JPS5849222B2 - Gluten fiber manufacturing method - Google Patents
Gluten fiber manufacturing methodInfo
- Publication number
- JPS5849222B2 JPS5849222B2 JP11831376A JP11831376A JPS5849222B2 JP S5849222 B2 JPS5849222 B2 JP S5849222B2 JP 11831376 A JP11831376 A JP 11831376A JP 11831376 A JP11831376 A JP 11831376A JP S5849222 B2 JPS5849222 B2 JP S5849222B2
- Authority
- JP
- Japan
- Prior art keywords
- gluten
- fibers
- gel
- metal chloride
- salt
- 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
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Description
【発明の詳細な説明】
本発明はグルテン蛋白質より紡糸法によらずに繊維グル
テン蛋白食品を製造する方法に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing a fibrous gluten protein food from gluten protein without using a spinning method.
動物性蛋白質、例えば畜肉類、魚介類は味覚、テクスチ
ャー、栄養等に於で好まれ、重要な食糧資源であるが、
その生産性が低いので将来の蛋白質食品源としては充分
な供給力を持たない。Animal proteins, such as meat and seafood, are preferred for their taste, texture, nutrition, etc., and are important food resources.
Due to its low productivity, it does not have sufficient supply capacity as a future protein food source.
この為従来、飼料、調味料原料等に用いられて食品とし
て利用される事の少なかった安価搾油粕蛋白、グルテン
等が次代の蛋白食品源として注目され、数多くの利用法
が提案されている。For this reason, inexpensive extracted oil cake proteins, gluten, etc., which have traditionally been used as raw materials for feed and seasonings and have rarely been used as foods, are attracting attention as next-generation protein food sources, and numerous uses have been proposed.
グルテン蛋白質は水に不溶でその水利物はグルテン分子
の分子間、分子内のSS結合に起因すると考えられる強
い粘着力を持った塊状の粘弾性ゲルを形戊し、そのゲル
は加熱によって凝固する。Gluten protein is insoluble in water, and its water products form a lumpy viscoelastic gel with strong adhesive force, which is thought to be due to the SS bonds between and within the gluten molecules, and the gel solidifies when heated. .
このグルテンゲルの性状を利用して内状の繊維構造を持
ったグルテン蛋白食品を得る数多くの試みがなされ提案
されているが、グルテン繊維を得るのは現在紡糸法以外
にはない。Many attempts have been made and proposed to utilize the properties of gluten gel to obtain gluten protein foods with an internal fibrous structure, but currently there is no method other than spinning to obtain gluten fibers.
例えばUSF3814823に開示されているように、
グルテンドウを加熱膨脹させる方法に於で膨脹方向を一
定方向に制御して、グルテンゲルに15〜2.5倍の延
伸力を与えながら同時に熱凝固させて方向性のある肉状
繊維組織を得る方法がある。For example, as disclosed in USF3814823,
A method of heating and expanding gluten dough, controlling the expansion direction in a fixed direction, applying a stretching force of 15 to 2.5 times to the gluten gel, and simultaneously thermally coagulating it to obtain a directional fleshy fiber structure. There is.
この方法は従来のカロ熱、加圧押出し法と同様、組織内
に気泡を含んだ海綿状の構造であって一部繊維化してい
ても大部分はグルテンゲルが結着して熱凝固しており紡
糸法のグルテン繊維に比して不満足なものである。This method is similar to the conventional Calo heat and pressure extrusion method, in which the tissue has a spongy structure containing air bubbles, and even though some of it has become fibrous, most of it is made up of gluten gel that is bound together and solidified by heat. This is unsatisfactory compared to gluten fiber produced by cage spinning.
また、USP3197310に開示されているように、
グルテン、卵白粉及び焙焼した大豆蛋白質の混合物をワ
ーリングブレンダーで攪拌し、生グルテンを強力な剪断
、引伸し作用でヒゲ状の繊維とし、生或した繊維を添加
した卵白粉、大豆蛋白質で被覆してグルテンの再結着を
防止して加熱凝固する方法がある。Also, as disclosed in USP3197310,
A mixture of gluten, egg white powder, and roasted soybean protein is stirred in a Waring blender, and the raw gluten is made into whisker-like fibers by strong shearing and stretching action, and then coated with egg white powder and soybean protein to which the raw gluten has been added. There is a method of heating and coagulating the gluten to prevent it from re-binding.
