JPS59196032A - Method for preventing denaturation of krill and for keeping its freshness - Google Patents
Method for preventing denaturation of krill and for keeping its freshnessInfo
- Publication number
- JPS59196032A JPS59196032A JP58072435A JP7243583A JPS59196032A JP S59196032 A JPS59196032 A JP S59196032A JP 58072435 A JP58072435 A JP 58072435A JP 7243583 A JP7243583 A JP 7243583A JP S59196032 A JPS59196032 A JP S59196032A
- Authority
- JP
- Japan
- Prior art keywords
- krill
- ethanol
- alcohol
- temperature
- protein
- 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.)
- Pending
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- Meat, Egg Or Seafood Products (AREA)
Abstract
Description
【発明の詳細な説明】
南氷洋のナンキョクオキアミ(E u p h a s
ia 5uPerba)の推定資源量は10億トンと
も50億1−ンとも云われ、適正漁獲量は5子方トン以
上とされる、人類最大の未利用蛋白資源であり、その利
用加工の為の開発がなされている。[Detailed description of the invention] Antarctic krill (Eupha s) of the Southern Ocean
The estimated resource amount of Perba (ia 5 u Perba) is said to be between 1 billion tons and 5 billion tons, and the appropriate catch is said to be more than 5 tons, making it the largest unused protein resource for humankind. development is underway.
古くからカニやエビの体組織特に肝臓はプロテアーゼ活
性が強いことが知られており、オキアミもこの種の酵素
やリパーゼが強いことがM察され、捕獲後4時間を経過
すると肉質の軟化、体色の劣化、エキス分の流失など自
己消化現象が生じてくる。この為、現在漁獲物の9割は
船上で海水によりボイルし、その後冷凍され(ボイル冷
凍)、1割は直ちに冷凍される(主冷凍)。現状の方法
ではオキアミのような小型漁獲物は、層厚く堆積した状
態で、凍結等の保存処理をすることになるが、支持組織
が魚類に比し軟弱なオキアミでは、その際に加わる外圧
により体組織が壊れ易く、この結果、内臓や血液の酵素
が肉組織に拡散して、自己消化を促進する為、冷凍貯蔵
中にも酸化系酵素チロシナーゼの働きにより、体成分チ
ロシンよりメラニンが生成され、体表面が黒変化し、商
品価値を著しく損なう等、鮮度保持が難しく、解凍時に
オキアミ特有の臭気の発生を防ぐ事が出来ない為に消費
者に敬遠され、陸上で行なう2次加工、又生鮮食料品と
しての消費拡大がなされておらず、遊魚用釣りエサとし
ての消費が大半を占めているのが現状である。ボイル処
理により自家酵素に基く自己消化や黒変を防止し、ドリ
ップを少なくする事が出来るが、完全なものではなく、
又蛋白を熱変性させる為、蛋白の変性度が大きく2次加
工利用の範囲が狭くなり、消費の拡大を図る事が出来な
い。即ちオキアミの大量消費を図るには、陸上における
2次加工方法の問題ではなく、洋上捕獲後から陸上にお
ける2次加工迄の数ケ月の期間の鮮度保持、変性防止の
方法が最大の問題である。It has been known for a long time that the body tissues of crabs and shrimp, especially the liver, have strong protease activity, and krill is also thought to have strong enzymes and lipase. Autolysis phenomena such as color deterioration and loss of extract components occur. For this reason, currently 90% of the catch is boiled in seawater on board and then frozen (boil freezing), and 10% is immediately frozen (main freezing). In the current method, small catches such as krill are preserved in a thick layer by freezing or other means, but krill, whose supporting tissue is softer than that of fish, suffers from the external pressure applied during this process. Body tissue is easily destroyed, and as a result, enzymes from internal organs and blood diffuse into the meat tissue and promote autolysis. Therefore, even during frozen storage, melanin is produced from body component tyrosine by the action of the oxidative enzyme tyrosinase. It is difficult to maintain freshness, such as the body surface turning black and a significant loss of product value, and it is not possible to prevent the generation of the odor characteristic of krill when thawing. Currently, consumption as a fresh food has not been expanded, and most of the consumption is as fishing bait for recreational fish. Boiling treatment can prevent autolysis and blackening caused by autologous enzymes and reduce dripping, but it is not perfect.
