JP2005130735A - Mushroom bed for breeding stag beetle larva, and method for producing the same - Google Patents
Mushroom bed for breeding stag beetle larva, and method for producing the same Download PDFInfo
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Abstract
Description
この発明は、製造後(キノコ菌糸の成育後)、雑菌に接触してもキノコ菌糸の抵抗力が強く、又高温に保持されてもキノコの菌糸が損傷を受けず、しかもキノコの子実体が発生しにくいクワガタムシ幼虫飼育用菌床、及びその製造方法に関するものである。 After the production (after mushroom hyphae growth), the mushroom mycelium has strong resistance to contact with various germs, and the mushroom hyphae are not damaged even when kept at a high temperature. The present invention relates to a fungus bed for raising stag beetle larvae that hardly occurs, and a method for producing the same.
従来、クワガタムシ幼虫飼育用菌床には、広葉樹のオガクズを主成分とする培地に、ヒラタケ科、キシメジ科、モエギタケ科のキノコの菌糸を接種・培養したものが用いられていた。
しかしながら、従来使用されているヒラタケ科、キシメジ科、モエギタケ科のキノコの菌糸(以下従来菌糸という)を使用した、クワガタムシ幼虫飼育用菌床には下記の欠点があった。
(イ)従来菌糸は、雑菌に接触すると抵抗力が弱く、キノコの菌糸が部分的若しくは完全に死滅してしまうことが多い。
(ロ)従来菌糸を接種・培養して、折角キノコ菌糸が良好に成育した菌床が得られても、夏季の30℃を越えるような高温に保持されると、キノコ菌糸が損傷を受け、菌床が劣化してしまう。そのため、常温での保存や輸送が困難である。
(ハ)従来菌糸は、温度又は湿度の変化により子実体が発生し易い。そしてクワガタムシは、その蛹時において、菌床(培養基)内に子実体の発生があると、しばしば羽化不全となり、商品価値がなくなる。
(ニ)この培養基内の子実体の発生を防止するために、特許文献1においては、従来菌糸から、一核菌糸を調製して用いているが、この操作は非常に煩雑で管理が難しい。
However, the mycelium for stag beetle larvae using mushroom mycelium (hereinafter referred to as conventional mycelium) of the oyster mushroom family, xylem family, and Moegiaceae family used conventionally has the following drawbacks.
(A) Conventional mycelia have low resistance when they come into contact with various germs, and mushroom mycelia are often partially or completely killed.
(B) Even if a mycelium in which the benthic mushroom mycelium is well grown is obtained by inoculating and culturing the mycelium conventionally, if it is kept at a high temperature exceeding 30 ° C in summer, the mushroom mycelium will be damaged, The fungus bed will deteriorate. Therefore, it is difficult to store and transport at room temperature.
(C) Conventional mycelium tends to generate fruit bodies due to changes in temperature or humidity. When stag beetles are found in the fungus bed (culture medium) at the time of drought, they often fail to emerge and lose commercial value.
(D) In order to prevent the occurrence of fruiting bodies in the culture medium, in Patent Document 1, mononuclear mycelia are prepared and used from conventional mycelia, but this operation is very complicated and difficult to manage.
発明者は、以上の欠点を解消するために、雑菌の侵入や高温に対し抵抗力が強く、しかも子実体が発生しにくいキノコを選別したところ、アガリクス属(Agaricus)のキノコの菌糸が、前記欠点を全て解消することを知り本発明を完成した。 In order to eliminate the above disadvantages, the inventor selected mushrooms that are highly resistant to invasion of germs and high temperatures, and that are unlikely to produce fruit bodies. As a result, the mycelium of the mushrooms of the genus Agaricus Knowing that all the drawbacks were eliminated, the present invention was completed.
