JPH09107912A - Seasoning containing globin peptide as an active ingredient and method of using hemoglobin as the seasoning - Google Patents
Seasoning containing globin peptide as an active ingredient and method of using hemoglobin as the seasoningInfo
- Publication number
- JPH09107912A JPH09107912A JP7293524A JP29352495A JPH09107912A JP H09107912 A JPH09107912 A JP H09107912A JP 7293524 A JP7293524 A JP 7293524A JP 29352495 A JP29352495 A JP 29352495A JP H09107912 A JPH09107912 A JP H09107912A
- Authority
- JP
- Japan
- Prior art keywords
- seasoning
- hemoglobin
- globin peptide
- blood
- active ingredient
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 235000011194 food seasoning agent Nutrition 0.000 title claims abstract description 33
- 108060003196 globin Proteins 0.000 title claims description 19
- 102000018146 globin Human genes 0.000 title claims description 19
- 108090000765 processed proteins & peptides Proteins 0.000 title claims description 18
- 238000000034 method Methods 0.000 title claims description 12
- 239000004480 active ingredient Substances 0.000 title claims description 5
- 108010036302 hemoglobin AS Proteins 0.000 title claims description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims abstract description 14
- 102000004190 Enzymes Human genes 0.000 claims abstract description 11
- 108090000790 Enzymes Proteins 0.000 claims abstract description 11
- 108010054147 Hemoglobins Proteins 0.000 claims abstract description 10
- 102000001554 Hemoglobins Human genes 0.000 claims abstract description 10
- 150000003278 haem Chemical class 0.000 claims abstract description 7
- 229910052742 iron Inorganic materials 0.000 claims abstract description 7
- 238000000354 decomposition reaction Methods 0.000 claims description 8
- 230000002255 enzymatic effect Effects 0.000 claims description 4
- 101710169606 Hemoglobin-2 Proteins 0.000 claims 1
- 210000004369 blood Anatomy 0.000 abstract description 14
- 239000008280 blood Substances 0.000 abstract description 13
- 235000013305 food Nutrition 0.000 abstract description 10
- 239000002699 waste material Substances 0.000 abstract description 9
- 102000004169 proteins and genes Human genes 0.000 abstract description 8
- 108090000623 proteins and genes Proteins 0.000 abstract description 8
- 150000004045 organic chlorine compounds Chemical class 0.000 abstract description 6
- 239000004278 EU approved seasoning Substances 0.000 abstract description 5
- 239000000463 material Substances 0.000 abstract description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 14
- 235000019640 taste Nutrition 0.000 description 14
- 238000006243 chemical reaction Methods 0.000 description 11
- 238000004519 manufacturing process Methods 0.000 description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 229940088598 enzyme Drugs 0.000 description 8
- 239000000306 component Substances 0.000 description 7
- 244000144972 livestock Species 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- 238000006911 enzymatic reaction Methods 0.000 description 6
- 108090000284 Pepsin A Proteins 0.000 description 5
- 102000057297 Pepsin A Human genes 0.000 description 5
- 108091005804 Peptidases Proteins 0.000 description 5
- 102000035195 Peptidases Human genes 0.000 description 5
- 210000000601 blood cell Anatomy 0.000 description 5
- 229940111202 pepsin Drugs 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- 239000004365 Protease Substances 0.000 description 4
- 239000006227 byproduct Substances 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- 108010019160 Pancreatin Proteins 0.000 description 3
- 235000019658 bitter taste Nutrition 0.000 description 3
- 239000007857 degradation product Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 229940055695 pancreatin Drugs 0.000 description 3
- 235000019600 saltiness Nutrition 0.000 description 3
- 230000001953 sensory effect Effects 0.000 description 3
- 239000001509 sodium citrate Substances 0.000 description 3
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 3
- 235000011121 sodium hydroxide Nutrition 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 238000004065 wastewater treatment Methods 0.000 description 3
- 102000005158 Subtilisins Human genes 0.000 description 2
