JPS6188862A - Method of molding edible structure from krill - Google Patents

Method of molding edible structure from krill

Info

Publication number
JPS6188862A
JPS6188862A JP59209513A JP20951384A JPS6188862A JP S6188862 A JPS6188862 A JP S6188862A JP 59209513 A JP59209513 A JP 59209513A JP 20951384 A JP20951384 A JP 20951384A JP S6188862 A JPS6188862 A JP S6188862A
Authority
JP
Japan
Prior art keywords
krill
concentration
sodium alginate
dope
liquid phase
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
JP59209513A
Other languages
Japanese (ja)
Other versions
JPH0461629B2 (en
Inventor
Hirohisa Omura
大村 浩久
Isao Hayakawa
功 早川
Michio Nonaka
野中 道夫
Yasuhiko Sasamoto
笹本 泰彦
Masakazu Hoshi
星 昌和
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)

Abstract

PURPOSE:To obtain the titled novel food having viscoelastic properties and improved balance of nutritive value, by blending krill with sodium alginate, processing the blend into specific dope, molding it into a specific shape and subjecting the molded article to liquid phase separation with a Ca or K salt. CONSTITUTION:Krill is directly used or pretreated, finely ground into preferably <=10mu, blended with sodium alginate to form dope having about 2-20wt% protein concentration, 0.5-3wt% sodium alginate concentration, and about 10.5-13.5pH, which is optionally filtered and deaerated, extruded into a fibrous state with about 0.1-4mm diameter, and molded, or molded into a flat, cylindrical, or flaky state, and the molded article is subjected to liquid phase separation with a liquid phase having about 0.2-12.0wt% Ca salt K salt concentration at about 2-9pH, to give the aimed food.

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・ったオキアミの
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 forming 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、広く南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1)
息するニーファーシア・スーペルバ(Euphausi
a 5uperba)種は、主にヒゲ鯨のエサとして知
られ、その資源量は数位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’amとして
1主目されている。
Krill is a type of zooplankton that is widely distributed in the Southern Ocean, and is a crustacean that resembles shrimp, especially in the Southern Ocean1).
Breathing Neifersia Superba (Euphausi)
The a. There is.

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a製品化されたり、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 to practical use, including turning it into cold a product 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〕[Problem that the invention seeks to solve]

然し乍ら、オキアミの食用化は、未だ、臭い、にがみ、
消化6ゲ素等の点で種々の問題が残っており、技術的に
も未解決な点が残っており、そのままの形で凍結させた
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。
However, the use of krill for food still has problems with odor, bitterness, and
Various problems remain in terms of digestive elements, etc., and there are still unresolved technical points.Frozen products that are frozen in their original form are difficult to use immediately after thawing, and frozen surimi There are various restrictions on obtaining this.

従って、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、径約O1)〜約4Il1)の繊維状に押
し出し成形するか、又は平板状、円筒状若しくはフレー
ク状に成形し、この成形物を、カルシウム塩或いはカリ
ウム塩濃度的0.2〜約12.0%、pl+約2〜約9
の液相にて、相分別させることによって、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 object 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% and the sodium alginate concentration is about 0.5 to about 3%. , forming a dope with a pH adjusted to about 10.5 to about 13.5, filtering and degassing this dope as necessary, and then extruding it into a fiber shape with a diameter of about O1) to about 4I1), or Or molded into a flat, cylindrical or flake shape, and the molded product is prepared with a calcium salt or potassium salt concentration of 0.2 to about 12.0%, pl+ about 2 to about 9
This was achieved by a method of molding edible structures from krill, which is characterized by phase separation in the liquid phase of krill to form a strong structure with viscoelasticity and mainly consisting of protein.

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ti構造物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 developed based on further studies on the method of forming edible Ti structures from fish etc. that the present inventors had previously proposed.
This work was completed by finding the 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、犀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1、脱殻等の加工
を施すことなく、且つ未利用部を生しさせずに全体をを
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、内部のみ)を用いることも
できる。
In the present invention, krill, which is a rhinoceros material, can be used as it is, and by using it as it is, 1. It is possible to effectively utilize the whole without undergoing processing such as shelling, and without creating unused parts, and it is nutritious. Although a well-balanced molded product can be obtained, a part of the molded product (for example, only the inside) can also be used.

本発明の実施に際しては、先ずオキアミを4・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, krill is pretreated as required in step 4 and then finely pulverized to, for example, 20 μm or less, preferably 10 μm or less.