本願発明は上記の欠点を解決するためになされたもので、下記の請求項1〜請求項7により構成されている。
請求項1: 広葉樹のオガクズを主原料とする培地に、アガリクス属のキノコの菌糸を成育させたことを特徴とするクワガタムシの幼虫飼育用菌床。
請求項2: アガリクス属のキノコが、カワリハラタケである請求項1に記載するクワガタムシの幼虫飼育用菌床。
請求項3: 広葉樹がクヌギ、エノキ、ブナ、ナラ、カシ、シイ、サクラ、又はクリである請求項1又は請求項2に記載するクワガタムシの幼虫飼育用菌床。
請求項4: 下記の(1)〜(3)の工程を順次経ることを特徴とするクワガタムシの幼虫飼育用菌床の製造方法。
(1)広葉樹のオガクズを主原料とする培地に、フスマ、小麦粉、おから、ビール粕、酵母エキス、ビタミン類、アミノ酸類等から選択される副原料の1種以上を加えた混合物を得る工程
(2)前記混合物を、耐熱性の容器に詰めて加圧蒸気殺菌する工程
(3)アガリクス属のキノコの菌糸を接種して培養する工程
請求項5: アガリクス属のキノコが、カワリハラタケである請求項4に記載するクワガタムシの幼虫飼育用菌床の製造方法。
請求項6: 培養温度が、20〜29℃、培養期間が50〜90日である請求項5に記載するクワガタムシの幼虫飼育用菌床の製造方法。
請求項7: 耐熱性の容器がガラス製、又は耐熱性プラスチック製である請求項5又は請求項6に記載するクワガタムシの幼虫飼育用菌床の製造方法。
The present invention has been made to solve the above-mentioned drawbacks, and is constituted by the following claims 1 to 7.
Claim 1: A fungus bed for breeding stag beetles, characterized in that a mycelium of mushrooms belonging to the genus Agaricus is grown in a medium mainly composed of hardwood sawdust.
[2] The fungus bed for stag beetle larva breeding according to [1], wherein the mushroom belonging to the genus Agaricus is Kawariharatake.
[3] The fungus bed for raising larvae of stag beetles as described in [1] or [2], wherein the broad-leaved tree is geese, enoki, beech, oak, oak, shii, cherry or chestnut.
[4] A method for producing a fungus bed for stag beetle larva rearing, which comprises sequentially performing the following steps (1) to (3):
(1) A step of obtaining a mixture obtained by adding one or more auxiliary materials selected from bran, flour, okara, beer lees, yeast extracts, vitamins, amino acids, etc., to a medium mainly composed of hardwood sawdust (2) A step of filling the mixture in a heat-resistant container and sterilizing under pressure steam (3) A step of inoculating and inoculating hyphae of agaricus mushrooms Claim 5: The agaricus mushrooms are Kawariharatake Item 5. A method for producing a fungus bed for stag beetle larva breeding according to Item 4.
[6] The method for producing a stag beetle larva breeding bed according to [5], wherein the culture temperature is 20 to 29 ° C. and the culture period is 50 to 90 days.
[7] The method for producing a fungus bed for stag beetle larvae according to [5] or [6], wherein the heat-resistant container is made of glass or heat-resistant plastic.
本願発明を以上のように構成する理由は、従来菌糸に代えてアガリクス属のキノコの菌糸、特にカワリハラタケ(Agaricus brazei)の菌糸を成育させたクワガタムシ幼虫飼育用菌床は、従来菌糸に比較して雑菌の侵入や高温に対し抵抗力が強く、長期間常温で保存可能であり、しかも子実体が発生しにくいためである。 The reason why the present invention is configured as described above is that the mycelium for raising stag beetles larvae in which hyphae of mushrooms of the genus Agaricus, in particular, mycelia of Agaricus brazei, are grown instead of the conventional mycelia is compared with the conventional mycelium. This is because it is highly resistant to invasion of bacteria and high temperatures, can be stored at room temperature for a long time, and fruit bodies are unlikely to occur.
