JPH0543340B2 - - Google Patents

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Publication number
JPH0543340B2
JPH0543340B2 JP59270712A JP27071284A JPH0543340B2 JP H0543340 B2 JPH0543340 B2 JP H0543340B2 JP 59270712 A JP59270712 A JP 59270712A JP 27071284 A JP27071284 A JP 27071284A JP H0543340 B2 JPH0543340 B2 JP H0543340B2
Authority
JP
Japan
Prior art keywords
egg white
solution
white solution
gel
heat
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
JP59270712A
Other languages
Japanese (ja)
Other versions
JPS61149070A (en
Inventor
Akira Sugisawa
Masanori Yamamoto
Mitsuru Yasuda
Yukihiro Nomura
Toshio Amano
Sayuri Ashida
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.)
House Foods Corp
Original Assignee
House Food Industrial Co Ltd
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 House Food Industrial Co Ltd filed Critical House Food Industrial Co Ltd
Priority to JP59270712A priority Critical patent/JPS61149070A/en
Publication of JPS61149070A publication Critical patent/JPS61149070A/en
Publication of JPH0543340B2 publication Critical patent/JPH0543340B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は、透明で、かつ粘稠状ないしゲル状を
呈する加工卵白の製造法に関する。
DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a method for producing processed egg white that is transparent and has a viscous or gel-like appearance.

(従来の技術) 元来、卵白は加熱によつて凝固する性質を有し
ており、この性質を利用して種々のゲル状ないし
凝固状食品が製造されているが、近時、この卵白
を酵素によつて加工処理する技術が研究、開発さ
れている。例えば、約1〜6%の蛋白質濃度の原
料卵白溶液にアスペルギルス属の生産する酸性蛋
白質分解酵素を作用させたのち、約80〜100℃に
加熱し、凝固物を除去する方法(特開昭58−
155048号)や、卵白液に所定量のパパインを添加
して酵素処理した後、常法通り乾燥する方法(特
開昭56−45176号)などがある。
(Prior art) Egg white originally has the property of coagulating when heated, and various gel-like or coagulated foods are manufactured using this property. Technology for processing using enzymes is being researched and developed. For example, there is a method in which a raw egg white solution with a protein concentration of about 1 to 6% is treated with an acidic proteolytic enzyme produced by Aspergillus, and then heated to about 80 to 100°C to remove the coagulum. −
155048), and a method in which a predetermined amount of papain is added to egg white liquid, treated with an enzyme, and then dried in a conventional manner (Japanese Patent Application Laid-Open No. 56-45176).

(発明が解決しようとする問題点) 前記特開昭58−155048号の方法は、加熱処理時
に凝固を起こさず、しかも、風味が良好で、種々
の飲料、栄養組成物の原料として使用できる卵白
加水分解物の製造法に関するものであり、また、
特開昭56−45176号の方法は、水戻しして加熱凝
固した際に、生卵白を加熱凝固させたものとほぼ
同様のゲル強度の高い卵白ゲルが得られるような
乾燥卵白を製造する方法に関するものであつて、
透明で、かつ粘稠状ないしゲル状を呈する加工卵
白の製造方法は知られていない。
(Problems to be Solved by the Invention) The method of JP-A-58-155048 produces egg whites that do not coagulate during heat treatment, have a good flavor, and can be used as raw materials for various beverages and nutritional compositions. It relates to a method for producing a hydrolyzate, and
The method disclosed in JP-A No. 56-45176 is a method for producing dried egg white that, when rehydrated and heat-coagulated, yields an egg white gel with a high gel strength similar to that obtained by heat-coagulating raw egg white. It is related to
There is no known method for producing processed egg white that is transparent and has a viscous or gel-like appearance.

