JPS6353983B2 - - Google Patents
Info
- Publication number
- JPS6353983B2 JPS6353983B2 JP1285281A JP1285281A JPS6353983B2 JP S6353983 B2 JPS6353983 B2 JP S6353983B2 JP 1285281 A JP1285281 A JP 1285281A JP 1285281 A JP1285281 A JP 1285281A JP S6353983 B2 JPS6353983 B2 JP S6353983B2
- Authority
- JP
- Japan
- Prior art keywords
- amino acid
- amino acids
- saccharide
- present
- mixture
- 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
Links
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Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
【発明の詳細な説明】
本発明はアミノ酸と糖類を含む合剤組成物に関
するものであり、殊に、アミノ酸と糖類との間の
所謂メイラード反応に基く褐変や品質変化の少な
いアミノ酸−糖類合剤組成物に関するものであ
る。
アミノ酸と糖類を含む合剤は、例えば医薬用、
食品用、および飼料用などの分野で広く使用され
ている。しかしながら、このアミノ酸−糖類含剤
は、その保存の期間中にアミノ酸と糖類との間の
メイラード反応によつて褐色に着色し、ひいては
カラメル臭の発生、溶解度の低下、還元価の増
加、二炭化炭素の発生、アミノ酸の減少および栄
養価の低下などを生じ、このため商品価値の低下
ないし喪失を生ずるという問題点を有している。
メイラート反応については、その利用法、例え
ばインスタントコーヒーの製造やパンや肉等にこ
げ目をつける工程などに利用することが知られて
いる。しかし、アミノ酸−糖類合剤におけるメイ
ラード反応を抑制する方法については、従来ほど
んど知られていない。
本発明の目的は、メイラード反応に基く褐変や
品質変化の少ないアミノ酸合剤組成物を提供する
ことにある。
本発明のアミノ酸合剤組成物は、アミノ酸と糖
類とを含む合剤のアミノ酸の表面をその重量の
0.1ないし30%の水溶性高分子物質にて被覆した
ことを特徴とするものである。
本発明の組成物に用いられるアミノ酸および糖
類には、格別の限定はなく、メイラート反応を呈
するようなアミノ酸および糖類はすべて本発明の
組成物に用いることができる。例えばアミノ酸と
しては、グリシン、アラニン、バリン、ロイシ
ン、イソロイシン、セリン、トレオニン、システ
イン、シスチン、メチオニン、アスパラギン酸、
ダルタミン酸、リシン、アルギニン、フエニルア
ラニン、チロシン、ヒスチジン、トリプトフア
ン、プロリン、オキシプロリン、アントラニル
酸、m−アミノ安息香酸、およびp−アミノ安息
香酸などを包含するものである。また、糖類とし
ては、例えばD−、L−およびDL−グルコース、
エリトロース、トレオース、リボース、アラビア
ノース、リキソース、マンノース、アルトロー
ス、アロース、ギユロース、イドース、ガラクト
ース、タロース、キシロース、などの単糖類及び
分解によつて上記単糖類が生成するラクトーズ、
サツカローズ、ラフイノースなどの多糖類及び澱
粉、グリコーゲン、セルローズなどを包含するも
のである。アミノ酸と糖類との配合比にも格別の
限定はなく任意の割合で混合したものであつても
い。
本発明の組成物においてアミノ酸を被覆するの
に用いられる水溶性高分子物質としては、アラビ
アガム、アラビノガラクタンガム、トラガカント
ガム、カラヤガム、グアーガム、ローカストビー
ンガム、タラガム、カラギーナンアルギン酸、フ
ア−セラン、寒天、ペクチン、デンプン、キサン
タンガス、ゼラチン、カゼイン、プルラン、デキ
ストリン等の動植物系多糖類及びソルブルスター
チ、カルボキシメチルセルロース(CMC)、アル
ギン酸ソーダ、アルギン酸プロピレングリコール
エステル等の誘導体並びにポリアクリル酸ソー
ダ、ポリビニルアルコール等の水溶性合成樹脂が
挙げられる。これらの化合物はいずれも食品添加
