JPH0438366B2 - - Google Patents
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- Publication number
- JPH0438366B2 JPH0438366B2 JP1094097A JP9409789A JPH0438366B2 JP H0438366 B2 JPH0438366 B2 JP H0438366B2 JP 1094097 A JP1094097 A JP 1094097A JP 9409789 A JP9409789 A JP 9409789A JP H0438366 B2 JPH0438366 B2 JP H0438366B2
- Authority
- JP
- Japan
- Prior art keywords
- culture medium
- mushroom
- culture
- bag
- culture bag
- 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
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- 235000001674 Agaricus brunnescens Nutrition 0.000 claims description 79
- 239000001963 growth medium Substances 0.000 claims description 74
- 238000004519 manufacturing process Methods 0.000 claims description 15
- 239000000463 material Substances 0.000 claims description 11
- 230000001954 sterilising effect Effects 0.000 description 33
- 238000004659 sterilization and disinfection Methods 0.000 description 29
- 238000001816 cooling Methods 0.000 description 16
- 241000894006 Bacteria Species 0.000 description 13
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- -1 polypropylene Polymers 0.000 description 9
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- 230000009545 invasion Effects 0.000 description 8
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- 238000009423 ventilation Methods 0.000 description 8
- 238000011109 contamination Methods 0.000 description 7
- 239000002054 inoculum Substances 0.000 description 7
- 230000001580 bacterial effect Effects 0.000 description 6
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- 244000052616 bacterial pathogen Species 0.000 description 4
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- 229920003023 plastic Polymers 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 241000233866 Fungi Species 0.000 description 3
- 241000209094 Oryza Species 0.000 description 3
- 235000007164 Oryza sativa Nutrition 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 3
- 235000009566 rice Nutrition 0.000 description 3
- 238000007789 sealing Methods 0.000 description 3
- 240000000599 Lentinula edodes Species 0.000 description 2
- 239000002390 adhesive tape Substances 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000012611 container material Substances 0.000 description 2
- 238000009776 industrial production Methods 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
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- 230000002265 prevention Effects 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 1
- 240000001080 Grifola frondosa Species 0.000 description 1
- 235000007710 Grifola frondosa Nutrition 0.000 description 1
- 235000001715 Lentinula edodes Nutrition 0.000 description 1
- 244000168667 Pholiota nameko Species 0.000 description 1
- 235000014528 Pholiota nameko Nutrition 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
