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JPS5823056B2 - How to prepare a protein that can be used in Thailand - Google Patents
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JPS5823056B2 - How to prepare a protein that can be used in Thailand - Google Patents

How to prepare a protein that can be used in Thailand

Info

Publication number
JPS5823056B2
JPS5823056B2 JP50126488A JP12648875A JPS5823056B2 JP S5823056 B2 JPS5823056 B2 JP S5823056B2 JP 50126488 A JP50126488 A JP 50126488A JP 12648875 A JP12648875 A JP 12648875A JP S5823056 B2 JPS5823056 B2 JP S5823056B2
Authority
JP
Japan
Prior art keywords
fibrous
added
protein
composition
gel
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
JP50126488A
Other languages
Japanese (ja)
Other versions
JPS5251058A (en
Inventor
宮中明子
金光永
中治十成
中村務
八木直樹
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.)
KURARE KK
MINAMINIPPON RAKUNO KYODO KK
Original Assignee
KURARE KK
MINAMINIPPON RAKUNO KYODO KK
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 KURARE KK, MINAMINIPPON RAKUNO KYODO KK filed Critical KURARE KK
Priority to JP50126488A priority Critical patent/JPS5823056B2/en
Publication of JPS5251058A publication Critical patent/JPS5251058A/en
Publication of JPS5823056B2 publication Critical patent/JPS5823056B2/en
Expired legal-status Critical Current

Links

Description

【発明の詳細な説明】 本発明は繊維状高たん白質食品の製造法、さらに詳しく
は耐熱軟化性に優れた繊維状高たん白質食品の製造法に
関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing a fibrous high-protein food, and more particularly to a method for producing a fibrous high-protein food with excellent heat softening resistance.

近年、いわゆる人工肉などの人工的な繊維状たん白質食
品に関する研究が進み、一部実用化も試みられている。
In recent years, research on artificial fibrous protein foods such as so-called artificial meat has progressed, and some attempts have been made to put them into practical use.

本発明者らも先に非繊維状たん白質を一定条件のもとに
たん白質分解酵素で処理し、これを延伸して繊維状たん
白質に改変し、畜肉様食感を付与した繊維状たん白質食
品を製造する方法を発明した(特公昭46−29780
)。
The present inventors have also previously treated non-fibrous proteins with proteolytic enzymes under certain conditions, stretched them and modified them into fibrous proteins, and produced fibrous proteins with a meat-like texture. Invented a method for producing white matter food (Special Publication No. 46-29780)
).

この方法では、非繊維状たん白質たとえばカゼインをC
a廿などでミセル化し、これをたん白質分解酵素で処理
してゲル化し、このゲルを延伸して配向したフィブリン
状組成物にしたのち酸で固定するが、このような方法で
えられる繊維状組成物は耐M幼二弱いため調理の際に熱
軟化し繊維形態を失うおそれがある。
In this method, non-fibrous proteins such as casein are
The fibrous material obtained by this method is made into micelles, treated with proteolytic enzymes to form a gel, and stretched to form an oriented fibrin-like composition, which is then fixed with acid. Since the composition has low resistance to M, there is a risk that it will be heat softened and lose its fiber form during cooking.

さらに、それ自体は充分に熱に対し安定な繊維状高たん
白質食品であっても、それを魚肉、畜肉類と混合した場
合に耐熱性が低下する場合があり、これを防止するため
多糖類溶液で処理する方法についても発明を行った(特
公昭48−35468)。
Furthermore, even if a fibrous high-protein food itself is sufficiently heat-stable, its heat resistance may decrease when mixed with fish or livestock meat, and to prevent this, polysaccharide He also invented a method for treatment with a solution (Japanese Patent Publication No. 35468/1973).

