JPH01202235A - Quality improving agent for starchy food - Google Patents

Quality improving agent for starchy food

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Publication number
JPH01202235A
JPH01202235A JP63026239A JP2623988A JPH01202235A JP H01202235 A JPH01202235 A JP H01202235A JP 63026239 A JP63026239 A JP 63026239A JP 2623988 A JP2623988 A JP 2623988A JP H01202235 A JPH01202235 A JP H01202235A
Authority
JP
Japan
Prior art keywords
product
quality improving
improving agent
partial decomposition
protein
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.)
Granted
Application number
JP63026239A
Other languages
Japanese (ja)
Other versions
JPH0746958B2 (en
Inventor
Atsushi Tsuda
津田 厚
Kenji Hanno
賢治 半埜
Sakae Katayama
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 Chemical Inc
Original Assignee
Katayama Chemical Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Katayama Chemical Inc filed Critical Katayama Chemical Inc
Priority to JP63026239A priority Critical patent/JPH0746958B2/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 JPH01202235A publication Critical patent/JPH01202235A/en
Priority to US07/593,289 priority patent/US5138038A/en
Priority to US07/869,793 priority patent/US5273773A/en
Publication of JPH0746958B2 publication Critical patent/JPH0746958B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Bakery Products And Manufacturing Methods Therefor (AREA)
  • General Preparation And Processing Of Foods (AREA)
  • Noodles (AREA)
  • Peptides Or Proteins (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:To obtain a quality improving agent for starchy foods having excellent quality improving effect, in safety and low cost, by using a partial decomposition product of a protein obtained by multi-stage partial decompositions containing alkali hydrolysis of a grain protein as an active ingredient. CONSTITUTION:A grain protein such as wheat gluten, corn gluten or soybean protein is subjected to multi-stage partial decompositions comprising a combination of hydrolysis by an alkali and one or more of decomposition treatments by an acid, an enzyme, an oxidizing agent and a reducing agent to give a partial decomposition product of protein. Solely said partial decomposition product or a mixture of said product with a surfactant of multihydric alcohol fatty ester type in a weight ratio 1:6-6:1 is used as a quality improve agent and added to starchy food materials such as breads and noodles in a ratio of 0.01-5wt.%.

Description

【発明の詳細な説明】 (イ)産業上の利用分野 この発明は、でんぷん質食品の品質改良剤に関する。さ
らに詳しくは、小麦グルテン、トウモロコノグルテン、
大豆蛋白などの穀物蛋白質の部分分解物からなり各種て
んぶん質食品素材に添加して用いる品質改良剤に関する
DETAILED DESCRIPTION OF THE INVENTION (a) Field of Industrial Application This invention relates to a quality improving agent for starchy foods. For more information, see wheat gluten, corn gluten,
This invention relates to a quality improver that is made of a partially decomposed product of grain proteins such as soybean protein and is used when added to various proteinaceous food materials.

(ロ)従来の技術 パン類やめん類は、でんぷんを主素材とするいわゆるて
んぶん質食品の代表的なものである。かかるでんぷん質
食品には各種の品質改良剤が添加されている。そしてそ
の代表例としてグリセリン脂肪酸エステル、プロピレン
グリコール脂肪酸エステル、ショ糖脂肪酸エステル等の
いわゆる多価アルコ・−ル脂肪酸エステル型界面活性剤
が汎用されており、さらにこれらの脂肪酸エステル型界
面活性剤にアスコルビン酸やグルコノラクトン類を併用
したり(特公昭56−42887号公報、特開昭55−
11333=1号及び55−118335号公報)、上
記グリセリン脂肪酸エステルを特定の処理に付して用い
る提案(特公昭59−41379号公報)がなされてい
る。
(b) Conventional technology Breads and noodles are typical so-called starchy foods whose main ingredient is starch. Various quality improving agents are added to such starchy foods. As typical examples, so-called polyhydric alcohol fatty acid ester type surfactants such as glycerin fatty acid ester, propylene glycol fatty acid ester, and sucrose fatty acid ester are widely used. Acids and gluconolactones are used in combination (Japanese Patent Publication No. 42887/1983, Japanese Patent Application Laid-Open No. 1983-1988)
11333=1 and No. 55-118335), and the use of the glycerin fatty acid ester after subjecting it to a specific treatment (Japanese Patent Publication No. 59-41379) has been proposed.

また1、最近、小麦グルテンをペプシンを固定化したバ
イオリアクターで処理することにより得ら ゛れるグル
テン部分加水分解物が、スポンジケーキ等の製菓、製パ
ン時の品質改良に応用できることも発表されている(化
学工業時報;昭和62年6月25日)。
1. It has recently been announced that gluten partial hydrolyzate obtained by treating wheat gluten in a bioreactor with immobilized pepsin can be applied to improve the quality of confectionery such as sponge cakes and bread. (Chemical Industry Times; June 25, 1986).

(ハ)発明が解決しようとする課題 しかしながら、多価アルコール脂肪酸エステル型界面活
性剤は食品添加物として認められているものの、それ自
体化学合成品であるため、毒性の点で不安が残るもので
ある。さらにこれらの界面活性剤はコスト及び品質改良
効果の点で、必ずしも満足できるものではなかった。
(c) Problems to be solved by the invention However, although polyhydric alcohol fatty acid ester type surfactants are recognized as food additives, they are themselves chemically synthesized products, so there are concerns about their toxicity. be. Furthermore, these surfactants have not always been satisfactory in terms of cost and quality improvement effects.

一方上記酵素分解により得られる小麦グルテン部分分解
物は、安全性が高いものであるが、コスト及び効果の点
で充分な期待は持てない。
On the other hand, the partial decomposition product of wheat gluten obtained by the enzymatic decomposition described above is highly safe, but does not have sufficient expectations in terms of cost and effectiveness.

この発明は、かかる状況に鑑みてなされたものであり、
ことに前記のごとく汎用されている多価アルコール脂肪
酸エステル型界面活性剤に代替できる安全かつ安価な添
加剤であって、しかし品質改良効果が浸れた新しいでん
ぷん質素品用品質改良剤を提供しようとするものである
This invention was made in view of this situation,
In particular, we would like to provide a new quality improver for starch raw materials that is a safe and inexpensive additive that can replace the widely used polyhydric alcohol fatty acid ester type surfactant as mentioned above, but also has a quality improvement effect. It is something to do.

(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、前記した小麦グルテン部
分分解物のごとき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解処理によって得
られる特定の蛋白質部分分解物が、(1)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、(11)単なるアルカリ分解物、酵素分解物、
酸化分解物等に比して優れたでんぷん質食品の品質改良
効果を奏する事実を見出した。
(d) Means for Solving the Problems From the above perspective, the present inventors have conducted various studies and examinations on partial decomposition methods for grain protein partial decomposition products such as the above-mentioned wheat gluten partial decomposition products, and have found that alkaline decomposition A specific protein partial decomposition product obtained by a sequential multi-stage decomposition treatment that requires treatment and is combined with a decomposition treatment using an acid, an enzyme, an oxidizing agent, or a reducing agent is (1) What is a normal protein partial decomposition product? In addition to being a new substance with completely different properties, (11) simple alkaline decomposition products, enzymatic decomposition products,
We have discovered the fact that this product has a superior quality improvement effect on starchy foods compared to oxidized decomposition products.