この方法は加熱凝固処理でグルテン繊維が軟化溶解して
得られたものは、やはり気泡を含んだ海綿状で紡糸法の
グルテン繊維に比して不満足なものである。In this method, the gluten fibers are softened and dissolved by heat coagulation treatment, and the resulting product is spongy and contains bubbles, which is unsatisfactory compared to gluten fibers obtained by spinning.
次に、特公昭50−2023に開示されているように、
弛緩したグルテンゲルを多糖類、蛋白質、合或高分子糊
剤を含む加熱水中で攪拌しつつ加熱凝固させ多糖類等の
溶液によりグルテンの再結着を防止してフレーク状又は
糸み\ず状の内状人造肉を得る方法がある。Next, as disclosed in Special Publication No. 50-2023,
The relaxed gluten gel is heated and coagulated by stirring in heated water containing polysaccharides, proteins, polymeric glue, etc., and the gluten is prevented from re-binding by a solution such as polysaccharides to form flakes or threads. There is a way to obtain internal artificial flesh.
この方法で得られたものは再結着を防止して海綿状構造
となる事を免かれるが、フレーク伏、糸み\ず状であっ
て挽肉状等以外に利用するには更に再加工が必要であり
利用価値が低い。The material obtained by this method prevents re-binding and avoids forming a spongy structure, but it has a flake-like or thread-like shape and requires further reprocessing to be used for purposes other than minced meat. It is necessary and has low utility value.
又紡糸法のグルテン繊維にくらべ繊維四が劣り全く不満
足なものである。Furthermore, compared to the gluten fiber produced by spinning, the fiber quality is inferior and is completely unsatisfactory.
更に特公昭47−24742で開示されるようにー、加
熱ゲル化と同時に攪拌、引伸しを行って繊維性を有する
生地を得、これを凍結、圧縮操作を施した後油熱する方
法があるが、加熱ゲル化で得られる繊維は油熱すること
により融解して再付着し得られた製品は方向性の繊維状
組織をとゾめるにすぎず満足できる繊維性を持たない。Furthermore, as disclosed in Japanese Patent Publication No. 47-24742, there is a method in which fibrous fabric is obtained by stirring and stretching at the same time as heating and gelling, which is then frozen, compressed, and then heated in oil. The fibers obtained by heating and gelling are melted and redeposited by heating with oil, and the resulting product only has a directional fibrous structure and does not have satisfactory fibrous properties.
本発明者は加熱凝固によって繊維を固定しようとするこ
の様な従来法ではグルテン繊維が加熱により融着して繊
維性を維持できず満足な繊維組織が得られないこと、多
くの融着防止作用を有する糊料、澱粉等を添加して食感
を低下させていること等の欠点を改良するには、グルテ
ン蛋白に添加する添加物は食感を良好にする為に必要最
少限にとどめるべきこと、加熱凝固法によらずに繊維化
をすることが必要であることを認め研究の結果、多糖類
を加えてグルテン蛋白質ゲルを改質再構戊し、アルカリ
金属の塩化物(食塩を除く)あるいはアルカリ土類金属
の塩化物中で圧延するとグルテン蛋白賞ゲル(以下グル
テンゲルという)は繊維化して離水し内部が全て繊維で
構或されたグルテン繊維束となり、得られたグルテン繊
維束は繊維束に包含される水分は多くてもグルテン繊維
の水分量が少なく細繊維化されており、塩による変性と
の相乗効果によって加熱によって繊維性を失うことがな
く、加熱調理後も更に長繊維な細繊維として分繊が可能
である事を発見して本発明を完威した。The inventor of the present invention discovered that in such a conventional method of fixing fibers by heating and coagulating, the gluten fibers are fused by heating and unable to maintain fibrous properties, making it impossible to obtain a satisfactory fiber structure, and that a satisfactory fibrous structure cannot be obtained. In order to improve the disadvantages such as the deterioration of texture due to the addition of thickeners and starches, etc., additives added to gluten protein should be kept to the minimum necessary to improve the texture. As a result of research, we recognized that it was necessary to form fibers without using heat coagulation, and as a result of our research, we added polysaccharides to modify and restructure the gluten protein gel, and added alkali metal chlorides (excluding table salt) to the gluten protein gel. ) or when rolled in an alkaline earth metal chloride, the gluten protein gel (hereinafter referred to as gluten gel) turns into fibers and releases water, forming gluten fiber bundles whose interior is entirely composed of fibers, and the resulting gluten fiber bundles are Although the fiber bundle contains a lot of water, the gluten fiber has a low water content and is made into fine fibers, and due to the synergistic effect with the denaturation with salt, it does not lose its fibrous properties when heated, and even after cooking, it remains a long fiber. He discovered that it was possible to split the fibers into fine fibers and completed the invention.