(問題を解決するための技術手段) 本発明者らは、従来法とは異なつた卵白の利用
法について研究した結果、特定の蛋白質濃度の非
凝固性の卵白溶液を使用すること、これを特定条
件下で加熱処理すること、その後、特定条件下で
エンドペプチダーゼ処理すること、以上の要件を
すべて同時に満足することによつて、透明で、か
つほとんど無味、無臭の粘稠物ないしゲル状物を
得ることができるという知見を得た。
(Technical means for solving the problem) As a result of research into a method of using egg white that is different from conventional methods, the present inventors have identified the use of a non-coagulable egg white solution with a specific protein concentration. By simultaneously satisfying all of the above requirements, heat treatment under certain conditions, followed by endopeptidase treatment under specific conditions, a transparent, almost tasteless and odorless viscous or gel-like substance can be produced. I have found that it is possible to obtain

上記の知見に基いて完成された本発明の要旨
は、蛋白質濃度2〜6重量%の非熱凝固性の卵白
溶液を、該卵白溶液中の蛋白質が加熱変性するに
充分な条件で加熱処理し、これをエンドペプチダ
ーゼを添加、混合し、35〜90℃で10時間〜1分の
範囲内で作用させて、上記卵白溶液を粘稠化ない
しゲル化させ、必要に応じて、さらに加熱処理す
ることを特徴とする加工卵白食品の製造法であ
る。
The gist of the present invention, which was completed based on the above findings, is to heat-treat a non-thermocoagulable egg white solution with a protein concentration of 2 to 6% by weight under conditions sufficient to heat-denature the proteins in the egg white solution. Add endopeptidase to this, mix, and let it act at 35 to 90°C for 10 hours to 1 minute to make the egg white solution viscous or gel, and if necessary, heat-treat it further. This is a method for producing processed egg white food characterized by the following.

以下、本発明の内容について詳しく説明する。 Hereinafter, the content of the present invention will be explained in detail.

本発明においては、まず卵白を溶解して特定の
蛋白質濃度を有する卵白溶液を得る。ここで使用
する卵白は、粉末状のものでもよく、あるいは液
状のものでもよいが、得られる卵白溶液は非熱凝
固性でなければならない。非熱凝固性の卵白溶液
の製造に関しては、常法に則つて実施すればよ
い。例えば、前述した特開昭58−155048号のよう
な方法、あるいは生卵白を凍結真空乾燥または減
圧乾燥し、粉末化した卵白を溶解して溶液化する
方法等がある。このような方法によつて得られた
卵白溶液の蛋白質濃度としては、2〜6重量%と
することが必要である。該卵白溶液の蛋白質濃度
が2重量%未満では、後の処理を本発明と同様に
実施しても、粘稠状ないしゲル状を呈するものが
得られない。反対に、該卵白溶液の蛋白質濃度が
6重量%を超えると、次の加熱処理時に凝固して
しまうので、その後の処理ができなくなつてく
る。
In the present invention, egg white is first dissolved to obtain an egg white solution having a specific protein concentration. The egg white used here may be in powder form or in liquid form, but the resulting egg white solution must be non-thermocoagulable. The production of a non-thermocoagulable egg white solution may be carried out according to a conventional method. For example, there is a method as described in Japanese Patent Application Laid-Open No. 58-155048 mentioned above, or a method in which raw egg white is freeze-vacuum dried or dried under reduced pressure and the powdered egg white is dissolved to form a solution. The protein concentration of the egg white solution obtained by such a method needs to be 2 to 6% by weight. If the protein concentration of the egg white solution is less than 2% by weight, even if the subsequent treatment is carried out in the same manner as in the present invention, a viscous or gel-like solution cannot be obtained. On the other hand, if the protein concentration of the egg white solution exceeds 6% by weight, it will coagulate during the next heat treatment, making subsequent treatments impossible.

