JP2009189333A - Powder made of sea cucumber entrails and method for producing the same - Google Patents

Powder made of sea cucumber entrails and method for producing the same Download PDF

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JP2009189333A
JP2009189333A JP2008035571A JP2008035571A JP2009189333A JP 2009189333 A JP2009189333 A JP 2009189333A JP 2008035571 A JP2008035571 A JP 2008035571A JP 2008035571 A JP2008035571 A JP 2008035571A JP 2009189333 A JP2009189333 A JP 2009189333A
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sea cucumber
powder
solid residue
viscera
liquid
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Kazuhiro Kumagai
一弘 熊谷
Hitoshi Kumagai
等 熊谷
Hiroyasu Tanaka
弘康 田中
Masuo Hasegawa
益男 長谷川
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KUMAKAN SHOTEN KK
MARINE CHEMICAL KENKYUSHO KK
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KUMAKAN SHOTEN KK
MARINE CHEMICAL KENKYUSHO KK
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Abstract

<P>PROBLEM TO BE SOLVED: To provide a powder of sea cucumber entrails which is easily mixed with other foods, is excellent in preservation stability and is easily treated, and a method for producing the same. <P>SOLUTION: The powder includes components prepared by decomposing sea cucumber entrails with a proteinase. The sea cucumber entrails are decomposed with the proteinase; the resultant liquid and solid residue are separated and the liquid is dried to a powder. Further, the above solid residue is decomposed with the proteinase; the resultant liquid and solid residue are separated and the above liquid is dried and brought to a powder. As the above proteinase, e.g., an autolytic enzyme of the sea cucumber is used. <P>COPYRIGHT: (C)2009,JPO&INPIT

Description

本発明は、食品添加物として用いられるナマコ内臓粉末及びその製造方法に関するものである。   The present invention relates to a sea cucumber visceral powder used as a food additive and a method for producing the same.

従来、ナマコの腸、生殖巣等の内臓は、加工工場から排出されるものの一部が食用に供されるに過ぎず、大部分が廃棄されている。前記食用に供されるものは、前記内臓を生のまま塩漬けにしたものであり、一般に「このわた」または「このこ」と称されている。しかし、前記「このわた」または「このこ」は独特の風味があり、また生ものであるために供給に限りがある。   Conventionally, part of the viscera such as sea cucumber intestines, gonads, etc. discharged from the processing plant is only used for food, and most of them are discarded. What is provided for edible use is the one in which the internal organs are salted as they are, and is generally referred to as “Kono Wata” or “Koko”. However, the “kotawa” or “koko” has a unique flavor and is raw, so its supply is limited.

そこで、前記「このわた」または「このこ」を他の食品に添加する食品添加物として利用することが検討されている。前記「このわた」または「このこ」を食品添加物として利用したものとして、例えば、切断した前記「このわた」または「このこ」を梅肉と混合したものが知られている(特許文献1参照)。   Therefore, it has been studied to use the above-mentioned “Konowa” or “Kokoko” as a food additive to be added to other foods. As what used said "this cotton" or "konoko" as a food additive, what mixed said cut "this cotton" or "konoko" with plum meat is known (refer patent document 1). .

しかしながら、前記「このわた」または「このこ」は、切断しただけでは他の食品と十分に混合できない場合があり、塩漬けとは言え生ものであるために長期の貯蔵が難しく、取り扱いにくいという不都合がある。
特開2003−274889号公報
However, there is a case where the above-mentioned “this cotton” or “koko” cannot be sufficiently mixed with other foods simply by cutting, and although it is salted, it is raw, so it is difficult to store for a long time and is difficult to handle. is there.
JP 2003-274889 A

本発明は、かかる不都合を解消して、他の食品と混合しやすく、貯蔵安定性に優れ取り扱いが容易なナマコ内臓粉末を提供することを目的とする。また、本発明の目的は、前記ナマコ内臓粉末の製造方法を提供することにもある。   An object of the present invention is to provide a sea cucumber visceral powder which can be easily mixed with other foods, has excellent storage stability and is easy to handle. Another object of the present invention is to provide a method for producing the sea cucumber viscera powder.

かかる目的を達成するために、本発明のナマコ内臓粉末は、ナマコの内臓をタンパク分解酵素で分解して得られた成分を含む粉末からなることを特徴とする。   In order to achieve this object, the sea cucumber viscera powder of the present invention is characterized by comprising a powder containing components obtained by degrading sea cucumber viscera with a proteolytic enzyme.

本発明のナマコ内臓粉末は、ナマコの内臓をタンパク分解酵素で分解しているので、タンパク質がペプチドまたはアミノ酸に低分子化されている。従って、水に易溶性であり、水に溶解することにより他の食品に容易に混合し、他の食品にこのわたの風味を付与することができる。   In the sea cucumber viscera powder of the present invention, the viscera viscera are decomposed by a proteolytic enzyme, so that the protein is reduced to a peptide or amino acid. Therefore, it is easily soluble in water, and can be easily mixed with other foods by dissolving in water to give this food flavor to other foods.