上記の前処理法としては、極カブロチアーゼの影響をさ
け、内蔵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っ
て酵素の活性を抑制する等の方法が好ましく、従って、
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 methods, in order to avoid the influence of polar cabrothiase and the peculiar odor of the internal organs and skin, the enzyme activity may be suppressed by heat inactivation, drying to change the flavor, or freezing and pulverization. The method of is preferable, 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
ホモシネイトでも可能である。
However, the molding method of the present invention is also possible with direct homogenates of raw krill.

次いで、上記の如く、必要に応じてiii+処理をした
オキアミの蛋白質の濃度を調整する。蛋白質濃度の調整
は水分等の調整により行い、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
響を受けるため一層には定められず、また、オキアミ原
料のlf’、 肋、目的とする成形物の形態の差異によ
って異なるが、約2.0〜約20.0%とすることによ
っ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 concentration of protein in the iii+-treated krill is adjusted as necessary. The protein concentration is adjusted by adjusting the water content, etc., and the preferred range of this protein concentration cannot be further determined because it is affected by the sodium alginate concentration and the alkali concentration. It varies depending on the shape of the molded product, but by setting the content to about 2.0 to about 20.0%, the desired product can be obtained in a good shape. If you try to get
It is preferably 2 to 5%.

また、上記のpl+の調整は通富苛性ソーダで行いpH
約1O05〜約13.5の高アルカリ性とすることによ
って本発明の目的を達成し得る。
In addition, the above pl+ adjustment was done with Tsutomi caustic soda and the pH
A high alkalinity of about 1005 to about 13.5 may achieve the objectives of the present invention.

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.

従って、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)4度の割合(看發基#)は、20.
1〜1:0.(15〜0.15が望ましく、このような
割合に調整することによって蛋白質の溶解、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i(C
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 protein concentration, sodium alginate concentration, and 4% alkali (caustic soda) ratio (care group #) is 20.
1-1:0. (15 to 0.15 is desirable; adjustment to such a ratio determines protein dissolution, interaction between protein and sodium alginate, and protease inactivation conditions; such adjustment results in fiber i ( C
is an important condition that determines the viscoelasticity and strength of

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
にて除去し史に好ましくはft〕し・力又は直空にて中
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l晶度のjPiI整を行う。
Impurities that may interfere with spinning are removed from the dope made of a mixture of protein and sodium alginate by filtration or centrifugation, and the air inside is removed by force or direct air. Preferably, this dope undergoes jPiI adjustment of l crystallinity to prevent gelation.

次いで、上記のドープを、1子0.1〜41の繊維状に
押し出し成形するか、又は平板状、円筒状若しくはフレ
ーク状に成形する。この成形法を、最も困難な押出成形
法により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、強度によっ
て選択されるが、上記ドープは、ノズル口径0.1〜4
.Olのスタッファ−から押出成形され、連続的無結節
ファイバー又は連続的結節状ファイバーとなる。この押
出方法は、ガス圧、スクリュー圧、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-mentioned dope is extruded into a fibrous shape of 0.1 to 41 particles, or formed into a flat plate, a cylinder, or a flake. To explain this molding method using the most difficult extrusion molding method as an example, the dope is selected depending on the viscosity of the dope and the viscoelasticity and strength of the desired molded product. 0.1-4
.. It is extruded from a stuffer of OL to form continuous knotless fibers or continuous knotted fibers. This extrusion method is possible by selecting an extrusion mechanism such as gas pressure, screw pressure, pump pressure, etc.

然る後、上記ファイバー(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って、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 to about 9.
By phase separation in a liquid phase (coagulation liquid), preferably at a pH of about 4 to about 7, a strong structure containing protein and sodium alginate as main components and having viscoelasticity is obtained.

尚、ファイバーの成形は、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、ファイバー径0.21程度で
はpH1,9にてlO秒程度で完了するが、ファイバー
の径、蛋白質、アルギン酸ナトリウムの濃度、液相のp
Hによって反応の速度、深部へのl止透程度、反応の強
弱が決定され、上記液相のpl+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ァイ
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 liquid phase described above is completed in about 10 seconds at pH 1.9 when the fiber diameter is about 0.21, but depending on the fiber diameter, protein, and sodium alginate concentration, the liquid phase p
H determines the rate of reaction, the extent to which l is sealed to the deep part, and the strength of the reaction, and the adjustment of pl+ of the liquid phase affects the viscoelasticity and strength of the fiber in relation to the protein concentration and sodium alginate concentration. This is an important condition to determine, and phase separation is completed by completion of the reaction in the liquid phase.