本願発明のクワガタムシの幼虫飼育用菌床に成育しているアガリクス属のキノコ菌糸は、従来菌糸に比較して雑菌の侵入や高温に対し抵抗力が強く、しかも子実体が発生しにくいので下記の優れた効果が得られる。
(イ)クワガタムシがその蛹時に子実体と共生する機会がないため、羽化不全障害を激減させることが可能となる。
(ロ)菌床が高温に保持されても変質・劣化しないので、夏季の高温時においても菌床(培養基)を冷蔵保存する必要がない。
(ハ)菌床が長期間にわたって変質・劣化せず、餌としての効果が長期間持続するので、餌交換の頻度をが減少させることができる。そのため餌交換によるクワガタムシの体重減少を防止することができ、良好に成長させることができる。
(ニ)前記(イ)〜(ハ)の技術的効果は、クワガタムシの幼虫飼育用菌床の製造コスト、及び流通コストを著しく軽減し、ひいては良質なクワガタムシの成虫個体を安価に提供することを可能にする。
The mushroom mycelium of the genus Agaricus that grows on the larva rearing stag beetle of the present invention is more resistant to invasion of bacteria and high temperatures than conventional hyphae, and is less likely to produce fruiting bodies. Excellent effect is obtained.
(B) Since the stag beetle does not have the opportunity to live with the fruiting body at the time of its drought, it is possible to drastically reduce the emergence failure.
(B) Since the fungus bed is kept at a high temperature and does not deteriorate or deteriorate, it is not necessary to store the fungus bed (culture medium) in a refrigerator even at high temperatures in summer.
(C) The fungus bed does not deteriorate or deteriorate over a long period of time, and the effect as a bait lasts for a long period of time, so the frequency of bait exchange can be reduced. Therefore, it is possible to prevent weight loss of stag beetles due to food exchange and to grow well.
(D) The technical effects (a) to (c) described above significantly reduce the production cost and the distribution cost of the stag beetle larvae breeding bed, and thus provide high-quality adult stag beetles at low cost. to enable.
本願発明において、広葉樹(特にクヌギ、エノキ、ブナ、ナラ、クリ、カシ、シイ、サクラ)のオガクズは、生のものを使用するのが好ましい。
本願発明に用いられるキノコの菌糸は、ハラタケ科のアガリクス属のキノコの菌糸である。
アガリクス属の菌糸としては、カワリハラタケ(Agaricus brazei)の他に、ツクリタケ(Agaricus bisporus)、シロオオハラタケ(Agaricus arvensis)が汎用される。
本願発明の菌床により飼育されるクワガタムシは、クワガタムシ科の昆虫をいう(特に市場性の良好なオオクワガタ、ノコギリクワガタ、ヒラタクワガタ、コクワガタ等の成育に適している。)。
本願発明に用いられる培養基(菌床)の広葉樹(オガクズ)以外の原料としては、小麦粉、フスマ、おから、ビール粕、酵母エキス、アミノ酸類、ビタミン類、無機塩類等が用いられる。
本願発明に用いられる培養基(菌床)は、通常上記培地原料に水を加えて、その水分含量を40〜70重量%に調整して用いる。
本願発明の培養基(菌床)の殺菌は加圧蒸気により行なわれ、通常耐熱性細菌の胞子(Bacillus)を死滅させる条件(例えば120℃で40分)が採用される。
本願発明の培養基(菌床)を詰める耐熱性の容器は、その内部を観察できるガラス容器が好ましいが、耐熱性プラスチック(例えばポリプロピレン)製でも全く支障がない。
本願発明において、培養基(菌床)にアガリクス属のキノコの菌糸を接種して培養する温度は、15〜30℃、より好ましくは20〜29℃であり、培養期間は20〜100日、より好ましくは50〜90日である。
In the present invention, it is preferable to use raw sawdust of hardwood (especially kunugi, enoki, beech, oak, chestnut, oak, shii, cherry).
The mycelium of the mushroom used in the present invention is a mycelium of a mushroom belonging to the genus Agaricus belonging to the family Agaricaceae.