また、本発明のナマコ内臓粉末は、粉末であるために長期に亘り安定に貯蔵することができ、容易に取り扱うことができる。   Moreover, since the sea cucumber visceral powder of this invention is a powder, it can be stably stored over a long period of time and can be handled easily.

本発明のナマコ内臓粉末は、ナマコの内臓をタンパク分解酵素で分解し、得られた液体と固形残渣とを分離し、該液体を乾燥して粉末化することにより製造することができる。前記タンパク分解酵素は、Bacillus subtilis 、Aspergillus oryzae 等より産生される市販のプロテアーゼを用いてもよく、ナマコの自己消化酵素を用いてもよい。ナマコの自己消化酵素を用いる場合には、分解が緩やかであるため、他の食品に添加した場合に風味を害するえぐ味、苦味等が発生しないという利点がある。   The sea cucumber viscera powder of the present invention can be produced by decomposing sea cucumber viscera with a proteolytic enzyme, separating the obtained liquid and solid residue, drying the liquid and pulverizing it. As the proteolytic enzyme, a commercially available protease produced from Bacillus subtilis, Aspergillus oryzae or the like may be used, or a sea cucumber self-digesting enzyme may be used. When using sea cucumber self-digesting enzymes, the degradation is slow, and there is an advantage that no pungent taste, bitterness, etc. occur when it is added to other foods.

前記固形残渣は、さらに、Bacillus subtilis 、Aspergillus oryzae 等より産生される市販のプロテアーゼからなるタンパク分解酵素で分解し、得られた液体と固形残渣とを分離し、該液体を乾燥して粉末化することにより、ナマコ内臓粉末としてもよい。   The solid residue is further decomposed by a proteolytic enzyme comprising a commercially available protease produced from Bacillus subtilis, Aspergillus oryzae, etc., and the resulting liquid and solid residue are separated, and the liquid is dried and powdered Depending on the situation, it may be a sea cucumber visceral powder.

次に、添付の図面を参照しながら本発明の実施の形態についてさらに詳しく説明する。図1乃至図5は本実施形態の製造方法においてナマコの内臓をタンパク分解酵素で分解して得られた液体の分子量分布を示す図である。   Next, embodiments of the present invention will be described in more detail with reference to the accompanying drawings. FIGS. 1 to 5 are diagrams showing the molecular weight distribution of a liquid obtained by decomposing sea cucumber viscera with a proteolytic enzyme in the production method of this embodiment.

本実施形態のナマコ内臓粉末は、ナマコの腸、生殖巣等の内臓をタンパク分解酵素で分解して得られた成分を含む粉末からなるものである。   The sea cucumber visceral powder of this embodiment is composed of a powder containing components obtained by decomposing viscera such as sea cucumber intestines and gonads with a proteolytic enzyme.

本実施形態のナマコ内臓粉末は、次のようにして製造することができる。   The sea cucumber viscera powder of this embodiment can be manufactured as follows.

まず、乾燥ナマコ等のナマコの加工品を製造する際に取出されたナマコの内臓のうち、腸と生殖巣とを分離し、塩水で洗浄してナマコ内臓粉末の原料とする。このとき、前記腸の内容物や砂等の異物を除去する。   First, the intestines and gonads are separated from sea cucumber viscera extracted when manufacturing processed sea cucumbers such as dried sea cucumbers, and washed with salt water to obtain raw materials for sea cucumber viscera powder. At this time, foreign matter such as the intestinal contents and sand is removed.

次に、前記塩水で洗浄した前記腸及び生殖巣(以下、「腸及び生殖巣」を「ナマコ内臓」と記載する)とを−10℃以下で冷凍し、冷凍状態のまま、磨砕機またはミンサーにより微細化してペースト状とする。前記ナマコ内臓は、常温では柔軟で弾性があるが、前記のように冷凍することにより容易に微細化することができる。   Next, the intestines and gonads washed with the salt water (hereinafter, “intestines and gonads” are described as “sea cucumber viscera”) are frozen at −10 ° C. or lower, and in a frozen state, a grinder or mincer. To make a paste. The sea cucumber viscera is soft and elastic at room temperature, but can be easily miniaturized by freezing as described above.

次に、ペースト状とされた前記ナマコ内臓を解凍し、水を添加したものをタンパク分解酵素で分解し、該ナマコ内臓を液化する。前記タンパク分解酵素は、Bacillus subtilis 、Aspergillus oryzae 等より産生される市販のプロテアーゼを用いてもよく、ナマコ自身が持っている自己消化酵素を用いてもよい。   Next, the sea cucumber viscera that has been made into a paste is thawed, and water-added one is decomposed by a proteolytic enzyme to liquefy the sea cucumber viscera. As the proteolytic enzyme, a commercially available protease produced from Bacillus subtilis, Aspergillus oryzae or the like may be used, or a self-digesting enzyme possessed by sea cucumber itself may be used.

