JP3158849B2 - Method for producing soy peptide mixture - Google Patents

Method for producing soy peptide mixture

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Publication number
JP3158849B2
JP3158849B2 JP06259094A JP6259094A JP3158849B2 JP 3158849 B2 JP3158849 B2 JP 3158849B2 JP 06259094 A JP06259094 A JP 06259094A JP 6259094 A JP6259094 A JP 6259094A JP 3158849 B2 JP3158849 B2 JP 3158849B2
Authority
JP
Japan
Prior art keywords
peptide mixture
solution
soybean
soybean protein
peptide
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 - Fee Related
Application number
JP06259094A
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Japanese (ja)
Other versions
JPH07264993A (en
Inventor
正行 松井
知子 鍛冶
実 木本
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.)
Fuji Oil Co Ltd
Original Assignee
Fuji Oil Co Ltd
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Publication date
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Priority to JP06259094A priority Critical patent/JP3158849B2/en
Publication of JPH07264993A publication Critical patent/JPH07264993A/en
Application granted granted Critical
Publication of JP3158849B2 publication Critical patent/JP3158849B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明は、風味良好な大豆ペプチ
ド混合物を高収率で生産出来る製造法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing a soybean peptide mixture having a good taste in a high yield.

【0002】[0002]

【従来の技術】通常、大豆蛋白を酵素により平均分子量
約100〜50000の範囲に加水分解して得られる大
豆ペプチド混合物でも、全てが水溶性になるほどに加水
分解することは困難で、どうしても一部水不溶の高分子
成分が残存する。
2. Description of the Related Art Generally, even a soybean peptide mixture obtained by hydrolyzing a soybean protein with an enzyme to an average molecular weight in the range of about 100 to 50,000 is difficult to hydrolyze so that the whole becomes water-soluble. Water-insoluble polymer components remain.

【0003】一方、従来知られている大豆ペプチド混合
物の製造方法は、大豆ペプチド混合物の有する不快な臭
いや苦味等の悪風味を除去する方法が殆どである。
On the other hand, most of the conventionally known methods for producing a soybean peptide mixture mostly remove unpleasant odors and bitter tastes of the soybean peptide mixture.

【0004】例えば、活性炭を用いる方法(特公昭56
−52543、特開平3−272694)、イオン交換
樹脂を用いる方法、合成吸着剤を用いる方法(特開平4
−190797、特開平4341193、特開平4−4
5750)等がそれである。
For example, a method using activated carbon (Japanese Patent Publication No. Sho 56
-52543, JP-A-3-272694), a method using an ion-exchange resin, and a method using a synthetic adsorbent (JP-A-Heisei 4).
-190797, JP-A-4341193, JP-A-4-4
5750).

【0005】これらの方法は、製造工程上、活性炭、イ
オン交換樹脂若しくは合成吸着剤の目詰まりを起こす原
因であると共に悪風味の源である水不溶の高分子成分を
分離除去する工程を含むものである。
[0005] These methods include a step of separating and removing a water-insoluble polymer component which causes clogging of activated carbon, an ion exchange resin or a synthetic adsorbent and which is a source of bad taste in the production process. .

【0006】ところが、水不溶の高分子成分を除去する
ことにより、風味は改良されるが、得られる大豆ペプチ
ド混合物の歩留りが低下し、その結果高価な物となり、
産業上利用が制限される問題を有している。
[0006] However, although the flavor is improved by removing the water-insoluble polymer component, the yield of the obtained soybean peptide mixture is reduced, and as a result, it becomes expensive.
There is a problem that industrial use is restricted.

【0007】[0007]

【発明が解決しようとする課題】そこで、本発明者等
は、歩留りが高く(換言すれば水不溶性成分を含む)且
つ不快な臭い、苦味等の悪風味のない風味良好な大豆ペ
プチド混合物を低コストで製造出来る実用的な大豆ペプ
チド混合物の製造法を目的とした。
Therefore, the present inventors have developed a low-yielding soybean peptide mixture having a high yield (in other words, containing a water-insoluble component) and no unpleasant odor or bitterness. The objective was to produce a practical soy peptide mixture that can be produced at low cost.

