JPS625572B2 - - Google Patents
Info
- Publication number
- JPS625572B2 JPS625572B2 JP54051699A JP5169979A JPS625572B2 JP S625572 B2 JPS625572 B2 JP S625572B2 JP 54051699 A JP54051699 A JP 54051699A JP 5169979 A JP5169979 A JP 5169979A JP S625572 B2 JPS625572 B2 JP S625572B2
- Authority
- JP
- Japan
- Prior art keywords
- egg
- liquid
- frozen
- egg yolk
- enzyme
- 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
Links
- 235000013601 eggs Nutrition 0.000 claims description 51
- 235000013345 egg yolk Nutrition 0.000 claims description 34
- 210000002969 egg yolk Anatomy 0.000 claims description 34
- 102000002322 Egg Proteins Human genes 0.000 claims description 32
- 108010000912 Egg Proteins Proteins 0.000 claims description 32
- 102000004190 Enzymes Human genes 0.000 claims description 32
- 108090000790 Enzymes Proteins 0.000 claims description 32
- 239000007788 liquid Substances 0.000 claims description 32
- 238000007710 freezing Methods 0.000 claims description 20
- 230000008014 freezing Effects 0.000 claims description 20
- 239000004365 Protease Substances 0.000 claims description 18
- 108091005804 Peptidases Proteins 0.000 claims description 14
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 claims description 10
- 238000004519 manufacturing process Methods 0.000 claims description 6
- 230000002779 inactivation Effects 0.000 claims description 2
- 229940088598 enzyme Drugs 0.000 description 31
- 238000004925 denaturation Methods 0.000 description 18
- 230000036425 denaturation Effects 0.000 description 18
- 239000012530 fluid Substances 0.000 description 16
- 238000000034 method Methods 0.000 description 12
- 235000019419 proteases Nutrition 0.000 description 8
- 238000010438 heat treatment Methods 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- 238000002474 experimental method Methods 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- 102000035195 Peptidases Human genes 0.000 description 4
- 230000000415 inactivating effect Effects 0.000 description 4
- 235000010746 mayonnaise Nutrition 0.000 description 4
- 239000008268 mayonnaise Substances 0.000 description 4
- 238000010257 thawing Methods 0.000 description 4
- 235000008429 bread Nutrition 0.000 description 3
- 235000009508 confectionery Nutrition 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- 235000014103 egg white Nutrition 0.000 description 3
- 210000000969 egg white Anatomy 0.000 description 3
- 230000002255 enzymatic effect Effects 0.000 description 3
- -1 fuicin Proteins 0.000 description 3
- 102000004169 proteins and genes Human genes 0.000 description 3
- 108090000623 proteins and genes Proteins 0.000 description 3
- 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 description 2
- 108010004032 Bromelains Proteins 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- 108010019160 Pancreatin Proteins 0.000 description 2
- 108090000526 Papain Proteins 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 235000019835 bromelain Nutrition 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 238000006911 enzymatic reaction Methods 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 244000005700 microbiome Species 0.000 description 2
- 229940055695 pancreatin Drugs 0.000 description 2
- 229940055729 papain Drugs 0.000 description 2
- 235000019834 papain Nutrition 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 235000011962 puddings Nutrition 0.000 description 2
- 230000001954 sterilising effect Effects 0.000 description 2