前記プロテアーゼを用いる場合は、前記ナマコ内臓の合計量に対し、100〜300重量%の範囲の水と、0.1〜0.5重量%の範囲の該プロテアーゼとを添加し、40〜60℃の範囲の温度で、2〜8時間の範囲の時間、反応させる。この結果、前記ナマコ内臓のタンパク質が分解されて低分子量のペプチドまたはアミノ酸となり、ナマコ内臓の65〜85重量%が液化される。   When using the protease, water in the range of 100 to 300% by weight and the protease in the range of 0.1 to 0.5% by weight are added to the total amount of the sea cucumber viscera, and 40 to 60 ° C. At a temperature in the range of 2 to 8 hours. As a result, the protein of the sea cucumber viscera is decomposed into a low molecular weight peptide or amino acid, and 65 to 85% by weight of the sea cucumber viscera is liquefied.

また、前記自己消化酵素を用いる場合は、前記ナマコ内臓の合計量に対し、100〜300重量%の範囲の水を添加し、40〜60℃の範囲の温度で、2〜8時間の範囲の時間、反応させる。この結果、前記プロテアーゼを用いる場合と同様に、前記ナマコ内臓のタンパク質が分解されて低分子量のペプチドまたはアミノ酸となり、ナマコ内臓の65〜70重量%が液化される。前記自己消化酵素を用いる場合には、前記プロテアーゼを用いる場合に比較して、タンパク質の分解が緩やかであるため、えぐ味、苦味等の発生を防止することができる。   Moreover, when using the said autodigestive enzyme, the water of the range of 100-300 weight% is added with respect to the total amount of the said sea cucumber internal organs, The temperature of the range of 40-60 degreeC is the range of 2-8 hours. Let react for hours. As a result, as in the case of using the protease, the protein of the sea cucumber viscera is decomposed into a low molecular weight peptide or amino acid, and 65 to 70% by weight of the sea cucumber viscera is liquefied. In the case of using the self-digesting enzyme, protein degradation is slower than in the case of using the protease, so that it is possible to prevent the occurrence of bitterness, bitterness and the like.

次に、前記ナマコ内臓をタンパク分解酵素で分解し、該ナマコ内臓を液化して得られた液体(以下、酵素分解液と略記する)を、遠心沈降機により5000〜10000Gの遠心力で5〜10分間処理して液体と固形残渣とを分離し、該固形残渣を除去する。次に、前記固形残渣を除去した酵素分解液を、真空下、60℃以下の温度に加熱して水分を蒸発させ、水分が50重量%になるまで濃縮する。前記酵素分解液は、真空下で濃縮することにより、ナマコ内臓の風味を形成する香り成分の分解を防止することができる。   Next, a liquid obtained by degrading the sea cucumber viscera with a proteolytic enzyme and liquefying the sea cucumber viscera (hereinafter abbreviated as “enzymatic degradation liquid”) is centrifuged at 5000 to 10,000 G with a centrifugal force of 5000 to 10000 G. Treat for 10 minutes to separate the liquid and solid residue and remove the solid residue. Next, the enzyme decomposition solution from which the solid residue has been removed is heated to a temperature of 60 ° C. or lower under vacuum to evaporate the water and is concentrated until the water reaches 50% by weight. By concentrating the enzyme decomposition solution under vacuum, it is possible to prevent decomposition of the scent component that forms the flavor of sea cucumber internal organs.

次に、前記のように濃縮された前記酵素分解液を、真空乾燥機により、真空下、50℃以下の温度に加熱するか、または凍結乾燥により、含有水分が10重量%以下、好ましくは5重量%以下になるまで乾燥し、固形物とする。次に、前記固形物を粉砕機で粉砕し、目開き300μmの篩により分級し、篩下の粉末を回収してナマコ内臓粉末とする。   Next, the enzyme decomposition solution concentrated as described above is heated to a temperature of 50 ° C. or less under vacuum by a vacuum dryer, or freeze-dried to contain 10% by weight or less, preferably 5%. Dry to weight% or less to make a solid. Next, the solid material is pulverized by a pulverizer, classified by a sieve having an opening of 300 μm, and the powder under the sieve is collected to obtain a sea cucumber visceral powder.

また、前記酵素分解液から除去された前記固形残渣は、前記プロテアーゼを用い、前記ナマコ内臓の場合と全く同一にして処理し、前記目開き300μmの篩下の粉末を回収してナマコ内臓粉末とすることができる。   The solid residue removed from the enzymatic decomposition solution is treated with the protease in exactly the same way as in the case of the sea cucumber viscera, and the powder under the sieve having an opening of 300 μm is recovered to obtain the sea cucumber visceral powder. can do.