【0008】[0008]

【課題を解決するための手段】本発明者等は前記目的を
達成すべく鋭意研究するなかで、特定の温度条件で水不
溶の高分子成分を含んだ大豆蛋白加水分解物溶液と吸着
剤を接触させたとき風味良好な大豆ペプチド混合物を得
ることが出来る知見を得て本発明を完成するに到った。
尚、水不溶の高分子成分を含んだ大豆蛋白加水分解物
は、具体的には15%トリクロル酢酸可溶率50〜90
を示す大豆蛋白加水分解物である。
Means for Solving the Problems The inventors of the present invention have conducted intensive studies to achieve the above object, and have found that a soybean protein hydrolyzate solution containing a water-insoluble polymer component under a specific temperature condition and an adsorbent are used. The present invention has been completed by obtaining the knowledge that a soybean peptide mixture having a good taste can be obtained when brought into contact.
In addition, the soybean protein hydrolyzate containing a water-insoluble polymer component specifically has a 15% trichloroacetic acid solubility of 50 to 90%.
And a soybean protein hydrolyzate.

【0009】即ち、本発明は、15%トリクロル酢酸可
溶率50〜90の大豆蛋白加水分解物溶液を50℃〜7
0℃で吸着剤処理することを特徴とする大豆ペプチド混
合物の製造法、である。
That is, the present invention provides a soybean protein hydrolyzate solution having a 15% trichloroacetic acid solubility of 50 to 90.
A method for producing a soybean peptide mixture, which comprises treating the soybean peptide mixture at 0 ° C.

【0010】本発明の15%トリクロル酢酸可溶率50
〜90の大豆蛋白加水分解物溶液は、大豆蛋白を水系下
にプロテア−ゼで加水分解した水不溶の高分子成分を含
んだ大豆蛋白加水分解物液である。
The solubility of 15% trichloroacetic acid of the present invention is 50%.
The soybean protein hydrolyzate solutions No. to No. 90 are soybean protein hydrolyzate solutions containing a water-insoluble polymer component obtained by hydrolyzing soybean protein with a protease in an aqueous system.

【0011】本発明の大豆蛋白は、丸大豆をヘキサン、
エタノール等の有機溶剤で脱脂した脱脂大豆から蛋白質
を水抽出した豆乳、更に豆乳より酸沈殿或いはアルコ−
ル沈殿等の方法により得られる分離大豆蛋白質、濃縮大
豆蛋白質等が適当である。
The soybean protein of the present invention is obtained by converting whole soybean into hexane,
Soymilk in which protein was extracted from defatted soybeans defatted with an organic solvent such as ethanol, and then acid precipitation or alcohol extraction from soymilk
Isolate soybean protein, concentrated soybean protein, and the like obtained by methods such as precipitation are suitable.

【0012】大豆蛋白を水系下にプロテア−ゼで加水分
解する。即ち、大豆蛋白は溶液或いは分散液となすこと
が適当であり、その濃度は、酵素分解可能な濃度範囲で
あれば特に限定しないが、通常、1〜10重量%溶液と
することが出来る。
The soybean protein is hydrolyzed with a protease in an aqueous system. That is, the soybean protein is suitably formed into a solution or a dispersion, and the concentration thereof is not particularly limited as long as it is within a concentration range capable of enzymatic degradation, but it can be usually a 1 to 10% by weight solution.

【0013】本発明に用いるプロテア−ゼは、エキソプ
ロテア−ゼ又はエンドプロテア−ゼを単独又は併用する
ことが出来、動物起源、植物起源或いは微生物起源は問
わない。具体的には、セリンプロテア−ゼ(動物由来の
トリプシン、キモトリプシン、微生物由来のズブチリシ
ン、カルボキシペプチダ−ゼ等)、チオ−ルプロテア−
ゼ(植物由来のパパイン、フィシン、ブロメライン
等)、カルボキシプロテア−ゼ(動物由来のペプシン
等)を用いることが出来る。更に具体的にはアスペルギ
ルス・オリ−ゼ起源の「プロチンFN」(大和化成株
製)、ストレプトマイセス・グリセウス起源の「アクチ
ナ−ゼ」(科研製薬株製)、バチルス・リケホルミス由
来の「アルカラ−ゼ」(ノボ社製)、バチルス・サブチ
ルス由来の「プロチンA」(大和化成株製)等を用いる
ことが出来る。
As the protease used in the present invention, exoprotease or endoprotease can be used alone or in combination, regardless of animal origin, plant origin or microbial origin. Specifically, serine proteases (trypsin, chymotrypsin derived from animals, subtilisin derived from microorganisms, carboxypeptidase, etc.), thiol-proteases
Zea (plant-derived papain, ficin, bromelain, etc.) and carboxyprotease (animal-derived pepsin, etc.) can be used. More specifically, “Protin FN” derived from Aspergillus oryzae (manufactured by Daiwa Kasei Co., Ltd.), “Actinase” derived from Streptomyces griseus (manufactured by Kaken Pharmaceutical Co., Ltd.), and “Alcala derived from Bacillus licheformis” ZE (manufactured by Novo), Bacillus subtilis-derived "protin A" (manufactured by Daiwa Kasei Co., Ltd.) and the like can be used.