- 108010056079 Subtilisins Proteins 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 150000001413 amino acids Chemical class 0.000 description 2
- 235000015249 blood sausages Nutrition 0.000 description 2
- 238000005119 centrifugation Methods 0.000 description 2
- 230000007515 enzymatic degradation Effects 0.000 description 2
- 210000003743 erythrocyte Anatomy 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 235000013372 meat Nutrition 0.000 description 2
- 210000004180 plasmocyte Anatomy 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 102000004196 processed proteins & peptides Human genes 0.000 description 2
- 239000003531 protein hydrolysate Substances 0.000 description 2
- 230000017854 proteolysis Effects 0.000 description 2
- 230000002797 proteolythic effect Effects 0.000 description 2
- 238000003307 slaughter Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000006228 supernatant Substances 0.000 description 2
- 241000251468 Actinopterygii Species 0.000 description 1
- 108091005658 Basic proteases Proteins 0.000 description 1
- 108010017384 Blood Proteins Proteins 0.000 description 1
- 102000004506 Blood Proteins Human genes 0.000 description 1
- 108010082495 Dietary Plant Proteins Proteins 0.000 description 1
- 241000287828 Gallus gallus Species 0.000 description 1
- 206010020710 Hyperphagia Diseases 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 241001494479 Pecora Species 0.000 description 1
- 241000282887 Suidae Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 235000011920 black pudding Nutrition 0.000 description 1
- 239000012503 blood component Substances 0.000 description 1
- 235000008429 bread Nutrition 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000013256 coordination polymer Substances 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 235000013601 eggs Nutrition 0.000 description 1
- 239000012156 elution solvent Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 235000020776 essential amino acid Nutrition 0.000 description 1
- 239000003797 essential amino acid Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 235000012041 food component Nutrition 0.000 description 1
- 239000005417 food ingredient Substances 0.000 description 1
- 238000001641 gel filtration chromatography Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 235000020830 overeating Nutrition 0.000 description 1
- 108010091748 peptide A Proteins 0.000 description 1
- 235000015277 pork Nutrition 0.000 description 1
- 244000144977 poultry Species 0.000 description 1
- 235000020991 processed meat Nutrition 0.000 description 1
- 229940024999 proteolytic enzymes for treatment of wounds and ulcers Drugs 0.000 description 1
- 235000011962 puddings Nutrition 0.000 description 1
- 235000013580 sausages Nutrition 0.000 description 1
- 239000011492 sheep wool Substances 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 235000019583 umami taste Nutrition 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
- 238000003911 water pollution Methods 0.000 description 1
Landscapes
- Seasonings (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Abstract
(57)【要約】
【課題】 廃棄された血液の利用により、廃棄蛋白質の
食材化あるいは有機塩素系化合物を含まない調味料、更
にはヘモグロビンの利用を得ること。
【解決手段】 ヘモグロビンあるいはヘモグロビンから
ヘム鉄を除いた殘渣を複数の酵素を用いて分子量300
0以下にまで分解する。(57) 【Abstract】 PROBLEM TO BE SOLVED: To obtain waste proteins by using waste blood as food materials or seasonings containing no organic chlorine compound, and further obtain hemoglobin. SOLUTION: Hemoglobin or a residue obtained by removing heme iron from hemoglobin is treated with a plurality of enzymes to give a molecular weight of 300.
Decomposes to 0 or less.
Description
【0001】[0001]
【発明の属する技術分野】本発明は、グロビンペプチド
を有効成分とする新規の調味料及び新規の調味料として
ヘモグロビンを利用する方法に関する。TECHNICAL FIELD The present invention relates to a novel seasoning containing a globin peptide as an active ingredient and a method for utilizing hemoglobin as a new seasoning.
【0002】[0002]
【従来の技術】近年の後進国における食糧危機にも拘ら
ず、世界の人口は恒常的に増加傾向にあり、世界の食糧
事情は今後とも更に厳しくなると考えられる。Despite the food crisis in the underdeveloped countries in recent years, the population of the world is constantly increasing, and the food situation in the world is expected to become more severe in the future.