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- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 238000012364 cultivation method Methods 0.000 description 1
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- 238000001704 evaporation Methods 0.000 description 1
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- 238000011176 pooling Methods 0.000 description 1
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- 239000002759 woven fabric Substances 0.000 description 1
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Landscapes
- Mushroom Cultivation (AREA)
Description
〔産業上の利用分野〕
本発明は、きのこ類の人工栽培に用いる信号培
養基の製造方法に関するものである。
〔従来の技術〕
近年、しいたけ等のきのこ類栽培に於て、次の
ような人工栽培が行われている。すなわち、まず
鋸屑・米糠等を混合し、水分を与えたきのこ培地
をポリプロピレン等のプラスチツク製培養袋に充
填し、殺菌して、きのこ類の人工培養基をつく
る。次に、このきのこ類の人工培養基に種菌を植
え付け、温度管理下で菌糸を蔓延させ、食用茸等
を大量に生産する。きのこ類の人工栽培のポイン
トは、いかにして雑菌の侵入を防止し、きのこ類
の生育に適した環境にするかであり、そのため、
殺菌釜を設置し、クリーンベンチ等の無菌環境内
で、種菌の植え付け作業を行つている。
しかし、殺菌釜で、せつかくきのこ培地を高圧
蒸気滅菌しても、高圧蒸気滅菌後、殺菌釜から90
℃程度の高温状態で取り出してきのこ培地の品温
が30℃以下になるまで、外気中で約半日かけて冷
却し、その後、種菌を接種するため、その間に雑
菌の侵入が生じる。このため、きのこ培地冷却用
に無菌室を設けたりしているが、多大な投資を必
要とし、また、多大な投資を行つても、作業者の
衣服、毛髪等に付着した雑菌が持ち込まれてしま
う。
そこで、きのこ類の人工培養基の製造方法とし
て、培養袋にきのこ培地を充填した後、キヤツプ
を固定するキヤツフ肩口、及び天板部分にスポン
ジが取り付けられた通気性キヤツプの両者を培養
袋の開口部に予め装着し、高圧蒸気滅菌、冷却を
行うことにより、設備投資を軽減し、雑菌汚染を
防止する方法が提案されている。すなわち、第7
図に示すようなポリプロピレンフイルム製の透明
な培養袋1を用い、その上部開口をリング状の肩
口キヤツプ2内に通して外側に折り返し、その状
態で、内部にフイルター3を有するキヤツプ4を
肩口キヤツプ2に嵌着して密封し、培養袋1内部
に雑菌を侵入させないようにして、高圧蒸気滅
菌、冷却を行う。この場合、通気は、蒸気キヤツ
プ4に設けられているフイルター3を通して行わ
れ、フイルター3によつて雑菌が除かれた空気が
培養袋1内に入るようになつている。しかしなが
ら、このように培養袋1の上部開口を肩口キヤツ
プ2内に入れたのち外側に折り返し、そこにフイ
ルター3内蔵のキヤツプ4を嵌着するという操作
は、煩雑で、自動化が極めて困難であるため、手
作業に頼つているのが実情である。これが製造コ
スト高の原因となり、また、キヤツプセツト自体
も高価である。
上記の培養袋1の代わりに第8図に示すような
培養袋の側面にフイルター3を装着した培養袋6
を用い、この培養袋6内に、きのこ培地5を充填
し、開口部をシールして密封した後、高圧蒸気滅
菌、冷却を行い、改めてハサミ等でシール部分を
切り取り、種菌を植え付けるという方法も提案さ
れている。しかしながら、使い捨てとなる培養袋
6にこのような高価なフイルター3を装着するこ
とは、培養袋6のコストが高くなる上に、高圧蒸
気滅菌中に通気不良による培養袋の破裂、或い
は、高圧蒸気滅菌時、培養袋6内及びきのこ培地
5内に含まれる空気の排気は行われるが、高圧蒸
気滅菌終了後、常圧に戻る際、吸気が十分に行わ
れず、きのこ培地5が培養袋6により真空パツク
状に圧縮される現象が多発し、安定なきのこ類の
人工培養基が製造できない。また、内圧により培
養袋6上部が膨れ、きのこ培地5上面と培養袋6
によつてヘツドスペース7が形成され、培養袋内
面の結露が甚だしくきのこ培地5に流れ落ちるた
め、雑菌汚染の要因となつた。
他方、上記のようにきのこ培養袋に工夫をこら
すのではなく、第9図に示すように、通常のポリ
プロピレン透明フイルム袋1内にきのこ培地5を
充填し、培養袋の開口部をゴム輪等の紐状体8で
くくる、或いは、ハサミ治具、粘着テープ等で留
めて、高圧蒸気滅菌し、冷却後、改めて培養袋を
開放して、種菌を植え付けるという方法も提案さ
れている。しかし、この方法も、必然的に煩雑な
手作業によらざるを得ず、また、上述した様な高
圧蒸気滅菌中の通気不良による培養袋の破裂、真
空パツク状の収縮、及びきのこ培地5上面と培養
袋1によつて形成されるヘツドスペースの解消は
出来なかつた。
このように、従来のきのこ類人工培養基の製造
方法では、高圧蒸気滅菌及び冷却を行う過程で雑
菌の侵入を防ぎ、しかも安価で人工培養基を得る
ことは困難であつた。
〔発明が解決しようとする課題〕
本発明は、このような事情に鑑みなされたもの
でその目的とするところは、従来の煩雑な手作業
を簡素化し、特別な高価である装置を必要とせ
ず、フイルター付キヤツプ等の原料費を軽減し、
しかも従来のきのこ類製造施設で実用できる、き
のこ類の人工培養基の製造方法を提供するにあ
る。
本発明の他の目的は高圧蒸気滅菌及び冷却を行
う過程において、雑菌の侵入を防ぎ、しかも高圧
蒸気滅菌中の人工培養基の培養袋の破裂、高圧蒸
気滅菌後の、真空パツク状の収縮、ヘツドスペー
スの形成が起こらないように適度な通気性と保形
性を与えられる、安定したきのこ類の人工培養基
の製造方法を提供するにある。
本発明の更に他の目的及び効果は以下の説明か
ら明らかにされよう。
〔課題を解決するための手段〕
上述の目的は、きのこ類の人工培養基を製造す
るに際し、フイルム状材からなる収容材にきのこ
培地を充填した後、開口面と平行な任意の一方向
を基準として上記収容材の対応する開口壁同士を
重ね合せて閉じ、該重ね合せた部分をきのこ培地
