JP2002165583A - Processed liquid whole egg and method for producing the same - Google Patents

Processed liquid whole egg and method for producing the same

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Publication number
JP2002165583A
JP2002165583A JP2000363120A JP2000363120A JP2002165583A JP 2002165583 A JP2002165583 A JP 2002165583A JP 2000363120 A JP2000363120 A JP 2000363120A JP 2000363120 A JP2000363120 A JP 2000363120A JP 2002165583 A JP2002165583 A JP 2002165583A
Authority
JP
Japan
Prior art keywords
whole egg
temperature
heating
solution
egg solution
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.)
Granted
Application number
JP2000363120A
Other languages
Japanese (ja)
Other versions
JP3560910B2 (en
Inventor
Tsukasa Ichimura
司 市村
Hideki Murakami
英樹 村上
Kenji Kurihara
健志 栗原
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.)
QP Corp
Original Assignee
QP Corp
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Filing date
Publication date
Application filed by QP Corp filed Critical QP Corp
Priority to JP2000363120A priority Critical patent/JP3560910B2/en
Publication of JP2002165583A publication Critical patent/JP2002165583A/en
Application granted granted Critical
Publication of JP3560910B2 publication Critical patent/JP3560910B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Meat, Egg Or Seafood Products (AREA)
  • Grain Derivatives (AREA)
  • Bakery Products And Manufacturing Methods Therefor (AREA)
  • Seeds, Soups, And Other Foods (AREA)

Abstract

PROBLEM TO BE SOLVED: To provide a new processed whole egg liquid decreased in the number of general live germs to the level same as that of a conventional sterilization method and also causing no lowering of function involved in the whole egg liquid before sterilized, and to provide a method for producing the liquid. SOLUTION: This method for producing a whole egg liquid comprises firstly heating a whole egg liquid at a given temperature for a given time and holding the resultant product for a given time at a temperature lower than the given temperature as a second heating.

Description

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

【0001】[0001]

【発明の属する技術分野】本発明は、加工液全卵、特に
殺菌前の全卵液と同等の機能性を有する殺菌された加工
液全卵及びその製造方法に関する。
[0001] The present invention relates to a processed liquid whole egg, and particularly to a sterilized processed liquid whole egg having the same functionality as that of a whole egg liquid before sterilization and a method for producing the same.

【0002】[0002]

【従来の技術】一般に、割卵して卵殻から分離されたば
かりの、またその後の殺菌処理を特別施していない全卵
液は、製造時の環境にもよるが一般生菌数が103〜1
5/g、大腸菌群数が10〜103/gほどであり、7
℃程度の温度に保管しても2〜3日間しか保存できな
い。また、食中毒の原因となるサルモネラ・エンティリ
ティディスが102〜103/g以上存在している場合も
あり、このような菌数レベルの全卵液をそのまま食品の
原料として使用した場合には作業環境を汚染し、さらに
広範囲の食中毒を引き起こす可能性が大きい。このよう
な状況下で、サルモネラ・エンティリティディスなどの
食中毒菌対策としては、従来よりプレートヒーターとホ
ールディングチューブより成る連続式の殺菌装置を用い
て60℃で3.5分間以上保持する方法や、加熱/冷却
ジャケットおよび攪拌装置を備えたタンク式のバッチタ
イプの殺菌装置を用いて58℃で10分間保持の条件等
で加熱処理することにより、特にサルモネラ・エンティ
リティディスを試料全卵液25gあたり陰性にすること
が行われている。
2. Description of the Related Art In general, whole egg liquid that has just been separated from an egg shell by breaking eggs and that has not been subjected to a special sterilization treatment has a general viable cell count of 10 3 to 1 depending on the environment at the time of production.
0 5 / g, the number of coliforms is about 10 to 10 3 / g, and 7
Even when stored at a temperature of about ℃, it can be stored for only a few days. In addition, Salmonella enteritidis causing food poisoning may be present in an amount of 10 2 to 10 3 / g or more. When whole egg solution having such a bacterial count is directly used as a raw material for food, It is likely to pollute the work environment and cause widespread food poisoning. Under such circumstances, as a countermeasure against food poisoning bacteria such as Salmonella enteritidis, there is conventionally a method of maintaining at a temperature of 60 ° C. for 3.5 minutes or more by using a continuous sterilizing apparatus comprising a plate heater and a holding tube, Using a tank-type batch-type sterilizer equipped with a heating / cooling jacket and a stirrer, heat-treating at 58 ° C. for 10 minutes, etc., in particular, Salmonella enteritidis per 25 g of the whole egg solution of the sample It has been done to make it negative.

【0003】また、特開昭51‐142567号公報に
は全卵液をそのままかあるいは糖を添加して55〜62
℃で20〜30分間の加熱を1回ないし数回繰り返すこ
とにより滅菌する方法が、さらに特表平3‐50252
7号公報には全卵液を2段階で加熱し、第2段階を直接
加熱にして殺菌する方法が記載されている。
[0003] Japanese Patent Application Laid-Open No. 51-142567 discloses 55-62 of whole egg solution as it is or by adding sugar.
The method of sterilization by repeating heating at 20 ° C. for 20 to 30 minutes once or several times is described in JP-A-3-50252.
No. 7 discloses a method in which whole egg liquid is heated in two stages, and the second stage is directly heated to sterilize.

