JPS58171401A - Treatment of cellulose-containing substance - Google Patents

Treatment of cellulose-containing substance

Info

Publication number
JPS58171401A
JPS58171401A JP3753782A JP3753782A JPS58171401A JP S58171401 A JPS58171401 A JP S58171401A JP 3753782 A JP3753782 A JP 3753782A JP 3753782 A JP3753782 A JP 3753782A JP S58171401 A JPS58171401 A JP S58171401A
Authority
JP
Japan
Prior art keywords
cellulose
containing substance
treatment
water
cellulase
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
Application number
JP3753782A
Other languages
Japanese (ja)
Other versions
JPS6318479B2 (en
Inventor
Yoshiyuki Takasaki
高崎 義幸
Hitoshi Yamabe
倫 山辺
Yasushi Mitsuishi
三石 安
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.)
National Institute of Advanced Industrial Science and Technology AIST
Original Assignee
Agency of Industrial Science and Technology
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 Agency of Industrial Science and Technology filed Critical Agency of Industrial Science and Technology
Priority to JP3753782A priority Critical patent/JPS58171401A/en
Publication of JPS58171401A publication Critical patent/JPS58171401A/en
Publication of JPS6318479B2 publication Critical patent/JPS6318479B2/ja
Granted legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Polysaccharides And Polysaccharide Derivatives (AREA)

Abstract

PURPOSE:A cellulose-containing substance is previously treated with polyethylene glycol, then saccharified with cellulose to effect markedly improved saccharification properties. CONSTITUTION:A cellulose-containing substance such as farm by-products is dipped in a polyethylene glycol or its derivative solution of usually 0.1-10%, preferably 0.1-1% concentration above room temperature, usually at 30-100 deg.C and 4-10pH. The mixture is filtered to recover the cellulose-containing substance and the substance is directly or, when necessary, after washed with water, dried to prepare the material to be saccharified. Then, a cellulose preparation such as from Trichoderma is made to act on the material for saccharification.

Description

【発明の詳細な説明】 本発明はセルp−ス含有物をセルラーゼに糖化するため
のセルリース含有物の前処理方法に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for pretreating a cellulase-containing material for saccharifying the cellulose-containing material into cellulase.

代替燃料としてのアルコールの生産と食糧資源Os保の
ために、セルーー・スを糖化してブドウ糖を製造しよう
とする研究が、最短、盛んに行なわれて−る。セル田−
入は天然では、リグニンやへζセ#レースと強固に結合
して存在して−るため。
In order to produce alcohol as an alternative fuel and conserve food resources, research is being actively conducted to produce glucose by saccharifying cellulose. Cell field
In nature, it exists in a strong bond with lignin and heliase.

そやま−ではセルラーゼによる分解を受けに(−0この
ため一セルラー(による分解を受けやすくするため、リ
グニンやヘミセ#−−スO除去やセルリースの結晶構造
を破壊する種々の方法が考案されて−る。たとえば、セ
ルレース含有物を、硫酸やリン酸のような酸や苛性ソー
ダのようなアルカリで処理するス法、r線で処理する方
法、ポール・ミルなどで微粉砕する方法あるーは凍結融
解法などが知られている。
In Soyama, various methods have been devised to remove lignin and hemicase O, and to destroy the crystal structure of cellulase, in order to make it more susceptible to decomposition by cellulase. For example, there are methods of treating cellulose-containing materials with acids such as sulfuric acid or phosphoric acid or alkalis such as caustic soda, methods of treating them with R-rays, and methods of pulverizing them with a pole mill. Freezing and thawing methods are known.

本発明者らは、セルロース含有物をセルラー(で糖化し
てグルコースを製造することを目的として、セルラーゼ
による糖化を促進するセルツース含有物の処理方法につ
いて檀々検討してきた結果セル胃−ス含□有物をポリエ
チレンダリコール又ハその誘導体で処理すると、セルラ
ーゼによる′糖、化性が著しく改善されることを詔めた
。本発明は、ζO知見にもとず−で1にされたものであ
る。
The present inventors have conducted extensive studies on a method for treating cellulose-containing materials that promotes saccharification by cellulase, with the aim of producing glucose by saccharifying cellulose-containing materials with cellulose. It has been stated that when organic matter is treated with polyethylene dalicol or its derivatives, the ability to convert sugar into sugar by cellulase is significantly improved.The present invention was made based on the knowledge of ζO be.

すなわち、本発明は七に勘−ス含有物をセルラーゼで糖
化するに際し、セルリース含有物をポリするものである
That is, the present invention is directed to, seventhly, polysizing the cellulose-containing material when saccharifying the cellulose-containing material with cellulase.

以下に本発明を更に具体的に説明する。The present invention will be explained in more detail below.

