JP2005040018A - Mushroom bed culture method - Google Patents

Mushroom bed culture method Download PDF

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Publication number
JP2005040018A
JP2005040018A JP2003200319A JP2003200319A JP2005040018A JP 2005040018 A JP2005040018 A JP 2005040018A JP 2003200319 A JP2003200319 A JP 2003200319A JP 2003200319 A JP2003200319 A JP 2003200319A JP 2005040018 A JP2005040018 A JP 2005040018A
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JP
Japan
Prior art keywords
culture bag
culture
bag
mushroom
mushroom bed
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Pending
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JP2003200319A
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Japanese (ja)
Inventor
Kaori Hamano
香織 浜野
Shigeki Tanimoto
茂樹 谷本
Yasuo Oneda
安雄 大根田
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MORI SANGYO KK
Original Assignee
MORI SANGYO KK
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Publication date
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Priority to JP2003200319A priority Critical patent/JP2005040018A/en
Publication of JP2005040018A publication Critical patent/JP2005040018A/en
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Abstract

<P>PROBLEM TO BE SOLVED: To provide a mushroom bed culture method by which breeding condition for mycelia is favorably maintained, moisture content in a mushroom bed can be suppressed at a lower level, carpophores are appropriately generated, minimization and deformation of mushrooms to be obtained are prevented, and big mushrooms can be harvested in large quantity. <P>SOLUTION: The mushroom bed culture method comprises charging spawned culture soil into a synthetic resin film culture bag to culture spawns. In the method, the mushroom bed and the culture bag is prevented from sticking to each other via air pressure under such a condition that the surface of the mushroom bed in the culture bag turns brown to the extent of nearly 80%, and the inner part of the culture bag is allowed to communicate with the outer air by cutting off part of the culture bag or making cuts in the culture bag. <P>COPYRIGHT: (C)2005,JPO&NCIPI

Description

【0001】
【発明の属する技術分野】
この発明は、きのこの菌床栽培、特に培養袋を使用するしいたけの床栽培に関するもので、きのこ栽培技術に属するものである。
【0002】
【従来の技術】
種菌を植付けた培地を培養袋に充填して行うきのこの菌床栽培は、培養瓶を使用する菌床栽培、さらには、原木を使用するほだ木栽培と共に広く行われている方法で、操作に熟練を必要とせず、手数も掛らないという優れた方法である。
【0003】
なかでも、しいたけの菌床栽培は、主として広葉樹を原料とした粒度の異なるオガコと、米ぬか又はふすま等の栄養分とを適当な割合で混合し、水分を60〜65%に調整した培地を、プラスチック製の培養袋に充填した後、高圧蒸気滅菌等にて培地を滅菌し、種菌を接種し、清浄な培養室内で、密閉した培養袋内で培養して、菌糸を蔓延させるというもので、菌糸が蔓延した菌床は、培養袋を破袋して取り出され、刺激を与えられ、子実体の発芽が促され、所定環境条件に保持されたきのこ栽培室で、きのこが生育・栽培される。