【0004】しかしながら、このような加熱殺菌方法で
製造された液全卵は、サルモネラ・エンティリティディ
スを25gあたり陰性にすることができる反面、その温
度条件での加熱中に全卵液の蛋白質の一部に熱変性が起
こり、生の全卵液が加熱殺菌前に有していた機能が低下
した。例えばこの方法で製造した殺菌全卵液を、卵の起
泡力を利用するスポンジケーキやカステラの原料として
用いた場合、泡立てに要する時間が長くなり、また、ス
ポンジケーキやカステラのボリュームが出ず、口溶けの
悪い、くちゃついた食感の製品となる。さらに、卵の熱
凝固性を利用する卵加工品(カスタードプリン、茶碗
蒸、卵豆腐など)の原料として用いると、組織が弱く、
ねっとりとしてやわらかすぎて、水っぽい食感の製品に
なる。
[0004] However, the liquid whole egg produced by such a heat sterilization method can make Salmonella enteritidis negative per 25 g, but the protein content of the whole egg liquid during heating at that temperature condition. Thermal denaturation occurred partially, and the function of the raw whole egg solution before heat sterilization was reduced. For example, when the pasteurized whole egg liquid produced by this method is used as a raw material for sponge cake or castella using the foaming power of eggs, the time required for whipping becomes longer, and the volume of the sponge cake or castella does not appear. It is a product with poor mouth melting and crunchy texture. Furthermore, when used as a raw material for processed egg products (eg custard pudding, chawanmushi, egg tofu, etc.) utilizing the heat coagulability of eggs, the tissue is weak,
It is a sticky, soft and watery product.

【0005】[0005]

【発明が解決しようとする課題】そこで、本発明は、卵
由来の食中毒菌であるサルモネラ・エンティリティディ
スが25gあたり陰性であり大腸菌群も1gあたり10
未満であると同時に、全卵液が加熱殺菌前に有していた
機能の低下が起きていない、新規な加工全卵液及びその
製造方法を提供することを目的になされたものである。
Therefore, the present invention relates to a method for producing a food poisoning bacterium derived from eggs, Salmonella enteritidis, which is negative per 25 g and whose coliform group is 10 g / g.
It is an object of the present invention to provide a novel processed whole egg solution and a method for producing the same, in which the functions of the whole egg solution before heat sterilization are not reduced at the same time.

【0006】[0006]

【課題を解決するための手段】本発明は、上記課題を解
決するために種々検討した結果、本発明に到達した。す
なわち、本発明は、(1)サルモネラ菌が陰性/25
g、大腸菌群が10未満/gであり、加熱殺菌前の全卵
液と同等の機能性を有し、かつ、アミラーゼ活性が加熱
殺菌前の全卵液よりも低減された加工全卵液、(2)全
卵液を、まず所定温度で所定時間第1加熱した後、該温
度より低い温度で所定時間保持して第2加熱する請求項
1記載の加工全卵液の製造方法、(3)全卵液を、まず
57〜60℃で1〜60秒間第1加熱した後、55〜5
8℃で3.5〜10分間第2加熱する加工全卵液の製造
方法、(4)全卵液を、まず所定温度で所定時間保持し
て第1加熱した後、一旦冷却し、第1加熱温度より低い
温度で所定時間保持して第2加熱する請求項1記載の加
工全卵液の製造方法、(5)全卵液を、まず57〜60
℃で1〜60秒間第1加熱した後、35℃以下に一旦冷
却し、再度55〜58℃で3.5〜10分間第2加熱す
る加工全卵液の製造方法、である。
Means for Solving the Problems The present invention has reached various aspects as a result of various studies to solve the above-mentioned problems. That is, the present invention provides (1) Salmonella negative / 25
g, E. coli group is less than 10 / g, has the same function as whole egg solution before heat sterilization, and has a reduced amylase activity than whole egg solution before heat sterilization, (2) The method for producing a processed whole egg liquid according to claim 1, wherein the whole egg liquid is first heated at a predetermined temperature for a first time and then kept at a temperature lower than the predetermined temperature for a second time. ) The whole egg solution was first heated at 57-60 ° C. for 1-60 seconds and then 55-5
A method for producing a processed whole egg liquid by second heating at 8 ° C. for 3.5 to 10 minutes, (4) first holding the whole egg liquid at a predetermined temperature for a predetermined time and then cooling it once, The method for producing a processed whole egg solution according to claim 1, wherein the second heating is performed while the temperature is lower than the heating temperature for a predetermined time, and (5) the whole egg solution is first subjected to 57-60.
After the first heating at 1 ° C. for 1 to 60 seconds, the mixture is once cooled to 35 ° C. or lower, and secondly heated again at 55 to 58 ° C. for 3.5 to 10 minutes.

【0007】[0007]

【発明の実施の形態】以下、本発明を詳述する。なお、
本発明において「%」は「質量%」をいう。まず、本発
明において全卵液とは、殻付卵を割卵して、卵殻を除い
て得た卵内容物を言うが、卵白液と卵黄液との混合の比
率が前記卵内容物の比率に近い限り、若干異なっても差
し支えない。態様としては、例えば割卵したままのも
の、割卵後ろ過したもの、卵白液と卵黄液を混合したも
のなどを挙げることができる。
DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention will be described below in detail. In addition,
In the present invention, “%” means “% by mass”. First, the whole egg solution in the present invention refers to the egg content obtained by breaking the eggs with a shell and removing the eggshell, and the mixing ratio of the egg white solution and the yolk solution is the ratio of the egg content. May be slightly different as long as Examples of the embodiment include those that have been broken, those that have been filtered after breaking, and those that have a mixture of egg white solution and egg yolk solution.