- 241000287828 Gallus gallus Species 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- 235000013527 bean curd Nutrition 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000013256 coordination polymer Substances 0.000 description 1
- 238000005138 cryopreservation Methods 0.000 description 1
- 235000011950 custard Nutrition 0.000 description 1
- 210000003278 egg shell Anatomy 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 235000012041 food component Nutrition 0.000 description 1
- 239000005417 food ingredient Substances 0.000 description 1
- 230000002538 fungal effect Effects 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 235000019600 saltiness Nutrition 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 235000019643 salty taste Nutrition 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 235000019605 sweet taste sensations Nutrition 0.000 description 1
- 235000019640 taste Nutrition 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 235000020138 yakult Nutrition 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L15/00—Egg products; Preparation or treatment thereof
- A23L15/25—Addition or treatment with microorganisms or enzymes
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Microbiology (AREA)
- Health & Medical Sciences (AREA)
- Nutrition Science (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
Description
本発明は凍結変性の少ない冷凍卵を製造する方
法に関する。
鶏卵の卵黄は、マヨネーズ、製菓・製パン原料
などとして広く利用され、腐敗を防止し鮮度を維
持して貯蔵する方法も種々開発されている。この
うち卵殻を除いて貯蔵する代表的方法として冷凍
法がある。
しかし割卵で得た卵黄液をそのまま凍結した冷
凍卵黄は、長期間の貯蔵中に凍結変性を起し、解
凍してもタンパク質が元に復さず、凝固を起して
しまう。そのため従来から卵黄液を加塩又は加糖
して凍結変性を防ぐことが行われているが、凍結
変性が十分防止される程度に塩分又は糖を添加す
ると、冷凍卵黄に塩味、甘味などの味のつくのは
避けられず、冷凍卵黄としての用途が制限される
こととなるという欠点があつた。この欠点は卵黄
液のみならず、全卵液などのような卵黄混有卵液
を冷凍したものにも同様見られるものである。
本発明者らはこのような従来の冷凍卵の製造方
法の欠点を克服し、長時間の貯蔵によつても凍結
変性が少なく、かつ凍結のさせ方などによる凍結
変性の度合いの差も少ない冷凍卵の製造方法を開
発するため鋭意研究を重ねた。その結果、卵黄液
又は卵黄混有卵液にあらかじめプロテアーゼを少
量添加して1時間以上酵素処理を行つたのち、加
熱失活させることによりその目的を満足しうるこ
とを見出し、本発明をなすに至つた。
すなわち本発明は、卵黄液又は卵黄混有卵液を
凍結させるに当り、あらかじめプロテアーゼを添
加して1時間以上酵素処理を行つたのち、加熱失
活させることを特徴とする冷凍卵の製造方法を提
供するものである。
本発明方法に用いる卵黄液としては、一般的に
は卵を割卵し、卵白と分離して得た卵黄液が、又
卵黄混有卵液としては、全卵液あるいは、卵黄液
と卵白液とを任意の割合で混合したものがあげら
れる。
本発明方法においてプロテアーゼとしては、動
植物・微生物の体外酵素・体内酵素として存在す
るものの中から適宜選択して用いられるが、好ま
しいものの例としては、植物中に存在するもので
はたとえばパパイン・フイシン・ブロメラインな
ど、動物体に由来するものではたとえばパンクレ
アチン・微生物に由来するものでは、たとえばプ
ロザイム「アマノ」P又はA〔商品名、天野製薬
(株)製〕・デナチームAP〔商品名、長瀬産業(株)製〕
などの糸状菌系プロテアーゼもしくはネオビタラ
ーゼNP又はAP(商品名、東和酵素(株)製〕・プロ
リシン5〔商品名、上田化学工業(株)製〕・アロア
ーゼK−2〔商品名、ヤクルト生化学(株)製〕など
の細菌系プロテアーゼがあげられる。卵黄液の
PHは5.8〜6.2位、全卵液のPH7.2〜7.8位であるか
ら、卵液として卵黄液、全卵液を用いる場合は、
至適PHが5.0〜9.0のプロテアーゼを用いるのが好
ましい。
本発明においてこれらのプロテアーゼの添加量
は、プロテアーゼの種類・卵液の組成・酵素処理
温度などの条件によつて異なるが、通常卵液に対
し0.0001〜0.5%の範囲、好ましくは0.001〜0.3%
の範囲で選ばれる。
この場合添加量が0.0001%未満では酵素分解反
応が進みにくく、0.5%を越えるとコストが高く
なり、また酵素を失活させる間にも酵素分解反応
が進行するので品質の一定のものを得るのが困難
となる。
上記の卵液にプロテアーゼを添加して、酵素処
理を1時間以上行なう。酵素処理時間は、1時間
以上行なわないと、凍結による卵液の変性が起き
易く、また凍結のしかたなどによつて起る凍結変
性の程度が大きく影響を受けて、品質の一定な製
品を得難くなるからである。また、酵素処理時の
温度は通常0〜55℃、好ましくは5〜50℃であ
り、酵素処理時間は通常長くても24時間までであ
る。処理時間は、温度が高くなる程短かくするこ
とができる。なお酵素処理の際の卵液のPHは上記
した理由により5〜9の範囲にあることが好まし
い。
なお本発明の酵素処理条件は、冷凍卵を解凍し
て得られた卵液の粘度が著しく増加しないことを
目安にして適宜定めることができる。
通常は、食品の原料として使うためには、冷凍
保存開始前に比較して、粘度が約10〜20倍位まで
であれば使い勝手が良い。次に酵素処理した卵液
を加熱して、殺菌と共にプロテアーゼを失活させ
る。このように加熱により殺菌失活させれば、解
凍の仕方などにより再度酵素による反応を受ける
ということもなく品質の安定した冷凍卵を得るこ
とができる。この殺菌・失活のための温度−時間
条件としては60〜65℃で2〜10分間行うのが好ま
しい。
本発明においては、このように酵素処理を行つ
たのち加熱失活させた卵黄液又は卵黄混有卵液を
常法に従つて通常−15℃〜−40℃の温度で凍結さ
せ、目的の冷凍卵を製造することができる。卵黄
液又は卵黄混有卵液を予め1時間以上プロテアー
ゼによる酵素処理を行つたのち加熱失活させてか
ら凍結した場合に、何故凍結保存中の変性が起き
にくくなり、かつ品質の安定した卵液になるのか
その機構作用については定かではないが、凍結変