面に沿つて折り曲げ、該折り曲げ部分を通気性を
有する押え器具で押さえ、押さえた状態で加熱殺
菌し、引き続いて冷却することを特徴とするきの
こ類の人工培養基の製造方法によつて達成され
る。
次に、本発明を図面に基づいて、詳しく説明す
る。
第1図は、本発明のきのこ類の人工培養基の製
造工程の一実施例の手順の一部を示す説明図、第
2図は、押さえ器具の使用例を示す説明図、第3
図は、第2図Aの一部拡大説明図であり、21は
きのこ培地、22は培養袋である。
本発明のきのこ類の人工培養基の製造方法は、
例えば次のようにして行う。まず、ポリプロピレ
ンフイルムからなる透明な培養袋22を準備し、
鋸屑,米糠等を混合して加水調整されたきのこ培
地を該培地袋22に充填し、全体の形を整える。
この時、使用する培養袋は、ポリプロピレン製等
のプラスチツクフイルム等の従来から用いられて
いる収容材から適宜選択して使用すればよく、そ
の形状も有底筒状のものだけに特に限定されるも
のではなく、例えば、筒状、有底角柱状等のもの
であつてもよい。
次に、第1図Aに示す様に、開口面と平行な任
意の一方向を基準として、きのこ培地21を入れ
た培養袋22の対応する開口壁同士23a,23
bを重ね合せて閉じ、第1図B,Cの順にきのこ
培地面に沿つて重ね合せた部分を折り曲げる。そ
の際、きのこ培地21の上面と培養袋22によつ
て形成されるヘツドスペース24は、なるべく小
さくなる様に折り曲げ、きのこ培地21上面と培
養袋22との間隙Xを好ましくは5mm以下とする
様に押さえ込む。ヘツドスペース24が大きく残
つていると、高圧蒸気滅菌後、培養袋22の内面
に多量の結露が起こり、流れ落ちる時、雑菌が侵
入するだけでなく、きのこ培地21上面の乾燥が
生じ、種菌を植え付けた時、活着不良となること
がある。
続いて、上記のようにして開口部を折り曲げた
ものを数個、第2図Aに示す様に、トレイ25に
並べ、培養袋の折り曲げ部分を押さえる様に押さ
え器具26を被せる。該押さえ器具26を被せた
状態でトレイ25ごと高圧蒸気滅菌し、終了後、
90℃程度の高温状態のまま殺菌釜より取り出し、
第2図Aの状態で30℃以下になるまで冷却するこ
とにより、きのこ類の人工培養基が得られる。
本発明の人工培養基の製造方法において、高圧
蒸気滅菌時の、殺菌釜内の雰囲気と培養袋内及び
きのこ培地内部の差圧による通気、並びに殺菌釜
搬出後のきのこ培地高温時の排気及び冷却過程で
の吸気等、培養袋内外の通気は、第3図に示す培
養袋折り曲げ部分27の壁面間の空隙を介して行
われる。折り曲げ部分27は、開口面と平行な任
意の一方向を基準として培養袋22の対応する開
口壁同士を重ね合せて、折り曲げただけである
が、該折り曲げ部分27の培養袋内面は、完全に
密着しておらず、培養袋22のしわ、袋素材自身
が表面に有する凹凸等によつて空隙を有してい
る。このような多様な空隙により、培養袋22内
部と外部が連通しており、空気が流通する。しか
し、上記空隙は、微小で直線的でないため、空気
の濾過作用を有し、雑菌の侵入が防がれる。
また、培養袋折り曲げ部分27の長さは、好ま
しくは20mm以上、より好ましくは50mm以上あれ
ば、充分雑菌の侵入が防がれ、冷却室の環境に応
じて、折り曲げ部分の長さを適宜調整すればよ
い。折り曲げ部の長さが20mm以下では、作業環境
により、雑菌の侵入が起こる恐れがある。培養袋
折り曲げ部分27は、28地点(培地の上面肩
部)で更に折り込み、きのこ培地21に沿つた方
が、より雑菌の侵入防止に効果があるが、きのこ
培地21の高さよりも長くして29地点(培地の
底面部)で再度折り込むことは、折り曲げ部分及
び内面に付着した水の蒸発を妨げ、種菌を植え付
ける際、結露と共にきのこ培地21内部に雑菌が
流れ込む危険性がある。
本発明の製造方法に用いる押さえ器具26は、
通気性を有した構造のものを用いる。このような
押さえ器具26を用いることにより、培養袋22
及び折り曲げ部分27の内面に付着した水分の蒸
散を効率的に行うことができ、雑菌の侵入を防止
できる。雑菌は、乾燥状態では繁殖できないが、
水分があると容易に繁殖し、また、空気中に浮遊
している胞子等は、水を伝わつてきのこ培地21
に滑り込むため、以上のことは極めて重要であ
る。
また、押さえ器具26の重さにより、きのこ培
地21の上面を加圧し、折り曲げ部分27が立ち
上がるのを防ぎ、更には、きのこ培地21の上面
と培養袋22とに囲まれてできるヘツドスペース
が形成されることを防止する。ここで、押さえ器
具26の重さは収容材の材質にもより一概に規定
できないが、例えばポリプロピレン製袋状物の場
合、きのこ培地21の上面1cm2面積当たり好まし
くは20g以上、より好ましは100g以下になるよ
うに設定する。20gを越えると、校閲蒸気滅菌
時、培地が押さえ器具の重さで圧縮される形とな
り、培養袋内外の通気が不充分で培養袋の破裂、
又は、真空パツク状の圧縮が生じたり、或いは、
きのこ培地21が緻密になつて、きのこ菌糸の生
長に悪影響を与えたりすることがある。
更に、この押さえ器具26を、第2図Aに示す
ようにすつぽり覆い被せることによつて、きのこ
培地の搬送時の変形を防ぐ。特に、高圧蒸気滅菌
後、殺菌釜から搬出する際、きのこ培地が高温で
変形し易いため効果的である。
なお、この押さえ器具26の材質は、耐熱性を
有しているものであれば、金属、プラスチツク等
特に限定されるものではない。また、その形状
は、第2図Aに示すように側板の高さが、きのこ
培地の高さより低く設定された籠状のものだけで
なく、第2図Bに示すような漁網状のものや、織
布、不織布、より糸、多孔質物質等通気性の構造
物を単独もしくは2種以上組み合わせたもの等を
用いることができる。更に、押さえ器具は、第2
図AもしくはBの様に、複数個まとめて被覆して
もよいし、Cの様に、個別に押さえ器具を準備し
てもよい。
以上のように、殺菌、冷却が完了して得られた
人工培養基は、開口部23をクリーンベンチ内で
再び開放し、シイタケ、マイタケ、ナメコ等のき
のこ類種菌を植え付け、その後、第10図の様に
培養袋の開口部をヒートシールするか、第11図
の様に糸で縫合する等、多様な培養形態に応用で
き、しかも連続的に工業生産することが可能とな
る。また、第4図に示す様に従来のフイルター付
キヤツプを利用する場合Aに比べ、本発明Bは、
きのこ種菌30を広範囲に植え付けることが出来
るため、より速く菌糸が蔓延し、培養期間が短縮
されることは言うまでもない。
本発明のきのこ類の人工培養基の製造方法は、
袋培養を行うあらゆるきのこ類の人工培養基の形
態に応用できるもので、例えば、第5図に示す様
