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JPH0724503B2 - Mushroom culture medium - Google Patents
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JPH0724503B2 - Mushroom culture medium - Google Patents

Mushroom culture medium

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Publication number
JPH0724503B2
JPH0724503B2 JP3081526A JP8152691A JPH0724503B2 JP H0724503 B2 JPH0724503 B2 JP H0724503B2 JP 3081526 A JP3081526 A JP 3081526A JP 8152691 A JP8152691 A JP 8152691A JP H0724503 B2 JPH0724503 B2 JP H0724503B2
Authority
JP
Japan
Prior art keywords
mycelium
growth
larch
water extract
addition
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
JP3081526A
Other languages
Japanese (ja)
Other versions
JPH04293430A (en
Inventor
幸司 高畠
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Toyama Prefecture
Original Assignee
Toyama Prefecture
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Toyama Prefecture filed Critical Toyama Prefecture
Priority to JP3081526A priority Critical patent/JPH0724503B2/en
Publication of JPH04293430A publication Critical patent/JPH04293430A/en
Publication of JPH0724503B2 publication Critical patent/JPH0724503B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Mushroom Cultivation (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明はヒラタケ、エノキタケ、
ヤナギマツタケ等で代表されるきのこの培養基に関す
る。
The present invention relates to oyster mushrooms, enoki mushrooms,
The present invention relates to a culture medium of mushrooms represented by Willow Matsutake.

【0002】[0002]

【従来の技術】わが国においては食生活の向上に伴ない
食用きのこの需要が急激に増大している。この需要に応
えるために食用きのこの人工栽培が広く行われている
が、近年原木の入手難の事情と安定生産の要請から、原
木栽培に代わって菌床栽培が急速に拡大しつつある。
2. Description of the Related Art In Japan, the demand for edible mushrooms is rapidly increasing with the improvement of eating habits. In order to meet this demand, artificial cultivation of edible mushrooms is widely carried out, but in recent years, fungal bed cultivation is rapidly expanding in place of the raw wood cultivation due to the difficulty of obtaining the raw wood and the demand for stable production.

【0003】菌床栽培は、一般的に鋸屑などの木質粉体
に米糠等の栄養剤を添加し、さらに栄養補助成分として
の窒素源や無機塩類を少量混合した培養基を滅菌し、菌
糸体を接種して培養(菌まわし)を行なって培地全体に
菌糸体を蔓延させた後、子実体を形成させ、それを収穫
するものである。
In bacterial bed cultivation, nutrients such as rice bran are generally added to wood powder such as sawdust, and a culture medium in which a small amount of a nitrogen source or an inorganic salt as a nutritional supplement component is mixed is sterilized to form a mycelium. After inoculating and culturing (rotating the fungus) to spread the mycelium over the entire medium, fruit bodies are formed and harvested.

【0004】[0004]

【発明が解決しようとする課題】しかしながら、上記の
ような従来行われている菌床栽培では、培養不良や害菌
汚染により子実体収率が低いので、高収穫量を得ること
はなかなか難しく、また栽培が長期間にわたるため生産
効率が充分でないという問題点があった。
However, in the conventional fungal bed cultivation as described above, it is difficult to obtain a high yield because the fruiting body yield is low due to poor culture or contamination with harmful bacteria. Further, there is a problem that the production efficiency is not sufficient because the cultivation is for a long period of time.

