JPH072095B2 - Protein food - Google Patents

Protein food

Info

Publication number
JPH072095B2
JPH072095B2 JP63110905A JP11090588A JPH072095B2 JP H072095 B2 JPH072095 B2 JP H072095B2 JP 63110905 A JP63110905 A JP 63110905A JP 11090588 A JP11090588 A JP 11090588A JP H072095 B2 JPH072095 B2 JP H072095B2
Authority
JP
Japan
Prior art keywords
protein
product
protein food
food according
weight
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 - Lifetime
Application number
JP63110905A
Other languages
Japanese (ja)
Other versions
JPH01281068A (en
Inventor
厚 津田
賢治 半埜
栄 片山
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.)
KATAYAMA KAGAKU KOGYO KENKYUSHO KK
Original Assignee
KATAYAMA KAGAKU KOGYO KENKYUSHO 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 KATAYAMA KAGAKU KOGYO KENKYUSHO KK filed Critical KATAYAMA KAGAKU KOGYO KENKYUSHO KK
Priority to JP63110905A priority Critical patent/JPH072095B2/en
Priority to ES198888110706T priority patent/ES2032902T3/en
Priority to EP88110706A priority patent/EP0298419B1/en
Priority to DE8888110706T priority patent/DE3871260D1/en
Priority to KR88008457A priority patent/KR960010398B1/en
Publication of JPH01281068A publication Critical patent/JPH01281068A/en
Priority to US07/593,289 priority patent/US5138038A/en
Priority to US07/869,793 priority patent/US5273773A/en
Publication of JPH072095B2 publication Critical patent/JPH072095B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Fish Paste Products (AREA)
  • Meat, Egg Or Seafood Products (AREA)
  • Formation And Processing Of Food Products (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Description

【発明の詳細な説明】 (イ)産業上の利用分野 この発明は、蛋白質食品に関する。さらに詳しくは、蒲
鉾、竹輪、ハム、ソーセージ、ハンバーグ、ミンチボー
ル等の魚肉、畜肉を主原料とした動物性蛋白質食品や、
豆腐類又は大豆蛋白、小麦グルテン等の蛋白質素材を主
原料とした植物性蛋白質食品に関する。
TECHNICAL FIELD The present invention relates to a protein food product. More specifically, fish protein such as kamaboko, bamboo rings, ham, sausage, hamburger, minced balls, animal protein foods mainly composed of livestock meat,
The present invention relates to a vegetable protein food mainly containing a protein material such as tofu or soybean protein and wheat gluten.

(ロ)従来の技術 蒲鉾、竹輪等の魚肉加工品やハム、ソーセージ、ハンバ
ーグ、ミンチボール等の畜肉加工品においては、通常、
テクスチャー(噛みごたえ)の改良のために澱粉が添加
されている。しかし、単に澱粉と肉素材とを混合して成
形しても形状保持性が劣ったり、またテクスチャーが不
充分である場合がしばしば生じている。ことに最近で
は、魚肉や畜肉の資源不足やコストの面から、澱粉に加
え、大豆蛋白や小麦グルテン等の植物性蛋白質を混合す
ることも行われているが、この植物性蛋白質の混和性や
分散性が不充分なためにテクスチャーの低下、硬さの低
下、形状保持性の劣化等の品質上の不都合が生じやす
く、とくに食感の低下を招く問題があった。
(B) Conventional technology For processed fish products such as kamaboko and bamboo rings, and processed meat products such as ham, sausage, hamburger and minced balls,
Starch has been added to improve the texture. However, even if the starch and the meat material are simply mixed and molded, the shape retention is often inferior and the texture is often insufficient. In particular, recently, from the viewpoint of resource shortage and cost of fish meat and livestock meat, in addition to starch, plant proteins such as soybean protein and wheat gluten have been mixed, but the miscibility of this plant protein and Due to insufficient dispersibility, inconveniences in quality such as deterioration of texture, hardness, deterioration of shape retention are likely to occur, and there is a problem that the texture particularly deteriorates.

この点の品質改良を意図して、従来から回転摩砕を用い
た特殊な物理的方法で肉にグルテンを混入する方法(特
開昭52−76453号公報参照)、大豆蛋白や小麦グルテン
にグアーガム、キサンタンガム等の増粘剤を添加した
り、さらにグリセリン脂肪酸エステルを添加し、魚肉・
畜肉に混合する方法(特開昭53−79058号公報、特開昭5
4−35240号、特開昭55−64782号各公報参照)、大豆蛋
白や小麦グルテンと大豆抽出残渣を魚肉すり身に混和す
る方法(特開昭53−118546号、特開昭55−39736号各公
報参照)や魚肉や畜肉の代わりに植物性蛋白を用い生澱
粉、α化澱粉及び可食性のアルカリ性物質(可溶化剤)
を含有させる方法(特開昭58−146260号公報参照)等が
知られている。
In order to improve the quality in this respect, a method of mixing gluten into meat by a special physical method using rotary grinding (see JP-A-52-76453), soybean protein, wheat gluten and guar gum are conventionally used. , A thickener such as xanthan gum, or a glycerin fatty acid ester,
Method of mixing with meat (JP-A-53-79058, JP-A-5
No. 4-35240, JP-A-55-64782), a method of mixing soybean protein, wheat gluten and soybean extract residue with fish meat surimi (JP-A-53-118546 and JP-A-55-39736). (See the official gazette) and vegetable protein in place of fish meat and meat, raw starch, pregelatinized starch and edible alkaline substance (solubilizer)
And the like (see JP-A-58-146260) are known.

また、特開昭56−137851号公報においては、植物性蛋白
をアルカリ処理し次いで中和する量の酸で処理する挽肉
様食品の製造法が開示されている。特開昭53−124654号
公報においては、塩酸酸性下で加水分解したグルテンを
粉末として肉加工品の製造に際して添加する方法が開示
されている。
Further, Japanese Patent Application Laid-Open No. 56-137851 discloses a method for producing a ground meat-like food by treating a vegetable protein with an alkali and then treating with a neutralizing amount of an acid. JP-A-53-124654 discloses a method in which gluten hydrolyzed under acidic conditions with hydrochloric acid is added as powder in the production of processed meat products.

(ハ)発明が解決しようとする課題 上記した従来の種々の方法は、いずれも魚肉や畜肉ある
いはこれらの代替となる植物性蛋白を用いた食品に品質
を向上することを意図した方法であり、ことに添加剤を
用いて品質向上を図る方法は比較的簡便な方法と考えら
れる。
(C) Problems to be Solved by the Invention The above-mentioned various conventional methods are methods intended to improve the quality of foods using plant protein, which is fish meat, livestock meat, or substitutes for them. Especially, the method of improving the quality by using the additive is considered to be a relatively simple method.

しかしながら、前記した従来の添加剤、すなわち、増粘
剤、グリセリン脂肪酸エステル、大豆抽出残渣、グルテ
ンの塩酸加水分解物を用いた際の品質改良効果は、必ず
しも充分なものといえなかった。ことに、グルテンの塩
酸加水分解物は、食品用添加剤としては安全性の点で理
想的なものであるが、品質改良効果の点で充分満足でき
るものではなかった。
However, the above-mentioned conventional additives, that is, the thickener, the glycerin fatty acid ester, the soybean extract residue, and the hydrochloric acid hydrolyzate of gluten, cannot be said to be sufficient in improving the quality. In particular, the hydrochloric acid hydrolyzate of gluten is ideal as a food additive in terms of safety, but it is not sufficiently satisfactory in terms of quality improvement effect.

この発明はかかる状況下なされたものであり、ことに安
全かつ安価でしかも各種品質改良効果が優れた蛋白質食
品用添加剤を提供しようとするものである。
The present invention has been made under such circumstances, and it is particularly intended to provide a safe and inexpensive additive for protein foods which is excellent in various quality improving effects.

(ニ)課題を解決するための手段 上記観点から、本発明者らは、穀物蛋白質部分分解物の
部分分解手法について種々研究、検討を行った結果、ア
ルカリ分解処理を必須とし、これに酸、酵素、酸化剤又
は還元剤による分解処理を組合わせた逐次的多段分処理
によって得られる特定の蛋白質部分解物が、(i)通常
の蛋白質部分分解物とはその性状等が全く異なる新規物
質であると共に、(ii)単なる酸分解物、アルカリ分解
物、酵素分解物、酸化分解物等に比して優れた蛋白質食
品の品質改良効果を奏する事実を見出した。
(D) Means for Solving the Problems From the above viewpoints, the present inventors have conducted various researches and studies on a partial decomposition method of a grain protein partial decomposed product, and as a result, require alkali decomposition treatment, and The specific protein degradation product obtained by the sequential multi-step treatment in combination with the degradation treatment with an enzyme, an oxidizing agent or a reducing agent is (i) a novel substance whose properties are completely different from those of ordinary protein degradation products. In addition, it has been found that (ii) it has an excellent quality improving effect on protein foods as compared with simple acid decomposition products, alkali decomposition products, enzymatic decomposition products, oxidative decomposition products, and the like.

