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JPH0233340B2 - - Google Patents
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JPH0233340B2 - - Google Patents

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Publication number
JPH0233340B2
JPH0233340B2 JP57198506A JP19850682A JPH0233340B2 JP H0233340 B2 JPH0233340 B2 JP H0233340B2 JP 57198506 A JP57198506 A JP 57198506A JP 19850682 A JP19850682 A JP 19850682A JP H0233340 B2 JPH0233340 B2 JP H0233340B2
Authority
JP
Japan
Prior art keywords
compost
pine
room
grain
added
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.)
Expired - Lifetime
Application number
JP57198506A
Other languages
Japanese (ja)
Other versions
JPS5988027A (en
Inventor
Kazuya Hashimoto
Hidekazu Imamura
Toyoaki Shinoki
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.)
Toyo Seikan Group Holdings Ltd
Original Assignee
Toyo Seikan Kaisha Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Toyo Seikan Kaisha Ltd filed Critical Toyo Seikan Kaisha Ltd
Priority to JP57198506A priority Critical patent/JPS5988027A/en
Publication of JPS5988027A publication Critical patent/JPS5988027A/en
Publication of JPH0233340B2 publication Critical patent/JPH0233340B2/ja
Granted legal-status Critical Current

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  • Micro-Organisms Or Cultivation Processes Thereof (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明はマツシユルーム種菌およびその製造方
法に関する。 マツシユルーム栽培に用いる種菌は、マツシユ
ルーム菌糸を培地に純粋培養したものであつて、
わが国で現在使用されているマツシユルーム種菌
は、馬きゆう肥または合成コンポストのような堆
肥にマツシユルーム菌糸を繁殖させた堆肥種菌
と、小麦、トーモロコシ、キビ、アワ等穀粒に菌
糸を繁殖させた穀粒種菌とに大別できる。 堆肥種菌は、耐熱性、耐病性、貯蔵性などの点
ですぐれ、高温時の保存や夏期の遠方への輸送を
安全に行なうことができ、しかもアンモニア分が
残つている菌床等不良コンポストへの活着性もす
ぐれている。一方菌床への接種に際しては、種菌
が大きな塊になつているために培養ビンからの取
出しが困難で(通常はピンをこわす)、また接種
前に手で種菌を細かくほぐさねばならない等取扱
いが面倒である。また接種は菌床に30cm四方に1
つぐらいの割合で表面から3cmぐらいの深さの穴
を掘つて種菌をこの穴に埋め込む点状接種法によ
つて行わねばならず、バルク方式等の機械播種が
不可能である。さらに種菌製造に要する培養期間
も比較的に長期間(約40日〜60日以上)を要す
る。 穀粒種菌は、穀粒の各々が独立して種菌保持体
であるため堆肥種菌に比べて発芽点が多く菌糸の
活着に適する。また接種はビンの口から穀粒種菌
を菌床の表面に散布する表面接種法又は混合接種
法により行うので取扱いが容易で、バルク方式等
機械播種に適する。さらに種菌製造に要する培養
日数は約20〜30日で比較的短い。しかし穀粒種菌
は一方において雑菌に侵され易く、穀粒の発酵熱
のため夏期の遠方への輸送が不可能であり、また
菌糸の老化が早く貯蔵性に乏しい上に不良コンポ
ストへの活着性が低く、さらに小動物等の食物と
なるためその被害も大きい等の欠点がある。 本発明は、このように従来の堆肥種菌と穀粒種
菌がそれぞれ長所とともに大きな欠点をも有する
点にかんがみなされたものであつて、それぞれの
長所を兼備しそれぞれの欠点を一掃した新規なマ
ツシユルーム種菌とその製造方法を提供すること
を目的とする。 特許請求の範囲第1項の発明にかかるマツシユ
ルーム種菌は、相互に分離独立した粒状に成形し
た堆肥の各粒にマツシユルーム菌糸を接種培養し
てなり、各粒は菌糸の成育に有効な栄養分を含む
糊剤を含有し、該糊剤は各粒の表面に被膜を形成
することなく、各粒内の堆肥を結合することを特
徴とするものである。また特許請求の範囲第2項
の発明にかかるマツシユルーム種菌の製造方法
は、堆肥を製造し、この堆肥に菌糸の成育に有効
な栄養分を含む糊剤を添加した後破砕して相互に
分離独立した粒状に成形し、かつ堆肥を粒状に成
形する前か後に、加熱殺菌によつて生じるアンモ
ニア、アミン等の有害アルカリ成分を堆肥の水洗
を行わずに中和捕捉するために充分な量の不揮発
性酸を添加し、該粒状となつた堆肥を培養容器に
充填して加熱殺菌したマツシユルーム菌糸をこの
粒状となつた堆肥に接種し培養するようにしたこ
とを特徴とするものである。 以下本発明にかかるマツシユルーム種菌および
その製造方法について詳細に説明する。 本発明にかかる粒状堆肥種菌の原料となる堆肥
は稲ワラ、麦ワラ、トウモロコシ、穂軸など植物
性廃棄物または馬きゆう肥を主原料として通常の
マツシユルーム用堆肥の製造に準じて製造する。 稲ワラを主原料とする場合の一例を示すと、稲
ワラを20cmに切断、1トン当り尿素10Kg、綿実カ
ス100Kgを混合し約2000の散水を行いながら硬
く積み込み高さ1.8m巾1.8mの堆積を造る。好気
性発酵を行う目的で8日目に通気、給水、混合の
ために切返しを行い、石膏25Kgを添加し硬く積み
込む。14日目に再び切返しを行い堆積の水分を65
%〜68%に調節する。堆積は通気性のよい疎積み
とする。18日目に最後の切返しを行い水分を68%
とする。馬きゆう肥の場合の一例を示すと、馬き
ゆう肥1トンにあらかじめ1000の吸水をさせて
おき、3日目に硫安4Kg、尿素2Kgを添加、散水
しながら疎積みする。6日目に炭酸カルシウム5
Kgを加えて切返し、8日目に最後の切返しを行つ
て水分を68%とする。いずれの堆肥の場合も浅箱
に入れて後発酵室内で空気を循環しながら50℃で
3日〜4日間保持する。冷却後の堆肥の水分は55
〜60%、窒素は1.8〜2.2%、PH6.8〜7.4のものが
好適である。 堆肥を培地として種菌を純粋培養するためには
高圧殺菌によつて堆肥中に存在する病害虫卵微生
物やその胞子を殺滅しなければならない。しかし
高圧殺菌を行うと堆肥中に蓄積された有効成分、
たとえば蛋白やバイオマスが熱分解しアンモニア
やアミン類を生ずる。これらはマツシユルーム菌
糸にとつて有害でその生育を阻害する。未熟な堆
肥にはもともとアンモニアが含まれており、殺菌
中に生成されるアンモニアとの相剰作用によつて
菌糸の生育はいつそう阻害される。堆肥中のアン
モニアは後発酵によつてある程度除去することは
可能であるが、加熱によりアルカリ成分を生ずる
物質の除去は充分ではない。そこで堆肥を培地と
して種菌を製造する際には殺菌前に堆肥を充分水
洗しアンモニア、アミンなどの有害アルカリ成分
およびそれらの給源を除去しなければならない。
しかし水洗によつてマツシユルーム菌糸の成長に
必要な養分、たとえば糖質、アミノ酸、ビタミン
類、無機成分、など水溶性成分の他、蛋白ヘミセ
ルローズ、リグニン、セルローズなど不溶性成分
も流失し成分的にも経済的にも損失である。 本発明にかかる種菌の製造方法においては、酒
石酸、クエン酸、リンゴ酸、フマール酸、シユウ
酸、リン酸等の不揮発性酸を殺菌前に堆肥に添加
しておくことにより、殺菌中に生成するアンモニ
アやアミン等の有害アルカリ成分を中和捕捉し、
水洗工程を省略するようにしている。これによつ
