JP2757106B2 - Microorganism for pulp bleaching and pulp bleaching method using the same - Google Patents

Microorganism for pulp bleaching and pulp bleaching method using the same

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Publication number
JP2757106B2
JP2757106B2 JP16612093A JP16612093A JP2757106B2 JP 2757106 B2 JP2757106 B2 JP 2757106B2 JP 16612093 A JP16612093 A JP 16612093A JP 16612093 A JP16612093 A JP 16612093A JP 2757106 B2 JP2757106 B2 JP 2757106B2
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JP
Japan
Prior art keywords
pulp
bleaching
pulp bleaching
microorganism
lignin
Prior art date
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Expired - Fee Related
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JP16612093A
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Japanese (ja)
Other versions
JPH06343460A (en
Inventor
令治 金子
武志 飯森
誠 町田
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Nippon Seishi KK
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Nippon Seishi KK
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  • Paper (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)

Description

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

【0001】[0001]

【産業上の利用分野】本発明は、パルプ漂白性能に優れ
た新規微生物及びその微生物を用いたパルプの漂白方法
に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a novel microorganism having excellent pulp bleaching performance and a method for bleaching pulp using the microorganism.

【0002】[0002]

【従来技術】従来、パルプの漂白には通常、塩素や二酸
化塩素等の塩素系薬品が使用されているが、これらの塩
素系薬品を用いて漂白した場合には極めて毒性の強い物
質であるダイオキシンを副成することが近年明らかにな
り、その使用量の削減が求められている。また、これら
の塩素系薬品に代わる漂白薬品として、いくつかの方法
が考案されているが、微生物あるいは酵素等によりパル
プの漂白を行うバイオブリーチング法も、それらの中で
有力な方法の一つとされている。
2. Description of the Related Art Conventionally, chlorinated chemicals such as chlorine and chlorine dioxide are usually used for bleaching pulp. However, dioxin, which is an extremely toxic substance, is bleached with these chlorinated chemicals. In recent years, it has become clear that by-products are produced, and there is a demand for a reduction in the amount used. In addition, several methods have been devised as bleaching chemicals to replace these chlorine-based chemicals, but biobleaching, in which pulp is bleached by microorganisms or enzymes, is one of the most effective methods among them. Have been.

【0003】バイオブリーチング法としては、特にリグ
ニンを分解する能力を有する白色腐朽菌をパルプ漂白に
用いる方法が検討されており、検討された白色腐朽菌の
具体例としては、例えば、カワラタケ(Coriolu
s versicolor)、カイガラタケ(Lenz
ites betuluna)、ヒラタケ(Pleur
otus ostreatus)、ファネロケーテ・ク
リソスポリウム(Phanerochaete chr
ysosporium)等が挙げられる。しかしなが
ら、上記のような菌では、そのリグニン分解活性が弱い
ため、バイオブリーチングに用いるには不十分であっ
た。
[0003] As a biobleaching method, a method of using, in particular, white rot fungi having the ability to degrade lignin for pulp bleaching has been studied. Specific examples of the white rot fungi that have been studied include, for example, Coriolus
versicolor, Kaitake mushroom (Lenz)
items betuluna, oyster mushroom (Pleur)
otus ostreatus, Fanelocate chrysosporium ( Phanerochaete chr)
yssoporium). However, the above-mentioned bacteria have insufficient lignin-decomposing activity, so that they were insufficient for use in biobleaching.

【0004】また、例えば特開平3−269188号公
報に示されるように、未漂白パルプを白色腐朽菌で処理
して漂白する場合の最適温度は28℃程度とされている
が、パルプの漂白工程を考慮すれば、さらに高い温度で
処理することが漂白時間短縮の点から望ましい。従っ
て、28℃程度で行う従来のパルプ漂白を目的として検
討されてきた上述の菌類は、パルプの工業的製造におけ
る漂白方法に用いるためには不十分であり、より高温条
件であってもリグニン分解活性が高く、白色度を大きく
向上させることができるような菌が求められていた。
Further, as shown in, for example, JP-A-3-269188, the optimum temperature for bleaching unbleached pulp by treating it with white rot fungi is about 28 ° C. In view of the above, processing at a higher temperature is desirable from the viewpoint of shortening the bleaching time. Therefore, the above-mentioned fungi, which have been studied for the purpose of conventional pulp bleaching at about 28 ° C., are insufficient for use in the bleaching method in industrial pulp production, and degrade lignin even under higher temperature conditions. Bacteria that have high activity and can greatly improve whiteness have been demanded.

