JPH01117724A - Artificial culture of mushroom - Google Patents
Artificial culture of mushroomInfo
- Publication number
- JPH01117724A JPH01117724A JP62274030A JP27403087A JPH01117724A JP H01117724 A JPH01117724 A JP H01117724A JP 62274030 A JP62274030 A JP 62274030A JP 27403087 A JP27403087 A JP 27403087A JP H01117724 A JPH01117724 A JP H01117724A
- Authority
- JP
- Japan
- Prior art keywords
- sawdust
- bran
- mushrooms
- medium
- mushroom
- 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.)
- Pending
Links
- 235000001674 Agaricus brunnescens Nutrition 0.000 title claims abstract description 73
- 240000007594 Oryza sativa Species 0.000 claims abstract description 21
- 235000007164 Oryza sativa Nutrition 0.000 claims abstract description 21
- 235000009566 rice Nutrition 0.000 claims abstract description 21
- 235000013339 cereals Nutrition 0.000 claims abstract description 10
- 239000000843 powder Substances 0.000 claims abstract description 10
- 235000015099 wheat brans Nutrition 0.000 claims abstract description 8
- 244000068988 Glycine max Species 0.000 claims abstract description 6
- 235000010469 Glycine max Nutrition 0.000 claims abstract description 6
- 240000008042 Zea mays Species 0.000 claims abstract description 6
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 claims abstract description 6
- 235000002017 Zea mays subsp mays Nutrition 0.000 claims abstract description 6
- 235000005822 corn Nutrition 0.000 claims abstract description 6
- 235000013527 bean curd Nutrition 0.000 claims abstract description 5
- 238000000034 method Methods 0.000 claims description 21
- 238000012364 cultivation method Methods 0.000 claims description 8
- 235000016709 nutrition Nutrition 0.000 claims description 7
- 235000012054 meals Nutrition 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 239000000463 material Substances 0.000 claims description 3
- 239000006227 byproduct Substances 0.000 claims description 2
- 239000000126 substance Substances 0.000 abstract description 19
- 230000012010 growth Effects 0.000 abstract description 18
- 235000015097 nutrients Nutrition 0.000 abstract description 12
- 230000002401 inhibitory effect Effects 0.000 abstract description 10
- 150000001875 compounds Chemical class 0.000 abstract description 2
- 240000000359 Triticum dicoccon Species 0.000 abstract 1
- 230000002950 deficient Effects 0.000 abstract 1
- 239000002609 medium Substances 0.000 description 26
- 240000001462 Pleurotus ostreatus Species 0.000 description 15
- 239000001963 growth medium Substances 0.000 description 7
- 239000000654 additive Substances 0.000 description 6
- 238000002156 mixing Methods 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 240000000731 Fagus sylvatica Species 0.000 description 5
- 235000010099 Fagus sylvatica Nutrition 0.000 description 5
- 235000001603 Pleurotus ostreatus Nutrition 0.000 description 5
- 241000233866 Fungi Species 0.000 description 4
- 239000002054 inoculum Substances 0.000 description 4
- 241000894007 species Species 0.000 description 4
- 239000002023 wood Substances 0.000 description 4
- 241000894006 Bacteria Species 0.000 description 3
- 241000218645 Cedrus Species 0.000 description 3
- 238000012258 culturing Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000035784 germination Effects 0.000 description 3
- 238000011081 inoculation Methods 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 244000168667 Pholiota nameko Species 0.000 description 2
- 235000014528 Pholiota nameko Nutrition 0.000 description 2
- 235000016976 Quercus macrolepis Nutrition 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000003306 harvesting Methods 0.000 description 2
- -1 milogerm Substances 0.000 description 2
- QCVGEOXPDFCNHA-UHFFFAOYSA-N 5,5-dimethyl-2,4-dioxo-1,3-oxazolidine-3-carboxamide Chemical compound CC1(C)OC(=O)N(C(N)=O)C1=O QCVGEOXPDFCNHA-UHFFFAOYSA-N 0.000 description 1
- 241001311476 Abies veitchii Species 0.000 description 1
- 241000208140 Acer Species 0.000 description 1
- 241000157282 Aesculus Species 0.000 description 1
- 241001070941 Castanea Species 0.000 description 1
- 235000014036 Castanea Nutrition 0.000 description 1
- 244000301850 Cupressus sempervirens Species 0.000 description 1