な底の閉じ込みの無い筒状の収容材31を準備
し、きのこ培地32に沿つた折り曲げ部分33を
2箇所設けることにより、きのこ種菌を多点に植
え付けることも可能となり、きのこ菌糸の培養期
間を大幅に短縮することも出来る。また、人工培
養基の形状も円柱形、直方体形等特に限定されな
い。さらに、本発明は、第8図に示すフイルター
3を装着した培養袋6にも応用可能で、シール等
の煩雑な作業を削除するだけでなく、培養袋の破
裂,真空パツク状の圧縮等の問題点も解消する。
〔発明の効果〕
以上の様に、本発明のきのこ類の人工培養基の
製造方法は、きのこ培地をフイルム状材からなる
収容材に充填し、高圧蒸気滅菌及び冷却するとい
う、きのこ種菌を接種する前工程に於て、開口面
と平行な任意の一方向を基準として上記収容材の
開口壁同士を重ね合せて折り曲げ、簡易な押さえ
器具を被せておくだけで、きのこ培養袋内に雑菌
が入らないように除菌し、しかも、適度な通気性
と保形性により、安定したきのこ類の人工培基を
製造しうるもので、培養袋の破裂,真空パツク状
の収縮,ヘツドスペースの形成等が起こらない。
また、従来の様なフイルター付きのキヤツプや、
袋の口元をゴム輪、ハサミ治具、粘着テープ等で
留めるというような複雑な操作を要せず、容易に
連続した工業的生産を可能とする。しかも、従来
から用いられていたポリプロピレン製等のプラス
チツクフイルム袋をそのまま用いることができる
ため、作業の簡略化、フイルター付キヤツプ等の
原料費の軽減により、大幅なコストダウンがはか
れるものである。
更に、製造された人工培養基に種菌を植え付け
る際に、広範囲に種菌の植え付けができるので、
より速く菌糸が蔓延し、培養期間が短縮される。
次に、実施例を挙げて本発明を具体的に説明す
る。
〔実施例 1〕
円筒形に押し出し成型された直径12cm、厚み
50μの透明プラスチツクフイルムを長さ35cmに切
断した。そして、その円筒フイルムを折り込み部
分が中央部で接触するようにガゼツト折り込みと
し、底部をヒートシールして密封することによ
り、透明ポリプロピレン製のきのこ培養袋をつく
つた。次に、このきのこ培養袋に、鋸屑4重量
部、米糠1重量部を加水混合し、含水率を70%に
調整したきのこ培地を1Kg充填し、直径12cm、高
さ14cmの円柱形に成型した。そして、開口面と平
行なある一方向を基準として培養袋の対応する開
口壁同士を重ね合せて密着させた後、きのこ培地
面に沿つて折り曲げ、第6図に示す様に、トレイ
34に9個並べた。ついで、培養袋の折り曲げ部
分を押さえる様に、側板及び底板に多数の通気孔
を有した上面開放型の押さえ器具35で固定し
た。この時、きのこ培地上面にかかる押さえ器具
35の重さは2g/cm2であり、培養袋の折り曲げ
部分の長さは9cmであつた。次に、これらを、高
圧蒸気滅菌釜内にそのままの状態で入れ、121℃、
90分間保持して滅菌した。滅菌後、殺菌釜内温度
90℃で取り出し、きのこ培地温度が25℃になるま
で冷却した。冷却には12時間を要し、冷却室内の
環境は、クラス10万レベルであつた。
〔実施例 2〕
透明プラスチツクフイルムの長さを30cmとし、
他は、実施例1と同様にして、きのこ培地の充
填、培養袋開口部の折り曲げ、押さえ器具の取り
付け、並びに、加熱蒸気滅菌,冷却を行つた。こ
の時、折り曲げ部分の長さは4cmであつた。
〔比較例 1〕
培養袋の開口部を密封せず、開口したままで加
熱蒸気滅菌及び冷却を行つた。なお、それ以外は
実施例1と同様の条件で実施した。
〔比較例 2〕
培養袋の開口部は、実施例1と同様にした重ね
合せて密着させた後、培地面に沿つて折り曲げを
行つたが、押さえ器具による押さえを行わなかつ
た。それ以外は実施例1と同様の条件で実施し
た。
〔比較例 3〕
押さえ器具を通気性の無いプラスチツクシート
とし、それ以外は実施例1と同様の条件で実施し
た。この時きのこ培地上面にかかる重さは、実施
例1と同じ2g/cm2であつた。
〔比較例 4〕
市販肩口キヤツプを使用すると共にスポンジフ
イルター付きキヤツプを用い、第7図に示す様に
して、トレイに並べ、加熱蒸気滅菌及び冷却を行
つた。但し押さえ器具による押さえは行わず、そ
の以外は実施例1と同様の条件で実施した。
以上の様にして製造した実施例及び比較例の人
工培養基の高圧蒸気滅菌後の培養袋破損数を調
べ、更に、実施例1、2及び比較例1、2、3の
人工培養基の培養袋上端をシートシールし、完全
に外気と遮断した後、25℃で10日間培養し、雑菌
汚染数を測定した。また、比較例4の人工培養基
を、冷却後、そのままの状態で、同様に25℃で10
日間培養し、雑菌汚染数を測定した。なお、それ
ぞれの実験は、270個の人工培養基で行つた。下
記の表に結果を示す。
[Industrial Application Field] The present invention relates to a method for producing a signal culture medium used for artificial cultivation of mushrooms. [Prior Art] In recent years, the following artificial cultivation methods have been used to cultivate mushrooms such as shiitake mushrooms. That is, first, a mushroom culture medium mixed with sawdust, rice bran, etc. and added with water is filled into a culture bag made of plastic such as polypropylene, and sterilized to create an artificial culture medium for mushrooms. Next, the inoculum is planted in an artificial culture medium for mushrooms, and the mycelium is spread under temperature control to produce a large amount of edible mushrooms. The key to artificially cultivating mushrooms is how to prevent the invasion of bacteria and create an environment suitable for mushroom growth.