Furthermore, since the protein is thermally denatured, the degree of denaturation of the protein is large, and the range of secondary processing and utilization is narrowed, making it impossible to increase consumption. In other words, in order to mass consume krill, the biggest issue is not the secondary processing method on land, but the method to maintain freshness and prevent denaturation during the several months period from capture at sea to secondary processing on land. .
洋上にて陸上における様な2次加工迄可能であれば、根
本的な解決が可能であるが、南氷洋の船上に於ける大量
処理という状況を考えた場合、これは不可能である。A fundamental solution would be possible if it were possible to perform secondary processing at sea as on land, but this is not possible when considering the situation of mass processing on board ships in the Southern Ocean.
本発明ではこの様な点を考慮して、従来のボイル冷凍法
に変る蛋白変性度の少ない、又確実に自己消化、黒変、
臭気発生等を防止し得る、簡便なる1次処理、保存法を
提供するものである。Taking these points into consideration, the present invention reduces the degree of protein denaturation compared to the conventional boil freezing method, and reliably eliminates autolysis, blackening, and
This provides a simple primary treatment and preservation method that can prevent odor generation and the like.
本発明を詳説すれば、エタノール等のアルコールを冷媒
及び蛋白−固、脱水、脱脂剤として使用するもので、保
存期間、2次加工処理方法等の目的の違いによりエタノ
ールの温度を5〜−50℃の間にて変化させ蛋白の変性
度等を調節する。冷却したエタノール中に採取した生鮮
オキアミを浸漬し、エタノールの比重によりオキアミを
懸垂した状態で急速冷凍を行なうと同時にエタノール浸
透による体表面の蛋白凝固、表面脱水、表面脱脂、酵素
失活を行ない、そのままの状態にて低温保存を行ないオ
キアミの変性防止及び鮮度を良好に保つオキアミの鮮度
保持方法である。To explain the present invention in detail, alcohol such as ethanol is used as a refrigerant and as a protein solidifying, dehydrating, and degreasing agent. ℃ to adjust the degree of protein denaturation, etc. The collected fresh krill is immersed in cooled ethanol, and the krill is rapidly frozen in a suspended state due to the specific gravity of the ethanol.At the same time, protein coagulation on the body surface, surface dehydration, surface defatting, and enzyme inactivation are performed by ethanol permeation. This is a method for maintaining the freshness of krill by storing it in its original state at a low temperature to prevent krill from denaturing and maintain good freshness.
本発明が従来の方法と異なる点は
(1)エタノールをオキアミの冷媒及び蛋白凝固、脱水
、脱脂、酵素失活剤として使用しエタノールの温度及び
濃度を調節してオキアミを浸漬させる事に依り冷凍速度
、蛋白の変性度、脱水度、脱脂底、酵素失活度を調整す
る事により良好な冷凍保存が可能となる。すなわち従来
カツオ漁船等に使用されているブライン浸漬式の食塩ブ
ラインでは22〜23%濃度で最低温度−17℃位迄冷
却している。この凍結カツオの皮下内への食塩の侵入は
皮下5閣位迄であり、この皮下5m+n迄の肉層の食塩
濃度は0.48〜3.75%である。そしてこの皮下5
+nm迄の内層の食塩濃度が2%以上の時には肉色の褐
変や脂質の酸敗が著しくなることが認められている。こ
の魚体内への食塩浸入の程度については、ブライン温度
の高低が影響している。The present invention differs from conventional methods in that (1) ethanol is used as a refrigerant for krill and as a protein coagulation, dehydration, defatting, and enzyme inactivation agent, and the temperature and concentration of ethanol are adjusted to allow the krill to be immersed in freezing; Good frozen storage is possible by adjusting the speed, degree of protein denaturation, degree of dehydration, degreased bottom, and degree of enzyme inactivation. That is, the salt brine of the brine immersion type conventionally used in skipjack fishing boats and the like has a concentration of 22 to 23% and is cooled to a minimum temperature of about -17°C. Salt infiltrates the frozen bonito subcutaneously up to the 5th subcutaneous level, and the salt concentration in the meat layer up to 5m+n subcutaneously is 0.48 to 3.75%. And this subcutaneous 5
It has been observed that when the salt concentration in the inner layer up to +nm is 2% or more, browning of the flesh color and rancidity of lipids become significant. The degree of salt infiltration into the fish body is influenced by the brine temperature.