【0014】本発明の加水分解の条件は用いるプロテア
ーゼの種類により異なり、そのプロテアーゼの作用pH
域、作用温度域で、大豆蛋白を加水分解するに充分な量
用いることが出来る。用いるプロテアーゼの種類にもよ
るが、通常、pHが6〜10、好ましくはpH7〜9で
あれば中和による塩の生成を軽減できるので、塩分制限
食(例えば、経管栄養食等)の用途に適したものとな
る。
The hydrolysis conditions of the present invention vary depending on the type of protease used, and the pH of the protease
It can be used in an amount sufficient to hydrolyze soybean protein in the temperature range and the working temperature range. Although depending on the type of protease to be used, if the pH is usually 6 to 10, preferably 7 to 9, the generation of salt by neutralization can be reduced, and thus the use of a salt-restricted diet (for example, a tube feeding diet). It becomes suitable for.

【0015】加水分解の程度は、大豆蛋白が分解率(蛋
白成分の15%トリクロロ酢酸可溶率で50〜90%程
度とすることが出来る。プロテアーゼによる加水分解時
間は、使用するプロテアーゼの活性や量によるが、通
常、30分〜24時間程度、好ましくは1〜10時間程
度とすることが出来る。酵素分解時間が長くなり過ぎる
と腐敗することがあるので短時間のほうが好ましい。
The degree of hydrolysis can be set so that the soybean protein is degraded (about 50-90% in terms of the solubility of 15% trichloroacetic acid in the protein component. Although it depends on the amount, it can be generally about 30 minutes to 24 hours, preferably about 1 to 10 hours.

【0016】加水分解した後、加熱処理(通常70〜1
50℃で30分乃至数秒)等して酵素失活することがで
きる。
After hydrolysis, heat treatment (usually 70 to 1)
(30 minutes to several seconds at 50 ° C.) to deactivate the enzyme.

【0017】このようにしてプロテアーゼで加水分解し
て得られる大豆蛋白加水分解物液は、水不溶の高分子成
分を含み、その量は、15%トリクロロ酢酸可溶率50
〜90%程度の酵素分解率のとき、約50〜10%(大
豆蛋白加水分解物中の割合)である。
The soybean protein hydrolyzate solution obtained by hydrolyzing with the protease in this manner contains a water-insoluble polymer component, and the amount thereof is 15% trichloroacetic acid solubility 50%.
When the enzyme degradation rate is about 90%, it is about 50 to 10% (the ratio in the soybean protein hydrolyzate).

【0018】水不溶の高分子成分は、ドデシル硫酸ナト
リウム(SDS)を含むリン酸緩衝液でのゲルろ過で評
価した分子量が約10000であり、脂質、配糖体等の
悪風味成分を含むものである。
The water-insoluble polymer component has a molecular weight of about 10,000 as evaluated by gel filtration using a phosphate buffer containing sodium dodecyl sulfate (SDS), and contains malodorous components such as lipids and glycosides. .

【0019】従来の技術では、この水不溶の高分子成分
を遠心分離等の方法で分離除去していたものを、本発明
においては、かかる水不溶の高分子成分を含んだままの
大豆蛋白加水分解物液を合成吸着剤に50℃〜70℃と
いう特定の温度範囲の条件で接触させるところに特徴が
ある。
In the prior art, the water-insoluble polymer component was separated and removed by a method such as centrifugation. However, in the present invention, the soybean protein hydrolyzate containing the water-insoluble polymer component is removed. It is characterized in that the decomposition product liquid is brought into contact with the synthetic adsorbent under the condition of a specific temperature range of 50 ° C to 70 ° C.

【0020】接触温度が50〜70℃のとき苦味成分、
臭い成分等の悪風味成分を除去でき、50℃以下では吸
着が不十分であり悪風味除去が充分でなく、70℃を越
えると吸着は十分であるが、焦げ味が付くので好ましく
ない。通常、温度が高くなると比例して吸着能は低下す
るものを、かかる特定温度範囲のとき大豆蛋白加水分解
物と合成吸着剤との相互作用が風味改良の点で最適の状
態になるものと推察される。
When the contact temperature is 50 to 70 ° C., a bitter component;
Bad flavor components such as odorous components can be removed. At 50 ° C. or less, adsorption is insufficient, and bad flavor removal is not sufficient. At 70 ° C. or more, adsorption is sufficient, but it is not preferable because it gives a burnt taste. Normally, the adsorption capacity decreases in proportion to the increase in temperature, but it is assumed that the interaction between the soybean protein hydrolyzate and the synthetic adsorbent becomes optimal in terms of flavor improvement in such a specific temperature range. Is done.