かくしてこの発明によれば、穀物蛋白質の部分分解物で
あって、以下の物性、 (a)重量平均分子量(ゲル濾過法による)が500〜900
00の範囲にある、 (b)紫外吸収λmaxが、260〜280nm付近で、かつ赤外
吸収が1400,1630及び3400cm-1付近である、 (c)等電点が、3.9〜5.0の範囲にある、 (d)pH緩衝性(本品の5重量%水溶液100mlのpHを6
から2まで低下させるのに1N−塩酸を2〜25ml必要とす
る)を有する、 (e)水に可溶であり、メタノール、エタノール、アセ
トン、エーテルに不溶である、 (f)外観は淡黄色ないし赤茶色の粉末である、 (g)キサントプロティン反応、ニンヒドリン反応によ
って呈色する、 (h)強い表面張力低下能(本品を25℃の純水に0.1重
量%添加することによって、純水の表面張力を50dyne/c
m以下(デュヌイの表面張力計で計測)に低下させる)
を有する。
Thus, according to the present invention, a grain protein partially decomposed product having the following physical properties: (a) weight average molecular weight (by gel filtration method) of 500 to 900
In the range of 00, (b) the ultraviolet absorption λmax is around 260 to 280 nm, and the infrared absorption is around 1400, 1630 and 3400 cm -1 , (c) the isoelectric point is in the range of 3.9 to 5.0. Yes, (d) pH buffering property (the pH of 100 ml of a 5 wt% aqueous solution of this product is 6%
To require 2 to 25 ml of 1N-hydrochloric acid to reduce to 2), (e) Soluble in water and insoluble in methanol, ethanol, acetone, ether, (f) Appearance is pale yellow To reddish brown powder, (g) Color develops by xanthoprotein reaction, ninhydrin reaction, (h) Strong surface tension reducing ability (by adding 0.1 wt% of this product to pure water at 25 ° C, The surface tension of water is 50 dyne / c
m or less (measured with Dunui's surface tensiometer)
Have.

(i)強い乳化能(本品1gの添加使用により少なくと
も、大豆油を30重量%含有する水−大豆油混合物100gを
完全乳化(均一な乳化状態を少なくとも10分、好ましく
は1時間以上維持することを意味する)しうる)を有す
る、 で特徴づけられる物質を蛋白食品素材に対して0.05〜10
重量%含有する蛋白質食品が提供される。
(I) Strong emulsifying ability (100 g of a water-soybean oil mixture containing at least 30% by weight of soybean oil is completely emulsified by the use of 1 g of this product (a uniform emulsified state is maintained for at least 10 minutes, preferably 1 hour or more). The substance characterized by having the meaning of
A protein food containing wt% is provided.

上記で特定される蛋白質部分分解物は、それ自体本願出
願前に文献未記載の新規物質であり、とくに上記表面張
力低下能(h)及び(i)の点で従来の穀物蛋白質部分
分解物とは区別されるものである。
The protein partial hydrolyzate specified above is a novel substance which has not yet been described in the literature before the application of the present invention, and in particular, in terms of the surface tension lowering ability (h) and (i), it is different from the conventional grain protein partial hydrolyzate. Are distinct.

また、この発明の添加対象の蛋白質食品とは、蛋白質を
主体(総固形分中に40重量%以上)とする食品を意味す
る。
The protein food to be added according to the present invention means a food mainly containing protein (40% by weight or more in the total solid content).

この発明の品質改良剤は蛋白質食品の製造時に添加して
用いられ、必要量の添加により各種の品質改良効果を発
揮するものである。
The quality improving agent of the present invention is used by adding it during the production of protein foods, and exhibits various quality improving effects by adding a necessary amount.

例えば、蒲鉾、竹輪等の魚肉を主原料とした動物性蛋白
質食品やハム、ソーセージ、ハンバーグ、ミンチボール
等の畜肉を主原料とした動物性蛋白質食品の製造時にお
いて、必要量添加することによって、その成形性が向上
し、形状保持性やテクスチャーが優れ、食感がより良好
な蛋白質食品を得ることができる。また、かかる品質改
良効果により、従来、その分散性の点で添加量に限界が
あった大豆蛋白等の植物蛋白質の混合量(従来せいぜい
10重量%程度)を増加することもできる。さらに、これ
らの動物性蛋白質食品に限らず、大豆蛋白食品や豆腐の
ごとき植物性蛋白質食品の製造時に添加することによ
り、大豆蛋白食品の安定性、形状保持性、テクスチャー
の向上や豆腐の弾力向上等の品質改良効果を発現するも
のである。
For example, kamaboko, ham, sausages, hamburgers, minced meat and other animal protein foods mainly made from animal protein foods mainly made of fish meat such as bamboo rings, at the time of production of animal protein foods mainly made by adding necessary amount, It is possible to obtain a protein food having improved moldability, excellent shape retention and texture, and a better texture. In addition, due to the quality improving effect, the amount of plant protein such as soybean protein, which has been conventionally limited in terms of dispersibility, has been limited (up to now.
10% by weight) can be increased. In addition to these animal protein foods, by adding them during the production of vegetable protein foods such as soybean protein foods and tofu, the stability, shape retention and texture of soybean protein foods are improved and the elasticity of tofu is improved. And the like, and the effect of improving quality is exhibited.

この発明で穀物蛋白質とは、穀物に含有される蛋白質を
意味し、ここで穀物としては、麦類(例えば、小麦)、
トウモロコシ類、豆類(例えば、大豆)などが挙げられ
る。かかる穀物に含まれる蛋白質のうち、例えば小麦蛋
白質は、グルテニンとグリアジンを主成分として含み、
通常小麦グルテンと称せられる。また、トウモロコシ蛋
白質は、ゼインを主成分として含み、通常トウモロコシ
グルテンと称せられる。これらはいずれも公知の物質で
あり、穀物から常法によって分離や抽出して得ることが
できる。例えば、小麦蛋白質(小麦グルテン)を得る場
合、小麦粉に少量の水を加えて固く練り、次いでこれを
多量の水中で練ると澱粉は水中に懸濁し、グルテン含有
分は粘着性のかたまりとなって残る。この操作を、水を
替えて数回行うと灰褐色、粘稠な塊状物となって得るこ
とができる。この発明の部分分解物の調製のためには、
このような塊状物をそのまま使用することができるが、
その乾燥品を用いてもよく、さらに精製したものや部分
変性品等を用いてもよい。例えば、小麦グルテンは、乾
燥品が市販されており容易に入手することができる。そ
の他市販のトウモロコシグルテンや大豆蛋白質を簡便に
使用することができる。
In the present invention, the grain protein means a protein contained in grains, where grains include wheat (eg wheat),
Examples include corn and beans (eg, soybean). Of the proteins contained in such grains, for example, wheat protein contains glutenin and gliadin as main components,
Usually called wheat gluten. Further, corn protein contains zein as a main component and is usually called corn gluten. These are all known substances, and can be obtained by separating or extracting from grains by a conventional method. For example, when obtaining wheat protein (wheat gluten), a small amount of water is added to wheat flour and kneaded firmly, and then this is kneaded in a large amount of water, the starch is suspended in water, and the gluten-containing content becomes a sticky mass. Remain. If this operation is repeated several times while changing water, a grayish brown viscous mass can be obtained. For the preparation of the partially degraded product of this invention,
Although such a lump can be used as it is,
The dried product may be used, or a further purified product or a partially modified product may be used. For example, wheat gluten is commercially available as a dried product and can be easily obtained. In addition, commercially available corn gluten and soybean protein can be easily used.

なお、かかる蛋白質は、粗製品を用いても精製品を用い
てもよいが、蛋白質を70%以上含有するものを用いるの
が好ましい。
Although such a protein may be a crude product or a purified product, it is preferable to use a protein containing 70% or more of the protein.

この発明の部分分解物は、穀物蛋白質を、アルカリによ
る加水分解処理と、酸、酵素、酸化剤又は還元剤を用い
た分解処理とを組合わせた多段分解処理に付すことによ
り得られる。即ち、アルカリ分解処理とこれ以外の分解
処理とを組合わせることにより得られる。
The partially decomposed product of the present invention is obtained by subjecting a grain protein to a multistage decomposition treatment in which hydrolysis treatment with an alkali and decomposition treatment with an acid, an enzyme, an oxidizing agent or a reducing agent are combined. That is, it can be obtained by combining the alkali decomposition treatment and the other decomposition treatments.

上記アルカリによる加水分解処理は、希アルカリ水溶液
中で加熱することにより行うのが適している。通常、加
水分解対象物の水溶液又は水分散液を、水酸化ナトリウ
ム、水酸化カリウム、水酸化カルシウム、炭酸ナトリウ
ム、炭酸カリウム等のアルカリ剤の存在下、約60〜180
℃下、約10〜600分撹拌して行うのが適している。ここ
で加水分解対象物の水溶液又は水分散液としては2〜40
重量%のものを用いるのが好ましく、また使用するアル
カリ剤の量は、加水分解対象物20gに対し0.1〜6gとする
のが好ましい。
The above-mentioned hydrolysis treatment with alkali is suitably performed by heating in a dilute aqueous alkali solution. Usually, an aqueous solution or aqueous dispersion of a substance to be hydrolyzed is added in the presence of an alkali agent such as sodium hydroxide, potassium hydroxide, calcium hydroxide, sodium carbonate, potassium carbonate to about 60 to 180.
It is suitable to carry out stirring at ℃ for about 10 to 600 minutes. Here, the aqueous solution or dispersion of the hydrolysis target is 2 to 40
It is preferable to use one by weight, and the amount of the alkaline agent used is preferably 0.1 to 6 g based on 20 g of the substance to be hydrolyzed.