次に、上記卵白溶液を加熱処理する。この加熱
の処理条件としては、上記卵白溶液中の蛋白質が
加熱変性するに充分な条件であることが必要であ
る。これによつて、次工程におけるエンドペプチ
ダーゼによる酵素分解が受けやすくなる。したが
つて、上記加熱処理の具体的条件としては、80〜
140℃で1時間〜5秒程度が好ましく、さらには
95〜100℃で10分〜5分程度が好ましい。
Next, the egg white solution is heat-treated. The conditions for this heating process need to be sufficient to denature the proteins in the egg white solution. This makes it more susceptible to enzymatic degradation by endopeptidase in the next step. Therefore, the specific conditions for the above heat treatment are 80~
Preferably at 140°C for about 1 hour to 5 seconds, and
Preferably, the temperature is 95 to 100°C for about 10 to 5 minutes.

このようにして卵白溶液中の蛋白質を加熱変性
させた後、エンドペプチダーゼを添加する。添加
するエンドペプチダーゼとしては、ブロメライン
(Bromelain)、フイシン(Ficin)などに代表さ
れる植物起源のもの、ストレプトマイセス・グリ
セウス(Streptomyces griceus)などの放線菌、
アスペルギルス・オリゼー(Aspergillus
oryzae)などの糸状菌、バシラス・ズブチルス
(Bacillus subutilis)のどの細菌から分離、精製
して得られるような微生物起源のものなどがあ
る。そして、その添加量は、卵白溶液中の蛋白質
に対して0.1重量%以上、好ましくは0.4〜3重量
%程度で充分である。その後、35〜90℃で10時間
〜10秒、好ましくは45〜80℃で2時間〜1分の範
囲内で作用させて、卵白溶液を粘稠化ないしゲル
化させる。ここにいう卵白溶液が粘稠化したと
は、B型粘度計(25℃、ローターNo.3、60rpm)
で測定した時の粘度が400cp以上を示すものをい
う。この場合、撹拌しながら酵素を作用させても
よいが、酵素を添加した後、該酵素を均一に分散
させるために撹拌し、その後、静置の状態で作用
させるのが本発明の目的を達成する上で好まし
い。
After the proteins in the egg white solution are denatured by heating in this manner, endopeptidase is added. The endopeptidases to be added include those of plant origin such as bromelain and ficin, actinomycetes such as Streptomyces griceus,
Aspergillus oryzae
They include those of microbial origin, such as those obtained by isolation and purification from filamentous fungi such as Bacillus subutilis and Bacillus subutilis. The addition amount is sufficient to be 0.1% by weight or more, preferably about 0.4 to 3% by weight, based on the protein in the egg white solution. Thereafter, the egg white solution is allowed to act at a temperature of 35 to 90°C for 10 hours to 10 seconds, preferably at 45 to 80°C for 2 hours to 1 minute, to make the egg white solution viscous or gel. When the egg white solution becomes viscous, it is measured using a B-type viscometer (25℃, rotor No. 3, 60rpm).
Refers to products with a viscosity of 400 cp or more when measured at In this case, the enzyme may be allowed to act while stirring, but the purpose of the present invention is achieved by adding the enzyme, stirring to uniformly disperse the enzyme, and then allowing the enzyme to act while standing still. It is preferable to do so.