【0008】本発明において、加熱前の全卵液と同等の
機能性とは、卵の持つ起泡性や熱凝固性が加熱殺菌前の
生の全卵液と同等であるということである。具体的に
は、卵の起泡力を利用するスポンジケーキやカステラの
原料として用いた場合、泡立てに要する時間が5%程度
長くなることはあっても、スポンジケーキやカステラの
ボリューム及び食感が同等であることや、卵の熱凝固性
を利用する卵加工品(カスタードプリン、茶碗蒸、卵豆
腐など)の原料として用いた場合、固まり方に差がなく
同等の食感の製品となることで判別できる。
[0008] In the present invention, the function equivalent to that of whole egg solution before heating means that the foaming property and the heat coagulation property of the egg are equivalent to those of raw whole egg solution before heat sterilization. Specifically, when used as a raw material for sponge cakes and castellas that use the foaming power of eggs, the volume and texture of sponge cakes and castellas may be increased even though the time required for whipping may be about 5% longer. When used as a raw material for processed eggs (such as custard pudding, chawanmushi, and egg tofu) that use the same heat-coagulability of eggs, there is no difference in the way they solidify, resulting in products with the same texture. Can be determined.

【0009】また、加熱殺菌前の全卵液には、アミラー
ゼ活性があるが、加熱殺菌を施すとアミラーゼが失活す
ることが知られており、殺菌品か無殺菌品かの鑑別に使
用されている。本発明品は、加熱殺菌により生の全卵液
よりアミラーゼ活性が低減しているものである。
[0009] Further, it is known that the whole egg solution before heat sterilization has an amylase activity, but it is known that heat sterilization deactivates amylase. ing. The product of the present invention has a lower amylase activity than that of a raw whole egg solution by heat sterilization.

【0010】本発明において、全卵液を、まず所定温度
で所定時間第1加熱した後、次いで所定温度で所定時間
保持して第2加熱する。まず、第1加熱を行う。加熱の
温度は57〜60℃が望ましい。これは、57℃未満で
あると全卵液に含まれるサルモネラ・エンティリティデ
ィスなどの食中毒菌にストレスを与え難く、また、60
℃を越えると全卵液の蛋白質の一部が変性して機能性が
低下するためである。加熱の時間は1〜60秒間程度が
望ましい。これは1秒未満であると全卵液に含まれるサ
ルモネラ・エンティリティディスなどの食中毒菌にスト
レスを与え難く、また、60秒を越えると、たとえ57
℃であっても全卵液の蛋白質の一部に変性が認められる
ためである。
[0010] In the present invention, the whole egg solution is first heated at a predetermined temperature for a first time and then held at a predetermined temperature for a predetermined time and second heated. First, the first heating is performed. The heating temperature is preferably from 57 to 60C. If the temperature is lower than 57 ° C., it is difficult to stress food poisoning bacteria such as Salmonella enteritidis contained in the whole egg solution,
If the temperature exceeds ℃, a part of the protein of the whole egg fluid is denatured and the functionality is reduced. The heating time is desirably about 1 to 60 seconds. When the time is less than 1 second, it is difficult to stress food poisoning bacteria such as Salmonella enteritidis contained in the whole egg fluid.
This is because denaturation is observed in a part of the protein of the whole egg fluid even at ℃.

【0011】次いで、第2加熱を行う。第2加熱は第1
加熱よりも低い温度で所定時間保持する。加熱の温度は
55〜58℃が望ましい。これは55℃未満であると充
分に殺菌され難く、また、58℃を越えると全卵液の蛋
白質の一部が変性しやすいからである。加熱の時間は
3.5分〜10分間程度が望ましい。これは、3.5分
未満だと充分に殺菌され難く、また、10分間を越える
とたとえ55℃の温度であっても全卵液の蛋白質の一部
に熱変性が起こり、機能性が低下するためである。第1
加熱と第2加熱の条件を逆にすると、全卵液に与えられ
る熱履歴は同じであっても殺菌効果に差が現れ、サルモ
ネラ・エンティリティディスを完全に陰性にすることは
できない。また、第1加熱と第2加熱を同じ温度で行っ
ても、本発明の効果は得られない。すなわち、サルモネ
ラ・エンティリティディスなどの食中毒菌は完全に死滅
することができないか、あるいは、全卵液の蛋白質の一
部に熱変性が起こって機能性が低下する。
Next, second heating is performed. The second heating is the first
Hold at a temperature lower than the heating for a predetermined time. The heating temperature is desirably 55 to 58 ° C. This is because if the temperature is lower than 55 ° C., it is difficult to sufficiently sterilize, and if the temperature is higher than 58 ° C., a part of the protein of the whole egg fluid is easily denatured. The heating time is desirably about 3.5 minutes to 10 minutes. This is because if it is less than 3.5 minutes, it is difficult to sufficiently sterilize, and if it exceeds 10 minutes, even if the temperature is 55 ° C., heat denaturation occurs in a part of the protein of the whole egg solution, and the functionality is reduced. To do that. First
When the conditions of the heating and the second heating are reversed, even though the heat histories given to the whole egg fluid are the same, there is a difference in the bactericidal effect, and Salmonella enteritidis cannot be made completely negative. Further, even if the first heating and the second heating are performed at the same temperature, the effect of the present invention cannot be obtained. That is, food poisoning bacteria such as Salmonella enteritidis cannot be completely killed, or a part of the protein in the whole egg fluid undergoes thermal denaturation, resulting in reduced functionality.