【0021】接触する際のpHは、通常は6〜7.5の
範囲が好適である。pHが5以下であると加水分解物中
の水不溶の高分子成分が沈殿し、pHが8より高いと合
成吸着剤による悪風味除去効果が低下する。
The pH at the time of contact is usually preferably in the range of 6 to 7.5. When the pH is 5 or less, the water-insoluble polymer component in the hydrolyzate precipitates. When the pH is higher than 8, the effect of removing the bad taste by the synthetic adsorbent decreases.

【0022】本発明においてかかる15%トリクロル酢
酸可溶率50〜90の大豆蛋白加水分解物溶液を50℃
〜70℃で吸着剤処理する際に用いる吸着剤は合成吸着
剤が適当である。
In the present invention, the soybean protein hydrolyzate solution having a 15% trichloroacetic acid solubility of 50 to 90 is heated to 50 ° C.
As the adsorbent used when the adsorbent is treated at a temperature of up to 70 ° C, a synthetic adsorbent is suitable.

【0023】本発明において合成吸着剤は、芳香族系、
アクリル系の疎水性吸着剤を利用することができる。本
発明に用いる合成吸着剤は、前記のものを用いることが
出来、その細孔分布が約30〜200オングストローム
のものが適当である。
In the present invention, the synthetic adsorbent is aromatic,
Acrylic hydrophobic adsorbents can be used. As the synthetic adsorbent used in the present invention, those described above can be used, and those having a pore distribution of about 30 to 200 angstroms are suitable.

【0024】本発明に用いる合成吸着剤は、より具体的
には、芳香族系としてスチレンジビニルベンゼン系の樹
脂(例えば、HP−20、HP−21、SP−825、
SP−206、SP−207、SP−800(いずれも
商標、三菱化成(株)製)等)、アクリル系の樹脂(H
P1MG、HP2MG(いずれも商標、三菱化成株製)
等)、フェノ−ル系の樹脂(S874、S861(いず
れも商標、住友化学工業(株)製)等)が適当である。
More specifically, the synthetic adsorbent used in the present invention is a styrene-divinylbenzene resin (for example, HP-20, HP-21, SP-825,
SP-206, SP-207, SP-800 (all are trademarks, manufactured by Mitsubishi Kasei Corporation) and the like, acrylic resin (H
P1MG, HP2MG (both trademarks, manufactured by Mitsubishi Kasei Corporation)
Etc.) and phenolic resins (S874, S861 (both are trademarks, manufactured by Sumitomo Chemical Co., Ltd.)) and the like.

【0025】本発明の接触方法は、合成吸着剤と接触さ
せる大豆蛋白加水分解物液が水不溶の高分子成分を含ん
でいる為、バッチ式の処理或いは連続カラムによる処理
でも上流式を利用すると樹脂の目詰りを回避出来好まし
い。。
In the contacting method of the present invention, since the soybean protein hydrolyzate solution to be brought into contact with the synthetic adsorbent contains a water-insoluble polymer component, the batch type treatment or the treatment with a continuous column can be carried out using the upstream method. This is preferable because clogging of the resin can be avoided. .

【0026】例えば、バッチ式で処理する場合には、使
用する合成吸着剤の量を大豆蛋白加水分解物乾燥物重量
の0.1〜2倍重量程度とし、5分〜2時間程度上記温
度範囲内で攪拌した後、水不溶の高分子成分は通過でき
るが樹脂は通過出来ない程度のフィルタ−でろ過するこ
とが出来る。
For example, when treating in a batch system, the amount of the synthetic adsorbent used is about 0.1 to 2 times the weight of the dried soybean protein hydrolyzate and about 5 minutes to 2 hours. After stirring, the mixture can be filtered with a filter that can pass the water-insoluble polymer component but cannot pass the resin.