この方法によれば、食品を構成する繊維状たん白質は多
糖類との水を包括する保護的結合によって、ばらけ性と
耐熱性に一段と優れた性能向上が見られるが、その反面
、本操作は付加的な工程を要し、かつ固定された繊維の
微細内面にまで多糖類溶液を充分浸透含浸させるために
処理時間、条件に煩雑な操作調整を要し、連続的な生産
が行い難いと言う欠点を有する。
According to this method, the fibrous proteins that make up foods have a protective bond with polysaccharides that envelops water, resulting in further improved properties in terms of disintegration and heat resistance. requires an additional process, and requires complicated operational adjustments to processing time and conditions in order to sufficiently penetrate and impregnate the fine inner surface of the fixed fibers with the polysaccharide solution, making continuous production difficult. It has the following disadvantages.

本発明者らは、上記の目的を以て酸性または中性多糖類
を最も効果的かつ能率的にたん白に投与結合させる工程
上の添加時期、添加条件について鋭意研究を重ねた結果
、ミセル化の形成途中もしくは少くとも繊維の形成固定
前に多糖類との結合を行わせることによって、従前の場
合よりも繊維状組成物の耐熱軟化性が著しく向上し、か
つ本性が後処理工程をほとんど要せず、簡単な操作によ
り効果を発現し得ることを見出し本発明を完成するにい
たった。
With the above-mentioned purpose, the present inventors have conducted intensive research on the timing and conditions of addition in the process of administering and bonding acidic or neutral polysaccharides to proteins in the most effective and efficient manner. By binding the polysaccharide during the process or at least before forming and fixing the fibers, the heat softening resistance of the fibrous composition is significantly improved compared to the conventional method, and the nature of the composition requires almost no post-processing steps. They discovered that the effect can be achieved through simple operations and completed the present invention.

一般に乳たん白質であるカゼインは乳中においてCan
や燐酸基またはクエン酸基と結合していわゆるカルシウ
ム−カゼイン−燐酸塩複合体としてミセル構造をとって
存在しており、このミセルにレンニンのような凝乳酵素
が作用すると、ミセ・ル構造を安定化するに一カゼイン
が分解されCanの存在下に凝集しゲル化すると考えら
れる。
Casein, which is generally a milk protein, can be found in milk.
It exists in a micelle structure as a so-called calcium-casein-phosphate complex by combining with a phosphoric acid group or a citric acid group, and when a milk-clotting enzyme such as rennin acts on this micelle, it forms a micellar structure. It is thought that for stabilization, casein is decomposed and aggregated in the presence of Can to form a gel.

しかして、このゲルは延伸などの応力により配向したフ
ィブリル化組成物となり、酸固定される。
As a result, this gel becomes a fibrillated composition oriented by stress such as stretching, and is acid-fixed.

しかしながら、このような酸固定物は熱安定性が充分と
は言えない面がある。
However, such acid fixatives have an aspect that their thermal stability is not sufficient.

例えば、各種の酸及び無水酸を使用した場合の繊維状組
成物の耐熱軟化性は第1表のようである。
For example, the heat softening properties of fibrous compositions using various acids and anhydrous acids are shown in Table 1.

上記第1表から明らかなように、無水酢酸による固定で
は高い熱安定性を示すが他の酸による固定では水分率6
0%以上で熱安定性に問題があることが分る。
As is clear from Table 1 above, fixation with acetic anhydride shows high thermal stability, but fixation with other acids shows a moisture content of 6.
It can be seen that there is a problem in thermal stability at 0% or more.

一方、特公昭48−35468によれば、多糖類を含む
溶液に繊維状たん白組酸物を浸漬後処理することにより
、下記の如き結果が得られている。
On the other hand, according to Japanese Patent Publication No. 48-35468, the following results were obtained by treating a fibrous protein composition after immersing it in a solution containing a polysaccharide.

しかし、上記結果は無水酢酸による固定化物に比し充分
対抗し得る成績を得ているとは言い難い。
However, the above results cannot be said to be sufficient to compete with those immobilized with acetic anhydride.

本発明者らは、特公昭48−35468に引続)き酸性
または中性多糖類の添加時期についてさらに詳細な研究
をおこなった結果、第3表の結果を得た。
The present inventors conducted further detailed research on the timing of addition of acidic or neutral polysaccharides following Japanese Patent Publication No. 48-35468, and obtained the results shown in Table 3.

