JPS63286270A - Feed for domestic animal - Google Patents
Feed for domestic animalInfo
- Publication number
- JPS63286270A JPS63286270A JP62123552A JP12355287A JPS63286270A JP S63286270 A JPS63286270 A JP S63286270A JP 62123552 A JP62123552 A JP 62123552A JP 12355287 A JP12355287 A JP 12355287A JP S63286270 A JPS63286270 A JP S63286270A
- Authority
- JP
- Japan
- Prior art keywords
- protein
- corpuscle
- added
- feed
- blood
- 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
- 241001465754 Metazoa Species 0.000 title abstract description 8
- 210000004369 blood Anatomy 0.000 claims abstract description 11
- 239000008280 blood Substances 0.000 claims abstract description 11
- 210000000601 blood cell Anatomy 0.000 claims description 16
- 102000004190 Enzymes Human genes 0.000 claims description 7
- 108090000790 Enzymes Proteins 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 6
- 244000144972 livestock Species 0.000 claims description 3
- 102000004169 proteins and genes Human genes 0.000 abstract description 13
- 108090000623 proteins and genes Proteins 0.000 abstract description 13
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 6
- 239000007788 liquid Substances 0.000 abstract description 5
- 108091005804 Peptidases Proteins 0.000 abstract description 3
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 abstract description 3
- 102000018146 globin Human genes 0.000 abstract description 3
- 108060003196 globin Proteins 0.000 abstract description 3
- 230000007062 hydrolysis Effects 0.000 abstract description 3
- 238000006460 hydrolysis reaction Methods 0.000 abstract description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 abstract description 3
- 239000011707 mineral Substances 0.000 abstract description 3
- 238000000926 separation method Methods 0.000 abstract description 3
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 abstract description 2
- 239000003513 alkali Substances 0.000 abstract description 2
- 239000011575 calcium Substances 0.000 abstract description 2
- 229910052791 calcium Inorganic materials 0.000 abstract description 2
- 102000004157 Hydrolases Human genes 0.000 abstract 2
- 108090000604 Hydrolases Proteins 0.000 abstract 2
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 abstract 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 abstract 1
- 239000003456 ion exchange resin Substances 0.000 abstract 1
- 229920003303 ion-exchange polymer Polymers 0.000 abstract 1
- 239000006228 supernatant Substances 0.000 abstract 1
- 230000002255 enzymatic effect Effects 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 238000005119 centrifugation Methods 0.000 description 5
- 238000001035 drying Methods 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 3
- 230000001186 cumulative effect Effects 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 230000003301 hydrolyzing effect Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000008267 milk Substances 0.000 description 2
- 210000004080 milk Anatomy 0.000 description 2
- 235000013336 milk Nutrition 0.000 description 2
- 239000000052 vinegar Substances 0.000 description 2
- 235000021419 vinegar Nutrition 0.000 description 2
- 230000004584 weight gain Effects 0.000 description 2
- 235000019786 weight gain Nutrition 0.000 description 2
- 241000473391 Archosargus rhomboidalis Species 0.000 description 1
- 239000005996 Blood meal Substances 0.000 description 1
- 241000283690 Bos taurus Species 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 102000001554 Hemoglobins Human genes 0.000 description 1