【0004】
この培養袋は、ヒートシールなどにより袋の開口部を密封した状態で使用されるが、菌の生育には空気が必要であるため、通常、培養袋の上部に、通気用の穴を設けられるとともに、この穴に、空気は通過するが雑菌は通過させない通気性フィルターが設けられ、雑菌や埃の侵入を阻止しながら、空気が供給されるように構成されている。
【0005】
【発明が解決しようとする課題】
培養袋内の培地に接種された菌は、菌床の下部に向かって、徐々に繁殖していくもので、菌糸が成長するために必要な空気の供給と、成長することによって排出される二酸化炭素の排除が効率的に行われる必要があるが、通気性フィルターに水分のある培地が接触すると、雑菌が侵入しやすいため、止むを得ない措置として、通気性フィルターが上部のみに設けられている。
【0006】
そのため、菌糸が菌床下部に繁殖していくに従って、空気の供給と二酸化炭素の排出が悪くなり、菌糸の繁殖条件が悪化し、菌糸の培養基間が長くなったり、菌糸の活力が低下するうえ、菌床内の含水率も高まり、培養袋から菌床を取り出した際、急激な水分の放出による刺激のため、子実体が大量に発生し、目的とするきのこの小型化や奇形化が著しいものとなることがある。
【0007】
これらの問題点を解消するため、種々の提案がなされているが、それらの一部を例示すると、以下のとおりである。
1)きのこの菌床栽培に使用する培養袋の、開口部から底部にかけて空気や水蒸気を通しバクテリア、菌糸、カビ類やきのこ類の胞子などをほとんど通さないフィルターと中孔を設け、培養袋の内部と外部とを空気や水蒸気が通過できるようにした培養袋を使用する(特許文献1参照)。
2)きのこの菌床栽培に使用する培養袋の材質を、ポリ4−メチル−1−ペンテン系重合体フィルムとする(特許文献2参照)。
【0008】
これらの提案は、上記問題点を解消せんとするものであるが、培養袋に特殊な材質のフィルムを使用する、あるいは特殊な構造とするもので、価格面での問題を発生させるばかりでなく、底部までフィルターを設けることは、上記したように、フィルターが水分を含む培地に接触することとなり、雑菌の侵入の恐れが発生するものである。
【0009】
【特許文献1】
特開平10−33058号(特許請求の範囲)
【特許文献2】
特開2002−188950号(特許請求の範囲)
【0010】
この発明はかかる現状に鑑み、培地に接種した種菌を培養袋の中で培養するに際し、きのこ菌床栽培の培養工程の途中、特に培養中の菌床の表面が概ね80%程度褐変化した状態で、培養袋の一部を切取り、又は切れ目を入れることにより、袋体内部を外気と強制的に連通させれば、含水率の上昇を抑制し、培養期間を短縮させることを見出して、この発明を完成したものである。
【0011】
【課題を解決するための手段】
すなわち、この発明の請求項1に記載の発明は、
種菌を接種した培地を、合成樹脂フィルム製の培養袋に充填して栽培するに際し、
培養袋内の菌床の表面が概ね80%程度褐変化した状態で、空気圧によって菌床と培養袋との張付きを解消し、かつ培養袋の一部を切取り、又は培養袋に切れ目を入れることによって、培養袋内部を外気と連通させること
を特徴とするきのこの菌床栽培方法である。
【0012】
また、この発明の請求項2に記載の発明は、
請求項1に記載のきのこの菌床栽培方法において、
前記空気圧によって菌床と培養袋との張付き解消は、
培養袋を変形させることによって行うこと
を特徴とするものである。
【0013】
また、この発明に請求項3に記載の発明は、
請求項1又は2に記載のきのこの菌床栽培方法において、
前記培養袋の一部の切取り、又は培養袋への切れ目は、
菌床の含水率を低下させるに十分な大きさに行うこと
を特徴とするものである。
【0014】
また、この発明に請求項4に記載の発明は、
請求項1乃至3のいずれかに記載のきのこの菌床栽培方法において、
前記培養袋の一部を切取りは、
培養袋に設けられたフィルターの除去によって行うこと
を特徴とするものである。
【0015】
また、この発明に請求項4に記載の発明は、
請求項1乃至3のいずれかに記載のきのこの菌床栽培方法において、
前記培養袋の一部への切れ目の形成は、
培養袋に設けられたフィルターの近傍に形成すること
を特徴とするものである。
【0016】
【発明の実施の形態】
以下、この発明のきのこ菌床栽培の好ましい実施形態を具体的に説明する。
<培地調製>
広葉樹のおが屑、チップダスト、コーンコブ等の基材と米ぬか、フスマ等の栄養源を、乾物重量比で3:4〜4:1の割合で攪拌混合すると共に含水率を60〜65%に調整することにより、培地を調製する。
<袋詰め>
上部に所要径の穴を形成し、この穴の内側に空気や水蒸気のみを通し、バクテリア、菌糸、カビ類やきのこ類の胞子などをほとんど通さないフィルターを貼着したポリプロピレン等のポリオレフィン製の培養袋に、調製した培地1〜3kgを詰める。
<殺 菌>
前記で得た培地の充填された培養袋を、温度120℃で60〜120分間蒸気加熱し、培地を殺菌する。
<接 種>
殺菌したのち放冷した培地の中央部にφ2〜3cm程度の穴を上下方向に形成し、この穴内に、例えば、ポテト・デキストロースブロス液体培地で温度25℃、2〜3週間培養したしいたけ菌株を、1袋あたり20〜30ml無菌的に植え付ける。
<培 養>
接種済みの培地(培養基)を温度25℃程度、湿度50〜70%の条件下に、通常30〜60日間かけて菌糸を蔓延させる。
菌糸の蔓延した培地(培養基)は、さらに同様な条件下に60〜120日間維持して、菌糸に原基形成能力を持たせる。この状態は、通常完熟と言われる。
