JPS6016216B2 - New dipeptide sweetener composition - Google Patents

New dipeptide sweetener composition

Info

Publication number
JPS6016216B2
JPS6016216B2 JP55136164A JP13616480A JPS6016216B2 JP S6016216 B2 JPS6016216 B2 JP S6016216B2 JP 55136164 A JP55136164 A JP 55136164A JP 13616480 A JP13616480 A JP 13616480A JP S6016216 B2 JPS6016216 B2 JP S6016216B2
Authority
JP
Japan
Prior art keywords
alanine
sweetness
sweetener composition
taste
sweeteners
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
Application number
JP55136164A
Other languages
Japanese (ja)
Other versions
JPS5763068A (en
Inventor
勇三 岡田
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.)
Ajinomoto Co Inc
Original Assignee
Ajinomoto Co Inc
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 Ajinomoto Co Inc filed Critical Ajinomoto Co Inc
Priority to JP55136164A priority Critical patent/JPS6016216B2/en
Publication of JPS5763068A publication Critical patent/JPS5763068A/en
Publication of JPS6016216B2 publication Critical patent/JPS6016216B2/en
Expired legal-status Critical Current

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Description

【発明の詳細な説明】 本発明は改良された甘味を有するジベプチド甘味料組成
物に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to dipeptide sweetener compositions with improved sweetness.

甘味料には、例えば、ショ糖をはじめとする糠類、ソル
ビツト、キシリツト、マルチツト、リカシン等の糖アル
コール、ジベプチド、トリプトフアン、グリシン等のア
ミノ酸、ベプチド系甘味料その他たん白質甘味料、人工
合成甘味料があり、この中、糖類特に砂糖は、苦味、異
味その他嫌味を感じさせず、良好な甘味を有するものと
して、最も広く普及している。
Sweeteners include, for example, brans such as sucrose, sugar alcohols such as sorbitate, xylitol, maltituto, and lycasin, amino acids such as dipeptide, tryptophan, and glycine, peptide sweeteners and other protein sweeteners, and artificially synthesized sweeteners. Among these, saccharides, particularly sugar, are the most widely used because they have a good sweet taste without causing bitterness, off-taste, or other unpleasant tastes.

一方、糖アルコール、ベプチド系甘味料などは、近年ダ
イエット等を目的として、注目を集めており、種々の開
発が行われているが、砂糖に比べ、呈味性その他の面に
おいて、必ずしも満足できないものが多い。これらの中
、ジベプチド甘味料は、星味性において、先味が品のよ
い甘味で特徴づけられる満足できる品質を有するが、反
面、甘味質として、若干、厚みやまろやかさを欠くとい
う問題がある。すなわち、ジベプチド独自の甘味質で先
味が強く特徴づけられ、かつ、それが品のよいスッキリ
した呈味性を示すものの、砂糖に比べ、甘味の持続がな
く、甘味質として単調で厚みを欠き更にはまるやかごを
欠く煩向にある。本発明者は、上記の如き呈味質を有す
るジベプチド甘味料につき、その呈味質の改善を図るべ
く種々検討を重ね、グリシン、DL−アラニン、Lーア
ラニン、Lーセリンから成る群から選ばれたアミノ酸を
ジベプチド甘味料に配合することにより、ジベプチド甘
味料の星味性が改善され、ジベプチド甘味料単独の場合
に比べ、呈味性に中を与えると共に、特徴的かつ良好な
甘味性を発現するという新たな知見に至り、本発明を完
成したものである。
On the other hand, sugar alcohols, peptide sweeteners, etc. have attracted attention in recent years for the purpose of dieting, etc., and various developments have been carried out, but compared to sugar, they are not necessarily satisfactory in terms of taste and other aspects. There are many things. Among these, dibeptide sweeteners have satisfactory quality in terms of star taste, characterized by a good sweet taste, but on the other hand, there is a problem that the sweetness quality is slightly lacking in thickness and mellowness. . In other words, although dibeptide has a unique sweetness with a strong fore-taste, and exhibits an elegant and refreshing taste, compared to sugar, the sweetness does not last long and the sweetness is monotonous and lacks depth. Moreover, they are suffering from lack of maroons and baskets. The present inventor conducted various studies in order to improve the taste quality of the dipeptide sweetener having the taste quality described above, and selected a dipeptide sweetener selected from the group consisting of glycine, DL-alanine, L-alanine, and L-serine. By blending amino acids into dipeptide sweeteners, the starry taste of the dipeptide sweeteners is improved, giving it a more neutral taste and developing characteristic and good sweetness compared to the case of dipeptide sweeteners alone. This new finding has led to the completion of the present invention.

