JPH06191977A - Method for high-speed composting of organic material - Google Patents

Method for high-speed composting of organic material

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Publication number
JPH06191977A
JPH06191977A JP4322578A JP32257892A JPH06191977A JP H06191977 A JPH06191977 A JP H06191977A JP 4322578 A JP4322578 A JP 4322578A JP 32257892 A JP32257892 A JP 32257892A JP H06191977 A JPH06191977 A JP H06191977A
Authority
JP
Japan
Prior art keywords
strain
thermophilic
culture
organic material
compost
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
JP4322578A
Other languages
Japanese (ja)
Other versions
JPH0742184B2 (en
Inventor
Hide Kume
秀 久米
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.)
NAKAMURA SANGYO KK
Original Assignee
NAKAMURA SANGYO KK
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 NAKAMURA SANGYO KK filed Critical NAKAMURA SANGYO KK
Priority to JP4322578A priority Critical patent/JPH0742184B2/en
Publication of JPH06191977A publication Critical patent/JPH06191977A/en
Publication of JPH0742184B2 publication Critical patent/JPH0742184B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Classifications

    • 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
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A40/00Adaptation technologies in agriculture, forestry, livestock or agroalimentary production
    • Y02A40/10Adaptation technologies in agriculture, forestry, livestock or agroalimentary production in agriculture
    • Y02A40/20Fertilizers of biological origin, e.g. guano or fertilizers made from animal corpses

Abstract

PURPOSE:To provide a method for high-speed conversion of an organic material such as a plant or an animal corpse into a compost and a manure in which the utilization and treatment of the organic substance can be enhanced. CONSTITUTION:A mixed culture obtained by subjecting thermophilic cellulolytic microorganisms Clostridium thermocellum biovar. SK522 (FERM P-3459) and Thermus aquaticus biovar. SK542 (FERM P-3382) to symbiotic mixed culture at >=60 deg.C under a thermophilic environment or a fermentation decomposing agent containing the mixed culture as an effective principal ingredient is applied to an organic material to provide a compost and a manure.

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、有用な菌を使用して、
有機資材、特にモミガラ・藁桿類・種皮やソバ殻・落葉
・樹皮・山野草・廃材・廃ホダ木・廃菌床・余剰汚泥等
の難分解性有機資材を高速に堆・厩肥、コンポストにす
る方法に関する。
BACKGROUND OF THE INVENTION The present invention uses a useful bacterium to
Organic materials, especially hard-to-decompose organic materials such as rice husks, straw rods, seed coats, buckwheat husks, deciduous leaves, bark, wild grass, waste wood, waste wood, waste fungi beds, excess sludge, etc., at high speed for composting, manure and composting. On how to do.

【0002】[0002]

【従来の技術】従来、植物・動物遺体の有機物は、古来
から長時間嫌気的条件の下で微生物の働きによって分解
され、堆・厩肥として使用されてきた。しかしながら、
古来からの嫌気的条件による堆・厩肥化は長い日数を要
し、迅速な処理、堆・厩肥の迅速且つ大量の生産が行え
ず、有機資材の短期処分と有効利用が図れなかった。
2. Description of the Related Art Conventionally, organic substances of plant and animal remains have been decomposed by the action of microorganisms under anaerobic conditions for a long time and used as compost or manure. However,
Since ancient times, it took a long time to convert compost / manure due to anaerobic conditions, rapid treatment, rapid and mass production of compost / manure, and short-term disposal and effective use of organic materials could not be achieved.

【0003】[0003]

【発明が解決しようとする課題】本発明が解決しようと
する課題は、植物・動物遺体の有機資材を堆・厩肥に高
速処理し、これら有機物の活用と処理を高めることがで
きる有機資材の高速堆・厩肥化を提供することにある。
The problem to be solved by the present invention is to process organic materials of plant / animal corpses at high speed into compost / manure, and to improve the utilization and processing of these organic materials. The purpose is to provide manure and manure.

【0004】[0004]

【課題を解決するための手段】かかる課題を解決した本
発明の要旨は、 1) 下記1記載の好熱性繊維素分解菌クロストリジュ
ウム・サーモセルムSK522(Clostriduim thermoce
llum biovar.SK522,微工研条寄第3459号)
と、下記2記載のサーマス・アクアティクスSK542
(Thermus aquaticus biovar SK542,微工研条寄
第3382号)とを60℃以上の好熱性環境下で共生的
混合培養させた混合培養物又はこれを有効主成分とする
有機資材の発酵分解剤を、有機資材に施用して堆・厩肥
にすることを特徴とする有機資材の高速堆肥化法 記1 リグニン可溶化能を有し、生育適温が65〜72℃で、
40〜80℃の温度範囲で生育し、繊維素を旺盛に発酵
する好熱性繊維素分解菌クロストリジュウム・サーモセ
ルムSK522(Clostriduim thermocellum biovar.S
K522,微工研条寄第3459号) 記2 絶対好気性、生育適温が72〜76℃で、40〜82℃
の温度範囲で通常濃度の培地に生育し、作用適温75〜
85℃、作用水素イオン濃度pH=4.0〜11.3の
高温性広域作用水素イオン濃度活性のタンパク質分解酵
素とカロチノイド系黄色色素を産生するサーマス・アク
アティクスSK542(Thermus aquaticus biovar S
K542,微工研条寄第3382号) 2) 有機資材がモミガラ・落葉・廃材・余剰汚泥等の
難分解性有機資材である1記載の有機資材の高速堆肥化
法にある。
[Means for Solving the Problems] The gist of the present invention which has solved the above problems is as follows: 1) Clostriduim thermocem SK522 (Clostriduim thermocem)
llum biovar.SK522, Micro Engineering Research Center No. 3459)
And Thermus Aquatics SK542 described in 2 below
(Thermus aquaticus biovar SK542, Mikokenjojo 3382 No.) and a mixed culture obtained by symbiotic mixed culture in a thermophilic environment of 60 ° C. or higher, or a fermentative decomposing agent for an organic material containing the mixed culture as an active ingredient. , A high-speed composting method for organic materials, characterized by applying it to organic materials to form compost / manure Note 1 It has a lignin-solubilizing ability, and a suitable growth temperature is 65 to 72 ° C.
A thermophilic fibrin-degrading bacterium that grows in the temperature range of 40 to 80 ° C. and ferments actively, Clostriduim thermocellum biovar.S
K522, Mikori Kenjo No. 3459) Note 2 Absolute aerobic, optimum growth temperature is 72 to 76 ° C, 40 to 82 ° C.
It grows in a medium of normal concentration in the temperature range of
Thermos aquaticus SK542 (Thermus aquaticus biovar S) which produces a proteolytic enzyme and a carotenoid-type yellow pigment with a thermophilic broad-range action hydrogen ion concentration of 85 ° C and a action hydrogen ion concentration pH = 4.0 to 11.3
K542, Mikori Kenjo No. 3382) 2) The high-speed composting method of organic materials according to 1, wherein the organic materials are persistent organic materials such as chaff, deciduous leaves, waste materials and excess sludge.

【0005】尚、本発明に使用する好熱性繊維素分解菌
クロストリジュウム・サーモセルムSK522(Clostr
iduim thermocellum biovar.SK522,微工研条寄第
3459号)とサーマス・アクアティクスSK542
(Thermus aquaticus biovarSK542,微工研条寄第
3382号)は、いずれも本発明者らの発見にかかるも
ので、以下それぞれ単にSK522菌株及びSK542
菌株と称する。
The thermophilic fibrinolytic bacterium used in the present invention, Clostridium thermocellum SK522 (Clostr
iduim thermocellum biovar. SK522, Micro Engineering Kenjoyori No. 3459) and Thermus Aquatics SK542
(Thermus aquaticus biovar SK542, Microtechnical Research Institute No. 3382) are all related to the discovery of the present inventors. In the following, they are simply referred to as SK522 strain and SK542, respectively.
It is called a strain.

【0006】[0006]

【作用】本発明では、新菌株のSK522はリグニンを
可溶化し、植物遺体に多く含まれる繊維素を分解し、又
新菌株のSK542はタンパク質の分解酵素を生成して
タンパク質を分解する。しかも、両新菌株は互いに共生
的関係にあって、互いに両者の活動を高めて有機資材を
強力に発酵して、短期的に堆・厩肥化してしまう。
In the present invention, the new strain SK522 solubilizes lignin and decomposes fibrin contained in a large amount of plant remains, and the new strain SK542 produces a protein-degrading enzyme to decompose the protein. Moreover, the two new strains have a symbiotic relationship with each other, which enhances the activities of each other and strongly ferments the organic material, resulting in short-term composting and manure.

【0007】以下、各新菌株の機能について説明する。
SK522菌株は旺盛なる繊維素分解力と弱又は微弱な
るリグニン可溶化能を有する。又、SK542菌株は絶
対好気性中等度好熱性細菌で、高温性広域作用水素イオ
ン濃度活性の強力なタンパク質分解酵素とカロチノイド
系黄色色素を産生する。 SK542菌株の産生するタンパク質分解酵素の理化学
的性質
The function of each new strain will be described below.
The SK522 strain has a strong fibrin-decomposing ability and a weak or weak lignin-solubilizing ability. The SK542 strain is an absolutely aerobic and moderately thermophilic bacterium, and produces a strong proteolytic enzyme having a thermophilic broad-acting hydrogen ion concentration activity and a carotenoid yellow pigment. Physicochemical properties of proteolytic enzyme produced by SK542 strain

【表4】 以上のような理化学的性質をもつ新規酵素と思われるプ
ロテアーゼAとプロテアーゼBの他に、不安定な数種の
酵素の複合体である。 SK542菌株の産生する色素の理化学的性質 本菌の産生する黄色色素は、カロチノイド系黄色色素
で、水には不溶、次のような溶剤に可溶である。メタ
ノール,エタノール,石油エーテル,ベンジン,
アセトン,クロロホルム,アセン+メタノール
(7:3)及びアセトン+エタノール(1:1)混液。
また、赤外線吸光度最大値450nm。その他430,
435,470nmに小さなピークがある。
[Table 4] It is a complex of several unstable enzymes in addition to protease A and protease B, which are considered to be novel enzymes having the above physicochemical properties. Physicochemical Properties of Pigment Produced by SK542 Strain The yellow pigment produced by this bacterium is a carotenoid yellow pigment, which is insoluble in water and soluble in the following solvents. Methanol, ethanol, petroleum ether, benzine,
A mixture of acetone, chloroform, acene + methanol (7: 3) and acetone + ethanol (1: 1).
Also, the infrared absorption maximum value is 450 nm. Other 430,
There is a small peak at 435,470 nm.

【0008】そして、この二つの新菌株の好熱的な共生
的混合培養は、各菌株の機能の相加的作用ではなく、相
互作用によって生ずる相乗的効果によるものであり、互
いにその機能を高め、強力かつ安定してリグニン,繊維
素,タンパク質等の有機成分を迅速かつ強力に分解す
る。
The thermophilic symbiotic mixed culture of these two new strains is not an additive action of the functions of the respective strains, but a synergistic effect produced by the interaction, and enhances the functions of each other. It strongly and stably decomposes organic components such as lignin, fibrin, and proteins quickly and strongly.