前記力ルンウム塩又はカリウム塩の1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ァ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 above-mentioned concentration of 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 structured fibers. In particular, a high concentration of 0.2 to 12% is required to insolubilize and dehydrate sodium alginate, and it is usually carried out at a concentration of 1 to 7%.

上述の如(して得られるファイバーは、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
浄することによって表面を滑らかにすることができる。
The fibers obtained as described above are finally washed with water. This washing may be done with water, but it is preferable to wash with dilute physiological saline and then wash with water at the end.
When washed with water, the surface may become rough due to rapid surface swelling; to prevent this phenomenon, the surface can be made smooth by washing with physiological saline.

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, and further dried or swollen slightly. Used as a material for processing into food.

(実施例) 以下に試験例及び実施例を挙げる。(Example) Test examples 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1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士数分ホモ
ノナイズしてドープを得た。
Test Example After pulverizing thawed krill, it was placed in an antifoam blender and homogenized for several to several minutes while varying the protein concentration, 1 degree caustic soda concentration, and sodium alginate concentration to obtain a dope.

得られたドープをノスルロ径0.2〜0.4のスフソフ
ァ−から窒素ガス圧にて圧出し、塩酸でpl+を調整し
た塩化カルシウムの水溶液槽に注入して凝集さ・ヒた後
、水洗して種々のファイバーを得た。
The obtained dope was extruded with nitrogen gas pressure from a sufusofa with a Nosullo diameter of 0.2 to 0.4, poured into an aqueous solution tank of calcium chloride whose PL+ was adjusted with hydrochloric acid, coagulated and heated, and then washed with water. Various fibers were obtained.

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ァ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ァイバーの粘弾性、強
度等の物性が変化することが判った。
From these results, it was found that fibers with viscoelastic properties can be obtained by selecting the following conditions (■ to ■), and that physical properties such as viscoelasticity and strength of the fibers can be changed by changing the following conditions (■ to ■). Ta.

■蛋白質濃度は、2.0〜5.0%が好ましい。(2) The protein concentration is preferably 2.0 to 5.0%.

■ドープのp)Iは、苛性ソーダでpl+ 10.5〜
13.5に調整する。
■ Dope p)I is pl+ 10.5 ~ with caustic soda
Adjust to 13.5.

■アルギン酸ナトリウム1度は、0.5〜3.0%とす
る。
■ Sodium alginate should be 0.5 to 3.0%.

■凝固浴はpHを2〜9に調整する。■Adjust the pH of the coagulation bath 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。
(2) 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(pl+約7)を用いることがで
きることも判った。
It has also been found that seawater (pl+about 7) can be used as the coagulation bath.

実施例1 IKg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のスタッファ−から窒素
ガス圧にて、塩酸でpn5に開整した塩化力ルソウム濃
度3.8%の水/8液槽に注入し、約10秒間反応させ
、リールに巻き取った(速度約25 m/1Ilin、
)後、水洗してファイバーを得た。得られたファイバー
は、スパゲティ状の粘弾性と弾力を有していた。
Example 1 I kg of raw shucked krill was ground as it was, then homogenized at 45°C with a protein concentration of 3.0%, a pH of 12.4 (caustic soda), and a sodium alginate concentration of 1.0%, followed by filtration and desorption. This dope was then injected into a water/8 liquid tank with a russium chloride concentration of 3.8%, which had been adjusted to pn5 with hydrochloric acid, through a stuffer with a nozzle diameter of 0.25 mm under nitrogen gas pressure. , reacted for about 10 seconds, and wound up on a reel (speed of about 25 m/1 line,
) and then washed with water to obtain fibers. 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40%、pH13,0、アルギン酸ナトリ
ウム1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。
Example 2 1Kg of raw krill rounds were ground as they were, then homogenized at 45°C with a protein concentration of 40%, pH 13.0, and sodium alginate 1.3%, and after filtration and degassing, It was dope.

このドープを実施例1と同様にしてファイバーを得た。A fiber was obtained using this dope in the same manner as in Example 1.

このファイバーは、実施例1のファイバーと較べ差異は
少なかった。
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%、p)1)1.9、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。
Example 3 After grinding 1Kg of thawed shelled krill, it was homogenized at 50°C with a protein concentration of 3.5%, p) 1) 1.9, and a sodium alginate concentration of 0.9%, and filtered. After degassing, it was made into a dope.