【0005】そこで本発明者は、菌床栽培において子実
体の収穫量の良否および栽培期間の長短は、きのこの菌
糸体をいかに充分に培養できるかにかかっており、菌糸
体の生育が不充分な場合には決して良好な結果を得るこ
とができないとの知見に基づき、培養基中でいかに早
く、しかも多量の菌糸体を生長させるかについて長年鋭
意研究を重ねてきた結果、菌糸体の生長速度が早めら
れ、培養日数の短縮と共に作業効率を高めた栽培が可能
となり、延いては収穫量の飛躍的増大が期待できる菌糸
体量が豊富で害菌の生長を抑制できるきのこの培養基を
得ることに成功したものである。
Therefore, the inventors of the present invention have found that the yield of fruiting bodies and the length of the cultivation period in the fungal bed cultivation depend on how well the mycelia of the mushroom can be cultivated, and the mycelia grow insufficiently. In many cases, based on the finding that good results can never be obtained, as a result of many years of earnest research on how to grow a large amount of mycelium in the culture medium, the growth rate of the mycelium It is possible to accelerate the cultivation, shortening the number of culturing days and cultivating with improved working efficiency, and further, it is possible to expect a drastic increase in the yield, and to obtain a mushroom culture medium that is rich in mycelium and can suppress the growth of harmful fungi It was successful.

【0006】[0006]

【課題を解決するための手段】本発明は新しく見出ださ
れたカラマツ材の水抽出物のきのこ菌糸体への生長促進
作用と害菌への生長抑制作用に着目し、この抽出物を人
工培養基に対して適正な濃度の割合で添加することを特
徴とするものである。
Means for Solving the Problems The present invention focuses on the newly found water extract of larch wood to promote the growth of mushroom mycelia and suppress the growth of harmful fungi. It is characterized in that it is added at an appropriate concentration ratio to the culture medium.

【0007】樹木の抽出成分には、きのこ菌糸体の生長
に対して、栄養となる成分、阻害となる成分、害菌のみ
の生育を抑える成分がある。カラマツ水抽出物は主要構
成成分がアラビノガラクタンであって、抽出物の90パ
ーセント以上を占めている。そして、このアラビノガラ
クタンは多くの樹木のうちカラマツに特異的に存在する
多糖類であり、これまで生薬や微生物由来のアラビノガ
ラクタンにはさまざまな生理活性機能があることが報告
されている(例えば、「山田陽城;漢方薬中の免疫賦活
アラビノガラクタン,東洋医学,Vo17,No1,1
986」「土師美惠子;樹葉多糖類の生理活性,農水省
森林総合研究所研究成果選集,1989」)。また、カ
ラマツ水抽出物には微量のタキシホリンが含まれてお
り、タキシホリンは抗菌作用のあるフラボノイドである
(善本知孝など編;木材利用の化学,共立出版,198
3)。
The extracted components of trees include a nutrient component, an inhibitory component, and a component that suppresses the growth of only harmful fungi with respect to the growth of mushroom mycelium. The main constituent of larch water extract is arabinogalactan, which accounts for over 90% of the extract. And, this arabinogalactan is a polysaccharide that specifically exists in larch among many trees, and it has been reported that arabinogalactan derived from crude drugs and microorganisms has various bioactive functions ( For example, "Yamada Yoshiro; Immunostimulating arabinogalactan in Chinese medicine, Oriental medicine, Vo17, No1,1
986 "," Mieko Hajii; Physiological activity of leaf polysaccharides, Forest Research Institute of the Ministry of Agriculture, Forestry and Fisheries, 1989 "). In addition, the larch water extract contains a trace amount of taxifolin, which is a flavonoid having an antibacterial action (edited by Tomotaka Yoshimoto et al .; Chemistry of Wood Utilization, Kyoritsu Shuppan, 198).
3).

【0008】この有効な生理活性機能があるとされるア
ラビノガラクタンを多量に含有するカラマツ水抽出物を
培地に添加して各種食用きのこを培養した結果、このカ
ラマツ水抽出物はきのこの菌糸体に顕著な伸長作用と重
量増大作用を与えていることが認められた。また、抗菌
作用のあるタキシホリンを微量に含有するカラマツ水抽
出物を添加した培地できのこ栽培の主要害菌を培養した
結果、カラマツ水抽出物には、害菌の生長を抑制する作
用が認められた。
The larch water extract containing a large amount of arabinogalactan, which is said to have this effective physiologically active function, was added to the medium to culture various edible mushrooms. As a result, the larch water extract mushroom mycelium was obtained. It was confirmed that the sucrose had a remarkable elongation effect and a weight increasing effect. In addition, as a result of culturing the main harmful fungi of mushroom cultivation in a medium containing a larch water extract containing a small amount of taxifolin having an antibacterial action, the larch water extract was found to have an action of suppressing the growth of the harmful fungus. It was