一方、上記アルカリによる加水分解処理に組合わせる他
の分解処理のうち、酸による分解処理は、希酸水溶液の
中で加熱して行うのが適している。通常、分解対象物の
水溶液や水分散液を、塩酸、硫酸等の無機酸や酢酸等の
有機酸の存在下約60〜120℃以下、約10〜600分撹拌して
行うのが適している。ここでの量的条件は前述したアル
カリ加水分解の際の条件と同一とするのが好ましい。
On the other hand, among other decomposition treatments to be combined with the above-mentioned hydrolysis treatment with alkali, the decomposition treatment with acid is suitably performed by heating in a dilute aqueous acid solution. Generally, it is suitable to stir an aqueous solution or aqueous dispersion of the decomposition target in the presence of an inorganic acid such as hydrochloric acid or sulfuric acid or an organic acid such as acetic acid at about 60 to 120 ° C. or less for about 10 to 600 minutes. . The quantitative conditions here are preferably the same as the above-mentioned conditions for the alkaline hydrolysis.

同じく、酵素による分解処理は、プロテアーゼ活性を有
する酵素の希水溶液中で行うのが適しており、通常、分
解対象物の水溶液や水分散液に、ペプシン、アルカリプ
ロテアーゼ、パパイン等の酵素を少量存在させた状態で
この酵素の至適pH条件下で約10〜60℃下、約60〜600分
行われる。ここで量的条件は分解対象物20gに対し酵素
使用量を0.02〜5gとする以外上記と同様とするのが好ま
しい。
Similarly, it is suitable to perform the decomposition treatment with an enzyme in a dilute aqueous solution of an enzyme having a protease activity. Usually, a small amount of an enzyme such as pepsin, alkaline protease, papain is present in an aqueous solution or aqueous dispersion of the decomposition target. In this state, it is carried out under the optimum pH condition of this enzyme at about 10 to 60 ° C for about 60 to 600 minutes. Here, the quantitative conditions are preferably the same as above except that the amount of enzyme used is 0.02 to 5 g per 20 g of the decomposition target.

同じく還元剤又は酸化剤による分解処理は、還元剤又は
酸化剤の希水溶液中で行うのが適しており、通常、分解
対象物の水溶液や水分散液に、亜硫酸塩、チオール系化
合物、エリソルビン酸、ヒドラジン等の還元剤又は過酸
化水素、次亜塩素酸塩等の酸化剤を少量存在させた状態
で、約10〜100℃下で、10〜600分行われる。この際の量
的条件は、分解対象物20gに対する還元剤又は酸化剤の
使用量を0.1〜5gとする以外上記と同様とするのが好ま
しい。
Similarly, the decomposition treatment with a reducing agent or an oxidizing agent is preferably performed in a dilute aqueous solution of a reducing agent or an oxidizing agent. Usually, an aqueous solution or aqueous dispersion of the decomposition target is treated with a sulfite, a thiol compound, or erythorbic acid. , A reducing agent such as hydrazine or a small amount of hydrogen peroxide or an oxidizing agent such as hypochlorite is present at about 10 to 100 ° C. for 10 to 600 minutes. The quantitative conditions at this time are preferably the same as those described above except that the amount of the reducing agent or the oxidizing agent used relative to 20 g of the decomposition target is 0.1 to 5 g.

上記多段分解処理の順序はとくに限定されない。即ち、
小麦グルテン等の原料を最初にアルカリ加水分解処理
(A)に付した後、上述した酸、酵素、還元剤及び酸化
剤を用いた分解処理(B)(アルカリ以外の分解処理)
のいずれか又はその二種以上の処理に付してもよく、ま
たこの逆の順で分解処理を行ってもよい。また、先にア
ルカリ以外の分解処理(B)に付した後、アルカリ加水
分解処理(A)に対し、再びアルカリ以外の分解処理
(B)に付すことにより得ることも可能である。また、
これらの各処理間では、適宜、中和処理がなされてもよ
い。
The order of the multistage decomposition process is not particularly limited. That is,
Raw materials such as wheat gluten are first subjected to alkaline hydrolysis treatment (A), and then decomposed using the above-mentioned acid, enzyme, reducing agent and oxidizing agent (B) (decomposition treatment other than alkali)
Any one of them or two or more thereof may be subjected to the treatment, or the decomposition treatment may be performed in the reverse order. Alternatively, it can be obtained by first subjecting it to a decomposition treatment other than alkali (B), and then again subjecting it to a hydrolysis treatment (A) other than alkali to a decomposition treatment (B) other than alkali. Also,
A neutralization treatment may be appropriately performed between these treatments.

この発明において、より優れた品質改良効果は、重量平
均分子量が500〜90000の範囲で認められ、さらに優れた
品質改良効果は同じく1000〜70000の範囲で認められ
る。これらの分子量は、前記した部分分解処理の条件を
調節することにより適宜制御することができる。
In the present invention, a more excellent quality improving effect is recognized in the weight average molecular weight range of 500 to 90,000, and a further excellent quality improving effect is recognized in the range of 1000 to 70,000. These molecular weights can be appropriately controlled by adjusting the conditions for the partial decomposition treatment described above.

なお、これらの分子量は、標準物質として1600,6500,16
000,65000,88000の分子量を有するポリスチレンスルホ
ン酸ソーダを溶媒として1重量%の食塩水を用い、ファ
ルマシア社製のセファデックスG−75又は−100を担体
として用いてゲル濾過法によって測定した値である。
The molecular weight of these substances is 1600,6500,16 as a standard substance.
1% by weight of sodium styrenesulfonate having a molecular weight of 000,65,000,88000 as a solvent, and a value measured by gel filtration using Sephadex G-75 or -100 manufactured by Pharmacia as a carrier. is there.

このようにして得られる蛋白質部分分解物は分解後の水
溶液の形態でそのまま蛋白質食品の品質改良剤として使
用できるが、乾燥後に粉末としても用いることもでき
る。また、例えば限外濾過法等による脱塩処理あるいは
脱色処理などによる精製品も良好に使用できる。
The partially decomposed protein thus obtained can be used as it is as a quality improving agent for protein food in the form of an aqueous solution after decomposition, but can also be used as a powder after drying. Further, for example, a purified product obtained by desalting treatment or decoloring treatment by an ultrafiltration method or the like can be favorably used.

この発明の品質改良剤は、前述のごとく各種蛋白質食品
の製造時に添加して用いられ、この際の添加量は通常、
添加対象の蛋白質食品素材に対して0.05〜10重量%とす
るのが適しており、0.2〜3重量%とするのが好まし
い。0.05重量%未満では、前述した種々の品質改良効果
が不充分で適さず、10重量%を越えると、添加量の増大
に見合う品質改良効果の向上が見られず好ましくない。
The quality improving agent of the present invention is used by adding it during the production of various protein foods as described above, and the addition amount at this time is usually
It is suitable to add 0.05 to 10% by weight, preferably 0.2 to 3% by weight, to the protein food material to be added. If it is less than 0.05% by weight, the above-mentioned various quality improving effects are insufficient and not suitable, and if it exceeds 10% by weight, the quality improving effect corresponding to the increase in the added amount is not improved, which is not preferable.

なお、この発明の品質改良剤中には、上記蛋白質部分分
解物以外に他の品質改良成分が含まれていてもよい。特
にショ糖脂肪酸エステルやグリセリン脂肪酸エステルの
ような多価アルコール脂肪酸エステル型界面活性剤と併
用するのが一つの好ましい態様である。この際蛋白質部
分分解物と界面活性剤との配合比を1:6〜6:1(重量比)
(好ましくは1:4〜4:1)とすると、相乗的な品質改良効
果が得られるので、より好ましい。
It should be noted that the quality improving agent of the present invention may contain other quality improving components in addition to the above-mentioned partially degraded protein. In particular, one preferred embodiment is to use together with a polyhydric alcohol fatty acid ester type surfactant such as sucrose fatty acid ester or glycerin fatty acid ester. At this time, the mixing ratio of the partially decomposed protein and the surfactant is 1: 6 to 6: 1 (weight ratio).
(Preferably 1: 4 to 4: 1) is more preferable because a synergistic quality improving effect can be obtained.

またエタノール、プロピオン酸、乳酸、ソルビン酸、デ
ヒドロ酢酸、食塩などの通常使用される防腐剤が併用さ
れていてもさしつかえはなく、これも一つの好ましい使
用態様である。
Further, a commonly used preservative such as ethanol, propionic acid, lactic acid, sorbic acid, dehydroacetic acid, and sodium salt may be used in combination, and this is also one preferable mode of use.

(ホ)実施例 この発明を実施例及び試験例によって詳細に説明する。(E) Examples The present invention will be described in detail with reference to Examples and Test Examples.

