JP2001238610A - Method for producing modified copra meal - Google Patents

Method for producing modified copra meal

Info

Publication number
JP2001238610A
JP2001238610A JP2000054719A JP2000054719A JP2001238610A JP 2001238610 A JP2001238610 A JP 2001238610A JP 2000054719 A JP2000054719 A JP 2000054719A JP 2000054719 A JP2000054719 A JP 2000054719A JP 2001238610 A JP2001238610 A JP 2001238610A
Authority
JP
Japan
Prior art keywords
copra meal
mannose
salts
copra
producing modified
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
Application number
JP2000054719A
Other languages
Japanese (ja)
Inventor
Futoshi Yokomizo
太 横溝
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Fuji Oil Co Ltd
Original Assignee
Fuji Oil Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Fuji Oil Co Ltd filed Critical Fuji Oil Co Ltd
Priority to JP2000054719A priority Critical patent/JP2001238610A/en
Priority to PCT/JP2001/000993 priority patent/WO2001064932A1/en
Priority to AU2001230615A priority patent/AU2001230615A1/en
Publication of JP2001238610A publication Critical patent/JP2001238610A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P19/00Preparation of compounds containing saccharide radicals
    • C12P19/14Preparation of compounds containing saccharide radicals produced by the action of a carbohydrase (EC 3.2.x), e.g. by alpha-amylase, e.g. by cellulase, hemicellulase
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23KFODDER
    • A23K10/00Animal feeding-stuffs
    • A23K10/10Animal feeding-stuffs obtained by microbiological or biochemical processes
    • A23K10/14Pretreatment of feeding-stuffs with enzymes
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23KFODDER
    • A23K20/00Accessory food factors for animal feeding-stuffs
    • A23K20/10Organic substances
    • A23K20/163Sugars; Polysaccharides
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P60/00Technologies relating to agriculture, livestock or agroalimentary industries
    • Y02P60/80Food processing, e.g. use of renewable energies or variable speed drives in handling, conveying or stacking
    • Y02P60/87Re-use of by-products of food processing for fodder production

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Zoology (AREA)
  • Polymers & Plastics (AREA)
  • Microbiology (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Food Science & Technology (AREA)
  • Biotechnology (AREA)
  • Wood Science & Technology (AREA)
  • Animal Husbandry (AREA)
  • Biomedical Technology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Physiology (AREA)
  • Molecular Biology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Fodder In General (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)

Abstract

PROBLEM TO BE SOLVED: To efficiently and economically isolate mannose by introducing salts in the reaction system. SOLUTION: This method for producing modified copra meal features acting mannanase upon copra meal in the coexistence of salts.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【産業上の利用分野】本発明は、飼料または飼料添加用
として特にサルモネラ菌排菌効果の期待されるマンノー
スを含有する改質コプラミールの製造法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a process for producing a modified copra meal containing mannose, which is expected to have a salmonella eradication effect, especially for feed or feed addition.

【0001】[0001]

【従来の技術】従来より、飼料にマンノース類を添加す
ることによりサルモネラ菌の排菌効果が期待されること
が知られている(Poultly Science 1989 68 1357)。
また、ヤシ油を搾った粕として産出されるコプラミール
にマンナンが豊富に含有されることも従来より知られて
おり、コプラミールなどガラクトマンナン類を含む原料
に酵素を作用させて得られるマンノース多糖体を家畜用
飼料に配合することにより、サルモネラ汚染防止に効果
があるとの報告もなされている(特開平8-173055)。
2. Description of the Related Art It has been conventionally known that the addition of mannoses to a feed is expected to have an effect of eliminating Salmonella bacteria (Poultly Science 1989 68 1357).
It has also been known that copra meal, which is produced as coconut oil pulp, is rich in mannan.Mannose polysaccharides obtained by the action of enzymes on raw materials containing galactomannans such as copra meal are also known. It has been reported that blending it with feed for livestock is effective in preventing Salmonella contamination (Japanese Patent Application Laid-Open No. 8-173055).

