JPH10204494A - Powdery enzyme preparation and granule using the same - Google Patents

Powdery enzyme preparation and granule using the same

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Publication number
JPH10204494A
JPH10204494A JP1235697A JP1235697A JPH10204494A JP H10204494 A JPH10204494 A JP H10204494A JP 1235697 A JP1235697 A JP 1235697A JP 1235697 A JP1235697 A JP 1235697A JP H10204494 A JPH10204494 A JP H10204494A
Authority
JP
Japan
Prior art keywords
enzyme
preparation
enzyme preparation
sulfate
powdery
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.)
Withdrawn
Application number
JP1235697A
Other languages
Japanese (ja)
Inventor
Takafumi Izawa
啓文 伊澤
Takaaki Watanabe
高明 渡邉
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.)
Kao Corp
Original Assignee
Kao Corp
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 Kao Corp filed Critical Kao Corp
Priority to JP1235697A priority Critical patent/JPH10204494A/en
Publication of JPH10204494A publication Critical patent/JPH10204494A/en
Withdrawn legal-status Critical Current

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  • Enzymes And Modification Thereof (AREA)
  • Detergent Compositions (AREA)

Abstract

PROBLEM TO BE SOLVED: To obtain a powdery enzyme preparation useful for a detergent for clothing, tableware, housing, etc., capable of exhibiting excellent free fluidity and aggregation resistance during preservation without deactivating an enzyme by including an enzyme and a specific amount of an ionic surfactant. SOLUTION: This preparation comprises (A) an enzyme such as protease, esterase, carbohydrase or lyase and (B) 0.2-10wt.% of the protein amount of the component A of an ionic surfactant [e.g. an alkyl (ether) sulfate or an alkenyl (ether) sulfate]. The preparation is obtained by spray-drying a slurried aqueous solution containing the component A and the component B in a fixed ratio, having 1-20wt.% of solid content concentration.

Description

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

【0001】[0001]

【発明の属する技術分野】本発明は、自由流動性、保存
時における凝集性が改善された粉末状酵素製剤及びこれ
を含有する造粒物に関する。
TECHNICAL FIELD The present invention relates to a powdery enzyme preparation having improved free-flowing properties and cohesiveness during storage and a granulated product containing the same.

【0002】[0002]

【従来の技術】衣料用の洗浄剤や漂白剤には、洗浄作用
を高める目的で各種の酵素が配合されることが多い。こ
れらの酵素は、保存中に失活せず、洗浄工程中で活性を
十分発揮させるために、通常、粉末状酵素製剤として又
はこれを顆粒状に造粒したものが配合されている。粉末
状酵素製剤は、通常、噴霧乾燥法により製造されるが、
酵素水溶液のような低濃度スラリーから粉末状酵素製剤
を製造した場合、得られる製剤の自由流動性が必ずしも
十分でなく、また、保存時に吸湿して凝集することが認
められている。このために、これを用いた造粒物を調製
する際及び/又は洗浄剤や漂白剤に配合する際のハンド
リングが困難になり、また酵素の失活が起こるといった
問題が発生する。
2. Description of the Related Art Various enzymes are often added to detergents and bleaching agents for clothing to enhance the washing effect. These enzymes are not deactivated during storage, and are sufficiently formulated as a powdered enzyme preparation or a granulated form thereof in order to sufficiently exhibit the activity during the washing step. Powdered enzyme preparations are usually produced by a spray drying method,
When a powdery enzyme preparation is produced from a low-concentration slurry such as an aqueous enzyme solution, it has been recognized that the resulting preparation does not always have sufficient free-flowing properties, and that it absorbs and aggregates during storage. For this reason, handling becomes difficult when preparing a granulated product using the same and / or when blending it into a detergent or a bleaching agent, and problems such as inactivation of enzymes occur.

【0003】一般に、粉末状製剤の物性は乾燥装置の運
転条件をコントロールすることにより調整されている
が、これには限界がある。また、噴霧するスラリーにつ
いては、これを高濃度化することによりその物性の改善
を図ることも可能であるが、過度にスラリー中の水分量
を減少させると、スラリーの粘度が上昇し、例えば噴霧
乾燥法にて乾燥を行うことによって酵素粉末を得る場
合、噴霧が困難になるという問題がある。また、スラリ
ーを高濃度化することにより酵素の析出が起こるため、
回収率の低下も認められる。他に、粉末状酵素製剤の物
性の改善には乾燥助剤の添加も効果はあるが、その添加
量に制限があり、大量に使用すると酵素活性が低下する
という問題がある。
[0003] In general, the physical properties of a powdery preparation are adjusted by controlling the operating conditions of a drying apparatus, but this has limitations. In addition, it is possible to improve the physical properties of the slurry to be sprayed by increasing the concentration of the slurry.However, if the amount of water in the slurry is excessively reduced, the viscosity of the slurry increases. When the enzyme powder is obtained by drying by a drying method, there is a problem that spraying becomes difficult. In addition, since the precipitation of the enzyme occurs by increasing the concentration of the slurry,
A decrease in recovery is also observed. In addition, although the addition of a drying aid is also effective for improving the physical properties of the powdered enzyme preparation, the amount of addition is limited, and there is a problem that the enzyme activity is reduced when used in a large amount.