As mycelium of the genus Agaricus, in addition to Agaricus brazei, agaricus bisporus and agaricus arvensis are widely used.
The stag beetle bred on the fungus bed of the present invention refers to an insect of the family Stag beetle (especially suitable for the growth of stag beetle, sawtooth stag beetle, stag beetle, stag beetle, etc. having good marketability).
As raw materials other than the broad-leaved tree (sawdust) of the culture medium (fungus bed) used in the present invention, flour, bran, okara, beer lees, yeast extract, amino acids, vitamins, inorganic salts and the like are used.
The culture medium (bacteria bed) used in the present invention is usually used by adding water to the medium raw material and adjusting the water content to 40 to 70% by weight.
Sterilization of the culture medium (bacteria bed) of the present invention is carried out with pressurized steam, and usually a condition for killing spores (Bacillus) of heat-resistant bacteria (for example, at 120 ° C. for 40 minutes) is employed.
The heat-resistant container filled with the culture medium (bacteria bed) of the present invention is preferably a glass container capable of observing the inside, but even when made of a heat-resistant plastic (for example, polypropylene), there is no problem.
In this invention, the temperature which inoculates a culture medium (mycelium bed) with the mycelium of the genus Agaricus genus is 15-30 degreeC, More preferably, it is 20-29 degreeC, The culture period is 20-100 days, More preferably Is 50-90 days.
下記の配合により原料を混合した。
ブナ:ナラ:クヌギ=1:1:1のオガクズ(水分41%) 50重量%
小麦粉(水分14%) 4重量%
フスマ(水分11%) 5重量%
酵母エキス 1重量%
水 40重量%
(TOTAL水分) (61重量%)
The raw materials were mixed according to the following formulation.
Beech: Nara: Knugi = 1: 1: 1 sawdust (41% moisture) 50% by weight
Flour (moisture 14%) 4% by weight
5% by weight (11% moisture)
1% by weight of yeast extract
40% by weight of water
(TOTAL moisture) (61 wt%)
前記混合物を、容量800mlのガラスビンに400g詰め、通気性のあるキャップをして、オートクレーブで120℃、40分間滅菌して、クワガタムシの幼虫飼育用培養基を200本得た。この培養基にカワリハラタケの菌糸を接種し、27℃で、65日間培養した。
前記200本の培養基内に、カワリハラタケの菌糸が蔓延した菌床は、199本であり、極めて成功率が高かった。
400 g of the mixture was put into a glass bottle with a capacity of 800 ml, a cap having air permeability was sterilized, and sterilized in an autoclave at 120 ° C. for 40 minutes to obtain 200 culture media for raising stag beetles. This culture medium was inoculated with the mycelium of Kawariharatake and cultured at 27 ° C. for 65 days.
The number of fungal beds in which the mycelium of Agaricus mushrooms spread in the 200 culture media was 199, and the success rate was extremely high.
前記段落0009及び段落0010と同一の方法で調製したカワリハラタケの菌糸が蔓延した菌床100本を、120日間屋内の常温で保存テストを実施したところ、外見から劣化したことを目測で判断できたものは1本もなかった。又カビの発生したもの及び子実体が発生したものも1本もなかった。
これに対し、前記段落0009及び段落0010と同一の方法で得た、従来菌糸のヒラタケ(Pleurotus ostreatus)の菌糸が蔓延した菌床100本を同一の条件で保存しところ、外見から劣化したと目測で判断できたものは16本であり、又カビの発生したものは1本、子実体が発生したものは27本であった。
A 100-bed mycelium infested with agaric mycelium prepared by the same method as in paragraphs 0009 and 0010 was subjected to a storage test at room temperature indoors for 120 days. There was no one. In addition, there was no mold and no fruiting body.
On the other hand, when 100 fungal beds infested with mycelia of oyster mushrooms (Pleurotus ostreatus) obtained by the same method as in paragraphs 0009 and 0010 were stored under the same conditions, it was estimated that they had deteriorated in appearance. The number of cases that could be judged was 16; the number of molds was 1; and the number of fruiting bodies was 27.