【0005】そこで本発明者らは、このようなパルプ漂
白微生物を自然界から分離スクリーニングする方法につ
いて検討を行い、新しい菌の分離方法及びスクリーニン
グ方法を開発(特願平5−85731等)すると共に、
これらの方法を用いてパルプ漂白活性の高い菌の探索を
行った結果、パルプの白色度を大きく向上させることが
できるのみならず、従来の微生物に比べ、高温でその活
性を示す新規微生物SKB−185株の分離に成功し、
本発明を完成させた。
Accordingly, the present inventors have studied methods for separating and screening such pulp bleached microorganisms from nature, and have developed new methods for separating and screening bacteria (Japanese Patent Application No. 5-85731).
As a result of searching for a bacterium having a high pulp bleaching activity using these methods, not only can the pulp whiteness be significantly improved, but also a new microorganism SKB- which exhibits its activity at a higher temperature than conventional microorganisms. Successful isolation of 185 strains,
The present invention has been completed.

【0006】[0006]

【発明が解決しようとする課題】従って本発明の第1の
目的は、高温において優れたパルプ漂白性能を有する新
規な微生物を提供することにある。本発明の第2の目的
は、塩素系薬品を用いることのない、工業的なパルプの
漂白方法を提供することにある。
Accordingly, it is a first object of the present invention to provide a novel microorganism having excellent pulp bleaching performance at high temperatures. A second object of the present invention is to provide an industrial pulp bleaching method without using a chlorine-based chemical.

【0007】[0007]

【課題を解決するための手段】本発明の上記の諸目的
は、パルプ漂白性能に優れた微生物SKB−185株及
びそれを用いたパルプの漂白方法によって達成された。
以下に本発明の、新規な微生物SKB−185株の菌学
的性質を示す。 (1)培地における生育状態
The above objects of the present invention have been attained by a microorganism SKB-185 strain excellent in pulp bleaching performance and a pulp bleaching method using the same.
The bacteriological properties of the novel microorganism SKB-185 of the present invention will be described below. (1) Growth state in medium

【0008】[0008]

【表1】 [Table 1]

【0009】(2) 生理、生態学的性質 生育のpH範囲:pH3〜9付近で生育し、pH2以下
及び10以上では生育しない。生育の最適pHは4〜7
付近である(ポテト煎汁・デキスト・ロース寒天培地、
30℃、4日間培養)。 生育の温度範囲:24〜40℃付近で生育し45℃以上
では生育しない(ポテト煎汁・デキストロース寒天培
地、pH5.6 、4日間培養)。 フェノールオキシダーゼ反応:陽性を示す(30℃、3
日間培養)。 菌叢の特徴:白色でフェルト状である(ポテト煎汁・デ
キストロース寒天培地、30℃、pH5.6 、4日間培
養)。
(2) Physiological and ecological properties Growth pH range: Growing around pH 3-9, not growing below pH 2 and above 10. The optimal pH for growth is 4-7
Around (potato decoction, dext, loin agar,
(Culture at 30 ° C for 4 days). Temperature range for growth: grows around 24-40 ° C and does not grow above 45 ° C (potato decoction / dextrose agar medium, pH 5.6, cultured for 4 days). Phenol oxidase reaction: positive (30 ° C, 3
Days culture). Characteristics of the flora: white and felt-like (potato decoction / dextrose agar medium, 30 ° C., pH 5.6, cultured for 4 days).

【0010】これらの生理的、生態的性質及び各培地に
おける生育状態等の菌学的性質を詳細に検討したが、既
知の菌と同定するには至らなかった。しかしながら、本
菌は後記する実施例から明らかなように、リグニン分解
菌として従来から知られている白色腐朽菌よりも、漂白
活性において優れており、その活性の差は、特に高温に
おいて顕著である。
The physiological and ecological properties and the mycological properties such as the growth state in each medium were examined in detail, but could not be identified with known bacteria. However, as is clear from the examples described later, the present bacterium is superior in bleaching activity to white rot fungi conventionally known as lignin-degrading bacteria, and the difference in the activity is particularly remarkable at high temperatures. .