【0012】このように第1段加熱で全卵液内のサルモ
ネラ・エンティリティディスなどの食中毒菌にストレス
を与えることにより、第2段加熱の温度が、従来法より
も低い、すなわち全卵液の蛋白質が変性し難い温度であ
っても、一般生菌数及び有害細菌数を減らすことができ
る。したがって、全卵液が加熱殺菌前に有していた機能
の低下が従来の殺菌全卵よりも起きていない新規な加工
液全卵を提供できる。
As described above, by applying stress to food poisoning bacteria such as Salmonella enteritidis in the whole egg solution by the first stage heating, the temperature of the second stage heating is lower than that of the conventional method, ie, the whole egg solution. Even at a temperature at which the protein is difficult to denature, the number of general viable bacteria and the number of harmful bacteria can be reduced. Therefore, it is possible to provide a novel processed liquid whole egg in which the function of the whole egg liquid before heat sterilization is not reduced as compared with the conventional sterilized whole egg.

【0013】また、本発明の殺菌効果をより増すため
に、第1段加熱後に冷却するとよい。本発明における冷
却とは第2加熱温度よりも低い温度まで品温をさげるこ
とである。これは、一旦加熱された全卵液を冷却するこ
とにより、加熱によってダメージを受けたサルモネラ・
エンティリティディスなどの食中毒菌が、冷却時及び第
2段加熱時の温度変化によってさらに大きなダメージを
受けるためである。冷却方法はどのような方法でも構わ
ないが、緩慢冷却よりも急速冷却が望ましい。この場
合、冷却温度は35℃以下が望ましい。冷却温度が例え
ば40〜45℃と高い場合には、温度変化が小さいため
効果は少なくなる。また、10℃以下まで冷却するとい
った極端な温度変化を与えるとさらに効果は増すが、実
際の製造を考えた場合は、次の第2加熱時の効率が悪く
なる。従って、この冷却は20〜35℃程度に冷却する
ことが望ましい。加熱後は、通常どおり冷却することが
望ましい。
Further, in order to further enhance the sterilizing effect of the present invention, it is preferable to cool after the first stage heating. Cooling in the present invention means lowering the product temperature to a temperature lower than the second heating temperature. This is because salmonella damaged by heating is cooled by cooling the whole heated egg solution.
This is because food poisoning bacteria such as an entity disc are more greatly damaged by temperature changes during cooling and second-stage heating. Although any cooling method may be used, rapid cooling is preferable to slow cooling. In this case, the cooling temperature is desirably 35 ° C. or less. When the cooling temperature is as high as, for example, 40 to 45 ° C., the effect is reduced because the temperature change is small. Further, when an extreme temperature change such as cooling to 10 ° C. or less is given, the effect is further increased, but when actual production is considered, the efficiency of the next second heating is deteriorated. Therefore, this cooling is desirably performed to about 20 to 35 ° C. After heating, it is desirable to cool as usual.

【0014】このように第一加熱で全卵液内のサルモネ
ラ・エンティリティディスなどの食中毒菌に加熱のダメ
ージを与え、さらに急速に冷却することによりダメージ
が倍増され、第2加熱の温度が食品衛生法に記載されて
いる60℃で3.5分間以上保持の条件よりも低い、す
なわち全卵液の蛋白質が変性し難い条件下で、サルモネ
ラ・エンティリティディスなどの食中毒菌を死滅させる
ことができる。また、全卵液中の蛋白質の熱変性が少な
いので、全卵液が加熱殺菌前に有していた機能の低下が
従来の殺菌全卵よりも起きていない新規な加工全卵液を
提供することができる。
[0014] Thus, the first heating causes heat damage to food poisoning bacteria such as Salmonella enteritidis in the whole egg solution, and furthermore, the damage is doubled by rapid cooling, and the temperature of the second heating is increased. It is possible to kill food poisoning bacteria such as Salmonella enteritidis under the condition of holding at 60 ° C. for 3.5 minutes or more as described in the Sanitation Law, that is, under the condition that the protein of whole egg fluid is hardly denatured. it can. In addition, since the protein in the whole egg solution is less thermally denatured, a new processed whole egg solution is provided in which the function of the whole egg solution before heat sterilization does not decrease compared to the conventional sterilized whole egg. be able to.

【0015】以上の製造工程は、従来法に基づき行えば
良いが、作業性を考え、連続式の殺菌装置を用いるとよ
い。また全行程終了後の全卵液は、二次的な微生物汚染
の無い条件下で容器に充填することが望ましい。容器は
密閉可能であればその材質や形態は問わない。
The above manufacturing steps may be performed based on a conventional method, but it is preferable to use a continuous sterilizer in consideration of workability. In addition, it is desirable that the whole egg solution after the completion of the entire process be filled in a container under conditions free of secondary microbial contamination. The material and form of the container are not limited as long as it can be sealed.