【0009】[0009]

【実施例】次に、本発明の実施例について説明する。カ
ラマツ材鋸屑1部に対して水5部(重量比)を加え、室
温で30分間攪拌しながら水溶性エキス分を抽出し、そ
の抽出液をろ過したろ液を減圧濃縮し、これを乾燥、粉
砕してカラマツ水抽出物を得る。
EXAMPLES Next, examples of the present invention will be described. Water (5 parts by weight) was added to larch sawdust (1 part), the water-soluble extract was extracted while stirring at room temperature for 30 minutes, and the filtrate obtained by filtering the extract was concentrated under reduced pressure and dried. Grind to obtain a larch water extract.

【0010】次に、人工培養基の主成分としてのポテト
・デキストロース寒天培地にカラマツ水抽出物を0〜1
5%の範囲内で添加し、きのこ菌糸体を接種した。これ
を25℃で6日間培養して菌糸体の伸長生長を測定し
た。測定した結果は表1のとおりである。
Next, 0 to 1 of larch water extract was added to potato-dextrose agar medium as a main component of the artificial culture medium.
It was added within the range of 5% and inoculated with mushroom mycelium. This was cultured at 25 ° C. for 6 days to measure the elongation growth of mycelium. The measured results are shown in Table 1.

【0011】[0011]

【表1】 [Table 1]

【0012】この表1から、ヒラタケにおいては1〜5
%の添加範囲で添加しないものに比べて15%前後の伸
長効果があり、また、エノキタケでは1〜2%の範囲の
添加量で伸長効果が認められ、さらにヤナギマツタケで
は1〜5%の添加条件で10〜15%程度の伸長促進効
果があることが認められた。
From Table 1, 1 to 5 for oyster mushrooms
%, There is an extension effect of about 15% compared to the case where it is not added, and the extension effect is recognized with the addition amount of 1 to 2% in Enokitake, and 1-5% addition is added to Willow Matsutake. It was confirmed that there was an elongation promoting effect of about 10 to 15% under the conditions.

【0013】次いで、前回と同様にポテト・デキストロ
ース寒天培地にカラマツ水抽出物を0〜15%の範囲内
で添加すると共にきのこ菌糸体を接種し、これを25℃
で10日間培養した後、寒天を溶解、除去して菌糸体の
重量を測定した。その測定の結果は表2に示すとおりで
ある。
Then, as in the previous time, the larch water extract was added to the potato-dextrose agar medium within the range of 0 to 15% and the mushroom mycelium was inoculated at 25 ° C.
After culturing for 10 days, the agar was dissolved and removed, and the weight of the mycelium was measured. The results of the measurement are shown in Table 2.

【0014】[0014]

【表2】 [Table 2]

【0015】表2から、ヒラタケ及びエノキタケにおい
ては、1〜10%の添加範囲内での添加量が増えるのに
伴なって重量が次第に増大し、いずれも10%の添加量
では添加しないものに比べて約3.4倍量と3.1倍量
に達して最大の数値を示た。ヤナギマツタケでは1〜5
%の添加範囲内で添加量が増えるのにしたがって増大
し、特に添加量が5%では添加しないものに比べて3.
2倍量と著しく増大していた。また、10%の添加であ
っても、全く添加しないものに比べて約2.3倍量の重
量増加が認められた。
From Table 2, in the case of Pleurotus ostreatus and Enoki mushroom, the weight gradually increased as the amount added in the addition range of 1 to 10% increased. In comparison, it reached the maximum value, reaching about 3.4 times and 3.1 times the quantity. 1-5 for Willow Matsutake
%, It increases as the addition amount increases within the addition range of 3%.
It was remarkably increased to double the amount. Further, even with 10% addition, a weight increase of about 2.3 times as much as that without addition was observed.

