JPH0533719B2 - - Google Patents

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Publication number
JPH0533719B2
JPH0533719B2 JP60149334A JP14933485A JPH0533719B2 JP H0533719 B2 JPH0533719 B2 JP H0533719B2 JP 60149334 A JP60149334 A JP 60149334A JP 14933485 A JP14933485 A JP 14933485A JP H0533719 B2 JPH0533719 B2 JP H0533719B2
Authority
JP
Japan
Prior art keywords
egg white
decomposition product
peptides
molecular weight
liquid
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
JP60149334A
Other languages
Japanese (ja)
Other versions
JPS6212727A (en
Inventor
Masato Shimohashi
Mineo Hasegawa
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.)
Kewpie Corp
Original Assignee
QP Corp
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 QP Corp filed Critical QP Corp
Priority to JP60149334A priority Critical patent/JPS6212727A/en
Publication of JPS6212727A publication Critical patent/JPS6212727A/en
Publication of JPH0533719B2 publication Critical patent/JPH0533719B2/ja
Granted legal-status Critical Current

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/64Proteins; Peptides; Derivatives or degradation products thereof

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Epidemiology (AREA)
  • Birds (AREA)
  • Dermatology (AREA)
  • Cosmetics (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)
  • Peptides Or Proteins (AREA)
  • Coloring Foods And Improving Nutritive Qualities (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