【0011】この様に優れた漂白活性を有する微生物は
従来において知られていないことから、本菌株を新菌株
と認定してSKB−185株と命名し、工業技術院生命
工学工業技術研究所特許微生物寄託センターに寄託した
(寄託番号:FERM−13530)。本菌株の分類学
上の正確な位置については、なお不明な点が幾つか残っ
ているため正確な同定が現時点においては困難であり、
今後の研究を待たなければならない。
Since microorganisms having such excellent bleaching activity have not been known so far, the present strain was identified as a new strain and named SKB-185 strain. Deposited at the Microbial Depositary Center (Deposit No .: FERM-13530). The exact location of this strain in the taxonomic system is still difficult to identify at this time due to some unclear points.
We have to wait for future research.

【0012】以下、本発明に使用するSKB−185株
の分離方法について説明する。SKB−185株は、リ
グニンあるいはリグニンが残存するパルプを含有する培
地に、腐朽材や土壌から分離した微生物源を接種して培
養し、培地の脱色帯部分から分離・選択される。ここで
リグニンとしては、クラフトリグニンやサルファイトリ
グニン等が、リグニン残存パルプとしてはクラフトパル
プのような化学パルプを用いることができる。
Hereinafter, a method for isolating the SKB-185 strain used in the present invention will be described. The SKB-185 strain is cultured by inoculating a medium containing lignin or a pulp in which lignin remains, with a microorganism source isolated from decay material or soil, and separating and selecting from a decolorized zone portion of the medium. Here, kraft lignin, sulfite lignin and the like can be used as lignin, and chemical pulp such as kraft pulp can be used as lignin residual pulp.

【0013】また、培地としては、パルプに培養液を添
加しただけの液体培地や、パルプを寒天等で固めた固体
培地等が挙げられる。なお、上記した分離・選択方法に
おける培地の調製、リグニン分解菌の選択は、従来公知
の方法に基づいて適宜行えば良い。上記の分離・選択方
法は、従来のフェノールオキシダーゼの検出による方法
に比較して、簡便かつ高精度であるのみならず、腐朽材
や土壌から分離した微生物源から、リグニン分解菌の分
離・選択が可能である点に特徴がある。
Examples of the medium include a liquid medium obtained by simply adding a culture solution to pulp and a solid medium obtained by solidifying pulp with agar or the like. The preparation of the culture medium and the selection of lignin-degrading bacteria in the above-mentioned separation / selection method may be appropriately performed based on a conventionally known method. The above separation / selection method is not only simpler and more accurate than the conventional method based on phenol oxidase detection, but also separates / selects lignin-degrading bacteria from microorganism sources separated from decay materials and soil. The feature is that it is possible.

【0014】次に、本発明の新規な微生物SKB−18
5株を用いたパルプの漂白方法について説明する。本菌
株を用いたパルプの漂白方法は、基本的には、菌をパル
プに接種して所定期間培養するものであり、その条件等
は特に限定されない。本発明において使用するパルプと
しては、化学パルプ、機械パルプ等その種類は問わな
い。
Next, the novel microorganism SKB-18 of the present invention is described.
The pulp bleaching method using five strains will be described. The pulp bleaching method using this strain is basically a method of inoculating pulp with a fungus and culturing it for a predetermined period, and the conditions and the like are not particularly limited. The pulp used in the present invention may be of any type such as chemical pulp and mechanical pulp.

【0015】パルプの形状は、菌が生育し漂白され易い
形状である限りいずれの形状であっても良い。また培養
時におけるパルプ濃度は、20ないし60%の範囲であ
ることが、通気性・菌の生育等の観点から好ましい。2
0%未満では、菌の生育は認められるがパルプの漂白効
率が低下し、他方60%以上では菌の生育が悪くなると
共に、パルプの漂白能力も低下する。
[0015] The shape of the pulp may be any shape as long as the bacteria grow and are easily bleached. Further, the pulp concentration during the culturing is preferably in the range of 20 to 60% from the viewpoints of air permeability and growth of bacteria. 2
If it is less than 0%, the growth of bacteria is observed, but the bleaching efficiency of the pulp is reduced. On the other hand, if it is more than 60%, the growth of the bacteria is deteriorated and the bleaching ability of the pulp is reduced.

【0016】培養時のpH及び温度は他の条件により相
違し、前述した本菌の生理学的性質に記載の範囲内であ
れば特に限定されないが、通常は、 pHが4〜7の範囲
内であり、培養温度は25℃ないし40℃の範囲内であ
ることが好ましく、特に37℃付近で良好な結果を得る
ことができる。更に、パルプの漂白に要する時間短縮の
ため、必要に応じて培養時に各種の栄養源を添加しても
良い。
The pH and temperature during the cultivation are different depending on other conditions and are not particularly limited as long as they are within the range described in the physiological properties of the present bacterium. Usually, the pH and the temperature are within the range of 4 to 7. Yes, the culture temperature is preferably in the range of 25 ° C. to 40 ° C., and particularly good results can be obtained at around 37 ° C. Further, various nutrients may be added at the time of culturing, if necessary, in order to shorten the time required for bleaching the pulp.

