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JPH0461629B2 - - Google Patents
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JPH0461629B2 - - Google Patents

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Publication number
JPH0461629B2
JPH0461629B2 JP59209513A JP20951384A JPH0461629B2 JP H0461629 B2 JPH0461629 B2 JP H0461629B2 JP 59209513 A JP59209513 A JP 59209513A JP 20951384 A JP20951384 A JP 20951384A JP H0461629 B2 JPH0461629 B2 JP H0461629B2
Authority
JP
Japan
Prior art keywords
krill
concentration
dope
fiber
sodium alginate
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
JP59209513A
Other languages
Japanese (ja)
Other versions
JPS6188862A (en
Inventor
Hirohisa Oomura
Isao Hayakawa
Michio Nonaka
Yasuhiko Sasamoto
Masakazu Hoshi
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.)
Maruha Nichiro Corp
Original Assignee
Taiyo Fishery 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 Taiyo Fishery Co Ltd filed Critical Taiyo Fishery Co Ltd
Priority to JP59209513A priority Critical patent/JPS6188862A/en
Publication of JPS6188862A publication Critical patent/JPS6188862A/en
Publication of JPH0461629B2 publication Critical patent/JPH0461629B2/ja
Granted legal-status Critical Current

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  • Meat, Egg Or Seafood Products (AREA)
  • Formation And Processing Of Food Products (AREA)

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、オキアミを原料として、粘弾性を有
し且つ栄養価のバランスの優れた新規な可食構造
物を提供すると共に、従来、十分に利用されてい
なかつたオキアミの有効利用を図り得る、オキア
ミからの可食構造物の成形法に関するものであ
る。
Detailed Description of the Invention [Field of Industrial Application] The present invention provides a novel edible structure using krill as a raw material, which has viscoelasticity and has an excellent balance of nutritional value. The present invention relates to a method for molding edible structures from krill, which makes it possible to effectively utilize krill that has not been used in the past.

〔従来の技術〕[Conventional technology]

オキアミは、広く海洋に分布する動物性プラン
クトンの一種でエビによく似た甲殻類であり、特
に南極海に棲息するユーフアーシア・スーペルバ
(Euphausia superba)種は、主にヒゲ鯨のエサ
として知られ、その資源量は数億トンとも数十億
トンともいわれており、その上味も良いので、将
来の蛋白資源として注目されている。
Krill is a type of zooplankton that is widely distributed in the ocean, and is a crustacean that resembles shrimp. In particular, the Euphausia superba species that lives in the Southern Ocean is mainly known as food for baleen whales. The resource amount is said to be in the hundreds of millions or even billions of tons, and because of its good taste, it is attracting attention as a future protein resource.

そこで、近年オキアミの利用に関する実用化が
種々試みられており、そのままの形で冷凍食品化
されたり、更に冷凍すり身とする試みも行われて
いる。
Therefore, in recent years, various attempts have been made to put krill into practical use, including turning it into a frozen food as it is, and even trying to turn it into frozen surimi.

〔発明が解決しようとする問題点〕 然し乍ら、オキアミの食用化は、未だ、臭い、
にがみ、消化酵素等の点で種々の問題が残つてお
り、技術的にも未解決な点が残つており、そのま
まの形で凍結された冷凍製品は解凍後直ちに利用
し難く、また、冷凍すり身を得るには種々の制限
を受ける。
[Problems to be solved by the invention] However, the use of krill for food still has problems such as odor,
Various problems remain regarding bittern, digestive enzymes, etc., and there are still unresolved technical points, and frozen products that are frozen in their original form are difficult to use immediately after thawing. Obtaining frozen surimi is subject to various restrictions.

従つて、本発明の目的は、上述の問題点を解決
した、オキアミの一層効果的な新規な利用方法を
提供することにある。
Therefore, an object of the present invention is to provide a new and more effective method for using krill that solves the above-mentioned problems.