【0004】[0004]

【発明が解決しようとする課題】従って、本発明の目的
は、酵素の失活も見られず、しかも、自由流動性及び保
存時における凝集性が改善された粉末状酵素製剤及びこ
れを用いた造粒物を提供することにある。
SUMMARY OF THE INVENTION Accordingly, an object of the present invention is to provide a powdery enzyme preparation which has no deactivation of the enzyme, and has improved free-flowing properties and improved cohesion during storage. It is to provide granules.

【0005】[0005]

【課題を解決するための手段】そこで、本発明者らは粉
末状酵素製剤の流動性向上につき種々検討した結果、全
く意外にも加水分解酵素等の酵素と少量のイオン性界面
活性剤とを均一に分散して共存させても当該酵素は失活
せず、しかも自由流動性及び保存時における凝集性が改
善された粉末状酵素製剤が得られることを見出し、本発
明を完成させるに至った。
The present inventors have made various studies on improving the flowability of a powdered enzyme preparation. As a result, the present inventors surprisingly found that an enzyme such as a hydrolase and a small amount of an ionic surfactant were used. It was found that the enzyme was not inactivated even when uniformly dispersed and coexisted, and that a powdery enzyme preparation with improved free-flowing properties and improved cohesiveness during storage was obtained, thereby completing the present invention. .

【0006】すなわち、本発明は、酵素及び該酵素タン
パク量の0.2〜10重量%のイオン性界面活性剤を含
有することを特徴とする粉末状酵素製剤を提供するもの
である。また、本発明は、酵素タンパク量の0.2〜1
0重量%のイオン性界面活性剤を含有する酵素水溶液を
噴霧乾燥することを特徴とする上記粉末状酵素製剤の製
造法を提供するものである。更に本発明は、上記粉末状
酵素製剤及びバインダーを含有することを特徴とする酵
素含有造粒物を提供するものである。
That is, the present invention provides a powdery enzyme preparation containing an enzyme and an ionic surfactant in an amount of 0.2 to 10% by weight based on the amount of the enzyme protein. In addition, the present invention relates to an enzyme protein amount of 0.2 to 1%.
It is intended to provide a method for producing the above-mentioned powdery enzyme preparation, which comprises spray-drying an enzyme aqueous solution containing 0% by weight of an ionic surfactant. Further, the present invention provides an enzyme-containing granule comprising the above-mentioned powdery enzyme preparation and a binder.

【0007】[0007]

【発明の実施の形態】本発明に用いられる酵素として
は、漂白剤や洗浄剤に配合される酵素であれば特に制限
されない。具体的にはプロテアーゼ、エステラーゼ、カ
ルボヒドラーゼ、リアーゼ等が挙げられる。
BEST MODE FOR CARRYING OUT THE INVENTION The enzyme used in the present invention is not particularly limited as long as it is an enzyme blended in a bleach or a detergent. Specific examples include protease, esterase, carbohydrase, lyase and the like.

【0008】プロテアーゼの具体例としては、ペプシ
ン、トリプシン、キモトリプシン、コラーゲナーゼ、ケ
ラチナーゼ、エラスターゼ、ズブチリシン、パパイン、
アミノペプチダーゼ、カルボキシペプチダーゼ等が挙げ
られる。
Specific examples of proteases include pepsin, trypsin, chymotrypsin, collagenase, keratinase, elastase, subtilisin, papain,
Examples include aminopeptidase, carboxypeptidase and the like.

【0009】エステラーゼの具体例としては、ガストリ
ックリパーゼ、パンクレアチックリパーゼ、植物リパー
ゼ類、ホスホリパーゼ類、コリンエステラーゼ類、ホス
ファターゼ類等が挙げられる。
Specific examples of esterases include gastric lipase, pancreatic lipase, plant lipases, phospholipases, cholinesterases, phosphatases and the like.

【0010】カルボヒドラーゼとしては、セルラーゼ、
マルターゼ、サッカラーゼ、アミラーゼ、ペクチナー
ゼ、α−及びβ−グリコシダーゼ等が挙げられる。リア
ーゼとしては、カルボキシ脱離酵素、アルデヒド脱離酵
素、オキソ酸脱離酵素、ヒドロリアーゼ、多糖に作用す
る脱離酵素、アンモニアリアーゼ等が挙げられる。
As carbohydrase, cellulase,
Examples include maltase, saccharase, amylase, pectinase, α- and β-glycosidase. Examples of lyases include carboxy lyase, aldehyde lyase, oxoacid lyase, hydrolyase, lyase that acts on polysaccharides, and ammonia lyase.