A sterilization pot has been installed, and the seeds are planted in a sterile environment such as a clean bench. However, even if the mushroom culture medium is sterilized using high-pressure steam in a sterilization pot, after sterilization, the 90%
The mushroom culture medium is taken out at a high temperature of about 30°C and cooled in the open air for about half a day until the temperature drops to below 30°C, and then the inoculum is inoculated, which causes the invasion of various bacteria. For this reason, sterile rooms are set up to cool the mushroom culture medium, but this requires a large amount of investment, and even with a large amount of investment, bacteria attached to workers' clothes, hair, etc. are brought in. Put it away. Therefore, as a method for producing an artificial culture medium for mushrooms, after filling a culture bag with a mushroom culture medium, both the shoulder of the cap, which fixes the cap, and the breathable cap, which has a sponge attached to the top plate, are inserted into the opening of the culture bag. A method has been proposed to reduce equipment investment and prevent bacterial contamination by attaching the device in advance, sterilizing it with high-pressure steam, and cooling it. That is, the seventh
Using a transparent culture bag 1 made of polypropylene film as shown in the figure, pass its upper opening into a ring-shaped shoulder cap 2 and fold it back to the outside.In this state, insert a cap 4 having a filter 3 inside into the shoulder cap. The culture bag 1 is fitted into the culture bag 2 and sealed, and the culture bag 1 is sterilized with high-pressure steam and cooled while preventing bacteria from entering the culture bag 1. In this case, ventilation is performed through a filter 3 provided in the steam cap 4, and air from which germs have been removed by the filter 3 enters the culture bag 1. However, the operation of inserting the upper opening of the culture bag 1 into the shoulder cap 2, folding it back to the outside, and fitting the cap 4 with the built-in filter 3 therein is complicated and extremely difficult to automate. The reality is that we rely on manual labor. This causes high manufacturing costs, and the capsule itself is also expensive. A culture bag 6 with a filter 3 attached to the side of the culture bag as shown in FIG. 8 instead of the culture bag 1 described above.
There is also a method of filling the culture bag 6 with the mushroom culture medium 5, sealing the opening, sterilizing it with high-pressure steam, cooling it, cutting out the sealed part with scissors, etc., and planting the seed fungus. Proposed. However, attaching such an expensive filter 3 to the disposable culture bag 6 not only increases the cost of the culture bag 6, but also increases the risk of the culture bag rupturing due to poor ventilation during high-pressure steam sterilization, or the high-pressure steam During sterilization, the air contained in the culture bag 6 and the mushroom culture medium 5 is exhausted, but when returning to normal pressure after high-pressure steam sterilization, sufficient air is not taken in, and the mushroom culture medium 5 is removed from the culture bag 6. The phenomenon of being compressed into vacuum packs occurs frequently, making it impossible to produce stable artificial culture media for mushrooms. In addition, the top of the culture bag 6 swells due to internal pressure, and the top surface of the mushroom culture medium 5 and the culture bag 6
As a result, a head space 7 was formed, and the condensation on the inner surface of the culture bag was extremely condensed into the mushroom culture medium 5, causing bacterial contamination. On the other hand, instead of devising the mushroom culture bag as described above, as shown in FIG. 9, a mushroom culture medium 5 is filled in a normal polypropylene transparent film bag 1, and the opening of the culture bag is secured with a rubber ring or the like. A method has also been proposed in which the culture bag is tied with a string-like body 8 or fastened with a scissor jig, adhesive tape, etc., sterilized with high-pressure steam, and after cooling, the culture bag is opened again and the inoculum is planted. However, this method also inevitably requires complicated manual work, and also causes problems such as rupture of the culture bag due to poor ventilation during high-pressure steam sterilization, shrinkage of the vacuum pack, and the top surface of the mushroom culture medium 5. The head space formed by the culture bag 1 could not be eliminated. As described above, in the conventional method for producing an artificial culture medium for mushrooms, it has been difficult to prevent the invasion of various bacteria during the process of high-pressure steam sterilization and cooling, and to obtain an artificial culture medium at a low cost. [Problems to be Solved by the Invention] The present invention was made in view of the above circumstances, and its purpose is to simplify the conventional complicated manual work and eliminate the need for special expensive equipment. , reduce raw material costs such as caps with filters,
Moreover, it is an object of the present invention to provide a method for producing an artificial culture medium for mushrooms that can be put to practical use in conventional mushroom production facilities. Another object of the present invention is to prevent the invasion of germs during the process of high-pressure steam sterilization and cooling, and to prevent the rupture of the culture bag of the artificial culture medium during high-pressure steam sterilization, the shrinkage of the vacuum pack-like shape after high-pressure steam sterilization, and the prevention of the head. To provide a method for producing a stable artificial culture medium for mushrooms, which can be given appropriate air permeability and shape retention to prevent the formation of spaces. Further objects and effects of the present invention will become apparent from the following description. [Means for solving the problem] The above object is to produce an artificial culture medium for mushrooms by filling a containing material made of a film-like material with a mushroom culture medium, and then using an arbitrary direction parallel to the opening surface as a reference. Then, the corresponding opening walls of the container material are overlapped and closed, the overlapped part is folded along the surface of the mushroom culture medium, the folded part is held down with an air permeable holding device, and heated and sterilized while being held down. , is achieved by a method for producing an artificial culture medium for mushrooms, which is characterized by successive cooling. Next, the present invention will be explained in detail based on the drawings. FIG. 1 is an explanatory diagram showing a part of the procedure of an embodiment of the manufacturing process of an artificial culture medium for mushrooms of the present invention, FIG. 2 is an explanatory diagram showing an example of the use of a holding device, and FIG.
The figure is a partially enlarged explanatory view of FIG. 2A, where 21 is a mushroom culture medium and 22 is a culture bag. The method for producing an artificial culture medium for mushrooms of the present invention includes:
For example, do it as follows. First, prepare a transparent culture bag 22 made of polypropylene film,
A mushroom culture medium mixed with sawdust, rice bran, etc. and hydrated is filled into the culture medium bag 22, and the entire shape is adjusted.
