JPH06253787A - Decoloring method of dark-fleshed fish - Google Patents
Decoloring method of dark-fleshed fishInfo
- Publication number
- JPH06253787A JPH06253787A JP5064877A JP6487793A JPH06253787A JP H06253787 A JPH06253787 A JP H06253787A JP 5064877 A JP5064877 A JP 5064877A JP 6487793 A JP6487793 A JP 6487793A JP H06253787 A JPH06253787 A JP H06253787A
- Authority
- JP
- Japan
- Prior art keywords
- pseudomonas
- fish
- dark
- cultured
- fleshed
- 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
Links
Landscapes
- Coloring Foods And Improving Nutritive Qualities (AREA)
- Fish Paste Products (AREA)
- Meat, Egg Or Seafood Products (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、赤身魚特有の身の色を
効果的に脱色する方法に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for effectively decolorizing the body color peculiar to red fish.
【0002】サバ、イワシ等赤身魚は、日本近海で多く
漁獲されているが、充分に有効利用されているとはいい
難い。その理由のひとつは、血液蛋白に由来する色にあ
り、赤身魚を含んだねり製品などは、その色が黒ずみ、
商品価値が低下するため、赤身魚利用上の大きな障害と
なっている。Red fish such as mackerel and sardines are often caught in the seas around Japan, but it cannot be said that they are sufficiently utilized. One of the reasons for this is the color derived from blood protein, and the color of red meat-containing fish products such as batter products is dark.
The decline in commercial value is a major obstacle to the use of red fish.
【0003】[0003]
【従来の技術】赤身魚特有の色の主因が血液蛋白(ミオ
グロビン、ヘモグロビン)であり、これらが水溶性であ
ることから、従来、水晒しやアルカリ晒しをくり返す方
法、遠心分離する方法といった物理的方法によってこれ
を除去することが行われてきた。しかしながら、このよ
うな処理は、くり返して行わなければならないし、それ
でも完全に脱色することはできない。それどころか、か
えって、残渣には、抽出のくり返しによる筋肉蛋白質の
変性に起因する赤褐色ないし灰褐色の着色が生じてい
る。2. Description of the Related Art Blood proteins (myoglobin and hemoglobin) are the main causes of the color peculiar to red fish, and since these are water-soluble, they have been physically exposed to water and alkali repeatedly, and are physically separated by centrifugation. It has been carried out by a selective method. However, such a treatment must be repeated, and the color cannot be completely decolorized. On the contrary, the residue is colored reddish brown or grayish brown due to the denaturation of muscle protein due to repeated extraction.
【0004】このような欠点を回避して赤身魚の色を効
率的に脱色する方法として、溶剤で処理する方法、特に
塩酸・エタノール混液を用い、赤身魚の色を酸で分解す
る方法が提案されているが(日本水産学会誌、46(1
0)、1269−1272(1980))、特に工業的
な面からみて未だ完全なものとはいい難い。As a method for efficiently decolorizing the color of red fish while avoiding such drawbacks, a method of treating with a solvent, particularly a method of decomposing the color of red fish with an acid using a hydrochloric acid / ethanol mixed solution has been proposed. There are (Journal of the Fisheries Society of Japan, 46 (1
0), 1269-1272 (1980)), and especially from an industrial viewpoint, it is hard to say that they are perfect.
【0005】[0005]
【発明が解決しようとする課題】本発明は、魚本来の味
や旨みを全く損うことなく、しかも食品公害上問題とな
るような化学物質を使用することなく、きわめて効率的
に赤身魚の特有な色を脱色するための方法を新たに開発
する目的でなされたものである。また、本発明は、血合
肉の色を脱色するための新しい方法も併せて開発する目
的でなされたものである。DISCLOSURE OF THE INVENTION The present invention is very efficient and peculiar to red fish without spoiling the original taste and taste of the fish and without using chemical substances that pose a problem in food pollution. It was made with the purpose of developing a new method for decolorizing various colors. Further, the present invention was made for the purpose of developing a new method for decolorizing the color of blood mixture.
【0006】[0006]
【課題を解決するための手段】本発明は、上記した目的
を達成するためになされたものであって、従来とは全く
別の発想でなされたものである。The present invention has been made in order to achieve the above-mentioned object, and has been made with a completely different idea from the conventional one.
【0007】すなわち、本発明者らは、微生物を利用す
るのが有利であるとの発想を新たに得、赤身魚の色の主
原因である、ミオグロビンに着目し、これを効果的に分
解する微生物のスクリーニングを行ったところ、有効な
菌を発見し、この新知見に基づき更に研究の結果、本発
明の完成に至ったものである。That is, the present inventors newly acquired the idea that it is advantageous to use a microorganism, and focused on myoglobin, which is the main cause of the color of red fish, and effectively decomposed it. As a result of the screening described above, an effective bacterium was found, and as a result of further research based on this new finding, the present invention was completed.