性し易い卵黄の蛋白質がプロテアーゼによりある
程度分解され変性を起しにくい構造のものに変
り、さらには、加熱処理によつて酵素が失活させ
られるので蛋白質の分解が一定以上に進まないこ
とによるからであろうと考えられる。
本発明方法によれば、塩味・甘味などの余計な
味がなく、長期間冷凍貯蔵しても凍結変性の少な
くかつ品質が安定した冷凍卵を得ることができ、
これはマヨネーズ・製菓・製パン原料などとして
広く使用することができる。
次に本発明を実施例に基づきさらに詳細に説明
する。
実施例 1
割卵して得た全卵液(PH7.6)をよくかきまぜ
て均一な乳濁液とし、さらにろ過処理したもの10
Kgにパパイン0.5g及びプロリシン5 0.25gを
添加し、5℃に冷却して酵素処理を行つた。16時
間後に63℃で4分間加熱処理し、殺菌と共に酵素
の失活処理を行つた。次いでこの全卵液を常温に
冷却後、1Kgずつポリエチレン製袋に詰め、−25
℃に調整した冷蔵庫中に凍結保存した。保存1箇
月ごとに凍結全卵液を取り出し、それを解凍し粘
度を測定して凍結変性の程度を測定した。なお粘
度の測定はB型粘度計(株式会社東京計器製造所
製)を用いて行つた。この結果を第1表に示し
た。
一方比較のために酵素を添加しない以外は上記
と全く同様にして調製した全卵液を、同様の条件
で冷凍し同様にして凍結変性の程度を測定した。
この結果を対照例として第1表に示した。
The present invention relates to a method for producing frozen eggs with less freeze denaturation. Egg yolks from chicken eggs are widely used as raw materials for mayonnaise, confectionery and bread making, and various methods have been developed to prevent spoilage and maintain freshness. Among these methods, the freezing method is a typical method for storing eggshells without removing them. However, frozen egg yolks, which are obtained by freezing the egg yolk liquid obtained by breaking eggs, undergo freezing denaturation during long-term storage, and even when thawed, the proteins do not return to their original state, resulting in coagulation. For this reason, egg yolk liquid has traditionally been salted or sweetened to prevent freeze denaturation, but if salt or sugar is added to an extent that sufficiently prevents freeze denaturation, frozen egg yolks will have a salty or sweet taste. This was unavoidable and had the disadvantage of limiting its use as frozen egg yolk. This drawback is found not only in egg yolk liquid, but also in frozen egg liquid containing egg yolk, such as whole egg liquid. The present inventors have overcome the shortcomings of the conventional frozen egg production method, and have developed a method of freezing eggs that causes less freeze denaturation even during long-term storage, and also reduces the difference in the degree of freeze denaturation depending on the method of freezing. He conducted extensive research to develop a method for producing eggs. As a result, it was discovered that the purpose could be achieved by adding a small amount of protease to egg yolk liquid or egg liquid containing egg yolk in advance, performing enzymatic treatment for one hour or more, and then inactivating it by heating. I've reached it. That is, the present invention provides a method for producing frozen eggs, which comprises adding protease in advance to freezing an egg yolk solution or an egg solution containing egg yolk, enzymatically treating the solution for at least one hour, and then inactivating it by heating. This is what we provide. The egg yolk liquid used in the method of the present invention is generally obtained by breaking the egg and separating it from the egg white, and the egg yolk mixed egg liquid can be whole egg liquid or egg yolk liquid and egg white liquid. Examples include mixtures of and in arbitrary proportions. In the method of the present invention, proteases are appropriately selected and used from those existing as extracorporeal enzymes and intracorporeal enzymes of animals, plants, and microorganisms. Preferred examples include those existing in plants such as papain, fuicin, and bromelain. Those derived from animal bodies, such as pancreatin, and those derived from microorganisms, such as Prozyme "Amano" P or A [trade name, Amano Pharmaceutical Co., Ltd.