前記段落0009及び段落0010と同一の方法で調製したカワリハラタケの菌糸が蔓延した菌床100本を、30日間、40℃で保存テストを実施したところ、外見から劣化したと目測で判断できたものは1本もなく、カワリハラタケの菌糸が確認できた。
これに対し、前記段落0009及び段落0010と同一の方法で得た、従来菌糸のヒラタケの菌糸が蔓延した菌床100本を同一の条件で保存しところ、外見から劣化したと目測で判断できたものは100本であった。
A storage test was carried out at 40 ° C. for 30 days, in which 100 hyphae mushroom hyphae infested, prepared by the same method as in paragraphs 0009 and 0010, was found to have been visually determined to have deteriorated from appearance. There was no one, and mycelia of Kawariharatake was confirmed.
On the other hand, when 100 fungal beds in which the mycelium of the oyster mushrooms of the conventional mycelium obtained by the same method as the above paragraphs 0009 and 0010 were stored under the same conditions, it could be judged by visual observation that the appearance was deteriorated. There were 100 items.
前記段落0009及び段落0010と同一の方法で調製したカワリハラタケの菌糸が蔓延した菌床100本を、温度ショックを与えるために24時間、5℃の低温にさらし、その後10日間常温に保持して、子実体が発生するや否やについて調べたところ、子実体が発生したものは1本もなかった。
これに対し、前記段落0009及び段落0010と同一の方法で得た、従来菌糸のヒラタケの菌糸が蔓延した菌床100本を同一の条件で保存したところ、子実体が発生したものは42本であった。
In order to give a temperature shock, 100 bacterial beds infested with mycelia of Kawariharatake prepared by the same method as in paragraphs 0009 and 0010 are exposed to a low temperature of 5 ° C. for 24 hours and then kept at a normal temperature for 10 days. As a result of investigating immediately after the occurrence of a child entity, none of the child entities occurred.
On the other hand, when 100 fungal beds in which the mycelium of oyster mushrooms in the conventional hyphae obtained by the same method as in paragraphs 0009 and 0010 were stored under the same conditions, 42 fruit bodies were generated. there were.
前記段落0010〜0013の結果によれば、本願発明に係るクワガタムシ幼虫飼育用菌床は、常温保存が可能であり、特に夏場の暑い時期にも冷蔵する必要がなく、子実体の発生もないことがわかる。 According to the results of the above paragraphs 0010 to 0013, the stag beetle larvae breeding bed according to the present invention can be stored at room temperature, and does not need to be refrigerated even in the hot summer season, and no fruiting body is generated. I understand.
前記段落0009及び段落0010で調製した菌床に、国産のオオクワガタ、ノコギリクワガタ、ヒラタクワガタ、コクワガタ等の幼虫を入れ、実際の飼育テストを行なった。
その結果、菌床へ初令幼虫を投入しても、幼虫の成長は極めて良好であった。
Larvae such as domestic stag beetle, sawtooth stag beetle, stag beetle, stag beetle, etc. were put into the fungus bed prepared in paragraphs 0009 and 0010, and an actual rearing test was performed.
As a result, the growth of larvae was extremely good even when the primary larvae were introduced into the fungus bed.
容量1500mlのガラスビンを使用する(培養基750g充填)以外は、前記段落0009及び段落0010と同じ方法で調製したカワリハラタケの菌糸が蔓延した菌床に、国産のオオクワガタ、ノコギリクワガタ、ヒラタクワガタ、コクワガタ等の幼虫を入れ、実際の飼育テストを行なったところ、初令幼虫から餌交換なしで、大型の個体を羽化させることができた。
Except for using a glass bottle with a capacity of 1500 ml (filled with 750 g of culture medium), larvae such as Japanese stag beetle, sawtooth stag beetle, stag beetle, stag beetle, etc. When the actual rearing test was carried out, large individuals could emerge from the early larvae without exchanging food.