【0008】本発明者らが新たに分離した微生物KB−
74株は、形態観察及び性状を試験した結果(下記する
表1)から、シュードモナスに属する細菌に分類され、
そして生理的性状を試験した結果(下記する表2)から
総合的に検討した結果、シュードモナス・サッカロフィ
ラと同定し、これをシュードモナス・サッカロフィラK
B−74(Pseudomonas saccharo
phila KB−74)と命名した。本菌株は、工業
技術院生命工学工業技術研究所にFERMP−1345
7として寄託されている。The microorganism KB- which was newly isolated by the present inventors
The 74 strains were classified as bacteria belonging to Pseudomonas, based on the results of morphological observation and properties (Table 1 below),
Then, as a result of comprehensively examining from the results of testing physiological properties (Table 2 below), it was identified as Pseudomonas saccharophila, and Pseudomonas saccharophila K was identified.
B-74 (Pseudomonas saccharo
phila KB-74). This strain is FERMP-1345 in the Institute of Biotechnology, Institute of Biotechnology, AIST.
Deposited as 7.
【0009】[0009]
【表1】 [Table 1]
【0010】[0010]
【表2】 [Table 2]
【0011】本発明を実施するには、シュードモナス属
に属するミオグロビン分解菌、例えばKB−74菌を培
養しその培養上清又はその濃縮物等を赤身魚とを接触せ
しめればよい。そのためには、シュードモナス属菌を培
養して得た培養物、培養物から分離して得た上清や遠心
分離液等の培養液、及び/又は、これらの乾燥物、ペー
スト状物、濃縮物、分離物、希釈物等の各種処理物が適
宜使用される。In order to carry out the present invention, a myoglobin-degrading bacterium belonging to the genus Pseudomonas, for example, KB-74 bacterium may be cultured and the culture supernatant or a concentrate thereof may be brought into contact with red fish. For that purpose, a culture obtained by culturing Pseudomonas sp., A culture fluid such as a supernatant or a centrifuge obtained by separating the culture, and / or a dried product, a paste-like product, or a concentrate thereof. , Various kinds of processed products such as separated products and diluted products are appropriately used.
【0012】菌の培養は、細菌の培養における常法にし
たがって適宜行えばよいが、培地にミオグロビン、ヘモ
グロビン等の血液蛋白を添加しておくと、更に効果が高
まる。Cultivation of the bacterium may be appropriately carried out according to a conventional method for culturing bacteria, but the effect is further enhanced by adding blood proteins such as myoglobin and hemoglobin to the medium.
【0013】本発明にしたがって赤身魚を脱色するに
は、赤身肉とシュードモナス属菌培養上清物等とを5〜
35℃、好ましくは常温で1時間〜3日間程度接触せし
めれば良く、例えば、シュードモナス属菌培養上清物等
を赤身肉にふりかけたり、スプレーしたり、すりこんだ
り、注入したり、赤身肉とともにミンチしたり、ねり込
んだり、あるいは赤身肉を漬け込んだりすればよい。In order to decolorize red fish according to the present invention, the red meat and Pseudomonas culture supernatant or the like are added to
It may be contacted at 35 ° C., preferably at room temperature for about 1 hour to 3 days. For example, sprinkling, spraying, rubbing, injecting, lean meat, etc. on the lean meat with the culture supernatant of Pseudomonas sp. It can be minced, kneaded, or pickled with red meat.
【0014】赤身肉は、赤身魚から赤身部分を分離して
処理してもよいし、赤身部分を分離することなく赤身魚
全体を微生物処理してもよく、後者の場合、白身部分に
は格別の影響を及ぼすことなく赤身部分のみが選択的に
脱色できる。したがって血合肉のついた魚肉も、血合肉
の部分のみを選択的に脱色することができる。The red meat may be processed by separating the red meat part from the red fish, or the whole red fish may be microbially treated without separating the red meat. In the latter case, the white meat is exceptionally treated. Only the lean part can be selectively decolorized without the effect of. Therefore, even in the fish meat with blood mixture, only the blood meat portion can be selectively decolorized.
【0015】赤身魚としては、サバ、イワシ、サンマ等
各種の赤身魚がすべて本発明の対象として処理脱色され
る。本発明は、脱色効果にすぐれているだけでなく、赤
身魚が本来有している風味、食感、旨み等にはいささか
も影響を及ぼさない点でも非常に卓越している。As red fish, various kinds of red fish such as mackerel, sardines and saury are all treated and decolorized as the object of the present invention. The present invention is not only excellent in decolorizing effect, but also extremely excellent in that it does not affect the flavor, texture, taste and the like that red fish originally have.