本実施形態のナマコ内臓粉末は食品添加物として用いることができ、例えば各種発酵食品に添加することにより、添加した発酵食品にこのわた風味を付与することができ、該発酵食品の本来の香気及び風味とは異なる独特の香気及び風味を有するものとすることができる。前記発酵食品は、このわた風味を付与するために、香気が全くないか、またはこのわた風味を害しない程度の香気を持つものが好ましい。このような発酵食品として、例えば、イカ塩辛を挙げることができる。   The sea cucumber viscera powder of the present embodiment can be used as a food additive. For example, by adding it to various fermented foods, this added flavor can be imparted to the fermented foods. The original flavor and flavor of the fermented foods It may have a unique aroma and flavor different from. The fermented food preferably has no aroma or imparts an aroma that does not harm this aroma in order to impart this aroma. Examples of such fermented foods include squid salt.

イカ塩辛に対する本実施形態のナマコ内臓粉末の添加量は、イカ塩辛の塩分濃度等によっても異なるが、イカ塩辛の全量の1〜5重量%とすることが適している。本実施形態のナマコ内臓粉末は、前述のようにタンパク質が酵素分解により低分子化したペプチドまたはアミノ酸が増加しているので、水に容易に溶解させることができ、少量であってもイカ塩辛に均一に混合することができる。   The addition amount of the sea cucumber viscera powder of the present embodiment to the squid salty salt is suitable to be 1 to 5% by weight of the total amount of the squid salty salt although it varies depending on the salt concentration of the squid salty salt. The sea cucumber viscera powder of this embodiment has a peptide or amino acid whose protein has been reduced in molecular weight by enzymatic degradation as described above, so it can be easily dissolved in water. Uniform mixing is possible.

本実施形態のナマコ内臓粉末を添加したイカ塩辛は、添加後0〜10℃の範囲の温度で1〜2週間熟成することにより該ナマコ内臓粉末がよく馴染み、このわた風味がよく出る。本実施形態のナマコ内臓粉末を添加したイカ塩辛は、瓶詰め等にして珍味として食用に供することができる。   The squid salty spice added with the sea cucumber visceral powder of this embodiment is well adapted to the sea cucumber visceral powder by aging at a temperature in the range of 0 to 10 ° C. for 1 to 2 weeks, and this cotton flavor is often produced. The squid salted fish to which the sea cucumber viscera powder of this embodiment is added can be used for food as a delicacy by bottling.

次に、本発明の実施例を示す。   Next, examples of the present invention will be described.

本実施例では、まず、塩水で洗浄し、腸内容物や砂等の異物を除去したナマコ内臓120kgを冷凍し、ダイス孔径5mmのミンサーで微細化した後、解凍し、ペースト状とした。   In this example, first, 120 kg of sea cucumber viscera from which foreign substances such as intestinal contents and sand were removed by washing with salt water was frozen, refined with a mincer having a die hole diameter of 5 mm, and then thawed to obtain a paste.

次に、前記のようにペースト状としたナマコ内臓300g(水分91.3重量%)を容量2リットルの三角フラスコに入れ、水900gを加えたものを12本用意し、自動振盪機にセットした。そして、50℃で4時間振盪することにより、ナマコ内蔵をその自己消化酵素で分解し、前記ナマコ内臓のタンパク質の67.1重量%が分解した酵素分解液を得た。前記酵素分解液の分子量分布をゲル浸透クロマトグラフィー(以下、GPCと略記する)で測定した結果を図1に示す。図1から、前記ナマコ内臓に含まれていたタンパク質のうち液化したものは、そのほとんどが分子量1000以下のペプチドまたはアミノ酸に分解されていることが明らかである。   Next, 300 g of the sea cucumber internal organs (water content: 91.3% by weight) made into a paste as described above was placed in a Erlenmeyer flask having a capacity of 2 liters, and 12 pieces with 900 g of water added thereto were prepared and set in an automatic shaker. . Then, by shaking at 50 ° C. for 4 hours, the built-in sea cucumber was decomposed by the self-digesting enzyme, and an enzyme decomposition solution in which 67.1 wt% of the sea cucumber visceral protein was decomposed was obtained. FIG. 1 shows the results of measuring the molecular weight distribution of the enzyme decomposition solution by gel permeation chromatography (hereinafter abbreviated as GPC). From FIG. 1, it is clear that most of the proteins contained in the sea cucumber viscera are decomposed into peptides or amino acids having a molecular weight of 1000 or less.

次に、前記酵素分解液を、遠心沈降機により10000Gの遠心力で10分間処理し、液体と固形残渣とに分離し、該固形残渣を除去した。次に、前記固形残渣を除去した前記酵素分解液を0.02MPaの真空下、60℃の温度に加熱して水分を蒸発させ、水分が50重量%になるまで濃縮した。   Next, the enzyme decomposition solution was treated with a centrifugal settling machine at a centrifugal force of 10,000 G for 10 minutes to separate into a liquid and a solid residue, and the solid residue was removed. Next, the enzyme decomposition solution from which the solid residue had been removed was heated to a temperature of 60 ° C. under a vacuum of 0.02 MPa to evaporate the moisture, and concentrated until the moisture became 50% by weight.