本発明者らは、さらに2種以上の組合せからなる多糖類
についての研究をおこない、Ca+1−反応性官能基を
有しない中性多糖類とCa+反応性官能基を有する中性
多糖類を組合せて用いると、耐熱軟化性が相剰的に増大
することを見出した。
The present inventors further conducted research on polysaccharides consisting of a combination of two or more types, and found a combination of a neutral polysaccharide that does not have a Ca+1-reactive functional group and a neutral polysaccharide that has a Ca+-reactive functional group. It has been found that the heat softening resistance increases additively when used.

この場合の多糖類の添加時期についての比較研究結果を
次に示す(多糖類の添加方法、酸固定化法、その他の条
件は第3表の条件と同じである)。
The results of a comparative study regarding the timing of polysaccharide addition in this case are shown below (the polysaccharide addition method, acid fixation method, and other conditions are the same as those in Table 3).

すなわち、上記、第3、第4表に明らかな如く多糖類を
1種類または2種類以上組合せて使用する場合に、固定
化した繊維を多糖類溶液で後処理するよりは、それ以前
の工程的地点に遡及して添加するほど得られる繊維の耐
熱性は向上し、特にゲル形成前望ましくはミセル形成開
始後の一定の時点で添加する場合、最大の耐熱性が得ら
れることが判明した。
That is, as is clear from Tables 3 and 4 above, when using one type or a combination of two or more polysaccharides, it is better to It has been found that the heat resistance of the resulting fibers improves the more retroactively it is added, and in particular, when it is added at a certain point before gel formation, preferably after the start of micelle formation, the maximum heat resistance can be obtained.

なお、この一定時点は原料たん白の組成その他の条件に
より可成り変動があり、定量化することは困難である。
Note that this fixed point in time varies considerably depending on the composition of the raw protein and other conditions, and is difficult to quantify.

また、ミセル形成前すなわち金属多価イオン添加前の均
一なゾル溶液または原料たん白質に直接多糖類を投与し
たところ、製品繊維のばらけ性は一応向上するものの、
耐熱性は多糖類溶液による後処理と同等程度の効果しか
得られなかった。
In addition, when polysaccharides were directly administered to a homogeneous sol solution or raw protein before micelle formation, that is, before addition of multivalent metal ions, the looseness of the product fibers improved to some extent;
Regarding heat resistance, the effect was only comparable to that obtained by post-treatment with a polysaccharide solution.

これは特開昭49−110854にみられる結果と一致
し、均−系への多糖類の投与は耐熱性向上に寄与する効
果が少ないものと判定される。
This is consistent with the results found in JP-A-49-110854, and it is determined that homogeneous administration of polysaccharides has little effect on improving heat resistance.

しかして、本発明は乳たん白質またはそれと他の非繊維
状動植物たん白質との混合液に金属多価イオンを作用さ
せてミセル化による不均一系の形成を開始させた後、少
(とも一種類の酸性または中性多糖類を含む多糖類を加
え、ついでそのミセルを破壊してゲルを形成させ、この
ゲルに応力を加え配向されたフィブリル組成物にしたの
ち、またはしつつ酸で固定することにより耐熱性のすぐ
れた熱軟化性の低い繊維状高たん白質食品の製法を提供
するものである。
Therefore, the present invention involves applying metal polyvalent ions to milk protein or a mixture of it and other non-fibrous animal and plant proteins to initiate the formation of a heterogeneous system through micellization. polysaccharides, including acidic or neutral polysaccharides of various types, are then disrupted to form a gel, which is then stressed into an oriented fibrillar composition and then fixed with acid. This provides a method for producing a fibrous high-protein food with excellent heat resistance and low heat softening property.