〔産業上の利用分野〕 本発明は化粧料の基材や医薬品の原料に適した
卵白分解物及びその製法に関する。 〔従来の技術〕 従来から、卵白分解物を化粧料の基材等に用い
る試みがなされており、この種の卵白分解物を得
るには、特公昭50−15851号や同57−45560号の提
案にあるように、予め酸性域に調整した卵白液を
1回だけプロテアーゼ処理する方法が採用されて
いる。 しかしながら、上記従来法によると、プロテア
ーゼ処理に使用する蛋白分解酵素は卵白の蛋白質
のペプタイドの鎖を無秩序に切断してしまう性質
があるため、得られた卵白分解物中には分子量が
1500を越えるような高分子量のペプタイドから、
アミノ酸のような低分子分解物まで含まれてお
り、その上、皮ふへの吸着性や消化・吸収性に優
れた分子量200〜400のペプタイドの占める割合が
非常に低いという問題があつた。 〔発明が解決しようとする問題点〕 したがつて、従来の卵白分解物は、化粧料の基
材や医薬品の原料には適していないという問題が
あつた。 本発明者等は、化粧料の基材や医薬原料に適し
た卵白分解物を得んと種々研究を重ねた結果、卵
白液を予めアルカリ域に調整し、これを2回プロ
テアーゼ処理するば所期の目的のものが得られる
との知見を得、この知見に基づき本発明を完成さ
せたものである。 〔問題点を解決するための手段〕 本発明は卵白分解物及びその製法に関し、本発
明の卵白分解物は、分子量1300以下のペプタイド
からなり、そのペプタイド全量に対して分子量
200〜400のペプタイドが60%以上を占めることを
特徴とし、また、本発明の卵白分解物の製法を予
め、PHをアルカリ域に調整した卵白液をプロテア
ーゼ処理して粗卵白分解物を得、この分解物を再
びプロテアーゼ処理した後、これを加熱処理し、
加熱により生じた固形物を除去し、分子量1300以
下のペプタイドからなり、そのペプタイド全量に
対して分子量200〜400のペプタイドが60%以上占
める卵白分解物を得ることを特徴とするものであ
る。 以下、本発明の卵白分解物とその製法について
詳細に説明する。 本発明の卵白分解物を得るに、まず、原料の卵
白液を用意する。この卵白液は、鶏卵等を割卵
し、卵黄を分離して得られる生状のもののほか、
冷凍状卵白を解凍したもの、乾燥状卵白を水に溶
解したもの或いはリゾチームを除去した卵白液で
あつても差し支えない。尚、卵白液中に卵黄分の
混入量が多いと、目的の卵白分解物が得にくくな
るので、卵黄分の混入が少ない卵白液を用いるこ
とが望ましい。 次に、卵白液に苛性ソーダ・苛性カリ等のアル
カリ剤を添加し、卵白液をアルカリ域に調整す
る。卵白液のPH後の試験例にも示すように、8.0
〜9.5の範囲内に調整すると分子量200〜400のペ
プタイドの含量が多い卵白分解物を得ることがで
きる。尚、使用する卵白液がはじめから所定のア
ルカリ域にあるときは、PHの調整をする必要はな
い。また、卵白液中には糖分が含まれているの
で、糖分が含まれない卵白分解物を製造したいと
きは、アルカリ調整工程の前に、卵白液を脱糖処
理しておくとよい。 次に、アルカリ域に調整した卵白液に蛋白
(質)分解酵素を添加し、一定温度条件下に一定
時保持してプロテアーゼ処理し、粗製の卵白分解
物を得る。この処理で用いる蛋白分解酵素として
は、パパイン・フイシン・プロメライン・ペプシ
ン等の、動・植物組織からの抽出酵素のほか、微
生物由来の酵素、例えば「アマノA」・「アマノ
P」(商品名;天野製薬(株)製)、デナチームAP(商
品名;長瀬産業(株)製)、ネオビタラーゼNP(商品
名;東和酵素(株)製)又はプロリシン5(商品名;
上田化学工業(株)製)等、種類を問わず使用するこ
とができる。蛋白分解酵素の添加量は、使用する
酵素の種類にもよるが、卵白液に対して0.1〜1.0
%が適当である。また、プロテアーゼ処理の温度
と時間は45〜55℃で20〜50時間の範囲が適当であ
る。 この1回目のプロテアーゼ処理により、卵白液
中に含まれている蛋白質が分解されることになる
が、卵白液のPHをアルカリ域に調整しているため
か蛋白質比較的分子量の大きなペプタイドに分解
される。そして、このプロテアーゼ処理によつて
粗卵白分解物が得られる。 次に、得られた粗卵白分解物に蛋白分解酵素を
添加し、再びプロテアーゼ処理を行う。使用する
蛋白分解酵素の種類・その添加量及びプロテアー
ゼ処理の条件(温度・時間)は、1回目のプロテ
アーゼ処理の場合と同じでよい。 この2回目のプロテアーゼ処理により、粗卵白
分解物中に含まれている比較的分子量の大きなペ
プタイドは、後の試験例にも示すように低分子量
のペプタイドに分解される。 最後に、このプロテアーゼ処理液を90〜100℃
で5〜20分間程度加熱処理し、液中に含まれてい
るリゾチーム等の蛋白分解酵素によつては分解さ
れにくい蛋白質を熱凝固させて、液中に固形物を
生じさせた後、この固形物を液から除去すれば、
卵白分解物を得ることができる。固形物の除去に
は、デカンター法や遠心分離法を採用するとよ
い。 このようにして得られた卵白分解物は、透明で
かつ無臭の液体であるが、常温に放置すると腐敗
しやすいため、保存に当つては−15℃以下に冷凍
することが望ましい。尚、この卵白分解物はスプ
レードライ法等により乾燥して粉末状に仕上げる
ことができ、このようにすれば、腐敗する心配が
ないので取扱い上便利である。 〔実施例〕 卵白液100Kgをタンクに投入し、これにイース
ト130gを添加し、卵液を35℃に保持し、ゆつく
り撹拌しながら4時間脱糖処理をした。 得られた脱糖卵白液を30r・p・mの速度で撹
拌しながら、卵液に10%苛性ソーダ水溶液1Kgを
少量ずつ添加して卵液のPHを9.0に調整した。 次に、このようにして得られた卵液にフイシン
120gと微生物由来酵素(天野製薬(株)製;商品名
「アマノP」)100gを添加した後、卵液を50℃に
保持し、ゆつくり撹拌しながら24時間プロテアー
ゼ処理を行なつた後、更にパパイン(前記のもの
と同じ)120gと微生物由来酵素(前記のものと
同じ)100gを加え、前記と同様に24時間酵素処
理を行なつた。 次に、酵素処理が終了した卵液をニーダーにて
97℃で10分間加熱した後、常温(20℃)に冷却
し、而る後、この加熱処理で生じた凝固物を固液
分離装置で取り除いた。 最後に、得られた卵液を加圧液(東洋紙No.
26を使用)した後、液をスプレードライヤーに
て乾燥したところ、粉末状の卵白分解物9.1Kgを
得ることができた。 〔作 用〕 以下、試験例を示し、本発明に係る卵白分解物
の特性を述べる。 試験例 1 次の4種の粉末状卵白分解物のサンプルを用意
した。 (1) テスト区(アルカリ調整、プロテアーゼ2回
処理) 上述の実施例で得られたもの (2) 対照区1(アルカリ調整、プロテアーゼ1回
処理) プロテアーゼ処理を1回で止め、2回目の処
理を省略したほかは、実施例と同じ方法で得ら
れたもの、 (3) 対照区2(酸調整、プロテアーゼ2回処理) 脱糖卵白液に20%クエン酸水溶液6Kgを添加
して卵液のPHを4.0としたほかは、実施例と同
じ方法で得られたもの (4) 対照区3(酸調整、プロテアーゼ1回処理) 脱糖卵白液に20%クエン液水溶液6Kgを添加
して卵液のPHを4.0とし、プロテアーゼ処理を
1回でやめ、2回目の処理を省略したほかは、
実施例と同じ方法で得られたもの この4種のサンプル0.1gずつをそれぞれ清水
3mlに溶解させ、ゲル過(フアルマシア社製;
商品名「セフアデツクスG−10及びG15」を使
用)を行ない、OD280nmの光の吸光度から分子
量の分布を求め、また原料卵白液100Kgからの収
量を測定したところ、表−1の結果が得られた。
[Industrial Application Field] The present invention relates to an egg white decomposition product suitable as a base material for cosmetics and a raw material for pharmaceuticals, and a method for producing the same. [Prior art] Previously, attempts have been made to use egg white decomposition products as base materials for cosmetics, etc., and in order to obtain this type of egg white decomposition products, the methods described in Japanese Patent Publication No. 50-15851 and No. 57-45560 have been made. As proposed, a method is adopted in which egg white liquid, which has been adjusted to an acidic range in advance, is treated with protease only once. However, according to the above conventional method, the proteolytic enzyme used for protease treatment has the property of randomly cleaving the peptide chains of egg white proteins, so the resulting egg white decomposition product has a low molecular weight.
From high molecular weight peptides exceeding 1500,