実施例1〜10(小麦グルテンの酸による部分分解と次い
で実施したアルカリによる部分分解による分解物の調
製) 塩化水素換算で0.5g,1g,2g及び4gに相当する塩酸水溶液
100gの入ったフラスコにそれぞれ和光純薬工業(株)製
の小麦グルテン(試薬品)20gを加え、80℃及び100℃に
て60分間加熱撹拌した。
Examples 1 to 10 (Preparation of Degradation Products by Partial Decomposition of Wheat Gluten with Acid and Subsequent Partial Decomposition with Alkali) Hydrochloric acid aqueous solution equivalent to 0.5 g, 1 g, 2 g and 4 g in terms of hydrogen chloride
20 g of wheat gluten (reagent product) manufactured by Wako Pure Chemical Industries, Ltd. was added to each flask containing 100 g, and the mixture was heated and stirred at 80 ° C. and 100 ° C. for 60 minutes.

その後、苛性ソーダで中和し純水で総量200gにして、小
麦グルテンの酸による部分分解物の10%水溶液を調製
し、その各100gをフラスコもしくはオートクレーブ10個
に入れ、これらに苛性ソーダ又は炭酸ナトリウム0.5〜2
gの範囲内の量を各別に加え、80℃〜150℃にて30分〜36
0分間加熱攪拌した。その後、塩酸にて中和し純水で総
量200gにしてこの発明の部分分解物である発明品No.1〜
10を得た。
Then, the total amount of pure water to neutralize with caustic soda to 200g, to prepare a 10% aqueous solution of the partial decomposition product of wheat gluten acid, 100g of each put into a flask or 10 autoclaves, caustic soda or sodium carbonate 0.5 ~ 2
Add an amount within the range of g separately, and at 80 ℃ to 150 ℃ for 30 minutes to 36 minutes.
The mixture was heated and stirred for 0 minutes. After that, it was neutralized with hydrochloric acid, and the total amount was 200 g with pure water.
Got 10.

表−1に分解条件と分解物の平均分子量を示す。Table 1 shows the decomposition conditions and the average molecular weight of the decomposition products.

なお、発明品No.1を等電点沈澱又は透析により脱塩した
ものは、ほとんど無味無臭であった。
Inventive product No. 1 was almost saltless and odorless when it was desalted by isoelectric precipitation or dialysis.

実施例11〜14(とうもろこしグルテン及び大豆蛋白の酸
による部分分解と次いで実施したアルカリによる部分分
解による分解物の調製) 日本食品化工(株)製とうもろこしグルテンを原料とし
実施例6及び1と同じ条件で酸及びアルカリを用いて順
次、部分分解を実施して発明品No.11,12を得た。平均分
子量はそれぞれ11800と27100であった。
Examples 11 to 14 (Preparation of corn gluten and soybean protein by partial decomposition with acid and subsequent partial decomposition with alkali carried out) Preparation of corn gluten manufactured by Nippon Shokuhin Kako Co., Ltd. as raw material and under the same conditions as in Examples 6 and 1. Inventive products Nos. 11 and 12 were obtained by sequentially carrying out partial decomposition with acid and alkali. The average molecular weights were 11800 and 27100, respectively.

また、市販の湯葉をアセトンで脱脂して得た大豆蛋白を
原料とし、実施例6及び1と同様の条件で酸及びアルカ
リを用いて順次部分分解を行い発明品No.13,14を得た。
In addition, the soybean protein obtained by defatting commercially available yuba with acetone was used as a raw material, and the partial decomposition was sequentially carried out using an acid and an alkali under the same conditions as in Examples 6 and 1 to obtain invention products No. 13 and 14. .

平均分子量はそれぞれ12000と29000であった。実施例1
5,16(小麦グルテンのアルカリによる部分分解と次いで
実施した酸による部分分解による分解物の調製) 苛性ソーダ2g又は4gを溶解した水溶液100gに実施例1〜
10で用いた小麦グルテン20gを加えて100℃にて60分間加
熱撹拌後、塩酸にて中和し、純水で総量200gにして小麦
グルテンのアルカリによる部分分解物の10%水溶液を調
製し、その100gに塩化水素換算で0.5g及び1gに相当する
塩酸を各別に加え、100℃にて60分間加熱撹拌した。そ
の後苛性ソーダで中和し、純水で総量200gにして発明品
No.15,16を得た。表−2に分解条件と分解物の平均分子
量を示す。
The average molecular weights were 12000 and 29,000, respectively. Example 1
5,16 (Preparation of Degradation Product by Partial Decomposition of Wheat Gluten with Alkali and Partial Decomposition with Acid Performed Then) Examples 1 to 1 in 100 g of an aqueous solution in which 2 g or 4 g of caustic soda was dissolved
After adding 20 g of wheat gluten used in 10 and heating and stirring at 100 ° C. for 60 minutes, the mixture was neutralized with hydrochloric acid, and a total amount of 200 g was prepared with pure water to prepare a 10% aqueous solution of partially decomposed product of wheat gluten with alkali, Hydrochloric acid equivalent to 0.5 g and 1 g in terms of hydrogen chloride was separately added to 100 g of the mixture, and the mixture was heated with stirring at 100 ° C. for 60 minutes. After that, it was neutralized with caustic soda and the total amount was 200g with pure water.
No.15 and 16 were obtained. Table 2 shows the decomposition conditions and the average molecular weight of the decomposed products.

実施例17(小麦グルテンの酵素による部分分解と次いで
実施したアルカリによる部分分解による分解物の調製) 実施例1〜10で用いた小麦グルテン20gを0.1N−塩酸液1
50gが入ったフラスコに加え、pH1.5の水溶液を得た。こ
れに和光純薬工業(株)製試薬ペプシン(1:10,000)0.
2gを加え37℃で90分間反応させた。その後、苛性ソーダ
で中和し純水で総量200gにして小麦グルテンの酵素によ
る部分分解物の10%水溶液を調製し、その100gに苛性ソ
ーダを1g加えフラスコ中で60分間加熱撹拌した。その後
塩酸にて中和して純水で総量200gとし発明品No.17を得
た。
Example 17 (Preparation of Degradation Products by Partial Decomposition of Wheat Gluten by Enzyme and Subsequent Partial Decomposition by Alkali) 20 g of wheat gluten used in Examples 1 to 10 was dissolved in 0.1N hydrochloric acid solution 1
It was added to a flask containing 50 g to obtain a pH 1.5 aqueous solution. Wako Pure Chemical Industries, Ltd. reagent pepsin (1: 10,000) 0.
2 g was added and reacted at 37 ° C. for 90 minutes. After that, a 10% aqueous solution of the partially decomposed product of wheat gluten by the enzyme was prepared by neutralizing with caustic soda to a total amount of 200 g with pure water, and 1 g of caustic soda was added to 100 g of the aqueous solution and heated and stirred in a flask for 60 minutes. After that, the product was neutralized with hydrochloric acid to obtain 200 g of pure water to obtain Inventive Product No. 17.

平均分子量は29000であった。The average molecular weight was 29,000.

実施例18(小麦グルテンの還元剤による部分分解と次い
で実施したアルカリによる部分分解による分解物の調
製) 亜硫酸ナトリウム4gを溶解した水溶液100gに実施例1〜
10で用いた小麦グルテン20gを加えて、30℃にて60分間
撹拌後、純水で総量200gにして小麦グルテンの還元剤に
よる部分分解物の10%水溶液を調製し、その100gに苛性
ソーダ1gを加え、フラスコ中で100℃で60分間加熱撹拌
した。その後、塩酸にて中和して純水で総量を200gとし
発明品No.18を得た。平均分子量は39500であった。
Example 18 (Preparation of Decomposition Product by Partial Decomposition of Wheat Gluten with Reducing Agent and Subsequent Partial Decomposition with Alkali) Examples 1 to 1 were added to 100 g of an aqueous solution containing 4 g of sodium sulfite.
20 g of wheat gluten used in 10 was added, and after stirring for 60 minutes at 30 ° C., a total amount of 200 g was prepared with pure water to prepare a 10% aqueous solution of a partial decomposition product of the reducing agent of wheat gluten, and 100 g of which was caustic soda 1 g. In addition, the mixture was heated and stirred in a flask at 100 ° C for 60 minutes. After that, the product was neutralized with hydrochloric acid to a total amount of 200 g with pure water to obtain an invention product No. 18. The average molecular weight was 39500.