【0011】本発明に用いられるイオン性界面活性剤の
うち、アニオン性界面活性剤としては、アルキルベンゼ
ンスルフォン酸塩、アルキル又はアルケニルエーテル硫
酸塩(AES)、アルキル又はアルケニル硫酸塩(A
S)、オレフィンスルフォン酸塩(AOS)、アルカン
スルフォン酸塩、飽和又は不飽和脂肪酸塩、アルキル又
はアルケニルエーテルカルボン酸塩、α−スルホ脂肪酸
塩又はエステル、アミノ酸型界面活性剤、N−アシルア
ミノ酸型界面活性剤、アルキル又はアルケニルリン酸エ
ステル又はその塩、カルボン酸型高分子界面活性剤など
が挙げられる。両性界面活性剤としては、カルボキシ又
はスルホベタイン型界面活性剤などが挙げられる。カチ
オン性界面活性剤としては、第4級アンモニウム塩など
が挙げられる。本発明においてはこれらのうちアルキル
又はアルケニルエーテル硫酸塩(AES)、アルキル又
はアルケニル硫酸塩(AS)が特に好ましい。
Among the ionic surfactants used in the present invention, examples of the anionic surfactant include alkylbenzene sulfonate, alkyl or alkenyl ether sulfate (AES), and alkyl or alkenyl sulfate (A
S), olefin sulfonate (AOS), alkane sulfonate, saturated or unsaturated fatty acid salt, alkyl or alkenyl ether carboxylate, α-sulfo fatty acid salt or ester, amino acid type surfactant, N-acyl amino acid type Examples thereof include a surfactant, an alkyl or alkenyl phosphate or a salt thereof, and a carboxylic acid type polymer surfactant. Examples of the amphoteric surfactant include a carboxy or sulfobetaine type surfactant. Examples of the cationic surfactant include a quaternary ammonium salt. In the present invention, alkyl or alkenyl ether sulfate (AES) and alkyl or alkenyl sulfate (AS) are particularly preferable.

【0012】本発明の粉末状酵素製剤においてイオン性
界面活性剤の含有量は酵素タンパク量の0.2〜10重
量%であるが、その添加量が0.2重量%未満では物性
の改善効果が得られず、また添加量が10重量%を超え
ると酵素の失活が起こるので好ましくない。なお、ノニ
オン性界面活性剤では物性の改善効果は認められなかっ
た。
In the powdered enzyme preparation of the present invention, the content of the ionic surfactant is from 0.2 to 10% by weight of the amount of the enzyme protein. Is not obtained, and when the added amount exceeds 10% by weight, the enzyme is inactivated, which is not preferable. In addition, the nonionic surfactant did not show the effect of improving the physical properties.

【0013】本発明の粉末状酵素製剤には、製剤の比活
性を一定に保つための希釈剤(例えば増量剤、充填剤
等)、乾燥促進剤、緩衝剤等を必要に応じて配合するこ
とができる。乾燥促進剤としては、例えば塩化カルシウ
ム、硫酸ナトリウム等が挙げられる。増量剤又は充填剤
としては例えば硫酸塩、ハロゲン化物、炭酸塩、リン酸
塩、ケイ酸塩、ホウ酸塩等が挙げられる。より具体的に
は以下の化合物が挙げられる。
The powdered enzyme preparation of the present invention may contain a diluent (eg, a bulking agent, a filler, etc.), a drying accelerator, a buffering agent, etc., as required, for keeping the specific activity of the preparation constant. Can be. Examples of the drying accelerator include calcium chloride and sodium sulfate. Examples of extenders or fillers include sulfates, halides, carbonates, phosphates, silicates, borates and the like. More specifically, the following compounds are mentioned.

【0014】硫酸塩:硫酸ナトリウム、硫酸カリウム、
硫酸カルシウム、硫酸マグネシウム、硫酸亜鉛、硫酸第
1鉄、チオ硫酸ナトリウム、硫酸アルミニウム ハロゲン化物:塩化ナトリウム、塩化カリウム、塩化カ
ルシウム、塩化マグネシウム、臭化カリウム 炭酸塩:炭酸ナトリウム、炭酸水素ナトリウム、炭酸カ
リウム、炭酸カルシウム、炭酸マグネシウム リン酸塩:リン酸ナトリウム、リン酸水素ナトリウム、
リン酸2水素ナトリウム、リン酸カリウム、リン酸2水
素カリウム、ピロリン酸ナトリウム ケイ酸塩:ケイ酸ナトリウム、メタケイ酸ナトリウム、
ケイ酸カリウム、ケイ酸カルシウム ホウ酸(塩):ホウ砂、ホウ酸カリウム、ホウ酸 糖類:全ての単糖、全ての2糖、例えばマルトース型2
糖類及びトレハロース型2糖類
Sulfates: sodium sulfate, potassium sulfate,
Calcium sulfate, magnesium sulfate, zinc sulfate, ferrous sulfate, sodium thiosulfate, aluminum sulfate Halogen: sodium chloride, potassium chloride, calcium chloride, magnesium chloride, potassium bromide Carbonate: sodium carbonate, sodium hydrogen carbonate, potassium carbonate , Calcium carbonate, magnesium carbonate Phosphate: sodium phosphate, sodium hydrogen phosphate,
Sodium dihydrogen phosphate, potassium phosphate, potassium dihydrogen phosphate, sodium pyrophosphate silicate: sodium silicate, sodium metasilicate,
Potassium silicate, calcium silicate Boric acid (salt): Borax, potassium borate, boric acid Saccharides: All monosaccharides, all disaccharides, for example, maltose type 2
Sugars and trehalose-type disaccharides