本発明方法で用いられる原料の乳たん白質は通常、水酸
化ナトリウム、炭酸カリウムなどのアルカリ金属塩、燐
酸ナトリウムなどのアルカリ性燐酸塩、アンモニアなど
の水溶液に溶解させた溶解液として用いられ、そのPH
値は6〜9で濃度は5〜30%が好適である。
Milk protein, the raw material used in the method of the present invention, is usually used as a solution dissolved in an aqueous solution of an alkali metal salt such as sodium hydroxide or potassium carbonate, an alkaline phosphate such as sodium phosphate, or ammonia.
A value of 6 to 9 and a concentration of 5 to 30% are preferred.

この乳たん白質は、他の非繊維状動植物性たん白質、た
とえば大豆たん白質、グルテンなどとの混合液の形で用
いてもよい。
This milk protein may be used in the form of a mixture with other non-fibrous animal and vegetable proteins, such as soybean protein and gluten.

この乳たん白質のミセル化に用いる金属多価イオンとし
ては、カルシウムイオン(Ca丑→、マグネシウムイオ
ン(Mg ” )があげられ、具体的例としては、塩化
カルシウム、臭化カルシウム、硝酸カルシウムなどの水
溶性カルシウム塩、塩化マグネシウム、臭化マグネシウ
ム、硝酸マグネシウム、硫酸マグネシウムなどの水溶性
マグネシウム塩などが用いられる。
Examples of multivalent metal ions used for micellization of milk proteins include calcium ions (Caₑ→) and magnesium ions (Mg''), and specific examples include calcium chloride, calcium bromide, calcium nitrate, etc. Water-soluble calcium salts, water-soluble magnesium salts such as magnesium chloride, magnesium bromide, magnesium nitrate, and magnesium sulfate are used.

添加される酸性または中性多糖類としては、デキストリ
ン、殿粉、アミロース、アミロペクチン、α化殿粉、グ
アーガム、λ−カラゲニン、アラビヤゴム、こんにゃく
粉、ペクチン、カルボキシメチルセルローズ、カルボキ
シメチル殿粉、アルギン酸、グルコン酸(またはデルタ
グルコラクトン)などが用いられる。
The acidic or neutral polysaccharides to be added include dextrin, starch, amylose, amylopectin, pregelatinized starch, guar gum, λ-carrageenan, gum arabic, konjac flour, pectin, carboxymethyl cellulose, carboxymethyl starch, alginic acid, Gluconic acid (or delta glucolactone), etc. are used.

これらのものは単独で用いる場合は、乳たん白質などの
混合物に対し0.5〜30%程度の範囲で添加し得る。
When these substances are used alone, they can be added in an amount of about 0.5 to 30% to the mixture of milk proteins and the like.

また多糖類として、2種以上の中性多糖類の混合物を使
用すると相剰的な耐熱軟化性が得られ好結果を与える。
Furthermore, when a mixture of two or more types of neutral polysaccharides is used as the polysaccharide, good results can be obtained since complementary heat softening resistance can be obtained.

このような中性多糖類の組合せとしては、Ca廿反応性
の官能基を有するものと有しないものの間の組合せが好
適である。
As a combination of such neutral polysaccharides, a combination of one having a Ca-reactive functional group and one not having a Ca-reactive functional group is suitable.

例えば、Ca廿反応性の官能基を有しない中性多糖類と
しては、重合度4〜25の各種デキストリン、殿粉、ア
ミロース、アミロペクチン、α化殿粉、グアーガムなど
が用いられ、Ca丑反応性官能基を有する中性多糖類と
しては、λ−カラゲニン、アラビヤゴム、こんにゃく粉
などがあげられる。
For example, as neutral polysaccharides that do not have Ca-reactive functional groups, various dextrins with a polymerization degree of 4 to 25, starch, amylose, amylopectin, pregelatinized starch, guar gum, etc. are used. Examples of the neutral polysaccharide having a functional group include λ-carrageenan, gum arabic, and konjac flour.