【0027】又、連続カラムによる方法では、合成吸着
剤1重量部に対して大豆蛋白加水分解物が乾燥物として
0.1〜2重量部となる量の大豆蛋白加水分解物液を通
液し、合成吸着剤との接触時間が5分以上取れる線速度
とすることが出来る。又、合成吸着剤の再生は、0.5
〜3Nの水酸化ナトリウム或いは30〜90%程度の有
機溶剤を用いることが出来、有機溶剤として、エタノー
ル、メタノ−ル、イソプロパノ−ル、アセトン等を、合
成吸着剤量の1〜20倍容量程度用いることが出来る。
In the method using a continuous column, a soybean protein hydrolyzate solution is passed through in an amount of 0.1 to 2 parts by weight as a dry matter of the soybean protein hydrolyzate per 1 part by weight of the synthetic adsorbent. And a linear velocity at which a contact time with the synthetic adsorbent can be taken for 5 minutes or more. The regeneration of the synthetic adsorbent is 0.5
Sodium hydroxide of about 3N or an organic solvent of about 30 to 90% can be used. As the organic solvent, ethanol, methanol, isopropanol, acetone or the like is used, and about 1 to 20 times the volume of the synthetic adsorbent. Can be used.

【0028】以上のようにして得られた大豆蛋白ペプチ
ド混合物液は、用途によりそのまま或いは濃縮して用い
ることも出来るが、通常、殺菌して粉霧乾燥、凍結乾燥
等して乾燥粉末の状態で利用することができる。
The soybean protein peptide mixture solution obtained as described above can be used as it is or in a concentrated form depending on the application. However, it is usually sterilized and then dried in a dry powder state by powder drying, freeze drying or the like. Can be used.

【0029】[0029]

【実施例】以下、実施例により発明の実施様態を説明す
る。 実施例1 分離大豆蛋白(不二製油(株)製、「ニュ−フジプロ−
R」)10kgをpH7の9%水溶液とし、エンドプロテ
ア−ゼを含有する蛋白分解酵素(大和化成株(株)製、
「プロチンAC−10」)400gを作用させ50℃で
5時間加水分解(15%TCA可溶率75%)した後、
80℃で30分間加熱して酵素失活させた。この溶液を
「A液」とする。
The embodiments of the present invention will be described below with reference to examples. Example 1 Isolated soybean protein (manufactured by Fuji Oil Co., Ltd., "New Fuji Pro-
R ") 10 kg of a 9% aqueous solution of pH 7 and a protease containing endoprotease (manufactured by Daiwa Kasei Co., Ltd .;
400 g of “protin AC-10”) was allowed to act thereon, and the mixture was hydrolyzed at 50 ° C. for 5 hours (15% TCA solubility: 75%).
The enzyme was inactivated by heating at 80 ° C. for 30 minutes. This solution is referred to as “Solution A”.

【0030】このA液を一部取り、凍結乾燥し、大豆ペ
プチド混合物を得た。この大豆ペプチド混合物をコント
ロールとして「ペプチドA」とした。A液10kg(固形
分9%)を取り、合成吸着剤(三菱化成(株)製、「S
P−207」)を0.9L(固形分割合約70%)添加
し液温65℃で1時間攪拌し、悪風味成分を吸着させた
後、100メッシュのステンレスフィルタ−でろ過し
て、樹脂を取り除いた。このろ液を凍結乾燥して大豆ペ
プチド混合物780gを得た。この大豆ペプチド混合物
を「ペプチドB」とした。
A part of the solution A was taken and freeze-dried to obtain a soybean peptide mixture. This soybean peptide mixture was designated as “peptide A” as a control. Take 10 kg (solid content 9%) of solution A and use a synthetic adsorbent (Mitsubishi Kasei Co., Ltd., "S
P-207 ") was added at 0.9 L (solid content ratio: about 70%), and the mixture was stirred at a liquid temperature of 65 ° C. for 1 hour to adsorb the bad taste component. Removed. This filtrate was freeze-dried to obtain 780 g of a soy peptide mixture. This soy peptide mixture was designated as “peptide B”.

【0031】実施例2 実施例1と同様にして得られたA液1.1kgを65℃に
加温して合成吸着剤(三菱化成(株)製、「HP−2
1」)200立方cm(固形分割合約70%)を詰めたカ
ラム(30mm径×600mm高)にLV=0.3m/hの
条件で通液し、悪風味成分を吸着させた。得られた溶出
液を「B液」とする。B液を凍結乾燥して大豆ペプチド
混合物75gを得た。この大豆ペプチド混合物を「ペプ
チドC」とした。
Example 2 1.1 kg of solution A obtained in the same manner as in Example 1 was heated to 65 ° C., and a synthetic adsorbent (“HP-2” manufactured by Mitsubishi Kasei KK) was used.
1)) The solution was passed through a column (30 mm diameter x 600 mm height) packed with 200 cubic cm (solid content ratio: about 70%) under the condition of LV = 0.3 m / h to adsorb bad flavor components. The obtained eluate is referred to as “Solution B”. The solution B was freeze-dried to obtain 75 g of a soy peptide mixture. This soy peptide mixture was designated as “peptide C”.