- 240000006055 Dacrydium cupressinum Species 0.000 description 1
- 235000018782 Dacrydium cupressinum Nutrition 0.000 description 1
- 102000002322 Egg Proteins Human genes 0.000 description 1
- 108010000912 Egg Proteins Proteins 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 235000019733 Fish meal Nutrition 0.000 description 1
- 240000006499 Flammulina velutipes Species 0.000 description 1
- 235000016640 Flammulina velutipes Nutrition 0.000 description 1
- 240000001080 Grifola frondosa Species 0.000 description 1
- 235000007710 Grifola frondosa Nutrition 0.000 description 1
- 241000534018 Larix kaempferi Species 0.000 description 1
- 241000039951 Lithocarpus glaber Species 0.000 description 1
- 244000103635 Lyophyllum ulmarium Species 0.000 description 1
- 235000015934 Lyophyllum ulmarium Nutrition 0.000 description 1
- 244000232885 Naematoloma sublateritium Species 0.000 description 1
- 235000016009 Naematoloma sublateritium Nutrition 0.000 description 1
- 239000001888 Peptone Substances 0.000 description 1
- 108010080698 Peptones Proteins 0.000 description 1
- 235000013697 Pinus resinosa Nutrition 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 244000141698 Prunus lannesiana Species 0.000 description 1
- 241000219492 Quercus Species 0.000 description 1
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 1
- 241001622901 Scomberomorus commerson Species 0.000 description 1
- 235000019764 Soybean Meal Nutrition 0.000 description 1
- 241000209140 Triticum Species 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 241000190021 Zelkova Species 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 235000019693 cherries Nutrition 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 235000014103 egg white Nutrition 0.000 description 1
- 210000000969 egg white Anatomy 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000004467 fishmeal Substances 0.000 description 1
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 1
- 230000002538 fungal effect Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 235000010181 horse chestnut Nutrition 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 238000011177 media preparation Methods 0.000 description 1
- 239000013028 medium composition Substances 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 235000019319 peptone Nutrition 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 235000021395 porridge Nutrition 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000007790 scraping Methods 0.000 description 1
- 238000006748 scratching Methods 0.000 description 1
- 230000002393 scratching effect Effects 0.000 description 1
- 238000011218 seed culture Methods 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000004455 soybean meal Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
Landscapes
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Mushroom Cultivation (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明はキノコ類の人工栽培方法に係り、特にオカラを
栄養源とした場合に、高いキノコ収量を与えるオガ屑に
よるキノコの人工栽培方法に関する。[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a method for artificially cultivating mushrooms, and in particular to a method for artificially cultivating mushrooms using sawdust that provides a high mushroom yield when okara is used as a nutritional source. .
キノコの瓶栽培法についてヒラタケ(市場には「シメン
」の名で出されている)を例に従来の栽培法を説明する
(大森清寿「ヒラタケ」農山魚村文化協会)。Regarding the method of growing mushrooms in bottles, I will explain the conventional cultivation method using oyster mushrooms (sold under the name ``Shimen'' on the market) as an example (Kiyohisa Omori, ``Oyster Mushrooms'', Rural Culture Association).
第3図にヒラタケ(以下「シメン」という)の瓶栽培に
関する従来プロセスを示す、原料としてオガ屑と米糠を
容量比的4:1で混合し、これに水を加えて混合して水
分含有率が約65%の培地が調製される。この培地は栽
培瓶中に充填され、瓶の中央部に先端部の直径が1.0
cm、上端部が1.5cm程度の棒を用いて穴があけら
れる。Figure 3 shows the conventional process for growing oyster mushrooms (hereinafter referred to as "shimen") in bottles. As raw materials, sawdust and rice bran are mixed at a volume ratio of 4:1, water is added to this, and the water content is increased. A medium with a concentration of about 65% is prepared. This medium is filled into a cultivation bottle, and the diameter of the tip is 1.0 mm in the center of the bottle.
cm, and a hole is made using a rod with an upper end of about 1.5 cm.