次に、前記のように濃縮された前記酵素分解液を、真空乾燥機により、0.0013MPaの真空下、50℃以下の温度に加熱して、含有水分が4.5重量%になるまで乾燥し、固形物を得た。次に、前記固形物を粉砕機で粉砕し、目開き300μmの篩により分級し、篩下の粉末205.5gを回収した。   Next, the enzyme decomposition solution concentrated as described above is heated to a temperature of 50 ° C. or lower under a vacuum of 0.0013 MPa by a vacuum dryer, and dried until the water content becomes 4.5% by weight. To obtain a solid. Next, the solid matter was pulverized with a pulverizer and classified with a sieve having an opening of 300 μm to recover 205.5 g of the powder under the sieve.

次に、前記酵素分解液を前記遠心沈降機により処理して除去された固形残渣(水分89.3重量%)900gに、水1800gとBacillus subtilisより産生される市販のプロテアーゼ4.5gとを加え、容量2リットルの三角フラスコ3本に入れ、自動振盪機にセットした。そして、50℃で4時間振盪することにより分解し、前記固形残渣のタンパク質の67.4重量%が分解した酵素分解液を得た。   Next, 1800 g of water and 4.5 g of commercially available protease produced from Bacillus subtilis are added to 900 g of the solid residue (water content: 89.3% by weight) removed by treating the enzyme digestion solution with the centrifugal settling machine. , Placed in three Erlenmeyer flasks with a capacity of 2 liters and set on an automatic shaker. And it decomposed | disassembled by shaking at 50 degreeC for 4 hours, and the enzyme decomposition liquid which 67.4 weight% of the protein of the said solid residue decomposed | disassembled was obtained.

次に、前記酵素分解液を、遠心沈降機により10000Gの遠心力で10分間処理し、液体と固形残渣とに分離し、該固形残渣を除去した。次に、前記固形残渣を除去した前記酵素分解液の分子量分布をGPCで測定した結果を図2に示す。図2から、前記固形残渣に含まれていたタンパク質のうち液化したものは、そのほとんどが分子量1000以下のペプチドまたはアミノ酸に分解されていることが明らかである。   Next, the enzyme decomposition solution was treated with a centrifugal settling machine at a centrifugal force of 10,000 G for 10 minutes to separate into a liquid and a solid residue, and the solid residue was removed. Next, the result of having measured the molecular weight distribution of the said enzyme decomposition liquid which removed the said solid residue by GPC is shown in FIG. From FIG. 2, it is clear that most of the protein contained in the solid residue is liquefied into peptides or amino acids having a molecular weight of 1000 or less.

次に、前記固形残渣を除去した前記酵素分解液を0.02MPaの真空下、60℃の温度に加熱して水分を蒸発させ、水分が50重量%になるまで濃縮した。   Next, the enzyme decomposition solution from which the solid residue had been removed was heated to a temperature of 60 ° C. under a vacuum of 0.02 MPa to evaporate the moisture, and concentrated until the moisture became 50% by weight.

次に、前記のように濃縮された前記酵素分解液を、真空乾燥機により、0.0013MPaの真空下、50℃以下の温度に加熱して、乾燥し、固形物を得た。次に、前記固形物を粉砕機で粉砕し、目開き300μmの篩により分級し、篩下の粉末63.5g(水分5.2重量%)を回収した。   Next, the enzyme decomposition solution concentrated as described above was heated to a temperature of 50 ° C. or less under a vacuum of 0.0013 MPa by a vacuum dryer, and dried to obtain a solid. Next, the solid matter was pulverized by a pulverizer and classified by a sieve having an opening of 300 μm, and 63.5 g (water content: 5.2% by weight) of the powder under the sieve was recovered.

前記ナマコ内臓の前記酵素分解液を加熱、乾燥して得られた粉末205.5gと、前記固形残渣の前記酵素分解液を加熱、乾燥して得られた粉末63.5gとを合わせて、ナマコ内臓粉末を得た。   A combination of 205.5 g of the powder obtained by heating and drying the enzyme decomposition solution of the sea cucumber viscera and 63.5 g of the powder obtained by heating and drying the enzyme decomposition solution of the solid residue, A visceral powder was obtained.

次に、本実施例で得られたナマコ内臓粉末を、全量に対して2〜4重量%添加したイカ塩辛100gを瓶詰めにし、このわた風味イカ塩辛食品を製造し、内部を−40℃の温度に保持した冷凍庫に保管し、1ヶ月ごとに色彩、臭気、香気、味覚を評価した。前記このわた風味イカ塩辛食品は、4ヶ月経過しても、色彩、臭気、香気、味覚のいずれにも変化がなく、長期保存が可能であることが確認された。   Next, the sea cucumber viscera powder obtained in the present example was bottled with 100 g of squid salted spice added with 2 to 4% by weight based on the total amount, and this savory squid salted food was produced. It stored in the hold | maintained freezer and the color, odor, aroma, and taste were evaluated every month. It was confirmed that the cotton-flavored squid salty food had no change in color, odor, aroma and taste even after 4 months, and could be stored for a long time.