【0009】[0009]

【実施例】以下、本発明及びその利用実施例について詳
しく説明する。本発明で使用する微生物は、新菌のSK
522菌株とSK542菌株である。新両菌株の諸性質
は下記の通りである。尚、以下記載の菌学的性質の試験
及び分類同定はすべてバージェーズ マニュアル オブ
デタミネイディブ バクテリオロジー 第7版(19
57),第8版(1974)及びバージェーズ マニュ
アル オブ システマテック バクテリオロジー 第1
巻(1984),第2巻(1986)(Bergey’s Manu
al ofDeterminative Bacteriology 7th. Ed.(1957),8t
h.Ed.(1974).Bergey’s Manualof Systematic Bacterio
logy Vol.1(1984), Vol.2(1986).)の記載に基づいて行
った。
EXAMPLES The present invention and examples of use thereof will be described in detail below. The microorganism used in the present invention is a new SK.
522 strain and SK542 strain. Properties of both new strains are as follows. In addition, all the tests and classification and identification of mycological properties described below are carried out by the Burgers Manual of Determinative Bacteriology 7th Edition (19
57), 8th Edition (1974) and Burgers Manual of Systematic Bacteriology No. 1
Volume (1984), Volume 2 (1986) (Bergey's Manu
al of Determinative Bacteriology 7th. Ed. (1957), 8t
h.Ed. (1974) .Bergey's Manualof Systematic Bacterio
logy Vol.1 (1984), Vol.2 (1986).).

【0010】[I]SK522菌株 (Clostridium thermocellum biovar SK522,微工
研条寄第3459号,FERM BP−3459) 菌学的性質 随伴菌なしで、単独では生育ができない。しかし、随伴
菌は、容易に単離純粋培養されるので、単離した随伴菌
を基礎とし、これと共生培養しながら、その諸性質を試
験した結果である。 形 態 直桿状、わずかに湾曲するものもある。単独、ときどき
2連。0.3〜0.5×2.2〜4.0μ。培養が古く
なると糸状に伸延し、長連鎖状、長さ5.7〜12.8
μ。周毛、室温懸滴標本では運動性がみられない。末端
に楕円、または円形の胞子を形成して細胞を膨張し棍棒
状。グラム陰性。
[I] SK522 strain (Clostridium thermocellum biovar SK522, Mikori Kenjojo No. 3459, FERM BP-3459) Mycological properties It cannot grow alone without a concomitant bacterium. However, since the associated bacteria are easily isolated and pure-cultured, it is the result of testing various properties of the isolated associated bacteria while co-culturing them with the isolated associated bacteria as a basis. Shape There are also straight rod shape and slightly curved shape. Alone, sometimes two. 0.3-0.5 × 2.2-4.0 μ. When the culture becomes old, it extends into filaments, long-chain, and lengths of 5.7 to 12.8.
μ. Motility is not observed in pericardium and room temperature hanging drop specimens. Oval or circular spores are formed at the ends to expand the cells and form a club. Gram negative.

【0011】培養的性質 (1) 平板培養 肉汁寒天、その他一般の常用培地による平板培養には生
育しない。しかし、ビルジョンら(Viljoen et al.)の
提示する培地テトロール(Tetrault)円形ろ紙寒天平板
培養に随伴菌と黄色斑点状のコロニーを形成するが、本
菌単独では作り得ない。 (2) 斜面培養,穿刺培養 シュワイツアー(Schweizer)の試薬処理ろ紙添加ビル
ジョンら(Viljoenet al.)培地寒天斜面培養,及び同
穿刺培養ともに生育しない。 (3) バレイショ培養,ゼラチン培養 表面,穿刺とも生育しない。 (4) 液体培養 ビルジョンらの(Viljoen et al.)培地,繊維素肉汁,
繊維素ペプトン水(生育僅少)等の繊維素を含有する培
地だけに生育が認められる。グルコース,キシロース等
の繊維素以外の物質を炭素源とすれば繊維素の分解力を
失う。
Culture characteristics (1) Plate culture It does not grow on plate culture using broth agar or other commonly used medium. However, while the medium presented by Viljoen et al., Tetrault circular filter paper agar plate forms colonies with associated bacteria and yellow spots, it cannot be produced by this bacterium alone. (2) Slope culture and stab culture Addition of Schweizer reagent-treated filter paper to Viljoe et al. Medium Agar slope culture and stab culture do not grow. (3) It does not grow on potato culture, gelatin culture surface, or puncture. (4) Liquid culture Viljoen et al. Medium, fibrin gravy,
Growth is observed only in a medium containing fibrin such as fibrin peptone water (poor growth). If a substance other than fibrin such as glucose or xylose is used as a carbon source, the degrading power of fibrin is lost.

【0012】生理生化学的性質 1.酵素作用等 (1) 繊維素分解 本菌のもつ繊維素分解酵素は、本質的にはいくつかのβ
−1,4−グルカナーゼの複合体である。細胞外に分泌
され、作用温度80℃以上、同水素イオン濃度pH=1
0.0以上の耐熱性,耐アルカリ性の酵素が数種含まれ
ていることを確認した。ミセル構造をなす繊維素の巨大
分子の末端から切断し、グルコース,セロビオース,セ
ロオリゴ糖類等を生成する。これらの酵素を作用する基
質を主体として示すと、 ろ紙を分解する FP−アーゼ:陽性 アビセルを分解する アビセラーゼ:陽性 セロビオースを2分子のグルコースに分解する セロビアーゼ:陽性 (2) リグニン分解 イナワラリグニン可溶化 :陽性 (弱,微弱) (3) タンパク質分解 プロテオリティック酵素(Proteolytic enzymes) :陰性 ペプチダーゼ(peptidase) :陽性 (4) デンプン加水分解テスト :僅かに陽性 (5) ヘミセルロース,キシラン,ペクチンの加水分解テスト :陰性 (6) インベルターゼ,マルターゼ :陽性 (7) 脂肪分解力テスト :陰性 (8) 酸化反応 ハイドロキノン反応 :陽性 チロシン反応 :陰性 (9) 還元作用 :陽性 2.生産物試験 (1) 繊維素発酵 発酵率78〜91%,繊維素を旺盛に発酵してエタノー
ル,メタノール,アセトアルデヒド,酢酸,乳酸,ギ
酸,ラク酸,コハク酸,フマル酸,酒石酸,グルコン
酸,グルコース,セロビオース,セロオリゴ糖類,セロ
デキストリン,多量の炭酸ガス,水素,及び硫化水素等
を生成する。 (2) その他の糖,及びアルコールより生酸 グルコース,ショ糖,マルトース,セロビオースより生
酸。 (3) ガス発生試験 繊維素より猛烈にガス発生するが、グルコース,ショ
糖,マルトース,セロビオースよりガス発生は認められ
ない。 (4) ペプトン水試験 アンモニヤ :僅かに反応あり インドール :陽性 スカトール :陽性 硫化水素 :陽性 (5) 色素生産 通常,カロチノイド黄色色素生産 3.生育条件 (1) 生育温度 至適温度は65〜72℃,温度範囲は40〜80℃,4
0℃以下では生育しない。 (2) 水素イオン濃度 至適水素イオン濃度pH=6.7〜8.0,その範囲は
5.6〜9.6。 (3) 窒素源 ペプトンが最も優れ,尿素,尿酸,アスパラギン,グル
タミン酸ナトリウム等も良好である。アンモニウム塩も
良好な無機窒素源となる。 (4) 炭素源 繊維素以外の炭水化物で継代培養を続けると、その生育
と発酵力を失う。 (5) 酸素との関係 Eh=200〜−250mVと推定され、嫌気性菌であ
る。 (6) 微量栄養素の要求 ビオチン,ピリドキサミン,ビタミンB12p−アミノ
安息香酸等の微量栄養素を要求する。 4.DNAのG+Cの含有量 G+Cのmol%=38〜40(Tm)と推定される。
Physiological and biochemical properties 1. Enzymatic action, etc. (1) Fibrinolysis The fibrinolytic enzyme possessed by this bacterium is essentially composed of some β
It is a complex of -1,4-glucanase. Secreted extracellularly, action temperature 80 ℃ or more, same hydrogen ion concentration pH = 1
It was confirmed that several kinds of enzymes having heat resistance and alkali resistance of 0.0 or more were contained. It cleaves from the ends of macromolecules of fibrin that form a micellar structure, producing glucose, cellobiose, cellooligosaccharides, and the like. When the substrates that act on these enzymes are mainly shown, it decomposes filter paper FP-ase: Positive Avicel is decomposed Avicelase: Positive Cellobiose is decomposed into two molecules of glucose Cellobiase: Positive (2) Lignin-decomposed Inawala lignin solubilization : Positive (weak, weak) (3) Proteolytic enzymes: Negative peptidase: Positive (4) Starch hydrolysis test: Slightly positive (5) Hemicellulose, xylan, pectin hydrolysis test : Negative (6) Invertase, Maltase: Positive (7) Lipolysis test: Negative (8) Oxidation reaction Hydroquinone reaction: Positive Tyrosine reaction: Negative (9) Reduction action: Positive 2. Product test (1) Fibrin fermentation 78-91% fermentation rate, fermenting fibrin actively and ethanol, methanol, acetaldehyde, acetic acid, lactic acid, formic acid, lactic acid, succinic acid, fumaric acid, tartaric acid, gluconic acid, It produces glucose, cellobiose, cellooligosaccharides, cellodextrin, large amounts of carbon dioxide, hydrogen, and hydrogen sulfide. (2) Produced acid from other sugars and alcohol Produced acid from glucose, sucrose, maltose, and cellobiose. (3) Gas generation test Although gas is generated more violently than fibrin, no gas generation is observed from glucose, sucrose, maltose, and cellobiose. (4) Peptone water test Ammonia: Slight reaction Indole: Positive skatole: Positive Hydrogen sulfide: Positive (5) Pigment production Usually, carotenoid yellow pigment production 3. Growth conditions (1) Growth temperature Optimum temperature is 65-72 ° C, temperature range is 40-80 ° C, 4
It does not grow below 0 ° C. (2) Hydrogen ion concentration Optimum hydrogen ion concentration pH = 6.7-8.0, the range is 5.6-9.6. (3) Nitrogen source Peptone is the best, and urea, uric acid, asparagine, sodium glutamate, etc. are also good. Ammonium salts are also good sources of inorganic nitrogen. (4) Carbon source When the subculture is continued with carbohydrates other than fibrin, its growth and fermenting power are lost. (5) Relationship with oxygen Eh = 200 to −250 mV, which is an anaerobic bacterium. (6) Requirement of micronutrients Micronutrients such as biotin, pyridoxamine, vitamin B 12 and p -aminobenzoic acid are required. 4. Content of G + C of DNA mol% of G + C = 38-40 (Tm) is estimated.