このドープをノズル口t’40.4 mmのスタッファ
−から実施例1と同様にpH5,0、塩化力ルンウム濃
度4%の水溶液槽に注入し、約10秒間反応さ一仕、リ
ールに巻き取った後、水洗してファイバーを得た。得ら
れたファイバーは、実施例1で得られたファイバーに較
べてやや弱い粘弾性を示したが、巻き取り速度約20m
/win、でリールに巻き取ることが可能であった。
This dope was injected into an aqueous solution tank with a pH of 5.0 and a chloride concentration of 4% as in Example 1 through a stuffer with a nozzle opening t' of 40.4 mm, reacted for about 10 seconds, and then wound onto a reel. After removing the fibers, they were washed with water to obtain fibers. The obtained fiber showed slightly weaker viscoelasticity than the fiber obtained in Example 1, but the winding speed was about 20 m.
/win, it was possible to wind it onto a reel.

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IKg
を磨砕した後、蛋白質濃度2.5%、p)1)3゜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io、25mmの
スタッファ−から、pH7−’fA 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
してファイバーを得た。
Example 4 Ikg of fallen krill collected from thawed frozen shucked krill
After grinding, the protein concentration was 2.5%, p) 1) 3゜1,
Assuming that the sodium alginate concentration is 1.2%, this is 45
The mixture was homogenized at ℃, filtered and degassed, and then used as a dope. In the same manner as in Example 1, this dope was mixed into a coagulation bath with a pH of 7-'fA and a calcium concentration of 5% through a nozzle opening io and a 25 mm stuffer, and after reacting for about 10 seconds, the fiber was washed with water. Obtained.

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、pl+を苛性
ソーダで1).5に爪整し、これらを40℃にてホモジ
ナイズし、濾過脱気後、ノズル口径0.21のスタッフ
ァ−から押し出し、pH5に調整した塩化力ルノウム濃
度3.5%の水溶液槽に注入し、5秒間反応後水洗して
ファイバーを得た。得られたファ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
/8液として、海水(pH7,2)にカルシウム塩を熔
解したものを用いた場合にもファイバーは凝固し、差異
は少なかった。
Example 5 After freezing and pulverizing the shelled krill, pl+ was mixed with caustic soda to prepare a protein concentration of 4% and a sodium alginate concentration of 1.0%. 5, homogenized at 40°C, filtered and deaerated, extruded through a stuffer with a nozzle diameter of 0.21, and poured into an aqueous solution tank with a 3.5% chloride concentration adjusted to pH 5. After reaction for 5 seconds, the fibers were washed with water to obtain fibers. The obtained fiber is a gluten
It had viscoelasticity and elasticity similar to that of somen noodles. Incidentally, even when seawater (pH 7.2) in which calcium salt was dissolved was used as the water/8 solution, the fibers coagulated, 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った
オキアミを、問題を生しることなく効果的に、fll用
でき、しかも、従来十分に利用できなかった未利用部分
、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 effectively used as a whole without causing any problems. In addition to the effective and complete intake and utilization of vitamins and minerals, the addition and mixing of sodium alginate provides a reinforcing effect of vitamins, etc. from the standpoint of nutritional health, and makes it possible to fully utilize krill protein. It is evaluated from both aspects of effective use.

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lli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、過去ゲル状ネットワークが
不可能であっ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 under the above-mentioned specific conditions, the interaction between proteins and polymorphisms, etc. The method allows fiber structuring from whole krill ground material, which was previously not possible from gel-like networks.

更に、本発明によれば、全オキアミを、しかも生の1に
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、全多糖質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 with a high yield from whole krill in the raw state, and the edible structure obtained by the present invention contains whole protein,
It is highly nutritious with all minerals, vitamins, and polysaccharides completely recovered.

Claims (2)

【特許請求の範囲】[Claims] (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、径
約0.1〜約4mmの繊維状に押し出し成形するか、又
は平板状、円筒状若しくはフレーク状に成形し、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
ることによって、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。
(1) After pre-treating the krill as necessary, add sodium alginate to it and mix to reduce the protein concentration to about 2~
about 20%, sodium alginate concentration about 0.5 to about 3
%, a dope with a pH adjusted to about 10.5 to about 13.5 is formed, and this dope is filtered and degassed as necessary, and then extruded into a fiber shape with a diameter of about 0.1 to about 4 mm. , or molded into a flat, cylindrical, or flake shape, and the molded product is treated with a calcium salt or potassium salt concentration of about 0.2 to
An edible structure from krill that is characterized by forming a strong structure mainly composed of protein and having viscoelasticity by phase separation in a liquid phase of about 12.0% and pH of about 2 to about 9. A method of forming things.
(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。
(2) A 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 true JPS6188862A (en) 1986-05-07
JPH0461629B2 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)

Citations (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

Patent Citations (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
JPH0461629B2 (en) 1992-10-01

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