- 108010054147 Hemoglobins Proteins 0.000 description 1
- 239000004365 Protease Substances 0.000 description 1
- 235000002597 Solanum melongena Nutrition 0.000 description 1
- 244000061458 Solanum melongena Species 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 244000309466 calf Species 0.000 description 1
- 210000004027 cell Anatomy 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 230000037213 diet Effects 0.000 description 1
- 235000005911 diet Nutrition 0.000 description 1
- 235000019621 digestibility Nutrition 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000007071 enzymatic hydrolysis Effects 0.000 description 1
- 238000006047 enzymatic hydrolysis reaction Methods 0.000 description 1
- 235000021050 feed intake Nutrition 0.000 description 1
- 238000013467 fragmentation Methods 0.000 description 1
- 238000006062 fragmentation reaction Methods 0.000 description 1
- 150000003278 haem Chemical class 0.000 description 1
- 210000003677 hemocyte Anatomy 0.000 description 1
- 229940000351 hemocyte Drugs 0.000 description 1
- 230000000415 inactivating effect Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 230000006651 lactation Effects 0.000 description 1
- 238000004811 liquid chromatography Methods 0.000 description 1
- 239000006166 lysate Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 210000004180 plasmocyte Anatomy 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 102220280971 rs1253463092 Human genes 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Landscapes
- Feed For Specific Animals (AREA)
- Fodder In General (AREA)
Abstract
Description
(産業上の利用分野)
本発明は、Jlt曲場より流出する層由血赦の有効的な
活用として、#!會血液中の血球全酵素で蛋白質加水分
解処理して得られる酵素加水分解物、又はこれと血漿と
の混合物を家畜用飼料に添加てることにより板曲の効率
的な成育ン行なうところにある。
(従来の技術)
層着血液の飼料への利用は従来から血粉と称し、他の物
質に吸収させたり、棟々σ)乾燥法によって粉末状にし
て原曲用飼料の副原料として用いられてい友が、消化性
、暗灯性、臭気等の間鞠点を有している。
又、層曲血液の他の利用法として、血iY遠心分離でる
ごとによって得られる上置数、いわゆる血漿画分ン食品
、医薬品といつに分野で広く利用している。
しかしながら、運上分離後、残潰物となる血球画分の利
#3は未だ確立されておらす溌莱されているのが塊状で
ある。
(本発明か解決しようとしている間親点)本発明は上記
の如く、血球の利用が木だ行なわれていない塊状におい
て、血球中に言句する高蛋白質の有用性に鑑み、酵素処
理によって得られる血球の酔糸加水分解物が家曲肖成、
特l二唾乳期、離乳期、肥育用jの家由の1要な蛋白質
源となることを見出し本酔累加水分解物の利用法を提供
するごとケ目的とてる。
さらに本発明は渚曲条者がかかえる盾會1111液の処
理に関する諸間和ン解決するもσ)である。
な活用法として、原曲用飼料へθ】利用を検討した結果
、従来よりある蛋白質加水分解酵素プロテアーゼン血球
に作用させに後、これを乾燥てることにより加水分解物
として白色の粉末品を得た口
この白色粉末品は、m球中l二せ44″′rる被合蛋白
質ヘモグロビンを蛋白貴加水分鱗#糸であるグロテアー
ゼで加水分解せしめるごとによって含有てるヘム分ン分
陥したものであり、大部分をグロビン蛋白質か占め、他
にカルシウム、燐といったミネラルン宮儒する◎
本発明をさらに詳しく説明すると、本発明で採取する渚
曲血液は牛、肱か一般的であるが水壷のf3II類に限
定でることはなく利用出来る。
これら採取血液を遠心分1Ij118機V#3いて沈澱
画分、丁なわち血球ケ得る。又、必要に応じて遠心分離
を繰り返てことによって血球の収曾増加が図れる。血球
ケ得る方法は遠心分片化機ケ用いる方法が簡便で最良の
方法であるがごれg二限定されるものではない。
血球の酵素による加水分解は、PHスタット法と叶ばれ
る方法(NEW FOOD INDDSTRYvo
l 、26 No、8 1984 )を用いて行なう
。
てなわち1血球に2〜5倍容の水ン加え血球浴数の蛋白
袈磯度ン調贅する。しかる恢アルカリを加え浴液のPH
を7〜10好ましくはP H8,2〜8.7に調gt、
てる。これに解糸ン皿球蛋臼買に対して0.1〜10%
加え、浴&温度40〜70℃の状態で加水分解ケ行なっ
た後1点心分離を行ない、上置徹を活性炭処理、あるい
はイオン交換側側を由いて精#する。
尚、遠心分離後の残渣に水を加え遠心分離を繰り返すこ
とにより酵素加水分解物の収量Y尚めることも出来る。
稍装後の酵素加水分解?I君−向浴赦は、このまま、あ
るいは血漿と混合し、酢液状で利用てることも可能であ
るが、得られた蛋日佃の経時変化、保存、及び輸送の点
から考えて、凍結乾燥、真を乾燥あるいは、スプレード
ライによって乾燥粉末化し利用することがより好ましい
。
かくして得られる酵素加水分解物は、原曲用納料に添加
するが唾乳期の人工乳、離乳期の代用乳、肥育期前期の
配合飼料に添加するのが好ましい、
絡加童は特に制限はないが、酵素加水分解物として、あ
るいは血漿と混合てることにより、水壷用銅料に対して
固形分換算で0.1〜10%添加することが適当である
か、ごれより多く添加しても何ら間組はない。
血球を酵素加水分解することにより得られた白色粉末品
の蛋白質構成は、e種のアミノ酸がペプチド結合したグ
ロビン蛋白質である。
液体クロマトマドグラフィー法で副足したグロビン蛋白
質の分子量は、1000〜2000に集中しているが、
広くは500〜5000に分布する。
又、本白色粉末品は獣皿%自の異臭もほとんどなし′O
この様にこの酵素加水分解された日色松末状蛋白寛は、
比較的、低分子量であり、カルシウム、勢といったミネ
ラルも多1it(二含有し、消化吸収性に優れ、栄養価