瓶の口にキャップが取付けられた後、120℃(飽和水
蒸気圧下)で1時間程度加熱して滅菌する。滅菌処理を
施した栽培瓶は、内容物が充分に(25°C以下)冷却
された後、砕いた種菌5〜20gが瓶中央部の穴と表面
に3〜5mm程度の厚さになるように添加される。接種
が完了した栽培瓶は速やかにキャップをし、温度20〜
25°C1湿度60〜70%の培養室に搬入され、ここ
で培地中に菌糸を伸長させる。この操作を「培養」とい
い、通常20〜35日を要する。After a cap is attached to the mouth of the bottle, it is sterilized by heating at 120°C (under saturated steam pressure) for about 1 hour. After the contents of the sterilized cultivation bottle have been sufficiently cooled (below 25°C), 5 to 20 g of crushed seed culture is placed in the hole in the center of the bottle and on the surface to a thickness of about 3 to 5 mm. added to. Immediately cap the cultivation bottle after inoculation and keep it at a temperature of 20~20℃.
The cells are transported to a culture room at 25° C. and 60-70% humidity, where the hyphae are allowed to grow in the medium. This operation is called "culturing" and usually takes 20 to 35 days.
培養が完了したところで瓶のキャップが取り外され、培
地表面の老化した種菌層が取り除かれる(この操作を「
画描」という)。菌種終了後の瓶は、発芽、生育室に搬
入され、温度10〜15°C1湿度90〜95%、照度
50〜200I!、uXの条件に置くと、通常10〜1
5日程度でキノコが発生し、採取可能となる。Once the culture is complete, the cap of the bottle is removed and the aged starter layer on the surface of the medium is removed (this operation is referred to as
(referred to as "painting"). After seeding, the bottles are carried into the germination and growth room, where the temperature is 10-15°C, the humidity is 90-95%, and the illuminance is 50-200I! , when placed under the conditions of uX, it is usually 10 to 1
Mushrooms will develop in about 5 days and can be collected.
なお、キノコの人工栽培においては米糠−オガ屑混合培
地が最もよく使用されているが、キノコの生産原価の低
減を図るためには培地材料であるオガ屑や米糠を安価に
購入する方策をとらなければならない、また、栄養源と
して米糠の代わりにフスマ、トウモロコシ粕、大豆粕な
どの使用が可能であり、豆腐製造時に副生ずるオカラを
栄養源として使用せんとする試みもなされている。In addition, rice bran and sawdust mixed medium is most commonly used in the artificial cultivation of mushrooms, but in order to reduce the production cost of mushrooms, it is necessary to purchase medium materials such as sawdust and rice bran at low cost. In addition, it is possible to use bran, corn meal, soybean meal, etc. in place of rice bran as a nutritional source, and attempts have also been made to use okara, which is a by-product during tofu production, as a nutritional source.
キノコ類の人工栽培法においては、米糠−オガ屑混合培
地が最も良く用いられるが、この場合、キノコの生育に
とって必要な栄養源を確保するととに生育阻害物質の含
有量を所定レベル以下に保たなければならない、米糠の
性状は概して一定と考えられるため、米糠−オガ屑培地
を用いる場合に重要な点はオガ屑樹種と種菌の種類の選
定にあり、栽培業者は自らの経験によって栽培ノウハウ
を蓄積している。In the artificial cultivation of mushrooms, a rice bran-sawdust mixed medium is most often used, but in this case, it is necessary to secure the nutrients necessary for mushroom growth and to keep the content of growth-inhibiting substances below a predetermined level. The properties of rice bran are generally considered to be constant, so when using a rice bran-sawdust culture medium, the important point is the selection of the sawdust tree species and the seed fungus. is accumulating.