【0016】さらに、人工培養基の主成分としてのポテ
ト・デキストロース液体培地を使用し、これにカラマツ
水抽出物を0〜15%の範囲内で添加した培養基におい
て、接種したきのこ菌糸体を24℃で10日間培養して
菌糸体の重量を測定した。測定した結果は表3のとおり
である。
Furthermore, using potato dextrose liquid medium as the main component of the artificial culture medium, to the culture medium in which the larch water extract was added within the range of 0 to 15%, the inoculated mushroom mycelium was grown at 24 ° C. After culturing for 10 days, the weight of mycelium was measured. The measured results are shown in Table 3.

【0017】[0017]

【表3】 [Table 3]

【0018】この表3からヒラタケでは、1%を添加し
ただけで2倍量以上の菌糸体が得られ、さらに10%の
添加範囲内では添加量が増えるのに伴なって菌糸体重量
が増加し、5〜10%の範囲内の添加では無添加のもの
に比べて2.9〜3.1倍量の菌糸体が得られ、また1
5%の添加であっても3倍量を超える重量増加が認めら
れた。
From Table 3, it is possible to obtain more than double the amount of mycelium by adding 1% to the oyster mushroom, and the mycelium weight increases with the increasing amount within the addition range of 10%. However, when added within the range of 5 to 10%, the mycelium was obtained in an amount of 2.9 to 3.1 times that of the non-added one.
Even with the addition of 5%, a weight increase exceeding 3 times was observed.

【0019】エノキタケでは、1〜10%の添加範囲内
で添加量が増えるのに従って菌糸体重量が増加し、特に
5〜10%の範囲では添加しないものに比べて2.3〜
3.6倍量になっており、また15%の添加でも3倍量
を超える重量増加が認められた。ヤナギマツタケでは、
1〜5%の添加範囲で添加量が増えるのに従って菌糸体
重量が増加し、殊に5%の添加では無添加のものに比べ
て約2.3倍量になっており、また10%では約2倍
量、15%でも1.7倍量の菌糸体の増量が認められ
た。
In the case of Enoki mushroom, the weight of mycelium increases as the amount added increases in the addition range of 1 to 10%, and particularly 2.3 to 10% in the range of 5 to 10% as compared with the one not added.
The amount was 3.6 times the amount, and even with the addition of 15%, the weight increase exceeding 3 times the amount was recognized. In Willow Matsutake,
The weight of mycelium increased as the amount of addition increased in the range of addition of 1 to 5%, and in particular, the amount of addition of 5% was about 2.3 times as much as that of no addition, and 10%. About twice the amount, and even at 15%, the amount of mycelia increased 1.7 times.

【0020】次に、スギ木粉3部に対して米糠1部を混
合(重量比)した木粉培地を人工培養基の主成分として
使用し、これに木粉培地の乾物重量に対してカラマツ水
抽出物を0〜15%の割合で添加し、含水率が約65%
になるように調整し、接種したきのこの菌糸体を24℃
にて20日間培養して菌糸体の伸長生長を測定した。測
定した結果は表4のとおりである。
Next, a wood flour medium in which 1 part of rice bran was mixed with 3 parts of cedar wood flour (weight ratio) was used as a main component of the artificial culture medium, and larch water was added to dry matter weight of the wood flour medium. The extract is added at a rate of 0 to 15%, and the water content is about 65%.
And adjust the mycelium of inoculated mushrooms to 24 ℃
The cells were cultured for 20 days at 20 ° C. and the growth of mycelia was measured. The measured results are shown in Table 4.