【0002】しかし、これらは使用される酵素がβ−マ
ンノシダーゼあるいはガラクトマンナナーゼ単体もしく
はα−ガラクトシダーゼとの組み合わせであり、目的成
分もマンノースのオリゴ糖ないしは多糖類であってマン
ノースではない。マンノース類は、単糖とオリゴ糖、多
糖類では効能に差があり、単糖のマンノースがサルモネ
ラ菌に対して最も有用に働くとの報告もあるが、マンノ
ースは高価であり飼料への添加は養鶏業界にとっては経
済的負担となる。このような事情から、効果と製造コス
トの面を考慮した上でさらに安価な飼料添加用のマンノ
ースを提供することが市場から求められている。
However, these enzymes use β-mannosidase or galactomannanase alone or in combination with α-galactosidase, and the target component is mannose oligosaccharide or polysaccharide, not mannose. Mannoses differ in efficacy between monosaccharides, oligosaccharides, and polysaccharides, and there are reports that the monosaccharide mannose works most effectively against Salmonella, but mannose is expensive and must be added to feed for poultry farming. It is an economic burden for the industry. Under these circumstances, there is a need in the market to provide a more inexpensive feed-adding mannose in consideration of the effects and production costs.

【0003】[0003]

【課題を解決するための手段】コプラミールはヤシ油を
搾った粕として産出され、それ自体が動物の飼料として
利用されている。しかし、その中に30〜36%含まれ
るコプラマンナンは難消化性である上、サルモネラ菌の
排菌効果もあまり無く、有効に利用されているとは言い
難い。本発明者はマンナナーゼをコプラミールに作用さ
せる際にNaCl、MgCl2などの塩類を添加する
と、塩類を用いない場合よりも多量の単糖のマンノース
が遊離することを見出し、本発明を完成するに至った。
すなわち、本発明は、コプラミールに、塩類の共存下、
マンナナーゼを作用させることを特徴とする改質コプラ
ミールの製造法である。
SUMMARY OF THE INVENTION Copra meal is produced as coconut oil squeezed cake, and is itself used as animal feed. However, copramannan, which is contained therein in an amount of 30 to 36%, is indigestible and has little effect on eradicating Salmonella. The present inventors have found that when salts such as NaCl and MgCl2 are added when mannanase is allowed to act on copra meal, a larger amount of monosaccharide mannose is released than when no salts are used, and the present invention has been completed. .
That is, the present invention, in copra meal, in the presence of salts,
This is a method for producing modified copra meal, which is characterized by allowing mannanase to act.

【0004】使用するマンナナーゼは、市販されている
もの(例えばヘミセルラーゼGM「アマノ」/天野製薬
株式会社製(商品名)、スミチームACH/新日本化学
工業株式会社製(商品名)、セルロシンGM5/阪急バ
イオインダストリー株式会社(商品名))で良い。尚、
これら市販品で入手可能なもののほとんどはAspergillu
s niger由来である。
The mannanase to be used is commercially available (for example, hemicellulase GM "Amano" / manufactured by Amano Pharmaceutical Co., Ltd. (trade name), Sumiteam ACH / Shin Nippon Chemical Co., Ltd. (trade name), cellulosin GM5 / Hankyu Bio-Industry Co., Ltd. (trade name) is good. still,
Most of these commercially available products are Aspergillu
s niger.

【0005】これら酵素を塩類の共存下でコプラミール
に作用させる。塩類は、塩化物塩または硫酸化物塩が好
ましく、NaCl、MgCl2、MgSO4のようなア
ルカリ金属やアルカリ土類金属の塩化物塩もしくは硫酸
化物塩、あるいは、NH4Clなどが入手のし易さ、値
段、安全性の面からさらに好ましい。これら塩類は予め
酵素液に溶解しておくのが簡便であり、酵素液中、0.00
01 〜 2.0 M(mol/litter)、好ましくは、
0.005 〜 0.5 M となるように調製するとよい。2.0 M
を越えると効果に乏しくなる。
[0005] These enzymes act on copra meal in the presence of salts. The salt is preferably a chloride salt or a sulfate salt, and a chloride salt or a sulfate salt of an alkali metal or an alkaline earth metal such as NaCl, MgCl2, or MgSO4, or NH4Cl is easily available, price, It is more preferable from the viewpoint of safety. It is convenient to dissolve these salts in the enzyme solution in advance, and in the enzyme solution,
01 to 2.0 M (mol / liter), preferably
It should be adjusted to be 0.005 to 0.5M. 2.0 M
If it exceeds, the effect will be poor.