<発 生>
完熟した培養基を袋から完全に取出し、表面を裸出させ(除袋)、散水により刺激を与え、温度10〜20℃、湿度80〜90%、照度150〜300ルクスの条件下で、子実体原基を形成させ、さらに成熟子実体を形成させる。
【0017】
この発明のきのこの菌床栽培方法においては、培地に接種した種菌を培養する工程途中に、培養袋の一部を切取り、又は培養袋に切れ目を入れて、培養袋内部を外気と連通させ、培養袋内の含水率の上昇を抑え、若しくは低下させ、除袋した培養基から大量の子実体を発生させ、小型化と奇形を軽減する。
【0018】
この培養袋の一部を切取り、又は培養袋に切れ目を入れる部位は、培養袋の切取りは任意の箇所で良いが、培養袋の大きさや培地の充填量などを勘案し、また、培養袋内の含水率の上昇を抑え、若しくは低下させるために、培養袋には、通常、長さ(高さ)約380mmの培養袋の場合には、下から約300mm程度の位置におよそφ25mm程度の通気穴を塞いでフィルターが設けられているため、そのフィルターを取外すことが、工程管理や品質の安定性などの面から好都合で、この発明にとり好ましいことである。
【0019】
なお、培養袋に入れる切り目は、上記と同様に、培養袋の大きさや培地の充填量などを勘案し、培養袋内の含水率の上昇を抑え、若しくは低下させることができるように、その位置や長さが決められるが、上記と同様に、フィルターを基準とし、当該フィルターに切り目を入れるのが好ましい。
【0020】
この工程は、通常、培養工程の後期で、より具体的には、除袋前20〜50日の間で、菌床表面が概ね80%程度褐変化するおよそ3週間程度前で、より具体的には、培養が90日間という短い場合は、除袋前20〜30日の間に、培養が180日間という長い場合は、除袋前30〜50日の間に行われる。
【0021】
すなわち、菌床の表面が概ね80%程度に褐変化すると、培養基の表面と培養袋の内面とが張付いて、培養袋内の空気の流通が阻害されるので、この時点で、培養袋内の空気圧を利用して、培養基の表面と培養袋の内面との張付きを解消させると同時に、培養袋内の含水率の上昇を抑え、若しくは低下させるために、培養袋の一部切取りもしくは培養袋の一部切開を行なうもので、前記張付きの解消は、培養袋の上部を折り畳むなどの手段で培養袋を変形させ、それによる空気圧を利用して、培地(培養基)の表面と培養袋との張付きを解除することが望ましい。
【0022】
【実施例】
以下、実施例により、この発明のきのこの菌床栽培方法を、より詳細に説明する。
【0023】
<実施例1〜4、比較例1>
広葉樹のおが屑で、粒径が2、36〜0、83mmと粒径が0.83mm以上の二種を、乾物重量比で1:1に混合したものに、菌床しいたけ用の栄養源(デルトップ:商品名)を、おが屑と栄養源が3:1(絶乾重量比)になるように混合し、20分間攪拌した。さらに、含水量が60〜64%になるように水を添加しながら40分間攪拌して培地を調製した。
調製した培地1300gを、高さ38cmのフィルター付き培養袋に充填し、加圧して高さが16〜17cmに収まるようにした。
培地温度118℃で45分間高圧殺菌した後放冷し、培地内温度が25℃以下になった時点で、しいたけ菌種(cg44)を15〜22cc接種した。
菌種の接種された培地を、平均温度22.1℃、平均湿度72.4%の培養室で培養した。
培養中に培養袋のフィルターを、それぞれ
a.接種後95日(除袋前40日:実施例1)
b.接種後105日(除袋前30日:実施例2)
c.接種後115日(除袋前20日:実施例3)
d.接種後125日(除袋前10日:実施例4)
に切除し、更に培養を続け、総計で135日培養した。
最後までフィルターを切除せずに、135日培養したものを比較例1とした。接種後135日培養した、実施例1〜4及び比較例1の培地(培養基)を培養袋から取り出し(除袋)、培養袋の除去による刺激により、子実体の発生を促し、温度15〜17℃に管理された発生室で、除袋後21日目、以下21日毎に浸水を行いながら、子実体を生育させた。
フィルターの切除の有無、切除日が異なる、実施例1〜4及び比較例における除袋時の菌床重量、菌床含水率、1床当りの平均収量、平均個数、1個当りの平均重量、45mm以上に生育した大型きのこの個数比率について、それぞれ測定した結果を表1に示す。
【0024】
【表1】

Figure 2005040018
【0025】
【発明の効果】
この発明のきのこ菌床栽培方法は、種菌の培養工程において、菌床の表面がおおむね80%程度に褐変化した段階で、培養袋の一部を切取り、又は培養袋に切れ目を入れるという簡単な操作、特に、培養袋に設けられているフィルターを培養途中で取り除くという簡単な操作で、菌糸の繁殖条件を良好に維持するうえ、菌床内の含水率を低めに抑えることができるもので、それにより、子実体が適正に発生し、目的とするきのこの小型化や奇形化が避けられ、大型のきのこを多量に収穫することを可能にするという優れた効果を奏するものである。[0001]
BACKGROUND OF THE INVENTION
The present invention relates to fungus bed cultivation of mushrooms, and particularly to floor cultivation of shiitake mushrooms using culture bags, and belongs to the mushroom cultivation technique.
[0002]
[Prior art]