実施例19(小麦グルテンのアルカリによる部分分解と次
いで実施した酵素による部分分解(実施例17と順次が
逆)による分解物の調製) 苛性ソーダ2gを溶解した水溶液100gに実施例1〜10で用
いた小麦グルテン20gを加えて100℃にて60分間加熱撹拌
後、塩酸にて中和し、純水で総量200gにして小麦グルテ
ンのアルカリによる部分分解物の10%水溶液を調製し、
その100gに試薬塩酸を加えpH1.5の水溶液を得、これを
フラスコ中で、和光純薬工業(株)製試薬ペプシン(1:
10,000)0.1gを加えて37℃で90分間反応させた。その
後、苛性ソーダで中和して純水で総量200gにし発明品N
o.19を得た。
Example 19 (Preparation of Degradation Product by Partial Decomposition of Wheat Gluten with Alkali and Partial Decomposition with Enzyme Performed Next (Sequential Reverse of Example 17)) Used in Examples 1 to 10 in 100 g of an aqueous solution in which 2 g of caustic soda was dissolved. After adding 20 g of wheat gluten and heating and stirring at 100 ° C. for 60 minutes, the mixture was neutralized with hydrochloric acid to a total amount of 200 g with pure water to prepare a 10% aqueous solution of partially decomposed product of wheat gluten with alkali,
Reagent hydrochloric acid was added to 100 g of the solution to obtain an aqueous solution having a pH of 1.5, which was placed in a flask in a reagent pepsin (1: 1,
10,000) 0.1 g was added and reacted at 37 ° C. for 90 minutes. After that, it was neutralized with caustic soda and the total amount was 200 g with pure water.
I got o.19.

平均分子量は24500であった。The average molecular weight was 24500.

実施例20(小麦グルテンのアルカリによる部分分解と次
いで実施した酸化剤による部分分解による分解物の調
製) 苛性ソーダ2gを溶解した水溶液100gに実施例1〜10で用
いた小麦グルテン20gを加えて100℃にて60分間加熱撹拌
後、塩酸にて中和し、純水で総量200gにして小麦グルテ
ンのアルカリによる部分分解物の10%水溶液を調製し、
その100gにH2O2換算で0.5gに相当する過酸化水素を加
え、40℃で60分間加熱撹拌した。その後、残存している
H2O2と当量のチオ硫酸ナトリウムを加え、純水で総量を
200gにして発明品20を得た。
Example 20 (Preparation of Decomposition Product by Partial Decomposition of Wheat Gluten with Alkali and Partial Decomposition with Oxidizing Agent Performed Next) To 100 g of an aqueous solution in which 2 g of caustic soda was dissolved, 20 g of wheat gluten used in Examples 1 to 10 was added, and 100 ° C was added. After heating and stirring for 60 minutes, neutralize with hydrochloric acid and make a total amount of 200 g with pure water to prepare a 10% aqueous solution of partially decomposed wheat gluten by alkali,
Hydrogen peroxide corresponding to 0.5 g in terms of H 2 O 2 was added to 100 g of the mixture, and the mixture was heated and stirred at 40 ° C. for 60 minutes. Then remains
Add H 2 O 2 and an equivalent amount of sodium thiosulfate, and add pure water to make the total amount.
Inventive product 20 was obtained in 200 g.

平均分子量は37000であった。The average molecular weight was 37,000.

以下に実施例1〜20によって得られたこの発明の蛋白質
部分分解物の諸物性及び粒子分散作用を表−3に、表面
張力及び乳化持続時間の測定結果を表−4に示す。
Various physical properties and particle dispersing action of the partially decomposed protein of the present invention obtained in Examples 1 to 20 are shown in Table 3 below, and the results of measuring surface tension and emulsion duration are shown in Table 4.

表中、原料欄のWは小麦グルテンを、Cはとうもろこし
グルテンを、Bは大豆蛋白をそれぞれ意味する。なお空
欄は、測定または試験せずを意味する。
In the table, W in the raw material column means wheat gluten, C means corn gluten, and B means soy protein. In addition, the blank means that the measurement or the test is not performed.

各諸物性及び粒子分散作用の測定方法、試験方法は以下
のとおりである。
The measurement methods and test methods for each physical property and particle dispersion action are as follows.

〔平均分子量〕[Average molecular weight]

これらの分子量は、標準物質として1600,6500,16000,65
000,88000の分子量を有するポリスチレンスルホン酸ソ
ーダを溶媒として1重量%の食塩水を用い、ファルマシ
ア社製のセファデックスG−75又はG−100を担体とし
て用いてゲル濾過法によって測定した値である。
These molecular weights are 1600,6500,16000,65 as standard substances.
It is the value measured by gel filtration method using sodium polystyrene sulfonate having a molecular weight of 000,88000 as a solvent, 1% by weight saline, and Sephadex G-75 or G-100 manufactured by Pharmacia as a carrier. .

〔等電点〕[Isoelectric point]

ビーカーにこの発明の実施例で得られた発明品1〜20を
各100gづつ取り、室温にて撹拌下、IN−HClを1mlづつ添
加し、pHを測定した。得られたpH曲線の傾きが最も緩や
かになるpH値を等電点とした。
100 g of each of the invention products 1 to 20 obtained in the examples of the present invention were placed in a beaker, IN-HCl was added in an amount of 1 ml under stirring at room temperature, and the pH was measured. The pH value at which the slope of the obtained pH curve was the most gentle was taken as the isoelectric point.

〔緩衝能〕[Buffer capacity]

等電点の測定方法と同様にして得られたpH曲線より、pH
を6から2まで低下させるのに必要な1Nの塩酸量を緩衝
能とした。なお、この際のpH中和曲線を、発明品No.1,N
o.7,No.11,及びNo.13について第1図(イ)〜(ニ)に
示した。
From the pH curve obtained in the same manner as the isoelectric point measurement method,
The buffering capacity was defined as the amount of 1N hydrochloric acid required to reduce the pH from 6 to 2. Incidentally, the pH neutralization curve at this time, invention product No. 1, N
o.7, No. 11, and No. 13 are shown in Fig. 1 (a) to (d).

〔UV〕(UV)

日立U−3200形分光光度計を用いて800〜200nmの範囲の
吸光度を測定した。
Absorbance in the range of 800 to 200 nm was measured using a Hitachi U-3200 spectrophotometer.

〔IR〕(IR)

日立260−10形赤外分光光度計を用いてKBr法で測定し
た。
It was measured by the KBr method using a Hitachi 260-10 type infrared spectrophotometer.

〔粒子分散力〕(炭酸カルシウムスラリー) ・ナショナルM1型ミキサーに発明品および水道水を計25
0g入れ、炭酸カルシウム(竹原化学工業製軽質炭酸カル
シウム)を250gを加え2分間混合し、50重量%スラリー
を調製する。その後直ちにスラリーをビーカーに移し、
東京計器製DVH−B型粘度計にて、回転数50rpm,ロータ
ーNo.3〜5にて粘度(cps)を測定する。ただし、その
発明の部分分解物の添加濃度は、総量500gに対して0.3
重量%である。
[Particle Dispersing Power] (Calcium Carbonate Slurry) ・ A total of 25 invention products and tap water in a National M1 type mixer
Add 0 g and add 250 g of calcium carbonate (light calcium carbonate manufactured by Takehara Chemical Industry Co., Ltd.) and mix for 2 minutes to prepare a 50 wt% slurry. Immediately after that, transfer the slurry to a beaker,
Viscosity (cps) is measured with a DVH-B type viscometer manufactured by Tokyo Keiki Co., Ltd. at a rotation speed of 50 rpm and a rotor No. 3 to 5. However, the addition concentration of the partially decomposed product of the invention is 0.3 with respect to the total amount of 500 g.
% By weight.

(カオリンスラリー) ・ナショナルM1型ミキサーに、この発明の部分分解物お
よび水道水を200g入れ、カオリン〔土屋カオリン工業
(株)製〕粉末を300gを加えて2分間混合し、60重量%
スラリーを調製する。その後直ちにスラリーをビーカー
に移し、東京計器製DVH−B型粘度計にて、回転数50rp
m,ローターNo.3〜5にて粘度を測定する。ただし、その
発明の部分分解物の添加濃度は、総量500gに対して0.3
重量%である。
(Kaolin slurry) -In a National M1 type mixer, 200 g of the partially decomposed product of the present invention and tap water are added, and 300 g of kaolin [manufactured by Tsuchiya Kaolin Industry Co., Ltd.] powder is added and mixed for 2 minutes to obtain 60% by weight.
Prepare a slurry. Immediately after that, the slurry was transferred to a beaker, and the rotation speed was 50 rp with a DVH-B viscometer manufactured by Tokyo Keiki.
Viscosity is measured with m, rotor No. 3-5. However, the addition concentration of the partially decomposed product of the invention is 0.3 with respect to the total amount of 500 g.
% By weight.

表面張力及び乳化持続時間の測定方法は以下のとおりで
ある。
The methods for measuring the surface tension and the duration of emulsification are as follows.

[表面張力の測定] 実施例で調製した発明品の表面張力を温度25℃で純水を
溶媒として用いてデュヌイの表面張力計によって測定し
た。
[Measurement of Surface Tension] The surface tension of the invention products prepared in the examples was measured at a temperature of 25 ° C. using pure water as a solvent with a surface tension meter manufactured by Dunui.

[乳化持続時間の測定] 実施例で調製した発明品の乳化持続時間を下記の試験方
法により測定した。
[Measurement of emulsification duration] The emulsification duration of the invention products prepared in the examples was measured by the following test method.