【0003】これに対し、食糧確保の方策としては、増
産,生産の効率化,過食割合の増大、即ち、廃棄部分の
可食化による摂取効率の向上などが考えられる。On the other hand, as measures for securing food, it is conceivable to increase production, improve production efficiency, increase the proportion of overeating, that is, improve intake efficiency by making waste portions edible.
【0004】廃棄物及び不可食成分の可食化についてみ
ると、ここ数年、植物性蛋白質の利用と同様に畜産副産
物の食材化にも多大なる関心が寄せられている。畜産副
産物とは、家畜家禽類の主要生産物である乳,肉,卵,
刈り取り羊毛等以外の屠体の構成成分の総称であり、そ
の総量は豚で50%を占めている。Regarding the edible use of wastes and inedible components, much interest has been paid to the use of livestock by-products as foodstuffs as well as the use of vegetable proteins in the past few years. Livestock by-products are the main products of livestock and poultry: milk, meat, eggs,
It is a general term for the constituent components of carcasses other than cut sheep wool, and the total amount is 50% for pigs.
【0005】これら畜産副産物のうち、屠畜血液は「液
体肉(liquid meat)」とも呼ばれ、欧州で
はブラッドソーセージ(血液ソーセージ)やブラックプ
リン(血液プリン)として食品に利用されている。しか
しながら、日本及びアメリカでは嗜好上あるいは宗教上
の理由から、一般に屠畜血液は食品原料からは除外され
ている。Of these livestock by-products, slaughtered blood is also called "liquid meat", and is used in Europe as blood sausage (blood sausage) or black pudding (blood pudding) in foods. However, in Japan and the United States, slaughtered blood is generally excluded from food ingredients for reasons of taste and religion.
【0006】それ故、屠畜血液は家畜の肥育頭数が多
く、飼料を自国で生産しているアメリカでは飼料原料と
して利用されているのに対して、家畜の肥育頭数が少な
く、飼料を輸入に頼っている日本では廃棄しているのが
現状である。[0006] Therefore, slaughtered blood has a large number of fattening heads of livestock and is used as a feed raw material in the United States where feed is produced in its own country. In Japan, which we rely on, it is currently discarded.
【0007】これら血液廃水は莫大な経費のかかる廃水
処理の対象となっており、又、垂れ流しによる環境問題
の原因ともなっている。このような状況下、近年畜産業
界では資源の有効利用,屠畜場における廃水処理の省力
化等の観点から、屠畜血液利用の気運が高まりつつあ
る。[0007] These blood wastewaters are subject to enormous costly wastewater treatments, and also cause environmental problems due to runoff. Under these circumstances, the livestock industry has recently been gaining momentum for using slaughter blood from the viewpoint of effective use of resources and labor saving of wastewater treatment at slaughterhouses.
【0008】屠畜血液はプラズマと血球部分に分けられ
る。最近では、屠畜血液中のプラズマは新しい乳化剤と
して注目されており、ソーセージ等の食肉加工品の原料
や菓子類のクリームやパン生地の原料等、食品としての
用途が広がりつつある。Slaughtered blood is divided into plasma and blood cells. Recently, plasma in slaughtered blood has been attracting attention as a new emulsifier, and its use as a food such as a raw material for processed meat products such as sausages, a raw material for cream and bread dough for confectionery is spreading.
【0009】[0009]
【発明が解決しようとする課題】プラズマ蛋白質中には
各種医薬品への利用が期待できる成分あるいは既に利用
されている成分も多い。それに対し、血球部分はその色
や不溶性等の理由から、ほとんど廃棄されているのが現
状である。わずかながら、ヘム鉄としての食材化が行な
われているが、ヘム鉄を製造した場合には廃棄蛋白質が
大量に殘渣として産出される。There are many components in plasma proteins that can be expected to be used in various pharmaceuticals or components that have already been used. On the other hand, most of the blood cells are currently discarded due to their color and insolubility. Although a small amount of heme iron is used as a food material, when heme iron is produced, a large amount of waste protein is produced as a residue.