The problem was that it contained even low-molecular decomposition products such as amino acids, and the proportion of peptides with a molecular weight of 200 to 400, which have excellent adsorption to the skin and excellent digestibility and absorption, was extremely low. [Problems to be Solved by the Invention] Therefore, there was a problem in that the conventional egg white decomposition product was not suitable as a base material for cosmetics or a raw material for pharmaceuticals. As a result of various studies aimed at obtaining an egg white decomposition product suitable for cosmetic base materials and pharmaceutical raw materials, the inventors of the present invention discovered that egg white liquid should be adjusted to an alkaline range in advance and then treated with protease twice. Based on this knowledge, the present invention was completed based on this knowledge. [Means for Solving the Problems] The present invention relates to an egg white decomposition product and a method for producing the same.
It is characterized in that 200 to 400 peptides account for 60% or more, and the method for producing an egg white decomposition product of the present invention includes obtaining a crude egg white decomposition product by treating an egg white liquid whose pH has been adjusted to an alkaline range with protease, After this decomposition product is treated with protease again, it is heated,
The method is characterized in that solid matter generated by heating is removed to obtain an egg white decomposition product consisting of peptides with a molecular weight of 1300 or less, in which peptides with a molecular weight of 200 to 400 account for 60% or more of the total amount of peptides. Hereinafter, the egg white decomposition product of the present invention and its production method will be explained in detail. To obtain the egg white decomposition product of the present invention, first, an egg white liquid as a raw material is prepared. This egg white liquid is available in raw form, which is obtained by breaking chicken eggs and separating the yolk, as well as
It may be thawed frozen egg white, dried egg white dissolved in water, or egg white liquid from which lysozyme has been removed. Note that if there is a large amount of egg yolk mixed into the egg white liquid, it will be difficult to obtain the desired egg white decomposition product, so it is desirable to use an egg white liquid with a small amount of egg yolk mixed in. Next, an alkaline agent such as caustic soda or caustic potash is added to the egg white liquid to adjust the egg white liquid to an alkaline range. As shown in the test example after PH of egg white liquid, 8.0
When adjusted within the range of ~9.5, an egg white decomposition product containing a high content of peptides with a molecular weight of 200 to 400 can be obtained. It should be noted that if the egg white solution used is already in the predetermined alkaline range, there is no need to adjust the pH. Furthermore, since egg white liquid contains sugar, if it is desired to produce an egg white decomposition product that does not contain sugar, it is advisable to desugarize the egg white liquid before the alkali adjustment step. Next, a proteolytic enzyme is added to the egg white liquid adjusted to an alkaline range, and the mixture is maintained at a constant temperature for a certain period of time to be treated with a protease to obtain a crude egg white decomposition product. The proteolytic enzymes used in this treatment include enzymes extracted from animal and plant tissues, such as papain, fuicin, promelain, and pepsin, as well as enzymes derived from microorganisms, such as "Amano A" and "Amano P" (trade name). manufactured by Amano Pharmaceutical Co., Ltd.), Denazyme AP (trade name; manufactured by Nagase Sangyo Co., Ltd.), Neovitalase NP (trade name; manufactured by Towa Koso Co., Ltd.), or Prolysin 5 (trade name;
(manufactured by Ueda Chemical Industry Co., Ltd.), etc., any type can be used. The amount of protease added depends on the type of enzyme used, but it is 0.1 to 1.0 to the egg white liquid.