て菌糸の成育に必要な養分を流失することなく有
効に利用することができる。 通常堆肥のPHは6.8〜7.4を示し、上記不揮発酸
を堆肥の重量に対し0.01〜0.2%添加すれば堆肥
のPHは6.8〜7.0に調整できるが、高圧殺菌中に蛋
白分解が起りアンモニア、アミンを生ずるため、
PHは上昇するので、実用的には不揮発性酸は0.2
〜2.0%添加するのが安全である。なお、不揮発
性酸の添加は殺菌前にすればよいのであつて、堆
肥を粒状化する以前とは限らない。粒状化して培
養ビンに充填した後で添加してもよい。 本発明の方法においては、後述の工程により堆
肥を粒状化した後種菌培養中に粒状物がマツシユ
ルーム菌糸によつて完全におおわれるまでその形
状を安定に保つため、また粒状物の製造中に不整
形や細粒が生じると菌糸の生育が遅くなる。また
歩留りの低下を防止するために、堆肥中に各種の
糊剤、たとえばグアーガム、ローカストビーンガ
ム、タマリンド、タラガム、アラビヤガム、トラ
ガントガム、カラヤガム、ガツテイガム、ペクチ
ン、アルギン酸、キサンタンガム、ゼラチン、カ
ゼイン、グルテン、ポリアクリル酸ナトリウム、
カルボキシメチルセルローズ等を単一又は二種以
上を複合的に添加して保形性を向上させるように
している。上記物質は保形性のみならず菌糸の栄
養源としても利用される。それらの糊剤の堆肥重
量に対する添加量は次のとおりである。 タマリンド 0.2 % ローカストビーンガム 0.1 グアーガム 0.05 トラガントガム 0.3 カルボキシメチルセルローズ 0.2 澱 粉 0.5 アルギン酸 0.05 なお、マツシユルーム菌糸の生育を促進するた
め、堆肥中に各種の栄養強化物(各種アミノ酸、
大豆粕、綿実粕、ブドウ糖、果糖、マンニツト、
ソルビツト等)を、また成長促進剤としてビタミ
ンB1、ビオチン、米ぬか、大豆油ら植物性油脂
等を添加することができる。 上記のように堆肥を熟成した後各種添加物を堆
肥に添加し、堆肥と添加物との混合物を適当な破
砕機(たとえば大型ブレンダー)で破砕し小片と
なし水分約60%に調節する。この小片を細孔(た
とえば2〜3mm径)から圧出させると径5mm程度
の棒状に成形された堆肥が連続的に作られる。圧
出された堆肥は自重によつて落下し粒状に崩壊す
る。上記圧出による方法のほか破砕機によつて粘
土状ゲル状(泥状)になつた堆肥を打抜成形法そ
の他適当な方法によつて径5mm程度の粒子として
もよい。粒子は必ずしも球形でなく、円柱形、楕
円、円錐、立方体など適当でよいが大きさは一定
にするのが好ましい。 粒状に成形した堆肥を培養ビンに充填する。粒
状であるため機械操作による充填が容易である。
ビン詰めした粒状堆肥は115℃〜121℃で60分〜
100分ぐらい殺菌する。121℃で100分の殺菌によ
つても粒状堆肥は安定で、殺菌中に生じるアンモ
ニア等の二次分解物はあらかじめ堆肥中に添加さ
れていた不揮発性酸によつて中和され安定化され
る。また殺菌中に発生したアンモニアの一部は各
堆肥粒子間から拡散によつて外部に放散される。 殺菌により無菌状態となつた粒状堆肥にあらか
じめ純粋保存培地に純粋培養してある接種菌を移
植し一定期間培養する。移植後約1週間後に菌糸
は接種点の周囲に繁茂するので培養ビン中の粒状
堆肥を撹拌混合そ繁茂菌糸が粒状堆肥の各粒子間
に均一に分布繁植するようにする。培養期間(菌
糸が蔓延するのに要する日数)は約20日である。
培養完了後粒状の堆肥種菌を紙、ポリエチレン、
セロハン等からなる他の容器に移し包装して出荷
する。 以下本発明の実施例を掲げる。 実施例 1 堆肥(水分63.5%、窒素1.93%、PH7.33)1000
Kgに酒石酸5Kg、ブドウ糖5Kg、綿実粕1Kg、タ
マリンド2Kgを加えて混合した後破砕機で堆肥の
長さを3mm以下に破砕し直径3mmの孔より圧出さ
せ直径4〜6mmの粒状物を得た。殺菌後のPHは
6.8を示した。 実施例 2 堆肥(水分59.6%、窒素1.97%、PH7.40)1000
Kgにカルボキシメチルセルローズ2Kg、大豆粕2
Kgを加えて混合した後実施例1に従い粒状物を得
た。培養ビンに700g充填した後重炭酸ソーダ2
%、クエン酸2%、マンニツト1%を含む液50ml
を加えた。殺菌後のPHは7.0を示した。 本発明にかかる粒状堆肥種菌は、従来の堆肥種
菌と穀粒種菌のそれぞれの長所を兼備し、その上
それぞれの欠点を一掃した理想的なマツシユルー
ム種菌である。すなわち、耐熱性、耐病性、貯蔵
性、菌床への活着性にすぐれ、高温時の保存や夏
期の遠方への輸送も安全に行える上に、菌床への
接種作業がきわめて容易であり、バルク方式など
機械播種に適し、種菌製造時の培養日数が短期間
ですむ。 本発明にかかる粒状堆肥種菌の純粋培養および
菌床栽培の際の培養日数および諸性能を従来の堆
肥種菌および穀粒種菌と対比して次表に示す。
TECHNICAL FIELD The present invention relates to a pine seed starter and a method for producing the same. The seed fungus used for pine room cultivation is a pure culture of pine room mycelium in a medium,
The pine room starters currently used in Japan are compost starters in which pine room mycelium is propagated in compost such as horse manure or synthetic compost, and grain starters in which pine room mycelia are propagated in grains such as wheat, corn, millet, and millet. It can be broadly classified into grain seed bacteria. Compost seed bacteria have excellent heat resistance, disease resistance, and storage stability, and can be safely stored at high temperatures and transported to long distances in the summer, and can be used to store bad compost such as fungal beds with residual ammonia content. It also has excellent rooting ability. On the other hand, when inoculating a fungal bed, the inoculum is in large clumps, making it difficult to remove it from the culture bottle (usually by breaking the pins), and the inoculum must be broken up by hand before inoculation, making it difficult to handle. It's a hassle. In addition, inoculation should be done once per 30 cm square on the fungal bed.
This must be done using the spot inoculation method, which involves digging holes approximately 3 cm deep from the surface and burying the inoculum into these holes, making mechanical sowing such as bulk methods impossible. Furthermore, the culture period required for seed culture production is relatively long (approximately 40 days to 60 days or more). Grain starters have more germination points than compost starters because each grain is an independent starter holder, making them suitable for hyphae to take root. Inoculation is carried out by a surface inoculation method or a mixed inoculation