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1 、(a)重量平均分子量(ゲル濾過法による)か500
〜90000の転回にある、 (b)紫外吸収λmaXが、260〜28Onm付近で
、かつ赤外吸収が1400.1630及び3400cm
−’付近である、(c)等電点が、3.9〜5.0の範
囲にある、(d) p H緩衝性(本品の5重量%水溶
液10h+(jのpHを6から2まで低下させるのにI
N〜塩酸を2〜25MQ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
+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01
重量%添加することによって、純水の表面張力を50d
yne/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。
Thus, according to the present invention, a partially decomposed product of grain protein has the following physical properties: (a) a weight average molecular weight (by gel filtration method) of 500;
~90000 turn, (b) UV absorption λmaX is around 260 to 28 Onm, and infrared absorption is 1400.1630 and 3400 cm
-', (c) Isoelectric point is in the range of 3.9 to 5.0, (d) pH buffering property (5% by weight aqueous solution of this product 10h + (j pH from 6 to 2 I to lower it to
(e) Soluble in water and insoluble in methanol, ethanol, acetone, and ether (f) Powder with pale yellow to reddish brown appearance (g)
Color develops due to xanthoprotein reaction and ninhydrin reaction. (h) Strong surface tension lowering ability (drink this product in pure water at 25°C).
By adding % by weight, the surface tension of pure water can be increased to 50d.
yne/cm (measured with a Dunui surface tension meter).

(i)強い乳化能(本品19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10
09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、 で特性づけられる物質からなるでんぷん質食品の品質改
良剤が提供される。
(i) Strong emulsifying ability (by using this product 19, water-soybean oil mixture 10 containing at least 30% by weight of soybean oil)
Completely emulsify 09 (keep it uniformly emulsified for at least 10 minutes,
There is provided an agent for improving the quality of starchy foods comprising a substance characterized by: (meaning that it can be maintained preferably for more than 1 hour).

上記で特定される蛋白質部分分解物:よ、それ自体本顆
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)及び乳化能(i)の点で従来の穀物蛋
白質部分分解物とは区別されろものである。
The protein partial decomposition product specified above is itself a new substance that had not been described in any literature prior to the filing of this application, and is particularly superior to conventional grain proteins in terms of the above-mentioned surface tension lowering ability (h) and emulsifying ability (i). It should be distinguished from partially decomposed products.

この発明の品質改良剤ばてんふん質食品の素材に添加し
て用いられ、必要量の添加により各種の品質改良効果を
発揮する乙のである。例えば、でん7S;んの変性によ
るパン類やめん類の硬化を防止又は抑制するいわゆる老
化防止効果、乾燥によって生じうるパン類やめん類の硬
化を防止又は遅延する保水性向上効果、製パンや製めん
時の生地のきめの細かさや粘りを適度に調整しさらに製
パン時においてはイースト醗酵による生地膨張を増進さ
け、かつ、「スダチ」がより細かくて均一なパンを提供
できる生地調整効果等の品質改良効果を得ることができ
る。そして、これらの品質改良効果;よ、いずれらアル
カリ分解、酵素分解、還元分解、酸化分解等によるもの
に比して向上されfこらのである。
The quality improving agent of this invention is used by being added to the raw materials of bulk foods, and when added in the required amount, it exhibits various quality improving effects. For example, the so-called anti-aging effect that prevents or suppresses the hardening of breads and noodles due to the denaturation of Denn 7S; The fineness and stickiness of the dough during noodle making can be adjusted to an appropriate level, and during bread making, dough expansion due to yeast fermentation can be prevented, and ``Sudachi'' can provide finer and more uniform bread. Quality improvement effects can be obtained. These quality improvement effects are much better than those achieved by alkaline decomposition, enzymatic decomposition, reductive decomposition, oxidative decomposition, etc.

この発明の対象となるでんぷん質食品としては、パン類
、めん類が代表的であるが、これ以外に例えば、クツキ
ー、スポンジケーキ等のでんぷん質を主たる素材とする
食品や食品原料が種々挙げられる。
Typical starchy foods that are the subject of this invention are breads and noodles, but other than these, there are also various other foods and food ingredients whose main ingredient is starch, such as kutsky and sponge cake.

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
グルテンと称仕られろ。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r二まりとなって残る。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かできる。
In this invention, grain protein refers to protein contained in grains, and examples of grains include barley (e.g., wheat),
Examples include corn and beans (eg, soybeans). Among the proteins contained in such grains, wheat protein, for example, contains glutenin and gliadin as main components,
Commonly referred to as wheat gluten. Corn protein contains zein as a main component and is usually referred to as corn gluten. These are all known substances and can be obtained by separating or extracting them from grains using conventional methods. For example, to obtain wheat protein (wheat gluten), if you add a small amount of water to wheat flour and knead it until hard, then knead it in a large amount of water, the starch will be suspended in the water and the gluten content will become a sticky lump. It remains. If this operation is repeated several times by changing the water, a grey-brown, viscous lump can be obtained. For the preparation of the partially decomposed product of this invention, such lumps can be used as they are, but their dried products may also be used, and further purified products, partially modified products, etc. may also be used. . For example, wheat gluten
Dried products are commercially available and can be easily obtained.

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。
Other 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。
The protein may be either a crude product or a purified product, but it is preferable to use one containing 70% or more 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 products of the present invention are obtained by subjecting grain proteins to a multistage decomposition treatment that combines hydrolysis treatment with an alkali and decomposition treatment using an acid, an enzyme, an oxidizing agent, or a reducing agent. That is, it can be obtained by combining alkaline decomposition treatment and other decomposition treatment.

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60〜1
80℃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0.1〜69とするのが好ましい。
The hydrolysis treatment with an alkali is suitably carried out by heating in a dilute aqueous alkali solution. Usually, an aqueous solution or aqueous dispersion of the substance to be hydrolyzed is prepared in the presence of an alkaline agent such as sodium hydroxide, potassium hydroxide, calcium hydroxide, sodium carbonate, potassium carbonate, etc.
It is suitable to carry out stirring at 80° C. for about 10 to 600 minutes. °The aqueous solution or aqueous dispersion of the substance to be hydrolyzed is preferably 2 to 40% by weight, and the amount of alkaline agent used is 0.1 to 69% by weight per 20 g of the substance to be hydrolyzed. It is preferable to do so.

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。
On the other hand, among the other decomposition treatments that can be combined with the hydrolysis treatment using an alkali, the decomposition treatment using an acid is preferably carried out by heating in a dilute aqueous acid solution.