【0013】分類学上の位置 生育至適温度65〜72℃,温度範囲40〜80℃とい
う高温に於いて、旺盛に繊維素を発酵する本SK522
菌株に類似するものとして、次のような好熱性繊維素分
解菌が上げられる。 クロストリジュウム・サーモセルム(Clostridium ther
mocellum Viljoen, Fred and Peterson,1926.: Jour. A
gr. Sci. (London),16,7(1926).) クロストリジュウム・ディゾルベンス(C. dissolvens
Bergey et al.1925,別名 Bacillus cellulose dessolve
ns Khouvine,1923.: Ann. Inst. Past.37,711(1923);Be
rgey’s Manual,2nd.Ed.(1925)p.344.) クロストリジュウム・セルラシウム(C.thermocellulas
eum Enebo,1951.:Bergey’s Manual,7th.Ed.(1957)p.68
9.) バチルス・サーモセルロリテックス(Bacillus thermoc
ellulolyticus Coolhaas,1928.:Cent Bakt.II,75,101
(1928),76,38(1929).) バチルス・サーモフィブリンコルス(B.thermofibrinco
lus Itano and Arakawa,1929:農化,5,816,921(1929);6,
248,257(1930).) これらの中で、特に次の4つの相違点を除けば形態学
的,培養的,生理生化学的試験において本菌株とよく類
似する細菌はクロストリジュウム・ディゾルベンスであ
る。 (1) 弱又は微弱ではあるが、リグニン可溶化能を有す
る。 (2) 生育適温65〜72℃,生育温度範囲40〜80
℃,40℃以下では生育しない。 (3) 繊維素を旺盛に発酵するが、ヘミセルロース,キシ
ラン,ペクチン等は発酵しない。 (4) リグニン可溶化能はサーマス属(genus Thermus)
のある種の細菌によって共生的に顕著に強調され、同時
に本菌の繊維素分解力,その他作用機能に対して好影響
が与えられる。 しかし現在、バージェーズマニアル(Bergsy’s Manual
of Systematic Bacteriology Vol.2(1986)p.1104,p.11
41.)において、好熱性分解菌として記載されているも
のはクロストリジュウム・サーモセルムのみである。ク
ロストリジュウム・ディゾルベンス以下全部当該菌の亜
種か変種として取り扱われ、又は研究不完全なものとさ
れている。そこで、本菌株の分類同定は、クロストリジ
ュウム・サーモセルムとその菌学的諸性質を比較検討す
ることとし、同時に他の好熱性繊維素分解菌についても
対比し、参考とした。
Taxonomic position: SK522 which actively ferments fibrin at an optimum growth temperature of 65 to 72 ° C. and a temperature range of 40 to 80 ° C.
The following thermophilic fibrinolytic bacteria are similar to the strains. Clostridium ther
mocellum Viljoen, Fred and Peterson, 1926 .: Jour. A
gr. Sci. (London), 16,7 (1926).) C. dissolvens
Bergey et al. 1925, aka Bacillus cellulose dessolve
ns Khouvine, 1923 .: Ann. Inst. Past.37,711 (1923); Be
rgey's Manual, 2nd.Ed. (1925) p.344.) C. thermocellulas
eum Enebo, 1951.: Bergey's Manual, 7th.Ed. (1957) p.68
9.) Bacillus thermocellolitex
ellulolyticus Coolhaas, 1928.: Cent Bakt.II, 75,101
(1928), 76,38 (1929).) Bacillus thermofibrinco
lus Itano and Arakawa, 1929: Farming, 5,816,921 (1929); 6,
248,257 (1930).) Among these, Clostridium disorbens is a bacterium that is very similar to this strain in morphological, culture, and physiological biochemical tests except for the following four differences. (1) It has a lignin-solubilizing ability although it is weak or weak. (2) Suitable growth temperature of 65 to 72 ° C, growth temperature range of 40 to 80
Does not grow at temperatures below 40 ° C. (3) Actively ferment fibrin, but not hemicellulose, xylan, pectin, etc. (4) Lignin solubilization ability is the genus Thermus
It is prominently symbiotically emphasized by certain types of bacteria, and at the same time has a positive effect on the fibrinolytic activity and other action functions of this bacterium. However, at present, Berges' Manual (Bergsy's Manual
of Systematic Bacteriology Vol.2 (1986) p.1104, p.11
In 41.), only Clostridium thermocellum is described as a thermophilic degrading bacterium. All of them are treated as subspecies or variants of Clostridium dissolvens, or incompletely studied. Therefore, for the classification and identification of this strain, it was decided to compare and examine Clostridium thermocellum and various mycological properties thereof, and at the same time, other thermophilic fibrinolytic bacteria were also compared for reference.

【0014】以上のようにして、菌学的諸性質を比較検
討した結果を総括すれば、本菌株と公知のクロストリジ
ュウム・サーモセルムをはじめ列挙した好熱性繊維素分
解菌との特徴的な性状の相違点として、前記の4項目が
あげられるが、その他各種炭水化物に対する作用,微量
栄養素の要求等,色々と数え上げることができるが、特
に強調したいことはリグニンに対する問題である。本菌
株がリグニン可溶化能をもち、その可溶化能がサーマス
・アクアティックスSK542(Thermus aquaticus bi
ovar SK542)との共生的混合培養によって顕著に
増強されることである。これに対して、クロストリジュ
ウム・サーモセルムをはじめその他の好熱性繊維素分解
菌のリグニンに関する記載(description)は全く見ら
れない。あったとしても、それは繊維素の分解に対する
阻害作用についてである。斯る理由によって、本菌株の
リグニン可溶化能の生理生化学的性質をひとつの根拠と
して新菌株(Strain)とし、クロストリジュウム・サー
モセルムSK522(Clostridium thermocellum biova
r SK522)と名称した。
As described above, the results of comparative examination of various mycological properties are summarized as follows. The characteristic properties of this strain and known thermophilic fibrinolytic bacteria including Clostridium thermocellum are listed. The differences are the above-mentioned four items, and they can be enumerated in various ways such as the action on various other carbohydrates, the requirement of micronutrients, etc., but what I would like to emphasize especially is the problem with lignin. This strain has a lignin solubilizing ability, and the solubilizing ability is thermus aquaticus SK542 (Thermus aquaticus bi
It is significantly enhanced by the symbiotic mixed culture with ovar SK542). In contrast, there is no description about lignin of other thermophilic fibrinolytic bacteria including Clostridium thermocellum. If so, it is about its inhibitory effect on fibrin degradation. For this reason, a new strain (Strain) was established based on the physiological and biochemical properties of the lignin-solubilizing ability of this strain as one basis, and Clostridium thermocellum SK522 (Clostridium thermocellum biova
r SK522).

【0015】微生物受託番号 本菌株の微生物受託番号は、微工研条寄第3459号
(FERMBP−3459)である。本菌株を標準的菌
株とし、クロストリジュウム・サーモセルム(Clostrid
ium thermocellum Viljoen, Fred and Peterson,192
6.)に属する菌種中、リグニン可溶化能を有し、サーマ
ス属(genus Thermus Brock and Freeze1969)に属する
ある種の細菌との共生的混合培養によって顕著にリグニ
ン可溶化能を増強することを特徴し、かつSK522菌
株及び自然並びに人工的変異株を抱括する生理生化学的
性状による新菌株である。
Microorganism Accession Number The microorganism accession number of this strain is Microtechnology Research Institute No. 3459 (FERMBP-3459). This strain is the standard strain, and Clostridium thermocellum (Clostrid
ium thermocellum Viljoen, Fred and Peterson, 192
It has the ability to solubilize lignin among bacterial species belonging to 6.), and significantly enhances the ability to solubilize lignin by symbiotic mixed culture with certain bacteria belonging to the genus Thermus Brock and Freeze1969. It is a novel strain with physiological and biochemical properties that characterizes the SK522 strain and natural and artificial mutants.

【0016】SK522菌株のスクリーニング 土壌,海浜汚泥,堆・厩肥,人・家畜糞便を分離源とし
て55〜65℃で数回濃縮培養を繰り返した後、ビルジ
ョンら(Viljoen et al.)の提示する培地テトロール
(Tetrault)円形ろ紙寒天平板培養等によって定法通り
分離する。又、本菌は実質的に純粋に分離できた。培地
としてビルジョンら(Viljoen et al.)の提示する塩類
組成が適当であるが、必要に応じて微量の無機金属塩
類,ビタミン類,生長促進因子,例えば酵母エキス等を
添加するとよい。 ビルジョンらの培地 (Viljoen,Fred and Peterson 1926) ペプトン 5.0g 炭酸カルシウム 過剰 リン酸アンモニウムナトリウム 2.0g 酸性リン酸カリウム 1.0g 硫酸マグネシウム 0.3g 塩化カルシウム 0.1g 塩化第二鉄 痕跡 繊維素(ろ紙) 15.0g 井水 1000ml
Screening of SK522 strain Soil, beach sludge, manure / manure, human / livestock faeces are used as separation sources, and concentrated culture is repeated several times at 55 to 65 ° C., then presented by Viljoen et al. Medium Tetrault circular filter paper Agar plates are used for isolation according to standard methods. The bacterium was able to be isolated substantially purely. The salt composition suggested by Viljoen et al. Is suitable as the medium, but if necessary, a trace amount of inorganic metal salts, vitamins, growth promoting factors such as yeast extract, etc. may be added. Viljoen, Fred and Peterson 1926 Peptone 5.0 g Calcium carbonate Excess ammonium phosphate sodium 2.0 g Potassium acid phosphate 1.0 g Magnesium sulfate 0.3 g Calcium chloride 0.1 g Ferric chloride Trace fiber Element (filter paper) 15.0 g Imizu 1000 ml

【0017】SK522菌株の有用性 本SK522菌株は、もともと旺盛なる繊維素分解菌で
ある。この菌株が弱又は微弱ではあるが、リグニン可溶
化能を有することを本発明者たちが見出し、更にその可
溶化能が本菌株とサーマス属(genus Thermus)のある
種の細菌との共生的混合培養によって顕著に増強される
と共に、本菌株の繊維素分解力、その他作用機能にも好
影響を与えた。又、この混合培養の成功は、多種類の難
分解性有機資材の分解利用を可能にして、その生産性を
向上させ、野積堆肥化法を確実なものにし、好熱性高速
分解方式による堆肥の製造法を確立した。そして、SK
522菌株とSK542菌株を主要菌とする健全活性あ
る土壌微生物フロラーの形成は、環境要因の変化に対し
て有効菌の生育と作用機能を安定させて、土壌病害や連
作障害の消滅,克服した。又、土壌や植物の葉面に直接
撒布する新技術や屎尿の脱臭分解,硬タンパク質の分解
等、新しい次元の微生物利用法の展開が期待される。
Utility of SK522 Strain The present SK522 strain is a fibrin-degrading bacterium that is originally active. The present inventors have found that this strain has a lignin solubilizing ability, although this strain is weak or weak, and the solubilizing ability of the strain is symbiotic mixing of this strain with a certain bacterium of the genus Thermus (genus Thermus). It was remarkably enhanced by culturing, and also had a favorable effect on the fibrinolytic activity and other action functions of this strain. In addition, the success of this mixed culturing enables the decomposition and utilization of many types of persistent organic materials, improves their productivity, and ensures the nodoko composting method. The manufacturing method was established. And SK
The formation of a healthy active soil microbial flora mainly consisting of the 522 strain and the SK542 strain stabilized the growth and action function of effective bacteria against changes in environmental factors, and eliminated or overcame soil diseases and continuous cropping disorders. In addition, it is expected that new technology of microbial utilization such as new technology of direct spraying on soil or leaf surface of plant and deodorization of human waste and decomposition of hard protein will be developed.

【0018】[II]SK542菌株 (Thermus aquaticus biovar SK542,微工研条寄
第3382号,FERM BP−3382) 菌学的性質 形 態 長桿状、0.4〜0.6×3.0〜5.0μ。ある条件
下、例えば培養が古くなると糸状、長さ20〜130
μ。鞭毛なし、室温懸滴標本では運動性がみられない。
内生胞子なし。グラム陰性。
[II] Strain SK542 (Thermus aquaticus biovar SK542, Microtechnical Lab Article 3382, FERM BP-3382) Mycological properties Long rod-shaped, 0.4-0.6 × 3.0-5 0.0μ. Under certain conditions, for example, when culture becomes old, filamentous, length 20 to 130
μ. No flagella and no motility in room temperature hanging drops.
No endospores. Gram negative.