物として飲食品に添加することを許された化合物
であり、アミノ酸−糖類合剤の広範な使用目的を
妨げるものではない。
本発明の組成物において着色抑制剤として用い
られる水溶性高分子物質は、アミノ酸の重量の
0.1〜30%、好ましくは、0.5〜5%、の量で用い
られる。水溶性高分子物質の使用量が0.1%より
少いと、着色抑制の効果が不十分であり、また、
30%より多くしても、着色抑制の効果が格別向上
しないばかりでなく、人間及び動物における味覚
に悪影響を与え、保存性は改善されるものの商品
価値を失うなどの欠点を生ずる。
本発明の組成物は、上記アミノ酸−糖類合剤お
よび水溶性高分子物質に加えて他の添加剤、例え
ば緩衝剤としてのクエン酸ナトリウム、電解質調
整剤としての塩化ナトリウムおよび/又は塩化カ
リウムその他アミノ酸−糖類合剤の使用目的に応
じ、香料、着色剤、呈味剤、保存剤など各種の物
質を含んでいてもよい。
本発明の水溶性高分子物質は被覆するアミノ酸
粒子の希望する粒径に応じて公知の各種の表面被
覆法、例えばパンコーチング法、流動コーチング
法、ドライコーチング法等適当な方法を用いて容
易にアミノ酸粒子の表面に被覆することができ
る。
本発明によつて既存のアミノ酸−糖類合剤の保
存性が著るしく高められ、かつ、その商品価値が
高められるばかりでなく、今まで実用不可能であ
つたアミノ酸−糖類合剤の実用化を可能になるな
ど、産業上の有用性は、はかり知れないものがあ
る。
以下本発明を代表的な実施例により説明する
が、これらは単なる例示であり、本発明はこれら
のみに制限されないことは言うまでもない。
実施例 1
粉末グルコース560g、被覆剤としてデキスト
リンを3%(7g)使用して被覆されたグリシン
242gをガラス容器中で十分混合し合剤を調製し
た。この合剤の混合直後の白度は81であつた。こ
の合剤を室温および50℃にて30日間保存した後、
その白度を測定したところ、80であつて、着色は
認められなかつた。
白度W(B、Y)は、青色反射率Bおよび視感
反射率Yから、下記式により算出した。
W(B、Y)=4B−3Y
比較例 1
上記実施例1と同様の実験を繰り返えした。但
しデキストリンで被覆しなかつた。合剤の白度変
化は下記の通りであつた。
混合直後 83
常温保存30日後 25(褐変顕著)
50℃保存4日後 63(褐変顕出)
実施例 2
実施例1と同様を行つた。但し、被覆剤として
ゼラチンを1.51使用した。白度は下記の通りであ
つた。
混合直後 81
30日後 81
着色は全く認められなかつた。
比較例 2
実施例2と同様の実験を行つた。但しゼラチン
で被覆しなかつた。白度は下記の通り、
混合直後 82
常温保存30日後 23(褐変顕著)
50℃〃 4日後 64(褐変顕出)
実施例 3
実施例1と同様の実験を行つた。但し、被覆剤
としてアラビアガムを1.5%使用した。又、165g
の塩化ナトリウムと40gの塩化カリウムが追加添
加された。
白度は下記の通りであつた。
混合直後 82
30日後 81(着色なし)
比較例 3
実施例3と同様の実験を行つた。但しアラビア
ガムで被覆しなかつた。白度の変化は下記の通
り。
混合直後 81
常温保存30日後 21(褐変顕著)
50℃保存4日後 64(褐変顕出)
実施例 4〜15
各種組成の被覆剤を用いて実施例1と同様の実
験を行つた結果を次表に示す。
【表】DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a combination composition containing an amino acid and a saccharide, and in particular to an amino acid-saccharide combination composition that exhibits little browning or quality change due to the so-called Maillard reaction between the amino acid and the saccharide. The present invention relates to a composition. A mixture containing amino acids and saccharides can be used for pharmaceutical purposes, for example.