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℃
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。
Usually, an aqueous solution or aqueous dispersion of the substance to be decomposed is heated to about 60 to 120°C in the presence of an inorganic acid such as hydrochloric acid or sulfuric acid or an organic acid such as acetic acid.
It is suitable to carry out stirring for about 10 to 600 minutes. The quantitative conditions here are preferably the same as those for the alkaline hydrolysis described above.

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。
Similarly, enzymatic decomposition treatment is suitably carried out in a dilute aqueous solution of an enzyme with protease activity, and usually a small amount of an enzyme such as pepsin, alkaline protease, or papain is present in the aqueous solution or aqueous dispersion of the substance to be decomposed. Under the optimal pH condition for this enzyme, at about 10 to 60°C, about 60°C
Runs for ~600 minutes.

ここで量的条件は分解対象物209に対し酵素使用量を
0.02〜59とする以外上記と同様とするのが好まし
い。
Here, the quantitative conditions are preferably the same as above except that the amount of enzyme used is 0.02 to 59% of the target substance 209 to be decomposed.

同じく還元剤は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、lO〜600分行われる
。この際の量的条件は、分解対象物209に対する還元
剤又は酸化剤の使用量を0,1〜59とする以外上記と
同様とするのが好ましい。
Similarly, decomposition treatment using a reducing agent or an oxidizing agent is suitably carried out in a dilute aqueous solution of the reducing agent or oxidizing agent, and usually sulfites, thiol compounds, and erythorbine are added to the aqueous solution or aqueous dispersion of the target substance. The reaction is carried out at about 10 to 100° C. for 10 to 600 minutes in the presence of a small amount of a reducing agent such as an acid or hydrazine or an oxidizing agent such as hydrogen peroxide or hypochlorite. The quantitative conditions at this time are preferably the same as those described above except that the amount of reducing agent or oxidizing agent used with respect to the object to be decomposed 209 is 0.1 to 59.

上記多段分解処理の順序はとくに限定されない。The order of the multi-stage decomposition processing is not particularly limited.

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)に付し、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。
That is, after first subjecting raw materials such as wheat gluten to alkaline hydrolysis treatment (A), any of the above-mentioned decomposition treatment using acids, enzymes, reducing agents, and oxidizing agents (B) (decomposition treatment other than alkali) Alternatively, the decomposition treatment may be performed in the reverse order. Alternatively, it can be obtained by first subjecting it to a non-alkali decomposition treatment (B), then subjecting it to an alkali hydrolysis treatment (A), and then again subjecting it to a non-alkali decomposition treatment (B).

また、これらの各処理間では、適宜、中和処理かなされ
てもよい。
In addition, neutralization treatment may be performed as appropriate 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500〜60000の範囲で認められる。
In this invention, more excellent quality improvement effects are observed when the weight average molecular weight is in the range of 500 to 60,000.

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。
These molecular weights can be appropriately controlled by adjusting the conditions of the above-mentioned partial decomposition treatment.

なお、これらの分子量は、標準物質として1600゜6
500、16000.6500G、 88,000の分
子量を有するボ°  リスチレンスルホン酸ソーダを用
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。
In addition, these molecular weights are 1600°6 as a standard substance.
Using sodium polystyrene sulfonate having a molecular weight of 500, 16000, 6500G, and 88,000, Sephadex G-75 or G manufactured by Pharmacia was used.
This is a value measured by a gel filtration method using -100 as a carrier.

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でんぷん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 protein partial decomposition product thus obtained can be used as a quality improver for starchy foods in the form of an aqueous solution after decomposition, but it can also be used as a powder after drying. In addition, purified products obtained by desalination treatment or decolorization treatment, such as ultrafiltration, can also be used satisfactorily.

この発明の品質改良剤は、通常パン類やめん類等のでん
ぷん質食品の製造工程において添加して用いられ、種々
の効果を発揮する。
The quality improving agent of this invention is usually added and used in the manufacturing process of starchy foods such as breads and noodles, and exhibits various effects.

製パンの方法は中種法、ストレート法等の方法があるが
、いづれに用いても良く、添加工程や時期は特に限定さ
れないか通常、生地調製時のミキシング工程において製
パン原料に添加すればよい。
Bread-making methods include the dough method and the straight method, but either method may be used, and the addition process and timing are not particularly limited. good.

一方、製めん時に用いる際も、添加工程や時期は特に限
定されないが、通常、めん生地の混練工程において製め
ん原料に添加すればよい。
On the other hand, when used in noodle making, the addition process and timing are not particularly limited, but it can usually be added to the noodle making raw materials in the noodle dough kneading process.

製パン時の添加量は、製パン原料の小麦粉に対し、0.
01〜5重量%とするのが適しにいる。このような添加
により、パン生地が滑らかとなって処理加工性や損傷回
復性が向上し、かつ得られたパンの保水性が向上し老化
が防止又は抑制されることとなる。さらに、得られたパ
ンのスダチら細かく均一となり、そのパン容積も従来の
品質改良剤に比して増加されることとなる。なお、添加
量が0.01ME1%未満であると十分な品質改良効果
が発揮されず、また5重量%以上添加しても経済的デメ
リットを打ち消す効果は発揮されないので好ましくない
。通常、総合的な品質改良効果及びコストの点で、添加
量は0.05〜3重量%とするのが好ましく、0.1−
1重量%とするのがより好ましい。
The amount added during bread making is 0.
A suitable content is 0.01 to 5% by weight. Such addition makes the bread dough smooth, improving processability and damage recovery properties, and improves the water retention of the resulting bread, thereby preventing or suppressing aging. Furthermore, the texture of the obtained bread will be fine and uniform, and the volume of the bread will be increased compared to conventional quality improvers. It should be noted that if the amount added is less than 0.01ME1%, a sufficient quality improvement effect will not be exhibited, and even if it is added in an amount of 5% by weight or more, the effect of negating the economic disadvantages will not be exhibited, which is not preferable. Normally, from the viewpoint of overall quality improvement effect and cost, the amount added is preferably 0.05 to 3% by weight, and 0.1-3% by weight.
More preferably, the content is 1% by weight.

ただし、生地調整やパン容積の増加を主目的とする場合
には、添加量は0.02〜t、oria%程度で充分で
あり、パンの老化防止性の向上を主目的とする場合には
0.05重量%以上とするのが好ましい。
However, if the main purpose is to adjust the dough or increase the volume of the bread, an amount of 0.02 to 0.02 tons or oria% is sufficient; if the main purpose is to improve the anti-aging properties of the bread, The content is preferably 0.05% by weight or more.