本発明の方法を説明するとグルテン例えば、粉末グルテ
ン・バイクルグルテン・生グルテン・コーングルテン等
に、調整するグルテンゲル量(以下係はグルテンゲル量
に対する重量饅で示す)に対して多糖類例えばペクチン
・アミ口ペクチン・カルボキシメチルセルローズ・加工
澱粉・カラギーナン・ローカストビーンガム等のガム質
等を0.5〜10φ好ましくは1〜5係、繊維強度を必
要とする場合は、更に食塩を1〜5φ添カロして混合し
、次に水を30〜90φ添加して後、アルカリ例えばア
ンモニア・苛性ソーダ等、又は酸例えば酢酸・蟻酸・乳
酸・炭酸・塩酸等、又は還元剤例えば硫化水素・硫化ナ
トリウム・硫化アンモニウム・亜硫酸ナトリウム等の亜
硫酸塩・2−メルカブトエタノール・グルタチオン・シ
スチン等を添加してよく混捏し、グルチン蛋白質の部分
的解膠、SS結合の還元切断を起させた水分30〜90
%の均質なグルテンゲルを調整する。To explain the method of the present invention, gluten, such as powdered gluten, bickle gluten, fresh gluten, corn gluten, etc., is mixed with polysaccharides such as pectin and the amount of gluten gel to be adjusted. Add gum such as pectin, carboxymethyl cellulose, modified starch, carrageenan, locust bean gum, etc. to 0.5 to 10 mm, preferably 1 to 5 mm, and if fiber strength is required, add 1 to 5 mm of salt. Stir and mix, then add 30 to 90 φ of water, then add an alkali such as ammonia, caustic soda, etc., an acid such as acetic acid, formic acid, lactic acid, carbonic acid, hydrochloric acid, etc., or a reducing agent such as hydrogen sulfide, sodium sulfide, sulfide. Ammonium, sulfites such as sodium sulfite, 2-mercabutoethanol, glutathione, cystine, etc. were added and kneaded well to cause partial peptization of glutin protein and reductive cleavage of SS bonds.
% homogeneous gluten gel.
酸、アルカリ、還元剤の添加量はグルテンゲルの水分、
添加物、希望するグルテン繊維の引張り強度等により一
概には規定できないが、例えばアンモニア水を加えてゲ
ルを調整する方法ではpH 9〜12が好ましい内状の
テクスチャーを得る。The amount of acid, alkali, and reducing agent added depends on the moisture content of the gluten gel,
Although it cannot be absolutely defined depending on the additives, the desired tensile strength of the gluten fibers, etc., for example, in a method of adjusting the gel by adding aqueous ammonia, an inner texture with a preferable pH of 9 to 12 can be obtained.
この様にして得られた水分30〜90%の均質なグルテ
ンゲルを次にアルカリ金属の塩化物(食塩を除く)ある
いはアルカリ土類金属の塩化物中又は該塩化物の水溶液
中で4倍以上、好ましくは10〜20倍の長さに展延し
て繊維化する。The thus obtained homogeneous gluten gel with a water content of 30 to 90% is then immersed in an alkali metal chloride (excluding common salt) or an alkaline earth metal chloride or an aqueous solution of the chloride for at least 4 times. , preferably 10 to 20 times the length to form a fiber.