該酵素処理時の作用条件が上記範囲内において
ゆるやかな条件の場合、すなわち、温度が低い
か、あるいは温度が高くても作用時間が極めて短
い場合、卵白溶液は粘稠物質となり、反対に上記
作用条件がきびしい場合、すなわち、作用温度が
高く時間が長くなると、卵白溶液はゲル状物質と
なる。したがつて、卵白溶液の酵素処理にあたつ
ては、実施者において最終的に希望する物性によ
つて、適宜その条件を決定すればよい。また、酵
素作用条件をゆるやかにして得られた粘稠物質
は、その後、さらに加熱することによつてゲル状
物質に変化する性質を有しているので、このよう
な性質も考慮して、上記酵素処理時の条件を決定
すればよい。例えば、卵白溶液の酵素処理後に何
らかの食品素材、添加物等を添加する場合、上記
酵素処理条件をゆるやかにして卵白溶液を粘稠物
質にした後、上記食品素材、添加物等を添加し、
その後、さらに加熱してゲル状物質を得る方法等
を採用してもよい。この場合の加熱条件として
は、60〜120℃で30分〜30秒、好ましくは80〜100
℃で10分〜1分で充分である。
If the action conditions during the enzyme treatment are gentle within the above range, that is, the temperature is low, or the action time is extremely short even if the temperature is high, the egg white solution will become a viscous substance, and the above action will be reversed. When the conditions are severe, ie, the working temperature is high and the time is long, the egg white solution becomes a gel-like substance. Therefore, when enzymatically treating an egg white solution, the conditions may be determined as appropriate depending on the final desired physical properties of the practitioner. In addition, the viscous substance obtained under mild enzyme action conditions has the property of changing into a gel-like substance by further heating. The conditions for enzyme treatment may be determined. For example, when adding some food materials, additives, etc. after enzymatic treatment of the egg white solution, the enzyme treatment conditions are made gentle to make the egg white solution viscous, and then the food materials, additives, etc. are added.
Thereafter, a method of further heating to obtain a gel-like substance may be adopted. In this case, the heating conditions are 60 to 120℃ for 30 minutes to 30 seconds, preferably 80 to 100℃.
10 minutes to 1 minute at ℃ is sufficient.

(発明の効果) このようにして処理された加工卵白は、透明な
粘稠物か、あるいは透明なゲル状物で、かつ無
味・無臭である。その結果、種々の増粘食品やゲ
ル状食品に使用しても、加熱凝固卵白特有の臭い
や味が付加されることがなく、また、上記食品の
色を変色することもない。さらに、上記増粘食品
やゲル状食品に使用される増粘剤やゲル化剤の添
加量を減少させることができると共に、卵白の有
する栄養を付加することが可能となる。
(Effects of the Invention) The processed egg white treated in this manner is a transparent viscous substance or a transparent gel-like substance, and is tasteless and odorless. As a result, even when used in various thickened foods and gel-like foods, the odor and taste peculiar to heat-coagulated egg whites are not added, and the color of the foods mentioned above does not change. Furthermore, it is possible to reduce the amount of thickeners and gelling agents used in the above-mentioned thickened foods and gelled foods, and it is also possible to add the nutrition of egg whites.

本発明では、得られる加工卵白を適宜乾燥手段
によつて粉末化し、それを増粘剤またはゲル化剤
として使用してもよく、あるいは本発明の他の実
施態様として、上記処理工程のいずれかの段階で
各種製品原料を添加してもよい。
In the present invention, the obtained processed egg white may be powdered by appropriate drying means and used as a thickening agent or gelling agent, or as another embodiment of the present invention, any of the above processing steps may be performed. Various product raw materials may be added at this stage.

(実施例) 実施例 1 生卵白を−20℃以下で凍結した後、減圧度が6
パスカル、棚温度が35℃の条件で20時間凍結真空
乾燥し、その後、コーヒーミルで粉砕して卵白粉
末を得た。次に、該卵白粉末を水に溶解して、蛋
白質濃度5重量%の非熱凝固性卵白溶液90gを
得、それを100℃で5分間加熱処理して該卵白溶
液中の蛋白質を加熱変性させた後、ブロメライン
(SIGMA製)1重量%溶液10gを添加、混合し、
60℃で15分間静置状態で作用させて、透明なゲル
を得た。
(Example) Example 1 After freezing raw egg whites at -20℃ or lower, the degree of vacuum was 6.
Pascal and vacuum-dried for 20 hours at a shelf temperature of 35°C, and then ground in a coffee mill to obtain egg white powder. Next, the egg white powder was dissolved in water to obtain 90 g of a non-thermocoagulable egg white solution with a protein concentration of 5% by weight, which was heat-treated at 100°C for 5 minutes to heat-denature the protein in the egg white solution. After that, 10g of bromelain (manufactured by SIGMA) 1% by weight solution was added and mixed.
A transparent gel was obtained by standing at 60°C for 15 minutes.