すなわちブライン温度が高い場合、食塩の浸入が高く、
又緩慢凍結になり、肉色の褐変、蛋白の変性などが進行
する。本発明においてはこの現象を積極的に利用し従来
のボイル冷凍に変る方法としてエタノール温度の高低及
び濃度の濃淡によりオキアミの凍結速度及びエタノール
の皮下浸入環を制御してエタノールによる蛋白の変性等
を行ない自家酵素に基く自己消化や黒変を防止し、ドリ
ップを少なくする処理方法である。In other words, when the brine temperature is high, salt penetration is high;
In addition, slow freezing occurs, resulting in browning of the meat color and denaturation of proteins. In the present invention, we actively utilize this phenomenon and, as an alternative to the conventional boil freezing method, we control the freezing rate of krill and the subcutaneous penetration ring of ethanol by controlling the temperature and concentration of ethanol to prevent protein denaturation by ethanol. This is a treatment method that prevents autolysis and blackening based on autologous enzymes and reduces dripping.
(2)エタノール中にオキアミを懸垂させながら冷凍す
る為、外圧による体組織の破壊がなく、内臓や血液の酵
素が肉組織に拡散しない為、自己消化を生ずる事がない
。(2) Since krill is frozen while suspended in ethanol, body tissues are not destroyed by external pressure, and enzymes from internal organs and blood do not diffuse into meat tissues, so autolysis does not occur.
(3)エタノールを冷媒として使用し、低温エタノール
にオキアミを浸漬する事により、瞬間的な急速冷凍が可
能となり、緩慢冷凍時に生ずる組織破壊、蛋白変性がな
い良好な冷凍保存が可能である。(3) By using ethanol as a refrigerant and immersing krill in low-temperature ethanol, instantaneous rapid freezing is possible, and good frozen preservation is possible without the tissue destruction and protein denaturation that occur during slow freezing.
(4)エタノールによる蛋白凝固である為、陸上におけ
る2次加工の利用度が高い。(4) Since protein coagulation is performed using ethanol, secondary processing on land is highly applicable.
(5)オキアミの冷凍状態においてエタノールが存在す
る為、スラリー状態であり、移送取扱いが容易となる。(5) Since ethanol is present in the frozen state of krill, it is in a slurry state and is easy to transport and handle.
(6)エタノールを冷媒として使用する為、冷凍操作が
容易に行なえる。(6) Since ethanol is used as a refrigerant, freezing operations can be performed easily.
(7)処理機械が簡単で、小型であり、船上におけるオ
キアミの大量処理が可能となる。(7) The processing machine is simple and small, making it possible to process large quantities of krill on board.
次に本発明の詳細な説明すると保冷材等により断熱され
たエタノール槽に濃度50〜95%のエタノールを約4
0%程度充たし、温度を5〜−50℃に冷却した後に、
漁獲されたオキアミを洗浄後光のままエタノール中に投
入する。Next, to explain the present invention in detail, approximately 40% of ethanol with a concentration of 50 to 95% is poured into an ethanol tank insulated with a cold insulating material, etc.
After filling the tank to about 0% and cooling the temperature to 5 to -50℃,
After washing, the caught krill is placed in ethanol while still being washed.