〔問題点を解決するための手段〕[Means for solving problems]

本発明は、上記目的を、オキアミを、必要に応
じ前処理した後、これにアルギン酸ナトリウムを
添加混和し、蛋白質濃度を約2〜約20%、アルギ
ン酸ナトリウム濃度を約0.5〜約3%、PHを約
10.5〜約13.5に調整したドープを形成し、このド
ープを、必要に応じ濾過脱気した後、平板状に成
形、円筒状に成形、フレーク状に成形、若しくは
径約0.1〜約4mmの繊維状に押し出し成形し、こ
の成形物を、カルシウム塩或いはカリウム塩濃度
約0.2〜約12.0%、PH約2〜約9の液相にて、相
分離させることによつて、蛋白質を主成分とし粘
弾性を有する強固な構造物とすることを特徴とす
るオキアミからの可食構造物の成形法により達成
したものである。
The present invention achieves the above-mentioned purpose by pre-treating krill as necessary and then adding and mixing sodium alginate to the krill so that the protein concentration is about 2 to about 20%, the sodium alginate concentration is about 0.5 to about 3%, and the PH Approximately
A dope adjusted to 10.5 to about 13.5 is formed, and this dope is filtered and deaerated as necessary, and then formed into a flat plate, a cylinder, a flake, or a fiber with a diameter of about 0.1 to about 4 mm. By extrusion molding and phase separation of this molded product in a liquid phase with a calcium salt or potassium salt concentration of about 0.2 to about 12.0% and a pH of about 2 to about 9, it is possible to form a viscoelastic product with protein as the main component. This has been achieved by a method for molding edible structures from krill, which is characterized by forming a strong structure with.

尚、本発明は、本発明者等が先に提案した魚類
等からの可食構造物の形成法について更に種々検
討した結果、原料としてオキアミを用いた場合の
最適条件を見出し完成したものである。
The present invention was completed by further investigating the method of forming edible structures from fish etc. that the present inventors had previously proposed, and as a result found optimal conditions when using krill as a raw material. .

以下、本発明のオキアミからの可食構造物の成
形法をその実施態様に基づいて詳述する。
Hereinafter, the method for forming an edible structure from krill according to the present invention will be described in detail based on its embodiments.

本発明では、原材料であるオキアミをそのまま
用いることができ、そのまま用いることにより、
脱殻等の加工を施すことなく、且つ未利用部を生
じさせずに全体を有効に活用でき、栄養上バラン
スの良い成形品が得られるが、それらの一部(例
えば、肉部のみ)を用いるいこともできる。
In the present invention, krill, which is a raw material, can be used as it is, and by using it as it is,
It is possible to effectively utilize the entire product without processing such as shelling, and without creating unused parts, resulting in a nutritionally well-balanced molded product. You can also do things.

本発明の実施に際しては、先ずオキアミを必要
に応じ、前処理後、例えば、20μ以下、好ましく
は10μ以下に微粉砕する。
In carrying out the present invention, first, if necessary, krill is pretreated and then pulverized to, for example, 20 μm or less, preferably 10 μm or less.

上記の前処理法としては、極力プロテアーゼの
影響をさけ、内臓や皮の特異臭を避ける為には、
加熱失活せしめるか乾燥してフレーバーを変える
か又は冷凍粉砕によつて酵素の活性を抑制する等
の方法が好ましく、従つて、本発明においては、
オキアミを乾燥して得た乾燥粉末、オキアミを凍
結粉砕して得たオキアミ粉末並びに加熱変性せし
めたオキアミ粉末を、原料オキアミとして用いる
ことができる。
As for the above pretreatment method, in order to avoid the influence of protease as much as possible and avoid the peculiar odor of internal organs and skin,
Methods such as heat inactivation, drying to change the flavor, or freezing and pulverization to suppress enzyme activity are preferred; therefore, in the present invention,
Dry powder obtained by drying krill, krill powder obtained by freeze-pulverizing krill, and heat-denatured krill powder can be used as raw material krill.

しかし、本発明の成形法は、生のオキアミのダ
イレクトホモジネイトでも可能である。
However, the molding method of the present invention is also possible with a direct homogenate of raw krill.