本発明を適用で自るセルリース含有物とは、木質又は非
木質(草木−)系の檜物体又はその派生物であって、例
えば、稲ワラ、モ之ガラ、バガスなどの農産副産物、そ
して、ナビャ、コゴンなどの雑草類、木材、パルプ、古
紙、センイ性%葉物などが挙げられ、乳中バガスなどの
草木−の物質に對しては特に有効である。これらセルリ
ース含有物は完全に脱すダ品ンヤ脱へ攬セAl田−スさ
れえ4のである必要はなく、軽度の化学的処珈や磨砕、
放射線処理、高温加熱処理、凍結融解処理など物理的処
理されたものに併用すゐと効果的であるO 本発明で−うポリエチレングリコールとは、例えば、市
販されて−るポリエチレンダリフールダOO,ポリエチ
レングリコール1ooo、プリエチレングリコール、2
000.ポリエチレンダリコールaooo、ポリエチレ
ンダリシール20000(以上−ずれも和光純薬工粱株
式金社販売)など(−0CHxCH* )  の構造を
単位とする種AltJ重今度のものである。
The cellulose-containing substances to which the present invention is applied are woody or non-woody (vegetable) cypress objects or derivatives thereof, such as agricultural by-products such as rice straw, Japanese mullet, and bagasse; Examples include weeds such as navy and cogon, wood, pulp, waste paper, and senile leafy materials, and are particularly effective against plant materials such as milk bagasse. These cellulose-containing substances do not need to be removed completely, and may be removed by mild chemical treatment, grinding, or
It is effective when used in combination with materials that have been subjected to physical treatments such as radiation treatment, high-temperature heat treatment, and freeze-thaw treatment. Polyethylene glycol 1ooo, preethylene glycol, 2
000. Polyethylene Dalycol aooo, Polyethylene Dalyseal 20000 (both sold by Wako Pure Chemical Industries, Ltd.), etc. (-0CHxCH*) are species AltJ heavy products having the structure as a unit.

ぎリエチレングリコー〃の誘導体としては、ツイーンJ
7.ツイーンダO,ツイーンdO1クイーンlO,ツイ
ーンtS(いずれもアメリカ アトラスパウダー カン
パニー製)あるいはトリトンz−tooやトリトンX−
亭01(以上いずれもアメリカ ローム アンド ハー
ス カンパニー構造)、ブリッジJj(花王アトラス株
式金社製造)など、(0CHsCH冨−)、を骨格とす
る誘導体である。
As a derivative of ethylene glycol, Tween J
7. Tween O, Tween dO1 Queen lO, Tween tS (all manufactured by Atlas Powder Company of America), or Triton Z-too or Triton X-
These are derivatives having a skeleton of (0CHsCH-), such as Tei 01 (all of the above structures are manufactured by Rohm and Haas Company of America) and Bridge Jj (manufactured by Kao Atlas Co., Ltd., Kinsha).

これら物質は、通常a/〜104、通常Q/〜l襲程度
の溶液でこれにセルリース含有物を浸漬させる。浸漬は
、室温以上の温度、通常JO−1OO℃で行な勤れゐが
、浸漬時間は浸漬温度が高−はど短縮することができる
。浸漬時OpHは高vhはど効果的であるが、通常pH
約ダ〜約10で行なわれる。
These materials are usually used in a solution of about a/~104, usually Q/~l, and the cellulose-containing material is immersed therein. The dipping can be carried out at a temperature above room temperature, usually JO-100°C, but the dipping time can be shortened if the dipping temperature is high. OpH during immersion is effective at high VH, but normal pH
It is carried out in about 10 to 10 days.

浸漬後、濾過してセルリース含有物を回収し、必要によ
や水て洗滌し、そのま−あるいは乾燥して糖化原料とす
る・ セルラーゼ酵素剤としては、例えば、トリコブ夛マ属、
アスペルギルス属、スボロトリクム属、イルペックス属
や細1、放4g111の生産するものなど種★微生物起
源のセルラー櫂が使用でき一必要によりこれらを混合し
て使用する。
After soaking, the cellulose-containing substances are collected by filtration, washed with water if necessary, and used as raw material for saccharification either as is or dried. Examples of cellulase enzyme preparations include Atricobium spp.
Cellular paddles of microbial origin can be used, such as those produced by the genus Aspergillus, Suborotrichum, and Irpex, and if necessary, these can be used in combination.

次に実施例により本発明を具体的に説明する。Next, the present invention will be specifically explained with reference to Examples.