【0016】尚、本発明の加工全卵液及びその製造方法
に際しては、本発明の目的を損なわない範囲で、任意の
原料・成分を添加することができる。そのような原料・
成分としては、塩類、単糖類、ニ糖類、多糖類、糖アル
コールなどをあげることができる。
In the processed whole egg solution and the method for producing the same according to the present invention, arbitrary raw materials and components can be added as long as the object of the present invention is not impaired. Such raw materials
Examples of the components include salts, monosaccharides, disaccharides, polysaccharides, sugar alcohols and the like.

【0017】以下、本発明の実施例と試験例を述べる。Hereinafter, examples and test examples of the present invention will be described.

【実施例】実施例1 以下の工程では連続式殺菌装置(岩井機械(株)製、D
HX型プレート式熱交換器)を用いた。鶏卵を割卵して
得た全卵液を第1加熱プレートに通して58.5℃の温
度に加熱し、該温度で3秒間保持した後、第1冷却プレ
ートで30℃に冷却した。
EXAMPLE 1 In the following steps, a continuous sterilizer (manufactured by Iwai Machine Co., Ltd., D
HX type plate heat exchanger). The whole egg solution obtained by breaking the eggs was passed through a first heating plate, heated to a temperature of 58.5 ° C., kept at that temperature for 3 seconds, and then cooled to 30 ° C. with a first cooling plate.

【0018】次いで、第2加熱プレートで56.5℃の
温度に加熱し、該温度で5分間保持した後、熱交換プレ
ートで17℃に冷却し、第2冷却プレートで10℃以下
に冷却して、加工全卵液を製造した。これを、微生物に
よる2次汚染のない環境下でナイロンポリ袋に10kgづ
つ充填し、冷蔵保存した。
Then, the mixture is heated to a temperature of 56.5 ° C. by the second heating plate and kept at the temperature for 5 minutes, cooled to 17 ° C. by the heat exchange plate, and cooled to 10 ° C. or less by the second cooling plate. Thus, a processed whole egg solution was produced. This was filled into nylon polybags in an amount of 10 kg each in an environment free from secondary contamination by microorganisms, and stored in a refrigerator.

【0019】この加工全卵液は、一般性菌数102/g
未満、サルモネラ菌陰性/25g、大腸菌群陰性/0.
1gであり、製菓適性に優れている等加熱殺菌前の全卵
液と同等の機能性を有し、かつ、アミラーゼ活性が加熱
殺菌前の全卵液よりも低減されたいた。
This processed whole egg solution has a general bacteria count of 10 2 / g.
Less than, Salmonella negative / 25g, coliform group negative / 0.
1 g, having the same functionality as whole egg solution before heat sterilization, such as being superior in confectionery suitability, and having a lower amylase activity than whole egg solution before heat sterilization.

【0020】[0020]

【試験例】試験例1(細菌試験) 菌添加原料液卵 鶏卵を割卵して得られた全卵液(一般性菌数104
g)に有害細菌の指標菌としてS.enteritid
isと、大腸菌として、E.coli、Ent.col
oacae、Citi.freundiiの3種類の混
液を、それぞれ106/gの濃度となるように添加し、
汚染された全卵液を調整した。
[Test Example] Test Example 1 (Bacterial test) Egg liquid with added bacteria Eggs obtained by breaking chicken eggs (general bacteria count 10 4 /
g) as an indicator of harmful bacteria; enteritid
and E. coli as E. coli. coli, Ent. col
oacae, Citi. Freundii's three kinds of mixed solutions were added so that the concentration of each mixture was 10 6 / g,
The contaminated whole egg fluid was prepared.

【0021】次の5種類のサンプルを準備した。 発明品 菌添加原料卵を実施例1と同様の方法と装置で加熱し、
加工全卵液とした。
The following five types of samples were prepared. Inventive product Bacteria-added raw material egg is heated by the same method and apparatus as in Example 1,
The whole egg solution was processed.

【0022】比較品1 菌添加原料卵を加熱プレートで56.5℃まで加熱後、
該温度で5分間保持することにより殺菌し、次いで冷却
プレートで8℃以下に冷却して殺菌全卵液を製造した。
装置は、実施例1と同様のものを使用した。
COMPARATIVE PRODUCT 1 After heating the raw material-added egg to 56.5 ° C. on a heating plate,
Sterilization was carried out by maintaining at this temperature for 5 minutes, and then cooled to 8 ° C. or lower on a cooling plate to produce a sterilized whole egg solution.
The device used was the same as in Example 1.

【0023】比較品2 菌添加原料卵を加熱プレートで60℃まで加熱後、該温
度で3.5分間保持することにより殺菌し、次いで冷却
プレートで8℃以下に冷却して殺菌全卵液を製造した。
装置は、実施例1と同様のものを使用した。
COMPARATIVE PRODUCT 2 The raw egg with the added bacteria is heated to 60 ° C. on a heating plate, sterilized by holding at that temperature for 3.5 minutes, and then cooled to 8 ° C. or less on a cooling plate to remove the sterilized whole egg solution. Manufactured.
The device used was the same as in Example 1.

【0024】比較品3 菌添加原料卵をプレート式熱交換機で56.5℃の温度
に加熱し、該温度で5分間保持した後、次いで、一次冷
却することなくで58.5℃の温度に加熱し、該温度で
3.5分間保持した後、冷却プレートで8℃以下に冷却
して殺菌全卵液を製造した。装置は、実施例1と同様の
ものを使用した。
Comparative product 3 The raw material egg added with the bacterium was heated to a temperature of 56.5 ° C. in a plate heat exchanger and kept at that temperature for 5 minutes, and then heated to a temperature of 58.5 ° C. without primary cooling. After heating and maintaining at this temperature for 3.5 minutes, the mixture was cooled to 8 ° C. or less on a cooling plate to produce a sterilized whole egg solution. The device used was the same as in Example 1.