method in which grain inoculum is sprayed onto the surface of the bacterial bed from the mouth of the bottle, making it easy to handle and suitable for mechanical sowing such as bulk methods. Furthermore, the number of culture days required to produce the seed culture is relatively short, about 20 to 30 days. However, grain inoculum is easily attacked by various bacteria, cannot be transported to long distances in the summer due to the heat of grain fermentation, and the mycelium ages quickly and has poor storage stability, as well as poor ability to take root in compost. There are drawbacks such as low yield, and the fact that it becomes food for small animals and causes great damage. The present invention has been made in consideration of the fact that the conventional compost starter and grain starter have both advantages and major drawbacks, and has developed a new pine room starter that combines the advantages of each and eliminates the drawbacks of each. The purpose is to provide a method for producing the same. The pine room seed fungus according to the invention of claim 1 is obtained by inoculating and culturing pine room mycelia into each grain of compost formed into mutually separated and independent granules, and each grain contains nutrients effective for the growth of the mycelia. It contains a sizing agent, and the sizing agent is characterized in that it binds the compost within each grain without forming a film on the surface of each grain. In addition, the method for producing a pine seed starter according to the invention of claim 2 includes producing compost, adding a glue containing nutrients effective for the growth of mycelia to the compost, and then crushing the compost to separate them from each other. A sufficient amount of non-volatile material to neutralize and capture harmful alkaline components such as ammonia and amines generated by heat sterilization before or after forming the compost into granules without washing the compost with water. This method is characterized in that the granulated compost is inoculated with pine room mycelium, which has been sterilized by heating the granular compost to which an acid has been added, and is then cultured. Hereinafter, the pine seed bacterium and the method for producing the same according to the present invention will be explained in detail. Compost, which is the raw material for the granular compost starter according to the present invention, is produced using plant waste such as rice straw, wheat straw, corn, and cobs, or horse manure as the main raw material, in accordance with the production of ordinary compost for pine room. An example of using rice straw as the main raw material is to cut rice straw into 20 cm pieces, mix 10 kg of urea and 100 kg of cottonseed scraps per ton, and load the mixture firmly while sprinkling water at approximately 20,000 m of water to a height of 1.8 m and a width of 1.8 m. Build a deposit of For the purpose of aerobic fermentation, on the 8th day, the tank was turned over for aeration, water supply, and mixing, and 25 kg of gypsum was added and loaded firmly. On the 14th day, cut again to remove 65% of the accumulated moisture.
Adjust to %~68%. The pile should be loosely stacked with good ventilation. On the 18th day, the final cut was made to reduce the moisture content to 68%.
shall be. To give an example of the case of Umaki Yuu Manure, 1 ton of Umaki Yuu Manure is made to absorb 1,000 ml of water in advance, and on the third day, 4 kg of ammonium sulfate and 2 kg of urea are added and loosely piled up while sprinkling water. Calcium carbonate 5 on day 6
Kg is added and cut back, and on the 8th day, a final cut is made to bring the moisture content to 68%. In either case, the compost is placed in a shallow box and kept at 50°C for 3 to 4 days while circulating air in the post-fermentation chamber. The moisture content of compost after cooling is 55