【0006】コプラミールはヤシ油を搾った粕、または
さらに油脂を溶剤抽出した残さとして産出するものが使
用でき、通常その中にマンナンを30〜36重量%程度
含有するものである。塩類を含有する酵素液はコプラミ
ールと均一に混合すればよいが、コプラミールは非常に
吸水性が高いため、均一混合に必要な反応系の水分量は
かなり必要である。しかし、マンノースの精製工程など
で水分を除去する必要から必要最小限にとどめるべきで
あり、適する水分量は、反応系中50〜70重量%、好
ましくは58〜62重量%である。
[0006] Copra meal can be used as a residue produced by squeezing palm oil or as a residue obtained by extracting oils and fats with a solvent, and usually contains mannan in an amount of about 30 to 36% by weight. The enzyme solution containing salts may be mixed uniformly with copra meal, but since copra meal has a very high water absorption, a considerable amount of water is required in the reaction system necessary for uniform mixing. However, it is necessary to remove the water in the mannose purification step and the like, so that the water content should be kept to the minimum necessary.

【0007】本法により処理したコプラミールは遊離の
単糖のマンノースを含んでおり、塩類を予め反応系内に
導入することで、酵素の失活を抑えることができ反応性
の向上をもたらす。コプラミールは、そのまま、あるい
は適宜乾燥させて飼料に配合するか、もしくは水溶性画
分を抽出して飼料に添加することにより、特にサルモネ
ラ菌の排菌効果を発揮することが出来る。
[0007] Copra meal treated by the present method contains free monosaccharide mannose, and by introducing salts into the reaction system in advance, the inactivation of the enzyme can be suppressed and the reactivity is improved. Copra meal can be particularly effective in eliminating Salmonella by mixing it with the feed as it is or by drying it appropriately or by extracting the water-soluble fraction and adding it to the feed.

【0008】例えば、コプラミール100gにβ−ガラク
トマンナナーゼ15000uを0.01MのNaCl水
溶液に溶解した酵素液150gを添加し60℃で72時間反
応させ、12〜15gのマンノースが生じる。この反応
処理後のコプラミールをそのまま乾燥した飼料等に配合
すればよい。その配合量を0.25〜1%程度とすれば
配合飼料でのマンノースの含量は0.01〜0.075
重量%となりサルモネラ菌など有害細菌の排除効果が得
られる。
For example, 150 g of an enzyme solution obtained by dissolving 15000 u of β-galactomannanase in an aqueous solution of 0.01 M NaCl is added to 100 g of copra meal and reacted at 60 ° C. for 72 hours to produce 12 to 15 g of mannose. The copra meal after the reaction treatment may be directly blended into a dried feed or the like. If the compounding amount is about 0.25 to 1%, the mannose content in the compound feed is 0.01 to 0.075.
% By weight, and an effect of eliminating harmful bacteria such as Salmonella can be obtained.

【0009】[0009]