更にこの展延、繊維化について詳述するとアルカリ金属
の塩化物(食塩を除く)あるいはアルカリ士類金属の塩
化物中で展延して繊維化する方法では、グルテンゲルに
該塩化物の結晶を撒布しながら麺棒で強く押しつけて延
すとグルテンゲルは表面より塩析効果で収縮すると共に
ミクロな構造においても分子同士が絡み合いながら、つ
ながった繊維の集合体として分離され、該塩化物の結晶
が繊維の間に喰込みながら分繊効果を高めると共に形或
されたグルテン繊維は塩析脱水され、塩によって変性を
起して加熱に安定なグルテン繊維が得られる。Further, to explain this spreading and fiberization in detail, in the method of spreading and fiberizing in an alkali metal chloride (excluding common salt) or an alkali metal chloride, the chloride crystals are added to the gluten gel. When spread by pressing strongly with a rolling pin while spreading, the gluten gel shrinks from the surface due to the salting-out effect, and even in the microstructure, the molecules are entangled with each other and separated as an aggregate of connected fibers, and the chloride crystals are separated. The gluten fibers are bitten between the fibers to enhance the splitting effect, and the formed gluten fibers are salted out and dehydrated, and the gluten fibers are denatured by the salt and are stable to heat.
この方法で該塩化物の結晶はグルテンゲルに圧着されて
、グルテン繊維の分繊とグルテン膜の破壊、脱水に大き
な効果を発揮する。In this method, the chloride crystals are pressed onto the gluten gel, and are highly effective in splitting gluten fibers, destroying gluten membranes, and dehydrating.
次に該塩化物の水溶液中で繊維化する方法では、塩濃度
を5φ以上好ましくは10φ以上とした該塩化物の水溶
液中でグルテンゲルを展延するとグルテンゲル表面は徐
々に繊維化されてくる。Next, in the method of forming fibers in an aqueous solution of the chloride, when the gluten gel is spread in the aqueous solution of the chloride with a salt concentration of 5φ or more, preferably 10φ or more, the surface of the gluten gel is gradually turned into fibers. .
この状態のま\加熱するとグルテンゲルは熱凝固を起し
て繊維化できなくなるので熱凝固以下の温度で行う必要
がある。If heated in this state, the gluten gel will undergo thermal coagulation and will no longer be able to form into fibers, so it must be heated at a temperature below thermal coagulation.
表面が繊維化したグルテンゲルは分子的には繊維性の配
向を持つが、三次元網目構造を保持しきれず、三次元構
造に水分を強く包含して膜伏を呈し容易に繊維化が進行
しないが展延方向に沿ってグルテンゲルを揉解するとグ
ルテンゲルは急速に収縮を始め繊維化する。Gluten gel with a fibrous surface has a fibrous orientation molecularly, but it cannot maintain its three-dimensional network structure, and the three-dimensional structure strongly traps water and exhibits a membrane-like structure that prevents it from easily becoming fibrous. When the gluten gel is rubbed along the spreading direction, the gluten gel begins to rapidly shrink and becomes fibrous.
このアルカリ金属の塩化物(食塩を除く)あるいはアル
カリ土類金属の塩化物中又は該塩化物の水溶液中での繊
維化は多糖類を加えて再構戊したことによって始めて達
戊されるものでグルテンのみで塩による処理を行っても
膜となって全く繊維性がない。This fiber formation in alkali metal chlorides (excluding common salt) or alkaline earth metal chlorides, or in an aqueous solution of these chlorides, can only be achieved by adding polysaccharides to reconstitute the structure. Even when gluten alone is treated with salt, it forms a film and has no fibrous properties.
塩による処理によって収縮して包含する水分を離水し、
繊維の集合体として分離、固定されたグルテン繊維は加
熱、調理によっても最早繊維性を失うことはなく、更に
細繊維に分離が可能である。By treatment with salt, it shrinks and removes the contained water,
Gluten fibers separated and fixed as a fiber aggregate no longer lose their fibrous properties even when heated or cooked, and can be further separated into fine fibers.