~60%, nitrogen 1.8~2.2%, and pH 6.8~7.4 are preferred. In order to pure culture the starter bacteria using compost as a medium, it is necessary to kill pests, egg microorganisms, and their spores present in the compost by high-pressure sterilization. However, when high-pressure sterilization is performed, the active ingredients accumulated in the compost,
For example, proteins and biomass are thermally decomposed to produce ammonia and amines. These are harmful to pine room mycelium and inhibit its growth. Immature compost naturally contains ammonia, and the interaction with the ammonia produced during sterilization often inhibits the growth of mycelium. Although ammonia in compost can be removed to some extent by post-fermentation, the removal of substances that produce alkaline components by heating is not sufficient. Therefore, when producing seed bacteria using compost as a medium, the compost must be sufficiently washed with water to remove harmful alkaline components such as ammonia and amines and their sources before sterilization.
However, by washing with water, nutrients necessary for the growth of pine room mycelium, such as water-soluble components such as carbohydrates, amino acids, vitamins, and inorganic components, as well as insoluble components such as protein hemicellulose, lignin, and cellulose, are washed away, resulting in a loss of composition. It is also an economic loss. In the inoculum production method according to the present invention, non-volatile acids such as tartaric acid, citric acid, malic acid, fumaric acid, oxalic acid, phosphoric acid, etc. are added to the compost before sterilization, so that the inoculum generated during sterilization is Neutralizes and captures harmful alkali components such as ammonia and amines,
The washing process is omitted. This allows the nutrients necessary for the growth of mycelia to be used effectively without being washed away. Normally, the pH of compost is 6.8 to 7.4, and if the nonvolatile acid mentioned above is added at 0.01 to 0.2% based on the weight of compost, the pH of compost can be adjusted to 6.8 to 7.0, but protein decomposition occurs during high-pressure sterilization, resulting in ammonia and amines. In order to cause
Since the PH increases, in practical terms non-volatile acids are 0.2
It is safe to add ~2.0%. Note that the nonvolatile acid may be added before sterilization, and not necessarily before granulating the compost. It may be added after being granulated and filled into culture bottles. In the method of the present invention, after the compost is granulated by the process described below, the shape of the granules is kept stable until they are completely covered with pine room mycelia during inoculum cultivation, and during the production of the granules, no The growth of hyphae is slowed down when formation of fine particles or formation of fine particles occurs. In order to prevent a decrease in yield, various thickening agents are added to the compost, such as guar gum, locust bean gum, tamarind, tara gum, gum arabic, tragacanth gum, karaya gum, guttay gum, pectin, alginic acid, xanthan gum, gelatin, casein, gluten, and polyester. sodium acrylate,
Carboxymethyl cellulose or the like is added singly or in combination of two or more to improve shape retention. The above substances are used not only for shape retention but also as a nutrient source for hyphae. The amounts of these glues added to the weight of compost are as follows. Tamarind 0.2% Locust bean gum 0.1 Guar gum 0.05 Gum tragacanth 0.3 Carboxymethyl cellulose 0.2 Starch 0.5 Alginic acid 0.05 In order to promote the growth of pine room mycelium, various nutritional enrichments (various amino acids,
Soybean meal, cottonseed meal, glucose, fructose, mannitrate,