【0021】[0021]

【表4】 [Table 4]

【0022】この表4からヒラタケでは、1〜10%の
添加範囲内で無添加のものに比べて4〜14%増の伸長
生長が認められ、またエノキタケでは、1〜5%の添加
範囲で無添加と比べて7〜9%増の伸長生長が認めら
れ、さらにヤナギマツタケでは1〜10%の添加条件下
で無添加のものに比べて3〜10%増の伸長効果が認め
られた。
From Table 4, in the oyster mushroom, an elongation growth of 4 to 14% was recognized in the addition range of 1 to 10% as compared with the non-added one, and in the enoki mushroom, the addition range was 1 to 5%. An elongation growth of 7 to 9% was observed as compared with that without addition, and a growth effect of Willow matsutake increased by 3 to 10% under the addition condition of 1 to 10% as compared with that without addition.

【0023】きのこ栽培において、害菌汚染の程度はき
のこの生産効率に大きく影響し、カラマツ水抽出物がき
のこ菌糸体以上に害菌をも生長促進させると結果的にカ
ラマツ水抽出物を添加する意味がなくなる。そこで、き
のこの健全な生長を阻害する害菌に対してカラマツ水抽
出物が及ぼす影響を実験した。
In mushroom cultivation, the degree of contamination of harmful bacteria greatly affects the production efficiency of mushrooms, and when the larch water extract promotes the growth of harmful bacteria more than the mushroom mycelium, the larch water extract is added as a result. It makes no sense. Therefore, the effect of the larch water extract on the harmful bacteria that inhibit the healthy growth of mushrooms was tested.

【0024】実験の方法としては、ポテト・デキストロ
ース寒天培地に、0〜15%の濃度範囲内でカラマツ水
抽出物を添加した後、主要害菌であるトリコデルマ菌を
接種し、24℃にて48時間乃至72時間培養して害菌
の菌糸体の伸長生長を測定した。その測定結果は表5に
示すとおりである。
As a method of experiment, after adding larch water extract in a concentration range of 0 to 15% to potato-dextrose agar medium, Trichoderma bacterium, which is a main harmful bacterium, was inoculated, and at 48 ° C. at 48 ° C. After culturing for 72 hours to 72 hours, the elongation growth of the mycelium of the harmful fungus was measured. The measurement results are as shown in Table 5.

【0025】[0025]

【表5】 [Table 5]

【0026】表5から明らかなように、添加量の増加に
伴なって概ねトリコデルマ菌の生長を抑制する作用が強
く働き、カラマツ水抽出物5%の添加では11〜17
%、10%の添加では24〜29%の抑制作用がそれぞ
れ認められた。
As is clear from Table 5, the effect of suppressing the growth of Trichoderma bacterium generally works strongly as the amount of addition increases, and 11 to 17 are obtained when 5% of the larch water extract is added.
%, 10% addition, the suppression effect of 24-29% was recognized, respectively.

【0027】以上の結果から、各種の培地にカラマツ水
抽出物を適正な範囲内で添加すれば、一方ではいずれも
菌糸体の生長を促進する作用があり、他方主要害菌に対
しては逆に生長を抑制する作用があることが判明した。
従って、カラマツ水抽出物は前記両作用による相乗効果
によって、きのこ菌糸体に対する生長速度を大いに促進
することが明らかである。
From the above results, when the larch water extract was added to various culture media within an appropriate range, on the one hand, both had the action of promoting the growth of mycelium, while on the other hand, it had the opposite effect on the main harmful bacteria. Was found to have the effect of suppressing growth.
Therefore, it is clear that the larch water extract greatly promotes the growth rate on the mycelium of mushrooms by the synergistic effect of the above two actions.