本実施例では、ナマコ内臓を酵素分解するために、反応槽に水45kgを入れ、実施例1と全く同一にしてペースト状としたナマコ内臓4.5kg(水分92.5重量%)を加え、50℃で4時間反応させることにより、該ナマコ内蔵をその自己消化酵素で分解し、該ナマコ内臓のタンパク質の67.0重量%が分解した酵素分解液を得た。前記酵素分解液の分子量分布をGPCで測定した結果を図3に示す。図3から、前記ナマコ内臓に含まれていたタンパク質のうち液化したものは、そのほとんどが分子量1000以下のペプチドまたはアミノ酸に分解されていることが明らかである。   In this example, in order to enzymatically decompose the sea cucumber viscera, 45 kg of water was put into the reaction tank, and 4.5 kg of sea cucumber viscera (water content 92.5 wt%) made into the same paste form as in Example 1 was added, By reacting at 50 ° C. for 4 hours, the built-in sea cucumber was decomposed by the autolytic enzyme to obtain an enzymatic degradation solution in which 67.0% by weight of the sea cucumber visceral protein was degraded. The result of measuring the molecular weight distribution of the enzyme decomposition solution by GPC is shown in FIG. From FIG. 3, it is clear that most of the proteins contained in the sea cucumber viscera are decomposed into peptides or amino acids having a molecular weight of 1000 or less.

次に、前記酵素分解液を、遠心沈降機により10000Gの遠心力で10分間処理し、液体と固形残渣とに分離し、該固形残渣を除去した。次に、前記固形残渣を除去した前記酵素分解液を0.02MPaの真空下、60℃の温度に加熱して水分を蒸発させ、水分が50重量%になるまで濃縮した。   Next, the enzyme decomposition solution was treated with a centrifugal settling machine at a centrifugal force of 10,000 G for 10 minutes to separate into a liquid and a solid residue, and the solid residue was removed. Next, the enzyme decomposition solution from which the solid residue had been removed was heated to a temperature of 60 ° C. under a vacuum of 0.02 MPa to evaporate the moisture, and concentrated until the moisture became 50% by weight.

次に、前記のように濃縮された前記酵素分解液を、真空乾燥機により、0.0013MPaの真空下、50℃以下の温度に加熱して、含有水分が4.7重量%になるまで乾燥し、固形物を得た。次に、前記固形物を粉砕機で粉砕し、目開き300μmの篩により分級し、篩下の粉末2.3kgを回収し、ナマコ内臓粉末を得た。   Next, the enzyme decomposition solution concentrated as described above is heated to a temperature of 50 ° C. or lower under a vacuum of 0.0013 MPa by a vacuum dryer, and dried until the water content becomes 4.7% by weight. To obtain a solid. Next, the solid was pulverized with a pulverizer and classified with a sieve having an opening of 300 μm, and 2.3 kg of the powder under the sieve was recovered to obtain a sea cucumber visceral powder.

次に、本実施例で得られたナマコ内臓粉末を用いた以外は実施例1と全く同一にして、このわた風味イカ塩辛食品を製造し、内部を−40℃の温度に保持した冷凍庫に保管し、1ヶ月ごとに色彩、臭気、香気、味覚を評価した。前記このわた風味イカ塩辛食品は、4ヶ月経過しても、色彩、臭気、香気、味覚のいずれにも変化がなく、長期保存が可能であることが確認された。   Next, except that the sea cucumber viscera powder obtained in this example was used, this savory squid salty food was produced in the same manner as in Example 1 and stored in a freezer maintained at a temperature of -40 ° C. The color, odor, aroma and taste were evaluated every month. It was confirmed that the cotton-flavored squid salty food had no change in color, odor, aroma and taste even after 4 months, and could be stored for a long time.

本実施例では、ナマコ内臓を酵素分解するために、反応槽に水60kgを入れ、実施例1と全く同一にしてペースト状としたナマコ内臓30kg(水分91.5重量%)と、Bacillus subtilisより産生される市販のプロテアーゼ150gとを加え、50℃で4時間反応させることにより、該ナマコ内蔵を分解し、該ナマコ内臓のタンパク質の88.2重量%が分解した酵素分解液を得た。前記酵素分解液の分子量分布をGPCで測定した結果を図4に示す。図4から、前記ナマコ内臓に含まれていたタンパク質のうち液化したものは、そのほとんどが分子量1000以下のペプチドまたはアミノ酸に分解されていることが明らかである。   In this example, in order to enzymatically decompose the sea cucumber viscera, 60 kg of water was put in the reaction tank, and the sea cucumber viscera 30 kg (moisture 91.5 wt%) made exactly the same as in Example 1 and Bacillus subtilis By adding 150 g of the commercially available protease to be produced and reacting at 50 ° C. for 4 hours, the built-in sea cucumber was decomposed to obtain an enzymatic degradation solution in which 88.2% by weight of the protein of the sea cucumber viscera was decomposed. FIG. 4 shows the results of measuring the molecular weight distribution of the enzyme decomposition solution by GPC. It is clear from FIG. 4 that most of the proteins contained in the sea cucumber viscera are decomposed into peptides or amino acids having a molecular weight of 1000 or less.