本発明の1つの特徴であるこの加熱安定性は塩によって
変性が起りグルテン繊維間の反応性が低下する事、及び
塩析効果によりグルテン繊維内に包含されていた水分が
グルテン繊維間に移行してグルテン繊維束組織内に保持
される為と考えられる。This heat stability, which is one of the features of the present invention, is due to denaturation caused by salt, which reduces the reactivity between gluten fibers, and due to the salting-out effect, water contained in gluten fibers migrates between gluten fibers. This is thought to be because the gluten is retained within the gluten fiber bundle tissue.
又、アルカリ金属の塩化物(食塩を除く)あるいはアル
カリ土類金属の塩化物に対してHLB7〜12の蔗糖脂
肪酸エステルを2〜10φ添加すると更に良好なグルテ
ン繊維を得ることができる。Furthermore, even better gluten fibers can be obtained by adding 2 to 10 φ of sucrose fatty acid ester with HLB of 7 to 12 to the chloride of an alkali metal (excluding salt) or the chloride of an alkaline earth metal.
賦香味料、着色料は自由に添加が可能であるが特にグル
テンゲルの調整工程で他の蛋白質例えば卵白アルフ゛ミ
ン、ラクトアルブミン、グロプリン、ゼラチン、卵白、
卵白粉、大豆蛋白質等を1〜10φ添加すると繊維及び
繊維束の強度を強くし、疎水性乳化剤例えば七ノー、ジ
ーグリセライド、ソルビタン脂肪酸エステル、プロピレ
ングリコール脂肪酸エステル、蔗糖脂肪酸エステル等を
0.1〜3φ、不飽和脂肪酸例えばオレイン酸、リノー
ル酸等を0.1〜5%添加すると展延性、繊維性、加工
性を改良することができる。Flavoring agents and coloring agents can be added freely, but other proteins such as egg white albumin, lactalbumin, globulin, gelatin, egg white,
Addition of egg white powder, soybean protein, etc. of 1 to 10 mm increases the strength of fibers and fiber bundles, and addition of hydrophobic emulsifiers such as 7-no, di-glyceride, sorbitan fatty acid ester, propylene glycol fatty acid ester, sucrose fatty acid ester, etc. of 0.1 to 10 mm Addition of 0.1 to 5% of 3φ, unsaturated fatty acids such as oleic acid and linoleic acid can improve spreadability, fibrous properties, and processability.
得られたグルテン繊維は利用目的により適宜分繊するこ
とにより微細でしかも繊維束の太さ、附着が不均一な網
目を形或した極めて畜肉、魚介類の蛋白組織と類似した
繊維組織を得るのでソシャク性がよく、又耐熱性、加工
性が優れていて従来法では得ることができなかったすぐ
れた特徴をもち、しかも紡糸法等に比べて製造工程が単
純な為、工業的に有利に製造することが可能である。By dividing the obtained gluten fibers as appropriate depending on the purpose of use, it is possible to obtain a fiber structure that is fine and has a network shape with uneven fiber bundle thickness and attachment, which is extremely similar to the protein structure of meat and seafood. It has excellent properties that could not be obtained by conventional methods, such as good elasticity, heat resistance, and processability.Moreover, the manufacturing process is simpler than spinning methods, etc., making it industrially advantageous. It is possible to do so.
添附参考写真は本発明によって得られるグルテン繊維の
組織を示す写真である。The attached reference photograph is a photograph showing the structure of gluten fibers obtained by the present invention.
次に実施例を記して説明する。Next, examples will be described.
実施例 1
水分65饅の生グルテン500g、ペクチン20g、ワ
キシースターチ10g、卵白粉15g,食塩ioy,水
150Ceを混合し、更にアンモニア水IQccを加え
て充分に捕潰して均質なグルテンゲルを調整した。Example 1 500 g of raw gluten with a moisture content of 65 g, 20 g of pectin, 10 g of waxy starch, 15 g of egg white powder, IOY of salt, and 150 Ce of water were mixed, and then IQcc of ammonia water was added and sufficiently crushed to prepare a homogeneous gluten gel. .