% is appropriate. Further, the temperature and time of the protease treatment are suitably in the range of 45 to 55°C for 20 to 50 hours. This first protease treatment breaks down the proteins contained in the egg white liquid, but perhaps because the pH of the egg white liquid is adjusted to an alkaline range, the proteins are broken down into peptides with relatively large molecular weights. Ru. A crude egg white decomposition product is obtained by this protease treatment. Next, a protease is added to the obtained crude egg white decomposition product, and the protease treatment is performed again. The type of protease used, the amount added, and the conditions for protease treatment (temperature and time) may be the same as in the first protease treatment. By this second protease treatment, the relatively large molecular weight peptides contained in the crude egg white decomposition product are decomposed into low molecular weight peptides, as will be shown in later test examples. Finally, heat this protease treatment solution to 90-100℃.
After heat treatment for about 5 to 20 minutes to coagulate proteins that are difficult to decompose by proteolytic enzymes such as lysozyme contained in the liquid and form solids in the liquid, this solid If you remove something from the liquid,
Egg white decomposition product can be obtained. A decanter method or a centrifugation method may be used to remove solids. The egg white decomposition product obtained in this way is a transparent and odorless liquid, but it is easily putrefied if left at room temperature, so it is preferable to freeze it at -15°C or lower for storage. Note that this egg white decomposition product can be dried into a powder form by spray drying or the like, and in this way, there is no risk of spoilage and it is convenient to handle. [Example] 100 kg of egg white liquid was put into a tank, 130 g of yeast was added thereto, and the egg white liquid was kept at 35°C and subjected to a desugar treatment for 4 hours with gentle stirring. While stirring the resulting desugared egg white solution at a speed of 30 r.p.m., 1 kg of a 10% aqueous solution of caustic soda was added little by little to the egg solution to adjust the pH of the egg solution to 9.0. Next, add hydrin to the egg liquid obtained in this way.
After adding 120g and 100g of microorganism-derived enzyme (manufactured by Amano Pharmaceutical Co., Ltd.; trade name "Amano P"), the egg solution was kept at 50°C and subjected to protease treatment for 24 hours with gentle stirring. Further, 120 g of papain (same as above) and 100 g of microbial enzyme (same as above) were added, and enzymatic treatment was carried out for 24 hours in the same manner as above. Next, the egg liquid that has undergone enzyme treatment is placed in a kneader.
After heating at 97°C for 10 minutes, it was cooled to room temperature (20°C), and then the solidified matter produced during this heating treatment was removed using a solid-liquid separator. Finally, add the obtained egg liquid to a pressurized liquid (Toyo Paper No.
After drying the solution using a spray dryer, 9.1 kg of powdered egg white decomposition product was obtained. [Function] Hereinafter, test examples will be shown and the characteristics of the egg white decomposition product according to the present invention will be described. Test Example 1 The following four samples of powdered egg white decomposition products were prepared. (1) Test group (alkaline adjustment, protease treatment twice) What was obtained in the above example (2) Control group 1 (alkaline adjustment, protease treatment once) Protease treatment was stopped after one time, and second treatment (3) Control group 2 (acid adjustment, protease treatment twice) 6 kg of 20% citric acid aqueous solution was added to the desugarized egg white liquid to make the egg liquid. Obtained in the same manner as in the example except that the pH was set to 4.0 (4) Control group 3 (acid adjustment, protease treatment once) Added 6 kg of 20% citric solution to the desugarized egg white liquid to make egg liquid. The pH of the sample was set to 4.0, the protease treatment was stopped after one treatment, and the second treatment was omitted.
Obtained by the same method as in the example. 0.1 g each of these four types of samples were dissolved in 3 ml of clear water, and gel filtration (manufactured by Pharmacia;
The molecular weight distribution was determined from the absorbance of light at OD280nm, and the yield from 100 kg of raw egg white liquid was measured, and the results shown in Table 1 were obtained. .