【実施例】圧搾コプラミール10gに対し、β−ガラクト
マンナナーゼ1/30gおよび様々な塩類(種類および添加
量は表1.に記載している)を溶解した酵素液15gを添
加混合した後、密閉容器に入れ、60℃に静置保管し72時
間反応させた。生成したマンノースの定量を次のように
行った。酵素処理コプラミールに50gの水を加え沸騰
浴中にて10分間保持し、酵素を失活させると同時に水
溶性成分を水層に溶解させた後、全体を100mlに定
容し、ろ過して水溶液を得た。この溶液を除たん白する
など適宜前処理し、イオン交換クロマトグラフィーを使
用してマンノース量を調べた。その結果、NaCl(0.001
〜0.01M)、MgCl2(0.001〜0.1M)、CuSO4(0.001M)な
どを添加した場合、対照区(無添加)よりマンノースの
生成量が多くなっていた(表1)。尚、β−ガラクトマ
ンナナーゼは、ヘミセルラーゼGM「アマノ」(天野製
薬株式会社製(商品名)、β−ガラクトマンナナーゼ活
性45000u/g)を使用した。
[Example] To 10 g of pressed copra meal, 1/30 g of β-galactomannanase and 15 g of an enzyme solution in which various salts (types and addition amounts are described in Table 1) were added and mixed. And allowed to react at 72 ° C. for 72 hours. The produced mannose was quantified as follows. 50 g of water was added to the enzyme-treated copra meal, and the mixture was kept in a boiling bath for 10 minutes to deactivate the enzyme and simultaneously dissolve the water-soluble component in the aqueous layer. I got The solution was appropriately pretreated, such as by protein removal, and the amount of mannose was determined using ion exchange chromatography. As a result, NaCl (0.001
-0.01M), MgCl2 (0.001-0.1M), CuSO4 (0.001M), etc., produced more mannose than the control (no addition) (Table 1). As the β-galactomannanase, hemicellulase GM “Amano” (trade name, manufactured by Amano Pharmaceutical Co., Ltd., 45000 u / g β-galactomannanase activity) was used.

【0010】 [0010]

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】コプラミールに、塩類の共存下、マンナナ
ーゼを作用させることを特徴とする改質コプラミールの
製造法。
1. A method for producing a modified copra meal, wherein mannanase is allowed to act on copra meal in the presence of salts.
【請求項2】塩類がNaCl、MgCl2、NH4Clなどの塩化物塩
ないしはMgSO4などの硫酸化物塩である請求項1記載の
製造法。
2. The method according to claim 1, wherein the salt is a chloride salt such as NaCl, MgCl2, NH4Cl or a sulfate salt such as MgSO4.
JP2000054719A 2000-02-29 2000-02-29 Method for producing modified copra meal Pending JP2001238610A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
JP2000054719A JP2001238610A (en) 2000-02-29 2000-02-29 Method for producing modified copra meal
PCT/JP2001/000993 WO2001064932A1 (en) 2000-02-29 2001-02-13 Process for producing modified copra meal
AU2001230615A AU2001230615A1 (en) 2000-02-29 2001-02-13 Process for producing modified copra meal

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2000054719A JP2001238610A (en) 2000-02-29 2000-02-29 Method for producing modified copra meal

Publications (1)

Publication Number Publication Date
JP2001238610A true JP2001238610A (en) 2001-09-04

Family

ID=18575933

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2000054719A Pending JP2001238610A (en) 2000-02-29 2000-02-29 Method for producing modified copra meal

Country Status (3)

Country Link
JP (1) JP2001238610A (en)
AU (1) AU2001230615A1 (en)
WO (1) WO2001064932A1 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2195796B1 (en) * 2002-05-30 2005-02-01 Institut De Recerca I Tecnologia Agroalimentaries NATURAL RUBBER BASED PREMIX FOR ANIMAL FEEDING.

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6349093A (en) * 1986-08-18 1988-03-01 Res Dev Corp Of Japan Production of mannosaccharide-containing glucide
JP2591948B2 (en) * 1987-02-27 1997-03-19 東和化成工業株式会社 Method for producing β-1,4-mannobiose
JPH08173055A (en) * 1994-12-21 1996-07-09 Shinichi Hoshida Mannose-based polysaccharide-containing feed
JPH099985A (en) * 1996-07-17 1997-01-14 Meiji Seika Kaisha Ltd Food containing low-viscosity hardly digestible polysaccharides
JPH11137288A (en) * 1997-02-17 1999-05-25 Osaka City Production of mannose

Also Published As

Publication number Publication date
WO2001064932A1 (en) 2001-09-07
AU2001230615A1 (en) 2001-09-12

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