Manufactured by Nagase Sangyo Co., Ltd. Denateam AP [Product name, manufactured by Nagase Sangyo Co., Ltd.]
Filamentous fungal proteases such as or neovitalase NP or AP (trade name, manufactured by Towa Koso Co., Ltd.), Prolysin 5 [trade name, manufactured by Ueda Chemical Co., Ltd.], Aloase K-2 [trade name, manufactured by Yakult Biochemical Co., Ltd.] Bacterial proteases such as those manufactured by Co., Ltd. are available.
The PH is 5.8 to 6.2, and the PH of whole egg fluid is 7.2 to 7.8, so when using egg yolk fluid or whole egg fluid as egg fluid,
It is preferable to use a protease with an optimum pH of 5.0 to 9.0. In the present invention, the amount of these proteases added varies depending on conditions such as the type of protease, the composition of the egg fluid, and the enzyme treatment temperature, but it is usually in the range of 0.0001 to 0.5%, preferably 0.001 to 0.3% based on the egg fluid.
selected within the range. In this case, if the amount added is less than 0.0001%, the enzymatic decomposition reaction will not progress, and if it exceeds 0.5%, the cost will increase, and the enzymatic decomposition reaction will continue even while the enzyme is deactivated, making it difficult to obtain products of constant quality. becomes difficult. Protease is added to the above egg fluid, and enzyme treatment is performed for 1 hour or more. If the enzyme treatment is not carried out for at least 1 hour, the egg fluid is likely to be denatured due to freezing, and the degree of freeze denaturation that occurs will be greatly affected by the freezing method, making it difficult to obtain products of consistent quality. This is because it becomes difficult. Further, the temperature during the enzyme treatment is usually 0 to 55°C, preferably 5 to 50°C, and the enzyme treatment time is usually up to 24 hours at the longest. The treatment time can be made shorter as the temperature increases. Note that the pH of the egg fluid during enzyme treatment is preferably in the range of 5 to 9 for the reasons described above. Note that the enzyme treatment conditions of the present invention can be determined as appropriate with the aim that the viscosity of the egg fluid obtained by thawing frozen eggs does not increase significantly. Normally, in order to use it as a food ingredient, it is convenient to use it if the viscosity is about 10 to 20 times higher than before freezing. Next, the enzyme-treated egg fluid is heated to sterilize it and deactivate the protease. By sterilizing and inactivating eggs by heating in this manner, frozen eggs of stable quality can be obtained without undergoing the enzyme reaction again depending on the method of thawing. The temperature and time conditions for this sterilization and inactivation are preferably 60 to 65°C for 2 to 10 minutes. In the present invention, the egg yolk liquid or egg yolk-containing egg liquid that has been heat-inactivated after the enzyme treatment is frozen at a temperature of usually -15°C to -40°C according to a conventional method, and the desired freezing temperature is obtained. Eggs can be produced. If egg yolk liquid or egg yolk-mixed egg liquid is enzymatically treated with protease for at least 1 hour and then heated to inactivate it before freezing, why does denaturation during cryopreservation become less likely to occur and the quality of the egg liquid remains stable? Although the mechanism and action of this phenomenon are not clear, the protein in the egg yolk, which is easily denatured by freezing, is degraded to some extent by protease and changed into a structure that is less susceptible to denaturation, and furthermore, the enzyme is deactivated by heat treatment. This is thought to be due to the fact that protein decomposition does not proceed beyond a certain level because of the According to the method of the present invention, it is possible to obtain frozen eggs that are free from unnecessary tastes such as saltiness and sweetness, have little freeze denaturation, and have stable quality even when frozen for a long period of time.