《試験方法》 ・ビーカーに試供薬剤および水道水を合計70g入れ、pH
を7.0に調整する。大豆油〔キシダ化学(株)製試薬〕3
0gを加え特殊幾化工業(株)製HV−M型ホモミキサーで
回転数8000rpmにて5分間混合する。混合後直ちに乳化
液を比色管に移し室温にて放置し、分離が始まるまでの
時間を乳化持続時間とする。乳化持続時間の測定は、放
置開始後1時間後までは10分毎に観察し、その後は1時
間毎に観察した。ただし、この発明の部分分解物の添加
濃度は、総量に対して1.0重量%である。
《Test method》 ・ Put a total of 70g of test chemicals and tap water in a beaker, and adjust the pH.
To 7.0. Soybean oil [Reagent manufactured by Kishida Chemical Co., Ltd.] 3
0 g was added, and the mixture was mixed for 5 minutes at a rotation speed of 8000 rpm with an HV-M type homomixer manufactured by Tokuyo Kogyo Co., Ltd. Immediately after mixing, the emulsified liquid is transferred to a colorimetric tube and left at room temperature, and the time until the start of separation is defined as the emulsification duration time. The measurement of the duration of emulsification was performed every 10 minutes until 1 hour after the start of standing and thereafter every 1 hour. However, the addition concentration of the partially decomposed product of the present invention is 1.0% by weight based on the total amount.

比較例1(小麦グルテンの調製) 実施例1〜10に用いた小麦グルテンを分解処理せずその
まま比較品No.1として用いた。
Comparative Example 1 (Preparation of Wheat Gluten) The wheat gluten used in Examples 1 to 10 was used as a comparative product No. 1 without being decomposed.

比較例2(小麦グルテンのアルカリによる部分分解物の
調製) 苛性ソーダ2gを溶解した水溶液100gに実施例1〜10で用
いた小麦グルテン20gを加えて100℃にて60分間加熱撹拌
後、塩酸で中和し、純水で総量200gとして比較品No.2を
得た。
Comparative Example 2 (Preparation of partially decomposed product of wheat gluten with alkali) 20 g of wheat gluten used in Examples 1 to 10 was added to 100 g of an aqueous solution in which 2 g of caustic soda was dissolved, and the mixture was heated with stirring at 100 ° C. for 60 minutes, and then with hydrochloric acid. Comparative product No. 2 was obtained by adding pure water to a total amount of 200 g.

平均分子量は47000であった。The average molecular weight was 47,000.

比較例3(小麦グルテンの酸による部分分解物の調製) 塩化水素換算で4gに相当する塩酸水溶液100gの入ったフ
ラスコに和光純薬工業(株)製の小麦グルテン(試薬
品)20gを加え、100℃、60分間加熱撹拌した。その後、
苛性ソーダで中和し純水で総量200gにして、比較品No.3
を得た。部分加水分解物の平均分子量は47000であっ
た。
Comparative Example 3 (Preparation of partially decomposed product of wheat gluten by acid) 20 g of wheat gluten (reagent product) manufactured by Wako Pure Chemical Industries, Ltd. was added to a flask containing 100 g of hydrochloric acid aqueous solution corresponding to 4 g in terms of hydrogen chloride, The mixture was heated and stirred at 100 ° C for 60 minutes. afterwards,
Comparative product No. 3 neutralized with caustic soda and made up to 200 g with pure water
Got The average molecular weight of the partial hydrolyzate was 47,000.

比較例4(小麦グルテンの酵素による部分分解の調製) 実施例1〜10で用いた小麦グルテン20gを0.1N−塩酸液1
50gが入ったフラスコに加え、pH1.5の水溶液を得た。こ
れに和光純薬工業(株)製試薬ペプシン(1:10,000)0.
2gを加え37℃で90分間反応させた。その後、苛性ソーダ
で中和し純水で総量200gにして比較品No.4を得た。部分
分解物の平均分子量は60000であった。
Comparative Example 4 (Preparation of partial enzymatic decomposition of wheat gluten) 20 g of wheat gluten used in Examples 1 to 10 was dissolved in 0.1N hydrochloric acid solution 1
It was added to a flask containing 50 g to obtain a pH 1.5 aqueous solution. Wako Pure Chemical Industries, Ltd. reagent pepsin (1: 10,000) 0.
2 g was added and reacted at 37 ° C. for 90 minutes. Then, it was neutralized with caustic soda and the total amount was 200 g with pure water to obtain a comparative product No. 4. The average molecular weight of the partially decomposed product was 60,000.

この発明の実施例の発明品No.1〜20、比較例の比較品N
o.1〜4、及び公知物質であるショ糖脂肪酸エステル
[第1工業製薬(株)製、商品名:DKエステルF−160
(HLB15)、比較品No.5]パルミチン酸モノグリセライ
ド[太陽化学(株)製、商品名:サンソフトNo.8001、
比較品No.6]について以下の試験例を実施した。
Inventive products No. 1 to 20 of the embodiment of the present invention, Comparative product N of the comparative example
o.1 to 4 and sucrose fatty acid ester which is a known substance [Daiichi Kogyo Seiyaku Co., Ltd., trade name: DK ester F-160
(HLB15), Comparative product No. 5] Palmitic acid monoglyceride [manufactured by Taiyo Kagaku Co., Ltd., trade name: Sunsoft No. 8001,
The following test example was carried out for the comparative product No. 6].

試験例1 (蒲鉾の品質改良効果) A.試験方法及び条件 下記に示す配合組成の混合物を擂潰し、蒲鉾用仕上りす
り身を製造する。このすり身をいくつかに分け、夫々別
個に試供品を添加して均一化した。得られた仕上りすり
身の硬さを測定後、塩化ビニリデン系チューブ(折径4.
5cm)に充填し、すわり処理(15℃、15hr)後、加熱(9
0℃、40分間)してチューブ詰蒲鉾を得た。
Test Example 1 (Kamaboko quality improving effect) A. Test method and conditions A mixture having the following composition is crushed to produce a finished fish paste for Kamaboko. This surimi was divided into several pieces, and the sample was added to each and homogenized. After measuring the hardness of the finished surimi obtained, vinylidene chloride tube (folding diameter 4.
5 cm), and after sitting (15 ℃, 15hr), heat (9
(0 ° C, 40 minutes) to obtain a tube-packed kamaboko.

得られた蒲鉾の破壊強度および破壊時の歪を測定した。
なお、すり身の硬さは成形性に関係し、得られた製品の
破壊強度および破壊歪は、その製品のテクスチャーを表
す。
The breaking strength and strain at the time of breaking of the obtained kamaboko were measured.
The hardness of the surimi is related to the formability, and the breaking strength and breaking strain of the obtained product represent the texture of the product.

〈配合組成〉 スケソウ冷凍すり身 2kg(100重量部) 食塩 44g(2.2 ) 砂糖 18g(0.9 〃 ) グルタミン酸ナトリウム 10g(0.5 〃 ) みりん 10g(0.5 〃 ) ばれいしょ澱粉 140g(7 〃 ) 〈すり身の硬さ〉 仕上りすり身を直径6cm、高さ5cmのガラス容器に詰めて
試料とし、不動工業製レオメーター(NRM−2010J・D−
CW)を使用して5mm圧縮したときの応力を「すり身の硬
さ」とした。
<Combined composition> Alaska pollack frozen surimi 2 kg (100 parts by weight) Salt 44 g (2.2) Sugar 18 g (0.9 〃) Sodium glutamate 10 g (0.5 〃) Mirin 10 g (0.5 〃) Potato starch 140 g (7 〃) <Surry hardness> The finished surimi was packed in a glass container with a diameter of 6 cm and a height of 5 cm to prepare a sample, which was made by Fudo Kogyo Rheometer (NRM-2010J ・ D-
CW) was used and the stress when compressed by 5 mm was defined as "hardness of surimi".

〈破壊強度、破壊時の歪〉 得られた蒲鉾を3cmの高さに切断して試料とし、同じレ
オメーターを用いて試料を圧縮し、破壊時の強度(破壊
時の応力(g)と破壊時の歪(mm)を測定する。
<Fracture strength, strain at fracture> The obtained kamaboko is cut into a sample with a height of 3 cm, and the sample is compressed using the same rheometer to obtain the strength at fracture (stress at fracture (g) and fracture). Measure the strain at time (mm).

B.結果 この結果を表5に示す。B. Results The results are shown in Table 5.

表5の結果に示されるように、この発明の蛋白質食品の
品質改良剤によれば、蒲鉾の形状保持性や硬さを著しく
向上することができる。
As shown in the results of Table 5, the quality improving agent for protein food of the present invention can remarkably improve the shape-retaining property and hardness of the kamaboko.

試験例2 発明品No.2と、比較品No.5又はNo.6で用いたショ糖脂肪
酸エステル又はパルミチン酸モノグリセリドを併用添加
して、試験例1と同様な試験を行った。
Test Example 2 Inventive product No. 2 and the sucrose fatty acid ester or palmitic acid monoglyceride used in Comparative product No. 5 or No. 6 were added together, and the same test as in Test Example 1 was conducted.

この結果を表6に示す。The results are shown in Table 6.

このように、ショ糖脂肪酸エステルやパルミチン酸グリ
セリド等を併用することにより、相乗的に優れた蛋白質
食品の品質改良効果が得られることが判る。
Thus, it is understood that the combined use of sucrose fatty acid ester, palmitic acid glyceride and the like can synergistically improve the quality of protein foods.

