JPH024258B2 - - Google Patents
Info
- Publication number
- JPH024258B2 JPH024258B2 JP59064539A JP6453984A JPH024258B2 JP H024258 B2 JPH024258 B2 JP H024258B2 JP 59064539 A JP59064539 A JP 59064539A JP 6453984 A JP6453984 A JP 6453984A JP H024258 B2 JPH024258 B2 JP H024258B2
- Authority
- JP
- Japan
- Prior art keywords
- shiitake
- extract
- seed
- fruiting body
- medium
- 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
Links
- 240000000599 Lentinula edodes Species 0.000 claims description 79
- 235000001715 Lentinula edodes Nutrition 0.000 claims description 48
- 239000000284 extract Substances 0.000 claims description 24
- 238000000034 method Methods 0.000 claims description 18
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 15
- 239000001963 growth medium Substances 0.000 claims description 12
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 10
- 239000004744 fabric Substances 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
- 239000002023 wood Substances 0.000 claims description 6
- 238000011218 seed culture Methods 0.000 claims description 4
- 238000012364 cultivation method Methods 0.000 claims description 3
- 239000002609 medium Substances 0.000 description 19
- 241000233866 Fungi Species 0.000 description 8
- 239000005720 sucrose Substances 0.000 description 8
- 241000894006 Bacteria Species 0.000 description 7
- 239000002026 chloroform extract Substances 0.000 description 5
- 229920001817 Agar Polymers 0.000 description 4
- 239000008272 agar Substances 0.000 description 4
- 239000000654 additive Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000001965 increasing effect Effects 0.000 description 3
- 239000007791 liquid phase Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000401 methanolic extract Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 235000001674 Agaricus brunnescens Nutrition 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 244000061456 Solanum tuberosum Species 0.000 description 2
- 235000002595 Solanum tuberosum Nutrition 0.000 description 2
- 229930006000 Sucrose Natural products 0.000 description 2
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 238000004026 adhesive bonding Methods 0.000 description 2
- 210000000476 body water Anatomy 0.000 description 2
- 238000012258 culturing Methods 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 238000011081 inoculation Methods 0.000 description 2
- 230000009545 invasion Effects 0.000 description 2
- 230000001737 promoting effect Effects 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- RQFCJASXJCIDSX-UHFFFAOYSA-N 14C-Guanosin-5'-monophosphat Natural products C1=2NC(N)=NC(=O)C=2N=CN1C1OC(COP(O)(O)=O)C(O)C1O RQFCJASXJCIDSX-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 101000993347 Gallus gallus Ciliary neurotrophic factor Proteins 0.000 description 1
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 102000014150 Interferons Human genes 0.000 description 1
- 108010050904 Interferons Proteins 0.000 description 1
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 1