次いで、上記の如く、必要に応じて前処理をし
たオキアミの蛋白質と濃度を調整する。蛋白質濃
度の調整は水分等と調整により行い、この蛋白質
濃度の好適な範囲は、アルギン酸ナトリウム濃度
及びアルカリ濃度に影響を受けるため一概には定
められず、また、オキアミ原料の種類、目的とす
る成形物の形態の差異によつて異なるが、約2.0
〜約20.0%とすることによつて目的とする製品を
良好な形態で得ることができ、生オキアミを用い
て繊維状の形成物を得ようとする場合、2〜5%
とするのが好ましい。
Next, as described above, the protein and concentration of the pretreated krill is adjusted as necessary. The protein concentration is adjusted by adjusting water, etc., and the preferred range of protein concentration cannot be determined unconditionally because it is affected by the sodium alginate concentration and alkali concentration, and also depends on the type of krill raw material and the intended shaping. Approximately 2.0, although it varies depending on the shape of the object.
~20.0%, the desired product can be obtained in good form, and when trying to obtain a fibrous product using raw krill, 2~5%
It is preferable that

また、上記のPHの調整は通常苛性ソーダで行い
PH約10.5〜約13.5の高アルカリ性とすることによ
つて本発明いの目的を達成し得る。
In addition, the above pH adjustment is usually done with caustic soda.
The object of the present invention can be achieved by making it highly alkaline with a pH of about 10.5 to about 13.5.

次いで、上述の如く蛋白質濃度及びPHを調整し
たドープに、アルギン酸ナトリウムを約0.5〜約
3%添加する。
Next, about 0.5 to about 3% sodium alginate is added to the dope whose protein concentration and pH have been adjusted as described above.

従つて、生のオキアミを用いて繊維状の成形物
を得る場合の蛋白質濃度、アルギン酸ナトリウム
濃度及びアルカリ(苛性ソーダ)濃度の割合(重
量基準)は、1:0.1〜1:0.05〜0.15が望まし
く、このような割合に調整することによつて蛋白
質の溶解、蛋白質とアルギン酸ナトリウムとの相
互作用並びにプロテアーゼの失活条件が決定さ
れ、斯る調整は、結果として繊維の粘弾性、強度
を決定する重要な条件となる。
Therefore, when obtaining a fibrous molded product using raw krill, the ratio (by weight) of protein concentration, sodium alginate concentration, and alkali (caustic soda) concentration is preferably 1:0.1 to 1:0.05 to 0.15. By adjusting these ratios, the conditions for protein dissolution, interaction between protein and sodium alginate, and protease inactivation are determined, and such adjustment is important in determining the viscoelasticity and strength of the fiber. This is the condition.

蛋白質及びアルギン酸ナトリウムの混和物から
なるドープから紡糸を妨げるような夾雑物を濾別
又は遠心分離等にて除去し更に好まくは遠心力又
は真空にて中の空気を除くことが望ましく、この
ドープは、ゲル化しないようにする為に温度の調
整を行う。
It is desirable to remove impurities that would interfere with spinning from a dope made of a mixture of protein and sodium alginate by filtration or centrifugation, and more preferably to remove air inside by centrifugal force or vacuum. Adjust the temperature to prevent gelation.

次いで、上記のドープを成形する。この成形法
を、最も困難な押出成形法により径約0.1〜約4
mmの繊維状に成形する場合を例に説明すると、ド
ープの粘度並びに目的とする成形品の粘弾性、強
度によつて選択されるが、上記ドープは、ノズル
口径0.1〜4.0mmのスタツフアーから押出成形さ
れ、連続的無結節フアイバー又は連続的結節状フ
アイバーとなる。この押出方法は、ガス圧、スク
リユー圧、ポンプ圧等、圧出のメカニズムの選択
により可能である。
Next, the above dope is molded. This molding method is performed using the most difficult extrusion molding method to create a mold with a diameter of about 0.1 to about 4
Taking as an example the case where the dope is molded into a fibrous shape of 0.1 mm in diameter, the dope is selected depending on the viscosity of the dope and the viscoelasticity and strength of the desired molded product. It is molded into continuous knotless fiber or continuous knotted fiber. This extrusion method is possible by selecting an extrusion mechanism such as gas pressure, screw pressure, pump pressure, etc.

然る後、上記フアイバー(成形物)は、PH約2
〜約9、好ましくはPH約4〜約7の液相(凝固
液)にて、相分離させることによつて、蛋白質及
びアルギン酸ナトリウムを主成分とし粘弾性を有
する強固な構造物となる。
After that, the fiber (molded product) has a pH of about 2.
By phase separation in a liquid phase (coagulation liquid) with a pH of about 9 to about 9, preferably about 4 to about 7, a strong structure containing protein and sodium alginate as main components and having viscoelasticity is obtained.