【0019】培養的性質 増殖が活発。ゼェネレーションタイムは20〜50分。 (1) 平板培養 3%寒天,60℃培養:黄色,比較的緻密,小円形コロ
ニー。 (2) 寒天穿刺培養 表面発育だけ,黄色わずかに拡張。 (3) 液体培養 表面に被膜状に生育(静置培養)。
Culture property Proliferation is active. Generation time is 20 to 50 minutes. (1) Plate culture 3% agar, 60 ° C culture: yellow, relatively dense, small round colonies. (2) Agar stab culture Only surface growth, yellow slightly expanded. (3) Liquid culture Grows in a film on the surface (static culture).

【0020】生理生化学的性質 1.酵素作用等 (1) タンパク質分解 プロテオリティック酵素 :陽性(強力) (proteolytic enzymes) ゼラチン加水分解 :陽性 ペプチダーゼ(peptidase) :陽性 (2) デンプン加水分解 :僅かに陽性 (3) ペクチン分解 :陽性(弱い) (4) 繊維素分解 :陰性 (5) リグニン分解 :陰性 繊維素及びリグニンの分解は共に陰性ではあるが、好熱
性繊維素分解菌SK522菌株との共生的混合培養によ
って、SK522菌株のリグニン可溶化能を顕著に増強
し、同時に繊維素分解力,その他の作用機能にも好影響
を与える。 (6) 脂肪分解 :陰性 (7) インベルターゼ,マルターゼ :陽性 (8) カタラーゼ,オキシダーゼ反応 :陽性 (9) 硫化水素生成 :陽性(弱い) (10) 硫酸還元反応 :陰性 2.生産物試験 (1) 糖,アルコールより生酸及びガス発生 ガス発生せず。グルコース,ガラクトース,マルトー
ス,ラクトース,グリセロールより生酸。 (2) インドール,スカトールの生成 :陰性 (3) 色素生産 黄色色素(カロチノイド系色素,吸光度最大値450n
m,その他430,435,470nmに小さなピーク
がある)を産生する。しかし、グルコース,その他の糖
類を炭素源とする合成培地ではほとんど産生されない。
Physiological and biochemical properties 1. Enzyme action, etc. (1) Proteolytic proteolytic enzyme: Positive (strong) (proteolytic enzymes) Gelatin hydrolysis: Positive peptidase: Positive (2) Starch hydrolysis: Slightly positive (3) Pectin degradation: Positive (weak) ) (4) Degradation of fibrin: Negative (5) Degradation of lignin: Negative Degradation of both fibrin and lignin is negative, but lignin digestion of SK522 strain is possible by symbiotic mixed culture with thermophilic fibrinolytic SK522 strain. It significantly enhances the solubilizing ability, and at the same time has a favorable effect on the fibrin decomposing power and other action functions. (6) Lipolysis: Negative (7) Invertase, maltase: Positive (8) Catalase, oxidase reaction: Positive (9) Hydrogen sulfide production: Positive (weak) (10) Sulfate reduction reaction: Negative 2. Product test (1) Raw acid and gas generation from sugar and alcohol No gas generation. A raw acid from glucose, galactose, maltose, lactose, and glycerol. (2) Formation of indole and skatole: Negative (3) Pigment production Yellow pigment (carotenoid pigment, maximum absorbance 450n
m, others with small peaks at 430, 435, 470 nm). However, it is scarcely produced in a synthetic medium containing glucose and other sugars as a carbon source.

【0021】3.生育条件 (1) 培地濃度 サーマス属(genus Thermus)の細菌は一般に有機物濃
度に感受性がある。栄養物は少なく、濃度が低い方がよ
いといわれている。しかし、本菌株はこれらと趣を異に
し、通常の濃度においてもよく生育する。 食塩NaCl 5%以上でも生育する。至適濃度2.
0〜3.0%。一般にサーマス属(genus Thermus)の
細菌は2%以上のNaCl存在下では生育しない。 グルタミン酸ナトリウム3%以上でも生育する。 ショ糖,又はマルトース5%以上でも生育する。 2%ペプトン+1%酵母エキスの存在下でも、その生
育が阻害されない。一般にサーマス属(genus Thermu
s)の細菌はトリプトン,酵母エキス濃度,それぞれ
0.1%前後が適当で、各々1%以上になると生育しな
い。 (2) 生育温度 最適温度は72〜76℃,生育温度範囲40〜82℃,
40℃以下では発育できない。 (3) 水素イオン濃度 最適水素イオン濃度pH=6.0〜10.0。生育水素
イオン濃度範囲pH=4.0〜11.0。 (4) 窒素源 ゼラチン等のタンパク質,グルタミン酸塩,尿素,それ
に無機窒素源としてアンモニウム塩がよく利用される。 (5) 炭素源 グルコース,ショ糖,マルトース,ガラクトース,セロ
ビオース,ラフィノース,スタキオース,デンプン,グ
リセロール,酢酸,ラク酸,リンゴ酸,グルタミン酸塩
を利用する。 (6) 酸素との関係 絶対好気性。 (7) 微量栄養素の要求 本菌株は微量栄養素の要求が高い。ビオチン,ニコチン
酸アミド,チアミン等のビタミン類が要求されるほか
に、本菌株の良好な発育には鉄,マンガン,カルシウム
等の金属イオンを比較的高濃度に要求する。そして、こ
れらのミネラル量にも敏感である。 (8) 抗生物質に対する感受性 一般のサーマス属(genus Thermus)の細菌と同様に、
ペニシリンG,クロラムフェニコール,テトラサイクリ
ン,ストレプトマイシン,カナマイシン,その他抗生物
質に高い感受性を示す。 4.DNAのG+Cの含有量 G+Cのmol%=68(Tm)と推定される。
3. Growth conditions (1) Medium concentration Bacteria of the genus Thermus are generally sensitive to organic matter concentrations. It is said that the less nutrients and the lower the concentration, the better. However, this strain is different from these in that it grows well even at normal concentrations. It grows even with salt NaCl 5% or more. Optimal concentration 2.
0-3.0%. In general, Genus Thermus bacteria do not grow in the presence of more than 2% NaCl. It grows even with sodium glutamate of 3% or more. It grows on sucrose or maltose 5% or more. Its growth is not inhibited even in the presence of 2% peptone + 1% yeast extract. Generally the genus Thermu
For the bacteria of s), trypton and yeast extract concentrations of about 0.1% are suitable, and they do not grow when they exceed 1%. (2) Growth temperature Optimum temperature is 72-76 ℃, growth temperature range is 40-82 ℃,
It cannot grow below 40 ° C. (3) Hydrogen ion concentration Optimal hydrogen ion concentration pH = 6.0 to 10.0. Growth hydrogen ion concentration range pH = 4.0 to 11.0. (4) Nitrogen source Proteins such as gelatin, glutamate, urea, and ammonium salt are often used as an inorganic nitrogen source. (5) Carbon source Glucose, sucrose, maltose, galactose, cellobiose, raffinose, stachyose, starch, glycerol, acetic acid, lactic acid, malic acid, glutamate are used. (6) Relationship with oxygen Absolutely aerobic. (7) Demand for micronutrients This strain has high demands for micronutrients. In addition to vitamins such as biotin, nicotinamide, and thiamine, a relatively high concentration of metal ions such as iron, manganese, and calcium is required for good growth of this strain. It is also sensitive to the amount of these minerals. (8) Susceptibility to antibiotics Like general Thermus genus (genus Thermus) bacteria,
It shows high sensitivity to penicillin G, chloramphenicol, tetracycline, streptomycin, kanamycin and other antibiotics. 4. Content of G + C of DNA mol% of G + C = 68 (Tm) is estimated.

【0022】分類学上の位置 本菌が絶対好気性,生育至適温度72〜76℃,生育温
度範囲40〜82℃,40℃以下では生育しない。無胞
子,グラム陰性の長桿菌であること等から、その他菌学
的諸性質を勘案して、サーマス属(genus Thermus Broc
k and Freege 1967)と同定される。そして、類似する
サーマス属(genus Thermus)の細菌として、 サーマス・アクアティックス(Thermus aquaticus Broc
k and Freege 1969.:Bergey’s Manual(1984)Vol.1,P.3
37.) サーマス・サーモフィルス(Thermus thermophilus Osh
ima and Imahori 1974.:Int.J.Bacteriol.,24,102(197
4)) サーマス・フラブス(Thermus Flavus Saiki,Kimura an
d Arima 1972.:Agr.Biol.Chem.,36,2357(1972)) 等が上げられるが、現在バーゼーズマニアル(Bergey’
s Manual of SystematicBacteriology Vol.1(1984)P.33
3)のサーマス属(genus Thermus Brock and Freeg 196
7)に属する細菌種はサーマス・アクアティックス(The
rmus aquaticusBrock and Freege 1969)だけであり、
しかも下記のような既知の菌種中に見出し得ない特徴的
な性状を有するので、本菌株をサーマス・アクアティッ
クスの新菌株(strain)として、サーマス・アクアティ
クスSK542(Thermus aquaticus biovar SK54
2)と名称するのが妥当であると結論する。
Taxonomic position The bacterium does not grow in absolute aerobic condition, optimum growth temperature of 72 to 76 ° C, growth temperature range of 40 to 82 ° C, 40 ° C or lower. Since it is a non-spore-free, Gram-negative long bacillus, etc., in consideration of other mycological properties, the genus Thermus (genus Thermus Broc
k and Freege 1967). And, as a similar bacterium of the genus Thermus, Thermus aquaticus Broc
k and Freege 1969.:Bergey's Manual (1984) Vol.1, P.3
37.) Thermus thermophilus Osh
ima and Imahori 1974.:Int.J.Bacteriol.,24,102(197
4)) Thermus Flavus Saiki, Kimura an
d Arima 1972.:Agr.Biol.Chem.,36,2357(1972)), etc., but currently Bersey's Manual
s Manual of Systematic Bacteriology Vol.1 (1984) P.33
3) Genus Thermus Brock and Freeg 196
Bacterial species belonging to 7) are Thermus aquatics (The
rmus aquaticusBrock and Freege 1969),
Moreover, since it has the characteristic properties that cannot be found in the known bacterial species as described below, this strain is used as a new strain (strain) of Thermus aquaticus SK542 (Thermus aquaticus biovar SK54).
We conclude that it is appropriate to name it 2).

【0023】下 記 (1) 好熱性繊維素分解菌SK522菌株との共生的混合
培養によって、そのリグニン可溶化能を顕著に増強す
る。と同時に繊維素分解力,その他の作用機能にも好影
響を与える。 (2) 広域の作用水素イオン濃度と作用温度を有する強い
タンパク質分解力を持つ。 (3) 有機物濃度の感受性が、既知のサーマス属(genus
Thermus)の細菌と異なり、非常に弱く、通常濃度の培
地においてもよく生育する。 (4) 微量栄養素の要求が強く、各種ビタミン類及び金属
イオンを要求し、それらのミネラル量にも敏感である。 (5) 黄色色素(カロチノイド系色素,吸光度最大値45
0nm,その他430,435,470nmに小さなピ
ークがある)を産生する。
(1) The lignin-solubilizing ability is remarkably enhanced by symbiotic mixed culture with the thermophilic fibrinolytic bacterium SK522 strain. At the same time, it has a positive effect on the ability to decompose fibrin and other functions. (2) It has a strong proteolytic activity with a wide range of working hydrogen ion concentration and working temperature. (3) The genus Thermus (genus
(Thermus) bacteria are very weak and grow well in medium of normal concentration. (4) Strong demand for micronutrients, demand for various vitamins and metal ions, and sensitivity to their mineral contents. (5) Yellow pigment (carotenoid pigment, maximum absorbance 45)
0 nm and others have small peaks at 430, 435 and 470 nm).