次に、前記酵素分解液を、遠心沈降機により10000Gの遠心力で10分間処理し、液体と固形残渣とに分離し、該固形残渣を除去した。次に、前記固形残渣を除去した前記酵素分解液を0.02MPaの真空下、60℃の温度に加熱して水分を蒸発させ、水分が50重量%になるまで濃縮した。   Next, the enzyme decomposition solution was treated with a centrifugal settling machine at a centrifugal force of 10,000 G for 10 minutes to separate into a liquid and a solid residue, and the solid residue was removed. Next, the enzyme decomposition solution from which the solid residue had been removed was heated to a temperature of 60 ° C. under a vacuum of 0.02 MPa to evaporate the moisture, and concentrated until the moisture became 50% by weight.

次に、前記のように濃縮された前記酵素分解液を、真空乾燥機により、0.0013MPaの真空下、50℃以下の温度に加熱して、含有水分が4.2重量%になるまで乾燥し、固形物を得た。次に、前記固形物を粉砕機で粉砕し、目開き300μmの篩により分級し、篩下の粉末2.1kgを回収し、ナマコ内臓粉末を得た。   Next, the enzyme decomposition solution concentrated as described above is heated to a temperature of 50 ° C. or less under a vacuum of 0.0013 MPa by a vacuum dryer, and dried until the moisture content becomes 4.2% by weight. To obtain a solid. Next, the solid was pulverized with a pulverizer and classified with a sieve having an opening of 300 μm, and 2.1 kg of the powder under the sieve was collected to obtain a sea cucumber visceral powder.

次に、本実施例で得られたナマコ内臓粉末を用いた以外は実施例1と全く同一にして、このわた風味イカ塩辛食品を製造し、内部を−40℃の温度に保持した冷凍庫に保管し、1ヶ月ごとに色彩、臭気、香気、味覚を評価した。前記このわた風味イカ塩辛食品は、4ヶ月経過しても、色彩、臭気、香気、味覚のいずれにも変化がなく、長期保存が可能であることが確認された。   Next, except that the sea cucumber viscera powder obtained in this example was used, this savory squid salty food was produced in the same manner as in Example 1 and stored in a freezer maintained at a temperature of -40 ° C. The color, odor, aroma and taste were evaluated every month. It was confirmed that the cotton-flavored squid salty food had no change in color, odor, aroma and taste even after 4 months, and could be stored for a long time.

本実施例では、ナマコ内臓を酵素分解するために、反応槽に水67.5kgを入れ、実施例1と全く同一にしてペースト状としたナマコ内臓22.5kg(水分92.6重量%)と、Aspergillus oryzaeより産生される市販のプロテアーゼ112gとを加え、50℃で4時間反応させることにより、該ナマコ内蔵を分解し、該ナマコ内臓のタンパク質の72.5重量%が分解した酵素分解液を得た。前記酵素分解液の分子量分布をGPCで測定した結果を図5に示す。図5から、前記ナマコ内臓に含まれていたタンパク質のうち液化したものは、そのほとんどが分子量1000以下のペプチドまたはアミノ酸に分解されていることが明らかである。   In this example, in order to enzymatically decompose the sea cucumber viscera, 67.5 kg of water was put into the reaction tank, and 22.5 kg of sea cucumber viscera (water content 92.6% by weight) made exactly the same as in Example 1 was obtained. And 112 g of a commercially available protease produced from Aspergillus oryzae and reacting at 50 ° C. for 4 hours, thereby decomposing the sea cucumber vigor and decomposing 72.5% by weight of the sea cucumber visceral protein Obtained. The result of measuring the molecular weight distribution of the enzyme decomposition solution by GPC is shown in FIG. From FIG. 5, it is clear that most of the proteins contained in the sea cucumber viscera are decomposed into peptides or amino acids having a molecular weight of 1000 or less.

次に、前記酵素分解液を、遠心沈降機により10000Gの遠心力で10分間処理し、液体と固形残渣とに分離し、該固形残渣を除去した。次に、前記固形残渣を除去した前記酵素分解液を0.02MPaの真空下、60℃の温度に加熱して水分を蒸発させ、水分が50重量%になるまで濃縮した。   Next, the enzyme decomposition solution was treated with a centrifugal settling machine at a centrifugal force of 10,000 G for 10 minutes to separate into a liquid and a solid residue, and the solid residue was removed. Next, the enzyme decomposition solution from which the solid residue had been removed was heated to a temperature of 60 ° C. under a vacuum of 0.02 MPa to evaporate the moisture, and concentrated until the moisture became 50% by weight.

次に、前記のように濃縮された前記酵素分解液を、真空乾燥機により、0.0013MPaの真空下、50℃以下の温度に加熱して、含有水分が4.7重量%になるまで乾燥し、固形物を得た。次に、前記固形物を粉砕機で粉砕し、目開き300μmの篩により分級し、篩下の粉末1.2kgを回収し、ナマコ内臓粉末を得た。   Next, the enzyme decomposition solution concentrated as described above is heated to a temperature of 50 ° C. or lower under a vacuum of 0.0013 MPa by a vacuum dryer, and dried until the water content becomes 4.7% by weight. To obtain a solid. Next, the solid was pulverized with a pulverizer and classified with a sieve having an opening of 300 μm, and 1.2 kg of the powder under the sieve was collected to obtain a sea cucumber visceral powder.