【0010】又、HAPとして塩酸分解により調味料化
した場合、DCPやMCP等の有害な有機塩素系化合物
が発生するため、食品の安全性の観点から近年問題にな
りつつある。これらの諸問題は血球の利用量に数量的な
制限を与え、ひいてはプラズマ部分の利用の足かせにも
なっている。Further, when HAP is used as a seasoning by decomposing hydrochloric acid, harmful organic chlorine compounds such as DCP and MCP are generated, which is becoming a problem from the viewpoint of food safety in recent years. These problems place a quantitative limit on the amount of blood cells used, which in turn impedes the use of plasma parts.
【0011】上記した現状の利用方法では、廃棄蛋白質
の産出あるいは有機塩素系化合物を含む調味料という好
ましくない食材の生産といった新たな問題が引き起こさ
れている。[0011] The above-mentioned current utilization method causes new problems such as production of waste protein or production of undesired foodstuffs such as seasonings containing organic chlorine compounds.
【0012】本発明は上記事情に鑑みてなされたもので
あり、廃棄されていた血液の利用により、廃棄蛋白質の
食材化あるいは有機塩素系化合物を含まない調味料の開
発を行ない、廃棄蛋白質の呈味性の改良及びそれを有効
成分とする調味料ならびに血液中のヘモグロビンの利用
方法を提供することを目的としている。The present invention has been made in view of the above circumstances, and by utilizing the blood that has been discarded, the waste protein is used as a food material or a seasoning containing no organochlorine compound is developed, and the waste protein is presented. It is an object of the present invention to provide an improved taste, a seasoning containing the same as an active ingredient, and a method for utilizing hemoglobin in blood.
【0013】[0013]
【課題を解決するための手段】本発明者は上記課題の解
決のために鋭意検討した結果、上記課題が解決され得る
ことを見出だしたので、以下にその発明の詳細を説明す
る。先ず、本発明が利用対象としているヘモグロビンは
牛,豚.羊,鶏,魚類等の動物の血液成分から得られる
物である。Means for Solving the Problems As a result of intensive studies for solving the above-mentioned problems, the present inventor has found that the above-mentioned problems can be solved. The details of the invention will be described below. First, the hemoglobin targeted for use in the present invention is cow or pig. It is obtained from blood components of animals such as sheep, chicken and fish.
【0014】これらの血液はクエン酸ナトリウム等を加
えた後に遠心分離することにより、プラズマと血球部分
とに分けられる。血球部分はヘモグロビンを主成分と
し、これを調味料の原料とする。These bloods are separated into plasma and blood cells by adding sodium citrate or the like and then centrifuging. The blood cell portion contains hemoglobin as a main component, and this is used as a raw material for seasonings.
【0015】先ず、ヘモグロビンを固形分として水に対
して5〜30重量%になるように分散させ、酸もしくは
アルカリによって酵素の至適pHに調整し、1種(例えば
ペプシン)あるいは2種(例えばペプシンとパンクレア
チン)以上の酵素を1度に又は逐次的に添加して、20
〜70℃の温度で3〜48時間酵素反応させて加水分解
する。加水分解終了後、得られた液を遠心分離あるいは
濾過等の通常公知の方法を用いて、蛋白分解物と不溶性
ペプチドあるいはヘム鉄に分離する。First, hemoglobin is dispersed as a solid content in water in an amount of 5 to 30% by weight, and the pH of the enzyme is adjusted to an optimum pH with an acid or an alkali, and one kind (for example, pepsin) or two kinds (for example, pepsin). Pepsin and pancreatin) or more enzymes are added at once or sequentially to give 20
It is hydrolyzed by enzymatic reaction at a temperature of ~ 70 ° C for 3 to 48 hours. After completion of hydrolysis, the obtained solution is separated into a proteolytic product and an insoluble peptide or heme iron by using a commonly known method such as centrifugation or filtration.