(1)オキアミの生鮮度を高く蛋白変性度を低く保つ場
合は、ブラインクーラー等の冷凍機により、エタノール
温度を−20〜−50℃に保ち、5℃から一20℃程度
迄の凍結通過時間を短くし、急速凍結を行なう事により
エタノールの浸入を皮下表面のみにし、エタノールによ
る蛋白の変性を表面のみにとどめる。冷凍時間は10分
〜2時間程度である。凍結凝固処理が終ると別のエタノ
ール槽にエタノールをポンプ等により移送し、凍結凝固
処理に使用していたエタノール槽は貯蔵用として使用し
、槽内を−30〜−50℃にまで下げそのまま冷凍貯蔵
する。(1) If you want to keep the freshness of krill high and the degree of protein denaturation low, use a freezer such as a brine cooler to keep the ethanol temperature at -20 to -50℃, and freeze the krill from 5℃ to about -20℃ for a long time. By shortening the time and performing rapid freezing, ethanol can only enter the subcutaneous surface, and denaturation of proteins by ethanol can be limited to the surface. Freezing time is about 10 minutes to 2 hours. After the freeze-coagulation process is completed, the ethanol is transferred to another ethanol tank using a pump, etc. The ethanol tank used for the freeze-coagulation process is used for storage, and the temperature inside the tank is lowered to -30 to -50℃ and then frozen. Store.
(2)オキアミを二次加工素材として鮮度保持貯蔵を行
なう場合は、エタノールによるオキアミの蛋白凝固、脱
水、脱脂、酵素失活を積極的に行なう為、浸漬時のエタ
ノール濃度を70〜95%とし温度を5〜−20℃位に
保つ。オキアミを浸漬させ無凍結又は部分凍結の状態で
10分〜1時間保持し、エタノールをオキアミに浸透さ
せて蛋白凝固、脱水、脱脂、酵素失活をさせた後にブラ
インクーラー等により一30℃位まで冷却し凍結凝固処
理を行ない、そのままエタノールに浸漬した状態で冷凍
貯蔵するか、又は別のエタノール槽にエタノールをポン
プ等により移送し、凍結凝固処理に使用していたエタノ
ール槽は貯蔵用として使用し、槽内を一30〜50℃に
まで下げ、そのまま冷凍貯蔵する。(2) When storing krill to maintain its freshness as a secondary processing material, the ethanol concentration during soaking should be 70-95% in order to actively coagulate the proteins, dehydrate, degrease, and deactivate the enzymes in the krill using ethanol. Keep the temperature between 5 and -20°C. Krill is soaked and kept in an unfrozen or partially frozen state for 10 minutes to 1 hour, and ethanol is infiltrated into the krill to cause protein coagulation, dehydration, defatting, and enzyme inactivation, and the temperature is then heated to around -30℃ in a brine cooler etc. Either cool and freeze-coagulate it, then store it in a frozen state immersed in ethanol, or transfer the ethanol to another ethanol tank using a pump, etc., and use the ethanol tank used for freeze-coagulation for storage. The inside of the tank is lowered to -30 to 50°C and stored frozen.