【0024】微生物受託番号 本菌株の微生物受託番号は、微工研条寄第3382号
(FERMBP−3382)である。SK542菌株と
は、本菌株を標準的菌株とし、サーマス・アクアティッ
クス(Thermus aquaticus Brock and Freege 1969)に
属する細菌種中、好熱性繊維素分解菌(SK522菌
株)との共生的混合培養によって、そのリグニン可溶化
能を顕著に増強し、同時に繊維素分解力にも好影響を与
えることを特徴とし、かつSK542菌株及び自然並び
に人工的変異株を抱括する生理生化学的性状による新菌
株(strain)である。
Microorganisms accession number The microorganisms accession number of this strain is Micro Engineering Research Article No. 3382 (FERMBP-3382). The SK542 strain is a standard strain of this strain, and by symbiotic mixed culture with a thermophilic fibrinolytic bacterium (SK522 strain) among bacterial species belonging to Thermus aquaticus Brock and Freege 1969, A new strain with a physiological and biochemical property that significantly enhances its lignin solubilizing ability and at the same time has a favorable effect on the fibrin degrading power, and has physiobiochemical properties that embraces the SK542 strain and natural and artificial mutants ( strain).

【0025】SK542菌株のスクリーニング 分離源は九州各地の温泉源及び温泉源付近の土壌,腐植
等である。分離試料を55〜60℃で前培養した後、定
法に従って3%寒天平板培養によって単離する。又、本
菌は実質的に純粋に分離できた。 分離用培地組成 (カステンホルツの培地:Castenholz,R.W.;Bacteriol.
Rev.,33,467(1969)) ニトリロ三酢酸 100mg CaSO4・2H2O 60mg MgSO4・7H2O 100mg NaCl 8mg KNO3 103mg NaNO3 689mg Na2HPO4 111mg FeCl3 0.28mg MnSO4・H2O 2.2mg ZnSO4・7H2O 0.5mg H3BO3 0.5mg CuSO4 0.016mg Na204・2H2O 0.025mg (イーストエキス 5000mg) (トリプトン 5000mg) (ショ糖 10000mg) 全量(純水で、pH=〜8) 1000ml 注:( )内の組成は発明者らが改変。
Screening of SK542 strain Isolate sources are hot spring sources in various places in Kyushu, soils near hot spring sources, humus and the like. The separated sample is precultured at 55 to 60 ° C. and then isolated by 3% agar plating according to a standard method. The bacterium was able to be isolated substantially purely. Separation medium composition (Castenholz medium: Castenholz, RW; Bacteriol.
Rev., 33, 467 (1969)) Nitrilotriacetic acid 100 mg CaSO 4 .2H 2 O 60 mg MgSO 4 .7H 2 O 100 mg NaCl 8 mg KNO 3 103 mg NaNO 3 689 mg Na 2 HPO 4 111 mg FeCl 3 0.28 mg MnSO 4 .H 2 O 2.2 mg ZnSO 4 .7H 2 O 0.5 mg H 3 BO 3 0.5 mg CuSO 4 0.016 mg Na 2 M 0 O 4 .2H 2 O 0.025 mg (yeast extract 5000 mg) (tryptone 5000 mg) (sucrose 10000 mg) ) Total volume (with pure water, pH = ~ 8) 1000 ml Note: The composition in () is modified by the inventors.

【0026】SK542菌株の有用性 本新菌株の有用性は、次の三つの作用機能によって特徴
づけられる。 (1) 好熱性繊維素分解菌(SK522菌株)との共生的
混合培養によって、該菌のもつリグニン分解能を顕著に
増強する。と同時に、その繊維素分解力、その他の作用
機能にも好影響を与える。 (2) 広域の作用水素イオン濃度と作用温度を有する強い
タンパク質分解力をもつ。 (3) 不溶性、カロチノイド系の黄色色素を産生する。菌
体中のこの黄色色素が他の微生物等による分解を受け水
溶性の低分子量体のものとなり、植物体に吸収されて、
果実の味、色沢、貯蔵性等の果実の品質の向上に役立
つ。又、本SK542菌株菌体を施用すると、これを基
質として繁殖する一般の従属栄養微生物や土壌有効菌の
増殖を促す。 以上のようなことが、既知のサーマス属(genus Thermu
s)の細菌と異なり有機物濃度の感受性の非常に弱いこ
とと相俟って、自然生態や農耕生態系において、多種類
の難分解性繊維物質,硬タンパク質や余剰汚泥、その他
広く各種の有機資材を利用できるようになった。更にこ
のことが、生産性向上、土壌病害や連作障害の克服、そ
して、屎尿の脱臭・分解、土壌又は植物葉面に直接撒布
する新技術の開発等、新次元の微生物利用法の発展へと
繋がる。
Utility of SK542 Strain The utility of this new strain is characterized by the following three functions. (1) By symbiotic mixed culture with a thermophilic fibrinolytic bacterium (SK522 strain), the lignin degrading ability of the bacterium is remarkably enhanced. At the same time, it also has a positive effect on its fibrin decomposing power and other action functions. (2) It has a strong proteolytic activity with a wide range of action hydrogen ion concentration and action temperature. (3) It produces an insoluble yellow carotenoid pigment. This yellow pigment in the fungus body is decomposed by other microorganisms and becomes a water-soluble low molecular weight substance, which is absorbed by the plant,
It helps improve the quality of fruits such as taste, color and storability. When the SK542 strain is applied, it promotes the growth of general heterotrophic microorganisms and soil-effective bacteria that propagate using this strain as a substrate. The above is the known genus Thermu (genus Thermu
In combination with the extremely weak sensitivity of organic matter concentration unlike bacteria of (s), in natural ecology and agricultural ecosystem, various kinds of persistent organic substances, hard proteins and surplus sludge, and various other organic materials are widely used. Is now available. Furthermore, this leads to the development of a new dimension of microbial utilization, such as productivity improvement, overcoming soil diseases and continuous crop damage, and deodorizing and decomposing human waste, and developing new technology for direct spraying on soil or plant foliage. Connect.

【0027】[III]SK522菌株とSK542菌
株の混合培養物 1.SK522菌株の多量培養物 前記ビルジョンら(Viljoen et al.,1926)の培地を用
い嫌気または半嫌気的条件下で、65〜70℃,48〜
60時間培養し、その培養液をもって菌体含有の培養物
とする。 2.SK542菌株の多量培養物 前記カステンホルツ(Castenholz,1969)の培地を用
い、通気または振盪等の好気的条件下で、70〜75
℃,24時間培養し、その培養液をもって培養物とす
る。
[III] Mixed culture of SK522 strain and SK542 strain 1. Large-scale culture of SK522 strain Using the medium of Viljoen et al., 1926 described above, under anaerobic or semi-anaerobic conditions, 65-70 ° C, 48-
After culturing for 60 hours, the culture solution is used as a culture containing cells. 2. Large-scale culture of SK542 strain Using the culture medium of Castenholz (1969), 70-75 under aerobic conditions such as aeration or shaking
Cultivate at 24 ° C for 24 hours, and use the culture solution as a culture.

【0028】3.SK522菌株とSK542菌株の混
合培養物 下記の培地を用い、SK522菌株及びSK542菌株
の多量培養物の適量をそれぞれ接種して、65〜70
℃,24〜36時間培養して、両菌株の混合培養物とす
る。そして、石灰岩岩粉,ドロマイト岩粉,貝化石粉
末,カニ・シャコ・貝殻等の甲殻・貝殻粉末,炭酸カル
シウム,消石灰,パーライト,バーミキュライト,ゼオ
ライト,けいそう土,塩基性岩粉,粉砕ピートモス,木
炭,くん炭末等の一種又は複数種の混合物の賦型剤を用
いて粉粒体となし、水分を5〜7%以下の製品にすると
2ケ年以上の保存に耐える。又、施用直前に両菌株の多
量培養物を等量にとってよく混和して、すぐに施用する
か、或いは賦型剤を用いて粉粒体に製造しても、その最
終製品の品質性能は全くかわらない。又、下記の共生混
合培養用E−培地を以下単にE−培地と称する。 下 記 共生混合培養用 E−培地 K2HPO4 5kg (NH42SO4 2kg 尿素 2kg ペプトン 5kg 酵母エキス 5kg ろ紙(繊維素) 15kg CaCO3 過剰 水(〜pH7.0) 1000l 4.両菌株の共生的混合培養のもたらす有用性 共に高温環境という条件下で、絶対好気性のサーマス属
(genus Thermus)のSK542菌株との共生的混合培
養は、嫌気性の好熱性繊維素分解菌SK522菌株単独
ではほとんど不可能な天然の難分解性有機資材の分解発
酵を顕著に高揚する。まず、SK542菌株の増殖はS
K522菌株の欠除するタンパク分解活性を充補する。
しかも、堆・厩肥をはじめ廃木材、都市下水汚泥等の難
分解性有機資材の分解発酵は、すべて固体発酵の状態
で、かなり通気のよい環境下におかれている。そして、
初期の段階におけるSK542菌株の増殖は高温嫌気的
環境へと変移せしめ、これによってSK522菌株の自
然界での生育を可能となる。
3. Mixed culture of SK522 strain and SK542 strain Using the following medium, appropriate amounts of large-scale cultures of the SK522 strain and the SK542 strain were inoculated, respectively, to obtain 65-70.
Cultivate at 24 ° C for 36 to 36 hours to obtain a mixed culture of both strains. And limestone rock powder, dolomite rock powder, shell fossil powder, crust, shellfish powder such as crab, shrimp, shell, calcium carbonate, slaked lime, perlite, vermiculite, zeolite, diatomaceous earth, basic rock powder, ground peat moss, charcoal , If it is made into powder and granules by using one or a mixture of plural kinds of charcoal powder or the like and the product has a water content of 5 to 7% or less, it can be stored for more than 2 years. In addition, just before application, a large amount of the cultures of both strains are mixed in equal amounts and mixed well, and immediately applied, or even if it is manufactured into a powder or granule using a excipient, the quality performance of the final product is completely Unchanged. Further, the following E-medium for mixed culture is simply referred to as E-medium. E-medium for co-cultivation mixed culture K 2 HPO 4 5 kg (NH 4 ) 2 SO 4 2 kg Urea 2 kg Peptone 5 kg Yeast extract 5 kg Filter paper (fibrin) 15 kg CaCO 3 excess water (~ pH 7.0) 1000l 4. Utility of symbiotic mixed culture of both strains Under the condition of high temperature environment, symbiotic mixed culture with SK542 strain of absolutely aerobic Genus Thermus is anaerobic thermophilic fibrinolytic bacterium SK522. It remarkably enhances the decomposition and fermentation of natural refractory organic materials, which is almost impossible with the strain alone. First, the growth of the SK542 strain is S
It complements the proteolytic activity of the K522 strain.
Moreover, the decomposition and fermentation of persistent organic materials such as waste wood, manure, waste wood, and municipal sewage sludge are all solid-state fermentations, and are in a well-ventilated environment. And
The growth of the SK542 strain in the early stages is transformed into a high temperature anaerobic environment, which allows the SK522 strain to grow in nature.