【表】 尚、表中の%の数値はサンプル中に含まれてい
る蛋白分解物全量に対しての含有量を示す。 試験例 2 卵白液100Kgをタンクに投入し、これにイース
ト130gを添加し、卵液を35℃に保持し、ゆつく
り攪拌しながら4時間脱糖した。 次にこの脱糖卵白液を5等分し、それぞれの卵
液に10%苛性ソーダ水溶液を添加して、表−2に
示すPHの異なる5種類の卵液を得た。 得られた5種類の卵液について、それぞれ実施
例を同じ処理を行ない5種類の粉末状の卵白分解
物を得た。 この卵白分解物について試験例1と同じテスト
を行つたところ、表−2の結果が得られた。
[Table] The % values in the table indicate the content relative to the total amount of protein decomposition products contained in the sample. Test Example 2 100 kg of egg white liquid was put into a tank, 130 g of yeast was added thereto, and the egg white liquid was maintained at 35°C and desugarized for 4 hours with gentle stirring. Next, this desugarized egg white liquid was divided into five equal parts, and a 10% caustic soda aqueous solution was added to each of the egg liquids to obtain five types of egg liquids with different pH values as shown in Table 2. The five types of egg fluid obtained were subjected to the same treatment as in the example to obtain five types of powdered egg white decomposition products. When this egg white decomposition product was subjected to the same test as Test Example 1, the results shown in Table 2 were obtained.