【0015】これらは1種を単独で又は2種以上を混合
して使用される。また、造粒又は酵素剤の分野で公知の
着色剤、安定剤等も適宜使用でき、更に、賦香剤、消香
剤、帯電防止剤等も使用できる。
These are used singly or as a mixture of two or more. In addition, known coloring agents and stabilizers in the field of granulation or enzyme agents can be used as appropriate, and further, flavoring agents, deodorants, antistatic agents and the like can be used.

【0016】本発明の粉末状酵素製剤は、所定量のイオ
ン性界面活性剤を含有する酵素水溶液を常法に従って処
理することにより製造されるが、1〜20%濃度のスラ
リーを噴霧乾燥により固形化する方法が特に好ましい。
ここで、当該酵素水溶液中には、目的とする粉末状酵素
製剤の組成に必要な成分が全て配合されていることが好
ましい。
The powdered enzyme preparation of the present invention is produced by treating an enzyme aqueous solution containing a predetermined amount of an ionic surfactant according to a conventional method. A slurry having a concentration of 1 to 20% is solidified by spray drying. Is particularly preferable.
Here, it is preferable that all the components necessary for the composition of the target powdery enzyme preparation are blended in the enzyme aqueous solution.

【0017】噴霧乾燥により本発明の粉末状酵素製剤を
製造するには、通常の噴霧乾燥機を用いて、上記酵素水
溶液を乾燥すればよい。噴霧乾燥機には、通常ノズル型
とディスク型とがあるが、目的とする酵素製剤の粒径に
より使い分けることができる。小さい粒径(1μm 以
下)の製剤を製造する場合はノズル型が好ましく、大き
い粒径の製剤を製造する場合はディスク型が好ましい。
In order to produce the powdered enzyme preparation of the present invention by spray drying, the enzyme aqueous solution may be dried using a conventional spray dryer. The spray dryer generally has a nozzle type and a disk type, and can be used properly depending on the particle size of a target enzyme preparation. A nozzle type is preferable when manufacturing a preparation having a small particle size (1 μm or less), and a disk type is preferable when manufacturing a preparation having a large particle size.

【0018】乾燥機における熱風温度は、100〜20
0℃、特に130〜170℃が好ましく、排風温度(酵
素水溶液の温度に相当する)は、50〜100℃、特に
60〜100℃が好ましい。
The hot air temperature in the dryer is 100 to 20.
The temperature is preferably 0 ° C, especially 130 to 170 ° C, and the exhaust air temperature (corresponding to the temperature of the enzyme aqueous solution) is preferably 50 to 100 ° C, particularly preferably 60 to 100 ° C.

【0019】このようにして得られる粉末状酵素製剤を
造粒するには、造粒に必要な添加剤を配合し、常法に従
って造粒すればよい。かかる添加剤としては、バインダ
ーが挙げられる。ここでバインダーとしては、水溶性有
機バインダー、特に(a)融点が35℃以上のポリエチ
レングリコール及びその誘導体、ポリオキシエチレン・
ポリオキシプロピレン共重合体からなる群より選ばれる
水溶性高分子、(b)融点或いは流動点が35℃以上の
ノニオン性界面活性剤、(c)平均分子量が4000以
上のポリカルボン酸塩等の一種或いは2種以上が挙げら
れる。
In order to granulate the powdery enzyme preparation thus obtained, additives necessary for granulation may be blended and granulated according to a conventional method. Such additives include binders. As the binder, a water-soluble organic binder, in particular, (a) polyethylene glycol having a melting point of 35 ° C. or more and its derivatives, polyoxyethylene.
Water-soluble polymers selected from the group consisting of polyoxypropylene copolymers, (b) nonionic surfactants having a melting point or pour point of 35 ° C. or higher, and (c) polycarboxylates having an average molecular weight of 4000 or higher. One type or two or more types may be mentioned.

【0020】特に好ましい水溶性有機バインダーとして
は、(a)のポリエチレングリコール及びその誘導体と
して、ポリエチレングリコール、ポリエチレングリコー
ル硫酸、メトキシポリエチレングリコール等が挙げら
れ、(b)のノニオン性界面活性剤としてはポリオキシ
エチレンアルキルエーテル等が挙げられ、(c)のポリ
カルボン酸塩としてはポリアクリル酸、アクリル酸マレ
イン酸共重合体、ポリアセタールカルボキシレート等の
アルカリ金属塩が挙げられる。
Particularly preferred water-soluble organic binders include polyethylene glycol (a) and derivatives thereof such as polyethylene glycol, polyethylene glycol sulfate, and methoxypolyethylene glycol, and (b) nonionic surfactants such as poly (ethylene glycol). Examples of the polycarboxylate (c) include alkali metal salts such as polyacrylic acid, acrylic acid-maleic acid copolymer, and polyacetal carboxylate.