- 229920001491 Lentinan Polymers 0.000 description 1
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 1
- 229920000057 Mannan Polymers 0.000 description 1
- GXCLVBGFBYZDAG-UHFFFAOYSA-N N-[2-(1H-indol-3-yl)ethyl]-N-methylprop-2-en-1-amine Chemical compound CN(CCC1=CNC2=C1C=CC=C2)CC=C GXCLVBGFBYZDAG-UHFFFAOYSA-N 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 241001480065 Quercus serrata Species 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 239000011358 absorbing material Substances 0.000 description 1
- 230000000259 anti-tumor effect Effects 0.000 description 1
- 239000006286 aqueous extract Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 210000003608 fece Anatomy 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 230000033937 fruiting body development Effects 0.000 description 1
- 230000002538 fungal effect Effects 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 235000013922 glutamic acid Nutrition 0.000 description 1
- 239000004220 glutamic acid Substances 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- RQFCJASXJCIDSX-UUOKFMHZSA-N guanosine 5'-monophosphate Chemical compound C1=2NC(N)=NC(=O)C=2N=CN1[C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]1O RQFCJASXJCIDSX-UUOKFMHZSA-N 0.000 description 1
- 235000013928 guanylic acid Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229940079322 interferon Drugs 0.000 description 1
- 229940115286 lentinan Drugs 0.000 description 1
- 235000020778 linoleic acid Nutrition 0.000 description 1
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000010871 livestock manure Substances 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 235000020939 nutritional additive Nutrition 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 230000035755 proliferation Effects 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 229920002477 rna polymer Polymers 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 238000010898 silica gel chromatography Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000004809 thin layer chromatography Methods 0.000 description 1
- 235000019583 umami taste Nutrition 0.000 description 1
Landscapes
- Mushroom Cultivation (AREA)
Description
〔産業上の利用分野〕
本発明はシイタケ菌糸の成長を著しく促進し、
極めて高能率に短期間でシイタケを栽培する方法
に関するものである。
〔従来技術〕
シイタケの栽培法は、シイタケ菌糸をおがくず
に培養した純粋培養種菌を原木に詰め込み、後そ
の上を樹皮で作つたふた又はワツクスで密封し、
この接種した原木とするか、或いは、クサビ型又
は棒型の木片或いは紙紐の複数本を束ねて糊をつ
けた布又は糸で結束した小円筒形の駒(実公昭55
−4989号公報)に上記純粋培養種菌を付着又は含
浸させた種駒を原木に穿孔した孔に詰め込んで接
種した原木とするかして得られた接種原木をシイ
タケの菌糸の発育温度大体5〜35℃で空中湿度75
%位の場所において原木に菌糸を繁殖させる(伏
込み)。この操作の終つた原木をキノコの発生に
適当な場所すなわち、光線が十分にあたり、温度
が大体15〜17℃、湿度が大体85%位の場所に両側
から立てかける(ほだ起し)。このほだ起し後春
秋のころは1〜2週間で正常な形にシイタケが生
育し、生シイタケとして採取する。
近時シイタケには薬効成分として、抗腫瘍活性
を示す多糖類レンチナンや、インターフエロン誘
導活性を示す2本鎖リボ核酸並びにペプチドマン
ナン、また旨み成分である5′−グアニル酸やグル
タミン酸が含まれ、その需要が激増している。そ
れに伴いシイタケの生産は人工接種、菌の選択、
ハウス栽培などの生産技術の向上とともに急上昇
している。しかしながら、その生産高の上昇とと
もに原木不足、害菌による被害並びに子実体発生
不良などの問題も増大して来た。
害菌対策としては現在、ほだ木の管理に重点が
置かれているが、環境制御は自然状態では困難で
あるのが現状である。
そこで、シイタケ菌糸が蔓延すると害菌は侵入
しにくくなるという現象に着目し、種駒を打つ際
栄養添加物を投与してシイタケ菌糸を早く蔓延さ
せる方法が考えられ、その栄養添加物として、に
んじん抽出物、大豆もやし抽出物、米糠抽出物、
パルプ排液成分などを吸水性物質例えば脱脂綿に