これに対し、栄養源としてオカラを用いる場合、栽培条
件に関する詳細検討は行われておらず、通常米糠−オガ
屑法により栽培されているシメジをオカラを栄養源とし
て栽培してみると採算点とも言える80g/瓶程度のキ
ノコの得られるオガ屑と種菌の組合わせは極く限られた
ものであった。On the other hand, when okara is used as a nutrient source, no detailed study has been conducted regarding the cultivation conditions, and if shimeji mushrooms, which are normally grown using the rice bran-sawdust method, are cultivated using okara as a nutrient source, it will not be profitable. The combinations of sawdust and inoculum that could yield about 80 g/bottle of mushrooms were extremely limited.
本発明の目的は、上記のようなオカラを栄養源としてキ
ノコを栽培する場合に採用可能な種菌やオガ屑の種類が
かなり制限されるという不具合を回避できる高効率なキ
ノコの人工栽培方法を提供することにある。The purpose of the present invention is to provide a highly efficient method for artificially cultivating mushrooms that can avoid the above-mentioned disadvantage that the types of seed bacteria and sawdust that can be used are considerably limited when cultivating mushrooms using okara as a nutritional source. It's about doing.
上記の目的は、培地個装に当たってオカラおよびオガ屑
とともにフスマ、米糠、トウモロコシ粕等の大豆以外の
穀類粉末を混合添加することによって達成される。The above object is achieved by mixing and adding grain powder other than soybean, such as bran, rice bran, and corn meal, together with okara and sawdust when individually packaging the culture medium.
シメジ、ナメコ、エノキタケなど木材腐朽菌といわれる
キノコ類は木材を分解することによって生育に必要な物
質を獲得する能力を持っている。Mushrooms called wood-destroying fungi, such as shimeji mushrooms, nameko mushrooms, and enokitake mushrooms, have the ability to acquire the substances necessary for growth by decomposing wood.
しかし、培地として米糠−オガ屑混合物を用いると、生
育に必要な物質は殆ど全てこの米糠から獲得され、かつ
その分解速度は木材の場合よりも大きいので短期間のう
ちにキノコの収穫が可能になる。However, when a mixture of rice bran and sawdust is used as a medium, almost all the substances necessary for growth are obtained from the rice bran, and its decomposition rate is greater than that of wood, making it possible to harvest mushrooms in a short period of time. Become.
栄養源としてオカラを添加した場合も同様であるが、所
期のキノコ収量を達成するためには培養期間中に培地中
に菌糸がまん延するだけでなく、培養後に発芽・生育に
とっても適切な条件が整わなければならない、この点、
オカラーオガ屑混合培地を用いる場合に所期のキノコ収
量を与えるオガ屑一種菌の組合わせがかなり限定される
のは、このオカラおよびオガ屑中にはキノコの菌糸伸長
および発芽・生育にとって抑制作用を示す物質が存在す
る、あるいはこれらの過程で必要とされる物質が欠落し
ているためと思われる。The same is true when okara is added as a nutrient source, but in order to achieve the desired mushroom yield, not only must mycelia spread in the medium during the cultivation period, but also appropriate conditions must be established for germination and growth after cultivation. This point must be taken care of,
When using a mixed medium of okara and sawdust, the combination of sawdust bacteria that gives the desired mushroom yield is quite limited. This may be due to the presence of substances that indicate these processes, or the lack of substances required for these processes.
これに対し、オカラーオガ屑混合培地に更にフスマ、米
糠等の大豆以外の穀類粉末を添加すると、この中に含ま
れる物質によって生育阻害物質が封鎖されるか、あるい
はオカラとオガ屑だけでは欠落する化合物がフスマ、米
糠等の大豆以外の穀類粉末によって供給されるためにキ
ノコ収量の増大が達成される。On the other hand, if grain powders other than soybeans such as wheat bran and rice bran are added to the okara sawdust mixed medium, the growth inhibiting substances may be sequestered by the substances contained therein, or compounds that are missing from okara and sawdust alone may be added. An increase in mushroom yield is achieved because the mushrooms are supplied by grain powders other than soybeans such as bran and rice bran.