【0017】以上の如く、本菌を従来法と同様に用いて
パルプの漂白処理をすれば良く、格別の配慮は何も必要
とされない点も、本発明の優れた特徴の一つである。ま
た、本菌はその漂白性能から明らかな如く、高いリグニ
ン分解活性をも有しているので、本菌をパルプ漂白以外
の脱リグニンを必要とする各種の木材利用工業に用いる
こともできる。その場合の処理方法も、パルプ漂白の場
合と同様に、本菌を、目的とする木質原料を含有する培
地に接種して所定期間培養すればよい。
As described above, the pulp may be bleached using the fungus in the same manner as in the conventional method, and no special consideration is required. In addition, as apparent from its bleaching performance, the present bacterium also has a high lignin-decomposing activity, so that the bacterium can be used in various wood utilization industries requiring delignification other than pulp bleaching. In this case, as in the case of pulp bleaching, the treatment may be carried out by inoculating the present bacterium into a medium containing the desired woody material and culturing it for a predetermined period.

【0018】[0018]

【発明の効果】本発明の微生物は、従来の菌よりも特に
高温領域で格段に優れたパルプ漂白性能を持つため、紙
パルプ製造工程において塩素系薬品を使用しないパルプ
の漂白方法として、工業的に利用することが可能であ
る。更に、パルプ漂白以外の、例えばパルプ製造工程や
パルプ排水処理工程、木材糖化工程などへの応用も可能
である。
Industrial Applicability The microorganism of the present invention has much better pulp bleaching performance especially in a high temperature region than conventional microorganisms. It is possible to use it. Further, applications other than pulp bleaching, such as pulp manufacturing processes, pulp wastewater treatment processes, and wood saccharification processes, are also possible.

【0019】[0019]

【実施例】以下、実施例によって本発明を更に詳細に説
明するが、本発明はこれによって限定されるものではな
い。
EXAMPLES The present invention will be described in more detail with reference to the following Examples, but it should not be construed that the present invention is limited thereto.

【0020】実施例1. ポテト煎汁0.4%グルコース2%を含んだポテトデキ
ストロースブロース液体培地(DIFCO社製)でSK
B−185株を1週間静置培養し、形成された菌体マッ
トをワーリングブレンダーで粉砕した後、120℃で1
5分間加熱殺菌した酸素漂白パルプ(山陽国策パルプ
製;OKP)に、最終的なパルプ濃度が20%になるよ
うに菌体懸濁液を加え、30℃で7日間放置した。その
後500mlの水を加え、ミキサーで解繊してから手抄
シートを作製した。シートの白色度をハンター白色度計
を用いて測定し(JIS P−8123)、同時にカッ
パー価(JISP−8211−1976)も測定した。
白色度の上昇ポイントは表2に示した通りである。
Embodiment 1 SK in potato dextrose broth liquid medium (manufactured by DIFCO) containing 0.4% potato decoction and 2% glucose
The B-185 strain was allowed to stand and cultured for one week, and the formed bacterial cell mat was pulverized with a Waring blender.
A bacterial cell suspension was added to oxygen bleached pulp (OKP, manufactured by Sanyo Kokusaku Pulp) sterilized by heating for 5 minutes so that the final pulp concentration was 20%, and the mixture was allowed to stand at 30 ° C for 7 days. Thereafter, 500 ml of water was added thereto, and the mixture was defibrated by a mixer to prepare a hand-made sheet. The whiteness of the sheet was measured using a Hunter whiteness meter (JIS P-8123), and at the same time, the kappa number (JISP-8211-1976) was also measured.
The points of increase in whiteness are as shown in Table 2.

【0021】[0021]

【表2】 [Table 2]

【0022】比較例1及び2.実施例1で使用したSK
B185株の代わりに、代表的なリグニン分解菌である
カワラタケ(Coriolus versicolor) (比較例1)及びフ
ァネロケ−テ・クリソスポリウム(Phanerochaete chry
sosporium )(比較例2)を夫々用いた他は、実施例1
と全く同様の操作を行った。白色度の白色度の上昇ポイ
ントは表2に示した通りである。
Comparative Examples 1 and 2. SK used in Example 1
Instead of the B185 strain, representative lignin-degrading bacteria, Coriolus versicolor (Comparative Example 1) and Phanerochaete chrysosporium (Phanerochaete chry)
sosporium) (Comparative Example 2), respectively.
The same operation as described above was performed. The points of increase in whiteness are shown in Table 2.