尚、フアイバーの成形は、通常、上記の液相中
に直接押出すことにより行われる。
Incidentally, the fiber is usually formed by directly extruding it into the above-mentioned liquid phase.

上記液相における反応は、フアイバー径0.2mm
程度ではPH7.0にて10秒程度で完了するが、フア
イバーの径、蛋白質、アルギン酸ナトリウムの濃
度、液相のPHによつて反応の速度、深部への浸透
程度、反応の強弱が形成され、上記液相のPHの調
整は、前記の蛋白質濃度、アルギン酸ナトリウム
の濃度と関連してフアイバーの粘弾性、強度を決
定する重要な条件であり、上記液相における反応
の完了により相分離が完成する。
The reaction in the above liquid phase is based on the fiber diameter of 0.2 mm.
Although it completes in about 10 seconds at a pH of 7.0, the speed of the reaction, the degree of deep penetration, and the strength of the reaction are determined by the diameter of the fiber, the concentration of protein, sodium alginate, and the pH of the liquid phase. Adjustment of the pH of the liquid phase is an important condition that determines the viscoelasticity and strength of the fiber in relation to the protein concentration and sodium alginate concentration, and phase separation is completed by completing the reaction in the liquid phase. .

前記カルシウム塩又はカリウム塩の濃度は、蛋
白質の凝集、アルギン酸ナトリウムの不溶化、ド
ープの構造化の為の反応、並びに構造化したフア
イバーの脱水の立場から重要な条件である。特に
アルギン酸ナトリウムの不溶化並びに脱水の為に
は0.2〜12%という高濃度を必要とし、通常1〜
7%で実施する。
The concentration of the calcium salt or potassium salt is an important condition from the standpoint of protein aggregation, insolubilization of sodium alginate, reactions for structuring the dope, and dehydration of the structured fiber. In particular, a high concentration of 0.2 to 12% is required for insolubilization and dehydration of sodium alginate, and usually 1 to 12%.
Implemented at 7%.

上述の如くして得られるフアイバーは、最後に
水洗される。この水洗は、通常「水」でも良いが
希薄な生理食塩水で洗浄後、最後に水洗すること
が望ましい。直ちに「水」で洗浄すると、急激な
表面の膨潤の為、表面が荒れることがあり、これ
等の現象を防ぐ為に生理食塩水で洗浄することに
よつて表面を滑らかにすることができる。
The fiber obtained as described above is finally washed with water. This rinsing may normally be done with water, but it is desirable to wash with dilute physiological saline and then wash with water at the end. Immediately washing with water may cause the surface to become rough due to rapid surface swelling; to prevent this phenomenon, the surface can be made smooth by washing with physiological saline.

また、前記のドープを、平板状に成形、円筒状
に成形、又はフレーク状に成形する場合には、通
常の成形法により容易に成形できる。
Further, when the dope is molded into a flat plate, a cylinder, or a flake, it can be easily molded by a normal molding method.

本発明のオキアミからの可食構造物の成形法に
より得られる可食構造物、例えば上述の繊維状成
形物は、そのまま又はバインダーにて結束して、
更には若干乾燥させるか又は膨化させて、食品に
加工する為の素材として利用される。
The edible structure obtained by the method of molding an edible structure from krill of the present invention, for example, the above-mentioned fibrous molded product, can be used as it is or bound with a binder,
It is then dried or expanded slightly and used as a material for processing into food.

(実施例) 以下に試験及び実施例を挙げる。(Example) Tests and examples are listed below.

試験例 解凍したオキアミをそのまま微粉砕した後、泡
止めブレンダーに入れ、蛋白質濃度、苛性ソーダ
濃度、及びアルギン酸ナトリウム濃度を種々変え
て数分乃至十数分ホモジナイズしてドープを得
た。得られたドープをノズル口径0.2〜0.4のスタ
ツフアーから窒素ガス圧して圧出し、塩酸でPHを
調整した塩化カルシウムと水溶液槽に注入して凝
集させた後、水洗して種々のフアイバーを得た。
Test Example After pulverizing thawed krill, it was placed in an anti-foam blender and homogenized for several to ten-odd minutes while varying the protein concentration, caustic soda concentration, and sodium alginate concentration to obtain a dope. The obtained dope was forced out with nitrogen gas pressure through a staff with a nozzle diameter of 0.2 to 0.4, poured into an aqueous solution tank with calcium chloride whose pH was adjusted with hydrochloric acid, and coagulated, and then washed with water to obtain various fibers.