〔発明の効果〕〔Effect of the invention〕

以上述べたように本発明によれば、分子量200
〜400のペプタイドの含有割合の高い新規な卵白
分解物を得ることができる。また、本発明の卵白
分解物の製法によれば、ペプタイド全量に対して
分子量200〜400のペプタイドが60%以上を占める
卵白分解物を好適に得ることができる。 そして、この卵白分解物は、溶液状態では透明
でかつ吸着性がよいため化粧料の基材に適してい
る。また、低分子のペプタイドの含有量が多いた
め、消化・吸収性がよく、経腸・経管栄養剤等の
医薬品・食品の原料にも使用できる。
As described above, according to the present invention, the molecular weight is 200
A novel egg white decomposition product containing a high content of ~400 peptides can be obtained. Further, according to the method for producing an egg white decomposition product of the present invention, an egg white decomposition product in which peptides having a molecular weight of 200 to 400 account for 60% or more of the total amount of peptides can be suitably obtained. Since this egg white decomposition product is transparent in a solution state and has good adsorption properties, it is suitable as a base material for cosmetics. In addition, because it contains a large amount of low-molecular peptides, it has good digestibility and absorption, and can be used as a raw material for pharmaceuticals and foods such as enteral and tube nutrition.

Claims (1)

【特許請求の範囲】 1 分子量1300以下のペプタイドからなり、その
ペプタイド全量に対して分子量200〜400のペプタ
イドが60%以上を占めることを特徴とする卵白分
解物。 2 予め、PHをアルカリ域に調製した卵白液をプ
ロテアーゼ処理して粗卵白分解物を得、この分解
物を再びプロテアーゼ処理した後、これを加熱処
理し、加熱により生じた固形物を除去し、分子量
1300以下のペプタイドからなり、そのペプタイド
全量に対して分子量200〜400のペプタイドが60%
以上を占める卵白分解物を得ることを特徴とする
卵白分解物の製法。 3 予め、PHを8.0〜9.5に調整した卵白液を用い
ることとした特許請求の範囲第2項記載の卵白分
解物の製法。
[Scope of Claims] 1. An egg white decomposition product comprising peptides with a molecular weight of 1300 or less, in which peptides with a molecular weight of 200 to 400 account for 60% or more of the total amount of peptides. 2. A crude egg white decomposition product is obtained by treating an egg white liquid whose pH has been adjusted to an alkaline range in advance with a protease, and after treating this decomposition product again with a protease, this is heat treated to remove solids generated by heating, molecular weight
Consists of peptides with a molecular weight of 1300 or less, and 60% of the total peptide weight is peptides with a molecular weight of 200 to 400.
A method for producing an egg white decomposition product characterized by obtaining an egg white decomposition product that accounts for the above. 3. The method for producing an egg white decomposition product according to claim 2, which uses an egg white liquid whose pH has been adjusted to 8.0 to 9.5 in advance.
JP60149334A 1985-07-09 1985-07-09 Decomposed albumen and production thereof Granted JPS6212727A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60149334A JPS6212727A (en) 1985-07-09 1985-07-09 Decomposed albumen and production thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60149334A JPS6212727A (en) 1985-07-09 1985-07-09 Decomposed albumen and production thereof

Publications (2)

Publication Number Publication Date
JPS6212727A JPS6212727A (en) 1987-01-21
JPH0533719B2 true JPH0533719B2 (en) 1993-05-20

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
JP60149334A Granted JPS6212727A (en) 1985-07-09 1985-07-09 Decomposed albumen and production thereof

Country Status (1)

Country Link
JP (1) JPS6212727A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2810336B1 (en) * 2000-06-19 2003-01-31 Prod Oenologiques J Laffort & PROCESS FOR THE MANUFACTURE OF AN ADJUSTED CLARIFICATION PRODUCT FROM A WINE AND CLARIFICATION PRODUCT OBTAINED
JP2007238515A (en) * 2006-03-09 2007-09-20 Mandom Corp Hair cosmetic

Also Published As

Publication number Publication date
JPS6212727A (en) 1987-01-21

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