比較例 1 酵素を添加しないこと以外は全て実施例1と同
様の処理を施したところ、ゲル状物は得られず
に、透明な溶液のままであつた。
Comparative Example 1 When the same treatment as in Example 1 was performed except that no enzyme was added, a gel-like substance was not obtained and a transparent solution remained.

実施例 2 実施例1と同様にして得られた卵白粉末を水に
溶解して、蛋白質濃度4重量%の非熱凝固性卵白
溶液90gを得、それを80℃で10分間加熱処理し
て、該卵白溶液中の蛋白質の加熱変性させた後、
プロテアーゼ「アマノ」A(天野製薬製)0.4重量
%溶液10gを添加、混合し、50℃で10分間静置状
態で作用させた。このようにして得られた卵白溶
液の粘度は550cpであつた。その後、100℃で5
分間さらに加熱し、透明なゲルを得た。
Example 2 Egg white powder obtained in the same manner as in Example 1 was dissolved in water to obtain 90 g of a non-thermocoagulable egg white solution with a protein concentration of 4% by weight, which was heat-treated at 80°C for 10 minutes. After heating and denaturing the proteins in the egg white solution,
10 g of a 0.4% by weight solution of protease "Amano" A (manufactured by Amano Pharmaceutical Co., Ltd.) was added, mixed, and left to act at 50° C. for 10 minutes. The viscosity of the egg white solution thus obtained was 550 cp. After that, 5 at 100℃
Further heating for minutes resulted in a clear gel.

比較例 2 酵素を作用させた後、さらに加熱しないこと以
外は全て実施例2と同様に処理したところ、ゲル
状物は得られず、透明な溶液のままであつた。
Comparative Example 2 The same procedure as in Example 2 was carried out except that no further heating was performed after the enzyme was applied. No gel-like material was obtained, and the solution remained as a transparent solution.

実施例 3 実施例1と同様の方法で得られた卵白粉末を水
に溶解して、蛋白質濃度5重量%の卵白溶液100
gを得、それを100℃で3分間加熱処理して、該
卵白溶液中の蛋白質を加熱変性させた後、ブロメ
ライン(SIGMA製)0.5重量%溶液10gを添加、
混合し、50℃で10分間静置状態で作用させた。こ
のようにして得られた卵白溶液の粘度は600cpで
あつた。次に、該卵白溶液にグルコース0.1gを
添加混合した後、20gずつシヤーレに分注し、
120℃で5分間加熱殺菌してゲルを形成させ培地
とした。この培地のゲル強度をレオメーターで測
定したところ70gであつた。なお、上記ゲル強度
の測定は、不動工業(株)製レオメーター(NRM−
3002D型)を使用し、圧偏、弾性用プランジヤー
(10φ)、上昇速度6cm/分という条件で実施し
た。
Example 3 Egg white powder obtained in the same manner as in Example 1 was dissolved in water to make an egg white solution with a protein concentration of 5% by weight.
After heating it at 100°C for 3 minutes to heat-denature the protein in the egg white solution, add 10g of a 0.5% by weight solution of bromelain (manufactured by SIGMA).
The mixture was mixed and allowed to stand at 50°C for 10 minutes. The viscosity of the egg white solution thus obtained was 600 cp. Next, 0.1 g of glucose was added to the egg white solution and mixed, and then dispensed into 20 g portions into a shear dish.
The mixture was heat sterilized at 120°C for 5 minutes to form a gel, which was then used as a culture medium. The gel strength of this medium was measured using a rheometer and was found to be 70 g. The above gel strength was measured using a rheometer (NRM-) manufactured by Fudo Kogyo Co., Ltd.
3002D type) under the conditions of a pressure bias, an elastic plunger (10φ), and a rising speed of 6 cm/min.