これらの添加量は乳たん白質溶液の重量に対し、Ca(
上皮応性の官能基を有しない中性多糖類では5〜30%
程度、好ましくは5〜20%、さらに好ましくは5〜1
0%、Ca丑反応性の官能基を有する中性多糖類では0
.05〜10%程度、好ましくは0.1〜5%、さらに
好ましくは0.5〜2%である。
The amount of these additions is based on the weight of the milk protein solution.
5-30% for neutral polysaccharides without epithelial-responsive functional groups
degree, preferably 5 to 20%, more preferably 5 to 1
0%, and 0 for neutral polysaccharides with Ca-reactive functional groups.
.. The amount is approximately 0.05 to 10%, preferably 0.1 to 5%, and more preferably 0.5 to 2%.

これらの多糖類の添加時期は、金属多価イオンによるミ
セル形成開始後から、ゲル化前の工程のある時点を自由
に選択することができる。
The timing of adding these polysaccharides can be freely selected from a certain point in the process after the start of micelle formation by multivalent metal ions to before gelation.

さらに形成されたミセルを破壊してゲルを形成させる方
法としては、たん白質分解酵素たとえば細菌性プロテア
ーゼ、カビプロテアーゼ、トリプシン、キモトリプシン
、パパインなどを加えて室温ないしは加温下(通常40
〜60°C)にて処理する方法が好適である。
Furthermore, as a method of destroying the formed micelles and forming a gel, a proteolytic enzyme such as bacterial protease, fungal protease, trypsin, chymotrypsin, papain, etc. is added to the gel at room temperature or under heating (usually at 40°C).
~60°C) is preferred.

か(して得られるゲルは、常法にしたがい、応力を加え
られて配向したフィブリル状組成物となり、ついでこれ
を酸で固定する。
The resulting gel is subjected to stress to form an oriented fibrillar composition according to a conventional method, which is then fixed with acid.

これらの応力のかけ方については、一般的な種々の機械
的応力−ローラー間延伸、ローラ圧延、スクリュー押し
出し、攪拌、高速押し出しくジェット流)などが使用さ
れる。
As for how to apply these stresses, various general mechanical stresses such as stretching between rollers, roller rolling, screw extrusion, stirring, high-speed extrusion, jet flow, etc. are used.

酸による固定化はこれらの応力による配向とフィブリル
化を進めながら同時に行うことも出来る。
Fixation with acid can be performed simultaneously while orientation and fibrillation due to these stresses are being promoted.

本発明方法によれば、得られる繊維状組成物は酸固定後
も耐熱性が良好であり、食品衛生上好ましくない無水酢
酸の使用が避けられろ。
According to the method of the present invention, the resulting fibrous composition has good heat resistance even after acid fixation, and the use of acetic anhydride, which is undesirable in terms of food hygiene, can be avoided.

本発明方法で用いられる固定用の酸としては、塩酸、硫
酸などの無機酸、乳酸、クエン酸、酢酸などの有機酸が
あげられ、これらは単独でも、またその2種以上の混合
物でも用いられる。
The fixing acids used in the method of the present invention include inorganic acids such as hydrochloric acid and sulfuric acid, and organic acids such as lactic acid, citric acid and acetic acid, and these may be used alone or in a mixture of two or more thereof. .

さらにこれらの酸を塩化ナトリウム、硫酸ナトリウムな
どの塩と混合して用いれば、さらに良好な固定効果が得
られる。
Furthermore, if these acids are used in combination with a salt such as sodium chloride or sodium sulfate, an even better fixing effect can be obtained.

本発明方法でえられる繊維状たん白質にさらに適当な色
素、調味料、フレーバーなどを添加して外観、触感、味
覚のすぐれた繊維状高たん白食品を得ることが出来る。
By further adding appropriate pigments, seasonings, flavors, etc. to the fibrous protein obtained by the method of the present invention, a fibrous high-protein food with excellent appearance, texture, and taste can be obtained.

つぎに実施例をあげて本発明方法をさらに具体的に説明
する。
Next, the method of the present invention will be explained in more detail with reference to Examples.

実施例 1 カゼイン100グを40℃の温水500rIllに懸濁
し、これに28%アンモニア水6.Omlを加えて溶解
させた。
Example 1 100g of casein was suspended in 500ml of 40°C warm water, and 28% ammonia water was added to the suspension.6. Oml was added and dissolved.