それらの結果から、下記条件〜を選択する
ことにより粘弾性を有するフアイバーが得られる
こと、及び下記条件〜を変えることによりフ
アイバーの粘弾性、強度等の物性が変化すること
が判つた。
From these results, it was found that by selecting the following conditions ~, a fiber having viscoelasticity could be obtained, and that by changing the following conditions ~, the physical properties of the fiber, such as viscoelasticity and strength, could be changed.

蛋白質濃度は、2.0〜5.0%が好ましい。 The protein concentration is preferably 2.0 to 5.0%.

ドープのPHは、苛性ソーダでPH10.5〜13.5に
調整する。
Adjust the PH of the dope to 10.5 to 13.5 with caustic soda.

アルギン酸ナトリウム濃度は、0.5〜3.0%と
する。
The sodium alginate concentration is 0.5-3.0%.

凝固浴はPHを2〜9に調整する。 The pH of the coagulation bath is adjusted to 2-9.

凝固浴中の塩化カルシウム或いは塩化カリウ
ム水溶液の濃度は、0.2〜12%とする。
The concentration of calcium chloride or potassium chloride aqueous solution in the coagulation bath is 0.2 to 12%.

尚、凝固浴として海水(PH約7)を用いること
ができることも判つた。
It has also been found that seawater (PH approximately 7) can be used as the coagulation bath.

実施例 1 1Kgの生のオキアミむき身をそのまま磨砕した
後、蛋白質濃度3.0%、PH12.4(苛性ソーダ)、ア
ルギン酸ナトリウム濃度1.0%として、これを45
℃にてホモジナイズし、濾過脱気後、ドープとし
た。このドープをノズル口径0.25mmのスタツフア
ーから窒素ガス圧にて、塩酸でPH5に調整した塩
化カルシウム濃度3.8%の水溶液槽に注入し、約
10秒間反応させ、リールに巻き取つた(速度約25
m/min.)後、水洗してフアイバーを得た。得
られたフアイバーは、スパゲテイ状の粘弾性と弾
力を有していた。
Example 1 After grinding 1Kg of raw shucked krill, it was ground to 45% with a protein concentration of 3.0%, a pH of 12.4 (caustic soda), and a sodium alginate concentration of 1.0%.
The mixture was homogenized at ℃, filtered and degassed, and then used as a dope. This dope was injected under nitrogen gas pressure through a staff with a nozzle diameter of 0.25 mm into an aqueous solution tank with a calcium chloride concentration of 3.8% that had been adjusted to pH 5 with hydrochloric acid.
Let it react for 10 seconds, then wind it onto a reel (speed about 25
m/min.) and then washed with water to obtain a fiber. The obtained fiber had spaghetti-like viscoelasticity and elasticity.

実施例 2 1Kgの生のオキアミ・ラウンドをそのまま磨砕
した後、蛋白質濃度4.0%、PH13.0、アルギン酸
ナトリウム濃度1.3%として、これを45℃にてホ
モジナイズし、濾過脱気後、ドープとした。この
ドープを実施例1と同様にしてフアイバーを得
た。このフアイバーは、実施例1のフアイバーと
較べ差異は少なかつた。
Example 2 1Kg of raw krill rounds were ground as they were, then homogenized at 45°C with a protein concentration of 4.0%, a pH of 13.0, and a sodium alginate concentration of 1.3%, and after filtration and degassing, a dope was obtained. . A fiber was obtained using this dope in the same manner as in Example 1. This fiber had fewer differences compared to the fiber of Example 1.