【0021】また特にこれらの水溶性有機バインダー
は、洗剤に使用される成分でもあるので有用である。通
常の水溶性有機バインダーの使用量は、バインダー毎に
性質の相違があるので一概にはいえないが、得られる酵
素造粒物の酵素活性をできるだけ高めるためにはできる
だけ少量でバインダー効果が発現するものが一般には好
ましい。そのため、これらの水溶性有機バインダーは、
酵素造粒物中、通常5〜50重量%、好ましくは10〜
30重量%含有される。
In particular, these water-soluble organic binders are useful because they are also components used in detergents. The amount of the ordinary water-soluble organic binder used cannot be unconditionally determined because there is a difference in properties between the binders. However, in order to enhance the enzymatic activity of the obtained enzyme granule as much as possible, the binder effect is expressed with as little as possible. Are generally preferred. Therefore, these water-soluble organic binders
In the enzyme granulated product, usually 5 to 50% by weight, preferably 10 to 10% by weight.
30% by weight is contained.

【0022】本発明においては、更に必要に応じて粉末
状の増量剤を添加することができる。増量剤としてはア
ルカリ金属或いはアルカリ土類金属の硫酸塩、炭酸塩、
塩酸塩からなる群より選ばれる一種或いは二種以上の無
機塩が用いられる。すなわち、なかでも硫酸ナトリウ
ム、炭酸ナトリウム、塩化ナトリウム等の水溶性無機ア
ルカリ金属塩が洗浄への影響等を考えると好ましい。ま
た他の増量剤としてクエン酸ナトリウム等の水溶性有機
酸塩、タルク、酸化チタン、炭酸カルシウム、ゼオライ
ト、炭酸マグネシウム、活性白土、カオリン、ケイソウ
土、ベントナイト、パーライト、酸性白土等が挙げられ
る。
In the present invention, a powdery extender can be further added, if necessary. As fillers, alkali metal or alkaline earth metal sulfates, carbonates,
One or more inorganic salts selected from the group consisting of hydrochlorides are used. That is, among them, water-soluble inorganic alkali metal salts such as sodium sulfate, sodium carbonate, and sodium chloride are preferable in consideration of the influence on washing and the like. Other extenders include water-soluble organic acid salts such as sodium citrate, talc, titanium oxide, calcium carbonate, zeolite, magnesium carbonate, activated clay, kaolin, diatomaceous earth, bentonite, perlite, acidic clay, and the like.

【0023】更に、本発明の造粒物には、各種のカルシ
ウム塩、マグネシウム塩等の無機塩、或いは界面活性
剤、糖、カルボキシメチルセルロース等の有機物を用い
ることも可能である。更に、合成ヘクトライトやセピオ
ライトを配合して、培養に由来する有臭成分を吸着させ
ることもできる。また、色素や染料を配合して、酵素顆
粒に着色することも任意である。
Further, in the granulated product of the present invention, various inorganic salts such as calcium salts and magnesium salts, or organic substances such as surfactants, sugars and carboxymethyl cellulose can be used. Furthermore, synthetic hectorite or sepiolite can be blended to adsorb odorous components derived from culture. It is also optional to add a dye or a dye to color the enzyme granules.

【0024】造粒手段としては特に制限されず、湿式造
粒、乾式造粒のいずれでもよく、造粒方法としては押し
出し造粒、転動造粒、解砕造粒、流動層造粒、噴霧造
粒、破砕造粒等が挙げられる。このうち、転動造粒法、
特に攪拌転動造粒法が好ましい。攪拌転動造粒機の具体
例としては、ヘンシェルミキサー(三井三池化工機
(株))、ハイスピードミキサー(深江工業(株))、
バーチカルグラニュレーター(富士産業(株))等を挙
げることができる。これらの共通点は、堅形の混合槽内
部に攪拌羽根を取付けた垂直な攪拌軸を持つことであ
る。水平の攪拌軸を有する模型の造粒機であるレディゲ
・ミキサー(レディゲ社)もまた同様に用いることがで
きる。
The granulation means is not particularly limited, and may be wet granulation or dry granulation. The granulation methods include extrusion granulation, tumbling granulation, pulverized granulation, fluidized bed granulation, and spraying. Granulation, crushing granulation and the like can be mentioned. Among them, rolling granulation,
In particular, the stirring rolling granulation method is preferable. Specific examples of the stirring tumbling granulator include Henschel mixer (Mitsui Miike Kakoki Co., Ltd.), high speed mixer (Fukae Kogyo Co., Ltd.),
Vertical granulator (Fuji Sangyo Co., Ltd.) and the like can be mentioned. The common feature is that they have a vertical stirring shaft with stirring blades mounted inside a rigid mixing tank. A Lodige mixer (Lodige), a model granulator with a horizontal stirring axis, can also be used.

