
.. A 5% aqueous solution (sodium citrate, sodium hexate alcohol, α, β, γ-zychlodextrin) was combined and the degree of improvement in the bitterness and unpleasant taste of the Stevia extract was compared using a sensory test IZJ.
その結果を第1表に示した。The results are shown in Table 1.
ム・1′1曲 J’、4 jll
Δ△・・苦味、lIF味、はぼ完全にマスクされている
。M・1'1 song J', 4 jll Δ△...Bitterness, lIF taste, are completely masked.
△・・・若干、苦味を感じるが、良好である。Δ: Slightly bitter taste, but good.
[(・・・やや効果あり。[(...somewhat effective.
0・・・効果なし。0...No effect.
尚α、β、γ−1ノイクロデキストリンは1木食品化工
(株)のものを使用した。(純度98.5%以上)
右+m MQ jMとβ−サイク0デキストリンを併用
したものに顕棺な効果が認められる。The α, β, and γ-1 neuculodextrins manufactured by Ichiki Foods Chemical Co., Ltd. were used. (Purity 98.5% or more) Right+m MQ jM and β-cyc0 dextrin are used in combination, and a remarkable effect is observed.
実施例−2
ステビア抽出物(ステビオサイド含fj4B0.7%)
0.5%水溶液の系にてfi1幾酸塩酸塩−リーイクロ
デキストリンの組合わせについて検討した。Example-2 Stevia extract (stevioside containing fj4B0.7%)
The combination of fi1 dihydrochloride and li clodextrin was investigated in a 0.5% aqueous solution system.
その結果を第2表に小した。The results are summarized in Table 2.
評価基準は実施例−1ど同様である。The evaluation criteria are the same as in Example-1.
注−1日本食品化工(株)製の水アメタイプのサイク[
1デキストリンである。ザイクロデキストリンmは20
%でα、β、γの混合物である。Note-1 A starch syrup type cyc made by Nihon Shokuhin Kako Co., Ltd. [
1 dextrin. Zychlodextrin m is 20
% is a mixture of α, β, and γ.
41機酸塩、」ノイクロデギストリンをそれぞれ用品で
使用して−し改善効果は認められないが、両者を併用す
ると顕著な改善効果が認められる。No improvement effect was observed when using ``41-functional acid salt'' and ``neuclodegistrin'' in their respective products, but when both were used in combination, a significant improvement effect was observed.
実施例−3
ステビア抽出物(ステビオサイド含1151.’8%)
の0.5%水溶液の系にて検討した。Example-3 Stevia extract (contains stevioside 1151.'8%)
The study was conducted using a 0.5% aqueous solution system.
その結果を第3表に示した。The results are shown in Table 3.
評価基準は実施例−1と同様である。The evaluation criteria are the same as in Example-1.
不純物の多い中純度のステビア抽出物でも有機酸塩と1
ノイクロデキストリンを併用ツることによりyll−八
な望味改善効果が認められる。Even medium-purity stevia extract with many impurities has organic acid salts and 1
When used in combination with neuclodextrin, an effect of improving YLL-8 taste is observed.
但し、不純物が多いためにステビオサイドあたりのサイ
クLJデキストリンの添加量は多く必要である。However, since there are many impurities, it is necessary to add a large amount of CycloLJ dextrin per stevioside.
実施例−71
通常重版されているステビオサイド製剤ど本発明品と比
較した。Example 71 A commonly reprinted stevioside preparation was compared with the product of the present invention.
その結果を第4表に示した。The results are shown in Table 4.
注−2・・ステビオサイド含pi 84.2%注−3・
・ 51.6%
テスt−N o、1.2,3.6は粉体混合にて各1バ
■1した。テストNO,4,5,7はスプレードライA
7−にて各I By調製した。(尚C1−1−20には
約25%の水分が含まれているので、無水物換算で80
%配合した。)
以」−7種類のサンプルを5.7,5.10%溶液にて
官能検査を行なったところ、有機酸塩と4ノイク1]デ
キス1ヘリンを(Jl用した本発明品(テストNo。Note-2... Contains stevioside pi 84.2% Note-3.
- 51.6% Test t-No. 1.2 and 3.6 were each mixed with 1 bar of powder. Test No. 4, 5, 7 is spray dry A
Each IBy was prepared at 7-. (Since C1-1-20 contains about 25% water, it is calculated as 80% in terms of anhydride.
% blended. ) - When a sensory test was conducted on 7 types of samples using 5.7 and 5.10% solutions, it was found that the product of the present invention (Test No.
3.4.5.6.7)のhが苦味、嫌味が除去され顕著
な呈味改善効果が認められた。3.4.5.6.7) h removed bitterness and sarcasm, and a remarkable taste improvement effect was observed.
Claims (1)
分とする甘味料において、ステ上オサ161重B部に対
して、酒石酸塩、クエンM塩、リンゴ酸塩又はその他の
有機酸塩の一種又は二種以上を0.2〜50車楢部、サ
イクロデキストリン0.5〜100m 8部の割合で併
用添加することを特徴とするステビオサイドの呈味改善
法。In sweeteners containing stevioside (including rebaudioide) as a taste component, one or two of tartrate, citric M salt, malate, or other organic acid salts are added to stevioside 161 heavy B part. A method for improving the taste of stevioside, characterized in that the above is added in combination at a ratio of 0.2 to 50 parts of car undercover and 0.5 to 100 parts of cyclodextrin and 8 parts.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59044537A JPS60188035A (en) | 1984-03-08 | 1984-03-08 | Taste improvement in stevioside |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59044537A JPS60188035A (en) | 1984-03-08 | 1984-03-08 | Taste improvement in stevioside |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS60188035A true JPS60188035A (en) | 1985-09-25 |
JPH05981B2 JPH05981B2 (en) | 1993-01-07 |
Family
ID=12694255
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP59044537A Granted JPS60188035A (en) | 1984-03-08 | 1984-03-08 | Taste improvement in stevioside |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS60188035A (en) |
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