実施例1 バガス(約12&n’)gに粉砕したもの)100w1
9を表に記載の1%ポリエチレングリコール又は界面活
性剤溶液−一に浸漬し、30℃−夜装置し之のち、ガラ
スフィルターで減UE、濾過し、次−で水で充分洗滌し
たのち乾燥した。
Example 1 Bagasse (pulverized to about 12 &n') g) 100w1
9 was immersed in the 1% polyethylene glycol or surfactant solution listed in the table, incubated overnight at 30°C, filtered through a glass filter, thoroughly washed with water, and then dried. .

このもの各SO■をQJM酢際緩勘液(pHよo>as
gLtに入れ、これに七ルラー((トリコデルマ・ビリ
デの七ルラーゼ酵素、剤(ヤクル)生化学株式会社製造
販売、セルラーゼ オノスカR−to’>iアスペルギ
ルス襦のセルラーゼ酵素剤(ナガセ生化学w造販売)の
それぞれ!11の混合酵素液lコ単位手を添加し、全量
水でコーとし。
Add each SO■ of this to QJM vinegar laxative solution (pH yo > as
gLt, and add to this seven rulers ((Trichoderma viride seven rulerase enzyme, agent (Yakuru) manufactured and sold by Seikagaku Co., Ltd., Cellulase Onosuka R-to' ) Add 1 unit of each of the 11 mixed enzyme solutions and mix with water.

℃で1日間反応させた。反応後、−過した上澄液につい
て趨元糖をソモギー・ネルラン法により、可溶性糖をフ
ェノール−硫酸法により、そしてグルツースをダルコー
スオキシダーセ法により走量表から明らかなように、ト
リトンx −t o 41四ツ トラトンX−参or、ブリッジJU、 絆幸イー+JA
1などポリオキシエチレン系の非表面活性剤を使用した
と電輪化率の著し一向上が−められた。・またぼりエチ
レングリコ−5tJooooによっても効果が認められ
た。
The reaction was allowed to take place at ℃ for 1 day. After the reaction, the filtered supernatant was extracted with triton x by the Somogyi-Nerlan method, soluble sugar by the phenol-sulfuric acid method, and glucose by the dulose oxidase method. -t o 41 Yotsu Toraton X-sanor, Bridge JU, Kizunayuki E+JA
When polyoxyethylene-based non-surfactants such as No. 1 were used, the conversion rate was significantly improved.・Effects were also observed with Matabori Ethylene Glyco-5tJoooo.

なお、セルラーゼ活性は下記の通り測定した。Note that cellulase activity was measured as follows.

QOjMfhWI緩後液(pHjO)にf#解させたa
jlcMc(カルボキシメチルセルロース)溶液aj@
tにセルテーセ酵素液を加え、蒸溜水で全量1gItと
し、50℃で反応させた。そして、この条件で1分間に
lマイクロモルのグルコースに相当する還元力を生成す
る酵素量をl単位とした。
QOjMfhWI lag solution (pHjO) was made to dissolve f#a
jlcMc (carboxymethylcellulose) solution aj@
Celltese enzyme solution was added to the solution, the total amount was made up to 1 gIt with distilled water, and the reaction was carried out at 50°C. The amount of enzyme that generates a reducing power equivalent to 1 micromole of glucose per minute under these conditions was defined as the unit of 1.

実施例コ バガス(約Qj%に粉砕したもの)100mI9を水コ
ーに浸漬させたもの、あるーは/%、5%、10GO)
リドンX−ダox溶液粂コーに浸aさせたもOを室温(
Jj”C)で−夜放置後、ガラスフィルターで減EE濾
過し、次−で水で充分洗滌し、乾燥した。
Example Kobagasu (pulverized to about Qj%) 100ml I9 soaked in water, 1%, 5%, 10GO)
Lydon
After being left overnight in Jj''C), it was filtered with a reduced EE filter using a glass filter, and then thoroughly washed with water and dried.

こOもO各j□s9について、実施例1に記載の方法に
より、事j℃で一日間糖化した・そして反応後、−過し
た上澄液につ−て、還元糖、可溶性糖とグルコースを定
量した。得られた結果を第2表に示す。
Each sample was saccharified at ℃ for one day by the method described in Example 1. After the reaction, the filtered supernatant was treated with reducing sugars, soluble sugars, and glucose. was quantified. The results obtained are shown in Table 2.

表#1ら明らかなように、バガスをあらかじめ、シリ)
kx−参〇jで処理してお−たものを使用す為と、本処
理のものに比、べ糖の収量は約2〜3割増加した。そし
て、トリトンX−参Ojの濃度ホ、/襲よりも!≦〜l
O襲の方が効果的であった・ 実施例J 実施例2にお−て、トリトンx−#osの代り#IJ表
に示す。
As is clear from Table #1, bagasse is prepared in advance)
The yield of be sugar was increased by about 20 to 30% when compared with the product treated with kx-san〇j and the product treated with this process. And the concentration of Triton X-san Oj is better than / attack! ≦〜l
O attack was more effective.Example J In Example 2, #IJ instead of Triton x-#os is shown in the table.