【0028】[0028]

【発明の効果】本発明による培養基は、きのこの菌糸体
の生長を促進させると共にきのこの主要害菌の生長を抑
制する作用を有するカラマツ材の水抽出物が添加されて
いるので、菌床栽培における培養日数が大幅に短縮で
き、収穫量の増大を図ることが可能となり得る菌糸体量
が豊富で然も害菌の生長を抑制する培養基を提供でき
る。したがって、きのこ栽培者にとっては作業効率の高
い栽培を行なうことができ、労力の軽減と共に収益の増
大を図ることができ、経営基盤の安定につながるもので
ある。
INDUSTRIAL APPLICABILITY The culture medium according to the present invention contains a water extract of larch wood, which has the effects of promoting the growth of mycelium of mushrooms and suppressing the growth of major harmful fungi of mushrooms. It is possible to provide a culture medium in which the number of culturing days in (1) can be significantly shortened and the amount of harvest can be increased, and the mycelium is abundant and the growth of harmful bacteria is suppressed. Therefore, for the mushroom grower, cultivation can be performed with high work efficiency, labor can be reduced, and profit can be increased, which leads to stable management base.

【0029】また、カラマツ水抽出物質の主要構成成分
であるアラビノガラクタンは、食品添加物として認めら
れており、安全性が極めて高く、市販の化学合成品に比
べてきのこの薬害汚染のおそれが全くない。さらに、カ
ラマツ材の水抽出物は、廃材から約10%(重量比)の
高収率で容易に製造できるため、コスト的にも極めて安
価な生長促進剤として提供できる。
Also, arabinogalactan, which is the main constituent of the larch water extract, is recognized as a food additive, has a very high safety, and is less likely to be contaminated with chemicals than commercial chemical synthetic products. Not at all. Furthermore, since the water extract of larch wood can be easily produced from waste wood with a high yield of about 10% (weight ratio), it can be provided as a growth promoter which is extremely inexpensive in terms of cost.

【0030】なお、従来より廃棄処分していた製材鋸屑
などの廃材から生長促進剤としてのカラマツ水抽出物が
得られるため、資源の高度な有効利用が図られ、国民経
済上の見地からも有用性の高いものである。
Since larch water extract as a growth promoter can be obtained from waste materials such as sawmill sawdust that have been conventionally disposed of, it is possible to use resources highly efficiently and is useful from the viewpoint of national economy. It has high quality.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 人工培養基の主成分に、カラマツ材の水
抽出液を濃縮、乾燥して得たカラマツ水抽出物を添加し
てなることを特徴とするきのこの培養基。
1. A mushroom culture medium comprising a larch water extract obtained by concentrating and drying a water extract of larch wood as a main component of the artificial culture medium.
JP3081526A 1991-03-19 1991-03-19 Mushroom culture medium Expired - Lifetime JPH0724503B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3081526A JPH0724503B2 (en) 1991-03-19 1991-03-19 Mushroom culture medium

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3081526A JPH0724503B2 (en) 1991-03-19 1991-03-19 Mushroom culture medium

Publications (2)

Publication Number Publication Date
JPH04293430A JPH04293430A (en) 1992-10-19
JPH0724503B2 true JPH0724503B2 (en) 1995-03-22

Family

ID=13748775

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3081526A Expired - Lifetime JPH0724503B2 (en) 1991-03-19 1991-03-19 Mushroom culture medium

Country Status (1)

Country Link
JP (1) JPH0724503B2 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006246819A (en) * 2005-03-11 2006-09-21 Sanwa Tekki Corp Mushroom growth accelerating agent comprising wood extract
CN106946623A (en) * 2017-03-14 2017-07-14 安徽米乐食品有限公司 The method that residue prepares edible fungus culturing base manure auxiliary material is extracted using purple sweet potato anthocyanin
JP6989914B2 (en) * 2018-03-23 2022-01-12 地方独立行政法人北海道立総合研究機構 Mushroom cultivation medium additive, mushroom cultivation medium, and mushroom cultivation method using the same medium

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5944396A (en) * 1982-09-08 1984-03-12 Kyowa Hakko Kogyo Co Ltd Method for cultivating mushroom

Also Published As

Publication number Publication date
JPH04293430A (en) 1992-10-19

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