【0016】次に、ここで得られた蛋白分解物あるいは
得られた蛋白分解物を上記と同様の方法で酵素分解する
ことを、1回あるいは2回以上繰り返すことにより得ら
れる方法により乾燥あるいは濃縮して、グロビンペプチ
ドを有効成分とする調味料を得る。ここで、得られた蛋
白分解物の分子量は3000以下まで分解されているこ
と、及び使用する酵素は3種以上であることが望まし
い。Next, the protein degradation product obtained here or the enzymatic degradation of the obtained protein degradation product in the same manner as above is dried or concentrated by a method obtained by repeating once or twice or more. Thus, a seasoning containing globin peptide as an active ingredient is obtained. Here, it is desirable that the obtained protein hydrolyzate has a molecular weight of 3000 or less and that the number of enzymes used is 3 or more.
【0017】上記の方法により、従来のヘモグロビン蛋
白分解物より、塩酸分解調味料と同等以上に呈味性の優
れた、有機塩素系化合物を含まない調味料(以下、本発
明調味料と記載する)の製造が可能となる。By the above-mentioned method, a seasoning containing no organochlorine compound, which is more excellent in taste than a conventional hemoglobin protein hydrolyzate and has a taste equal to or better than a hydrochloric acid-decomposing seasoning (hereinafter referred to as the seasoning of the present invention). ) Can be manufactured.
【0018】[0018]
【発明の実施の形態】以下に実施例を記載して本発明を
更に具体的に説明する。 実施例1 本発明調味料の製造 衛生的に採血された新鮮な豚血液に、クエン酸ナトリウ
ムを終濃度0.5%になるよう加えた後、2000rp
mで10分間遠心分離した。BEST MODE FOR CARRYING OUT THE INVENTION The present invention will be described in more detail with reference to the following examples. Example 1 Production of seasoning of the present invention After adding sodium citrate to a final concentration of 0.5% to freshly collected hog blood which had been sanitarily collected, 2000 rp was obtained.
Centrifuge for 10 minutes at m.
【0019】得られた赤血球に等量の水を加えた後、苛
性ソーダを用いてpH8.5に調整し、アルカリ性プロテ
アーゼ(アルカラーゼ2.4L,ノボインダストリー社
製)を加えて55℃で、3時間酵素反応させた。反応終
了後、反応液を80℃以上で30分保持することにより
酵素を失活させた。After adding an equal amount of water to the obtained red blood cells, the pH was adjusted to 8.5 with caustic soda, alkaline protease (Alcalase 2.4 L, manufactured by Novo Industry) was added, and the mixture was heated at 55 ° C. for 3 hours. Enzyme reaction was performed. After completion of the reaction, the reaction solution was kept at 80 ° C. or higher for 30 minutes to deactivate the enzyme.
【0020】反応液を冷却後、塩酸を用いてpH4.0に
調整し、析出するヘム鉄を除くため5000rpmで1
0分間遠心分離した。得られた上澄を塩酸を用いてpH
2.0に調整し、酸性プロテアーゼ(ペプシン、和光純
薬製)を加えて40℃で、3時間酵素反応させた。After cooling the reaction solution, the pH was adjusted to 4.0 with hydrochloric acid, and 1 hour at 5000 rpm to remove the heme iron that had precipitated.
Centrifuge for 0 minutes. The pH of the obtained supernatant was adjusted with hydrochloric acid.
The pH was adjusted to 2.0, acidic protease (pepsin, manufactured by Wako Pure Chemical Industries, Ltd.) was added, and the enzyme reaction was carried out at 40 ° C. for 3 hours.
【0021】反応終了後、反応液を80℃以上で30分
保持することにより酵素を失活させ、苛性ソーダを用い
てpH8.0に調整した。次に、プロテアーゼ(パンクレ
アチン、和光純薬製)を加えて40℃で、6時間酵素反
応させた。After completion of the reaction, the reaction solution was kept at 80 ° C. or higher for 30 minutes to inactivate the enzyme, and the pH was adjusted to 8.0 using caustic soda. Next, protease (pancreatin, manufactured by Wako Pure Chemical Industries, Ltd.) was added, and the enzyme reaction was carried out at 40 ° C. for 6 hours.
