JPS585185A - Medium for cultivating fruit body of basidiomycetes - Google Patents
Medium for cultivating fruit body of basidiomycetesInfo
- Publication number
- JPS585185A JPS585185A JP56103420A JP10342081A JPS585185A JP S585185 A JPS585185 A JP S585185A JP 56103420 A JP56103420 A JP 56103420A JP 10342081 A JP10342081 A JP 10342081A JP S585185 A JPS585185 A JP S585185A
- Authority
- JP
- Japan
- Prior art keywords
- medium
- crushed
- dry weight
- present
- basidiomycetes
- 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.)
- Granted
Links
Landscapes
- Mushroom Cultivation (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Abstract
Description
【発明の詳細な説明】 本発明は、担子菌類子実体栽培用培地に関する。[Detailed description of the invention] The present invention relates to a medium for cultivating basidiomycete fruiting bodies.
従来、ナメコ、エノキタケ、ヒラタケ等の食用茸は、鋸
屑を主体とし、これに必要により米糠等の栄養源を適当
量配合した培地に、これら食用茸の種菌を接種、培養し
て得られている。Traditionally, edible mushrooms such as nameko, enokitake, and oyster mushrooms have been obtained by inoculating and culturing the inoculum of these edible mushrooms in a medium containing sawdust as the main ingredient and, if necessary, an appropriate amount of nutrients such as rice bran. .
しかしながら、食用茸の需要拡大によシ、上述の培地原
料となりうる良質の鋸屑(広葉樹及び針葉樹のうち特に
広葉樹が適する。)が不足し、しかも該鋸屑の価格が高
騰しているため良質の鋸屑の入手が著しく困難であるの
が実情である。However, due to the increasing demand for edible mushrooms, there is a shortage of high-quality sawdust (hardwoods are especially suitable among hardwoods and coniferous trees) that can be used as a raw material for the above-mentioned culture medium, and the price of sawdust is soaring. The reality is that it is extremely difficult to obtain.
一方、落花生の種子は、食用に供されている反面、その
莢は、はとんど何の有用な用途もなく焼却されているの
が実情である。On the other hand, while peanut seeds are edible, the reality is that the pods have no useful use and are incinerated.
そこで、本発明者等は、上記実情に鑑み種々検討した結
果、鋸屑と米糠及び/又はトウモロコシ糠を含有する培
地に粉砕落花先天を配合したものに、ナメコ、シイタケ
等の担子菌を接種、培養すれば、高収率で子実体を得る
ことが出来ること、更に、鋸虐の添加量を著しく軽減す
ることが出来ること等の知見を得、本発明を完成した。Therefore, as a result of various studies in view of the above-mentioned circumstances, the present inventors inoculated and cultured basidiomycetes such as nameko and shiitake mushrooms into a medium containing sawdust and rice bran and/or corn bran mixed with crushed peanuts. The present invention was completed based on the findings that fruit bodies can be obtained in high yield and the amount of sawdust added can be significantly reduced.
すなわち、本発明は、粉砕落花先天と粉砕、割培地であ
る。That is, the present invention is a crushed ground peanut and a crushed and split culture medium.
以下、本発明の詳細な説明する。The present invention will be explained in detail below.
先ず、本発明に使用される原料としては、如何なる品種
の落花先天であってもよい。First, the raw material used in the present invention may be any variety of fallen flowers.
また、落花先天は、そのま\(未加熱焙煎処理物)もし
くは常法により加熱焙煎処理を施したもの等如何なる処
理を施したものであっても良い。In addition, the peanuts may be used as they are (unheated and roasted) or may be subjected to any treatment such as heated and roasted in a conventional manner.
そして、前記落花先天を、莢と種子に常法により分別し
該莢を得る。Then, the fallen flower is separated into pods and seeds by a conventional method to obtain the pods.
次いで、前記莢を粉砕する。The pods are then crushed.