次にこのグルテンゲルに塩化マグネシウムを添加しなが
ら巾Loomm、厚さ51rL11L1長さ約5mの帯
状に展延してグルテン繊維を得た。Next, while adding magnesium chloride to this gluten gel, it was spread into a belt shape with a width of 51 mm, a thickness of 51 mm, a thickness of 51 mm, and a length of about 5 meters to obtain gluten fibers.
次に120℃で5分間処理して、スルメ様の組織と食感
を持つグルテン繊維を得た。Next, it was treated at 120°C for 5 minutes to obtain gluten fibers having a squid-like structure and texture.
実施例 2
バイタルグルテン20011ペクチン25g、食塩15
gをよく混合し、水500CC,酢酸125ccを加え
て捏合せグルテンゲルを得た。Example 2 Vital Gluten 20011 Pectin 25g, Salt 15
500 cc of water and 125 cc of acetic acid were added and kneaded to obtain a gluten gel.
次に巾2 0 0 mm,厚さ5間の約1,5倍に展延
して繊維化したグルテンゲルを10多塩化カルシウム溶
液中で展延方向に沿って揉解しながら分繊しグルテン繊
維を得た。Next, the gluten gel, which has been spread to a width of 200 mm and about 1.5 times the thickness of 5 mm and made into fibers, is divided into fibers while being rubbed along the spreading direction in a 100 mm polycalcium chloride solution. Obtained fiber.
得たグルテン繊維は3〜10分間、80〜120゜Cで
処理することにより、種々な食感を賦与することができ
る。Various textures can be imparted to the obtained gluten fibers by treating them at 80 to 120°C for 3 to 10 minutes.
例えば80℃で約5分間加熱処理して貝肉様、100℃
で約7分間加熱処理してカニ身様、1000Cで約10
分間加熱処理して牛肉様、シート状に延ばして後120
℃で約10分間加熱処理をしてスルメ様の食感および組
織を有するグルテン繊維が得られた。For example, heat treated at 80℃ for about 5 minutes to produce shellfish-like meat, then heated to 100℃.
Heat-treated for about 7 minutes at 1000C to resemble crab meat, about 10 minutes at 1000C.
Beef-like after heat treatment for 120 minutes and rolled out into a sheet shape.
After heat treatment at ℃ for about 10 minutes, gluten fibers having squid-like texture and structure were obtained.
実施例 3
コーングルテン100g、ワ¥シースターチ6g1カル
ボキシメチルセルロース4g、卵白粉6gをよく混合し
水160CC,アンモニア水4ccを加えて充分捏和し
て均質なグルテンゲルを得た。Example 3 100 g of corn gluten, 6 g of waxy starch, 4 g of carboxymethyl cellulose, and 6 g of egg white powder were thoroughly mixed, 160 cc of water and 4 cc of aqueous ammonia were added, and thoroughly kneaded to obtain a homogeneous gluten gel.
次にこのグルテンゲルに塩化マグネシウムを撒布しなが
ら約20倍に展延してグルテン繊維を得た。Next, this gluten gel was spread to about 20 times its size while being sprinkled with magnesium chloride to obtain gluten fibers.
次に長さ20關、巾8間に切断してカニエキスを加え1
20℃で約5分間加熱調理してカニ身様組織と食感を有
するグルテン繊維した。Next, cut into 20 pieces in length and 8 pieces in width, add crab extract and 1
The gluten fibers were cooked at 20° C. for about 5 minutes to form gluten fibers with a crab-like structure and texture.
実施例 4
水分70φの生グルテン1000,9にペクチン4 0
.91卵白粉20gを加えて混合し、次に亜硫酸水素
ナトリウム100■を加えて充分捏合せ、均質なグルテ
ンゲルを調整した。Example 4 Raw gluten 1000.9 with water content 70φ and pectin 40
.. 20 g of 91 egg white powder was added and mixed, and then 100 μ of sodium bisulfite was added and kneaded thoroughly to prepare a homogeneous gluten gel.