【0032】実施例3 分離大豆蛋白(不二製油(株)製、「ニュ−フジプロ−
R」)10kgをpH7の9%水溶液とし、エンドプロテ
ア−ゼを含有する蛋白分解酵素(大和化成(株)製、
「プロチンAC−10」)300gとエンドプロテア−
ゼとエキソプロテア−ゼを含有する蛋白分解酵素(天野
製薬株製、プロテア−ゼA)100gを作用させ50℃
で5時間加水分解(15%TCA可溶率85%)した
後、80℃で30分間加熱して酵素失活させた。この溶
液を「C液」とした。
Example 3 Isolated soybean protein (manufactured by Fuji Oil Co., Ltd., "New Fuji Pro-
R ") is a 9% aqueous solution having a pH of 7 and a protease containing endoprotease (manufactured by Daiwa Kasei Co., Ltd.)
"Protin AC-10") 300g and endoprotea-
100 g of a protease (protease A, manufactured by Amano Pharmaceutical Co., Ltd.) containing the enzyme and exoprotease was allowed to act at 50 ° C.
For 5 hours (85% of 15% TCA solubility), and then heated at 80 ° C. for 30 minutes to inactivate the enzyme. This solution was designated as “solution C”.

【0033】このC液を一部取り、凍結乾燥し、大豆ペ
プチド混合物を得た。この大豆ペプチド混合物を「ペプ
チドD」とした。C液50kg(固形分9%)を取り、合
成吸着剤(三菱化成(株)製、「HP−1MG」)を
9.0L(固形分割合約70%)添加し液温60℃で3
0分間攪拌し、悪風味成分を吸着させた後、100メッ
シュのステンレスフィルタ−でろ過して、樹脂を取り除
いた。この液を凍結乾燥してペプチド混合物3.9kgを
得た。このペプチド混合物を「ペプチドE」とした。
A part of the solution C was taken and freeze-dried to obtain a soybean peptide mixture. This soy peptide mixture was designated as “peptide D”. Take 50 kg (solid content 9%) of Liquid C, add 9.0 L (solid content ratio about 70%) of a synthetic adsorbent ("HP-1MG", manufactured by Mitsubishi Kasei Co., Ltd.) and add 3 L at a liquid temperature of 60 ° C.
After stirring for 0 minutes to adsorb the bad flavor components, the mixture was filtered through a 100-mesh stainless steel filter to remove the resin. This solution was freeze-dried to obtain 3.9 kg of the peptide mixture. This peptide mixture was designated as “peptide E”.

【0034】実施例4 実施例3と同様にして得られたC液4.4kgを70℃に
加温して合成吸着剤(三菱化成(株)製、「SP−20
6」)200立方cm(固形分割合約70%)を詰めたカ
ラム(30mm径×600mm高)にLV=3.6m/hの
条件で通液し、悪風味成分を吸着させた。得られた溶出
液を「D液」とした。D液を凍結乾燥して大豆ペプチド
混合物360gを得た。この大豆ペプチド混合物を「ペ
プチドF」とした。
Example 4 4.4 kg of the C solution obtained in the same manner as in Example 3 was heated to 70 ° C., and a synthetic adsorbent (“SP-20” manufactured by Mitsubishi Kasei Co., Ltd.) was used.
6 ") The solution was passed through a column (30 mm diameter x 600 mm height) packed with 200 cubic cm (solid content ratio: about 70%) under the condition of LV = 3.6 m / h to adsorb the bad flavor components. The obtained eluate was designated as "solution D". The solution D was freeze-dried to obtain 360 g of a soy peptide mixture. This soy peptide mixture was designated as “peptide F”.

【0035】比較例1 実施例1と同様にして得られたA液10kgに合成吸着剤
(三菱化成(株)製、「SP−207」)を0.9L
(固形分割合約 %)添加し液温15℃で1時間攪拌
し、悪風味成分を吸着させた後、100メッシュのステ
ンレスフィルタ−でろ過して、樹脂を取り除いた。この
液を凍結乾燥して大豆ペプチド混合物850gを得た。
この大豆ペプチド混合物を「ペプチドG」とした。
Comparative Example 1 0.9 L of a synthetic adsorbent ("SP-207", manufactured by Mitsubishi Kasei Co., Ltd.) was added to 10 kg of Solution A obtained in the same manner as in Example 1.
The mixture was stirred at a liquid temperature of 15 ° C. for 1 hour to adsorb bad flavor components, and then filtered through a 100-mesh stainless steel filter to remove the resin. This solution was freeze-dried to obtain 850 g of a soy peptide mixture.
This soybean peptide mixture was designated as “peptide G”.