これにλ−カラゲニン1グおよびテキストリン(重合度
15)11と塩化カルシウム(IOP)の混合水溶液を
加えてミセルを形成させた。
To this was added 1 g of λ-carrageenan, 11 g of textrin (degree of polymerization), and a mixed aqueous solution of calcium chloride (IOP) to form micelles.

ミセル溶液にプロテアーゼ200m9を加え、約lO分
間保持後ゲルを得た。
Protease 200m9 was added to the micelle solution, and a gel was obtained after holding for about 10 minutes.

このゲルをスリットから押し出し、さらにローラー間で
3倍に延伸して配向したフィブリル組成物にし、これを
5%硫酸ナトリウムを含む5%酢酸水溶液に浸漬して、
酵素の失活と繊維の固定化をおこなった。
This gel is extruded through a slit and further stretched three times between rollers to form an oriented fibril composition, which is immersed in a 5% acetic acid aqueous solution containing 5% sodium sulfate.
The enzyme was inactivated and the fibers were immobilized.

これを水洗しアルカリで中和後PH6,0にし水分約7
0%の繊維状たん白質的2801を得た。
After washing with water and neutralizing with alkali, the pH was adjusted to 6.0 and the water content was approximately 7.
0% fibrous proteinaceous 2801 was obtained.

得られた繊維状たん白質組成物は80℃で20分間加熱
後も大部分のフィブリルが良好な繊維形態を保持し、軟
化消失を起すようなことはなかった。
Even after heating the obtained fibrous protein composition at 80° C. for 20 minutes, most of the fibrils maintained good fiber morphology and did not soften or disappear.

本組成物は食肉様の食感を有する食品に好適であった。This composition was suitable for foods having a meat-like texture.

比較例 1 実施例1においてλ−カラゲニン1グとデキストリン1
0グを添加せず塩化カルシウムによるミセル化を行い、
以下実施例1と同様の操作をおこなった。
Comparative Example 1 In Example 1, 1 g of λ-carrageenan and 1 g of dextrin
Micelleization with calcium chloride is performed without adding 0g,
Thereafter, the same operations as in Example 1 were performed.

得られた繊維状組成物を2%混合多糖類水溶液(デキス
トリン(重合度15)/アラビヤゴムー10/1重量比
)に5分間浸漬し、水分率約70%の繊維状組成物を得
た。
The obtained fibrous composition was immersed for 5 minutes in a 2% mixed polysaccharide aqueous solution (dextrin (degree of polymerization 15)/gum arabic - 10/1 weight ratio) to obtain a fibrous composition with a moisture content of about 70%.

このものは80’C20分間の加熱で若干軟化しフィブ
リル構造の部分的消失を起した。
This material was slightly softened by heating at 80'C for 20 minutes, causing partial disappearance of the fibril structure.

実施例 2 カゼイン100グを50℃の温水500TLlに懸濁し
これに101のグリシニンを加え、28%アンモニア水
6.5 mlを加えて溶解させた。
Example 2 100 g of casein was suspended in 500 TL of 50° C. warm water, 101 glycinin was added thereto, and 6.5 ml of 28% aqueous ammonia was added to dissolve the suspension.

これに10グの塩化カルシウムを含む水溶液を加えてミ
セルを形成し、さらにデキストリン(重合度15)10
1とアラビヤゴム1グを加え攪拌溶解した。
To this, an aqueous solution containing 10 g of calcium chloride was added to form micelles, and 10 g of dextrin (degree of polymerization 15) was added.
1 and 1 g of gum arabic were added and stirred to dissolve.

このミセル溶液にプロテアーゼ200■を加えゲルを得
た。
200 μl of protease was added to this micelle solution to obtain a gel.

このゲルをスリットよりリボン状に押し出しさらにロー
ラー間で2倍に延伸し配向したフィブリル状組成物を得
た。
This gel was extruded into a ribbon shape through a slit and further stretched to double the length between rollers to obtain an oriented fibrillar composition.