実施例 3 1Kgの解凍したオキアミむき身をそのまま磨砕
した後、蛋白質濃度3.5%、PH11.9、アルギン酸
ナトリウム濃度0.9%として、これを50℃にてホ
モジナイズし、濾過脱気後、ドープとした。この
ドープをノズル口径0.4mmのスタツフアーから実
施例1と同様にPH5.0、塩化カルシウム濃度4%
の水溶液槽に注入し、約10秒間反応させ、リール
に巻き取つた後、水洗してフアイバーを得た。得
られたフアイバーは、実施例1で得られたフアイ
バーに較べてやや弱い粘弾性を示したが、巻き取
り速度約20m/min.でリールに巻き取ることが
可能であつた。
Example 3 After grinding 1 kg of thawed shelled krill, it was homogenized at 50° C. with a protein concentration of 3.5%, a pH of 11.9, and a sodium alginate concentration of 0.9%, and after filtration and degassing, it was made into a dope. This dope was poured from a staff with a nozzle diameter of 0.4 mm at a pH of 5.0 and a calcium chloride concentration of 4% as in Example 1.
The fiber was injected into an aqueous solution tank, reacted for about 10 seconds, wound up on a reel, and washed with water to obtain a fiber. Although the obtained fiber exhibited slightly weaker viscoelasticity than the fiber obtained in Example 1, it was possible to wind it onto a reel at a winding speed of about 20 m/min.

実施例 4 解凍した冷凍オキアミむき身より採取した落し
身1Kgを磨砕した後、蛋白質濃度2.5%、PH13.1、
アルギン酸ナトリウム濃度1.2%としてこれを、
45℃にホモジナイズし、濾過脱気後、ドープとし
た。このドープを実施例1と同様に、ノズル口径
0.25mmのスタツフアーから、PH7、塩化カルシウ
ム濃度5%の凝固槽に混入し、約10秒間反応させ
た後、水洗してフアイバーを得た。
Example 4 After grinding 1 kg of ground krill collected from thawed frozen shucked krill, the protein concentration was 2.5%, the pH was 13.1,
Assuming the sodium alginate concentration to be 1.2%,
The mixture was homogenized at 45°C, filtered and degassed, and then used as a dope. This dope was applied to the nozzle diameter in the same manner as in Example 1.
A 0.25 mm thick fiber was mixed into a coagulation bath with a pH of 7 and a calcium chloride concentration of 5%, reacted for about 10 seconds, and then washed with water to obtain a fiber.

実施例 5 オキアミむき身を凍結粉砕した後、蛋白質濃度
4%、アルギン酸ナトリウム濃度1.0%として、
PHを苛性ソーダで11.5に調整し、これらを40℃に
てホモジナイズし、濾過脱気後、ノズル口径0.2
mmのスタツフアーから押し出し、PH6に調整した
塩化カルシウム濃度3.5%の水溶液槽に注入し、
5秒間反応後水洗してフアイバーを得た。得られ
たフアイバーはグルテンの「そうめん」状の粘弾
性と弾力を有していた。尚、上記水溶液として、
海水(PH7.2)にカルシウム塩を溶解したものを
用いた場合にもフアイバーは凝固し、差異は少な
かつた。
Example 5 After freezing and crushing the shelled krill, the protein concentration was 4% and the sodium alginate concentration was 1.0%.
Adjust the pH to 11.5 with caustic soda, homogenize at 40℃, filter and degas, and use a nozzle diameter of 0.2.
It is extruded from a 3.5 mm statuf and injected into an aqueous solution tank with a calcium chloride concentration of 3.5% adjusted to pH 6.
After reaction for 5 seconds, the fiber was washed with water to obtain a fiber. The obtained fiber had viscoelasticity and elasticity similar to gluten noodles. In addition, as the above aqueous solution,
The fibers also coagulated when calcium salts were dissolved in seawater (PH7.2), and there was little difference.

〔発明の効果〕〔Effect of the invention〕

本発明によれば、食用化を図る上で種々の問題
のあつたオキアミを、問題を生じることなく効果
的に利用でき、しかも、従来十分に利用できなか
つた未利用部分、特にビタミン、ミネラルの有効
完全摂取利用、更には、アルギン酸ナトリウムの
添加混合による栄養保健の立場からビタミン等の
補強効果と併せて、オキアミ蛋白質の完全利用を
可能としたものであり、栄養上並びに資源の有効
利用の両側面から評価される。
According to the present invention, krill, which has had various problems in making it edible, can be used effectively without causing any problems, and moreover, it is possible to effectively utilize krill without causing any problems. In addition to the effective and complete intake and utilization of krill protein, the addition and mixing of sodium alginate has the effect of reinforcing vitamins, etc. from the standpoint of nutrition and health, and the complete utilization of krill protein is possible. It is evaluated from the aspect.