一方、製めん時の添加料は、小麦、そば、米、ライ麦、
ライ小麦、とうもろこし等の製めん原料に対し、0.0
1〜5重量%添加すればよく、好ましくは0.05〜3
重量%であり、0,1〜1重量%とするのがより好まし
い。
On the other hand, additives used in noodle making include wheat, buckwheat, rice, rye,
0.0 for noodle raw materials such as triticale and corn
It is sufficient to add 1 to 5% by weight, preferably 0.05 to 3% by weight.
The amount is preferably 0.1 to 1% by weight.

この添加により、めんの老化が防止又は抑制され、食感
、はぐれ性等を向上することができ、製めん時の歩留ま
り、保存性を向上することができる。また乾めんや即席
めんの場合には、戻りを促進することができ、さらに包
装ゆでめんの場合には、包装材への付着性を防止するこ
とができる。
This addition prevents or suppresses aging of the noodles, improves the texture, flakiness, etc., and improves the yield and storage stability during noodle production. Further, in the case of dry noodles or instant noodles, it can promote the return of the noodles, and in the case of packaged boiled noodles, it can prevent adhesion to the packaging material.

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やレ
シチン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:l(重量比)(好ましくは1:4〜4;l)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。
The quality improving agent of the present invention may contain other quality improving components in addition to the above-mentioned protein partial decomposition products. In particular, one preferred embodiment is to use it in combination with a polyhydric alcohol fatty acid ester type surfactant such as sucrose fatty acid ester or glycerin fatty acid ester, or lecithin. At this time, the blending ratio of protein partial decomposition product and surfactant is 1 = 6 ~
A ratio of 6:l (weight ratio) (preferably 1:4 to 4:l) is more preferable because a synergistic quality improvement 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、一つの好ましい使用@様
である。
Further, commonly used preservatives such as ethanol, propionic acid, lactic acid, sorbic acid, dehydroacetic acid, and common salt may be used in combination, and this is a preferred 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 This invention will be explained in detail by 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0.59. Ig、 ’29及び4gに
相当する塩酸水溶液【00gの入ったフラスコにそれぞ
れ和光純薬工業(昧)製の小麦グルテン(試薬品)20
gを加え、80℃及び100℃にて60分間加熱撹拌し
た。
Examples 1 to 10 (Preparation of decomposition products by partial decomposition of wheat gluten with acid and subsequent partial decomposition with alkali) 0.59 in terms of hydrogen chloride. Wheat gluten (reagent) manufactured by Wako Pure Chemical Industries (Madhi) 20 in flasks containing 00 g of hydrochloric acid aqueous solution corresponding to Ig, 29 and 4 g, respectively.
g was added thereto, 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2009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1009をフラスコもしくはオートクレ
ーブl0IIIに入れ、これらに苛性ソーダ又は炭酸ナ
トリウム0.5〜29の範囲内の量を各別に加え、80
℃〜150℃にて30分〜360分間加熱撹拌した。そ
の後、塩酸にて中和し純水で総fi2009にしてこの
発明の部分分解物である発明品No、1〜IOを得L0 表−1に分解条件と分解物の平均分子量を示す。
Thereafter, neutralize with caustic soda and bring the total amount to 2009 with pure water to prepare a 10% aqueous solution of the partial decomposition product of wheat gluten with acid, put each 1009 into a flask or autoclave 10III, and add 0.00% of caustic soda or sodium carbonate. Add amounts within the range of 5 to 29 separately to 80
The mixture was heated and stirred at 150° C. for 30 minutes to 360 minutes. Thereafter, the mixture was neutralized with hydrochloric acid and purified to a total fi of 2009 with pure water to obtain invention products No. 1 to IO, which are partial decomposition products of the present invention. Table 1 shows the decomposition conditions and the average molecular weight of the decomposition products.

(以下余白) 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、はとんど無味無臭であった。
(The following is a blank space) Invention product No. '1 which was desalted by isoelectric precipitation or dialysis was almost tasteless and odorless.

実施例II〜+4(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(味)製とう
もろこしグルテンを原料とし実施例6及びl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。
Examples II to +4 (Preparation of decomposed products by partial decomposition of corn gluten and soybean protein with acid and then partial decomposition with alkali) Using corn gluten manufactured by Nihon Shokuhin Kako (Aji) as raw material, same conditions as in Examples 6 and 1. Partial decomposition was carried out sequentially using acid and alkali to produce Invention Product No.

11.12を得た。平均分子量はそれぞれ11800と
27100であった。
11.12 was obtained. The average molecular weights were 11,800 and 27,100, 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I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!io、L3,1
4を得た。
In addition, using soybean protein obtained by defatting commercially available yuba with acetone as a raw material, partial decomposition was performed sequentially using acid and alkali under the same conditions as in Examples 6 and I to produce an invention! io,L3,1
I got 4.

平均分子量はそれぞれ12000と29000であっ1
こ。
The average molecular weights are 12,000 and 29,000, respectively.
child.

実施例15.16(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29又は49を溶解した水溶液1009に実
施例1−10で用いた小麦グルテン209を加えて10
0℃にて60分間加熱撹拌後、塩酸にて中和し、純水で
重量2aog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1009に塩化水
素換算で0.53及び1り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32009にして発明品No、1
5.16を得た。表−2に分解条件と分解物の平均分子
量を示す。
Example 15.16 (Preparation of decomposed product by partial decomposition of wheat gluten with alkali and subsequent partial decomposition with acid) Wheat gluten 209 used in Example 1-10 was added to aqueous solution 1009 in which caustic soda 29 or 49 was dissolved. te10
After heating and stirring at 0°C for 60 minutes, the mixture was neutralized with hydrochloric acid, and the weight was adjusted to 2 aog with pure water to prepare a 10% aqueous solution of partially decomposed wheat gluten with an alkali. Hydrochloric acid equivalent to 1 and 1 were added separately, and the mixture was heated and stirred at 100° C. for 60 minutes. After that, it was neutralized with caustic soda and made into a total of 32009 with pure water, making it Invention No. 1.
5.16 was 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209を0.IN
−塩酸液1509が入ったフラスコに加え、pH1,5
の水溶液を得fこ。これに0.29のペプシンを加え3
7℃で90分間反応させた。その後、苛性ソーダで中和
し純水て総ff12009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1009
に苛性ソーダを19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N0817を得た。
Example 17 (Preparation of decomposed product by enzymatic partial decomposition of wheat gluten followed by alkali partial decomposition) Wheat gluten 209 used in Examples 1 to 10 was mixed with 0. IN
-Add to a flask containing hydrochloric acid solution 1509, pH 1.5
Obtain an aqueous solution of. Add 0.29 pepsin to this and 3
The reaction was carried out at 7°C for 90 minutes. Thereafter, a 10% aqueous solution of enzymatic partial decomposition of wheat gluten was prepared by neutralizing with caustic soda and adding pure water to a total of 12,009 ff.
19 g of caustic soda was added to the flask, and the mixture was heated and stirred for 60 minutes. Thereafter, the mixture was neutralized with hydrochloric acid and the total amount was adjusted to 200 g with pure water to obtain invention product N0817.