【0029】(1) リグニンの可溶化 ここで、特に注目されることは、SK542菌株によっ
てSK522菌株のリグニン可溶化能が顕著に発揮され
ることです。難分解性有機資材は、実際には繊維素がリ
グニン、その他の有機成分と強く結合した状態で存在す
る。こうした天然のリグノセルロースは繊維素分解力の
旺盛なSK522菌株の単独施用ではほとんど分解が不
可能である。リグニンの化学構造は、未だ完全に明らか
にされていないが、ベンゼン環に炭素数3つの側鎖を持
つフエニルプロパンが基本単位になって、この単位体が
パーオキシダーゼによって触媒されるラジカル反応によ
りランダムに三次元的に重合した高分子化合物である。
微生物の分解に対する抵抗がきわめて強く、きわめて分
解困難であることは多くの研究者・技術者の認める一致
した見解である。ところが、本願発明で使用するSK5
22菌株は弱又は微弱ではあるが、リグニンを可溶化す
る。そして、このリグニン可溶化能が、SK542菌株
と共生的混合培養することによって、たとえば、イナワ
ラリグニンの50%以上が10日前後の短日時において
可溶化されるということが、今回、本願発明において、
はじめて明らかにされた。その実際的な施用が本願発明
の重要なる特徴的態様で、その作用効果は50〜80℃
以上という高温期段階で発揮され、分解発酵へその腐植
化が急速に進行する。
(1) Solubilization of lignin Here, it is particularly noted that the SK542 strain exerts a remarkable lignin-solubilizing ability of the SK522 strain. The persistent organic material actually exists in a state in which the fibrin is strongly bound to lignin and other organic components. Such natural lignocellulose can hardly be decomposed by the single application of the SK522 strain having a strong fibrinolytic activity. Although the chemical structure of lignin has not been completely clarified yet, phenylpropane, which has a side chain with three carbon atoms in the benzene ring, serves as the basic unit, and this unit is formed by a radical reaction catalyzed by peroxidase. It is a polymer compound that is randomly and three-dimensionally polymerized.
It is a consensus view of many researchers and engineers that resistance to microbial decomposition is extremely strong and extremely difficult to decompose. However, SK5 used in the present invention
Twenty-two strains solubilize lignin, though weakly or weakly. And, this lignin solubilizing ability, by symbiotic mixed culture with the SK542 strain, for example, that 50% or more of Inawara lignin is solubilized in a short time around 10 days, this time, in the present invention,
It was revealed for the first time. Its practical application is an important characteristic aspect of the present invention, and its action and effect are 50 to 80 ° C.
It is exerted at the high temperature stage mentioned above, and the humification progresses rapidly to the decomposition fermentation.

【0030】(2) 黄色色素の産生 SK542菌株をはじめ、サーマス属(genus Thermu
s)の産生する黄色色素はカロチノイド系不溶性色素で
ある。菌体中のこの黄色色素が他の微生物等による分解
を受け水溶性の低分子量体のものとなり、植物体に吸収
され、必要部位に移行し、丁度都合の良い前駆物質とな
る。すなわち、このような黄色色素が、ほかの溶菌した
細胞内容物や分泌物、それに発酵生産物等とともに根茎
葉部位の増大繁茂を促すだけでなく、花芽の形成,着
果,果実の肥大等の生殖生長の代謝系に深く関与してい
ることが分子生物学的レベルで行なわれた研究によって
も明らかにされ、その応用利用へと発展し、すでに果実
の味,色沢,貯蔵性等品質向上に役立っている。
(2) Production of yellow pigments The genus Thermu including the SK542 strain
The yellow pigment produced by s) is a carotenoid insoluble pigment. This yellow pigment in the bacterial cells is decomposed by other microorganisms to become a water-soluble low molecular weight substance, which is absorbed by the plant body and transferred to a necessary site, which is just a convenient precursor. That is, such a yellow pigment not only promotes the growth and proliferation of rhizomes along with other lysed cell contents and secretions, and fermentation products, but also causes the formation of flower buds, fruit set, fruit enlargement, etc. It has been clarified by research conducted at the molecular biological level that it is deeply involved in the metabolic system of reproductive growth, and it has been developed into its application and has already been improved in quality such as fruit taste, color and storage quality. Is useful to.

【0031】(3) 微生物生態系の混合複合化 また、この黄色色素を含むSK542菌株の菌体を施用
すると、それを基質として繁殖する一般の従属栄養微生
物,土壌有効菌等の増殖を促す。さらに重要なことは、
自然界の堆肥製造のような現場では、SK522菌株の
ような好熱性微生物が、すぐに増殖活性化するわけでは
ない。当初は、一般の常温性従属栄養微生物が増殖し、
これらの作用による発酵熱が蓄積されて品温の上昇に役
立つものであり、単一菌株の好熱性繊維素分解菌や少数
の微生物のみが、天然の難分解性有機資材の腐植化に関
与するわけではない。微生物フロラーの混合複合化多様
化が求められる。さまざまなタイプの有効菌が多く、さ
らに「エサ(基質)」も適度にあるという複合的内容が
望ましい。こうして、難分解性有機物の高温分解は、S
K522菌株を中心とする細菌フロラーがまず形成さ
れ、その腐植化過程が単純な構成成分の変化だけでな
く、きわめて複雑な微生物フロラーの相互作用やその変
遷等が、深い関わりをもって最も効率よく進行するので
ある。SK522菌株とSK542菌株に混合する他の
有効菌としては下記のものがある。
(3) Mixed Complexation of Microbial Ecosystem Further, when the bacterial cells of the SK542 strain containing the yellow pigment are applied, the growth of general heterotrophic microorganisms, soil effective bacteria and the like that propagate using the same as substrates is promoted. More importantly,
In the field such as compost production in the natural world, thermophilic microorganisms such as the SK522 strain do not immediately proliferate and activate. Initially, general room temperature heterotrophic microorganisms grow,
Fermentation heat due to these actions is accumulated to help increase product temperature, and only a single strain of thermophilic fibrinolytic bacteria and a small number of microorganisms are involved in the humification of natural persistent organic materials. Do not mean. It is required to mix and diversify the microbial flora. It is desirable to have a complex content that there are many effective bacteria of various types and that "feed (substrate)" is also appropriate. Thus, the high-temperature decomposition of persistent organic matter is
The bacterial flora centering on the K522 strain is formed first, and the humification process not only involves simple changes in the constituent components, but also the extremely complex interactions and transitions of the microbial flora, which are most efficiently and closely related. Of. Other effective bacteria to be mixed with the SK522 strain and the SK542 strain include the following.

【0032】(1) ヘミセルロースの分解菌の培養物 ヘミセルロースは繊維素とともに植物体(細胞壁)を形
成し、これを構成する糖類によって、キシラン,アラバ
ン,デキストラン,マンナン,ガラクタン等と称せられ
る。ヘミセルロース分解菌の培養物は、イナワラキシラ
ン約1%の濃度に加えた岩田の培地(1936)を使用
し、30〜38℃,通性嫌気的に集殖する。通常、バク
テリウム・ブルガトゥス(Bacterium vulgatus),バク
テリウム・プロディギオサム(Bac. prodigiosum),バ
クテリウム・メセンテリクスルバー(Bac. mesentericu
s ruber),ミクロスピラ・アガーリクェフィセンス(M
icrospira ager-liquefaciens)等の1株又は2株以上
の混合培養物が獲得される。 (2) ペクチン物質分解菌の培養物 ペクチン物質を強力に分解する細菌は、好気性のもので
は枯草菌群細菌及びエタノール・アセトン菌に、又嫌気
性ではラク酸菌に属するものが多い。本発明では、モリ
シュの培地(Molisch1939)を用い、土壌,堆肥,
馬糞,バガスやチョ麻等の腐敗物を分離源として、27
〜35℃,培養日数3〜5日,厚層及び薄層で数回の集
殖培養で種菌を獲得する。本発明では、その1株以上の
数株の培養物を用いる。
(1) Culture of Hemicellulose Degrading Bacteria Hemicellulose forms a plant (cell wall) with fibrin, and is called xylan, araban, dextran, mannan, galactan, etc. depending on the sugars that compose this. As a culture of hemicellulose-decomposing bacteria, Iwata's medium (1936) added to a concentration of rice xylan about 1% was used, and the cells were facultatively and anaerobically collected at 30 to 38 ° C. Usually Bacterium vulgatus, Bac. Prodigiosum, Bacteria mesentericu
s ruber), Microspyra Agariquefisense (M
A mixed culture of one or more strains such as icrospira ager-liquefaciens) is obtained. (2) Cultures of pectin substance-degrading bacteria Many of the bacteria that strongly decompose pectin substances belong to the Bacillus subtilis group bacteria and ethanol / acetone bacteria when they are aerobic, and to the lactic acid bacteria when they are anaerobic. In the present invention, using a Morish medium (Molisch 1939), soil, compost,
Separation sources such as horse manure, bagasse and chomp are 27
The inoculum is obtained by collecting culture several times in a thick layer and a thin layer at ˜35 ° C. for 3 to 5 days of culturing. In the present invention, cultures of one or more strains are used.

【0033】(3) 土壌放線菌の培養物 放線菌(Actinomycetales Buchanan,1917)の土壌
中の働きについて一般的に言うことが難しい。しかし、
各種の有機性物質、特に難分解性の繊維素,リグニン等
を他の微生物とともに分解し、土壌肥沃のもとになる腐
植の生成に重要な働きをしており、又抗生物質の産生を
通してのミクロフローラ・コントロール面で重要な意義
をもつことは確かである。放線菌の培養は、ワックスマ
ンの培地(Waksman1919),分離源に肥沃な土壌,
又堆・厩肥を用い強力菌を集殖する。 (4) 土壌糸状菌及び酵母の培養物 土壌糸状菌の最も多く存在する場所は、細菌,放線菌と
同様土壌で、土壌中の糸状菌は当然植物根のある耕作土
に多く、特に根圏ではその働きも活発である。植物遺体
等の有機性物質の分解にあずかり、土壌の肥沃度に関係
する。糸状菌は主として分解の初期段階で活躍している
と考えられる。次に土壌酵母の働きについては不明の点
が多い。しかし、土壌中には相当数の酵母菌が存在し、
かつその含有する豊富なビタミン類や生育因子をめぐっ
て他微生物との共存共棲や土壌活性等に影響のあること
は確かである。土壌糸状菌や酵母の培養物は、ツアペッ
ク・ドックスの培地(Czapek & Dox,1910)を用
い、土壌或いは堆・厩肥より分離,培養する。
(3) Soil actinomycete culture It is generally difficult to say about the action of actinomycetes (Actinomycetales Buchanan, 1917) in soil. But,
It decomposes various organic substances, especially incombustible fibrin and lignin, together with other microorganisms, and plays an important role in the formation of humus, which is the source of soil fertility. Certainly, it has important significance in terms of microflora control. The culture of actinomycetes is Waxman's medium (Waksman 1919), fertilized soil as a separation source,
In addition, strong bacteria are collected by using the manure and manure. (4) Cultures of soil filamentous fungi and yeasts The most abundant locations of soil filamentous fungi are soils like bacteria and actinomycetes, and filamentous fungi in soils are naturally abundant in cultivated soil with plant roots, especially rhizosphere. Then, the work is also active. It is involved in the decomposition of organic substances such as plant remains and is related to soil fertility. It is considered that filamentous fungi are mainly active in the initial stage of decomposition. Next, there are many unclear points about the function of soil yeast. However, there are quite a few yeasts in the soil,
In addition, it is certain that the abundant vitamins and growth factors contained therein will affect coexistence with other microorganisms and soil activity. Soil filamentous fungi and yeast cultures are separated and cultured from soil or manure / manure using a Tuapeck Dox medium (Czapek & Dox, 1910).