At this time, the culture bag used may be appropriately selected from conventionally used storage materials such as plastic film made of polypropylene, etc., and its shape is particularly limited to a cylindrical one with a bottom. For example, the shape may be cylindrical or prismatic with a bottom. Next, as shown in FIG. 1A, the corresponding opening walls 23a, 23 of the culture bag 22 containing the mushroom culture medium 21 are aligned with each other with respect to an arbitrary direction parallel to the opening surface.
1. Overlap and close the parts 2 and 3, and fold the overlapping parts along the mushroom culture surface in the order shown in Figure 1 B and C. At this time, the head space 24 formed by the top surface of the mushroom medium 21 and the culture bag 22 is bent to be as small as possible, so that the gap X between the top surface of the mushroom medium 21 and the culture bag 22 is preferably 5 mm or less. hold it down. If a large head space 24 remains, a large amount of dew condensation will occur on the inner surface of the culture bag 22 after high-pressure steam sterilization, and when it drips off, not only will bacteria enter, but the top surface of the mushroom culture medium 21 will dry out, allowing the seed to be planted. In some cases, poor attachment may occur. Subsequently, several culture bags with their openings bent as described above are arranged on a tray 25 as shown in FIG. 2A, and a pressing device 26 is placed over the culture bags so as to press the bent portions. The tray 25 is sterilized with high pressure steam with the holding device 26 covered, and after completion,
Remove from the sterilization pot while still at a high temperature of about 90℃,
An artificial culture medium for mushrooms can be obtained by cooling the mixture under the condition shown in Figure 2A to 30°C or lower. In the method for producing an artificial culture medium of the present invention, during high-pressure steam sterilization, ventilation is performed by the pressure difference between the atmosphere inside the sterilization pot, the culture bag, and the inside of the mushroom culture medium, and the exhaust and cooling process when the mushroom culture medium is at high temperature after being carried out from the sterilization pot. Ventilation inside and outside the culture bag, such as air intake, is performed through the gap between the walls of the culture bag folded portion 27 shown in FIG. The folded portion 27 is simply made by overlapping and bending the corresponding opening walls of the culture bag 22 based on an arbitrary direction parallel to the opening surface, but the inner surface of the culture bag at the folded portion 27 is completely They are not in close contact and have gaps due to wrinkles in the culture bag 22, unevenness on the surface of the bag material itself, and the like. These various voids communicate the inside and outside of the culture bag 22, allowing air to circulate therein. However, since the above-mentioned voids are minute and not linear, they have an air filtering effect and prevent the invasion of various germs. In addition, the length of the culture bag folded portion 27 should preferably be 20 mm or more, more preferably 50 mm or more, to sufficiently prevent the invasion of bacteria, and adjust the length of the bent portion as appropriate depending on the environment of the cooling room. do it. If the length of the bent part is less than 20 mm, there is a risk of bacteria entering depending on the working environment. The folded part 27 of the culture bag should be further folded at the 28th point (shoulder part of the upper surface of the medium) so that it runs along the mushroom culture medium 21, which is more effective in preventing the invasion of bacteria, but it should be made longer than the height of the mushroom culture medium 21. Folding again at point 29 (bottom part of the medium) prevents evaporation of water adhering to the folded part and the inner surface, and there is a risk that condensation and contaminants may flow into the inside of the mushroom medium 21 when planting the inoculum. The holding device 26 used in the manufacturing method of the present invention is
Use one with a breathable structure. By using such a holding device 26, the culture bag 22
Also, the moisture adhering to the inner surface of the bent portion 27 can be efficiently evaporated, and the invasion of various germs can be prevented. Bacteria cannot grow in dry conditions, but
Mushroom culture medium 21 The spores, etc. that are floating in the air can be easily propagated in the presence of moisture.
The above is extremely important in order to slip into the In addition, the weight of the holding device 26 pressurizes the top surface of the mushroom culture medium 21 to prevent the bent portion 27 from standing up, and furthermore, a head space is formed between the top surface of the mushroom culture medium 21 and the culture bag 22. to prevent it from happening. Here, the weight of the holding device 26 cannot be absolutely defined depending on the material of the containing material, but for example, in the case of a bag made of polypropylene, the weight is preferably 20 g or more per 1 cm 2 of the upper surface of the mushroom culture medium 21, and more preferably Set it so that it is 100g or less. If it exceeds 20g, the culture medium will be compressed by the weight of the holding device during proof steam sterilization, and ventilation inside and outside the culture bag will be insufficient, causing the culture bag to rupture.