Mushroom bed cultivation, which is performed by filling the culture medium inoculated with the inoculum into a culture bag, is a method widely used with fungus bed cultivation using culture bottles, and further with sardine cultivation using raw wood. It is an excellent method that does not require skill and labor.
[0003]
Among them, Shiitake fungus bed cultivation is mainly made of broad-leaved tree raw sawfish with different particle sizes mixed with nutrients such as rice bran or bran at a suitable ratio, and a medium adjusted to 60-65% moisture is made of plastic. After filling a culture bag made of sterilization, the medium is sterilized by high-pressure steam sterilization, etc., inoculated with inoculum, and cultured in a sealed culture bag in a clean culture chamber to spread the mycelium. The fungus bed that has spread is taken out by breaking the culture bag, stimulated, encouraged to germinate the fruit body, and grown and cultivated in a mushroom cultivation room maintained at a predetermined environmental condition.
[0004]
This culture bag is used in a state in which the opening of the bag is sealed by heat sealing or the like, but since air is necessary for the growth of bacteria, a vent hole is usually provided in the upper part of the culture bag. In addition, an air-permeable filter that allows air to pass through but does not allow germs to pass therethrough is provided in the hole, so that air is supplied while preventing invasion of germs and dust.
[0005]
[Problems to be solved by the invention]
The fungus inoculated in the culture medium in the culture bag gradually grows toward the bottom of the fungus bed. The supply of air necessary for the growth of mycelia and the dioxide emitted by the growth. It is necessary to eliminate carbon efficiently, but if a medium with moisture comes into contact with the air-permeable filter, it is easy for bacteria to enter. Yes.
[0006]
Therefore, as the mycelium propagates in the lower part of the mycelium, the supply of air and the discharge of carbon dioxide become worse, the hyphal growth conditions worsen, the length of the mycelium culture medium becomes longer, and the hyphal viability decreases. The moisture content in the fungus bed is also increased, and when the fungus bed is taken out of the culture bag, a large amount of fruiting bodies are generated due to stimulation by sudden release of moisture, and the target mushrooms are significantly reduced in size and deformed It can be a thing.
[0007]
In order to solve these problems, various proposals have been made, and some of them are exemplified as follows.