【0016】以下、本発明の実施例について述べる。Examples of the present invention will be described below.
【0017】[0017]
【実施例1】Pseudomonas sacchar
ophila KB−74(FERM P−1345
7)をポリペプトン3%、イーストエキス0.5%、食
塩0.5%(pH7.0)なる培地で30℃、3日間培
養した。本培養液0.1mlを、ミオグロビン0.12
5%を含む1/15Mリン酸バッファー(PH7.0)
溶液9mlに接種し、更に30℃、3日間培養した。培
養後、遠心分離によって、菌体を分離し、その上清を、
高速液体クロマトグラフィーによって、分析した。分析
条件は、以下の通りである。 機種 :島津 LC−6A カラム :Waco beads G−30 溶媒 :1/15Mリン酸バッファー、pH7.0 流速 :0.5ml/min 測定波長:280nm、500nm 測定結果は、図1、2に示した。Example 1 Pseudomonas sacchar
optila KB-74 (FERM P-1345
7) was cultivated in a medium containing 3% polypeptone, 0.5% yeast extract and 0.5% sodium chloride (pH 7.0) at 30 ° C. for 3 days. 0.1 ml of the main culture solution was added to myoglobin 0.12
1/15 M phosphate buffer (PH 7.0) containing 5%
9 ml of the solution was inoculated and further cultured at 30 ° C. for 3 days. After culturing, the cells were separated by centrifugation and the supernatant was
It was analyzed by high performance liquid chromatography. The analysis conditions are as follows. Model: Shimadzu LC-6A column: Waco beads G-30 solvent: 1 / 15M phosphate buffer, pH 7.0 flow rate: 0.5 ml / min measurement wavelength: 280 nm, 500 nm The measurement results are shown in FIGS.
【0018】[0018]
【実施例2】イワシの赤身部分を取り出し、その10g
に対し、実施例1で得た培養液1mlを充分に混合し、
室温に1日間放置した。その結果、赤身の色素が脱色さ
れて、各種加工にも適するような色となった。脱色後の
赤身肉を加熱処理して食したところ、イワシ本来の味、
旨み、食感は、脱色処理しなかったイワシのそれと比較
しても全くそん色のないものであった。[Example 2] Taking out the red meat part of the sardine, 10 g thereof
On the other hand, 1 ml of the culture solution obtained in Example 1 was mixed thoroughly,
It was left at room temperature for 1 day. As a result, the red pigment was decolorized and became a color suitable for various types of processing. When the red meat after decolorization was heat-treated and eaten, the original taste of the sardines,
The taste and texture of the sardines that had not been decolorized were completely neutral.
【0019】[0019]
【実施例3】マグロの血合肉1kgに実施例1で得た培
養液100mlを減圧濃縮して約半量とした濃縮液を混
合してミンチにかけ、これを10℃に2日間維持した。
その結果、血合肉中の色素が脱色され、これをすり身に
したけれども、製品の黒ずみが認められず、ねり製品の
原料として使用できることが確認された。[Example 3] To 1 kg of tuna blood mixed meat, 100 ml of the culture solution obtained in Example 1 was concentrated under reduced pressure to a concentration of about half, and the mixture was minced and maintained at 10 ° C for 2 days.
As a result, the pigment in the blood mixture was decolored, and although it was ground into surimi, it was confirmed that the product was not darkened and could be used as a raw material for paste products.
【0020】[0020]
【発明の効果】本発明によって、きわめて効率的に赤身
魚の脱色が可能となり、しかもその際、赤身魚本来の風
味、食感はいささかも損われず、そのうえ有害な添加物
を使用しないために食品衛生上もきわめて安全性が高い
という著効も奏される。Industrial Applicability According to the present invention, it is possible to decolorize red fish very efficiently, and at that time, the original taste and texture of the red fish are not impaired, and no harmful additives are used. It also has the outstanding effect of being extremely safe in terms of hygiene.
【0021】したがって本発明によれば、用途が限定さ
れていたサバやイワシ等の赤身魚の用途が広がるのみで
なく、血合肉も更に有効に利用できることとなった。Therefore, according to the present invention, not only the applications of red fish such as mackerel and sardines whose applications have been limited are widened, but also blood meat can be used more effectively.
【図1】本菌培養上清とコントロ−ルのHPLCパタ−
ン(280nm)の比較図である。FIG. 1 HPLC pattern of the culture supernatant of this bacterium and control
FIG. 4 is a comparative diagram of the wavelength range (280 nm).