含浸させて種駒接種穴に挿入し、その上に種駒を
直接打ち込む方法が考えられた。
しかしながら、これらの栄養物の添加ではシイ
タケ菌糸の早期の蔓延が十分でなく、かつその操
作も繁雑であつた。
〔発明の目的〕
本発明はシイタケの菌糸生長促進物質としてシ
イタケ子実体の抽出物とシイタケ培養基をシイタ
ケ種菌培地に添加して後通常のシイタケ栽培法を
行うことにより、シイタケ菌糸が速やかに蔓延
し、害菌の侵入を防止すると共に特に紙紐の複数
本を束ねて糊づけした布、糸で結束した種駒に該
シイタケ子実体の抽出物とシイタケ培養基を含浸
せしめて栽培した場合は、シイタケ栽培の操作も
簡便でシイタケ栽培効率も増大する方法を提供す
ることを目的とする。
〔発明の構成〕
本発明はシイタケ栽培において、シイタケ種菌
培地にシイタケ子実体抽出物とシイタケ培養基を
添加することによつて、害菌の侵入を防止しかつ
シイタケの発育を促進させて高能率にシイタケを
接種することができるシイタケの栽培法である。
本発明の方法が適用されるシイタケ栽培は、純
粋に培養したシイタケ種菌を原木に接種し、伏込
み、ほだ起し、シイタケの採取をする工程よりな
る一般のシイタケ栽培であつて、本発明の特徴は
シイタケ種菌を培養する段階においてシイタケ子
実体の抽出物とシイタケ培養基を用いる点にあ
る。
本発明に用いるシイタケ子実体の抽出物は、シ
イタケ子実体より水、メタノール又はクロロホル
ムで抽出し、さらにシリカゲルクロマトグラフイ
ーで分離精製した物質で、本体は脂質類と推定さ
れる。クロロホルム抽出物をさらにシリカゲル薄
層クロマトグラフイーで分画したところ、5個の
スポツトが表われ(展開溶媒はクロロホルム:メ
タノール=5:1)、その中下から2番目のスポ
ツトの画分が最も生長促進活性が得られたので、
このスポツトの画分をガスクロマトグラフイーで
構成脂肪酸を検索したところ、リノール酸とパル
ミチン酸が圧倒的に多かつた。
以上の如く、本発明に用いるシイタケ子実体の
抽出物は水、アルコール、クロロホルム何れの抽
出物でもシイタケ菌糸成長促進活性があるが、実
用的には水抽出物が好適である。
本発明に用いるシイタケ培養基は馬糞煎汁培
地、ペプトン加用寒天培地、アスパラギン加用寒
天培地、麦芽煎汁寒天培地、マイエル氏培地、リ
チヤード氏培地、ベツフアー氏培地、バレイシヨ
−寒天培地、木材腐朽菌用培地、バレイシヨ−蔗
糖培地などのキノコ類特にシイタケが培養し得る
培地が含まれる。そのうち、バレイシヨ−蔗糖培
地が好適である。
この培養基に添加するシイタケ子実体抽出物の
添加量は大体10〜0.1%位が好適である。
このシイタケ子実体抽出物とシイタケ培養基を
使用するには、シイタケ栽培を純粋培養したシイ
タケ種菌を原木の穿孔中に詰め込んで樹皮又はワ
ツクスなどで蓋をして、接種する場合は種菌を培
養する例えばオガクズ中に含浸せしめる。また、
クサビ形、円筒形の木片にシイタケ種菌を付着さ
せて種駒とする場合は、木片に塗布又は含浸させ
るか、本発明において好適の使用は、紙紐の複数
本を束ねて糊づけした布又は糸をもつて結束した
小円筒の駒に含浸させて種駒を得る方法による。
上記の種駒とした場合はこの種駒を原木の穿孔
に詰め込んで接種する。
以上の如く接種した原木は以下常法により大体
5〜35℃、空中湿度75%位の場所に傾斜をもつて
横置する(伏込み)。この伏込みにより原木のシ
イタケ菌糸が繁殖する。本発明の方法により接種
した原木は伏込み工程におけるシイタケ菌糸の繁
殖が著しく促進され、一般の方法の場合の約5倍
に繁殖が促進される。
以上の如くして原木にシイタケ菌糸の繁殖した
ものを光線が十分当たる15〜17℃、空中湿度85%
前後の天然又は人工環境において、原木を両側か
ら60゜位の角度で立てかけて1〜2週間でシイタ
ケが正常な形となる(ほだ起し)。この工程を終
了し、原木上に生育したシイタケを採取する。
〔実施例〕
例 1
シイタケ子実体40gを240mlの水に入れ、24時
間室温で撹拌し、得られた抽出液を遠心分離し、
液相を減圧で濃縮しシイタケ子実体水抽出物40ml
を得る。
かくして得られたシイタケ子実体水抽出物40ml
をバレイシヨ−蔗糖培地(バレイシヨ250gを細
片し、約20分間煮沸し、布で濾過し濾液を1に
する。それに蔗糖20gを加えて調整する)360ml
に加え、その液に紙紐を100〜200mmの長さに截断
し、10本位を20mm位の円筒状に束ねた上に、デン
プン糊をつけた布で巻いて固着結束した駒(以下
ヒモ駒と称す)1000個を浸漬し含浸させ、後殺菌
してこの駒にシイタケ菌を接種する。この種駒を
原木の穿孔に詰め込み接種し、後常法により伏込
み、ほだ起しを行いシイタケを採取した。
例 2
シイタケ子実体80gを240mlのメタノールに入
れ、60℃に加熱下撹拌しつつ3時間抽出する。得
られた抽出液を遠心分離し、液相を減圧で濃縮し
シイタケ子実体メタノール抽出物40mlを得る。
かくして得られたシイタケ子実体メタノール抽
出物40mlをバレイシヨ−蔗糖培地360mlに加え、
以下実施例1と同様のヒモ駒に含浸せしめて種駒
としてシイタケを栽培する。
例 3
シイタケ子実体80gを240mlのクロロホルムに
入れ、60℃に加熱下撹拌しつつ3時間抽出する。
得られた抽出液を遠心分離し、液相を減圧で濃縮
しシイタケ子実体クロロホルム抽出物40mlを得
る。
かくして得られたシイタケ子実体クロロホルム
抽出物40mlをバレイシヨ−蔗糖培地360mlに加え、
以下実施例1と同様のヒモ駒に含浸せしめて種駒
としてシイタケを栽培する。
〔発明の効果〕
実施例1,2,3で得られたシイタケ子実水、
メタノール、クロロホルム抽出物をバレイシヨ−
蔗糖培地にそれぞれ10%、0.3%、0.1%添加した
本発明のシイタケ子実体抽出物を含有する試料と
対照として無添加の培地におけるシイタケ菌糸生
長を菌体重量測定法により測定し、対照を100と
した生長率を判定した結果は表1の通りであつ
た。
[Industrial Application Field] The present invention significantly promotes the growth of shiitake mushroom mycelia,
This invention relates to a method of cultivating shiitake mushrooms with extremely high efficiency and in a short period of time. [Prior art] The method of cultivating shiitake mushrooms is to fill logs with pure cultured seed fungi obtained by culturing shiitake mycelium on sawdust, and then seal the top with a lid made of bark or wax.