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49を溶解した水溶液1009に実施
例1〜10で用いた小麦グルテン209を加えて、30
℃にて60分間撹拌後、純水で総量z009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1009に苛性ソーダ19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2009とし発明品No、 i
llを得L0平均分子量は39500であった。
Example 18 (Preparation of decomposed product by partial decomposition of wheat gluten with a reducing agent and then partial decomposition with an alkali) Wheat gluten 209 used in Examples 1 to 10 was added to an aqueous solution 1009 in which sodium sulfite 49 was dissolved, 30
After stirring at ℃ for 60 minutes, prepare a 10% aqueous solution of partially decomposed wheat gluten with a reducing agent by adjusting the total amount to z009 with pure water, add 19 of caustic soda to the 1009, and heat and stir in a flask at 100℃ for 60 minutes. did. After that, it was neutralized with hydrochloric acid and the total amount was adjusted to 2009 with pure water. Invention product No. i
11 was obtained, and the L0 average molecular weight was 39,500.

実施例19(小麦グルテンのアルカリにょる部分分解と
次いで実施した酵素に上る部分分解(実施例+7と順次
が逆)による分解物の!IXI製)苛性ソーダ2gを溶
解した水溶液1009に実施例1〜10で用いた小麦グ
ルテン209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fi2009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1009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、0.19のペプシンを加
えて37℃で90分間反応さ仕た。その後、苛性ソーダ
で中和し純水で総量2009にし発明品)o、19を得
た。
Example 19 (Produced by IXI, a decomposition product obtained by partial decomposition of wheat gluten with alkali and then enzymatic partial decomposition (the order is reversed from Example +7)) Examples 1 to 1 in an aqueous solution 1009 in which 2 g of caustic soda was dissolved. Add the wheat gluten 209 used in step 10, heat and stir at 100°C for 60 minutes, neutralize with hydrochloric acid, and make a total fi of 2009 with pure water to prepare a 10% aqueous solution of the partial decomposition product of wheat gluten with alkali. The reagent hydrochloric acid was added to the 1009 to obtain an aqueous solution with a pH of 1.5, and this was reacted in a flask at 37° C. for 90 minutes with the addition of 0.19 pepsin. Thereafter, the mixture was neutralized with caustic soda and purified with pure water to give a total amount of 2009 (invention product) o, 19.

平均分子mは24:)00であった。The average molecular m was 24:)00.

実施例20(小麦グルテンのアルカリによ7.部分分解
と次いで実施しl二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f三水溶液100りに実施fu
l11−10で用いた小麦グルテン20り・鷹I][1
えてl OO’Cにて60分間加熱撹拌後、塩酸にて中
和し、純水でtさ量2009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1
009にHt Oを換算で0.59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H t Otと当量のチオ硫酸ナトリウムを
加え、純水で総量200gにして発明品20を得た。
Example 20 (Partial decomposition of wheat gluten with an alkali and subsequent partial decomposition with a carbon dioxide agent) Preparation of a decomposed product by dissolving 2 g of caustic soda and adding 100 g of an aqueous solution.
20 ml of wheat gluten used in l11-10/Taka I] [1
After heating and stirring at OO'C for 60 minutes, neutralize with hydrochloric acid and adjust the weight to 2009 with pure water to prepare a 10% aqueous solution of partially decomposed wheat gluten with alkali.
Hydrogen peroxide equivalent to 0.59 in terms of Ht 2 O was added to 009, and the mixture was heated and stirred at 40° C. for 60 minutes. Thereafter, sodium thiosulfate in an amount equivalent to the remaining H t Ot was added, and the total amount was adjusted to 200 g with pure water to obtain Invention Product 20.

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。
Below, various physical properties and particle dispersion effects of the partially degraded proteins of the present invention obtained in Examples 1 to 20 are shown in Table 3, and measurement results of surface tension and emulsification duration are shown in Table 4.

(以下余白) 表3(つづき) 表中、原料側の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、測定まには試験せずを意味する。
(Margin below) Table 3 (Continued) In the table, W on the raw material side means wheat gluten, C means corn gluten, and B means soybean protein. Note that a blank column means that no test was performed during measurement.

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 effect 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
゜16000.65000.88000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 and 6500 as standard substances.
This value was measured by a gel filtration method using sodium polystyrene sulfonate having a molecular weight of 16,000.65,000.88,000 and using Sephadex G-75 or G-100 manufactured by Pharmacia as a carrier.

〔等電点〕[Isoelectric point]

ビー力にこの発明の実施例で得られた発明品I〜20を
各1009づつ取り、室温にて撹拌下、lN−HCl2
を1maづつ添加し、l)Hを測定した。得られたpl
(曲線の傾きが緩やかになるpH1tiを等電点とした
1009 pieces of each of the invention products I to 20 obtained in the examples of the present invention were placed in a beaker, and 1N-HCl2 was added under stirring at room temperature.
was added 1 ma at a time, and l) H was measured. Obtained pl
(The pH 1ti at which the slope of the curve becomes gentle was defined 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I)+(曲線よ
り、pnを6から2まで低下させるのに必要なlNの塩
酸量を緩衝能とした。なお、この際のpn中和曲線を、
発明品No、l、No、7.No、11.及びNo、1
3について第1図(イ)〜(ニ)に示した。
From the I) + (curve obtained in the same manner as the isoelectric point measurement method, the amount of lN hydrochloric acid required to lower pn from 6 to 2 was defined as the buffering capacity. In addition, pn neutralization at this time curve,
Invention No. 1, No. 7. No, 11. and No. 1
3 are shown in Figures 1 (a) to (d).

(UV) 日立U −3200形分光光度計を用いて800〜20
0nmの範囲の吸光度を測定した。
(UV) 800 to 20 using a Hitachi U-3200 spectrophotometer
Absorbance was measured in the 0 nm range.

(rR) 日立260−10形赤外分光光度計を用いてKBr法で
測定した。
(rR) Measured by the KBr method using a Hitachi 260-10 infrared spectrophotometer.

〔粒子分散力〕 (炭酸カルシウムスラリー)・ナショ
ナルMI型ミキサーに発明品および水道水を計250g
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2509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DV)I−B型帖文計にて、回転数5O
rpm、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5009に対して0.3重量−である。
[Particle dispersion power] (Calcium carbonate slurry) - A total of 250 g of the invention and tap water in a National MI mixer
Add calcium carbonate (light calcium carbonate manufactured by Takehara Chemical Industry Co., Ltd.) 2509 and mix for 2 minutes to prepare a 50% by weight slurry. Immediately thereafter, the slurry was transferred to a beaker, and the rotation speed was 50 using a Tokyo Keiki DV) I-B model meter.
Measure the viscosity (cps) at rpm, rotor No. 3-5. However, the concentration of the partially decomposed product of the invention is
The weight is 0.3 based on the total amount of 5009.