sorbitol, etc.), and vitamin B 1 , biotin, rice bran, soybean oil, and other vegetable oils and fats can be added as growth promoters. After the compost is aged as described above, various additives are added to the compost, and the mixture of compost and additives is crushed with a suitable crusher (for example, a large blender) to form small pieces and the moisture content is adjusted to about 60%. When these small pieces are squeezed out through pores (for example, 2 to 3 mm in diameter), a rod-shaped compost with a diameter of about 5 mm is continuously produced. The pressed compost falls under its own weight and collapses into granules. In addition to the extrusion method described above, the compost made into a clay-like gel (sludge) by a crusher may be formed into particles with a diameter of about 5 mm by a punching method or other suitable method. The particles are not necessarily spherical and may have any suitable shape such as a cylinder, an ellipse, a cone, or a cube, but it is preferable that the size is constant. Fill the culture bottle with granulated compost. Since it is granular, it is easy to fill by mechanical operation.
Bottled granular compost is heated at 115℃ to 121℃ for 60 minutes.
Sterilize for about 100 minutes. Granular compost remains stable even after 100 minutes of sterilization at 121℃, and secondary decomposition products such as ammonia generated during sterilization are neutralized and stabilized by the non-volatile acid added to the compost in advance. . Further, a part of the ammonia generated during sterilization is released to the outside by diffusion from between each compost particle. The inoculum, which has been pure cultured in a pure preservation medium, is transplanted to the granular compost that has been rendered sterile by sterilization and cultured for a certain period of time. Approximately one week after transplantation, the hyphae will grow around the inoculation point, so the granular compost in the culture bottle is stirred and mixed so that the hyphae are evenly distributed and planted between each particle of the granular compost. The culture period (the number of days required for mycelia to spread) is approximately 20 days.
After culturing is complete, transfer the granular compost starter to paper, polyethylene,
Transfer to another container made of cellophane, etc., wrap and ship. Examples of the present invention are listed below. Example 1 Compost (moisture 63.5%, nitrogen 1.93%, PH7.33) 1000
After adding and mixing 5 kg of tartaric acid, 5 kg of glucose, 1 kg of cottonseed meal, and 2 kg of tamarind, the compost is crushed into pieces with a length of 3 mm or less using a crusher and extruded through holes with a diameter of 3 mm to produce granules with a diameter of 4 to 6 mm. Obtained. The pH after sterilization is
It showed 6.8. Example 2 Compost (moisture 59.6%, nitrogen 1.97%, PH7.40) 1000
Kg to carboxymethyl cellulose 2Kg, soybean meal 2Kg
After adding Kg and mixing, granules were obtained according to Example 1. After filling 700g into the culture bottle, add bicarbonate of soda 2
%, 2% citric acid, 1% mannitol 50ml
added. The pH after sterilization was 7.0. The granular compost starter according to the present invention is an ideal pine room starter that combines the advantages of conventional compost starters and grain starters, and eliminates the drawbacks of each. In other words, it has excellent heat resistance, disease resistance, storage stability, and ability to adhere to fungal beds, and can be safely stored at high temperatures and transported to long distances in summer, and is extremely easy to inoculate onto fungal beds. Suitable for mechanical seeding, such as bulk methods, and requires only a short period of time for culturing during seed production. The number of culture days and various performances of the granular compost starter according to the present invention during pure culture and fungal bed cultivation are shown in the following table in comparison with conventional compost starters and grain starters.