か高い定め%成宵途中、つまり比軟的蛋白質′多3摂取
f7) C、、、t ’a”Jb賛とする時期の原曲の
鯛料ン添加し給与したところ、水壷の体1増加および納
科効率の改善に後れた効果があつ友。
以下に、本発明の実施例〉示すが゛、本発明はかかる実
施例に限定され少ものではない。
実施例1゜
層會場から採取し友妨糾な豚皿101に、25ラクエン
鍍ナトリウム水鹸液ン添加俊、理心分F@ン行ない血漿
および血球(二分離でる。得られkm球に3倍答の水を
加えて、かつ5規足Nap)[′j¥用いてPRケ8.
5に調竪する。これにプロテアーセを血球浴数に対して
3%加え、温度ケ55cで3時間保持てる。この間PH
は一定の値を保ち続ける。次いで礎牛MCIをを用いて
酵素失活後、5規足N30HにてPHを5.01m調歪
し、遠心分離を行ない上世液に活性炭ケ加えて1口過、
乾燥することにより1.1kgの白色粉末状乾燥物ケ得
た。この乾燥物中の蛋白質量ンケルダール法により御」
足したところ約85%含有されていた。
以上の様な操作ン叙回繰り換えてことによって得られた
酢累加水分解物ン、市販飼料に1%、3%、5%の割合
で添加しkものをそれぞれ試験区に、市Jl12鶴料の
みン対照区に阪足し、体皿6喀前後の哺乳期子豚に21
g1向給与し哺乳期子豚の増俸量および飼料要求率の比
較を行なった。
各区の哺乳期子豚は体重分布が平均にl(Industrial Application Field) The present invention provides #! Efficient growth of planks can be achieved by adding to livestock feed an enzymatic hydrolyzate obtained by hydrolyzing proteins using whole blood cell enzymes in the animal's blood, or a mixture of this and plasma. (Prior art) The use of layered blood for feed has traditionally been called blood meal, which has been absorbed into other substances or made into a powder using a drying method and used as an auxiliary raw material for raw feed. It has different characteristics such as digestibility, darkness, and odor. In addition, as another use of layered blood, the so-called plasma fraction obtained by blood iY centrifugation is widely used in the fields of foods, medicines, and other fields. However, the usefulness of the hemocyte fraction #3, which remains after separation, has not yet been established and is in the form of a lump. (The main point to be solved by the present invention) As mentioned above, in view of the usefulness of high protein contained in blood cells in the form of lumps in which the utilization of blood cells is not carried out, the present invention is based on the fact that high protein can be obtained by enzyme treatment. The hydrolyzate of blood cells produced by the blood cells is
In particular, we have discovered that this product can serve as an important protein source for animals during the lactation period, weaning period, and for fattening, and our purpose is to provide a method for utilizing the cumulative hydrolyzate. Furthermore, the present invention also solves various problems regarding the treatment of the 1111 liquid that is carried by beach users. As a practical use, we investigated the use of θ] in the original feed, and found that a white powder product was obtained as a hydrolyzate by allowing the conventional protein hydrolase protease to act on blood cells and then drying it. This white powder product is obtained by hydrolyzing hemoglobin, which is a conjugated protein in m bulbs, with grotease, which is a protein-rich hydrolyzed scale, to remove the heme content. ◎ To explain the present invention in more detail, the blood collected in the present invention can be collected from cows, calves, or commonly used in water bottles. The collected blood can be used without being limited to the f3II class.The collected blood is centrifuged to obtain a precipitate fraction, that is, blood cells.If necessary, by repeating centrifugation, blood cells can be obtained. The method for obtaining blood cells is to use a centrifugal fragmentation machine, which is simple and best, but the method is not limited to dirt. The law and the way it is fulfilled (NEW FOOD INDDSTERVo)
1, 26 No. 8 1984). In other words, add 2 to 5 times the volume of water to each blood cell and adjust the amount of protein in the blood cell bath. Add alkali to adjust the pH of the bath liquid.