【0034】(5) 好熱性バチルス属の培養物 一般に好気性,運動性,内生胞子を有する桿菌で、土
壌,葉面,枯草等自然界に広く分布する一群の細菌で、
ほとんどの菌株が強い熱抵抗性をもち、55℃以上でも
生育できるものが多いことから堆肥製造中の主要な微生
物であるという報告もある。又、バシトラシンやバシリ
シン等の抗菌物質を分泌することが、近年土壌植物病理
学の分野で注目されている。このようなことから、本菌
群が作物生産に利用しようとする試みが可能で、肥沃な
土壌や堆・厩肥等の懸濁液を80℃,10分間,加熱処
理して分離源とする。ワックスマンの培地(Waksman,19
22)を用い、50〜60℃,好気的に本菌群を集殖す
る。本発明では、これらの菌の単独又は混合培養を用い
る。 (6) 黄色色素産生菌の培養物 細菌の産生する黄色色素はカロチノイド系の色素であ
る。特に完熟堆肥中に数多く存在し、種類も多い。また
植物葉面にもよく存在する。これらを分離源とし、通常
の肉エキス培地又はペプトン・酵母エキス培地を用い、
25〜35℃,好気的条件下で培養,分離する。黄緑
色,黄色,黄褐色,紅色等の呈色によって容易に識別さ
れ、一般にフラボバクテリウム(Flavobacterium),ク
ロモバクテリウム(Chromobacterium),シュドモナス
(Pseudomonas),セラテラ(Serratia),光合成細菌
(Phototrophic bacteria)等に属する1株又は2株以
上の培養物が獲得される。
(5) Culture of thermophilic Bacillus genus Bacillus which is generally aerobic, motile, and has endospores, and is a group of bacteria widely distributed in the natural world such as soil, leaf surface, and hay.
It is also reported that most of the bacterial strains have strong heat resistance and can grow even at 55 ° C. or higher, and thus are major microorganisms during compost production. In addition, secreting antibacterial substances such as bacitracin and basilicin has attracted attention in the field of soil plant pathology in recent years. From these reasons, it is possible to try to utilize this bacterial group for crop production, and fertilized soil or a suspension of manure / manure is heat treated at 80 ° C. for 10 minutes to be used as a separation source. Waxman's medium (Waksman, 19
22), and aerobically collect the bacterial group at 50 to 60 ° C. In the present invention, single or mixed culture of these bacteria is used. (6) Culture of yellow pigment-producing bacteria Yellow pigment produced by bacteria is a carotenoid pigment. There are many types of ripe compost, and many types. It is also often found on the leaves of plants. Using these as a separation source, a normal meat extract medium or peptone-yeast extract medium,
Incubate and separate at 25-35 ° C under aerobic conditions. It is easily identified by colors such as yellow-green, yellow, yellow-brown, and red, and is generally flavobacterium (Flavobacterium), chromobacterium (Chromobacterium), pseudomonas (Pseudomonas), serratia (Serratia), phototrophic bacteria (Phototrophic bacteria) A culture of one or more strains belonging to, etc. is obtained.

【0035】以下、本発明の実施例の応用例について説
明する。 応用例.難分解性有機資材の高速コンポスト化
An application example of the embodiment of the present invention will be described below. Application example. High-speed composting of persistent organic materials

【0036】本発明で云うコンポストとは、compo
st,堆肥のことである。古来堆肥は、植物性有機物を
長時間嫌気的条件下で微生物的に分解したのに対し、現
在、なかでも本発明などにおける難分解性有機資材を対
象としたコンポスト化では、可能なかぎり好気的条件を
維持し、高温においてできるだけ短時間に微生物分解を
進めることを目的としてプロセスが組みたてられてい
る。このようなコンポスト化を高速コンポスト化と呼
ぶ。
The compost referred to in the present invention is compo.
st, compost. Since ancient times, compost decomposed plant organic matter microbially under anaerobic conditions for a long time, but nowadays, composting of persistent organic materials such as in the present invention is aerobic as far as possible. The process is designed to maintain microbial conditions and promote microbial degradation at high temperature in the shortest possible time. Such composting is called high-speed composting.

【0037】1.発酵分解剤 この応用例で施用した発酵分解剤は下記のような原材料
の配合割合である。 原材料の配合割合 (賦型剤:石灰岩岩粉1000kg当り) SK522菌株の多量培養物 4kg (0027記載の多量培養物) SK542菌株の多量培養物 4kg (0027記載の多量培養物) 土壌放線菌の培養物 2kg (0033記載の培養物) 好熱性バチルス属の培養物 2kg (0034記載の培養物) 黄色色素産生菌の培養物 2kg (0034記載の培養物) イーストエキス 500g
1. Fermentative decomposing agent The fermenting decomposing agent applied in this application example has the following blending ratio of raw materials. Mixing ratio of raw materials (vehicle: per 1000 kg of limestone rock powder) Large-scale culture of SK522 strain 4 kg (large-scale culture described in 0027) Large-scale culture of SK542 strain 4 kg (large-scale culture described in 0027) Culture of soil actinomycetes 2 kg (culture described in 0033) Culture of thermophilic Bacillus 2 kg (culture described in 0034) Culture of yellow pigment-producing bacterium 2 kg (culture described in 0034) Yeast extract 500 g

【0038】2.コンポストの製造 (1)製造装置:堅型減圧併流発酵槽、200l容、サ
クションによって給気し好気的条件で、加温および保
温、そして冷却も可能。 (2)試料:難分解性有機資材として、スギ,ヒノキ,
カシ,クヌギ等の針葉樹,広葉樹の混合ノコクズ。粒子
の大きさ8〜3mm。 ノコクズの成分組成(乾物当り%) ヘミセルロース 繊維素 リグニン 全窒素 灰分 C/N 13.5 45.4 27.3 0.15 1.7 287 (3)原材料の配合 ノコクズ 100kg 米ヌカ 10kg 硫安 1kg 尿素 1kg 過リン酸石灰(1kgを切り返し時に添加) 1kg+1kg 発酵分解剤 2kg 水分 約60%に調整 (4)コンポストの積込み ノコクズ100kgに、本発明の発酵分解剤、その他を
よく混合しながら水分が約60%になるように給水し発
酵槽中に積込む。 (5)製造経過 積込んだ原材料中に装着したサクション用パイプによっ
て可能な限り好気的条件で微生物分解を進める。2日目
で78〜85℃の最高温に達し、爾後10日間継続す
る。途中、1回切り返しを行ない、1kgの過リン酸石
灰を添加する。主発酵は2週間で終わる。35〜40
℃,2週間で後熟発酵が終了し、白色の放線菌で表面が
覆われる。
2. Manufacture of compost (1) Manufacturing equipment: rigid vacuum co-flow fermentation tank, 200 liters, can be heated, kept warm and cooled under aerobic conditions by supplying air by suction. (2) Sample: As a persistent organic material, cedar, cypress,
Mixed sawdust of conifers and broad-leaved trees such as oak and kunugi. Particle size 8-3 mm. Composition of Sawdust (% on dry matter) Hemicellulose Fibrin Lignin Total Nitrogen Ash Content C / N 13.5 45.4 27.3 0.15 1.7 287 (3) Blend of raw materials Sawdust 100kg Rice bran 10kg Ammonium sulfate 1kg Urea 1kg Calcium superphosphate (1 kg is added at the time of turning back) 1 kg + 1 kg Fermentation decomposing agent 2 kg Water content adjusted to about 60% (4) Loading of compost 100 kg of sawdust and the fermenting decomposing agent of the present invention and other water content are about 60%. And feed it to the fermenter. (5) Manufacturing process Microbiological degradation proceeds under aerobic conditions as much as possible by the suction pipe installed in the loaded raw materials. The maximum temperature of 78 to 85 ° C. is reached on the second day, and it continues for 10 days after that. On the way, cut back once and add 1 kg of lime superphosphate. Main fermentation ends in 2 weeks. 35-40
The post-ripening fermentation is completed at 2 ° C for 2 weeks, and the surface is covered with white actinomycetes.

【0039】3.結果および結論 有機資材の分解発酵は、野積または発酵槽内で行なわれ
る。分解発酵は微生物の作用によるが、コンポスト化
(堆肥化)の促進は、空気の流通をよくして好気性菌を
増殖させプロセス過程高温段階で分解,堆肥化する方
が、積んだまま放置して嫌気性菌による分解よりも、は
るかに速く分解腐熟化する。コンポストの腐熟過程で、
高温段階を経過さすか、また温度の上昇をおさえて低温
経過をとるかは、コンポストの品質との関連で一概に結
論できず、未だ論議の余地が残されている。しかし、す
くなくとも藁稈類の繊維素は微生物により分解されて低
分子化され、切れやすくなり、またノコクズ、その他の
木材質や資材ではボロボロになって取扱いが容易にな
る。そして、この高温段階で有機資材の分解腐熟化が急
速に進む。そのうえ、蓄熱し80℃前後の高温を経過す
ることが病害・病原菌・虫や雑草の種子を死滅させる。
さらに最近問題となっているコンポスト化の過程で発生
する悪臭も本発明の好気性高温高速コンポスト化方式で
はその心配がない。
3. Results and conclusions Degradation and fermentation of organic materials takes place in open-field or fermenters. Decomposition and fermentation are due to the action of microorganisms, but to promote composting (composting), it is better to improve the circulation of air to grow aerobic bacteria and decompose and compost at the high temperature stage of the process. It decomposes and ripens much faster than decomposition by anaerobes. During the compost ripening process,
Whether to go through the high-temperature stage or the low-temperature process by suppressing the temperature rise cannot be unequivocally concluded in relation to the quality of compost, and there is still room for debate. However, the fibrin of straw culm is decomposed by microorganisms to have a low molecular weight and easily cut, and at least sawdust and other wood materials and materials are fragile and easy to handle. Then, at this high temperature stage, decomposition and maturation of the organic material rapidly progresses. In addition, heat storage and high temperatures around 80 ° C kill the seeds of diseases, pathogens, insects and weeds.
Furthermore, the bad odor generated in the process of composting, which has recently become a problem, does not occur in the aerobic high temperature and high speed composting method of the present invention.

