JPH0533719B2 - - Google Patents
Info
- 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
Links
- 102000002322 Egg Proteins Human genes 0.000 claims description 70
- 108010000912 Egg Proteins Proteins 0.000 claims description 70
- QCVGEOXPDFCNHA-UHFFFAOYSA-N 5,5-dimethyl-2,4-dioxo-1,3-oxazolidine-3-carboxamide Chemical compound CC1(C)OC(=O)N(C(N)=O)C1=O QCVGEOXPDFCNHA-UHFFFAOYSA-N 0.000 claims description 67
- 235000014103 egg white Nutrition 0.000 claims description 67
- 210000000969 egg white Anatomy 0.000 claims description 67
- 238000000354 decomposition reaction Methods 0.000 claims description 40
- 239000007788 liquid Substances 0.000 claims description 40
- 108091005804 Peptidases Proteins 0.000 claims description 30
- 239000004365 Protease Substances 0.000 claims description 28
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 claims description 26
- 108090000765 processed proteins & peptides Proteins 0.000 claims description 21
- 102000004196 processed proteins & peptides Human genes 0.000 claims description 19
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 238000010438 heat treatment Methods 0.000 claims description 5
- 239000007787 solid Substances 0.000 claims description 5
- 235000019419 proteases Nutrition 0.000 description 24
- 235000013601 eggs Nutrition 0.000 description 12
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 239000000243 solution Substances 0.000 description 9
- 102000004190 Enzymes Human genes 0.000 description 6
- 108090000790 Enzymes Proteins 0.000 description 6
- 229940088598 enzyme Drugs 0.000 description 6
- 239000002585 base Substances 0.000 description 5
- 239000002537 cosmetic Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- 102000035195 Peptidases Human genes 0.000 description 4
- 102000004169 proteins and genes Human genes 0.000 description 4
- 108090000623 proteins and genes Proteins 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- 210000002969 egg yolk Anatomy 0.000 description 3
- 235000011121 sodium hydroxide Nutrition 0.000 description 3
- 102000016943 Muramidase Human genes 0.000 description 2
- 108010014251 Muramidase Proteins 0.000 description 2
- 108010062010 N-Acetylmuramoyl-L-alanine Amidase Proteins 0.000 description 2
- 108090000526 Papain Proteins 0.000 description 2
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 235000019621 digestibility Nutrition 0.000 description 2
- 235000013345 egg yolk Nutrition 0.000 description 2
- 229960000274 lysozyme Drugs 0.000 description 2
- 239000004325 lysozyme Substances 0.000 description 2
- 235000010335 lysozyme Nutrition 0.000 description 2
- 244000005700 microbiome Species 0.000 description 2
- 229940055729 papain Drugs 0.000 description 2
- 235000019834 papain Nutrition 0.000 description 2
- 229940024999 proteolytic enzymes for treatment of wounds and ulcers Drugs 0.000 description 2
- 238000001179 sorption measurement Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 1
- 241000287828 Gallus gallus Species 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 102000057297 Pepsin A Human genes 0.000 description 1
- 108090000284 Pepsin A Proteins 0.000 description 1
- 238000002835 absorbance Methods 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000002255 enzymatic effect Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 238000002523 gelfiltration Methods 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 235000016709 nutrition Nutrition 0.000 description 1
- 230000035764 nutrition Effects 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 229940111202 pepsin Drugs 0.000 description 1
- 235000011118 potassium hydroxide Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/64—Proteins; Peptides; Derivatives or degradation products thereof
Landscapes
- 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
〔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.
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)
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.
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
ID=15472834
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)
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 |
-
1985
- 1985-07-09 JP JP60149334A patent/JPS6212727A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS6212727A (en) | 1987-01-21 |
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