また、本発明の成形法により得られる可食構造
物の構造は、上述の特定の条件下でのプロテアー
ゼの失活並びに蛋白質と多糖類の相互作用等によ
り得られるもので、本発明の成形法によれば、過
去ゲル状ネツトワークが不可能であつた全オキア
ミ粉砕物からの繊維構造化が可能となる。
Furthermore, the structure of the edible structure obtained by the molding method of the present invention is obtained by the inactivation of protease and the interaction between protein and polysaccharide under the above-mentioned specific conditions. According to the authors, it is now possible to create a fiber structure from crushed whole krill, which was previously impossible to create a gel-like network.

更に、本発明によれば、全オキアミを、しかも
生の状態で高い歩留りで粘弾性を有する可食構造
物を得ることができ、本発明により得られる可食
構造物は、全蛋白、全ミネラル、全ビタミン、全
多糖類を完全に回収した高度の栄養を含むもので
ある。
Further, according to the present invention, it is possible to obtain an edible structure having viscoelasticity from whole krill in a high yield in a raw state, and the edible structure obtained by the present invention contains all protein, all minerals, and the like. It is highly nutritious, with all vitamins and polysaccharides completely recovered.

Claims (1)

【特許請求の範囲】 1 オキアミを、必要に応じ前処理した後、これ
にアルギン酸ナトリウムを添加混和し、蛋白質濃
度を約2〜約20%、アルギン酸ナトリウム濃度を
約0.5〜約3%、PHを約10.5〜約13.5に調整したド
ープを形成し、このドープを、必要に応じ濾過脱
気した後、平板状に成形、円筒状に成形、フレー
ク状に成形、若しくは径約0.1〜約4mmの繊維状
に押し出し成形し、この成形物を、カルシウム塩
或いはカリウム塩濃度約0.2〜約12.0%、PH約2
〜約9の液相にて、相分離させることによつて、
蛋白質を主成分とし粘弾性を有する強固な構造物
とすることを特徴とするオキアミからの可食構造
物の成形法。 2 ドープの蛋白質濃度が2〜5%で、成形物が
繊維状である、特許請求の範囲第1項記載のオキ
アミからの可食構造物の成形法。
[Claims] 1. After pretreating krill as necessary, sodium alginate is added and mixed to adjust the protein concentration to about 2 to about 20%, the sodium alginate concentration to about 0.5 to about 3%, and the pH to A dope adjusted to about 10.5 to about 13.5 is formed, and this dope is filtered and deaerated as necessary, and then formed into a flat plate, a cylinder, a flake, or a fiber with a diameter of about 0.1 to about 4 mm. This molded product is extruded into a shape with a calcium salt or potassium salt concentration of about 0.2 to about 12.0% and a pH of about 2.
~ By phase separation in the liquid phase of about 9,
A method for forming an edible structure from krill, which is characterized by forming a strong structure containing protein as a main component and having viscoelasticity. 2. The method for molding an edible structure from krill according to claim 1, wherein the protein concentration of the dope is 2 to 5% and the molded product is fibrous.
JP59209513A 1984-10-05 1984-10-05 Method of molding edible structure from krill Granted JPS6188862A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59209513A JPS6188862A (en) 1984-10-05 1984-10-05 Method of molding edible structure from krill

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59209513A JPS6188862A (en) 1984-10-05 1984-10-05 Method of molding edible structure from krill

Publications (2)

Publication Number Publication Date
JPS6188862A JPS6188862A (en) 1986-05-07
JPH0461629B2 true JPH0461629B2 (en) 1992-10-01

Family

ID=16574037

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59209513A Granted JPS6188862A (en) 1984-10-05 1984-10-05 Method of molding edible structure from krill

Country Status (1)

Country Link
JP (1) JPS6188862A (en)

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5264453A (en) * 1975-11-21 1977-05-27 Kiyokuyou Kk Method of separating protein from euphausiid
JPS577704A (en) * 1980-06-12 1982-01-14 Jitsuo Asakawa Tire
JPS5750848A (en) * 1980-09-13 1982-03-25 Suisanchiyou Chokan Preparation of new protein food ingredient using krill

Also Published As

Publication number Publication date
JPS6188862A (en) 1986-05-07

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