莢の粉砕程度は、如何なる粒度でも良く、例えば、j〜
/≠メツシュ、好ましくはt〜/2メツシュである。The degree of crushing of the pods may be of any particle size, for example, j~
/≠ mesh, preferably t~/2 mesh.
なお、前記粉砕程度が、≠メツシュを越える場合及び/
≠メツシュ未満の場合には、担子菌類子実体形成が、著
しく長期に及ぶ等のため好ましくない。In addition, when the degree of pulverization exceeds ≠ mesh and/
If it is less than ≠Metsu, the formation of basidiomycete fruiting bodies takes an extremely long time, which is not preferable.
粉砕手段としては、如何なる手段であっても良く、例エ
バ、ハンマーミル、カッターミル、ロータリークラッシ
ャー、挽臼等を用いる方法が挙げられる。Any means may be used as the crushing means, and examples thereof include methods using an evaporator, hammer mill, cutter mill, rotary crusher, mill, and the like.
次いで、このようにして得た粉砕落花生糞に、粉砕、割
砕もしくは薄片とした木質原料と米糠及び/又はトウモ
ロコシ糠を均質に配合して担子菌類子実体栽培用培地と
して用いることが出来るが、更に、これに必要により、
水;コーンステープリカー、皺、アミノ酸類、大豆ミー
ル、醤油粕等の窒素源;グルコース、マルツェ叡ス等の
炭素源;燐酸−カリウム、炭酸石灰、硫酸マグネシウム
、等のミネラル;ビタミン等より選ばれた7種以上を配
合して使用することも出来る。Next, the ground peanut manure obtained in this way can be homogeneously mixed with wood raw materials that have been ground, split, or sliced, and rice bran and/or corn bran, and used as a medium for cultivating basidiomycete fruiting bodies. Furthermore, if necessary,
Water: Nitrogen sources such as cornstap liquor, wrinkles, amino acids, soybean meal, soy sauce lees; Carbon sources such as glucose and maltose; Minerals such as potassium phosphate, lime carbonate, magnesium sulfate; Vitamins, etc. It is also possible to use a combination of seven or more types.
本発明に使用される木質原料は、通常担子菌の栽培に用
い°られるものであれば、如何なる樹種でも良く、例え
ば、ブナ、コナラ、ミズナラ、ダチカンバ、クヌギ、シ
ブ、サクシ、エゴノキ、ポプラ、ハンノキ、カシ、シイ
、タブ、チーク等の木質原料が挙げら庇る。The wood material used in the present invention may be of any tree species as long as it is normally used for cultivating basidiomycetes, such as beech, Quercus serrata, Quercus oak, Japanese birch, Japanese oak, Japanese oak, Japanese oak, Japanese oak, poplar, and alder. , oak, chinquapin, tab, teak, and other woody materials.
前記木質原料を通常の粉砕機もしくは割砕機により粉砕
もしくは割砕するが、あるいは鉋、スライサー等により
薄片状とする。この際、粉砕もしくは割砕した場合の粒
度としては約≠メツシュ、好適には?メツシュよりも細
粒のものが好ましく、また薄片状としたものは、厚さが
約3tnm以下、好適には/胴板下のものが好ましい。The wood raw material is crushed or crushed using a conventional crusher or crusher, or it is made into flakes using a plane, a slicer, or the like. At this time, the particle size when crushed or crushed is approximately ≠ mesh, which is the preferred size? Preferably, the particles are finer than mesh, and the flakes have a thickness of about 3 tnm or less, preferably under the shell plate.
なお、粉砕落花生糞の配合割合は、如何なる菫でも良く
、例えば落花生糞乾物重量%として培地総重量当りj〜
、2?チ、好ましくは7〜/、2チとなる如く配合する
ことが望ましい。In addition, the blending ratio of crushed peanut excrement may be any violet, for example, the proportion of groundnut excrement dry weight is j~ per total medium weight.
, 2? It is desirable to mix the amount so that the amount is 7 to 2, preferably 7 to 2.