1) A culture bag used for mushroom fungus bed cultivation is provided with a filter and a medium hole through which air and water vapor are passed from the opening to the bottom so that bacteria, mycelia, fungi and mushroom spores are hardly passed. A culture bag in which air and water vapor can pass between the inside and the outside is used (see Patent Document 1).
2) The material of the culture bag used for fungus bed cultivation of mushrooms is a poly-4-methyl-1-pentene polymer film (see Patent Document 2).
[0008]
These proposals are intended to eliminate the above-mentioned problems, but they use a special material film for the culture bag or have a special structure, which not only causes problems in terms of price. When the filter is provided up to the bottom, as described above, the filter comes into contact with the medium containing moisture, and there is a risk of invasion of various bacteria.
[0009]
[Patent Document 1]
JP-A-10-33058 (Claims)
[Patent Document 2]
JP 2002-188950 (Claims)
[0010]
In view of the present situation, the present invention, when cultivating the inoculum inoculated in the culture medium in the culture bag, during the cultivation process of the mushroom fungus bed cultivation, in particular, the state that the surface of the fungus bed during the cultivation is browned by about 80% Then, by cutting a part of the culture bag or making a cut, it is found that if the bag body is forced to communicate with the outside air, the increase in the moisture content is suppressed and the culture period is shortened. The invention has been completed.
[0011]
[Means for Solving the Problems]
That is, the invention according to claim 1 of the present invention is
When cultivating the culture medium inoculated with the inoculum in a culture bag made of synthetic resin film,
With the surface of the fungus bed in the culture bag browned by about 80%, the sticking between the fungus bed and the culture bag is eliminated by air pressure, and a part of the culture bag is cut or cut into the culture bag By this, it is a fungus bed cultivation method of the mushroom characterized by making the inside of a culture bag communicate with outside air.
[0012]
The invention according to claim 2 of the present invention is
In the method for cultivating the mushroom fungus according to claim 1,
Release of sticking between the bacteria bed and the culture bag by the air pressure,
This is performed by deforming the culture bag.
[0013]
Further, the invention according to claim 3 is the present invention.
In the fungus bed cultivation method of the mushroom according to claim 1 or 2,
Cutting a part of the culture bag, or a break in the culture bag,
It is characterized by being performed in a size sufficient to reduce the moisture content of the fungus bed.
[0014]
Further, the invention according to claim 4 is the present invention.
In the mushroom bed cultivation method in any one of Claims 1 thru | or 3,
Cutting out a part of the culture bag,
This is performed by removing the filter provided in the culture bag.
[0015]
Further, the invention according to claim 4 is the present invention.
In the mushroom bed cultivation method in any one of Claims 1 thru | or 3,
The formation of a cut in a part of the culture bag,
It is characterized by being formed in the vicinity of a filter provided in the culture bag.
[0016]
DETAILED DESCRIPTION OF THE INVENTION
Hereinafter, preferred embodiments of the mushroom fungus bed cultivation of the present invention will be specifically described.
<Medium preparation>
A base material such as hardwood sawdust, chip dust, and corn cob and a nutrient source such as rice bran and bran are stirred and mixed at a weight ratio of 3: 4 to 4: 1 and the water content is adjusted to 60 to 65%. Prepare the medium.
<Packing>
A culture made of polyolefin, such as polypropylene, with a hole of the required diameter formed in the upper part, a filter that passes only air and water vapor inside this hole, and hardly passes bacteria, mycelia, fungi and mushroom spores, etc. A bag is filled with 1-3 kg of the prepared medium.
<Bactericidal>
The culture bag filled with the medium obtained above is steam-heated at 120 ° C. for 60 to 120 minutes to sterilize the medium.
<Kind>
A hole with a diameter of about 2 to 3 cm is formed vertically in the center of the sterilized and allowed to cool, and in this hole, for example, a shiitake strain cultured in a potato-dextrose broth liquid medium at a temperature of 25 ° C. for 2-3 weeks. Aseptically plant 20-30 ml per bag.
<Culture>
The inoculated medium (culture medium) is allowed to spread over 30 to 60 days under conditions of a temperature of about 25 ° C. and a humidity of 50 to 70%.
The medium (culture medium) in which the mycelium has spread is further maintained under similar conditions for 60 to 120 days so that the mycelium has the ability to form a primordium. This state is usually said to be ripe.