This can be widely used as a raw material for mayonnaise, confectionery, bread, etc. Next, the present invention will be explained in more detail based on examples. Example 1 Whole egg liquid (PH7.6) obtained by breaking eggs was stirred well to make a homogeneous emulsion, and then filtered10
0.5 g of papain and 0.25 g of prolysine 5 were added to Kg, and the mixture was cooled to 5°C and subjected to enzyme treatment. After 16 hours, it was heat-treated at 63°C for 4 minutes to sterilize and deactivate the enzyme. Next, after cooling this whole egg liquid to room temperature, 1 kg each was packed in polyethylene bags, and -25
It was stored frozen in a refrigerator adjusted to ℃. The frozen whole egg fluid was taken out every month of storage, thawed, and its viscosity was measured to determine the degree of freeze denaturation. The viscosity was measured using a B-type viscometer (manufactured by Tokyo Keiki Seisakusho Co., Ltd.). The results are shown in Table 1. On the other hand, for comparison, whole egg fluid prepared in exactly the same manner as above except that no enzyme was added was frozen under the same conditions and the degree of freeze denaturation was measured in the same manner.
The results are shown in Table 1 as a control example.
【表】
この表の結果より酵素処理しない場合(実験番
号2)は1箇月の冷凍保存で急激に粘度が冷凍保
存開始前に比較して293.5倍に上昇し、冷凍変性
が著るしいのに対し、本発明の場合(実験番号
1)は粘度上昇は冷凍保存開始前に比較してわず
かに13倍と、はるかに小さいことがわかる。
なお、実験番号1に於て、卵液に酵素を添加し
て、酵素処理のための時間をとらずに、すぐに、
−10℃と−25℃に1ケ月間冷凍保存した後解凍し
た卵液の粘度を測定したところ、−10℃で保存し
たものは、1500cpであり、−25℃で保存したもの
は、3100cpを示した。一方表−1に示されてい
る、実験番号1(−25℃で保管)において、1ケ
月間保存したものの粘度は、260cpであり、更に
−10℃で1ケ月間保存したものは、250cpであつ
た。このことより、酵素処理を行つたのち加熱失
活させた本発明の方法は、凍結温度の相違などと
いう凍結のさせ方、また凍結解凍の仕方などによ
り、再度酵素による反応を受けるということ等の
影響が少く品質が一定の冷凍卵が得られることが
わかる。
実施例 2
割卵し卵白と分離して得た卵黄液10Kgをろ過し
たのち、50℃に昇温し、プロザイム「アマノ」P
又はA及びデナチームAPをそれぞれ2gずつ加
え、撹拌しながら50℃で5時間酵素処理を行つ
た。次に、65℃で10分間加熱処理し、殺菌と酵素
の失活を行つた。次いで、この卵黄液を常温にま
で冷却後1Kgずつポリエチレン製袋に詰め、実施
例1と同様に−25℃の冷蔵庫に凍結保存し、実施
例1と同様にして凍結変性の程度を試験した。こ
の結果を第2表に示す。なお酵素を添加しない以
外は上記と全く同様にして調製した卵黄液につい
ても全く同様の試験を行つた。この結果をあわせ
て第2表に示した。[Table] The results of this table show that in the case of no enzyme treatment (experiment number 2), the viscosity rapidly increased by 293.5 times after one month of frozen storage compared to before the start of frozen storage, and freezing denaturation was significant. On the other hand, it can be seen that in the case of the present invention (experiment number 1), the viscosity increase was only 13 times that before the start of frozen storage, which was much smaller. In addition, in experiment number 1, the enzyme was added to the egg fluid and immediately, without taking time for enzyme treatment,