Or, a vacuum pack-like compression occurs, or
The mushroom medium 21 may become dense, which may adversely affect the growth of mushroom mycelia. Furthermore, by completely covering the holding device 26 as shown in FIG. 2A, deformation of the mushroom culture medium during transportation is prevented. This is particularly effective since the mushroom culture medium is easily deformed at high temperatures when being removed from the sterilization pot after high-pressure steam sterilization. Note that the material of this holding device 26 is not particularly limited, as long as it has heat resistance, such as metal or plastic. In addition, the shape is not limited to a cage-like one with the height of the side plate set lower than the height of the mushroom culture medium as shown in Figure 2A, but also a fishing net-like shape as shown in Figure 2B. , woven fabrics, nonwoven fabrics, twine, porous materials, and other breathable structures may be used alone or in combination of two or more types. Furthermore, the holding device has a second
As shown in Figures A or B, multiple pieces may be covered together, or as shown in Figure C, pressers may be prepared individually. As described above, the artificial culture medium obtained after sterilization and cooling is completed, the opening 23 is opened again in the clean bench, mushroom inoculum such as shiitake, maitake, nameko, etc. is inoculated, and then, as shown in FIG. It can be applied to various culture formats, such as heat-sealing the opening of the culture bag as shown in FIG. 11, or suturing it with thread as shown in FIG. 11, and also enables continuous industrial production. Furthermore, as shown in FIG. 4, compared to case A in which a conventional cap with a filter is used, the present invention B has the following advantages:
Needless to say, since the mushroom seed fungus 30 can be planted over a wide area, the mycelium spreads more quickly and the cultivation period is shortened. The method for producing an artificial culture medium for mushrooms of the present invention includes:
This can be applied to the form of artificial culture medium for all kinds of mushrooms that are cultured in bags. For example, by preparing a cylindrical container 31 with no confinement at the bottom as shown in FIG. 5, and folding it along the mushroom culture medium 32. By providing two portions 33, it becomes possible to plant mushroom seed fungi at multiple points, and it is also possible to significantly shorten the cultivation period of mushroom hyphae. Furthermore, the shape of the artificial culture medium is not particularly limited, such as a cylindrical shape or a rectangular parallelepiped shape. Furthermore, the present invention can be applied to a culture bag 6 equipped with a filter 3 as shown in FIG. It also solves problems. [Effects of the Invention] As described above, the method for producing an artificial culture medium for mushrooms of the present invention involves filling a mushroom culture medium into a containing material made of a film-like material, sterilizing it with high-pressure steam, and cooling it. In the pre-process, the opening walls of the container material are overlapped and bent in any direction parallel to the opening surface, and simply covered with a simple holding device to prevent bacteria from entering the mushroom culture bag. It can be used to sterilize the mushrooms to prevent them from sterilizing, and to produce stable artificial culture for mushrooms due to its appropriate air permeability and shape retention, which prevents the rupture of culture bags, shrinkage of vacuum packs, and the formation of head spaces. does not occur.
In addition, a conventional cap with a filter,
To easily enable continuous industrial production without requiring complicated operations such as fixing the opening of a bag with a rubber ring, a scissor jig, adhesive tape, etc. Moreover, since conventionally used plastic film bags made of polypropylene or the like can be used as is, the cost can be significantly reduced by simplifying the work and reducing the cost of raw materials such as caps with filters. Furthermore, when inoculating the inoculum into the manufactured artificial culture medium, the inoculum can be planted over a wide area.
The mycelium spreads faster and the culture period is shortened. Next, the present invention will be specifically explained with reference to Examples. [Example 1] Cylindrical extrusion molded with a diameter of 12 cm and a thickness
A 50 μm transparent plastic film was cut into a length of 35 cm. Then, the cylindrical film was folded into a gusset so that the folded parts touched at the center, and the bottom was heat-sealed to make a mushroom culture bag made of transparent polypropylene. Next, this mushroom culture bag was filled with 1 kg of mushroom culture medium, which had been mixed with 4 parts by weight of sawdust and 1 part by weight of rice bran to adjust the moisture content to 70%, and formed into a cylinder with a diameter of 12 cm and a height of 14 cm. . Then, the corresponding opening walls of the culture bag are overlapped and brought into close contact with each other with reference to a certain direction parallel to the opening surface, and then folded along the mushroom culture surface, and placed in the tray 34 as shown in FIG. I arranged them. Next, the culture bag was fixed with a presser 35 having an open top and having a large number of ventilation holes in the side and bottom plates so as to press the bent portion of the culture bag. At this time, the weight of the holding device 35 placed on the top surface of the mushroom culture medium was 2 g/cm 2 , and the length of the bent portion of the culture bag was 9 cm. Next, these were placed as they were in a high-pressure steam sterilization pot and heated to 121°C.
Sterilized by holding for 90 minutes. After sterilization, temperature inside the sterilization pot
It was taken out at 90°C and cooled until the mushroom medium temperature reached 25°C. Cooling took 12 hours, and the environment inside the cooling room was at a class 100,000 level. [Example 2] The length of the transparent plastic film was 30 cm,
Other than that, filling with mushroom culture medium, bending the opening of the culture bag, attaching a holding device, heating steam sterilization, and cooling were carried out in the same manner as in Example 1. At this time, the length of the folded portion was 4 cm. [Comparative Example 1] The opening of the culture bag was not sealed, but steam sterilization and cooling were carried out with it left open. Note that the other conditions were the same as in Example 1. [Comparative Example 2] The opening of the culture bag was stacked and brought into close contact in the same manner as in Example 1, and then bent along the culture medium surface, but was not pressed with a pressing device. The other conditions were the same as in Example 1. [Comparative Example 3] A non-air permeable plastic sheet was used as the holding device, and the test was carried out under the same conditions as in Example 1 except for that. At this time, the weight applied to the top surface of the mushroom medium was 2 g/cm 2 , the same as in Example 1. [Comparative Example 4] Using a commercially available shoulder cap and a cap with a sponge filter, the caps were arranged on a tray as shown in FIG. 7, and heated and steam sterilized and cooled. However, pressing with a pressing device was not performed, and the other conditions were the same as in Example 1. The number of broken culture bags after high-pressure steam sterilization of the artificial culture media of Examples and Comparative Examples produced as described above was investigated, and the top end of the culture bags of the artificial culture media of Examples 1, 2 and Comparative Examples 1, 2, and 3 was investigated. After sealing the cells in a sheet and completely shutting them off from the outside air, they were cultured at 25°C for 10 days, and the number of bacterial contamination was measured. In addition, the artificial culture medium of Comparative Example 4 was cooled and kept as it was for 10 days at 25°C.
After culturing for days, the number of bacterial contamination was measured. Each experiment was conducted using 270 artificial culture media. The results are shown in the table below.