【0025】かくして得られた造粒物の粒径は特に制限
されないが、平均粒径として200〜3000μm、特
に350〜1500μmが好ましい。
The particle size of the granules thus obtained is not particularly limited, but the average particle size is preferably from 200 to 3000 μm, particularly preferably from 350 to 1500 μm.

【0026】本発明酵素含有造粒物は、被覆しなくても
用いることができるが、被覆をすると更に安定性が向上
するので望ましい。本発明酵素含有造粒物の被覆剤とし
ては、特に制限されないが、ポリエチレングリコール、
ポリアクリル酸塩、ポリビニルアルコール、ポリビニル
ピロリドン、セルロース誘導体、デンプン誘導体等の水
溶性被膜形成ポリマー;これらのポリマーとタルク、ク
レー、酸化チタン、炭酸カルシウム等の水溶性又は難溶
性無機粒子又はアルカリ金属ケイ酸塩、アルカリ金属炭
酸塩等の保護剤等との組み合わせが挙げられる。被覆剤
は酵素含有造粒物に対し重量比で0.01〜0.7、特
に0.05〜0.6の割合で用いるのが好ましい。
The enzyme-containing granules of the present invention can be used without coating, but coating is desirable because the stability is further improved. The coating agent for the enzyme-containing granules of the present invention is not particularly limited, but polyethylene glycol,
Water-soluble film-forming polymers such as polyacrylates, polyvinyl alcohol, polyvinylpyrrolidone, cellulose derivatives, starch derivatives, etc .; these polymers and water-soluble or hardly soluble inorganic particles such as talc, clay, titanium oxide, calcium carbonate, etc., or alkali metal silicon And combinations with protecting agents such as acid salts and alkali metal carbonates. The coating agent is preferably used in a weight ratio of 0.01 to 0.7, particularly 0.05 to 0.6, based on the enzyme-containing granules.

【0027】本発明酵素含有造粒物の被覆方法として
は、流動層造粒機、コーティングパン式造粒機、攪拌造
粒機等の装置により常法により被覆する方法が挙げられ
る。
The method for coating the enzyme-containing granulated product of the present invention includes a method of coating with an apparatus such as a fluidized bed granulator, a coating pan granulator, and a stirring granulator by a conventional method.

【0028】本発明の酵素含有造粒物は、洗浄剤組成物
の配合成分として有用であり、これを配合した洗浄剤組
成物は、衣料用、食器用、住居用等の洗浄剤として使用
することができる。
The enzyme-containing granule of the present invention is useful as a component of a detergent composition, and the detergent composition containing the granule is used as a detergent for clothing, tableware, residence, and the like. be able to.

【0029】[0029]

【実施例】以下、実施例を挙げて更に詳細に説明する
が、本発明はこれらに限定されるものではない。
EXAMPLES Hereinafter, the present invention will be described in more detail with reference to examples, but the present invention is not limited thereto.

【0030】実施例1 (1)酵素水溶液として、プロテアーゼ活性を有する粗
酵素(Bacillus sp. KSM-K16(FERM P-3367)由来)を含
む水溶液(酵素タンパク濃度:7.5重量%)を用い
た。この水溶液に、水溶液中の酵素タンパク量に対し、
10重量%となるように表1に示す各種界面活性剤を添
加し、酵素水溶液を調製した。 (2)コントロール(界面活性剤なし)及び(1)で得
た酵素水溶液をアトマイザー式噴霧乾燥機にて熱風温度
150℃、排風温度75℃で噴霧乾燥し、粉末状酵素製
剤(粒径10〜50μm )を得、以下の方法により安息
角、崩潰角、差角及び凝集度を測定した。結果を表1に
示す。これらはすべてパウダテスタ(ホリカワミクロン
(株)製)を用いて測定した。残存酵素活性はいずれの
粉末状酵素製剤も約92%であった。
Example 1 (1) As an enzyme aqueous solution, an aqueous solution containing a crude enzyme having protease activity (derived from Bacillus sp. KSM-K16 (FERM P-3367)) (enzyme protein concentration: 7.5% by weight) was used. Was. In this aqueous solution, relative to the amount of enzyme protein in the aqueous solution,
Various surfactants shown in Table 1 were added so as to be 10% by weight to prepare an aqueous enzyme solution. (2) The enzyme aqueous solution obtained in the control (no surfactant) and the enzyme aqueous solution obtained in (1) was spray-dried with an atomizer type spray dryer at a hot air temperature of 150 ° C. and an exhaust air temperature of 75 ° C. 5050 μm), and the angle of repose, the angle of collapse, the angle of difference and the degree of cohesion were measured by the following methods. Table 1 shows the results. These were all measured using a powder tester (manufactured by Horikawa Micron Corporation). The residual enzyme activity was about 92% for all powdered enzyme preparations.