【0025】それぞれ、一般性菌数、サルモネラ菌数、
および大腸菌群数を測定した。
The number of general bacteria, the number of Salmonella,
And the number of coliforms was measured.

【0026】試験結果 表1に示すとおりである。すなわち表より、本発明品
は、一般性菌数が減少しており、サルモネラ菌が陰性/
25g、大腸菌群が10/gであり、加熱殺菌前の全卵
液と同等の機能性を有し、かつ、アミラーゼ活性が加熱
殺菌前の全卵液よりも低減されていることが理解でき
る。
Test results are as shown in Table 1. That is, from the table, the product of the present invention has a reduced number of general bacteria and is negative for Salmonella.
It can be understood that 25 g, the coliform bacterium is 10 / g, which has the same functionality as whole egg solution before heat sterilization, and that the amylase activity is lower than that of whole egg solution before heat sterilization.

【0027】[0027]

【表1】 [Table 1]

【0028】注1)一般生菌数の測定 標準寒天培
地で検出した。
Note 1) Measurement of general viable cell count Detected on a standard agar medium.

【0029】注2)サルモネラ菌数の測定 原液を
そのままXLD平板培地に直接塗沫し、36℃で1〜2
日間培養し、検出されるか否かを測定した。
Note 2) Measurement of Salmonella count The stock solution was directly applied to an XLD plate medium as it was,
After culturing for a day, it was measured whether or not it was detected.

【0030】注3)大腸菌群数の測定 デスオキシ
コーレート培地で検出した。
Note 3) Measurement of the number of coliforms The number was detected in a desoxycholate medium.

【0031】注4)アミラーゼ活性 今井の変法
(C. Imai : Poultry Science, 58(4)815-823(1979))
に準じて測定した。すなわち、試料全卵液15gを試験
管に採り45℃加温した。そこに予め45℃に加温して
おいた0.7%可溶性澱粉液15mlを加え、混合した
後に45℃で30分間保持した。保持後、15%トリク
ロロ酢酸溶液5mlを加えて反応を休止させて反応液を
得た。この反応液をろ過し、ろ液2.5mlに対して1
/1000mol/lのヨウ素溶液0.5mlを加えて発
色させた。この反応液の585nmにおける吸光度を分光
光度計で測定して判別した。試料全卵中にアミラーゼ活
性が残っている場合は、加えた可溶性澱粉は分解され、
ヨウ素液を加えても発色せず吸光度は小さくなる。逆
に、殺菌処理によってアミラーゼ活性が失活もしくは低
減されている場合は、加えた可溶性澱粉は分解されず、
ヨウ素澱粉反応により青紫色を呈し吸光度は大きくな
る。
Note 4) Amylase activity Imai's modified method (C. Imai: Poultry Science, 58 (4) 815-823 (1979))
It measured according to. That is, 15 g of the whole sample egg solution was placed in a test tube and heated at 45 ° C. Thereto was added 15 ml of a 0.7% soluble starch solution preliminarily heated to 45 ° C., and after mixing, the mixture was kept at 45 ° C. for 30 minutes. After the holding, 5 ml of a 15% trichloroacetic acid solution was added to stop the reaction, thereby obtaining a reaction solution. This reaction solution was filtered, and 2.5 mL of the filtrate was added to 1 mL.
A color was developed by adding 0.5 ml of a / 1000 mol / l iodine solution. The absorbance of the reaction solution at 585 nm was determined by measuring with a spectrophotometer. If the amylase activity remains in the whole sample egg, the added soluble starch is degraded,
Even if an iodine solution is added, no color develops and the absorbance decreases. Conversely, when the amylase activity is inactivated or reduced by the sterilization treatment, the added soluble starch is not decomposed,
Due to the iodine-starch reaction, a blue-violet color is exhibited and the absorbance increases.

【0032】試験例2(スポンジケーキ) 試験例1で用いた本発明品と比較例1〜3の全卵液およ
び割卵して得た全卵液(一般生菌数104/g)(対照
品)を用いて下記の配合割合および製造方法でスポンジ
ケーキを製造し、全卵の泡立ち性とスポンジケーキの品
位(容積、比容積、やわらかさ、および食感)を調べ
た。
Test Example 2 (Sponge cake) The whole egg solution of the product of the present invention used in Test Example 1 and Comparative Examples 1 to 3 and the whole egg solution obtained by breaking eggs (general viable cell count: 10 4 / g) ( A sponge cake was produced using the control product) according to the following mixing ratio and production method, and the foaming properties of whole eggs and the quality (volume, specific volume, softness, and texture) of the sponge cake were examined.