これを5%硫酸ナトリウムを含む5%酢酸水溶液に浸漬
し、繊維の固定化をおこなった。
This was immersed in a 5% acetic acid aqueous solution containing 5% sodium sulfate to fix the fibers.

さらに、稀アルカリ水溶液で中和しP H6,0にし、
水分約68%の繊維状組成物的3202を得た。
Furthermore, neutralize with dilute alkaline aqueous solution to pH 6.0,
A fibrous composition 3202 having a water content of about 68% was obtained.

得られた繊維状組成物は80℃20分間加熱しても、大
部分のフィブリルがその形態を保持し、消失するような
ことはなかった。
Even when the obtained fibrous composition was heated at 80° C. for 20 minutes, most of the fibrils retained their shape and did not disappear.

このものは食肉様食品に適するものであった。This product was suitable for meat-like foods.

比較例 実施例2においてテキストリンとアラビヤゴムをミセル
形成前にたん自溶液に添加した後に塩化カルシウムを加
えミセル化を行い、他は実施例2と同様の操作をおこな
った。
Comparative Example In Example 2, texturin and gum arabic were added to the sputum solution before forming micelles, and then calcium chloride was added to form micelles, and the other operations were the same as in Example 2.

得られた繊維状組成物は80℃20分間の加熱により若
干軟化し、フィブリル繊維がかなり膠着し消失した。
The obtained fibrous composition was slightly softened by heating at 80° C. for 20 minutes, and the fibril fibers were considerably stuck and disappeared.

実施例 3 50℃の温水600rrLlに1002のカゼインを加
えさらに28%アンモニア水4.5 mlを加えカゼイ
ンを溶解させた。
Example 3 1002 casein was added to 600 rrLl of 50°C warm water, and 4.5 ml of 28% ammonia water was added to dissolve the casein.

これに塩化カルシウム水溶液(CaC12として10グ
含有)とグアーガムlOV、λ−カラゲニン1,07を
含む水溶液を同時に添加し、ミセル溶液を得た。
A calcium chloride aqueous solution (containing 10 g of CaC12) and an aqueous solution containing 1 OV of guar gum and 1,07 mL of λ-carrageenan were simultaneously added to this to obtain a micelle solution.

これにプロテアーゼ1807/9を加えゲルを得た。Protease 1807/9 was added to this to obtain a gel.

これをスリットより押し出しローラー間で2倍に延伸し
、さらに0.3%酢酸水溶液中で1.3倍に延伸しつつ
固定化を進めた後、5%硫酸ナトリウムを含む5%酢酸
水溶液に浸漬し固定化をおこなった。
This was extruded through a slit, stretched to 2 times between rollers, further stretched to 1.3 times in a 0.3% acetic acid aqueous solution to proceed with fixation, and then immersed in a 5% acetic acid aqueous solution containing 5% sodium sulfate. and fixed it.

これをさらに稀アルカリ水溶液で中和し、PH6,4に
し水分約70%の繊維状組成物を得た。
This was further neutralized with a dilute alkaline aqueous solution to obtain a fibrous composition with a pH of 6.4 and a water content of about 70%.

本繊維状組成物は80℃20分間加熱によっても各繊維
間のばらけ性も良好で軟化や膠着によるフィブリル構造
の消失を起すことが少(、食肉様・食品に好適であった
Even when heated at 80° C. for 20 minutes, this fibrous composition had good disassembly between the fibers and was less likely to lose its fibril structure due to softening or adhesion (and was suitable for meat-like and food products).

実施例 4 50℃の温水6001111に1001のカゼインを加
え28%アンモニア水6.0 mlを加えカゼイン溶液
を得た。
Example 4 1001 casein was added to 50°C warm water 6001111, and 6.0 ml of 28% ammonia water was added to obtain a casein solution.

これに塩化カルシウム10.0Pを含む水溶液を添加し
ミセルを形成させた。
An aqueous solution containing 10.0 P of calcium chloride was added to this to form micelles.