(カオリンスラリー) ・ナショナルMI型ミキサーに、この発明の部分分解物
および水道水を2009入れ、カオリン〔上屋カオリン
工業(PI8)製〕粉末を3009加えて2分間混合し
、60重g15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DV)I−B型帖度
計にて、回転数5Orpm、ローターNo、3〜5にて
粘度を測定する。ただし、こ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fi%である。
(Kaolin slurry) - Put 2009 of the partially decomposed product of this invention and tap water into a National MI mixer, add 3009 of kaolin [manufactured by Ueya Kaolin Kogyo (PI8)] powder and mix for 2 minutes to make 60 g of 15 slurry. Prepare. Immediately thereafter, the slurry is transferred to a beaker, and the viscosity is measured using a DV) I-B type meter manufactured by Tokyo Keiki at a rotational speed of 5 Orpm and a rotor number of 3 to 5. However, the concentration of the partially decomposed product of this invention is 0.3% by weight based on the total amount of 500g.

(以下余白) 表−4 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。
(Margins below) Table 4 The methods for measuring surface tension and emulsification duration 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 Examples was measured using a Dunuy surface tension meter at a temperature of 25° C. using pure water as a solvent.

[乳化持続時間の測定コ 実施例で調製しfこ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 product prepared in Example 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709入れ、
pHを7.0に調整する。大豆油〔キシダ化学(株)製
試薬〕309を加え特殊機化工業・(抹)製HV−M型
ホモミキサーで回転数800Orpm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) -Pour a total of 709 samples of drug and tap water into a beaker,
Adjust pH to 7.0. Soybean oil (reagent manufactured by Kishida Kagaku Co., Ltd.) 309 was added and mixed for 5 minutes at 800 rpm using an HV-M homomixer manufactured by Tokushu Kika Kogyo Co., Ltd. Immediately after mixing, the emulsion is transferred to a colorimetric tube and left at room temperature, and the time until separation begins is defined as the emulsification duration. The emulsification duration was measured every 10 minutes until 1 hour after the start of standing, and thereafter every 1 hour. However, the concentration of the partially decomposed product of this invention added is 1.0% by weight based on the total amount.

比較例!(小麦グルテンの調11Sり 実施例1〜lOに用いた小麦グルテンを分解処理せずそ
のまま比較具No、Lとして用いた。
Comparative example! (Preparation of Wheat Gluten 11S) The wheat gluten used in Examples 1 to 1O was used as it was as Comparative Samples No. 1 and L without being subjected to decomposition treatment.

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29を溶解した水溶液too9に実施例1〜
!0で用いた小麦グルテン209を加えて100℃で6
0分間加熱撹拌後、塩酸で中和し、純水で総量200g
として比較具No、2を得た。
Comparative Example 2 (Preparation of partially decomposed product of wheat gluten with alkali) Examples 1 to 9 were added to an aqueous solution too9 in which caustic soda 29 was dissolved.
! Add wheat gluten 209 used in step 0 and heat at 100°C.
After heating and stirring for 0 minutes, neutralize with hydrochloric acid and add pure water to a total amount of 200g.
Comparative device No. 2 was obtained.

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

比較例3(小麦グルテンの酵素による部分分解物の調製
) 実施例1−toで用いた小麦グルテン209を0.1N
−塩酸液150gか入ったフラスコに加え、pH1,5
の水溶液を得た。これに0.29のペプシンを加え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2009にして比較具N013を得た。部分
分解物の平均分子量は60000であった。
Comparative Example 3 (Preparation of enzymatic partial decomposition product of wheat gluten) 0.1N of wheat gluten 209 used in Example 1-to
-Add to a flask containing 150g of hydrochloric acid solution, pH 1.5
An aqueous solution of was obtained. Add 0.29 pepsin to this and 37
The reaction was carried out at ℃ for 90 minutes. Thereafter, the mixture was neutralized with caustic soda and the total amount was adjusted to 2009 with pure water to obtain comparative sample No. 013. The average molecular weight of the partially decomposed product was 60,000.

比較例4(小麦グルテンの還元剤による部分分解と次い
で実施した酵素による部分分解による分解物の調製)) 亜硫酸ナトリウム49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209を加え、30℃
にて60分間撹拌後、塩酸を加えてpH1,5の水溶液
を得、これに0.29のペプシンを加え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ff
12009にして比較具No、4を得た。
Comparative Example 4 (Preparation of decomposed product by partial decomposition of wheat gluten with a reducing agent and subsequent partial decomposition with an enzyme) Wheat gluten 209 used in Examples 1 to 10 was added to 100 g of an aqueous solution in which sodium sulfite 49 was dissolved, 30℃
After stirring for 60 minutes at , hydrochloric acid was added to obtain an aqueous solution with a pH of 1.5, to which 0.29 pepsin was added and reacted at 37° C. for 90 minutes. After that, neutralize with caustic soda and completely ff with pure water.
12009 to obtain comparison tool No. 4.

平均分子量は36000であった。The average molecular weight was 36,000.

この発明の実施例の発明品N011〜20、比較例の比
較具No、 1〜4、及び公知の品質改良剤であるショ
糖脂肪酸エステル[第1工業製薬(味)製、商品名:D
KエステルF−160(HLB15) 、比較具No。
Inventive products No. 1 to 20 of Examples of this invention, Comparative devices No. 1 to 4 of Comparative examples, and sucrose fatty acid ester which is a known quality improver [manufactured by Daiichi Kogyo Seiyaku (Aji), trade name: D
K-ester F-160 (HLB15), Comparison No.

5j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
コを用いて以下の試験例を実施した。
5j Palmitic acid monoglyceride [manufactured by Taiyo Kagaku Co., Ltd., trade name: Sunsoft No. 8001. Comparison product No. 6
The following test examples were carried out using

試験例1(製パン試験) A、製パン方法 ナショナル製ホームベーカリ−を用いて製パンし、温度
25℃に放置した。製パン条件を以下に示す。
Test Example 1 (Bread making test) A. Bread making method Bread was made using a National home bakery and left at a temperature of 25°C. The bread making conditions are shown below.

・製パン機・・・・・・ナショナルホームベーカリ−3
D−Br3型・原料 強力粉・・・・・・2809 砂糖・・・・・・179 スキムミルク ・・・・・・  69 塩   ・・・・・・ 59 バター・・・・・・ tt9 水   ・・・・・・2109 ドライイースト・・・・・・ 2.79・製パン時間・
・・・・・300分 但し、各発明品及び比較具は、原料に混和して添加した
。また、表中の添加濃度は、強力粉に対する重量%であ
る。
・Bread making machine・・・National Home Bakery-3
D-Br3 type/Ingredients Strong flour...2809 Sugar...179 Skim milk...69 Salt...59 Butter...tt9 Water... ...2109 Dry yeast...2.79・Bread making time・
...300 minutes However, each invention product and comparative device were mixed and added to the raw materials. Moreover, the addition concentration in the table is weight % based on strong flour.