更に、米糠対トウモロコシ糠の配合比は、如何なる比率
でも良い。Furthermore, the blending ratio of rice bran to corn bran may be any ratio.
次に、上記担子菌類子実体栽培用培地を適当な容器に入
れ、通常の殺菌処理を施しだのち、これに、担子菌の種
菌を接種し、その後は、通常の培養法に従って培養し、
担子菌子実体を得る。Next, the above-mentioned basidiomycete fruiting body cultivation medium is placed in a suitable container, subjected to a normal sterilization treatment, and then inoculated with a basidiomycete inoculum, and then cultured according to a normal culture method.
Obtain basidiomycete fruiting bodies.
本発明に適用可能な担子菌としては、例えば、スギタケ
属、シイタケ属、エノキタケ属、ヒラタケ属、マイタケ
属等に属するものであれば如何なる種別のものでも良く
、それらの内、ナメコ、シイタケ、エノキタケ、εラタ
ケ、マイタケ等は特に好適である。As the basidiomycete that can be applied to the present invention, any type of basidiomycete may be used as long as it belongs to the genus Sugitake, Shiitake, Enokitake, Oyster mushroom, Maitake, etc. Among them, Nameko, Shiitake, and Enokitake can be used. , ε-ratake, maitake, etc. are particularly suitable.
以上の如く、本発明は、担子菌類子実体を高収率で得る
ことが出来、しかも従来用いられていた以下、本発明を
実施例を挙げて詳細に説明する。As described above, the present invention makes it possible to obtain basidiomycete fruiting bodies in high yield, and in addition, the present invention will be described in detail with reference to Examples.
実施例1
ブナ鋸屑3109 (乾物重量)に、トウモロコシ糠t
0? (乾物重量)を配合したものに、水分、gl(W
/W)となる如く加水しイ更に、これに、水分63%(
W/W )の粉砕落花生糞(粉砕粒度/θメツシュ)を
9%(乾物重量%)となる如く添加した。Example 1 Beech sawdust 3109 (dry weight), corn bran t
0? (dry weight), water, gl(W
/W), and then add water to this to give a water content of 63% (
W/W ) crushed peanut manure (pulverized particle size/θ mesh) was added to the mixture at a concentration of 9% (dry weight %).
このようにして得た加水物を栽培袋に充填し、常法によ
り密栓したものを、圧力/Ky/crA(ゲージ圧力)
で温度/2θ℃の飽和水蒸気を9θ分間作用させて殺菌
したのち、室温迄冷却して培地を得た(本発明)。The hydrate obtained in this way was filled into a cultivation bag and sealed in a conventional manner, and the pressure/Ky/crA (gauge pressure)
After sterilizing the cells by applying saturated steam at temperature/2θ°C for 9θ minutes, the cells were cooled to room temperature to obtain a culture medium (the present invention).
なお、比較のだめの対照は、ブナ鋸屑310?(乾物重
量)に、トウモロコシ糠乙θf(乾物重量)を配合した
ものに、水分、1%(W/W)となる如く加水して得だ
ものを栽培袋に入れ、あとは本発明の調製法と全く同様
に加熱殺菌して得たものである。In addition, the control for comparison is beech sawdust 310? (dry weight) and corn bran θf (dry weight), add water to 1% (W/W), put the obtained product in a cultivation bag, and then prepare according to the present invention. It was obtained by heat sterilization in exactly the same manner as the method.
次いで、上記培地に夫々ナメコ種菌を接種し、温度23
℃で湿度60〜70%の条件下で3チ月間培養し、その
後子実体発生室に移し、温度/j℃で湿度−tθ〜9Q
チの条件下でλケ月間子実体を発生させて得た収量を第
1表に示す。Next, nameko inoculum was inoculated into each of the above-mentioned media, and the temperature was increased to 23°C.
The cells were cultured for 3 months at a temperature of 60 to 70% humidity, and then transferred to a fruiting body generation chamber at a temperature of /j°C and a humidity of -tθ to 9Q.