さらにこれにテキストリン(重合度15)5.1’とこ
んにや(粉2.02を含む水溶液を加え十分攪拌をおこ
なった。
Further, an aqueous solution containing 5.1' of Texturin (degree of polymerization: 15) and 2.02% of Konniya (powder) was added to this and thoroughly stirred.

これにグロテアーゼ200■を加え10分間後ゲルを得
た。
200 μl of Grotease was added to this and a gel was obtained after 10 minutes.

これをスリットより押し出しローラー間で2倍に延伸し
、5%酢酸カルシウム水溶液を含む5%酢酸水溶液に浸
漬固定し、繊維の配向方向と直角方向に力をかげて解繊
した。
This was extruded through a slit and stretched to double the length between extrusion rollers, fixed by immersion in a 5% acetic acid aqueous solution containing a 5% calcium acetate aqueous solution, and defibrated by applying force in a direction perpendicular to the fiber orientation direction.

これを種水酸化カルシウム水溶液で中和後水洗し、P
H6,5の繊維状組成物を得た。
This was neutralized with aqueous calcium hydroxide solution, washed with water, and P
A fibrous composition of H6,5 was obtained.

本繊維状組成物は80℃20分間の加熱により良好な耐
熱軟化性を示し、繊維構造の消失は少い。
This fibrous composition exhibits good heat softening resistance when heated at 80° C. for 20 minutes, with little loss of the fibrous structure.

実施例 5 実施例1に於てλ−カラゲニンとデキストリンを使用す
る代りに、デキストリン(重合度15)lO′?のみを
使用し、実施例1と同様の操作をおこなった。
Example 5 Instead of using λ-carrageenan and dextrin in Example 1, dextrin (degree of polymerization 15) lO'? The same operation as in Example 1 was performed using only

得られた繊維状組成物は80℃20分間の加熱によりフ
ィブリル構造が80%程度消失するが少量の繊維構造は
保持される。
When the obtained fibrous composition is heated at 80° C. for 20 minutes, about 80% of the fibril structure disappears, but a small amount of the fibrous structure is retained.

Claims (1)

【特許請求の範囲】[Claims] 1 乳たん白質またはこれと他の非繊維状動植物たん白
質との混合液に金属多価イオンを作用させてミセル化に
よる不均一系の形成を開始させた後、少くとも一種類の
酸性または中性多糖類を含む多糖類を添加し、ついでそ
のミセルを破壊してゲルを形成させ、このゲルに応力を
加え配向したフィブリル構造を有する繊維状組成物にし
た後、またはしつつ酸で固定することを特徴とする、耐
熱軟化性に優れた繊維状高たん白食品の製造法。
1. After starting the formation of a heterogeneous system through micellization by applying metal multivalent ions to milk protein or a mixture of this and other non-fibrous animal and plant proteins, at least one type of acidic or neutral Adding a polysaccharide including a polysaccharide, then destroying the micelles to form a gel, applying stress to the gel to form a fibrous composition having an oriented fibril structure, and then fixing with an acid. A method for producing a fibrous high-protein food with excellent heat-resistant softening properties.
JP50126488A 1975-10-21 1975-10-21 How to prepare a protein that can be used in Thailand Expired JPS5823056B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP50126488A JPS5823056B2 (en) 1975-10-21 1975-10-21 How to prepare a protein that can be used in Thailand

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP50126488A JPS5823056B2 (en) 1975-10-21 1975-10-21 How to prepare a protein that can be used in Thailand

Publications (2)

Publication Number Publication Date
JPS5251058A JPS5251058A (en) 1977-04-23
JPS5823056B2 true JPS5823056B2 (en) 1983-05-12

Family

ID=14936435

Family Applications (1)

Application Number Title Priority Date Filing Date
JP50126488A Expired JPS5823056B2 (en) 1975-10-21 1975-10-21 How to prepare a protein that can be used in Thailand

Country Status (1)

Country Link
JP (1) JPS5823056B2 (en)

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS49110854A (en) * 1973-03-06 1974-10-22
JPS50126852A (en) * 1974-03-27 1975-10-06

Also Published As

Publication number Publication date
JPS5251058A (en) 1977-04-23

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