When we measured the viscosity of egg fluid that had been frozen and stored at -10°C and -25°C for one month and then thawed, the viscosity of the egg fluid stored at -10°C was 1500 cp, and that stored at -25°C was 3100 cp. Indicated. On the other hand, in Experiment No. 1 (stored at -25℃) shown in Table 1, the viscosity of the sample stored for one month was 260cp, and the viscosity of the sample stored at -10℃ for another month was 250cp. It was hot. From this, the method of the present invention, in which the enzyme is treated and then inactivated by heating, can be subject to the enzyme reaction again depending on the way of freezing, such as the difference in freezing temperature, and the way of freezing and thawing. It can be seen that frozen eggs with little influence and constant quality can be obtained. Example 2 After filtering 10 kg of egg yolk liquid obtained by breaking eggs and separating them from egg whites, the temperature was raised to 50°C, and Prozyme "Amano" P
Alternatively, 2 g each of A and Denazyme AP were added, and enzyme treatment was performed at 50° C. for 5 hours with stirring. Next, it was heat-treated at 65°C for 10 minutes to sterilize and deactivate the enzyme. Next, this egg yolk liquid was cooled to room temperature, packed in polyethylene bags in 1 kg portions, stored frozen in a -25°C refrigerator in the same manner as in Example 1, and tested for the degree of freeze denaturation in the same manner as in Example 1. The results are shown in Table 2. Exactly the same test was also conducted on an egg yolk solution prepared in exactly the same manner as above except that no enzyme was added. The results are also shown in Table 2.
【表】
この結果より、酵素処理しない場合(実験番号
2)保存1箇月で冷凍変性が著しく、解凍しても
冷凍保存開始前に比較して粘度が約2000倍以上に
なつて通常の卵黄液として使用できないのに対
し、本発明の場合保存8箇月でも3500CPであ
り、製菓・製パン・マヨネーズ材料として利用で
きた。
実施例 3
PH7.6の殺菌全卵液の乳濁液2000Kgに、タシナ
ーゼN−11−100 200g及びアロアーゼK−2100
gを加えてよく混合し、温度を35℃に維持して2
時間酵素処理を行つた。次いでこの全卵液を、63
℃で3分間加熱処理して酵素を失活させたのち、
常温に冷却し16Kgずつ5ガロン缶(約19容)に
詰め、−40℃に調整した冷凍庫中に入れ凍結させ
た。このようにして得られた冷凍卵黄を、8箇月
保存後取り出して解凍しても、変性度は小さく、
変性カードが生じてないのでホモゲナイズするこ
となくカスタードプリン・卵豆腐・茶碗蒸しの原
料として使用することができた。
実施例 4
PH6.2の卵黄液1000Kgを50℃まで昇温させ、こ
れにパンクレアチン50g及びブロメライン50gを
加えよくかきまぜ、上記温度を維持しながら5時
間酵素処理を行つた。次いで65℃で10分間加熱処
理し、酵素を失活させたのち、常温にまで冷却
し、16Kgずつ5ガロン缶に詰め、これを−20℃に
調整した冷凍庫に入れ冷凍保管した。得られた冷
凍卵黄は、凍結変性が小さく、保存8箇月後でも
マヨネーズ原料として使用できた。
実施例 5
PH6.2の卵黄液1000Kgを5℃に冷却し、デナチ
ームAP200g及びプロザイム「アマノ」A100g
を添加してよく混合したのち、ただちに5ガロン
缶に16Kg詰めとし、これを約10℃以下に調整した
冷蔵庫に入れて16時間保管すると同時に酵素処理
を行なつた。次いで加熱による酵素の失活を行わ
ないで−40℃の急速凍結を行い、凍結変性の少な
い冷凍卵黄を得た。このものは保存8箇月後でも
解凍により、ミルクプリン原料として利用できる
卵黄液を与えた。[Table] From this result, when enzyme treatment is not performed (experiment number 2), freezing denaturation is significant after 1 month of storage, and even after thawing, the viscosity is approximately 2000 times higher than before starting frozen storage, and the viscosity is more than 2000 times that of normal egg yolk liquid. On the other hand, in the case of the present invention, it had a CP of 3500 even after 8 months of storage, and could be used as an ingredient for confectionery, bread, and mayonnaise. Example 3 To 2000 kg of emulsion of sterilized whole egg liquid with pH 7.6, 200 g of Tacinase N-11-100 and Aroase K-2100 were added.