【0022】反応終了後、反応液を80℃以上で30分
保持することにより酵素を失活させ、塩酸を用いてpH
5.5に調整した後、1/100容の活性炭を加えた。
室温で30分攪拌後、得られた濾液を固形分が30%と
なるまで濃縮した後、噴霧乾燥し、白色のグロビンペプ
チドの粉末を得た。After completion of the reaction, the reaction solution is kept at 80 ° C. or higher for 30 minutes to inactivate the enzyme, and the pH is adjusted with hydrochloric acid.
After adjusting to 5.5, 1/100 volume of activated carbon was added.
After stirring at room temperature for 30 minutes, the obtained filtrate was concentrated to a solid content of 30% and then spray-dried to obtain a white globin peptide powder.
【0023】得られたグロビンペプチドの成分分析値を
表1に、アミノ酸組成を表2に示した。これらの結果か
らグロビンペプチドは、通常市販されている調味料と同
様の成分からなる必須アミノ酸を多く含む良好な調味料
であると考えられた。The component analysis values of the obtained globin peptide are shown in Table 1, and the amino acid composition is shown in Table 2. From these results, it was considered that globin peptide is a good seasoning containing a large amount of essential amino acids composed of the same components as those of commercially available seasonings.
【0024】[0024]
【表1】 [Table 1]
【0025】[0025]
【表2】 [Table 2]
【0026】実施例2 本発明調味料の呈味性 得られたグロビンペプチド及び各種蛋白分解物を蛋白濃
度2%になるよう水に溶解したものを調整し、官能検査
を行なった。10名の熟練のパネラーの参加により、旨
味,甘味,苦み,塩味,酸味について評価させた。その
結果、表3に示した通り、グロビンペプチドは他の蛋白
酵素分解物より全ての点で優れた、又、グロビン塩酸分
解物と同等の呈味性を示した。Example 2 Taste of the seasoning of the present invention The globin peptide and various proteolytic products obtained were dissolved in water to a protein concentration of 2%, and a sensory test was conducted. Ten expert panelists participated in the evaluation of umami, sweetness, bitterness, saltiness and sourness. As a result, as shown in Table 3, the globin peptide was superior in all respects to other proteolytic enzymes, and showed the same taste as the globin-hydrolyzate.
【0027】[0027]
【表3】 [Table 3]
【0028】実施例3 グロビンペプチドの製造時にお
ける呈味性の変化 実施例1に示した製造工程中の各段階におけるグロビン
酵素分解物について、官能検査を行なった。10名の熟
練のパネラーにより、旨味,甘味,苦み,塩味,酸味に
ついて評価させた。その結果、表4に示した通り、分子
量3000以下にまで分解することにより、グロビン塩
酸分解物と同程度の呈味性を示すことが明らかとなっ
た。Example 3 Change in Taste during Production of Globin Peptide A sensory test was conducted on the globin enzymatic degradation product at each stage in the production process shown in Example 1. Ten skilled panelists evaluated the taste, sweetness, bitterness, saltiness and sourness. As a result, as shown in Table 4, it was revealed that by decomposing to a molecular weight of 3,000 or less, the same level of taste as the globin-hydrolyzed product was exhibited.
【0029】[0029]
【表4】 [Table 4]
【0030】以上のことから、分子量3000以上では
分解が不充分であり、アミノ酸や呈味性を有するペプチ
ドの遊離が少ないため呈味性が低いと考えられた。した
がってグロビン分解物を塩酸分解物よりも優れた調味料
とするためには、分子量3000以下まで分解すること
が必須条件と考えられた。なお、分子量分布はゲル濾過
クロマトグラフィーを用い、以下の条件で調べた。From the above, it was considered that when the molecular weight is 3,000 or more, the decomposition is insufficient, and the release of amino acids and taste-imparting peptides is small, so that the taste is low. Therefore, in order to make the globin decomposition product a seasoning superior to the hydrochloric acid decomposition product, it was considered that decomposition to a molecular weight of 3000 or less is an essential condition. The molecular weight distribution was examined by gel filtration chromatography under the following conditions.