【表】 また本発明にかかる粒状堆肥種菌の製造方法に
よれば、従来の堆肥種菌製造法と異り、殺菌工程
前に堆肥に不揮発性酸を添加しておくことにより
水洗を行うことなく有害アルカリ成分を中和する
ようにしたので、菌糸の成長に必要な養分が流失
することがなく、培養ビンにおける接種菌の粒状
堆肥培地への活着は極めてすぐれている。また従
来は堆肥を培養ビンに充填する場合は無定形の長
い繊維の堆肥を培養ビンに硬く充填する(硬くし
ないと弾力性で規定量だけ充填できない)ため通
気性が悪くなり、それを改善するためビン詰めし
た後で中心に穴を開けるなど多くの労力や時間を
費したが、本発明の方法においては堆肥を粒状化
してから培養ビンに充填するために機械充填も可
能となり、粒子間に間隙を生ずるため空気の流通
が良くなり穴開けなどの手間が省ける。 さらに、本発明の方法においては、接種菌を培
養ビン中の粒状堆肥に移植する際接種菌は表面層
の粒子にとどまらずビン中央部の粒子にまで移動
し易いので活着はいつそう容易となる。また従来
の堆肥種菌では培養ビン中での撹拌混合は不可能
であつたが、粒状の場合には接種後約1週間後に
撹拌混合すれば接種点が培養ビン全体に広がるの
で菌糸の全体への繁殖が著しく促進される。
[Table] Also, according to the method for producing granular compost starter according to the present invention, unlike conventional methods for producing compost starter, a non-volatile acid is added to the compost before the sterilization process, which eliminates the need for washing with water. Since the alkaline component is neutralized, the nutrients necessary for the growth of mycelia are not washed away, and the inoculated bacteria in the culture bottle adhere to the granular compost medium very well. In addition, conventionally, when filling compost into culture bottles, amorphous long-fiber compost is hardly filled into the culture bottle (if it is not hard, it cannot be filled with the specified amount due to its elasticity), which results in poor air permeability, which can be improved. However, with the method of the present invention, mechanical filling is also possible because the compost is granulated and then filled into culture bottles, and there is no space between the particles. The gap allows for better air circulation and eliminates the need for drilling holes. Furthermore, in the method of the present invention, when the inoculated bacteria are transplanted to the granular compost in the culture bottle, the inoculated bacteria easily move not only to the particles on the surface layer but also to the particles in the center of the bottle, so that it is easy to take root. . In addition, with conventional compost starters, stirring and mixing in the culture bottle was impossible, but in the case of granular forms, if you stir and mix about a week after inoculation, the inoculation point will spread throughout the culture bottle, so it will be possible to spread the inoculation point throughout the culture bottle. Reproduction is significantly promoted.