Claims (7)
(1)広葉樹のオガクズを主原料とする培地に、フスマ、小麦粉、おから、ビール粕、酵母エキス、ビタミン類、アミノ酸類等から選択される副原料の1種以上を加えた混合物を得る工程
(2)前記混合物を、耐熱性の容器に詰めて加圧蒸気殺菌する工程
(3)アガリクス属のキノコの菌糸を接種して培養する工程 A method for producing a fungus bed for raising larvae of stag beetles characterized by sequentially performing the following steps (1) to (3):
(1) A step of obtaining a mixture obtained by adding one or more auxiliary materials selected from bran, flour, okara, beer lees, yeast extracts, vitamins, amino acids, etc., to a medium mainly composed of hardwood sawdust (2) Step of filling the mixture in a heat-resistant container and sterilizing under pressure steam (3) Step of inoculating and inoculating mycelia of mushrooms belonging to the genus Agaricus
The method for producing a stag beetle larva breeding bed according to claim 5 or 6, wherein the heat-resistant container is made of glass or heat-resistant plastic.
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Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007312686A (en) * | 2006-05-26 | 2007-12-06 | General Environmental Technos Co Ltd | Method and material for accelerating growth of beetle larva |
CN104225636A (en) * | 2014-09-28 | 2014-12-24 | 天津农学院 | Programmed temperature rise sterilization method of edible fungi culture material |
CN106234312A (en) * | 2016-08-05 | 2016-12-21 | 云南省烟草公司昆明市公司 | A kind of save space, low cost, a confession kind method for the aphidius gifuensis of economical and efficient |
CN106962298A (en) * | 2017-05-26 | 2017-07-21 | 何振贤 | A kind of method of the grizzled bar longicorn in utilization Kazakhstan Zhong Tuifengfang Zhiduo County |
CN107660426A (en) * | 2017-12-05 | 2018-02-06 | 登封市绿奥农林科技有限公司 | A kind of method for the leg honeybee preventing and treating control of Apriona swainsoni that swollen using Kazakhstan |
CN109744205A (en) * | 2017-11-08 | 2019-05-14 | 丹阳市长富农业技术有限公司 | A kind of breeding method of beans pellet |
CN110896929A (en) * | 2019-12-09 | 2020-03-24 | 元谋联展农业科技有限公司 | American cockroach cultivation method and cultivation system |
-
2003
- 2003-10-29 JP JP2003368281A patent/JP2005130735A/en active Pending
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2007312686A (en) * | 2006-05-26 | 2007-12-06 | General Environmental Technos Co Ltd | Method and material for accelerating growth of beetle larva |
CN104225636A (en) * | 2014-09-28 | 2014-12-24 | 天津农学院 | Programmed temperature rise sterilization method of edible fungi culture material |
CN106234312A (en) * | 2016-08-05 | 2016-12-21 | 云南省烟草公司昆明市公司 | A kind of save space, low cost, a confession kind method for the aphidius gifuensis of economical and efficient |
CN106234312B (en) * | 2016-08-05 | 2019-02-26 | 云南省烟草公司昆明市公司 | A kind of save space, low cost, the aphidius gifuensis of economical and efficient for kind of a method |
CN106962298A (en) * | 2017-05-26 | 2017-07-21 | 何振贤 | A kind of method of the grizzled bar longicorn in utilization Kazakhstan Zhong Tuifengfang Zhiduo County |
CN109744205A (en) * | 2017-11-08 | 2019-05-14 | 丹阳市长富农业技术有限公司 | A kind of breeding method of beans pellet |
CN107660426A (en) * | 2017-12-05 | 2018-02-06 | 登封市绿奥农林科技有限公司 | A kind of method for the leg honeybee preventing and treating control of Apriona swainsoni that swollen using Kazakhstan |
CN110896929A (en) * | 2019-12-09 | 2020-03-24 | 元谋联展农业科技有限公司 | American cockroach cultivation method and cultivation system |
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