【0040】一般に好気性野積堆肥化法では主発酵6〜
8週間、後熟期間2〜3ケ月を要する。また古来の放置
したまま空気を流通しない、いわゆる嫌気性野積堆肥化
法では最低4〜6ケ月、あるいはそれ以上1ケ年以上放
置する必要がある。しかし、本発酵分解剤を使用する野
積堆肥化法では、2ケ月でほぼ完熟した製品となり、そ
の分析値も日本バーク堆肥協会および全国バーク堆肥工
業会の統一基準を上まる優れた品質のものとなる。そし
て、本応用例では、本発明の発酵分解剤の添加、およ
び堅型減圧併流発酵槽を使用することによって蓄熱
し、高温高速コンポスト化方式を確立した。すなわち、
主発酵10〜14日、80℃前後の高温が8〜10日間
継続する。この高温処理によって急速なる微生物分解が
進行し、ほぼ完熟の状態となるが、さらに2週間の後熟
発酵を続行し、それぞれの施用目的に適合する高品質の
製品とすることができた。なお、この新方式では発生す
る悪臭は顕著に低減され、その心配がなくなる。
In the aerobic open-air composting method, the main fermentation is generally 6 to
It requires 8 weeks and a post-ripening period of 2-3 months. Further, in the so-called anaerobic open-air composting method, in which air is not circulated as it has been for a long time, it is necessary to leave it for at least 4 to 6 months, or more than 1 year. However, in the Nozomi composting method using this fermenting decomposer, the product becomes almost ripe in two months, and the analysis value is of excellent quality that exceeds the unified standards of the Japan Burk Compost Association and the National Burk Compost Industry Association. Become. Then, in this application example, heat was accumulated by adding the fermentation decomposing agent of the present invention and using the rigid vacuum co-flow fermentation tank, and a high-temperature high-speed composting system was established. That is,
Main fermentation 10 to 14 days, high temperature around 80 ° C continues for 8 to 10 days. By this high-temperature treatment, rapid microbial decomposition proceeded and almost ripened state was reached, but after further ripening fermentation for 2 weeks, a high quality product suitable for each application purpose could be obtained. It should be noted that the bad smell generated by this new method is remarkably reduced, and there is no fear of it.

【0041】本発明の高温高速コンポスト化方式は、微
生物生理生態学の基礎的原理に基づくもので、堅型発酵
槽というひとつの閉鎖系内に添加された好熱性繊維素発
酵菌を主要菌とする有効菌群の生態系が誕生し、その健
全なる生育と旺盛なる増殖、そして有機物質の分解低分
子化にともなう微生物生態系の遷移を自然に、効果的か
つ確実、急速に進めるものである。以上のことを結論し
た主要なデータを次に示す。
The high-temperature high-speed composting method of the present invention is based on the basic principle of microbial physiology and ecology, and the thermophilic fibrin-fermenting bacterium added in one closed system called a rigid fermenter is the main bacterium. A new ecosystem of effective bacterial groups is born, which promotes the healthy growth, vigorous growth, and transition of the microbial ecosystem that accompanies the decomposition and low-molecularization of organic substances, effectively, reliably, and rapidly. . The main data that conclude the above are shown below.

【0042】4.主要な試験データ 表1.はコンポスト熟成にともなう色彩の変化、表2.
は積込み1ケ月後、後熟2週間後の製品の分析値であ
る。また表3.はコンポストの分解熟成にあたって出現
する微生群の動態をみたものである。
4. Main test data Table 1. Indicates the change in color with aging compost, Table 2.
Is the analysis value of the product one month after loading and two weeks after ripening. In addition, Table 3. Shows the dynamics of microbiomes that appear during decomposition and aging of compost.

【表1】 堆肥の品質を現場等で評価する場合、堆肥やコンポスト
の色彩、臭気、水分状態、堆積期間中の品温の経過等の
観察結果を総合的に判断すると、手軽に比較的正確に判
定を下すことができる。表1.は、コンポストの熟成に
伴う色の変化をマンセルの色彩図表を用いて記載した結
果である。積込み2週間後、主発酵の終了時、すでに完
熟堆肥の色彩を示し、同時に行なった品温の経過、水分
状態、臭気等からの判断の結果を総合的に勘案して、本
発明の高温高速コンポスト化方式では、積込み2週間後
の主発酵終了時まで、すでに完熟の状態にあることを示
している。
[Table 1] When assessing the quality of compost on-site, etc., it is easy and relatively accurate to make a judgment by comprehensively observing the observation results such as color of compost and compost, odor, moisture condition, and product temperature during the deposition period. be able to. Table 1. Is the result of describing the change of color with aging of compost using Munsell's color chart. Two weeks after loading, at the end of main fermentation, the color of the fully-ripened compost has already been shown, and the high temperature and high speed of the present invention is comprehensively considered in consideration of the results of the judgment of the temperature of the product, water condition, odor, etc. The composting method indicates that the plant is already in a mature state until the end of main fermentation 2 weeks after loading.

【表2】 この表は日本バーク堆肥協会と全国バーク堆肥工業会、
両協会の依頼によって提案された新品質基準(昭和55
年6月)によって測定した分析値を示したもので、その
結果はどの分析値も、この新規準を上まわり、本発明の
高温高速コンポスト化方式によると優良なる高品質のコ
ンポストを製造できることを示している。
[Table 2] This table shows the Japan Bark Compost Association and the National Bark Compost Industry Association,
New quality standards (Showa 55
June, 2006), and the results show that any analysis value exceeds this new level, and that the high temperature and high speed composting method of the present invention can produce excellent high quality compost. Shows.

【表3】 本表はコンポストの分解熟成にあたって出現する微生物
の動態をみたものである。積込み時、菌数が少なく、ま
た種類も少ない。分解熟成にともなって有効菌の数も増
え、種類も多くなり、複雑なものとなり、主発酵終了時
には最高となる。後熟終了時には好熱性細菌は胞子また
耐久体になり、そして放線菌の存在が最高となる。
[Table 3] This table shows the dynamics of microorganisms that appear during decomposition and aging of compost. When loaded, the number of bacteria is small and the variety is small. With decomposition and aging, the number of effective bacteria increases, the number of types increases, and it becomes complicated, and it becomes the highest at the end of main fermentation. At the end of post-ripening, the thermophilic bacterium becomes spores and is durable, and the presence of actinomycetes is highest.

【0043】[0043]

【発明の効果】以上の様に、本発明によれば、植物遺体
・動物遺体の有機資材を数週間から数ケ月でもって分解
発酵し、完熟した堆・厩肥にすることができ、有機資材
の高速処理、高速堆・厩肥化を可能とした。又、難分解
性有機資材をも高速に堆・厩肥化することができる。し
かも、悪臭の発生を少なく、完熟した堆・厩肥を大量生
産できるものとしている。
INDUSTRIAL APPLICABILITY As described above, according to the present invention, organic materials of plant and animal remains can be decomposed and fermented for several weeks to several months to produce a matured compost or manure. Enables high-speed processing, high-speed composting and manure conversion. In addition, it is possible to rapidly compost persistent organic materials even at high speed. In addition, it is possible to mass-produce fully matured manure and manure with less foul odor.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 下記1記載の好熱性繊維素分解菌クロス
トリジュウム・サーモセルムSK522(Clostriduim
thermocellum biovar.SK522,微工研条寄第345
9号)と、下記2記載のサーマス・アクアティクスSK
542(Thermus aquaticus biovar SK542,微工
研条寄第3382号)とを60℃以上の好熱性環境下で
共生的混合培養させた混合培養物又はこれを有効主成分
とする有機資材の発酵分解剤を、有機資材に施用して堆
・厩肥にすることを特徴とする有機資材の高速堆肥化
法。 記1 リグニン可溶化能を有し、生育適温が65〜72℃で、
40〜80℃の温度範囲で生育し、繊維素を旺盛に発酵
する好熱性繊維素分解菌クロストリジュウム・サーモセ
ルムSK522(Clostriduim thermocellum biovar.S
K522,微工研条寄第3459号) 記2 絶対好気性、生育適温が72〜76℃で、40〜82℃
の温度範囲で通常濃度の培地に生育し、作用適温75〜
85℃、作用水素イオン濃度pH=4.0〜11.3の
高温性広域作用水素イオン濃度活性のタンパク質分解酵
素とカロチノイド系黄色色素を産生するサーマス・アク
アティクスSK542(Thermus aquaticus biovar S
K542,微工研条寄第3382号)
1. A thermophilic fibrinolytic bacterium as described in 1 below, Clostridium thermocellum SK522 (Clostriduim).
thermocellum biovar.SK522, Micro Engineering Kenjiro 345
9) and Thermus Aquatics SK described in 2 below.
542 (Thermus aquaticus biovar SK542, Mikokenjoyori No. 3382) and a mixed culture obtained by symbiotic mixed culture in a thermophilic environment of 60 ° C. or higher, or a fermentative decomposition agent for an organic material containing the mixed culture as an active ingredient. A high-speed composting method for organic materials, characterized by applying to the organic materials to form compost / manure. Note 1 having a lignin solubilizing ability, a suitable growth temperature is 65 to 72 ° C.,
A thermophilic fibrin-degrading bacterium that grows in the temperature range of 40 to 80 ° C. and ferments actively, Clostriduim thermocellum biovar.S
K522, Mikori Kenjo No. 3459) Note 2 Absolute aerobic, optimum growth temperature is 72 to 76 ° C, 40 to 82 ° C.
It grows in a medium of normal concentration in the temperature range of
Thermos aquaticus SK542 (Thermus aquaticus biovar S) which produces a proteolytic enzyme and a carotenoid-type yellow pigment with a thermophilic broad-range action hydrogen ion concentration of 85 ° C and a action hydrogen ion concentration pH = 4.0 to 11.3
(K542, Micro Engineering Research Center No. 3382)
【請求項2】 有機資材がモミガラ・落葉・廃材・余剰
汚泥等の難分解性有機資材である請求項1記載の有機資
材の高速堆肥化法。
2. The high-speed composting method for an organic material according to claim 1, wherein the organic material is a hard-to-decompose organic material such as rice husk, defoliation, waste material, and excess sludge.
JP4322578A 1992-11-06 1992-11-06 High-speed composting method for organic materials Expired - Fee Related JPH0742184B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4322578A JPH0742184B2 (en) 1992-11-06 1992-11-06 High-speed composting method for organic materials

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4322578A JPH0742184B2 (en) 1992-11-06 1992-11-06 High-speed composting method for organic materials

Publications (2)

Publication Number Publication Date
JPH06191977A true JPH06191977A (en) 1994-07-12
JPH0742184B2 JPH0742184B2 (en) 1995-05-10

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ID=18145257

Family Applications (1)

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Country Link
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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1995013997A1 (en) * 1993-11-15 1995-05-26 Organic Gold Pty. Limited Fertiliser
WO2003055985A1 (en) * 2001-12-25 2003-07-10 Kabushiki Kaisha Sanyu Novel microorganism
CN107759397A (en) * 2016-08-18 2018-03-06 曹芳 A kind of agrochemical
CN115466140A (en) * 2022-10-20 2022-12-13 轩凯生物科技(山东)有限公司 Straw decomposition agent for improving water uniformity of organic fertilizer stack and application thereof

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1995013997A1 (en) * 1993-11-15 1995-05-26 Organic Gold Pty. Limited Fertiliser
WO2003055985A1 (en) * 2001-12-25 2003-07-10 Kabushiki Kaisha Sanyu Novel microorganism
KR100702258B1 (en) * 2001-12-25 2007-04-03 가부시끼가이샤 산유 Novel microorganism
US7371556B2 (en) 2001-12-25 2008-05-13 Kabushiki Kaisha Sanyu Microorganism
CN107759397A (en) * 2016-08-18 2018-03-06 曹芳 A kind of agrochemical
CN115466140A (en) * 2022-10-20 2022-12-13 轩凯生物科技(山东)有限公司 Straw decomposition agent for improving water uniformity of organic fertilizer stack and application thereof
CN115466140B (en) * 2022-10-20 2023-09-22 轩凯生物科技(山东)有限公司 Straw decomposition agent for improving moisture uniformity of organic fertilizer stack and application thereof

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