Adjust to 7 to 10, preferably pH 8, 2 to 8.7,
Teru. This is added to 0.1-10% of the amount of lysate and cylindrical protein purchased.
In addition, after hydrolysis is carried out in a bath and at a temperature of 40 to 70°C, single-point separation is carried out, and the upper plate is treated with activated carbon or purified via the ion exchange side. The yield Y of the enzymatic hydrolyzate can also be determined by adding water to the residue after centrifugation and repeating centrifugation. Enzyme hydrolysis after modification? Although it is possible to use I-Kun-Kouyakusha as it is or in the form of a vinegar liquid by mixing it with plasma, it is recommended to freeze-dry it from the viewpoint of changes over time, storage, and transportation of the obtained eggplant. It is more preferable to use the powder by drying or spray drying the powder. The enzymatic hydrolyzate obtained in this way is added to the original feed, but it is preferable to add it to artificial milk during the lactating period, milk replacer during the weaning period, and mixed feed during the early fattening period. However, it is appropriate to add 0.1 to 10% in terms of solid content to the copper material for water jars as an enzymatic hydrolyzate or by mixing it with plasma, or add more than dirt. However, there is no intermission. The protein composition of the white powder product obtained by enzymatic hydrolysis of blood cells is a globin protein in which e-type amino acids are peptide-bonded. The molecular weight of globin protein added by liquid chromatography is concentrated in the range of 1000 to 2000,
Broadly distributed between 500 and 5000. In addition, this white powdered product has almost no off-odor of natural animal odor.
It has a relatively low molecular weight and is high in minerals such as calcium and minerals. When I added the sea bream ingredients from the period when T'a''Jb San was added to the diet, the effect of increasing Mizuho's body by 1 and improving the efficiency of medical treatment was delayed.The following describes the present invention. However, the present invention is not limited to such an example and is not limited to the above. , plasma and blood cells (separate into two. Add three times the amount of water to the obtained km cells, and use five times Nap) ['j\ to PR case 8.
Tune to 5. To this, protease was added at 3% based on the number of blood cells in the bath, and the mixture was kept at a temperature of 55°C for 3 hours. During this time PH
continues to maintain a constant value. Next, after inactivating the enzyme using Kogyu MCI, the pH was adjusted to 5.01 m using 5-meter N30H, centrifugation was performed, and activated charcoal was added to the Joisei liquid, followed by 1 sip.
By drying, 1.1 kg of white powdery dried material was obtained. The amount of protein in this dried product can be determined by the Schönkeldahl method.
The total content was about 85%. The vinegar cumulative hydrolyzate obtained by repeating the above procedures was added to commercially available feed at a ratio of 1%, 3%, and 5%, and the mixture was added to the test plots at Ichi Jl 12 Tsuru. The feed was added to the control group, and the lactating piglets, which were around 6 months old, were given 21
The increase in pay and feed conversion rate of suckling piglets fed g1 were compared. The weight distribution of suckling piglets in each area is on average.