These inoculated logs can be used, or small cylindrical pieces made by bundling multiple wedge-shaped or stick-shaped pieces of wood or paper strings and binding them with glued cloth or thread (Jikko 55
-4989 Publication) with the above-mentioned pure culture seed fungi attached or impregnated with the seed pieces, which are packed into holes drilled in the log to obtain inoculated logs. Air humidity 75 at 35℃
Propagate mycelium on logs in approximately 100% of locations (propagation). Once this process has been completed, the log is propped up on both sides in a location suitable for mushroom growth, i.e., a location with sufficient sunlight, a temperature of approximately 15 to 17 degrees Celsius, and a humidity of approximately 85%. In spring and autumn, the shiitake mushrooms grow into a normal shape in 1 to 2 weeks after hodging and are collected as raw shiitake mushrooms. Recently, shiitake mushrooms contain medicinal ingredients such as the polysaccharide lentinan, which exhibits antitumor activity, double-stranded ribonucleic acid and peptide mannan, which exhibit interferon-inducing activity, and 5'-guanylic acid and glutamic acid, which are umami components. The demand for it is increasing rapidly. Along with this, shiitake production involves artificial inoculation, selection of bacteria,
It is rapidly increasing with the improvement of production technology such as greenhouse cultivation. However, with the increase in production, problems such as a shortage of logs, damage caused by harmful bacteria, and poor fruiting body development have also increased. Currently, emphasis is placed on the management of hodagi as a countermeasure against harmful bacteria, but environmental control is currently difficult under natural conditions. Therefore, we focused on the phenomenon that when shiitake mushroom mycelium spreads, it becomes difficult for harmful bacteria to invade, and we devised a method to quickly spread shiitake mushroom mycelium by administering nutritional additives when seeding. extract, soybean sprout extract, rice bran extract,
A method has been considered in which a water-absorbing material such as absorbent cotton is impregnated with pulp drainage components and the like is inserted into a seed seed inoculation hole, and the seed seed is directly driven onto it. However, the early spread of shiitake mycelium was not sufficient with the addition of these nutrients, and the operation was complicated. [Object of the Invention] The present invention provides a method for rapidly spreading shiitake mushroom mycelium by adding an extract of shiitake fruiting body and a shiitake culture medium as a mycelium growth promoting substance to a shiitake seed culture medium and then carrying out the usual shiitake cultivation method. In addition to preventing the invasion of harmful bacteria, Shiitake mushrooms can be cultivated by impregnating extracts of the Shiitake fruiting body and Shiitake culture medium into seed pieces bound with cloth or thread made by bundling and gluing multiple paper strings together. The purpose of the present invention is to provide a method that allows easy cultivation operations and increases Shiitake mushroom cultivation efficiency. [Structure of the Invention] The present invention prevents the invasion of harmful bacteria and promotes the growth of shiitake mushrooms, resulting in high efficiency in shiitake cultivation by adding shiitake fruiting body extract and shiitake culture medium to shiitake seed culture medium. This is a method of cultivating shiitake mushrooms that can be inoculated with shiitake mushrooms. Shiitake cultivation to which the method of the present invention is applied is a general shiitake cultivation that consists of the steps of inoculating a purely cultured shiitake seed fungus onto logs, laying down, hoisting, and collecting shiitake mushrooms, and the method of the present invention The feature of this method is that an extract of the fruiting body of the shiitake mushroom and a shiitake culture medium are used in the stage of culturing the shiitake seed fungus. The extract of the shiitake fruiting body used in the present invention is a substance extracted from the shiitake fruiting body with water, methanol, or chloroform, and further separated and purified by silica gel chromatography, and the main substance is presumed to be lipids. When the chloroform extract was further fractionated by silica gel thin layer chromatography, five spots appeared (developing solvent was chloroform:methanol = 5:1), and the second spot from the bottom was the most Since growth promoting activity was obtained,