【表】【table】
【表】
上記の結果より、実施例1、2は、培養袋の破
損及び雑菌の汚染のない良好な人工培養基が得ら
れた。すなわち、実施例1、2は、高圧蒸気滅
菌・冷却工程前後で、人工培養基の形状に差異は
なかつた。しかし、比較例3の人工培養基は、高
圧蒸気滅菌後、きのこ培養袋全数の上面に多量の
結露が見られ、真空パツク状に培地が圧縮された
ものが多発した。これは高圧蒸気滅菌中に、プラ
スチツクシートと培養袋上面との間に水の溜りが
出来、培養袋折り曲げ部分内面の水結着を促した
結果、培養袋内外の通気不良が生じたものと考え
られた。また実施例1、2の人工培養基は、培養
袋折り曲げ部分の長さの違いによるものである
が、作業環境の清浄度の差異に応じて、袋の折り
曲げ部分の長さを調節することにより、雑菌汚染
を完全に阻止出来ることが示された。
更に、実施例1、2の人工培養基は、落下菌に
よる雑菌汚染が無く、外観的な人工培養基の状態
も市販肩口キヤツプを使用した比較例4の人工培
養基と変わらなかつた。すなわち、本発明によれ
ば極めて簡単な操作により、市販肩口キヤツプを
使用したものと同等の雑菌防止効果が得られ、植
菌後に、袋開口部をシートシール、或いは、糸で
縫合等を行い、培養することが可能で、製造価格
の大幅なコストダウンが実現しうるものである。[Table] From the above results, in Examples 1 and 2, a good artificial culture medium was obtained without breakage of the culture bag or contamination with various bacteria. That is, in Examples 1 and 2, there was no difference in the shape of the artificial culture medium before and after the high-pressure steam sterilization/cooling process. However, in the artificial culture medium of Comparative Example 3, after high-pressure steam sterilization, a large amount of dew condensation was observed on the top surfaces of all the mushroom culture bags, and the culture medium was frequently compressed into vacuum packs. This is thought to be due to water pooling between the plastic sheet and the top of the culture bag during high-pressure steam sterilization, which promoted water condensation on the inner surface of the culture bag's folded part, resulting in poor ventilation inside and outside the culture bag. It was done. In addition, the artificial culture media of Examples 1 and 2 are due to the difference in the length of the folded part of the culture bag, but by adjusting the length of the folded part of the bag according to the difference in the cleanliness of the working environment, It has been shown that bacterial contamination can be completely prevented. Furthermore, the artificial culture media of Examples 1 and 2 were free from bacterial contamination due to fallen bacteria, and the appearance of the artificial culture media was the same as that of Comparative Example 4 using commercially available shoulder caps. That is, according to the present invention, with extremely simple operations, the same germ prevention effect as that obtained using commercially available shoulder caps can be obtained, and after inoculation, the bag opening is sealed with a sheet or sutured with thread, etc. It can be cultured and the manufacturing cost can be significantly reduced.
第1図は、本発明の一実施例の説明図、第2図
は、押さえ器具の使用例を示す説明図、第3図
は、第2図Aの一部拡大説明図、第4図は、従来
方法Aと本発明Bとを比較する説明図、第5図
は、他の実施例を示す説明図、第6図は、実施例
を示す説明図、第7図、第8図、第9図、第10
図、第11図は、従来方法を示す説明図である。
21……きのこ培地、22……培養袋、25…
…トレイ、26……押さえ器具。
FIG. 1 is an explanatory diagram of one embodiment of the present invention, FIG. 2 is an explanatory diagram showing an example of the use of the holding device, FIG. 3 is a partially enlarged explanatory diagram of FIG. 2A, and FIG. , an explanatory diagram comparing the conventional method A and the present invention B, FIG. 5 is an explanatory diagram showing another embodiment, FIG. 6 is an explanatory diagram showing the embodiment, FIGS. Figures 9 and 10
11 are explanatory diagrams showing the conventional method. 21...Mushroom medium, 22...Culture bag, 25...
...Tray, 26...pressing device.
Claims (1)
イルム状材からなる収容材にきのこ培地を充填し
た後、開口面と平行な任意の一方向を基準として
上記収容材の対応する開口壁同士を重ね合せて閉
じ、該重ね合せた部分をきのこ培地面に沿つて折
り曲げ、該折り曲げ部分を通気性を有する押え器
具で押さえ、押さえた状態で加熱殺菌し、引き続
いて冷却することを特徴とするきのこ類の人工培
養基の製造方法。1. When producing an artificial culture medium for mushrooms, after filling a containing material made of a film-like material with a mushroom culture medium, corresponding opening walls of the containing material are overlapped with each other with respect to an arbitrary direction parallel to the opening surface. the overlapping portion is folded along the surface of the mushroom culture medium, the folded portion is held down with a breathable holding device, heat sterilized while being held down, and subsequently cooled. Method for producing artificial culture medium.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1094097A JPH02273125A (en) | 1989-04-13 | 1989-04-13 | Production of artificial culture medium of mushroom |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1094097A JPH02273125A (en) | 1989-04-13 | 1989-04-13 | Production of artificial culture medium of mushroom |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH02273125A JPH02273125A (en) | 1990-11-07 |
| JPH0438366B2 true JPH0438366B2 (en) | 1992-06-24 |
Family
ID=14100948
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1094097A Granted JPH02273125A (en) | 1989-04-13 | 1989-04-13 | Production of artificial culture medium of mushroom |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH02273125A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2014008048A (en) * | 2012-07-03 | 2014-01-20 | Ueda Sangyo Kk | Method for artificially cultivating flammulina velutipes mushrooms |
-
1989
- 1989-04-13 JP JP1094097A patent/JPH02273125A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPH02273125A (en) | 1990-11-07 |
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