B、試験結果 パン体積、含水率及びその経日変化、軟らかさ及びデン
プン老化度を測定した結果、この発明の実施例である発
明品No、1〜20においては、いづれも無添加時及び
比較具と比べて、同等以上の品質改良効果を示した。そ
の代表例を比較例とともに表−5に示す。
B. Test results As a result of measuring bread volume, moisture content, its change over time, softness, and degree of starch aging, it was found that for invention products Nos. 1 to 20, which are examples of this invention, both without additives and in comparison. Compared to ingredients, it showed the same or better quality improvement effect. Typical examples are shown in Table 5 along with comparative examples.

表中の評価項目は下記の様に測定した。The evaluation items in the table were measured as follows.

・含水率(%) : 105℃、2時間乾燥前後の重量
差より求めた。
- Moisture content (%): Calculated from the difference in weight before and after drying at 105°C for 2 hours.

・含水率変化分(%):(製パン時の含水率)−(放置
後の含水率)・軟うカサ(97cm):不動工業製レオ
メータ−(NRM−2010J、D−CW)を用いて、
引張り強度として求めた。
・Moisture content change (%): (moisture content during bread making) - (moisture content after standing) ・Softening crust (97cm): Using a rheometer manufactured by Fudo Kogyo (NRM-2010J, D-CW) ,
It was determined as tensile strength.

・デンプン老化!(%):β−アミラーゼとプルラナー
ゼを用いるBAP法(f生物化学実験法t9−澱粉・関
連糖質実験法」 [学会出版センター])により、糊化
度を求める事により算出した。
・Starch aging! (%): Calculated by determining the degree of gelatinization using the BAP method (F Biochemical Experimental Methods T9-Starch and Related Carbohydrate Experimental Methods [Gakkai Publishing Center]) using β-amylase and pullulanase.

(以下余白) 表−5(続き) なお、上記発明品!及び11の部分分解物とショv1脂
肪酸エステル又はパルミチン酸モノグリセリドとを併用
した結果についても以下の表−6に示した。
(Margins below) Table 5 (Continued) In addition, the above invention! The results of using the partial decomposition product of No. 1 and No. 11 in combination with Sho v1 fatty acid ester or palmitic acid monoglyceride are also shown in Table 6 below.

C9考察 [パン体積] 上記試験No、2〜17に示されるように、この発明の
発明品を0.5重量%添加することによりパン体積を7
〜18%増加さけることができ、各比較品の増加効果O
〜8%に比して明らかに浸れている。
C9 Consideration [Bread Volume] As shown in Test Nos. 2 to 17 above, by adding 0.5% by weight of the invention product of this invention, the bread volume was increased to 7% by weight.
~18% increase can be avoided, and the increase effect of each comparison product O
It is clearly soaked compared to ~8%.

また、試験例No、18〜21に示されるように、ショ
糖脂肪酸エステルやパルミチン酸モノグリセリドと併用
することにより、パン体積がより増加されることがイっ
かる。
Furthermore, as shown in Test Examples Nos. 18 to 21, it was found that the bread volume was further increased when used in combination with sucrose fatty acid ester and palmitic acid monoglyceride.

[保水性、軟らかさ] 各発明品を用いて製パンされた乙のは、含水率の低下度
がブランクや比較品によるらのに比して少なく、保水性
が浸れている。また軟らかさも同様に改善されている。
[Water retention and softness] Bread made using each invention product had a lower degree of decrease in water content than the blank or comparison product, and had a high water retention property. The softness has also been improved as well.

[デンプン老化度] 各発明品を用いて製パンされたものは、その老化度がブ
ランクに比して明確に抑制されてお一〕、眼して1〜2
日程度、耐久性か向上しでいる。
[Starch retrogradation degree] The retrogradation degree of the bread made using each invention product was clearly suppressed compared to the blank], and was visually 1 to 2.
Durability has improved over time.

試験例2 (製めん試験) めんは製造後品質か徐々低下し、食感・歯ざわりが悪く
なっていく。また、はぐれ性も悪くなって行く。そこで
、本発明品の効果を比較検討した。
Test Example 2 (Noodle manufacturing test) After the noodles are manufactured, the quality gradually deteriorates, and the texture and texture become worse. In addition, the tendency to separate becomes worse. Therefore, the effects of the products of the present invention were compared and studied.

A、製めん方法 中力小麦粉foo9、食塩29および水359に所定量
の供試品を加え、混練して得ためん生地を製めんロール
を用いて約1.2xm厚のめん帯とした。このめん帯を
角力ツタ−No、20を用いて切断してめん線とし、約
30cm長に切断したものを約5分間ゆで上げ、約5℃
の冷蔵庫に保存した。
A. Noodle making method: A predetermined amount of the sample was added to 99 grams of all-purpose wheat flour, 29 grams of salt, and 359 grams of water, and the resulting noodle dough was kneaded into a noodle dough about 1.2 x m thick using a noodle making roll. This noodle strip was cut into noodle strips using Kakuriki Tsuta No. 20, and the cut pieces were cut into lengths of about 30 cm and boiled for about 5 minutes at about 5°C.
stored in the refrigerator.

その後、沸騰水中で撹拌什ずに約1分間鳩洗いし、はぐ
れ状態を観察し、同時に感応試験を行った。
Thereafter, they were washed in boiling water for about 1 minute without stirring, and the state of separation was observed, and a sensitivity test was conducted at the same time.

B、試験結果 この発明の実施例である発明品No、1〜2oにおいて
は、いずれも比較品と比べて、はぐれ状態及び食感性が
良好でめった。その代表例を比較例とともに表−7に示
す。
B. Test Results Inventive products No. 1 to 2o, which are examples of the present invention, were all successful in terms of peeling and texture compared to the comparative products. Typical examples are shown in Table 7 along with comparative examples.

表中の濃度(%)は、小麦粉に対する供試品の重量%で
ある。また、感応試験は、10人のパネラ−により行い
、その結果を総合的にまとめたものである。
The concentration (%) in the table is the weight % of the sample relative to the wheat flour. The sensitivity test was conducted by 10 panelists, and the results are comprehensively summarized.

(以下余白) (へ)発明の効果 この発明の品質改良剤によれば、各種でんぷん質食品の
生地調整時の粘りやきめの細かさを付与できると共に、
得られたでんぷん質食品の保水性を著しく向上でき優れ
た老化防止性を付与することができる。そして例えば、
パン類については、従来の品質改良剤に比してその容積
をより増大することができ、上記効果と相俟って軟らか
さか長期間維持されたパンを効率良く提供することが可
能となる。また例えばめん類についても生地調整用に有
効であり、老化防止作用や保水性作用により、長期間良
好なほぐれ性や食感を維持できるめんを提供できること
となる。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。
(The following is a blank space) (F) Effects of the Invention According to the quality improving agent of the present invention, it is possible to impart stickiness and fineness of texture when preparing the dough of various starchy foods, and
The water retention properties of the resulting starchy food can be significantly improved and excellent anti-aging properties can be imparted. And for example,
As for bread, the volume can be increased compared to conventional quality improving agents, and in combination with the above effects, it becomes possible to efficiently provide bread that maintains its softness for a long period of time. It is also effective for adjusting the dough of noodles, for example, and can provide noodles that maintain good loosening properties and texture for a long period of time due to anti-aging and water-retaining effects. Since the active ingredient, the partial decomposition product of grain protein, is food or food-like, it is extremely advantageous in that it is non-toxic and has improved safety as a food additive.
Moreover, it is inexpensive.