特許出願人 西用文男 山本隆司 田口益文Patent applicant Fumio Nishiyo Takashi Yamamoto Masufumi Taguchi
Claims (1)
アルコールに浸漬し、アルコールの比重により懸垂保持
した状態で、オキアミの急速冷凍を行なうと同時に、ア
ルコール浸透によるオキアミ体表面の蛋白凝固、表面脱
水、表面脱脂、酵素失活を行なう。この際にアルコール
の温度を変化させる事により、オキアミの冷凍速度及び
アルコールの浸透の深さを変えオキアミ体表面の蛋白凝
固、表面脱水、表面脱脂、酵素失活を′@整しそのまま
の状態又はアルコール除去後、低温保存を行なう事を特
徴とするオキアミの変性防止及び鮮度保持の方法。Fresh krill is immersed in alcohol such as ethanol cooled to 5 to -50°C, and kept suspended due to the specific gravity of the alcohol. At the same time, the krill is rapidly frozen, and at the same time, protein coagulation on the surface of the krill body due to alcohol penetration and surface dehydration. , surface degreasing, and enzyme deactivation. At this time, by changing the temperature of the alcohol, the freezing rate of the krill and the depth of penetration of the alcohol can be changed to adjust the protein coagulation, surface dehydration, surface degreasing, and enzyme deactivation on the surface of the krill body. A method for preventing denaturation and maintaining freshness of krill, which is characterized by storing krill at a low temperature after removing alcohol.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58072435A JPS59196032A (en) | 1983-04-23 | 1983-04-23 | Method for preventing denaturation of krill and for keeping its freshness |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58072435A JPS59196032A (en) | 1983-04-23 | 1983-04-23 | Method for preventing denaturation of krill and for keeping its freshness |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS59196032A true JPS59196032A (en) | 1984-11-07 |
Family
ID=13489218
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58072435A Pending JPS59196032A (en) | 1983-04-23 | 1983-04-23 | Method for preventing denaturation of krill and for keeping its freshness |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59196032A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2000023546A1 (en) * | 1998-10-21 | 2000-04-27 | Universite De Sherbrooke | Method of extracting lipids from marine and aquatic animal tissues |
US8278351B2 (en) | 2001-07-27 | 2012-10-02 | Neptune Technologies & Bioressources, Inc. | Natural marine source phospholipids comprising polyunsaturated fatty acids and their applications |
US8586567B2 (en) | 2009-10-29 | 2013-11-19 | Acasti Pharma, Inc. | Concentrated therapeutic phospholipid compositions |
WO2016161575A1 (en) * | 2015-04-08 | 2016-10-13 | 江南大学 | Method for dehydrating antarctic krill and extracting shrimp oil |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5063542A (en) * | 1973-10-11 | 1975-05-30 | ||
JPS5765173A (en) * | 1980-10-11 | 1982-04-20 | Kisai Food Kogyo Kk | Method of freezing fresh food |
-
1983
- 1983-04-23 JP JP58072435A patent/JPS59196032A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5063542A (en) * | 1973-10-11 | 1975-05-30 | ||
JPS5765173A (en) * | 1980-10-11 | 1982-04-20 | Kisai Food Kogyo Kk | Method of freezing fresh food |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2000023546A1 (en) * | 1998-10-21 | 2000-04-27 | Universite De Sherbrooke | Method of extracting lipids from marine and aquatic animal tissues |
US8278351B2 (en) | 2001-07-27 | 2012-10-02 | Neptune Technologies & Bioressources, Inc. | Natural marine source phospholipids comprising polyunsaturated fatty acids and their applications |
US8383675B2 (en) | 2001-07-27 | 2013-02-26 | Neptune Technologies & Bioressources, Inc. | Natural marine source phospholipids comprising polyunsaturated fatty acids and their applications |
US8680080B2 (en) | 2001-07-27 | 2014-03-25 | Neptune Technologies & Bioressources, Inc. | Natural marine source phospholipids comprising polyunsaturated fatty acids and their applications |
US10028968B2 (en) | 2001-07-27 | 2018-07-24 | Aker Biomarine Antarctic As | Natural marine source phospholipids comprising polyunsaturated fatty acids and their applications |
US8586567B2 (en) | 2009-10-29 | 2013-11-19 | Acasti Pharma, Inc. | Concentrated therapeutic phospholipid compositions |
US9475830B2 (en) | 2009-10-29 | 2016-10-25 | Acasti Pharma Inc. | Concentrated therapeutic phospholipid compositions |
US10130644B2 (en) | 2009-10-29 | 2018-11-20 | Acasti Pharma Inc. | Concentrated therapeutic phospholipid compositions |
US10617702B2 (en) | 2009-10-29 | 2020-04-14 | Acasti Pharma Inc. | Concentrated therapeutic phospholipid compositions |
WO2016161575A1 (en) * | 2015-04-08 | 2016-10-13 | 江南大学 | Method for dehydrating antarctic krill and extracting shrimp oil |
US10492508B2 (en) * | 2015-04-08 | 2019-12-03 | Jiangnan University | Method for extracting oil from dehydrated Euphausia superba |
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