<Development>
Remove the fully-ripened culture medium from the bag, expose the surface naked (unbag removal), stimulate with watering, and under the conditions of temperature 10-20 ° C, humidity 80-90%, illuminance 150-300 lux A primordial group is formed, and a mature fruit body is formed.
[0017]
In the mushroom bed cultivation method of the present invention, in the middle of the step of culturing the inoculum inoculated on the medium, a part of the culture bag is cut or a cut is made in the culture bag to communicate the inside of the culture bag with the outside air, Suppressing or reducing the moisture content in the culture bag, generating a large number of fruiting bodies from the removed culture medium, and reducing size and malformation.
[0018]
A part of this culture bag is cut or cut into the culture bag. The culture bag may be cut off at any location, but considering the size of the culture bag and the filling amount of the medium, etc. In order to suppress or reduce the increase in the moisture content of the culture bag, normally, in the case of a culture bag having a length (height) of about 380 mm, an aeration of about φ25 mm at a position of about 300 mm from the bottom. Since the filter is provided by closing the hole, removing the filter is advantageous in terms of process control and quality stability, and is preferable for the present invention.
[0019]
In the same way as above, the cut in the culture bag is positioned so that the increase in the moisture content in the culture bag can be suppressed or reduced in consideration of the size of the culture bag and the filling amount of the culture medium. Although the length is determined, it is preferable to make a cut in the filter based on the filter as described above.
[0020]
This step is usually more late in the culturing step, more specifically, about 20 to 50 days before unpacking, about 3 weeks before the surface of the fungus bed changes by about 80%, and more specifically. When the culture is as short as 90 days, it is performed between 20 and 30 days before unpacking, and when the culture is as long as 180 days, it is performed between 30 and 50 days before unpacking.
[0021]
That is, when the surface of the fungus bed changes to approximately 80% browning, the surface of the culture medium and the inner surface of the culture bag stick to each other and the air flow in the culture bag is inhibited. In order to eliminate the sticking between the surface of the culture medium and the inner surface of the culture bag by using the air pressure of the culture bag, the culture bag is partially cut or cultivated in order to suppress or reduce the increase in the moisture content in the culture bag. The bag is partially incised. To eliminate the sticking, the culture bag is deformed by means such as folding the upper part of the culture bag, and the air pressure is applied to the surface of the culture medium (culture medium) and the culture bag. It is desirable to release the sticking.
[0022]
【Example】
Hereinafter, the fungus bed cultivation method of the mushroom of the present invention will be described in more detail with reference to examples.
[0023]
<Examples 1-4, Comparative Example 1>
Hardwood sawdust, mixed with two kinds of particles with a particle size of 2, 36-0, 83 mm and a particle size of 0.83 mm or more in a dry matter weight ratio of 1: 1. Top: trade name) was mixed so that sawdust and nutrients were 3: 1 (absolute dry weight ratio) and stirred for 20 minutes. Further, the medium was prepared by stirring for 40 minutes while adding water so that the water content was 60 to 64%.
The prepared culture medium (1300 g) was filled in a culture bag with a filter having a height of 38 cm and pressurized so that the height was 16 to 17 cm.
After sterilizing under high pressure at a medium temperature of 118 ° C. for 45 minutes, the mixture was allowed to cool and when the temperature in the medium reached 25 ° C. or lower, 15-22 cc of Shiitake fungus species (cg44) was inoculated.
The medium inoculated with the bacterial species was cultured in a culture room having an average temperature of 22.1 ° C. and an average humidity of 72.4%.
During culture, each of the culture bag filters was a. 95 days after inoculation (40 days before bag removal: Example 1)
b. 105 days after inoculation (30 days before bag removal: Example 2)
c. 115 days after inoculation (20 days before bag removal: Example 3)
d. 125 days after inoculation (10 days before bag removal: Example 4)
The culture was further continued and cultured for a total of 135 days.
A sample that was cultured for 135 days without removing the filter to the end was designated as Comparative Example 1. The culture medium (culture medium) of Examples 1 to 4 and Comparative Example 1 cultured for 135 days after inoculation was removed from the culture bag (bag removal), and the generation of fruiting bodies was promoted by stimulation by removing the culture bag, and the temperature was 15 to 17 In the generation room controlled at 0 ° C., fruiting bodies were grown on the 21st day after the bag removal, while being submerged every 21 days thereafter.