When we searched for the constituent fatty acids of this spot fraction using gas chromatography, we found that linoleic acid and palmitic acid were overwhelmingly present. As described above, the extract of the fruiting body of Shiitake mushroom used in the present invention has the activity of promoting the growth of Shiitake mycelium in the form of water, alcohol, or chloroform, but an aqueous extract is practically preferred. The shiitake culture medium used in the present invention is horse manure decoction medium, peptone-added agar medium, asparagine-added agar medium, malt decoction agar medium, Mayer's medium, Richard's medium, Bettsfur's medium, potato agar medium, and wood rot fungi. The medium includes a medium in which mushrooms, especially shiitake, can be cultured, such as a potato-sucrose medium and a potato-sucrose medium. Among these, potato-sucrose medium is preferred. The amount of shiitake fruiting body extract added to this culture medium is preferably about 10 to 0.1%. To use this Shiitake fruiting body extract and Shiitake culture medium, the Shiitake seed fungus that has been pure cultured for Shiitake cultivation is stuffed into the hole in the log, covered with bark or wax, etc., and when inoculating, the seed fungus must be cultured, for example. Impregnate it in sawdust. Also,
When attaching shiitake seed fungi to a wedge-shaped or cylindrical piece of wood and using it as a seed piece, the piece of wood is coated or impregnated, or preferably used in the present invention is a cloth made by bundling and gluing a plurality of paper strings together. A method is used to obtain seed pieces by impregnating small cylindrical pieces tied together with thread. When using the seed pieces mentioned above, the seeds are stuffed into the holes of the logs and inoculated. The logs inoculated as described above are then placed horizontally at an angle at a temperature of approximately 5 to 35° C. and an atmospheric humidity of approximately 75% (laying down) using a conventional method. This bowing allows shiitake mycelium to propagate on the log. In the logs inoculated by the method of the present invention, the propagation of shiitake mushroom mycelium during the laying down process is significantly promoted, and the propagation is promoted approximately five times as much as in the case of a general method. As described above, the shiitake mycelia have grown on the logs and are exposed to sufficient light at 15-17℃ and the air humidity is 85%.
In a natural or artificial environment, the shiitake mushrooms will take a normal shape in one to two weeks by leaning logs at an angle of about 60 degrees from both sides (hoda-ori). After this process is completed, the shiitake mushrooms grown on the logs are collected. [Example] Example 1 40g of shiitake fruiting bodies were placed in 240ml of water, stirred at room temperature for 24 hours, and the resulting extract was centrifuged.
Concentrate the liquid phase under reduced pressure to obtain 40ml of shiitake fruiting body water extract.
get. 40 ml of the thus obtained shiitake fruiting body water extract
Potato-sucrose medium (cut 250 g of potato into small pieces, boil for about 20 minutes, filter through a cloth and make the filtrate 1. Adjust by adding 20 g of sucrose) 360 ml
In addition, paper strings were cut into 100 to 200 mm lengths and tied into a cylindrical shape of about 20 mm in the liquid, and pieces (hereinafter referred to as string strings) were tied together by wrapping them in a cloth coated with starch glue. 1,000 pieces are dipped and impregnated, then sterilized and inoculated with shiitake bacteria. These seed pieces were stuffed into the holes of the logs and inoculated, and then the shiitake mushrooms were harvested by laying down and raising the wood using the usual method. Example 2 Put 80 g of shiitake mushroom fruiting bodies into 240 ml of methanol and extract with stirring while heating at 60°C for 3 hours. The obtained extract is centrifuged, and the liquid phase is concentrated under reduced pressure to obtain 40 ml of a methanol extract of shiitake fruiting body. Add 40 ml of the thus obtained methanol extract of the shiitake fruiting body to 360 ml of potato-sucrose medium,
Thereafter, shiitake mushrooms are cultivated by impregnating the same string pieces as in Example 1 and using them as seed pieces. Example 3 Put 80 g of Shiitake mushroom fruiting bodies into 240 ml of chloroform and extract with stirring at 60°C for 3 hours.