【0031】装置:高速液体クロマトグラフ(wate
rs. LC module 1) カラム:ULTRASPHEROGEL SEC 20
00, BECKMAN社) 溶出溶媒:0.1%TFA/50%アセトニトリル 検出波長:220nm 流速:1m1/minApparatus: high performance liquid chromatograph (weight)
rs. LC module 1) Column: ULTRASPHEROGEL SEC 20
00, BECKMAN) Elution solvent: 0.1% TFA / 50% acetonitrile Detection wavelength: 220 nm Flow rate: 1 m1 / min
【0032】実施例4 酵素分解の方法を変えた本発明
調味料の製造 衛生的に採血された新鮮な豚赤液に、クエン酸ナトリウ
ムを終濃度0.5%になるよう加えた後、2000rp
mで10分間遠心分離した。得られた赤血球に等量の水
を加えた後、塩酸を用いてpH2.0に調整し、酸性プロ
テアーゼ(ペプシン、和光純薬製)を加えて40℃で、
3時間酵素反応させた。Example 4 Manufacture of seasoning of the present invention in which the method of enzymatic decomposition was changed. To fresh pork red liquor collected sanitarily, sodium citrate was added to a final concentration of 0.5%, and then 2000 rp.
Centrifuge for 10 minutes at m. After adding an equal amount of water to the obtained red blood cells, the pH was adjusted to 2.0 with hydrochloric acid, an acidic protease (pepsin, manufactured by Wako Pure Chemical Industries, Ltd.) was added, and at 40 ° C.,
The enzyme reaction was carried out for 3 hours.
【0033】反応終了後、反応液を80℃以上で30分
保持することにより、酵素を失活させ、苛性ソーダを用
いてpH8.0に調整した後、5000rpmで10分間
遠心分離した。得られた上澄にプロテアーゼ(アルカラ
ーゼ2.0L、ノボインダストリー社製、パンクレアチ
ン、和光純薬製)を加えて50℃で、12時間酵素反応
させた。After the reaction was completed, the reaction solution was kept at 80 ° C. or higher for 30 minutes to inactivate the enzyme, and the pH was adjusted to 8.0 using caustic soda, followed by centrifugation at 5000 rpm for 10 minutes. Protease (Alcalase 2.0 L, manufactured by Novo Industry Co., Pancreatin, manufactured by Wako Pure Chemical Industries, Ltd.) was added to the obtained supernatant, and an enzyme reaction was carried out at 50 ° C. for 12 hours.
【0034】反応終了後、反応液を80℃以上で30分
保持することにより、酵素を失活させ、塩酸を用いてpH
5.5に調整した後、1/100容の活性炭を加えた。
室温で30分攪拌後、濾過し、得られた濾液を固形分3
0%となるまで濃縮した淡黄色のグロビンペプチドを含
む調味料を得た。After completion of the reaction, the reaction solution is kept at 80 ° C. or higher for 30 minutes to inactivate the enzyme, and the pH is adjusted with hydrochloric acid.
After adjusting to 5.5, 1/100 volume of activated carbon was added.
After stirring at room temperature for 30 minutes, the mixture was filtered, and the obtained filtrate was mixed with solids 3
A seasoning containing a pale yellow globin peptide concentrated to 0% was obtained.
【0035】実施例5 酵素分解の方法を変えた本発明
調味料の呈味性 実施例1で得られたグロビンペプチドの粉末及び実施例
4で得られたグロビンペプチドを含む調味料を蛋白濃度
2%になるよう水に溶解したものを調整し、官能検査を
行なった。Example 5 Taste of the seasoning of the present invention obtained by changing the enzymatic decomposition method The powder of the globin peptide obtained in Example 1 and the seasoning containing the globin peptide obtained in Example 4 were used for protein concentration 2 What was melt | dissolved in water was adjusted so that it might become%, and sensory test was performed.