【0031】(安息角の測定)粉末状酵素製剤を、フル
イ(目開き710μm )に乗せ、フルイを振動させ、製
剤をロートを通じて注入法により測定し、安息角とし
た。安息角が小さいものほど自由流動性に優れ、大きい
ものほど自由流動性が劣る。
(Measurement of angle of repose) The powdered enzyme preparation was placed on a sieve (opening: 710 μm), the sieve was vibrated, and the preparation was measured by an injection method through a funnel to obtain the angle of repose. The smaller the angle of repose is, the better the free flowing property is, and the larger the angle of repose is, the lower the free flowing property is.

【0032】(崩潰角の測定)安息角を前記の方法で測
定した後、粉粒体に一定の衝撃を与えて崩潰したときの
角度を測定し、崩潰角とした。崩潰角が小さいものほど
自由流動性に優れ、大きいものほど自由流動性は劣る。
(Measurement of collapse angle) After the angle of repose was measured by the above-described method, the angle at which the granular material was collapsed by applying a certain impact was measured and defined as the collapse angle. The smaller the collapse angle is, the better the free flowing property is, and the larger the collapse angle is, the lower the free flowing property is.

【0033】(差角の算出)安息角と崩潰角の差を差角
として算出した。
(Calculation of Difference Angle) The difference between the angle of repose and the collapse angle was calculated as the difference angle.

【0034】(凝集度の測定)粉末状酵素製剤を2g秤
量し、3つのフルイ(目開き149、250、350μ
m )を重ねた上に乗せ、フルイを振動させ、停止後3つ
のフルイ上に残った粉体を秤量する。これより凝集度を
測定した。凝集度が小さいものほど自由流動性に優れ、
大きいものほど自由流動性が劣る。
(Measurement of Aggregation Degree) 2 g of the powdered enzyme preparation was weighed, and three sieves (mesh 149, 250, 350 μm) were weighed.
m) is placed on the pile, the sieve is vibrated, and the powder remaining on the three sieves after stopping is weighed. From this, the degree of aggregation was measured. The smaller the degree of cohesion, the better the free flowing property,
Larger ones are less free flowing.

【0035】[0035]

【表1】 [Table 1]

【0036】実施例2 下記組成の原料をハイスピードミキサー(深江工業
(株)製、FS−5型)により造粒し、酵素含有造粒物
を得た。
Example 2 A raw material having the following composition was granulated with a high-speed mixer (FS-5, manufactured by Fukae Kogyo Co., Ltd.) to obtain an enzyme-containing granule.

【0037】[0037]

【表2】 実施例1で得た粉末状酵素製剤 18(重量%) 核物質(粒子径500μm以下の粒子を11重量%、 粒子径700μm以上の粒子を9重量%含み、 平均粒子径が610μmの塩化ナトリウム) 55 バインダー(ポリエチレングリコール6000 (花王(株)製)) 6.5 酸化チタン 2 硫酸ナトリウム バランスTable 2 Powdery enzyme preparation obtained in Example 1 18 (% by weight) Nuclear substance (11% by weight of particles having a particle diameter of 500 μm or less, 9% by weight of particles having a particle diameter of 700 μm or more, and an average particle diameter of 610 μm) Sodium binder) 55 Binder (polyethylene glycol 6000 (manufactured by Kao Corporation)) 6.5 Titanium oxide 2 Sodium sulfate Balance

【0038】すなわち、上記原料(合計3.5kg)を全
てミキサーに投入し、ジャケットに70℃の温水を流し
ながら、アジテーター480rpm、チョッパー900rpm
で攪拌混合を行い、内容物を60℃まで上昇させた後温
水を止めた。原料投入から約15分の造粒操作により、
酵素含有造粒物(粒径350μm 以上1000μm 以下
が98%以上)を得た。
That is, the above-mentioned raw materials (total 3.5 kg) were all charged into a mixer, and agitator 480 rpm, chopper 900 rpm while flowing hot water at 70 ° C. through the jacket.
The contents were heated to 60 ° C., and the hot water was stopped. By granulation operation for about 15 minutes from the input of raw materials,
An enzyme-containing granulated product (98% or more in particle diameter of 350 μm or more and 1000 μm or less) was obtained.

【0039】[0039]

【表3】 [Table 3]

【0040】実施例3 界面活性剤としてラウリル硫酸ナトリウム(花王(株)
製、エマール10)を用い、酵素タンパク量に対する界
面活性剤の量を2、5、10重量%とした以外は実施例
1と同様にして粉末状酵素製剤及びコントロール(界面
活性剤なし)を製造した。表2に示した原料組成におい
て粉末状酵素製剤をこれらのものに代え、バインダー添
加量を6.7重量%とした以外は同様に配合し、実施例
2と同様の方法により酵素含有造粒物を得た。
Example 3 As a surfactant, sodium lauryl sulfate (Kao Corporation)
And Emul 10) in the same manner as in Example 1 except that the amount of the surfactant relative to the amount of the enzyme protein was changed to 2, 5, and 10% by weight to produce a powdered enzyme preparation and a control (without a surfactant). did. In the raw material composition shown in Table 2, the powdery enzyme preparation was replaced with these, and the mixture was blended in the same manner except that the amount of the binder was changed to 6.7% by weight. I got

【0041】[0041]

【表4】 [Table 4]