すなわち、本発明は、ジベプチド甘味料と、ジベプチド
甘味料重量の10〜1000%のグリシン、DL−アラ
ニン、Lーアラニン又はL−セリンを含有して成るジベ
プチド甘味料組成物でありジベプチド甘味料の欠点であ
る甘味の持続性がなく、単調に煩るといった点を補い、
より砂糖の甘味質に近づくことができるとともに、特徴
的かつ良好な甘味を有する甘味料組成物を提供するもの
である。
That is, the present invention is a diptide sweetener composition comprising a dipeptide sweetener and 10 to 1000% of glycine, DL-alanine, L-alanine, or L-serine by weight of the dipeptide sweetener, and which eliminates the drawbacks of the dipeptide sweetener. It compensates for the lack of long-lasting sweetness and the monotonous feeling of sweetness,
The present invention provides a sweetener composition that can more closely resemble the sweetness of sugar and has a characteristic and good sweetness.

また、甘味料は、いわゆる卓上甘味料として使用された
り、コーヒー、紅茶など飲料用その他に分包されたりす
る場合も多いが、この場合に計量等の便宜上要求される
増量剤の添加を省略若しくは減量でき、更にまた賦形剤
としての効果も発現できる等の副次的効果を奏すること
ができる。本発明で使用するジベプチド甘味料は、Q−
Lーアス/ぐルチル−Lーフヱニルアラニン−メチルェ
ステル又はエチルェステル(以下、APと略記する)で
ある。AP‘こ対し、グリシン、DLーアラニン、Lー
アラニン又はL−セリンを紐合せるが、これらのアミノ
酸をAPに対し、2種以上併用してもかまわない。また
、グリシン及びDL−アラニンは、Lーアラニン、L−
セリンに比べより高い効果を挙げることができる。AP
と上記アミノ酸の組成比はAPに対し、APの重量の1
0〜1000%好ましくは75〜500%のアミノ酸量
である。アミノ酸量がAPの重量の10%以下の場合に
は、甘味に砂糖にあるような厚みを欠く煩向が顕著とな
り、逆に1000%を越える場合には、甘味がぼけ、濃
厚感、異味感が感ぜられる。従って、上記10〜100
0%重量好ましくは75〜500%重量が、ジベプチド
甘味料として、砂糖により近い甘味質を呈し、あらゆる
用途に対応できるものとして、至通の範囲である。本発
明のジベプチド甘味料組成物は、例えば粉末、錠剤或い
はシロップ等、あらゆる態様で使用できる。
In addition, sweeteners are often used as so-called tabletop sweeteners or packaged for beverages such as coffee and tea, but in these cases, the addition of bulking agents, which is required for convenience such as measurement, may be omitted or It can have secondary effects such as being able to reduce the amount and also acting as an excipient. The dibeptide sweetener used in the present invention is Q-
It is L-as/glutyl-L-phenylalanine-methyl ester or ethyl ester (hereinafter abbreviated as AP). For AP', glycine, DL-alanine, L-alanine, or L-serine is combined, but two or more of these amino acids may be used in combination for AP. In addition, glycine and DL-alanine are L-alanine, L-
It can be more effective than serine. AP
The composition ratio of the above amino acids to AP is 1 of the weight of AP.
The amount of amino acids is 0-1000%, preferably 75-500%. If the amount of amino acids is less than 10% of the weight of AP, the sweetness will lack the thickness found in sugar, and on the other hand, if it exceeds 1000%, the sweetness will be dull, rich, and have a strange taste. I can feel it. Therefore, the above 10 to 100
0% by weight, preferably 75 to 500% by weight, is a common range for diptide sweeteners as they exhibit a sweetness quality closer to that of sugar and can be used in all kinds of applications. The dipeptide sweetener composition of the present invention can be used in any form, such as powder, tablet or syrup.