【0036】10名の熟練のパネラーにより、旨味,甘
味,苦味,塩味,酸味について評価させた。その結果、
表5に示した通り、グロビンペプチドは両製法とも同等
の呈味性を示した。以上の結果から、酵素分解の方法及
び濃縮方法の如何に拘らず、同等の調味料が製造できる
と考えられる。Ten skilled panelists evaluated the taste, sweetness, bitterness, saltiness and sourness. as a result,
As shown in Table 5, the globin peptides exhibited equivalent taste in both production methods. From the above results, it is considered that the same seasoning can be produced regardless of the enzymatic decomposition method and the concentration method.
【0037】[0037]
【表5】 [Table 5]
【0038】[0038]
【発明の効果】以上説明したように、本発明によれば塩
酸分解調味料と比べても、呈味性の優れた、DCPやM
CP等の有機塩素系化合物を含まないヘモグロビンから
の調味料の製造が可能となる。又、ヘム鉄製造時に産出
される廃棄蛋白質の調味料としての利用が可能となる。
更に、今まで廃棄されてきた畜産副産物である屠畜血液
の食材としての有効利用が可能となることから、廃水処
理にかかる経費の削減あるいは周辺環境の水質汚染の軽
減が可能となる。INDUSTRIAL APPLICABILITY As described above, according to the present invention, DCP and M, which are excellent in taste even when compared with hydrochloric acid-decomposing seasonings, are used.
It is possible to produce a seasoning from hemoglobin that does not contain an organic chlorine compound such as CP. Further, it becomes possible to use the waste protein produced during the production of heme iron as a seasoning.
Further, since the slaughtering blood, which is a by-product of livestock that has been discarded so far, can be effectively used as a food material, it is possible to reduce the cost for wastewater treatment or reduce water pollution in the surrounding environment.
Claims (6)
を特徴とする調味料。1. A seasoning comprising a globin peptide as an active ingredient.
素で分解して製造され、分子量が3000以下であるこ
とを特徴とする請求項1記載の調味料。2. The seasoning according to claim 1, wherein the globin peptide is produced by decomposing hemoglobin with an enzyme and has a molecular weight of 3000 or less.
は2種以上であることを特徴とする請求項2記載の調味
料。3. The seasoning according to claim 2, wherein the enzyme decomposing hemoglobin is one kind or two or more kinds.
0〜70℃で、3〜48時間の条件で酵素分解にて得ら
れたものであることを特徴とする請求項2又は請求項3
記載の調味料。4. The globin peptide is hemoglobin 2.
It was obtained by enzymatic decomposition under conditions of 0 to 70 ° C. for 3 to 48 hours.
Seasoning listed.
して得られたものであることを特徴とする請求項1又は
請求項2又は請求項3又は請求項4記載の調味料。5. The seasoning according to claim 1, wherein the globin peptide is obtained as a heme iron-producing residue.
法。6. A method of using hemoglobin as a seasoning.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7293524A JPH09107912A (en) | 1995-10-17 | 1995-10-17 | Seasoning containing globin peptide as an active ingredient and method of using hemoglobin as the seasoning |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7293524A JPH09107912A (en) | 1995-10-17 | 1995-10-17 | Seasoning containing globin peptide as an active ingredient and method of using hemoglobin as the seasoning |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH09107912A true JPH09107912A (en) | 1997-04-28 |
Family
ID=17795861
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP7293524A Pending JPH09107912A (en) | 1995-10-17 | 1995-10-17 | Seasoning containing globin peptide as an active ingredient and method of using hemoglobin as the seasoning |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH09107912A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106929554A (en) * | 2015-12-31 | 2017-07-07 | 上海杰隆生物制品股份有限公司 | A kind of preparation method of globin peptide |
| CN109567073A (en) * | 2019-01-08 | 2019-04-05 | 广东海洋大学 | A kind of hemoglobinated fish blood product of richness and its production method |
-
1995
- 1995-10-17 JP JP7293524A patent/JPH09107912A/en active Pending
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106929554A (en) * | 2015-12-31 | 2017-07-07 | 上海杰隆生物制品股份有限公司 | A kind of preparation method of globin peptide |
| CN109567073A (en) * | 2019-01-08 | 2019-04-05 | 广东海洋大学 | A kind of hemoglobinated fish blood product of richness and its production method |
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