【0042】実施例4 界面活性剤としてラウリル硫酸ナトリウム(花王(株)
製、エマール10)を用い、実施例1と同様にして粉末
状酵素製剤及びコントロール(界面活性剤なし)を製造
した。表2に示した原料組成において粉末状酵素製剤を
これらのものに代え、バインダー量を6.7、7.4、
8.1重量%とした以外は同様に配合し、実施例2と同
様の方法により酵素含有造粒物を得た。造粒歩留(%)
を表5に示す。
Example 4 As a surfactant, sodium lauryl sulfate (Kao Corporation)
And Emul 10) in the same manner as in Example 1 to produce a powdered enzyme preparation and a control (without surfactant). In the raw material composition shown in Table 2, the powdery enzyme preparation was replaced with these, and the binder amount was changed to 6.7, 7.4,
Except for using 8.1% by weight, the same blending was carried out, and an enzyme-containing granulated product was obtained in the same manner as in Example 2. Granulation yield (%)
Are shown in Table 5.

【0043】[0043]

【表5】 [Table 5]

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 酵素及び該酵素タンパク量の0.2〜1
0重量%のイオン性界面活性剤を含有することを特徴と
する粉末状酵素製剤。
1. An enzyme and the amount of the enzyme protein of 0.2 to 1
A powdery enzyme preparation comprising 0% by weight of an ionic surfactant.
【請求項2】 酵素タンパク量の0.2〜10重量%の
イオン性界面活性剤を含有する酵素水溶液を噴霧乾燥す
ることを特徴とする請求項1記載の粉末状酵素製剤の製
造法。
2. The method for producing a powdery enzyme preparation according to claim 1, wherein an enzyme aqueous solution containing an ionic surfactant in an amount of 0.2 to 10% by weight of the enzyme protein is spray-dried.
【請求項3】 請求項1記載の粉末状酵素製剤及びバイ
ンダーを含有することを特徴とする酵素含有造粒物。
3. An enzyme-containing granulated product comprising the powdered enzyme preparation according to claim 1 and a binder.
JP1235697A 1997-01-27 1997-01-27 Powdery enzyme preparation and granule using the same Withdrawn JPH10204494A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
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Application Number Priority Date Filing Date Title
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Publications (1)

Publication Number Publication Date
JPH10204494A true JPH10204494A (en) 1998-08-04

Family

ID=11803008

Family Applications (1)

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Country Link
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Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000022104A1 (en) * 1998-10-09 2000-04-20 Kao Corporation Enzyme particles
WO2006030889A1 (en) * 2004-09-16 2006-03-23 The Nisshin Oillio Group, Ltd. Lipase powder, method for producing same and use thereof
US7998715B2 (en) 2005-09-20 2011-08-16 Asahi Breweries, Ltd. Method of producing liquid koji having enhanced plant fiber degeneration enzyme, liquid koji obtained by the method and use thereof
US8124374B2 (en) 2005-10-12 2012-02-28 Asahi Breweries, Ltd. Method of producing recombinant protein
JP2012527506A (en) * 2009-05-20 2012-11-08 ビーエーエスエフ ソシエタス・ヨーロピア Method for producing a spray powder comprising one or more glycine-N, N-diacetic acid derivatives and method for using the spray powder for producing a compressed mass
US8715979B2 (en) 2005-10-05 2014-05-06 Asahi Breweries, Ltd. Method of producing filamentous fungus culture product
US8802170B2 (en) 2004-04-09 2014-08-12 Asahi Breweries, Ltd. Method of manufacturing liquid koji

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000022104A1 (en) * 1998-10-09 2000-04-20 Kao Corporation Enzyme particles
US6410287B1 (en) 1998-10-09 2002-06-25 Kao Corporation Enzyme particles
US6544763B2 (en) 1998-10-09 2003-04-08 Kao Corporation Enzyme particles
US8802170B2 (en) 2004-04-09 2014-08-12 Asahi Breweries, Ltd. Method of manufacturing liquid koji
WO2006030889A1 (en) * 2004-09-16 2006-03-23 The Nisshin Oillio Group, Ltd. Lipase powder, method for producing same and use thereof
US8580550B2 (en) 2004-09-16 2013-11-12 The Nisshin Oillio Group, Ltd. Lipase powder, method for manufacture thereof, and use thereof
US7998715B2 (en) 2005-09-20 2011-08-16 Asahi Breweries, Ltd. Method of producing liquid koji having enhanced plant fiber degeneration enzyme, liquid koji obtained by the method and use thereof
US8715979B2 (en) 2005-10-05 2014-05-06 Asahi Breweries, Ltd. Method of producing filamentous fungus culture product
US8124374B2 (en) 2005-10-12 2012-02-28 Asahi Breweries, Ltd. Method of producing recombinant protein
JP2012527506A (en) * 2009-05-20 2012-11-08 ビーエーエスエフ ソシエタス・ヨーロピア Method for producing a spray powder comprising one or more glycine-N, N-diacetic acid derivatives and method for using the spray powder for producing a compressed mass

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