【0023】実施例2.ポテト煎汁0.4%グルコース
2%を含んだポテトデキストロースブロース液体培地
(DIFCO社製)でSKB−185株を1週間静置培
養し、形成された菌体マットをワーリングブレンダーで
粉砕した後、120℃で15分間加熱殺菌した酸素漂白
パルプ(山陽国策パルプ製;OKP)に、最終的なパル
プ濃度が20%になるように菌体懸濁液を加え、37℃
で7日間放置した。その後500mlの水を加え、ミキ
サーで解繊してから手抄シートを作製した。シートの白
色度及びカッパー価を実施例1と同様の方法で測定し
た。白色度の白色度の上昇ポイントは表2に示した通り
である。
Embodiment 2 FIG. The SKB-185 strain was statically cultured for one week in a potato dextrose broth liquid medium (manufactured by DIFCO) containing 0.4% potato decoction and 2% glucose, and the resulting cell mat was pulverized with a Waring blender. A bacterial cell suspension was added to oxygen bleached pulp (OKP, manufactured by Sanyo Kokusaku Pulp) sterilized by heating at 120 ° C. for 15 minutes so that the final pulp concentration was 20%.
For 7 days. Thereafter, 500 ml of water was added thereto, and the mixture was defibrated by a mixer to prepare a hand-made sheet. The whiteness and kappa number of the sheet were measured in the same manner as in Example 1. The points of increase in whiteness are shown in Table 2.

【0024】比較例3及び4. 実施例2で使用したSKB−185株の代わりに、代表
的なリグニン分解菌であるカワラタケ(Coriolu
s versicolor)(比較例3)及びファネロ
ケーテ・クリソスポリウム(Phanerochaet
e chrysosporium)(比較例4)を夫々
用いた他は、実施例2と全く同様の操作を行った。白色
度の上昇ポイントは表2に示した通りである。上記表
の結果から明らかなように、本発明の新規な微生物は、
その漂白活性が従来の菌よりも著しく優れており、白色
度の大幅な向上を実現できることがわかる。
Comparative Examples 3 and 4. Instead of the SKB-185 strain used in Example 2, a typical lignin-degrading bacterium, Kawatake (Coriolu) was used.
s versicolor) (Comparative Example 3) and Fanelocate chrysosporium (Phanerochaet)
e chrysosporium) (Comparative Example 4), except that the same operation as in Example 2 was performed. The points of increase in whiteness are as shown in Table 2. Table 2 above
As is clear from the results, the novel microorganism of the present invention
The bleaching activity is remarkably superior to the conventional bacteria, and it can be seen that the whiteness can be greatly improved.

───────────────────────────────────────────────────── フロントページの続き (58)調査した分野(Int.Cl.6,DB名) C12N 1/14 - 1/15 D21C 9/10 C02F 3/34 BIOSIS(DIALOG) WPI(DIALOG)────────────────────────────────────────────────── ─── Continued on the front page (58) Field surveyed (Int. Cl. 6 , DB name) C12N 1/14-1/15 D21C 9/10 C02F 3/34 BIOSIS (DIALOG) WPI (DIALOG)

Claims (2)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】パルプ漂白性能に優れた微生物SKB−1
85株。
A microorganism SKB-1 having excellent pulp bleaching performance.
85 shares.
【請求項2】パルプ漂白性能に優れた微生物SKB−1
85株をパルプに接種培養することを特徴とするパルプ
の漂白方法。
2. A microorganism SKB-1 having excellent pulp bleaching performance.
A pulp bleaching method comprising inoculating and cultivating 85 strains of pulp.
JP16612093A 1993-06-11 1993-06-11 Microorganism for pulp bleaching and pulp bleaching method using the same Expired - Fee Related JP2757106B2 (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0726485A (en) * 1993-07-09 1995-01-27 Nippon Paper Ind Co Ltd Method for bleaching pulp

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0726485A (en) * 1993-07-09 1995-01-27 Nippon Paper Ind Co Ltd Method for bleaching pulp

Also Published As

Publication number Publication date
JPH06343460A (en) 1994-12-20

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