試験例3 スケソウ冷凍すり身2kgのうち、300gを小麦グルテンに
代替する以外、試験例1と同様にして発明品No.2,No.6
及びNo.14についての品質改良効果を評価した。
Test Example 3 Inventive products No. 2 and No. 6 were the same as Test Example 1 except that wheat gluten was substituted for 300 g of 2 kg of Alaska pollack frozen surimi.
And the quality improvement effect of No. 14 was evaluated.

この結果を表7に示す。The results are shown in Table 7.

試験例4 (ハンバーグの品質改良効果) 下記に示す小麦グルテン入りハンバーグ原料に供試品を
加えてハンバーグを製造した。その結果を表8に示す。
Test Example 4 (Hamburger quality improving effect) A hamburger was manufactured by adding a test sample to the hamburger raw material containing wheat gluten shown below. The results are shown in Table 8.

なお食感及び風味の評価は小麦グルテンが入っていない
原料から製造したハンバーグを標準品として用い、それ
と比較した結果である(10人のパネラーによって行い、
その結果を総合的にまとめたものである)。
The texture and flavor of the evaluation is the result of comparison with that using a hamburger made from a raw material that does not contain wheat gluten as a standard product (10 panelists,
It is a comprehensive summary of the results).

このように、この発明の品質改良剤によれば、食感、風
味等の品質を向上させることが判る。
Thus, it can be seen that the quality improving agent of the present invention improves quality such as texture and flavor.

試験例5 (大豆蛋白素材の品質改良効果) 粉末状分離大豆タンパク・フジプロR(不二製油(株)
製)に水を加えて溶解し、8%の水溶液とする。これに
供試品を所定濃度添加し撹拌混合後、噴霧乾燥して粉末
品を得た。
Test Example 5 (Quality improvement effect of soybean protein material) Powdered soybean protein / Fujipro R (Fuji Oil Co., Ltd.)
(Manufactured by Mitsui Chemical Co., Ltd.) and water to dissolve it into an 8% aqueous solution. A test product was added thereto at a predetermined concentration, mixed with stirring, and then spray-dried to obtain a powder product.

得られた粉末を密封して、25℃の恒温室で放置し溶解性
(NSI:Nitorogen Solubility Index)の経日変化を測定
した。
The obtained powder was sealed and left standing in a thermostatic chamber at 25 ° C., and the change with time of solubility (NSI: Nitorogen Solubility Index) was measured.

この結果を表9に示す。The results are shown in Table 9.

このように、この発明の品質改良剤は、大豆蛋白素材の
経時的溶解性を抑制し、より安定に保ち、例えば焼きち
ぢみを抑制するよう作用することも判明した。
As described above, it was also found that the quality improving agent of the present invention suppresses the temporal solubility of the soybean protein material, keeps it more stable, and acts, for example, to suppress baking.

また、ショ糖脂肪酸エステル(比較品No.5)又はパルミ
チン酸モノグリセリド(比較品No.6)と併用した際の結
果を表10に示した。このように併用により上記安定化効
果もより向上することが判る。
Table 10 shows the results when used in combination with sucrose fatty acid ester (Comparative Product No. 5) or palmitic acid monoglyceride (Comparative Product No. 6). Thus, it can be seen that the stabilizing effect is further improved by the combined use.

なお、上記大豆蛋白素材は、小麦蛋白と共に、ミートボ
ール・ハンバーグ等の肉ねり製品の増量剤としても用い
られており、それら蛋白素材を添加すると食感がソフト
化する事も言われている。しかし、この素材を肉ねり製
品に添加する場合、均一化が非常に困難であり、大きな
問題となっている。
The soybean protein material is also used as a bulking agent for meat-battered products such as meatballs and hamburgers together with wheat protein, and it is said that addition of these protein materials softens the texture. However, when this material is added to meat-battered products, it is very difficult to make it uniform, which is a big problem.

上記表9及び表10において、発明品No.2及びNo.12並び
に発明品No.2と比較品No.5との併用により、調製した粉
末品は、ハンバーグの増量剤として添加混合し易く、ま
た均一化が容易である事が確認された。このように発明
品は大豆タンパク素材の品質改良剤として非常に有用で
ある事がわかる。
In Tables 9 and 10 above, the invention products No. 2 and No. 12, and the invention product No. 2 and the comparative product No. 5 were used in combination, so that the prepared powder product was easy to add and mix as a hamburger bulking agent. It was also confirmed that homogenization was easy. Thus, it can be seen that the invention product is very useful as a quality improving agent for soybean protein materials.

試験例6 (豆腐の品質改良効果) 原料大豆100gを水洗し、約10℃の水に15時間浸漬し約25
0gとする。これに250gの水を更に加えながら摩砕してな
ま「ご」とし、供試品を加えて加熱沸騰する。加熱開始
後5分後の泡の高さを測定し、10分間煮沸する。その後
加水量を10倍(計1000g)に調製する。この煮沸「ご」
を搾汁して豆乳とオカラに分け、豆乳の温度が75℃にな
ったら、硫酸カルシウム3gを懸濁させた30mlの湯(40
℃)を加えて凝固させる。そのまま10分間放置し、凝固
させて豆腐を製造した。
Test Example 6 (tofu quality improving effect) 100 g of raw material soybean was washed with water and immersed in water at about 10 ° C for 15 hours to about 25
Set to 0g. 250 g of water is further added to this to grind it into sesame “go”, the test sample is added and the mixture is heated to boiling. 5 minutes after the start of heating, measure the height of the foam and boil for 10 minutes. After that, adjust the amount of water 10 times (total 1000 g). This boiling "go"
Is squeezed and divided into soy milk and okara, and when the temperature of soy milk reaches 75 ℃, 30 ml of hot water (40
℃) to solidify. It was left as it was for 10 minutes and coagulated to produce tofu.

煮沸時の泡の高さおよび得られた豆腐の重量、品質(弾
力,固形分)を表11に示す。
Table 11 shows the height of foam during boiling, the weight and quality (elasticity, solid content) of the obtained tofu.

このように、この発明の品質改良剤によれば、豆腐の弾
力や重力を向上させると共に、製造時において不都合な
泡の発生を抑制するよう作用することが判る。そしてこ
れらの効果はパルミチン酸モノグリセリドとの併用によ
りさらに相乗的に向上することが判る。
As described above, it is understood that the quality improving agent of the present invention acts to improve the elasticity and gravity of tofu and suppress the generation of inconvenient bubbles during production. It is also found that these effects are further synergistically improved by the combined use of palmitic acid monoglyceride.

試験例7(ソーセージの品質改良効果) 〈処方〉 豚肉 50.0部 豚脂 25.0〃 水(氷) 20.0〃 ゼラチン*1 0.5〃 食塩 1.7〃 ピロリン酸ナトリウム 0.16〃 亜硝酸ナトリウム 0.04〃 香辛料 0.3〃 検体 0.5〃 *1:ゼラチン:湘南ゼラチン(株)製 「コラーゲンパウダーGP」 〈調製方法〉 ○上記処方のものを、サイレントカッターにて混合後、
直径10mmの半腸ケーシングに詰め、82℃にて15分間加熱
し、ウインナソーセージを調製した。
Test Example 7 (Sausage quality improving effect) <Prescription> Pork 50.0 parts Pig fat 25.0〃 Water (ice) 20.0〃 Gelatin * 1 0.5〃 Salt 1.7〃 Sodium pyrophosphate 0.16〃 Sodium nitrite 0.04〃 Spice 0.3〃 Sample 0.5〃 * 1: Gelatin: "Collagen powder GP" manufactured by Shonan Gelatin Co., Ltd. <Preparation method> ○ After mixing the above formulations with a silent cutter,
It was packed in a semi-intestinal casing having a diameter of 10 mm and heated at 82 ° C. for 15 minutes to prepare a wiener sausage.

〈評価方法〉 加熱前後の重量差により、次式に依り歩留りを算出
した。
<Evaluation method> The yield was calculated according to the following formula from the weight difference before and after heating.

10人のパネラーにより、食感の評価を実施した。 The texture was evaluated by 10 panelists.

それらの結果を表12に示す。The results are shown in Table 12.

(へ)発明の効果 この発明の蛋白食品に含有される穀物蛋白質の部分分解
物は、品質改良剤として、各種蛋白質食品の優れた品質
改良効果、例えば、形状保持性、テクスチャー、安定
性、弾力、食感等の向上効果を奏するものである。そし
て、有効成分である穀物蛋白質の部分分解物は食品又は
食品に類するものゆえ、毒性がない点で極めて有利であ
り、食品添加用として安全性も向上され、しかも安価で
ある。
(H) Effect of the invention The partially decomposed product of grain protein contained in the protein food of the present invention, as a quality improving agent, has an excellent quality improving effect on various protein foods, such as shape retention, texture, stability and elasticity. The effect of improving texture and the like is achieved. Since the partially decomposed product of grain protein as an active ingredient is a food or a food-like product, it is extremely advantageous in that it is not toxic, has improved safety as a food additive, and is inexpensive.