Claims (1)

【特許請求の範囲】 1 相互に分離独立した粒状に成形した堆肥の各
粒にマツシユルーム菌糸を接種培養してなり、各
粒内の堆肥は菌糸の成育に有効な栄養分を含む糊
剤によつて結合されていることを特徴とするマツ
シユルーム種菌。 2 堆肥を製造し、この堆肥に菌糸の成育に有効
な栄養分を含む糊剤を添加した後破砕して相互に
分離独立した粒状に成形し、かつ堆肥を粒状に成
形する前か後に、加熱殺菌によつて生じるアンモ
ニア、アミン等の有害アルカリ成分を堆肥の水洗
を行わずに中和捕捉するために充分な量の不揮発
性酸を添加し、該粒状となつた堆肥を培養容器に
充填して加熱殺菌した後マツシユルーム菌糸をこ
の粒状となつた堆肥に接種し培養するようにした
マツシユルーム種菌の製造方法。
[Scope of Claims] 1. Pine room mycelium is inoculated and cultured in each grain of compost formed into separate and independent grains, and the compost inside each grain is treated with a sizing agent containing nutrients effective for the growth of mycelia. A pine mushroom seed fungus characterized by being combined. 2. Compost is produced, a sizing agent containing nutrients effective for the growth of mycelia is added to this compost, and then crushed and formed into mutually separated and independent granules, and heat sterilized either before or after forming the compost into granules. A sufficient amount of non-volatile acid is added to neutralize and capture harmful alkali components such as ammonia and amines produced by the compost without washing the compost, and the granulated compost is filled into a culture container. A method for producing a pine room seed fungus, which comprises inoculating the granular compost with pine room mycelium after heat sterilization and culturing it.
JP57198506A 1982-11-12 1982-11-12 Mushroom seed strain and production thereof Granted JPS5988027A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57198506A JPS5988027A (en) 1982-11-12 1982-11-12 Mushroom seed strain and production thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57198506A JPS5988027A (en) 1982-11-12 1982-11-12 Mushroom seed strain and production thereof

Publications (2)

Publication Number Publication Date
JPS5988027A JPS5988027A (en) 1984-05-21
JPH0233340B2 true JPH0233340B2 (en) 1990-07-26

Family

ID=16392262

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57198506A Granted JPS5988027A (en) 1982-11-12 1982-11-12 Mushroom seed strain and production thereof

Country Status (1)

Country Link
JP (1) JPS5988027A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH078B2 (en) * 1987-12-15 1995-01-11 寳酒造株式会社 Mushroom artificial cultivation method

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5561730A (en) * 1978-10-31 1980-05-09 Saito Chiyouichi Production of seed germ for mashroom cultivation

Also Published As

Publication number Publication date
JPS5988027A (en) 1984-05-21

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