【0036】比較例2 実施例1と同様にして得られたA液10kgに合成吸着剤
(三菱化成(株)製、「SP−207」)を0.9L
(固形分割合約70%)添加し液温85℃で30分間攪
拌し、悪風味成分を吸着させた後、100メッシュのス
テンレスフィルタ−でろ過して、樹脂を取り除いた。こ
の液を凍結乾燥して大豆ペプチド混合物780gを得
た。この大豆ペプチド混合物を「ペプチドH」とした。
Comparative Example 2 0.9 L of a synthetic adsorbent ("SP-207" manufactured by Mitsubishi Kasei Co., Ltd.) was added to 10 kg of Solution A obtained in the same manner as in Example 1.
(A solid content ratio of about 70%) was added, and the mixture was stirred at a liquid temperature of 85 ° C. for 30 minutes to adsorb bad flavor components, and then filtered through a 100-mesh stainless steel filter to remove the resin. This solution was freeze-dried to obtain 780 g of a soybean peptide mixture. This soy peptide mixture was designated as “peptide H”.

【0037】比較例3 実施例1と同様にして得られたA液10kgを遠心分離機
((株)日立工作機製、「SCR20B」、ロ−タ−,
「RPR9−2」)にかけ、水不溶の高分子成分を分離
除去した。得られた上澄み(固形分600g)に合成吸
着剤(三菱化成(株)製、「SP−207」)を0.6
L添加し液温15℃で1時間攪拌し、悪風味成分を吸着
させた後、100メッシュのステンレスフィルタ−でろ
過して、樹脂を取り除いた。この液を凍結乾燥して大豆
ペプチド混合物780gを得た。この大豆ペプチド混合
物を「ペプチドI」とした。
Comparative Example 3 10 kg of the solution A obtained in the same manner as in Example 1 was centrifuged (SCR20B, manufactured by Hitachi Koki Co., Ltd., rotor,
"RPR9-2") to separate and remove water-insoluble polymer components. The obtained supernatant (solid content: 600 g) was mixed with a synthetic adsorbent ("SP-207", manufactured by Mitsubishi Kasei Corporation) for 0.6 minute.
L was added, and the mixture was stirred at a liquid temperature of 15 ° C. for 1 hour to adsorb a bad flavor component, and then filtered through a 100-mesh stainless steel filter to remove the resin. This solution was freeze-dried to obtain 780 g of a soybean peptide mixture. This soy peptide mixture was designated as “peptide I”.

【0038】実験例1 前述実施例及び比較例と同様にして得たペプチドA〜H
を5%水溶液とし、10人のパネラーにより風味評価を
行った。結果を下記表1に示す。
Experimental Example 1 Peptides A to H obtained in the same manner as in the above Examples and Comparative Examples
Was made into a 5% aqueous solution, and the flavor was evaluated by 10 panelists. The results are shown in Table 1 below.

【0039】[0039]

【表1】 [Table 1]

【0040】以上のように、実施例1〜4と同様にして
得られたペプチドB、C、E、Fはコントロールである
ペプチドA,Dや比較例のペプチドG、H、Iに比べて
風味の優れた大豆ペプチド混合物とすることが出来た。
As described above, peptides B, C, E, and F obtained in the same manner as in Examples 1 to 4 are more flavorful than peptides A, D as controls and peptides G, H, and I as comparative examples. The soy peptide mixture was excellent in the above.

【0041】比較例1,2と同様にして得えられたペプ
チドG、Hは、苦味が強かったり、焦げ味が生じたりし
て風味の悪いものであった。又、比較例3と同様にして
得られたペプチドIは、風味が優れるものの次記表2に
示すように歩留まりの悪い方法であり、工業上の生産に
はコストがかかる欠点がある。これは、比較例3の方法
は酵素分解した後生じる水不溶成分を分離除去したため
である。尚、表2にはペプチドB、ペプチドG及びペプ
チドIを比較して示す。
Peptides G and H obtained in the same manner as in Comparative Examples 1 and 2 had a bad taste due to strong bitterness and burning. Peptide I obtained in the same manner as in Comparative Example 3 has a good taste, but has a low yield as shown in Table 2 below, and has a disadvantage in that industrial production is costly. This is because the water-insoluble component generated after the enzymatic decomposition was separated and removed in the method of Comparative Example 3. Table 2 shows a comparison of peptide B, peptide G and peptide I.