Existence of excision of filter, excision date is different, bacteria bed weight at the time of bag removal in Examples 1 to 4 and Comparative Example, moisture content of bacteria bed, average yield per bed, average number, average weight per piece, Table 1 shows the measurement results of the number ratio of large mushrooms grown to 45 mm or more.
[0024]
[Table 1]
Figure 2005040018
[0025]
【The invention's effect】
The mushroom fungus bed cultivation method of the present invention is a simple method in which a part of the culture bag is cut or a cut is made in the culture bag when the surface of the fungus bed is browned to about 80% in the inoculum culture process. The operation, especially the simple operation of removing the filter provided in the culture bag in the middle of the culture, to maintain good hyphae growth conditions, and to keep the moisture content in the fungus bed low, As a result, fruit bodies are properly generated, miniaturization and malformation of the target mushroom can be avoided, and a large amount of large mushrooms can be harvested.

Claims (5)

種菌を接種した培地を、合成樹脂フィルム製の培養袋に充填して栽培するに際し、
培養袋内の菌床の表面が概ね80%程度褐変化した状態で、空気圧によって菌床と培養袋との張付きを解消し、かつ培養袋の一部を切取り、又は培養袋に切れ目を入れることによって、培養袋内部を外気と連通させること
を特徴とするきのこの菌床栽培方法。
When cultivating the culture medium inoculated with the inoculum in a culture bag made of synthetic resin film,
With the surface of the fungus bed in the culture bag browned by about 80%, the sticking between the fungus bed and the culture bag is eliminated by air pressure, and a part of the culture bag is cut or cut into the culture bag The fungus bed cultivation method of the mushroom characterized by making the inside of a culture bag connect with external air by this.
前記空気圧によって菌床と培養袋との張付き解消は、
培養袋を変形させることによって行うこと
を特徴とする請求項1に記載のきのこの菌床栽培方法。
Release of sticking between the bacteria bed and the culture bag by the air pressure,
The mushroom bed cultivation method according to claim 1, wherein the cultivation is performed by deforming the culture bag.
前記培養袋の一部の切取り、又は培養袋への切れ目は、
菌床の含水率を低下させるに十分な大きさに行うこと
を特徴とする請求項1又は2に記載のきのこの菌床栽培方法。
Cutting a part of the culture bag, or a break in the culture bag,
The mushroom bed cultivation method according to claim 1 or 2, wherein the cultivation is performed in a size sufficient to reduce the moisture content of the fungus bed.
前記培養袋の一部を切取りは、
培養袋に設けられたフィルターの除去によって行うこと
を特徴とする請求項1乃至3のいずれかに記載のきのこの菌床栽培方法。
Cutting out a part of the culture bag,
The mushroom bed cultivation method according to any one of claims 1 to 3, wherein the method is performed by removing a filter provided in the culture bag.
前記培養袋の一部への切れ目の形成は、
培養袋に設けられたフィルターの近傍に形成すること
を特徴とする請求項1乃至3のいずれかに記載のきのこの菌床栽培方法。
The formation of a cut in a part of the culture bag,
It forms in the vicinity of the filter provided in the culture bag, The mushroom bed cultivation method in any one of the Claims 1 thru | or 3 characterized by the above-mentioned.
JP2003200319A 2003-07-23 2003-07-23 Mushroom bed culture method Pending JP2005040018A (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007195432A (en) * 2006-01-25 2007-08-09 Hokken Co Ltd Method for culturing lyphyllum decastes and carpophore thereof
CN104381024A (en) * 2014-12-10 2015-03-04 罗源县岐峰山水生态农业农民专业合作社 Planting method of flower mushrooms

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007195432A (en) * 2006-01-25 2007-08-09 Hokken Co Ltd Method for culturing lyphyllum decastes and carpophore thereof
CN104381024A (en) * 2014-12-10 2015-03-04 罗源县岐峰山水生态农业农民专业合作社 Planting method of flower mushrooms

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