従って、この発明の蛋白食品に含有される穀物蛋白質の
部分分解物は、蛋白質食品用添加剤として極めて有用な
ものであり、優れた形状保持性、テクスチャー、安定
性、弾力、食感等を有する各種蛋白質食品を得ることが
できる。
Therefore, the partially decomposed product of grain protein contained in the protein food of the present invention is extremely useful as an additive for protein food, and has excellent shape retention, texture, stability, elasticity, texture and the like. Various protein foods can be obtained.

【図面の簡単な説明】[Brief description of drawings]

第1図(イ)〜(ニ)は、この発明に用いる部分加水分
解物についてのpH中和曲線を例示するグラフ図である。
FIGS. 1 (A) to 1 (D) are graphs illustrating the pH neutralization curve for the partial hydrolyzate used in the present invention.

フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 A23L 1/325 101 D // C08L 89/00 LSE C12P 21/06 9282−4B (56)参考文献 特開 昭56−25093(JP,A) 特開 昭64−14274(JP,A)Continuation of the front page (51) Int.Cl. 6 Identification number Office reference number FI technical display location A23L 1/325 101 D // C08L 89/00 LSE C12P 21/06 9282-4B (56) References 56-25093 (JP, A) JP 64-14274 (JP, A)

Claims (10)

【特許請求の範囲】[Claims] 【請求項1】穀物蛋白質の部分分解物であって、以下の
物性、 (a)重量平均分子量(ゲル濾過法による)が500〜900
00の範囲にある、 (b)紫外吸収λmaxが、260〜280nm付近で、かつ赤外
吸収が1400、1630及び3400cm-1付近である、 (c)等電点が、3.9〜5.0の範囲にある、 (d)pH緩衝性(本品の5重量%水溶液100mlのpHを6
から2まで低下させるのに1N−塩酸を2〜25ml必要とす
る)を有する、 (e)水に可溶であり、メタノール、エタノール、アセ
トン、エーテルに不溶である、 (f)外観は淡黄色ないし赤茶色の粉末である、 (g)キサントプロテイン反応、ニンヒドリン反応によ
って呈色する、 (h)強い表面張力低下能(本品を25℃の純水に0.1重
量%添加することによって純水の表面張力を50dyne/cm
以下(デュヌイの表面張力計で計測)に低下させる)を
有する、 (i)強い乳化能(本品1gの添加使用により少なくと
も、大豆油を30重量%含有する水−大豆油混合物100gを
完全乳化(均一な乳化状態を少なくとも10分、好ましく
は1時間以上維持することを意味する)しうる)を有す
る、 で特徴づけられる物質を蛋白質食品素材に対して0.05〜
10重量%含有することを特徴とする蛋白質食品。
1. A partially degraded product of grain protein, which has the following physical properties: (a) a weight average molecular weight (by gel filtration method) of 500 to 900.
In the range of 00, (b) the ultraviolet absorption λmax is around 260 to 280 nm and the infrared absorption is around 1400, 1630 and 3400 cm -1 , (c) the isoelectric point is in the range of 3.9 to 5.0 Yes, (d) pH buffering property (the pH of 100 ml of a 5 wt% aqueous solution of this product is 6%
2 to 25 ml of 1N-hydrochloric acid is required to reduce from 2 to 2), (e) Soluble in water, insoluble in methanol, ethanol, acetone, ether, (f) Appearance is pale yellow To reddish brown powder, (g) Color develops by xanthoprotein reaction, ninhydrin reaction, (h) Strong surface tension lowering ability (pure water by adding 0.1 wt% of this product to pure water at 25 ° C) Surface tension of 50dyne / cm
It has the following (measured by Dunui's surface tensiometer): (i) Strong emulsification capacity (100 g of a water-soybean oil mixture containing at least 30% by weight of soybean oil is completely emulsified by adding 1 g of this product). (Meaning that a uniform emulsified state is maintained for at least 10 minutes, preferably for 1 hour or more)), the substance characterized by
A protein food characterized by containing 10% by weight.
【請求項2】部分分解物が、穀物蛋白質を(A)アルカ
リによる加水分解処理と、(B)酸、酵素、酸化剤又は
還元剤を用いた分解処理の1種又は2種以上との組み合
わせによる多段部分分解処理に付して得られた物質であ
る請求項1に記載の蛋白質食品。
2. A partially decomposed product, which is a combination of (A) an alkali hydrolysis treatment of grain protein and (B) one or more decomposition treatments using an acid, an enzyme, an oxidizing agent or a reducing agent. The protein food according to claim 1, which is a substance obtained by subjecting to a multistage partial decomposition treatment with.
【請求項3】部分分解物が、アルカリによる加水分解処
理と、酸による加水分解処理との組み合わせによる二段
部分分解処理により得られたものである請求項2に記載
の蛋白質食品。
3. The protein food according to claim 2, wherein the partially decomposed product is obtained by a two-step partial decomposition treatment by a combination of a hydrolysis treatment with an alkali and a hydrolysis treatment with an acid.
【請求項4】穀物が、小麦グルテン、とうもろこしグル
テン又は大豆蛋白である請求項1〜3のいずれかに記載
の蛋白質食品。
4. The protein food according to claim 1, wherein the grain is wheat gluten, corn gluten or soybean protein.
【請求項5】蛋白質食品が動物性蛋白質食品又は植物性
蛋白質食品である請求項1〜4のいずれかに記載の蛋白
質食品。
5. The protein food according to claim 1, which is an animal protein food or a vegetable protein food.
【請求項6】蛋白質食品が蒲鉾、竹輪、ハム、ソーセー
ジ、ハンバーグ又は大豆蛋白である請求項1〜4のいず
れかに記載の蛋白質食品。
6. The protein food according to claim 1, wherein the protein food is kamaboko, bamboo shoot, ham, sausage, hamburger or soybean protein.
【請求項7】多価アルコール脂肪酸エステル型界面活性
剤がさらに併用されてなる請求項1の蛋白質食品。
7. The protein food according to claim 1, which further comprises a polyhydric alcohol fatty acid ester type surfactant.
【請求項8】蛋白質部分分解物と多価アルコール脂肪酸
エステル型界面活性剤が重量比1:6〜6:1で配合されてな
る請求項7の蛋白質食品。
8. The protein food according to claim 7, wherein the partially decomposed protein and the polyhydric alcohol fatty acid ester type surfactant are mixed in a weight ratio of 1: 6 to 6: 1.
【請求項9】多価アルコール脂肪酸エステル型界面活性
剤が、ショ糖脂肪酸エステル及び/又はグリセリン脂肪
酸エステルである請求項8の蛋白質食品。
9. The protein food according to claim 8, wherein the polyhydric alcohol fatty acid ester type surfactant is sucrose fatty acid ester and / or glycerin fatty acid ester.
【請求項10】蛋白質食品素材に対して、0.01〜10重量
%添加して用いられる請求項1又は7記載の蛋白質食
品。
10. The protein food according to claim 1 or 7, which is used by adding 0.01 to 10% by weight to the protein food material.
JP63110905A 1987-07-06 1988-05-06 Protein food Expired - Lifetime JPH072095B2 (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
JP63110905A JPH072095B2 (en) 1988-05-06 1988-05-06 Protein food
ES198888110706T ES2032902T3 (en) 1987-07-06 1988-07-05 A PRODUCT OF PARTIAL DEGRADATION OF PROTEINS, PROCEDURE TO PREPARE IT AND ITS USE.
EP88110706A EP0298419B1 (en) 1987-07-06 1988-07-05 A protein partial degradation product, process for preparing it and its use
DE8888110706T DE3871260D1 (en) 1987-07-06 1988-07-05 PARTIAL DEGRADATION PRODUCT OF PROTEINS, METHOD FOR THE PRODUCTION THEREOF AND ITS USE.
KR88008457A KR960010398B1 (en) 1987-07-06 1988-07-06 A protein partial degradation product, process for preparing it and its use
US07/593,289 US5138038A (en) 1987-07-06 1990-10-04 Protein partial degradation product, process for preparing it and its use
US07/869,793 US5273773A (en) 1987-07-06 1992-04-16 Protein partial degradation products

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63110905A JPH072095B2 (en) 1988-05-06 1988-05-06 Protein food

Publications (2)

Publication Number Publication Date
JPH01281068A JPH01281068A (en) 1989-11-13
JPH072095B2 true JPH072095B2 (en) 1995-01-18

Family

ID=14547634

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63110905A Expired - Lifetime JPH072095B2 (en) 1987-07-06 1988-05-06 Protein food

Country Status (1)

Country Link
JP (1) JPH072095B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03133361A (en) * 1989-10-19 1991-06-06 Fuji Oil Co Ltd Processed edible meat product
JP2007267652A (en) * 2006-03-31 2007-10-18 Katayama Chem Works Co Ltd Quality improving agent for meat processed food, and method for improving quality of meat processed food

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5625093A (en) * 1979-08-02 1981-03-10 Toshiba Corp Transporting method of package plant
JPH0691793B2 (en) * 1987-07-06 1994-11-16 株式会社片山化学工業研究所 Partially decomposed protein, its production method and use

Also Published As

Publication number Publication date
JPH01281068A (en) 1989-11-13

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