次に、本実施例で得られたナマコ内臓粉末を用いた以外は実施例1と全く同一にして、このわた風味イカ塩辛食品を製造し、内部を−40℃の温度に保持した冷凍庫に保管し、1ヶ月ごとに色彩、臭気、香気、味覚を評価した。前記このわた風味イカ塩辛食品は、4ヶ月経過しても、色彩、臭気、香気、味覚のいずれにも変化がなく、長期保存が可能であることが確認された。   Next, except that the sea cucumber viscera powder obtained in this example was used, this savory squid salty food was produced in the same manner as in Example 1 and stored in a freezer maintained at a temperature of -40 ° C. The color, odor, aroma and taste were evaluated every month. It was confirmed that the cotton-flavored squid salty food had no change in color, odor, aroma and taste even after 4 months, and could be stored for a long time.

本発明の製造方法におけるナマコ内臓の酵素分解液の分子量分布を示す図。The figure which shows the molecular weight distribution of the enzymatic decomposition liquid of the sea cucumber internal organs in the manufacturing method of this invention. 本発明の製造方法におけるナマコ内臓の酵素分解液の分子量分布を示す図。The figure which shows the molecular weight distribution of the enzymatic decomposition liquid of the sea cucumber internal organs in the manufacturing method of this invention. 本発明の製造方法におけるナマコ内臓の酵素分解液の分子量分布を示す図。The figure which shows the molecular weight distribution of the enzymatic decomposition liquid of the sea cucumber internal organs in the manufacturing method of this invention. 本発明の製造方法におけるナマコ内臓の酵素分解液の分子量分布を示す図。The figure which shows the molecular weight distribution of the enzymatic decomposition liquid of the sea cucumber internal organs in the manufacturing method of this invention. 本発明の製造方法におけるナマコ内臓の酵素分解液の分子量分布を示す図。The figure which shows the molecular weight distribution of the enzymatic decomposition liquid of the sea cucumber internal organs in the manufacturing method of this invention.

Claims (4)

ナマコの内臓をタンパク分解酵素で分解して得られた成分を含む粉末からなることを特徴とするナマコ内臓粉末。   A sea cucumber visceral powder comprising a powder containing components obtained by decomposing sea cucumber viscera with a proteolytic enzyme. ナマコの内臓をタンパク分解酵素で分解し、得られた液体と固形残渣とを分離し、該液体を乾燥して粉末化することを特徴とするナマコ内臓粉末の製造方法。   A method for producing sea cucumber visceral powder, comprising decomposing sea cucumber viscera with a proteolytic enzyme, separating the obtained liquid and solid residue, and drying the liquid into powder. 前記タンパク分解酵素として、ナマコの自己消化酵素を用いることを特徴とする請求項2記載のナマコ内臓粉末の製造方法。   The sea cucumber visceral powder manufacturing method according to claim 2, wherein a sea cucumber autolysis enzyme is used as the proteolytic enzyme. 前記固形残渣をタンパク分解酵素で分解し、得られた液体と固形残渣とを分離し、該液体を乾燥して粉末化することを特徴とする請求項2または請求項3記載のナマコ内臓粉末の製造方法。   4. The sea cucumber visceral powder according to claim 2, wherein the solid residue is decomposed with a proteolytic enzyme, the obtained liquid and the solid residue are separated, and the liquid is dried and pulverized. Production method.
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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2014504160A (en) * 2011-12-22 2014-02-20 大連工業大学 Production method of active material by self-digestion of sea cucumber intestine
CN105533740A (en) * 2015-12-24 2016-05-04 广西北部湾海皇生物科技有限公司 Sea cucumber-traditional Chinese medicine extract with kidney-invigorating and essence-replenishing functions as well as preparation technology thereof
KR101829527B1 (en) 2016-03-04 2018-02-19 류병환 Coffee With Scent Of Sea And Its Manufacturing Method
CN108514084A (en) * 2018-03-14 2018-09-11 大连工业大学 A method of based on biological enzyme tenderizing sea cucumber

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2014504160A (en) * 2011-12-22 2014-02-20 大連工業大学 Production method of active material by self-digestion of sea cucumber intestine
CN105533740A (en) * 2015-12-24 2016-05-04 广西北部湾海皇生物科技有限公司 Sea cucumber-traditional Chinese medicine extract with kidney-invigorating and essence-replenishing functions as well as preparation technology thereof
KR101829527B1 (en) 2016-03-04 2018-02-19 류병환 Coffee With Scent Of Sea And Its Manufacturing Method
CN108514084A (en) * 2018-03-14 2018-09-11 大连工业大学 A method of based on biological enzyme tenderizing sea cucumber

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