また、粉末、錠剤、シロップ等のジベプチド甘味料に、
粉末、顕粒、液状等あらゆる態様での上記アミノ酸を添
加するなどして、ジベプチド甘味料とアミノ酸成分を共
存させてもよい。本発明のジベプチド甘味料組成物の代
表的使用例としては、いわゆるテーフルュースとしての
調味料、パン、デザート、ケーキ、キヤンデイー、チョ
コレート、チューインガム、クッキー、氷巣、プリン等
の製パン・製菓原料、コーヒーホワイトナー、泡立トッ
ピング等の乳製造乃至は乳製品代替品、粉末果汁、濃縮
果汁などの飲料等、甘味を有するすべての食品が対象と
なる。以下、実施例により、本発明を更に説明する。実
施例 1APO.05夕と、グリシン、DLーアラニン
、L−アラニン又はLーセリン各0.04夕をそれぞれ
ld‘の水に溶解し、甘味溶液を調整した。
In addition, dibeptide sweeteners such as powders, tablets, syrups, etc.
The diptide sweetener and the amino acid component may coexist by adding the above-mentioned amino acid in any form such as powder, granules, or liquid. Typical examples of the use of the dipeptide sweetener composition of the present invention include seasonings such as so-called tafurus, raw materials for bread and confectionery products such as bread, desserts, cakes, candy, chocolate, chewing gum, cookies, ice cubes, and puddings, and coffee. This applies to all foods with a sweet taste, such as milk products or dairy substitutes such as whiteners and foaming toppings, and beverages such as powdered fruit juices and concentrated fruit juices. The present invention will be further explained below with reference to Examples. Example 1APO. A sweetening solution was prepared by dissolving 0.05 ml of each of glycine, DL-alanine, L-alanine, or L-serine in 1d' of water.

(試験区)別に、APO.05夕をld‘の水に熔解し
たAP甘味溶液を調整した(対照区)。上記各試験区と
対照区の溶液につき、よく訓練された味覚パネル20名
を用いて2点階好試験法により官能評価を行った。結果
を第1表に示す。第1表 ※※※ 危険率0.1※で有意差あり ※※ 〃 1% ″ ※ 〃 5多 ″ 実施例 2 インスタントコーヒー1人前各2夕を熱湯各150の‘
に溶解し、コーヒー液を調製した。
(Test area) APO. An AP sweetening solution was prepared by dissolving 0.05 min. in ld' water (control group). The solutions of each test group and control group were subjected to sensory evaluation using a two-point scale test method using 20 well-trained taste panelists. The results are shown in Table 1. Table 1 ※※※ There is a significant difference with a risk rate of 0.1※※ 〃 1% '' ※ 〃 5 more '' Example 2 1 serving of instant coffee 2 times each with 150 ml of boiling water each
to prepare a coffee liquid.