第  J  表 表から明らかなよう輪、バガスをポリエチレンダリ=−
ルで処理することにより還元糖の生成量は約l参囁、可
溶性糖の生成量は約7襲増加した。
It is clear from Table J that the ring and bagasse are made of polyethylene = -
The amount of reducing sugars produced increased by about 1.3 times, and the amount of soluble sugars produced increased by about 7 times.

実施例ダ バガス(約Ojtに粉砕し念もの)100■をl襲ト9
)ンX−参〇j コーに浸漬したものを30℃、参〇℃
、30℃、70℃では各7日間処理し、100℃と12
0℃のものは各io分間加熱処理した。処理後、−過し
、水で洗滌後、乾燥した。なお、バガスtoow9を水
2−に、30℃i1日間浸漬後、−過、水で洗滌、乾燥
したもO:対照とした。
Example: 100 pieces of dabbagas (pulverized to about 0.000 kg) as a precautionary measure.9
) N
, 30°C and 70°C for 7 days each, and 100°C and 12°C.
Those at 0°C were heat-treated for each IO minute. After treatment, it was filtered, washed with water, and dried. In addition, bagasse tow 9 was immersed in water at 30° C. for 1 day, filtered, washed with water, and dried, which was used as a control.

こ0%0各jtOI+9’kQ2M酢酸緩極液(pHふ
O)ユj−に入れ、これに実施例!で使用したと同じゃ
素剤を添加し、全量を水でj−として、参5゛Cで2日
間反応させた。反応後、−過した上澄液につ−て、還元
糖、可溶性糖、グルコースを定量した。得られたIal
Aを第参表に示す。
This 0% 0 each jtOI + 9'kQ2M acetic acid mild polar solution (pHfO) was added to the Example! The same base material as used in 1 was added, the whole amount was diluted with water, and the mixture was reacted at 5°C for 2 days. After the reaction, reducing sugars, soluble sugars, and glucose were determined in the filtered supernatant. The obtained Ial
A is shown in the table below.

Claims (1)

【特許請求の範囲】[Claims] セルロース含有物をセルラーゼで糖化するに際し、セル
ロース含有物をあらかじめポリエチレンとV特徴とする
セルレース含有物の処理キ法。
A method for treating a cellulose-containing material, in which the cellulose-containing material is preliminarily characterized by polyethylene and V when the cellulose-containing material is saccharified with cellulase.
JP3753782A 1982-03-09 1982-03-09 Treatment of cellulose-containing substance Granted JPS58171401A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3753782A JPS58171401A (en) 1982-03-09 1982-03-09 Treatment of cellulose-containing substance

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3753782A JPS58171401A (en) 1982-03-09 1982-03-09 Treatment of cellulose-containing substance

Publications (2)

Publication Number Publication Date
JPS58171401A true JPS58171401A (en) 1983-10-08
JPS6318479B2 JPS6318479B2 (en) 1988-04-19

Family

ID=12500270

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3753782A Granted JPS58171401A (en) 1982-03-09 1982-03-09 Treatment of cellulose-containing substance

Country Status (1)

Country Link
JP (1) JPS58171401A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006519606A (en) * 2003-03-07 2006-08-31 アセニクス コーポレイション Method for promoting the activity of lignocellulolytic enzymes
JP2013530826A (en) * 2010-06-08 2013-08-01 バックマン・ラボラトリーズ・インターナショナル・インコーポレーテッド Method for decomposing sludge from pulp and paper manufacture

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2011109965A (en) * 2009-11-27 2011-06-09 Tokai Senko Kk Saccharification pretreatment method for cellulose-containing fiber material, and method for saccharifying the cellulose-containing fiber material, having the saccharification pretreatment method
JP5850608B2 (en) * 2010-10-18 2016-02-03 株式会社ダスキン Bioethanol production method
JP2013215187A (en) * 2012-03-15 2013-10-24 Kao Corp Method for producing saccharide

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS51136842A (en) * 1975-05-22 1976-11-26 Bio Research Center Co Method of enzymatic inversion of cellulose

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS51136842A (en) * 1975-05-22 1976-11-26 Bio Research Center Co Method of enzymatic inversion of cellulose

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006519606A (en) * 2003-03-07 2006-08-31 アセニクス コーポレイション Method for promoting the activity of lignocellulolytic enzymes
JP2013530826A (en) * 2010-06-08 2013-08-01 バックマン・ラボラトリーズ・インターナショナル・インコーポレーテッド Method for decomposing sludge from pulp and paper manufacture

Also Published As

Publication number Publication date
JPS6318479B2 (en) 1988-04-19

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