次に5%塩化カルシウム溶液中で揉解しながら約10倍
に展延してグルテン繊維を得、120℃で約5分間加熱
処理して畜肉様食感を有するグルテン繊維を得た。Next, gluten fibers were obtained by spreading the fibers about 10 times while being crushed in a 5% calcium chloride solution, and heat-treated at 120° C. for about 5 minutes to obtain gluten fibers having a meat-like texture.
Claims (1)
添加し更にアルカリあるいは酸あるいは還元剤を加えて
水分30〜c+o%の均質なグルテンゲルを調整し、次
にこのグルテンゲルをアルカリ金属の塩化物(食塩を除
く)あるいはアルカリ土類金属の塩化物で揉解、展延す
ることを特徴とするグルテン繊維の製法。 2 多糖類としてペクチン・アミ口ペクチン・カルボキ
シメチルセルローズ・加工澱粉・カラギーナン・ローカ
ストビーンガム等のガム質を単独または2種以上併用す
る特許請求の範囲第1項記載のグルテン繊維の製法。 3 グルテンゲルにアルカリ金属の塩化物(食塩を除く
)あるいはアルカリ土類金属の塩化物を撒布して揉解、
展延する特許請求の範囲第1項記載のグルテン繊維の製
法。 4 グルテンゲルをアルカリ金属の塩化物(食塩を除く
)あるいはアルカリ土類金属の塩化物の水溶液中で揉解
、展延する特許請求の範囲第1項記載のグルテン繊維の
製法。[Claims] 1 Adding polysaccharide to gluten or raw gluten by 0.5 to 10φ
A homogeneous gluten gel with a moisture content of 30 to C+O% is prepared by adding an alkali, an acid, or a reducing agent, and then this gluten gel is mixed with an alkali metal chloride (excluding common salt) or an alkaline earth metal chloride. A manufacturing method for gluten fibers, which is characterized by rolling and spreading the fibers. 2. The method for producing gluten fibers according to claim 1, in which, as the polysaccharide, gummy substances such as pectin, amino pectin, carboxymethyl cellulose, modified starch, carrageenan, and locust bean gum are used alone or in combination of two or more. 3. Sprinkle alkali metal chloride (excluding salt) or alkaline earth metal chloride on the gluten gel and rub it.
A method for producing gluten fibers according to claim 1. 4. The method for producing gluten fibers according to claim 1, wherein gluten gel is massaged and spread in an aqueous solution of an alkali metal chloride (excluding common salt) or an alkaline earth metal chloride.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11831376A JPS5849222B2 (en) | 1976-09-30 | 1976-09-30 | Gluten fiber manufacturing method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11831376A JPS5849222B2 (en) | 1976-09-30 | 1976-09-30 | Gluten fiber manufacturing method |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5344651A JPS5344651A (en) | 1978-04-21 |
JPS5849222B2 true JPS5849222B2 (en) | 1983-11-02 |
Family
ID=14733575
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP11831376A Expired JPS5849222B2 (en) | 1976-09-30 | 1976-09-30 | Gluten fiber manufacturing method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5849222B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20190047133A1 (en) * | 2016-04-06 | 2019-02-14 | Hilti Aktiengesellschaft | Application-optimized deactivation behavior of an electronic slipping clutch |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IL54096A (en) * | 1978-02-22 | 1981-07-31 | Shemer M | Physical form of gluten comprising inert material in gluten matrix,method for its manufacture and its use in food products |
JPH06217703A (en) * | 1992-04-08 | 1994-08-09 | Taiichiro Iwakura | Food with gluten as chief material |
JP6906766B2 (en) | 2017-11-30 | 2021-07-21 | 株式会社神戸製鋼所 | Gas treatment method and gas treatment equipment |
-
1976
- 1976-09-30 JP JP11831376A patent/JPS5849222B2/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20190047133A1 (en) * | 2016-04-06 | 2019-02-14 | Hilti Aktiengesellschaft | Application-optimized deactivation behavior of an electronic slipping clutch |
Also Published As
Publication number | Publication date |
---|---|
JPS5344651A (en) | 1978-04-21 |
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