【るように6〜
79Aずつ供試した。その結果ケ第1表に示す。
尚1表中の飼料要求率とは一足体重増加曾に対し%摂取
しり飼料の輩を表わしたものであり1次式の様に示され
る。
坏皇増加賃
第1表
第1表からも明らかな様に得られた酵素加水分解物を市
販飼料に添加して使用した場合体重増加および飼料効率
の改善に者しく優れた効果力ぐあっに0
実施例2゜
、 実施例1と同様にして得られた酵素加水分解物に
血漿乾燥物V1:1の割合で混合し、これを市販飼料に
1%、3%、5%の割合で添加したものをそれぞれ試験
区に設足し、実施例1の方法に基づき体M6−前後の哺
乳期子豚に2週間給与し、哺乳期子豚の増俸量および゛
飼料要求率の比較を行なっL0
各区の踊乳期子豚は、体重分布が平均になる様に6〜7
頭ずつ供試し友。その結果を第2表に示す。
第2衣からも明らかな様に酵素加水分解物と血漿乾燥物
の混合物ケ市版鋼料に添加して使用し定損合体及増加お
よび飼料効率σ】改善に者しく優れ定効果があった。[Like 6~
I tried each 79A. The results are shown in Table 1. The feed conversion ratio in Table 1 represents the percentage of feed intake per paw weight gain, and is expressed as a linear equation. As is clear from Table 1 of Table 1, when the obtained enzymatic hydrolyzate is added to commercially available feed, it is extremely effective in improving weight gain and feed efficiency. Example 2゜The enzymatic hydrolyzate obtained in the same manner as in Example 1 was mixed with dried plasma V at a ratio of 1:1, and this was added to commercial feed at ratios of 1%, 3%, and 5%. Each of the following was added to the test plots, and fed to suckling piglets around body M6 for two weeks based on the method of Example 1, and the pay increase and feed conversion rate of the suckling piglets were compared. The lactating piglets should be kept at 6 to 7 lbs. so that the weight distribution is average.
A head-to-head friend. The results are shown in Table 2. As is clear from the second coating, when the mixture of enzyme hydrolyzate and dried plasma was used by adding it to the commercial steel feed, it was clearly effective in improving constant loss and increasing feed efficiency. .
Claims (2)
水分解物を添加することを特徴とする家畜用飼料。(1) A livestock feed characterized by adding an enzyme hydrolyzate obtained by enzymatically treating blood cells in slaughtered blood.
水分解物と血漿とを混合し、これを添加することを特徴
とする家畜用飼料。(2) A feed for livestock, characterized in that an enzyme hydrolyzate obtained by enzymatically treating blood cells in slaughtered blood is mixed with plasma and added to the mixture.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62123552A JPH0817663B2 (en) | 1987-05-20 | 1987-05-20 | Livestock feed |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62123552A JPH0817663B2 (en) | 1987-05-20 | 1987-05-20 | Livestock feed |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63286270A true JPS63286270A (en) | 1988-11-22 |
JPH0817663B2 JPH0817663B2 (en) | 1996-02-28 |
Family
ID=14863424
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62123552A Expired - Lifetime JPH0817663B2 (en) | 1987-05-20 | 1987-05-20 | Livestock feed |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0817663B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2010209046A (en) * | 2009-03-12 | 2010-09-24 | Nippon Meat Packers Inc | Immunity-activating peptide and feed containing the same |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5327575A (en) * | 1976-08-02 | 1978-03-14 | Mars Ltd | Edible protein products |
-
1987
- 1987-05-20 JP JP62123552A patent/JPH0817663B2/en not_active Expired - Lifetime
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5327575A (en) * | 1976-08-02 | 1978-03-14 | Mars Ltd | Edible protein products |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2010209046A (en) * | 2009-03-12 | 2010-09-24 | Nippon Meat Packers Inc | Immunity-activating peptide and feed containing the same |
Also Published As
Publication number | Publication date |
---|---|
JPH0817663B2 (en) | 1996-02-28 |
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