【0033】<配合> 全卵液 1500g 上白糖 1400g 薄力粉 1000g 牛 乳 300g とかしバター 100g ベーキングパウダー 6g<Blending> 1500 g of whole egg solution 1400 g of white sucrose 1 flour flour 1000 g Milk 300 g Milk butter 100 g Baking powder 6 g

【0034】<製造方法>全卵液と上白糖を混合し、2
5℃に加温した後、ワイヤーホイッパーを付けたミキサ
ーで所定の泡比重になるまで攪拌した。次いで予め混合
しておいた薄力粉とベーキングパウダーを加え、牛乳、
とかしバターを加えて、種比重が0.45〜0.47g
/mlの生地にした。直径18cmのスポンジ型に35
0gずつ充填し、180℃のオーブンで30分間焼成
し、スポンジケーキを調製した。
<Production method> The whole egg solution and the upper sucrose are mixed and mixed.
After heating to 5 ° C., the mixture was stirred with a mixer equipped with a wire whipper until a predetermined foam specific gravity was reached. Then add the flour and baking powder that have been mixed in advance,
Add the comb butter and the seed specific gravity is 0.45-0.47g
/ Ml dough. 35 for 18cm diameter sponge type
The sponge cake was prepared by filling 0 g each and baking in an oven at 180 ° C. for 30 minutes.

【0035】試験結果 表2に示すとおりである。すなわち表より、本発明品を
スポンジケーキの製造に用いると、泡立てに要する時間
が短く、スポンジケーキのボリュウームがあり、かつ、
ほどよいやわらかさで、口どけが良く、くちゃつきのな
い、食感の良好なスポンジケーキとなることが理解でき
る。
Test Results Table 2 shows the results. That is, from the table, when the product of the present invention is used for producing a sponge cake, the time required for whipping is short, and there is a sponge cake volume, and
It can be understood that the sponge cake is moderately soft, has a good mouthfeel, has no crumble, and has a good texture.

【0036】[0036]

【表2】 [Table 2]

【0037】注4)泡立ち性の測定方法 スポンジケ
ーキの製造に適する泡比重と言われている、0.28〜
0.30(g/ml)になるまでの時間を測定した。
Note 4) Method for measuring foaming property It is said that the foam specific gravity suitable for producing sponge cake is 0.28 to
The time until it reached 0.30 (g / ml) was measured.

【0038】注5)泡比重の測定方法 泡立てた生地
をぬきとり、次式により計算した。[(容器+生地)質
量(g)−容器質量(g)]/容器の容量(ml)
Note 5) Method of measuring foam specific gravity The foamed dough was wiped off and calculated by the following equation. [(Container + dough) mass (g) -container mass (g)] / capacity of container (ml)

【0039】注6)容積の測定方法 菜種を用いた容
積置換法により測定した。
Note 6) Method of measuring volume The volume was measured by a volume replacement method using rapeseed.

【0040】注7)比容積の測定方法 焼きあがった
スポンジケーキの質量に対する容積の比率を計算した。
数値が大きいほどふくらみが良好であることを示す。
Note 7) Method of measuring specific volume The ratio of the volume to the mass of the baked sponge cake was calculated.
The larger the value, the better the swelling.

【0041】注8)やわらかさの測定方法 スポンジ
ケーキの中央部分から、5cm×5cm×5cmの試料
片を切り出しして、レオメーター(不動工業(株)製N
RM−2010J−CW型レオメーター)で弾力性(g
/cm)を測定した。数値が大きいほどやわらかいこと
を示す。 レオメーター測定条件 プランジャー:20mmφ円盤型 フルスケール:200g 上昇スピード:6cm/min
Note 8) Method of measuring softness A 5 cm × 5 cm × 5 cm sample piece was cut out from the center of the sponge cake, and a rheometer (Nudo manufactured by Fudo Kogyo Co., Ltd.) was used.
Elasticity (g) with RM-2010J-CW type rheometer
/ Cm) was measured. The larger the value, the softer it is. Rheometer measurement conditions Plunger: 20mmφ disk type Full scale: 200g Ascending speed: 6cm / min

【0042】注9)食感の評価方法 よく訓練された
パネラー15名が5点満点法で評価し、平均値を点数と
した。数値が大きいほど食感が良好であることを示す。
Note 9) Evaluation method of texture 15 well-trained panelists evaluated by the 5 points scale method, and the average value was scored. The larger the value, the better the texture.

【0043】試験例3(カスタ−ドクリーム、茶碗蒸
し) 試験例2で用いた本発明品と比較例1〜3の全卵液およ
び対照卵を用いて、次の卵加工品を製造し、食感を調べ
た。
Test Example 3 (Custard cream, chawanmushi) Using the product of the present invention used in Test Example 2, the whole egg solution of Comparative Examples 1 to 3 and the control egg, the following processed egg products were produced, and I checked the feeling.

【0044】A.カスタードクリーム <配合> 牛乳 600g 全卵液 250g 上白糖 130g バニラエッセンス 少量A. Custard cream <Blend> Milk 600g Whole egg liquid 250g Upper sugar 130g Vanilla essence Small amount

【0045】<製造方法>全原料を混合溶解後、プリン
カップに70gずつ充填し、スチームボックスで85℃
で30分間加熱した。
<Manufacturing method> After mixing and dissolving all the raw materials, the pudding cup was filled with 70 g each, and the mixture was placed in a steam box at 85 ° C.
For 30 minutes.

【0046】B.茶碗蒸し <配合> だし汁 600.0g 全卵液 150.0g 薄口醤油 15.0g みりん 5.0g 食塩 2.5gB. Chawanmushi <Blend> Dashi soup 600.0g Whole egg solution 150.0g Thin soy sauce 15.0g Mirin 5.0g Salt 2.5g

【0047】<製造方法>全原料を混合溶解後、茶碗蒸
し容器に一定量ずつ充填し、蒸し器を使用して85℃で
30分間過熱凝固させた。
<Production method> After mixing and dissolving all the raw materials, a certain amount was filled into a bowl of steamed teacup, and the mixture was coagulated by heating at 85 ° C for 30 minutes using a steamer.