実施例 4 実施例1と同様の方法で得られた卵白粉末を水
に溶解して、蛋白質濃度4重量%の卵白溶液500
gを得、それを95℃で5分間加熱処理して、該卵
白溶液中の蛋白質を加熱変性させた後、ブロメラ
イン(SIGMA製)0.8重量%溶液50gを添加、混
合し、65℃で20分間静置状態で作用させてゲルを
形成させた。これを−20℃以下で凍結処理した
後、減圧度6パスカル、棚温度35℃で20時間乾燥
し、これをコーヒーミルで粉砕した。このように
して得られた粉末をコーヒー粉末6g、砂糖10g
と共に粉体混合し、水100gを添加して溶解させ
た後、1時間静置してコーヒーゼリーを得た。
Example 4 Egg white powder obtained in the same manner as in Example 1 was dissolved in water to make an egg white solution with a protein concentration of 4% by weight.
After heating it at 95°C for 5 minutes to heat-denature the protein in the egg white solution, 50g of a 0.8% by weight solution of bromelain (manufactured by SIGMA) was added and mixed, and the mixture was heated at 65°C for 20 minutes. A gel was formed by standing still. This was frozen at -20°C or below, dried for 20 hours at a vacuum of 6 Pascals and a shelf temperature of 35°C, and ground in a coffee mill. The powder thus obtained is 6g of coffee powder and 10g of sugar.
The powders were mixed together, 100 g of water was added and dissolved, and the mixture was allowed to stand for 1 hour to obtain coffee jelly.

Claims (1)

【特許請求の範囲】 1 蛋白質濃度2〜6重量%の非熱凝固性の卵白
溶液を、該卵白溶液中の蛋白質が加熱変性するに
充分な条件で加熱処理し、これにエンドペプチダ
ーゼを添加、混合し、35〜90℃で10時間〜1分の
範囲内で作用させて、上記卵白溶液を粘稠化ない
しゲル化させることを特徴とする加工卵白の製造
法。 2 卵白溶液中の蛋白質が加熱変性するに充分な
条件での加熱処理条件が80〜140℃で1時間〜5
秒である特許請求の範囲第1項記載の加工卵白の
製造法。 3 エンドペプチダーゼの作用条件が45〜80℃で
2時間〜1分である特許請求の範囲第1項記載の
加工卵白の製造法。
[Scope of Claims] 1. A non-thermocoagulable egg white solution with a protein concentration of 2 to 6% by weight is heat-treated under conditions sufficient to denature the proteins in the egg white solution, and endopeptidase is added thereto; A method for producing processed egg whites, which comprises mixing and reacting at 35 to 90°C for 10 hours to 1 minute to make the egg white solution viscous or gel. 2 The heat treatment conditions are sufficient for heat denaturation of the proteins in the egg white solution at 80 to 140°C for 1 hour to 5.
2. The method for producing processed egg white according to claim 1, wherein the process is as follows. 3. The method for producing processed egg white according to claim 1, wherein the endopeptidase action conditions are 45 to 80°C and 2 hours to 1 minute.
JP59270712A 1984-12-24 1984-12-24 Production of processed albumen Granted JPS61149070A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59270712A JPS61149070A (en) 1984-12-24 1984-12-24 Production of processed albumen

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59270712A JPS61149070A (en) 1984-12-24 1984-12-24 Production of processed albumen

Publications (2)

Publication Number Publication Date
JPS61149070A JPS61149070A (en) 1986-07-07
JPH0543340B2 true JPH0543340B2 (en) 1993-07-01

Family

ID=17489909

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59270712A Granted JPS61149070A (en) 1984-12-24 1984-12-24 Production of processed albumen

Country Status (1)

Country Link
JP (1) JPS61149070A (en)

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5998655A (en) * 1982-11-30 1984-06-07 Otsuka Shokuhin Kogyo Kk Food protein and its preparation

Also Published As

Publication number Publication date
JPS61149070A (en) 1986-07-07

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