このコーヒー液にAPO.04夕、クリーミングパウダ
ー(味の素■製「マリームJ)4夕及びグリシン、DL
ーア0ラニン、L、アラニン若しくはLーセリン各0.
03夕を溶解したもの(試験区)並びにAPO.04夕
及びクリーミングパウダー4夕を溶解ししたもの(対照
区)をそれぞれ調製し、実施例1と同様にパネル20名
を用いて官能評価に供した。結果を第夕2表に示す。第
2表 ※ 危険率5多で有意差あり 実施例 3 グレープフルーツ果汁を低温濃縮し、乾燥粉末化したも
の30%、クエン酸2.5%、乳糖66%APO.5%
並びにグリシン、DLーアラニン、L−アラニン若しく
はL−セリン1.0%の重量組成からなる粉末グレープ
フルーツジュースを水各200の‘に溶解し、グレープ
フルーツジュースを調整した(試験区)。
This coffee liquid contains APO. 04 Yu, creaming powder (Ajinomoto ■ "Marime J") 4 Yu and glycine, DL
-A0lanine, L, alanine or L-serine each 0.
03 Yu dissolved (test plot) and APO. A solution of Creaming Powder No. 04 and Creaming Powder No. 4 (control group) was prepared, respectively, and subjected to sensory evaluation using a panel of 20 people in the same manner as in Example 1. The results are shown in Table 2. Table 2 * Significant difference at risk level 5 Example 3 Grapefruit juice concentrated at low temperature and made into dry powder 30%, citric acid 2.5%, lactose 66% APO. 5%
Grapefruit juice was prepared by dissolving powdered grapefruit juice containing 1.0% by weight of glycine, DL-alanine, L-alanine, or L-serine in 200 g of water (test group).

対照区として、上記と同一の配合でアミノ酸を添加しな
いグレープフルーツジュースを調製し、実施例1と同様
に、よく訓練された味覚パネル20名を用いて官能評価
を実施した。結果を3表に示す。第3表 ※※危険率1※で有意差あり ※ 〃 5※ 〃 以上の結果から明らかな如く、本発明のジベプチド甘味
料組成物は、AP単独の場合に比べ、甘味の質が改善さ
れ、満足できる品質であった。
As a control, grapefruit juice without the addition of amino acids was prepared with the same formulation as above, and sensory evaluation was performed in the same manner as in Example 1 using 20 well-trained taste panels. The results are shown in Table 3. Table 3** Significant difference at risk rate 1* 〃 5※ 〃 As is clear from the above results, the diptide sweetener composition of the present invention improves the quality of sweetness compared to the case of AP alone, The quality was satisfactory.

Claims (1)

【特許請求の範囲】[Claims] 1 α−L−アスパルチル−L−フエニルアラニンメチ
ルエステル及び/又はα−L−アスパルチル−L−フエ
ニルアラニンエチルエステル並びに該エステルの10〜
1000重量%のグリシン、DL−アラニン、L−アラ
ニン又はL−セリンを含有することを特徴とする新ジペ
プチド甘味料組成物。
1 α-L-aspartyl-L-phenylalanine methyl ester and/or α-L-aspartyl-L-phenylalanine ethyl ester and 10 to 10 of the ester
A new dipeptide sweetener composition containing 1000% by weight of glycine, DL-alanine, L-alanine or L-serine.
JP55136164A 1980-09-30 1980-09-30 New dipeptide sweetener composition Expired JPS6016216B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP55136164A JPS6016216B2 (en) 1980-09-30 1980-09-30 New dipeptide sweetener composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP55136164A JPS6016216B2 (en) 1980-09-30 1980-09-30 New dipeptide sweetener composition

Publications (2)

Publication Number Publication Date
JPS5763068A JPS5763068A (en) 1982-04-16
JPS6016216B2 true JPS6016216B2 (en) 1985-04-24

Family

ID=15168812

Family Applications (1)

Application Number Title Priority Date Filing Date
JP55136164A Expired JPS6016216B2 (en) 1980-09-30 1980-09-30 New dipeptide sweetener composition

Country Status (1)

Country Link
JP (1) JPS6016216B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0101756A1 (en) * 1982-08-31 1984-03-07 Chimicasa Gmbh Water-soluble sweetening tablet
WO1995027408A1 (en) * 1994-04-11 1995-10-19 East Wellsum Industries(S) Pte. Ltd. Sweetening agent containing glycine, l-proline and/or l-hydroxyproline

Also Published As

Publication number Publication date
JPS5763068A (en) 1982-04-16

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