【0042】[0042]

【表2】 [Table 2]

【0043】以上より、ペプチドBは歩留まりも風味も
優れていたが、ペプチドGは歩留まりは優れても風味が
悪く、ペプチドIは風味は優れていても歩留まりが悪い
ものであった。
As described above, peptide B was excellent in yield and flavor, but peptide G was excellent in yield but bad in taste, and peptide I was excellent in flavor but poor in yield.

【0044】[0044]

【発明の効果】以上説明したように、本発明の方法によ
り風味に優れた大豆ペプチド混合物を高歩留まりで製造
出来るようになったものである。
As described above, according to the method of the present invention, a soybean peptide mixture having excellent flavor can be produced at a high yield.

【0045】その他の効果としては、従来の低温域での
樹脂との接触方法に比べ合成吸着剤への吸着量が増加
し、その結果、従来より少ない合成吸着剤量で風味良好
な大豆ペプチド混合物を得ることができるようにまっ
た。
Another effect is that the amount of adsorption to the synthetic adsorbent is increased as compared with the conventional method of contacting with a resin in a low temperature range. Can be obtained.

【0046】さらに、従来法で必要であった水不溶の高
分子成分の遠心分離等による除去工程が不要な工程が可
能になり、歩留りの向上と併せて経済的な製造方法が可
能になり、安価に風味良好な大豆ペプチド混合物の製造
が可能になったものである。
Furthermore, a step that does not require a step of removing water-insoluble polymer components by centrifugation or the like, which is required in the conventional method, becomes possible, and an economical production method becomes possible in addition to an improvement in yield. This makes it possible to produce a soybean peptide mixture having a good taste at low cost.

───────────────────────────────────────────────────── フロントページの続き (58)調査した分野(Int.Cl.7,DB名) A23J 3/00 - 3/34 C07K 1/22 ──────────────────────────────────────────────────続 き Continued on the front page (58) Fields surveyed (Int. Cl. 7 , DB name) A23J 3/00-3/34 C07K 1/22

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】15%トリクロル酢酸可溶率50〜90の
大豆蛋白加水分解物溶液を50℃〜70℃で芳香族系、
アクリル系の疎水性吸着剤で処理することを特徴とする
大豆ペプチド混合物の製造法。
A soybean protein hydrolyzate solution having a solubility of 50% to 90% of 15% trichloroacetic acid in an aromatic system at 50 ° C to 70 ° C.
A method for producing a soybean peptide mixture, wherein the mixture is treated with an acrylic hydrophobic adsorbent .
JP06259094A 1994-03-31 1994-03-31 Method for producing soy peptide mixture Expired - Fee Related JP3158849B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
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Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
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Publications (2)

Publication Number Publication Date
JPH07264993A JPH07264993A (en) 1995-10-17
JP3158849B2 true JP3158849B2 (en) 2001-04-23

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Country Link
JP (1) JP3158849B2 (en)

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* Cited by examiner, † Cited by third party
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JP4678619B2 (en) * 1999-06-30 2011-04-27 武田薬品工業株式会社 Method for purifying LH-RH derivatives
CN1239513C (en) * 2000-03-13 2006-02-01 森永乳业株式会社 Protein hydrolyzates, process for producing the same and drinks and foods containing protein hydrolyzates
WO2004103391A1 (en) * 2003-05-22 2004-12-02 Fuji Oil Company, Limited Hepatic lipid metabolism accelerating agent, hepatic lipid metabolism accelerating health food and process for producing peptide mixture as active ingredient thereof
CN100338224C (en) * 2004-04-01 2007-09-19 广西大学 Method for preparing peptide of soybean through continuous enzyme membrane reaction of soyabean protein
CN101124314A (en) * 2004-12-21 2008-02-13 不二制油株式会社 Method of producing beers and soybean peptide for producing beers
JPWO2012115144A1 (en) * 2011-02-22 2014-07-07 三菱化学フーズ株式会社 Oil-in-water emulsion, oil-in-water foam-containing emulsion and enzyme-degraded milk protein mixture
CN102511648A (en) * 2011-12-28 2012-06-27 天津滨海诺奥酶工程技术有限公司 Method for producing soybean polypeptide powder
CN106455625B (en) * 2015-04-30 2020-02-07 中国食品发酵工业研究院 Hypoallergenic low-bitter soybean oligopeptide and preparation method and application thereof

Also Published As

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