Add g and mix well, maintain the temperature at 35℃ and cook for 2 hours.
A time enzyme treatment was performed. Next, this whole egg liquid was heated to 63
After inactivating the enzyme by heat treatment at ℃ for 3 minutes,
The mixture was cooled to room temperature, packed in 5-gallon cans (approximately 19 volumes) in 16 kg portions, and placed in a freezer adjusted to -40°C to freeze. Even if the frozen egg yolk obtained in this way is taken out and thawed after being stored for 8 months, the degree of denaturation is small.
Since no denatured curd was produced, it could be used as a raw material for custard pudding, egg tofu, and chawanmushi without homogenization. Example 4 1000 kg of egg yolk liquid with pH 6.2 was heated to 50°C, 50 g of pancreatin and 50 g of bromelain were added thereto, stirred well, and enzyme treatment was performed for 5 hours while maintaining the above temperature. The enzyme was then heat-treated at 65°C for 10 minutes to inactivate the enzyme, and then cooled to room temperature, packed in 16kg portions into 5-gallon cans, and stored frozen in a freezer adjusted to -20°C. The obtained frozen egg yolk had little freezing denaturation and could be used as a raw material for mayonnaise even after 8 months of storage. Example 5 1000 kg of egg yolk liquid with pH 6.2 was cooled to 5°C, and 200 g of Denazyme AP and 100 g of Prozyme "Amano" A were added.
After adding and mixing well, the mixture was immediately packed into 5-gallon cans at 16 kg, and the mixture was stored in a refrigerator adjusted to below 10°C for 16 hours, and at the same time enzyme treatment was performed. Next, rapid freezing was performed at -40°C without deactivating the enzyme by heating, to obtain frozen egg yolks with little freeze denaturation. Even after 8 months of storage, this product gave egg yolk liquid that could be used as a raw material for milk pudding when thawed.
Claims (1)
り、あらかじめプロテアーゼを添加して、1時間
以上酵素処理を行つたのち、加熱失活させること
を特徴とする冷凍卵の製造方法。 2 卵黄液又は卵黄混有卵液に添加するプロテア
ーゼの量が、卵液の重量に対して0.0001〜0.5%
である特許請求の範囲第1項記載の冷凍卵の製造
方法。[Scope of Claims] 1. A frozen egg characterized in that when freezing egg yolk liquid or egg yolk mixed egg liquid, protease is added in advance, enzyme treatment is performed for one hour or more, and then heat inactivation is performed. manufacturing method. 2 The amount of protease added to egg yolk liquid or egg yolk mixed egg liquid is 0.0001 to 0.5% of the weight of egg liquid.
A method for producing frozen eggs according to claim 1.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5169979A JPS55144846A (en) | 1979-04-26 | 1979-04-26 | Preparation of frozen egg |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5169979A JPS55144846A (en) | 1979-04-26 | 1979-04-26 | Preparation of frozen egg |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS55144846A JPS55144846A (en) | 1980-11-12 |
JPS625572B2 true JPS625572B2 (en) | 1987-02-05 |
Family
ID=12894139
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP5169979A Granted JPS55144846A (en) | 1979-04-26 | 1979-04-26 | Preparation of frozen egg |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS55144846A (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61139335A (en) * | 1984-12-10 | 1986-06-26 | Akiyoshi Yamane | Aging and storage of liquid egg |
JPS6455141A (en) * | 1987-08-26 | 1989-03-02 | Sanyo Shokuhin Kogyo Kk | Production of refrigerated egg yolk |
US6660321B2 (en) | 2001-06-27 | 2003-12-09 | Cargill, Incorporated | Frozen concentrated liquid whole egg and method of making same |
-
1979
- 1979-04-26 JP JP5169979A patent/JPS55144846A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS55144846A (en) | 1980-11-12 |
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