Widely used in fields such as food and feed. However, this amino acid-saccharide-containing agent becomes brown due to the Maillard reaction between the amino acid and the saccharide during its storage, resulting in the generation of caramel odor, decrease in solubility, increase in reducing value, and carbonization. This causes problems such as generation of carbon, decrease in amino acids, and decrease in nutritional value, resulting in a decrease or loss of commercial value. The Maylert reaction is known for its use in, for example, the production of instant coffee and the process of browning bread, meat, etc. However, little is known about the method of suppressing the Maillard reaction in amino acid-saccharide mixtures. An object of the present invention is to provide an amino acid mixture composition that exhibits less browning and quality changes due to the Maillard reaction. The amino acid mixture composition of the present invention covers the surface of the amino acid in the mixture containing amino acids and saccharides by weight.
It is characterized by being coated with 0.1 to 30% water-soluble polymer material. There are no particular limitations on the amino acids and saccharides used in the composition of the present invention, and all amino acids and saccharides that exhibit a Maylert reaction can be used in the composition of the present invention. For example, amino acids include glycine, alanine, valine, leucine, isoleucine, serine, threonine, cysteine, cystine, methionine, aspartic acid,
These include daltamic acid, lysine, arginine, phenylalanine, tyrosine, histidine, tryptophan, proline, oxyproline, anthranilic acid, m-aminobenzoic acid, p-aminobenzoic acid, and the like. In addition, examples of sugars include D-, L- and DL-glucose,
Monosaccharides such as erythrose, threose, ribose, arabinose, lyxose, mannose, altrose, allose, gyulose, idose, galactose, talose, xylose, and lactose produced by the above monosaccharides through decomposition;
It includes polysaccharides such as sugar rose and raffinose, starch, glycogen, cellulose, and the like. There is no particular limitation on the blending ratio of amino acids and sugars, and they may be mixed in any ratio. Water-soluble polymeric substances used to coat the amino acids in the composition of the present invention include gum arabic, gum arabinogalactan, gum tragacanth, gum karaya, guar gum, locust bean gum, tara gum, carrageenan alginate, fur-celan, and agar. , pectin, starch, xanthan gas, gelatin, casein, pullulan, dextrin and other animal and plant polysaccharides, soluble starch, carboxymethyl cellulose (CMC), sodium alginate, alginate propylene glycol ester and other derivatives, sodium polyacrylate, polyvinyl alcohol Water-soluble synthetic resins such as All of these compounds are permitted to be added to foods and drinks as food additives, and do not interfere with the wide range of uses of the amino acid-saccharide mixture. The water-soluble polymeric substance used as a coloring inhibitor in the composition of the present invention is based on the weight of amino acids.