Table 1 shows the yield obtained by developing fruiting bodies for λ months under the conditions described above.
第 1 表
上表よシ明らかな如く、本発明は、対照に比し、子実体
収量が著しく増加することがわかる。As is clear from Table 1, the fruiting body yield of the present invention is significantly increased compared to the control.
実施例2
ブナ鋸屑3/θt(乾物重量)に、米糠10グ(乾物重
量)を配合したものに、水分ご3%(W/W) とな
る如く加水し、更に、これに水分43%(W/W)の粉
砕落花生′莢(粉砕粒度/θメツシュ)を9チ(乾物重
量%)となる如く添加した。Example 2 To a mixture of 3/θt (dry weight) of beech sawdust and 10 g (dry weight) of rice bran, water was added to make the water content 3% (W/W). Pulverized peanut pods (pulverized particle size/θ mesh) of W/W) were added at a concentration of 9 g (dry weight %).
このようにして得た加水物を栽培袋に充填し、圧力)で
温度/2θ℃の飽和水蒸気を9θ分間作用させて殺菌し
たのち、室温迄冷却して培地を得た。The thus obtained hydrate was filled into a cultivation bag, sterilized by applying saturated steam at temperature/2θ° C. for 9θ minutes under pressure), and then cooled to room temperature to obtain a culture medium.
なお、比較のための対照培地はブナ鋸屑3/θf(乾物
重量)に米糠tOf(乾物重量)を配合したものに、水
分4j%(W/W)となる如く加水し、あとは本発明の
培地の調製法と全く同様に加熱殺菌して得たものである
。The control medium for comparison was a mixture of beech sawdust 3/θf (dry weight) and rice bran tOf (dry weight), water was added to give a moisture content of 4j% (W/W), and the rest was prepared using the method of the present invention. It was obtained by heat sterilization in exactly the same manner as the culture medium preparation method.
次いで、上記培地に夫々シイタケ種菌を接種し、温度、
23℃で湿度60〜7θチの条件下でjケガ間培養し、
その後子実体発生室に移し、温度1j−℃で湿度?θ〜
90%の条件下にグヶ月間子実体を発生させて得た収量
を第2表に示す。Next, each of the above-mentioned media was inoculated with shiitake seed fungi, and the temperature and
Cultured at 23°C and humidity of 60 to 7θ,
Afterwards, it is transferred to the fruiting body generation chamber, at a temperature of 1J-℃ and humidity? θ〜
Table 2 shows the yield obtained after fruiting bodies were allowed to develop for several months under 90% conditions.
第 2 表
上表より明らかな如く、本発明は、対照に比し、子実体
収量が著しく増加することがわかる。As is clear from Table 2, the fruiting body yield of the present invention is significantly increased compared to the control.
実施例3
ブナ鋸屑3101(乾物重量)に、トウモロコシ糠≠2
1(乾物重量)及び米糠/2v(乾物重量)を夫々配合
したものに、水分、g3%(W/W)となる如く加水し
、更に、これに水分、<J%(、・W/W) の粉砕
落花生糞(粉砕粒度lθメツシュ)を9%(乾物重量%
)となる如く添加した。Example 3 Beech sawdust 3101 (dry weight) and corn bran≠2
1 (dry weight) and rice bran/2v (dry weight), water was added to give a moisture content of 3% (W/W), and further water was added to this mixture, <J% (, W/W). ) of ground peanut manure (pulverized particle size lθ mesh) was added to 9% (dry weight %).
) was added.