【0048】試験結果 表3に示すとおりである。すなわち表より、本発明品を
卵加工品の例としてカスタードプリンおよび茶碗蒸しの
製造に用いると、食感の良好な製品となることが理解で
きる。
Test results Table 3 shows the results. That is, from the table, it can be understood that when the product of the present invention is used as an example of a processed egg product for the production of custard pudding and chawanmushi, the product has a good texture.

【0049】[0049]

【表3】 [Table 3]

【0050】注10)食感の評価方法 よく訓練され
たパネラー10名が5点満点法で評価し、その平均値を
点数とした。数値が大きいほど食感が良好であることを
示す。
Note 10) Evaluation method of texture Ten well-trained panelists evaluated the score on a scale of 1 to 5, and the average value was used as the score. The larger the value, the better the texture.

【0051】[0051]

【発明の効果】以上述べたように、本発明によると、一
般生菌数が減少していると同時に、サルモネラ菌、大腸
菌群などの有害細菌も死滅しており、かつ、全卵液が加
熱殺菌前に有していた機能の低下が起こっておらず、例
えば起泡性の要求されるスポンジケーキの製造や、熱凝
固性の要求される卵加工品(カスタードプリン、茶碗蒸
しなど)の製造にも適した加工全卵液及びその製造方法
を提供することができる。
As described above, according to the present invention, the harmful bacteria such as Salmonella and Escherichia coli are killed at the same time as the number of general viable bacteria is reduced, and the whole egg solution is sterilized by heat. There is no decline in the functions it had before, such as in the production of sponge cakes that require foaming properties, and in the manufacture of processed egg products (such as custard pudding and chawanmushi) that require heat-coagulability. A suitable processed whole egg solution and a method for producing the same can be provided.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) A23L 1/187 A23L 1/48 1/48 A23B 5/00 Z Fターム(参考) 4B025 LB17 LE08 LG26 LG52 LG53 LP01 LP16 4B032 DB06 DK12 DK42 DK47 DP08 4B036 LE05 LF19 LH41 LH44 LP01 4B042 AC07 AD40 AE08 AH09 AP02 AP03 AP18 ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 7 Identification symbol FI Theme coat ゛ (Reference) A23L 1/187 A23L 1/48 1/48 A23B 5/00 Z F-term (Reference) 4B025 LB17 LE08 LG26 LG52 LG53 LP01 LP16 4B032 DB06 DK12 DK42 DK47 DP08 4B036 LE05 LF19 LH41 LH44 LP01 4B042 AC07 AD40 AE08 AH09 AP02 AP03 AP18

Claims (5)

【特許請求の範囲】[Claims] 【請求項1】サルモネラ菌が陰性/25g、大腸菌群が
10未満/gであり、加熱殺菌前の全卵液と同等の機能
性を有し、かつ、アミラーゼ活性が加熱殺菌前の全卵液
よりも低減された加工全卵液。
(1) Salmonella is negative / 25 g, E. coli group is less than 10 / g, has the same function as whole egg solution before heat sterilization, and has amylase activity of whole egg solution before heat sterilization. Also reduced processed whole egg fluid.
【請求項2】全卵液を、まず所定温度で所定時間第1加
熱した後、該温度より低い温度で所定時間保持して第2
加熱する請求項1記載の加工全卵液の製造方法。
2. The whole egg solution is first heated at a predetermined temperature for a first time and then kept at a temperature lower than the first temperature for a second time.
The method for producing a processed whole egg solution according to claim 1, wherein the heating is performed.
【請求項3】全卵液を、まず57〜60℃で1〜60秒
間第1加熱した後、55〜58℃で3.5〜10分間第
2加熱する加工全卵液の製造方法。
3. A method for producing a processed whole egg solution, wherein the whole egg solution is first heated at 57 to 60 ° C. for 1 to 60 seconds, and then secondly heated at 55 to 58 ° C. for 3.5 to 10 minutes.
【請求項4】全卵液を、まず所定温度で所定時間保持し
て第1加熱した後、一旦冷却し、第1加熱温度より低い
温度で所定時間保持して第2加熱する請求項1記載の加
工全卵液の製造方法。
4. The method of claim 1, wherein the whole egg solution is first held at a predetermined temperature for a predetermined time and first heated, and then cooled once, and then held at a temperature lower than the first heating temperature for a predetermined time and second heated. Process of producing whole egg solution.
【請求項5】全卵液を、まず57〜60℃で1〜60秒
間第1加熱した後、35℃以下に一旦冷却し、再度55
〜58℃で3.5〜10分間第2加熱する加工全卵液の
製造方法。
5. The whole egg solution is first heated at 57 to 60 ° C. for 1 to 60 seconds, cooled once to 35 ° C. or lower, and then cooled again to 55 ° C.
A method for producing a processed whole egg solution in which a second heating is performed at -58 ° C for 3.5-10 minutes.
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JP2014045690A (en) * 2012-08-30 2014-03-17 Fron Tier Engineering Co Ltd Method and device for heat treating liquid egg
JP5879002B1 (en) * 2015-03-02 2016-03-08 キユーピー株式会社 Manufacturing method of whole egg

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* Cited by examiner, † Cited by third party
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