【図2】本菌培養上清とコントロ−ルのHPLCパタ−
ン(500nm)の比較図である。FIG. 2 HPLC pattern of the culture supernatant of the present bacterium and control
FIG. 4 is a comparative diagram of the wavelength range (500 nm).
Claims (2)
物、培養液、及び/又は処理物で処理することを特徴と
する赤身魚の脱色方法。1. A method for decolorizing red fish, which comprises treating the red fish with a Pseudomonas genus, a culture thereof, a culture solution, and / or a treated product.
サッカロフィラであることを特徴とする請求項1に記載
の脱色方法。2. A Pseudomonas spp.
The bleaching method according to claim 1, which is Saccharophila.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP06487793A JP3224630B2 (en) | 1993-03-02 | 1993-03-02 | How to decolor red fish |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP06487793A JP3224630B2 (en) | 1993-03-02 | 1993-03-02 | How to decolor red fish |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH06253787A true JPH06253787A (en) | 1994-09-13 |
JP3224630B2 JP3224630B2 (en) | 2001-11-05 |
Family
ID=13270799
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP06487793A Expired - Fee Related JP3224630B2 (en) | 1993-03-02 | 1993-03-02 | How to decolor red fish |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3224630B2 (en) |
-
1993
- 1993-03-02 JP JP06487793A patent/JP3224630B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JP3224630B2 (en) | 2001-11-05 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE60007655T2 (en) | PROTEIN HYDROLYSATE PRODUCED USING MARINE PROTEASES | |
Arancibia et al. | Antimicrobial and antioxidant chitosan solutions enriched with active shrimp (Litopenaeus vannamei) waste materials | |
Armenta‐López et al. | Astaxanthin extraction from shrimp waste by lactic fermentation and enzymatic hydrolysis of the carotenoprotein complex | |
Sila et al. | Characterisation of trypsin purified from the viscera of Tunisian barbel (Barbus callensis) and its application for recovery of carotenoproteins from shrimp wastes | |
DE2314984C3 (en) | Process for the production of protein hydrolyzate with a high content of free amino acids and its use as a condiment or food additive | |
JP4226299B2 (en) | Method for producing fish-derived gelatin peptide | |
Jabeur et al. | Statistical Experimental design optimization of microbial proteases production under co-culture conditions for chitin recovery from speckled shrimp Metapenaeus monoceros by-product | |
FR2401996A1 (en) | CONCENTRATED COMPOSITION OF MICROCOCCUS VARIANS AND A LACTIC ACID-PRODUCING BACTERIA, AND ITS APPLICATION TO THE TREATMENT OF MEAL-BASED PRODUCTS, IN PARTICULAR SAUSAGES AND SAUSAGES | |
WO1994026132A1 (en) | Method and composition for inhibiting escherichia coli in food products | |
Shaibani et al. | Antioxidant and antibactrial properties of protein hydrolysate from Persian Gulf Crab (Grapsus albacarinous) as affected by progress of hydrolysis | |
Wenno et al. | Physico-chemical characteristics and amino acid profile of fermented sauce made from tuna loin by-product | |
JPH06253787A (en) | Decoloring method of dark-fleshed fish | |
Hus et al. | The stability of Clostridium botulinum type E toxin in salty and/or acid environment | |
US5543325A (en) | Two-step method of hypo-osmotic shock for reducing viability of bacteria | |
EP0290716A2 (en) | Preservation process for poultry and fresh meat products using bacteriolytic enzyme product from streptomyces | |
DE69918951T2 (en) | Surimi product and process for its preparation | |
Kusumarwati et al. | Production and characterization of bacteriocin produced by lactic acid bacteria isolated from rusip | |
KR100476112B1 (en) | Seasoning food-stuff using side-products by Ammodytes personatus Girard sauce fermentation and method for production thereof | |
JP4446637B2 (en) | Method for producing extract from soy sauce cake | |
DE2345013A1 (en) | METHOD FOR MANUFACTURING FUNCTIONAL FOOD PROTEINS | |
Booth | A method for removal of some epiphytic diatoms | |
Fik et al. | Application of superchilling to prolong the keeping time of rainbow trout | |
JP4270798B2 (en) | Antibacterial peptide composition | |
JPH07327666A (en) | Microorganism having high activity to produce thiol protease inhibiting substance, production of the substance using the microorganism, preparation of food using the substance and quality improver composed of the substance | |
JP2696485B2 (en) | Extraction method of fish and shellfish algae extract containing large amount of mineral components |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
LAPS | Cancellation because of no payment of annual fees |