このようにして得た加水物lK9を栽培袋に充填し、常
法により密栓したものを、圧力/Ks+/c1A(ゲー
ジ圧力)で温度12θ℃の飽和水蒸気を90分間作用さ
せて殺菌したのち、室温迄冷却して培地を得た。(本発
明)
なお、比較のだめの対照培地は、上記本発明培地の調製
法のうち、ブナ鋸屑310ftC乾物重量)にトウモロ
コシ糠11.jr9 (乾物重量)及び米糠/2f(乾
物重量)を夫々配合したものに、水分j3%(W/W)
となる如く加水する以外は、本発明培地の調製法と全く
同様にして得たものである。The thus obtained hydrate lK9 was filled into a cultivation bag, which was sealed in a conventional manner, and the bag was sterilized by applying saturated steam at a temperature of 12θ°C for 90 minutes at a pressure of /Ks+/c1A (gauge pressure). A medium was obtained by cooling to room temperature. (The present invention) The control medium for comparison was prepared by adding 310 ftC of beech sawdust (dry weight) and corn bran to 11% of the method for preparing the medium of the present invention. jr9 (dry weight) and rice bran/2f (dry weight), with a moisture content of j3% (W/W).
It was obtained in exactly the same manner as the method for preparing the culture medium of the present invention, except that water was added as shown below.
次いで、上記培地に夫々ナメコ種菌を接種し、温度23
℃で湿度60〜70%の条件下で3チ月間培養し、その
後、子実体発生室に移し、温度第 3
表
上表より明らかな如く、本発明は、対照に比し、子実体
収量が著しく増加することがわかる。Next, nameko inoculum was inoculated into each of the above-mentioned media, and the temperature was increased to 23°C.
℃ for 3 months at a humidity of 60 to 70%, then transferred to a fruiting body generation chamber and incubated at a temperature of 3.
As is clear from the table above, it can be seen that the fruiting body yield of the present invention is significantly increased compared to the control.
Claims (1)
と米糠及び/又はトウモロコシ糠を均質に含有する担子
菌類子実体栽培用培地。A culture medium for cultivating basidiomycete fruiting bodies homogeneously containing crushed ground peanuts, crushed, crushed or thinly sliced wood material, and rice bran and/or corn bran.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56103420A JPS585185A (en) | 1981-07-03 | 1981-07-03 | Medium for cultivating fruit body of basidiomycetes |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56103420A JPS585185A (en) | 1981-07-03 | 1981-07-03 | Medium for cultivating fruit body of basidiomycetes |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS585185A true JPS585185A (en) | 1983-01-12 |
| JPS6352879B2 JPS6352879B2 (en) | 1988-10-20 |
Family
ID=14353541
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP56103420A Granted JPS585185A (en) | 1981-07-03 | 1981-07-03 | Medium for cultivating fruit body of basidiomycetes |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS585185A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS63237744A (en) * | 1987-03-25 | 1988-10-04 | Noukou Sanshiya:Kk | Feed for domestic animal |
| JPH01137921A (en) * | 1987-08-22 | 1989-05-30 | Morito Hitsujito Tsuchinokai:Kk | Culture medium for mushroom |
| JPH02142465A (en) * | 1988-11-24 | 1990-05-31 | Kikkoman Corp | Solid culture medium |
| CN104311168A (en) * | 2014-11-14 | 2015-01-28 | 内蒙古风水梁菌业有限公司 | Edible wood rotting fungus culture medium, edible wood rotting fungus culture bar and preparation method thereof |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP6572376B1 (en) | 2018-11-30 | 2019-09-11 | 上村工業株式会社 | Electroless plating bath |
-
1981
- 1981-07-03 JP JP56103420A patent/JPS585185A/en active Granted
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS63237744A (en) * | 1987-03-25 | 1988-10-04 | Noukou Sanshiya:Kk | Feed for domestic animal |
| JPH01137921A (en) * | 1987-08-22 | 1989-05-30 | Morito Hitsujito Tsuchinokai:Kk | Culture medium for mushroom |
| JPH02142465A (en) * | 1988-11-24 | 1990-05-31 | Kikkoman Corp | Solid culture medium |
| CN104311168A (en) * | 2014-11-14 | 2015-01-28 | 内蒙古风水梁菌业有限公司 | Edible wood rotting fungus culture medium, edible wood rotting fungus culture bar and preparation method thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6352879B2 (en) | 1988-10-20 |
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