It is used in amounts of 0.1-30%, preferably 0.5-5%. If the amount of water-soluble polymer substance used is less than 0.1%, the effect of suppressing coloring will be insufficient, and
If the amount exceeds 30%, not only will the effect of suppressing coloration not be particularly improved, but it will also have a negative impact on the taste of humans and animals, and although storage stability will be improved, there will be disadvantages such as loss of commercial value. The composition of the present invention contains, in addition to the above amino acid-saccharide mixture and water-soluble polymeric substance, other additives, such as sodium citrate as a buffer, sodium chloride and/or potassium chloride as an electrolyte regulator, and other amino acids. - Depending on the intended use of the saccharide mixture, it may contain various substances such as fragrances, colorants, flavoring agents, and preservatives. The water-soluble polymeric substance of the present invention can be easily coated using various known surface coating methods, such as pan coating, fluid coating, dry coating, etc., depending on the desired particle size of the amino acid particles to be coated. The surface of amino acid particles can be coated. The present invention not only significantly improves the shelf life of existing amino acid-saccharide mixtures and increases their commercial value, but also brings amino acid-saccharide mixtures to practical use, which has been impossible until now. The industrial usefulness is immeasurable, such as making it possible to The present invention will be explained below using typical examples, but these are merely illustrative and it goes without saying that the present invention is not limited to these. Example 1 560 g of powdered glucose, coated with glycine using 3% (7 g) of dextrin as coating agent
242 g was thoroughly mixed in a glass container to prepare a mixture. The whiteness of this mixture immediately after mixing was 81. After storing this mixture at room temperature and 50℃ for 30 days,
When the whiteness was measured, it was 80, and no coloration was observed. The whiteness W (B, Y) was calculated from the blue reflectance B and the luminous reflectance Y using the following formula. W(B, Y)=4B-3Y Comparative Example 1 The same experiment as in Example 1 above was repeated. However, it was not coated with dextrin. The whiteness change of the mixture was as follows. Immediately after mixing 83 After 30 days of storage at room temperature 25 (significant browning) After 4 days of storage at 50°C 63 (obvious browning) Example 2 The same procedure as in Example 1 was carried out. However, 1.51 gelatin was used as the coating agent. The whiteness was as follows. Immediately after mixing 81 30 days later 81 No coloration was observed. Comparative Example 2 An experiment similar to Example 2 was conducted. However, it was not coated with gelatin. The whiteness was as follows: Immediately after mixing 82 After 30 days of storage at room temperature 23 (significant browning) 50°C After 4 days 64 (obvious browning) Example 3 An experiment similar to Example 1 was conducted. However, 1.5% gum arabic was used as the coating material. Also, 165g
of sodium chloride and 40 g of potassium chloride were added. The whiteness was as follows. Immediately after mixing 82 After 30 days 81 (no coloring) Comparative Example 3 An experiment similar to Example 3 was conducted. However, it was not covered with gum arabic. The changes in whiteness are as follows. Immediately after mixing 81 After 30 days of storage at room temperature 21 (significant browning) After 4 days of storage at 50°C 64 (obvious browning) Examples 4 to 15 The results of experiments similar to those in Example 1 using coating materials of various compositions are shown in the table below. Shown below. 【table】
Claims (1)
アミノ酸の表面を水溶性高分子物質にて被覆して
なるアミノ酸合剤組成物。1. In a combination composition containing amino acids and saccharides,
An amino acid mixture composition in which the surface of amino acids is coated with a water-soluble polymer substance.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1285281A JPS57128662A (en) | 1981-02-02 | 1981-02-02 | Amino acid mixture composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1285281A JPS57128662A (en) | 1981-02-02 | 1981-02-02 | Amino acid mixture composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS57128662A JPS57128662A (en) | 1982-08-10 |
JPS6353983B2 true JPS6353983B2 (en) | 1988-10-26 |
Family
ID=11816922
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1285281A Granted JPS57128662A (en) | 1981-02-02 | 1981-02-02 | Amino acid mixture composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS57128662A (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2651128A1 (en) * | 1989-08-30 | 1991-03-01 | Chevance Leon | NEW USE OF ANTI-COMPONENTS FOR THE TREATMENT OF PERIODONTOSIS. |
FR2651127B1 (en) * | 1989-08-30 | 1994-06-03 | Chevance Leon | NOVEL USE OF SUBSTANCES AS ANTI-COMPONENTS AND MEDICINES CONTAINING SUCH A SUBSTANCE. |
US5888568A (en) * | 1998-06-25 | 1999-03-30 | Nestec S.A. | Limitation of browning |
-
1981
- 1981-02-02 JP JP1285281A patent/JPS57128662A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS57128662A (en) | 1982-08-10 |
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