従って、この発明の品質改良剤はでんぷん質素品用添加
剤として極めて有用なものである。
Therefore, the quality improver of the present invention is extremely useful as an additive for starchy raw materials.

【図面の簡単な説明】[Brief explanation of the drawing]

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中和曲線を各々例示するグラフ図で
ある。 (イ) (ハ) IN HCl(ml) 図 (ニ) I N−HCl (ml)
FIGS. 1(a) to 1(d) are graphs illustrating pH neutralization curves for partial hydrolysates used in the present invention. (B) (C) IN HCl (ml) Figure (d) IN-HCl (ml)

Claims (1)

【特許請求の範囲】 (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〜
90000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lN
−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50
dyne/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10
0g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、 で特性づけられる物質からなるでんぷん質食品の品質改
良剤。 (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)に記載の品質改良剤。 (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)に記載の品
質改良剤。 (1)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
載の品質改良剤。 (5)でんぷん質食品が、パン類又はめん類である請求
項(1)〜(4)のいずれかに記載の品質改良剤。 (6)でんぷん質食品が、パン類である請求項(5)に
記載の品質改良剤。 (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)の品質改良剤。 (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)記載の品質改良剤。 (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)記載の品質改良剤。 (10)でんぷん質食品素材に対して、0.01〜5重
量%添加して用いられる請求項(1)又は(7)記載の
品質改良剤。
[Scope of Claims] (1) A partial decomposition product of grain protein, which has the following physical properties: (a) a weight average molecular weight (by gel filtration method) of 500 to 500;
(b) UV absorption λmax is around 260 to 280 nm, and infrared absorption is 1400, 1630 and 3400 cm.
(c) Isoelectric point is around ^-^1, 3.9 to 5.0
(d) pH buffering property (1N to lower the pH of 100ml of a 5% aqueous solution of this product from 6 to 2)
(requires 2 to 25 ml of hydrochloric acid); (e) is soluble in water and insoluble in methanol, ethanol, acetone, and ether; (f) is a pale yellow to reddish brown powder in appearance; (g)
Color develops due to xanthoprotein reaction and ninhydrin reaction. (h) Strong surface tension lowering ability (this product is added to pure water at 25°C for 0.00 min.
By adding 1% by weight, the surface tension of pure water increases by 50%.
dyne/cm (measured with a Dunui surface tension meter). (i) Strong emulsifying ability (by adding 1 g of this product, a water-soybean oil mixture containing at least 30% by weight of soybean oil)
Completely emulsify 0g (keep it uniformly emulsified for at least 10 minutes,
A quality improving agent for starchy foods comprising a substance characterized by: (meaning that it can be maintained preferably for 1 hour or more). (2) The partial decomposition product is produced by a combination of one or more of the following: (A) hydrolysis treatment with an alkali and (B) decomposition treatment using an acid, an enzyme, an oxidizing agent, or a reducing agent. The quality improver according to claim (1), which is a substance obtained by subjecting it to multi-stage partial decomposition treatment. (3) The partially decomposed product undergoes hydrolysis treatment with an alkali,
The quality improving agent according to claim 2, which is obtained by a two-stage partial decomposition treatment in combination with an acid hydrolysis treatment. (1) The quality improving agent according to any one of claims (1) to (3), wherein the grain is wheat gluten, corn gluten, or soybean protein. (5) The quality improving agent according to any one of claims (1) to (4), wherein the starchy food is bread or noodles. (6) The quality improver according to claim (5), wherein the starchy food is bread. (7) The quality improving agent according to claim (1), further comprising a polyhydric alcohol fatty acid ester type surfactant. (8) The quality improving agent according to claim (7), wherein the protein partial decomposition product and the polyhydric alcohol fatty acid ester type surfactant are blended in a weight ratio of 1:6 to 6:1. (9) The polyhydric alcohol fatty acid ester type surfactant is
The quality improving agent according to claim 8, which is a sucrose fatty acid ester and/or a glycerin fatty acid ester. (10) The quality improving agent according to claim (1) or (7), which is used by adding 0.01 to 5% by weight to the starchy food material.
JP63026239A 1987-07-06 1988-02-05 Quality improver for starchy foods Expired - Lifetime JPH0746958B2 (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
JP63026239A JPH0746958B2 (en) 1988-02-05 1988-02-05 Quality improver for starchy foods
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
JP63026239A JPH0746958B2 (en) 1988-02-05 1988-02-05 Quality improver for starchy foods

Publications (2)

Publication Number Publication Date
JPH01202235A true JPH01202235A (en) 1989-08-15
JPH0746958B2 JPH0746958B2 (en) 1995-05-24

Family

ID=12187759

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63026239A Expired - Lifetime JPH0746958B2 (en) 1987-07-06 1988-02-05 Quality improver for starchy foods

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03111453A (en) * 1989-09-25 1991-05-13 Nitta Gelatin Inc Modifier for synthetic resin, modified resin material, modified resin film and modified surface-treated product
JPH05252859A (en) * 1992-03-13 1993-10-05 Nisshin Oil Mills Ltd:The Starchy frozen food and its production
KR100364586B1 (en) * 2000-06-27 2002-12-12 주식회사농심 Method for producing noodles with improved restoration
KR100542261B1 (en) * 2002-11-15 2006-01-11 주식회사농심 Method for manufacturing noodles with rapid rehydration rate

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6326238A (en) * 1986-07-19 1988-02-03 Kawasaki Steel Corp Production of clad steel ingot by insert casting

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6326238A (en) * 1986-07-19 1988-02-03 Kawasaki Steel Corp Production of clad steel ingot by insert casting

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03111453A (en) * 1989-09-25 1991-05-13 Nitta Gelatin Inc Modifier for synthetic resin, modified resin material, modified resin film and modified surface-treated product
JPH05252859A (en) * 1992-03-13 1993-10-05 Nisshin Oil Mills Ltd:The Starchy frozen food and its production
KR100364586B1 (en) * 2000-06-27 2002-12-12 주식회사농심 Method for producing noodles with improved restoration
KR100542261B1 (en) * 2002-11-15 2006-01-11 주식회사농심 Method for manufacturing noodles with rapid rehydration rate

Also Published As

Publication number Publication date
JPH0746958B2 (en) 1995-05-24

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