The obtained extract is centrifuged, and the liquid phase is concentrated under reduced pressure to obtain 40 ml of a chloroform extract of shiitake fruiting body. Add 40 ml of the shiitake fruiting body chloroform extract thus obtained to 360 ml of potato-sucrose medium,
Thereafter, shiitake mushrooms are cultivated by impregnating the same string pieces as in Example 1 and using them as seed pieces. [Effect of the invention] Shiitake mushroom seed water obtained in Examples 1, 2, and 3,
Methanol, chloroform extract
Shiitake mycelial growth in a sample containing the shiitake fruiting body extract of the present invention added to a sucrose medium at 10%, 0.3%, and 0.1%, respectively, and in a medium without additives as a control was measured by the fungal weight measurement method. The results of determining the growth rate are shown in Table 1.
【表】
以上の如く、水抽出物は10%添加により無添加
区の5倍、メタノール抽出物は0.3%添加により
2倍、クロロホルム抽出物は0.1%添加により5
倍の生長活性が得られた。
さらに、実施例1の方法によりえられたヒモ駒
をコナラに接種し、370日間伏込み、剥皮面及び
木口面のシイタケ菌繁殖を算出した。
なお、実施例1のヒモ駒の乾燥防止にグリセリ
ン1%を添加したヒモ駒も試料とした。なお対照
に無添加の培地を含浸させ、シイタケ菌を接種し
たヒモ駒を用いた。
その結果は表2の通りであつた。[Table] As shown above, the water extract is 5 times that of the non-additive group when 10% is added, the methanol extract is 2 times that of the non-additive area when 0.3% is added, and the chloroform extract is 5 times the amount when 0.1% is added.
Double growth activity was obtained. Furthermore, the string pieces obtained by the method of Example 1 were inoculated into Quercus serrata and allowed to lie down for 370 days, and the proliferation of Shiitake fungi on the peeled surface and the end surface was calculated. In addition, the string piece of Example 1 to which 1% glycerin was added to prevent drying was also used as a sample. In addition, as a control, Himokoma impregnated with an additive-free medium and inoculated with Shiitake fungi was used. The results were as shown in Table 2.
【表】
表2に示すように、シイタケ子実体抽出物添加
により剥皮面、木口面とも良好な結果が得られ
た。[Table] As shown in Table 2, good results were obtained on both the peeled surface and the end surface by adding the shiitake fruiting body extract.
Claims (1)
シイタケ子実体抽出物とシイタケ培養基を添加す
ることを特徴とするシケタケ栽培法。 2 シイタケ種菌培地が木片又は紙紐の複数本を
束ねて糊をつけた布又は糸で結束した種駒である
特許請求の範囲第1項記載のシイタケ栽培法。 3 シイタケ子実体抽出物がシイタケ子実体を
水、メタノール又はクロロホルムで抽出した抽出
物である特許請求の範囲第1項記載のシイタケ栽
培法。[Scope of Claims] 1. A method for cultivating shiitake mushrooms, which comprises adding a shiitake fruiting body extract and a shiitake culture medium to a shiitake seed culture medium. 2. The shiitake mushroom cultivation method according to claim 1, wherein the shiitake seed culture medium is a seed piece made by bundling a plurality of wood chips or paper strings and binding them with glued cloth or thread. 3. The shiitake mushroom cultivation method according to claim 1, wherein the shiitake fruiting body extract is an extract obtained by extracting the shiitake fruiting body with water, methanol, or chloroform.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59064539A JPS60207520A (en) | 1984-03-30 | 1984-03-30 | Culture of mushroom (shiitake) |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59064539A JPS60207520A (en) | 1984-03-30 | 1984-03-30 | Culture of mushroom (shiitake) |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS60207520A JPS60207520A (en) | 1985-10-19 |
| JPH024258B2 true JPH024258B2 (en) | 1990-01-26 |
Family
ID=13261125
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP59064539A Granted JPS60207520A (en) | 1984-03-30 | 1984-03-30 | Culture of mushroom (shiitake) |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS60207520A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4759715B2 (en) * | 2005-11-04 | 2011-08-31 | 徳島県 | Mushroom cultivation method and mushroom cultivation medium |
| JP7770043B2 (en) * | 2021-04-08 | 2025-11-14 | 国立研究開発法人農業・食品産業技術総合研究機構 | Hydroponic cultivation method |
-
1984
- 1984-03-30 JP JP59064539A patent/JPS60207520A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS60207520A (en) | 1985-10-19 |
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