以下、本発明を更に詳細に説明する。The present invention will be explained in more detail below.
次にオカラを栄養源、フスマを補助添加物とするシメジ
の容器栽培法を例にとって本発明を説明する。第1図は
シメジの瓶栽培法の操作の概要を示したものであり、培
地調製を除けば従来の栽培法と同一に行われる。Next, the present invention will be explained by taking as an example a container cultivation method for shimeji mushrooms using okara as a nutrient source and bran as an auxiliary additive. FIG. 1 shows an overview of the operation of the bottle cultivation method for shimeji mushrooms, which is carried out in the same manner as the conventional cultivation method except for the preparation of the medium.
培地調製に当たっては、所定量のオガ屑、オカラ、フス
マおよび水を加えてよく混合して水分含有率60〜70
%程度の培地とする。オカラーフスマーオガ屑の混合比
は乾燥重量基準で10〜40%:5〜40%=60〜8
0%程度にするのが望ましい。When preparing the culture medium, add a predetermined amount of sawdust, okara, wheat bran, and water and mix well to reach a moisture content of 60 to 70.
% of the medium. The mixing ratio of sawdust is 10-40% on a dry weight basis: 5-40% = 60-8
It is desirable to set it to about 0%.
この混合比は使用するオカラの品質、オガ屑や栽培する
キノコの種類によっても異なるが、栄養源となるオカラ
とフスマの合計量は内容積850m1の栽培瓶を用いる
場合にはこの1本当たり30〜100g、培地重量(乾
燥基準)の20〜50%程度に調整するのが望ましい、
添加量が少ないと栄養分が不足するために当然キノコ収
量が低下し、一方添加量が多過ぎると空気保持容量の大
きなオガ屑の量が少なくなったり、また菌糸が伸長した
部分の菌糸体濃度が高くなり過ぎて空気供給が抑制され
、層全体への菌糸の伸長が不可能になったりするので好
ましくない。This mixing ratio varies depending on the quality of okara used, the sawdust, and the type of mushrooms being cultivated, but the total amount of okara and bran that serve as nutrients is 30% per bottle when using a cultivation bottle with an internal volume of 850 m1. ~100g, preferably adjusted to about 20-50% of the medium weight (dry basis).
If the amount added is too small, the mushroom yield will naturally decrease due to a lack of nutrients, while if the amount added is too high, the amount of sawdust, which has a large air holding capacity, will decrease, and the mycelium concentration in the part where the mycelium has grown will decrease. If it becomes too high, air supply will be suppressed, making it impossible for hyphae to extend throughout the layer, which is not preferable.
フスマはオガ屑との混合培地として使用する場合には3
0〜50%程度の混合比率の時に最大のキノコ収量が得
られる。しかし、オカラを主栄養源として使用する場合
にはフスマ等の添加量は出来る限り少なくすることが望
ましく、この点から判断されるフスマ添加量の適正値は
培地中の乾物重量基準で5〜15%である。When bran is used as a mixed medium with sawdust,
The maximum mushroom yield is obtained at a mixing ratio of about 0 to 50%. However, when okara is used as the main nutrient source, it is desirable to keep the amount of bran added as low as possible, and from this point of view, the appropriate amount of bran added is 5 to 15% based on the dry weight of the medium. %.
オガ屑の樹種としては、種菌の種類等によっても異なる
ものの、シメジの場合には本発明の方法を利用すること
によって赤松、杉、栗、ケヤキ、ナラ、ヒノキ、ブナ、
サワラ、カラ松、カシ、トチ、モミ、カエデ、桜など極
めて広範囲のものを使用できるようになる。この点が本
発明の大きな特徴であり、オカラとフスマ等の補助添加
物とを組合わせることによって極めて多くの樹種の使用
が可能となる。なお、このように補助添加物の使用によ
ってオカラーオガ屑混合培地におけるキノコの生育特性
が著しく改善されるのはオガ屑に起因するキノコに対す
る生育阻害物質が補助添加物中に含まれている物質によ
って封鎖されるか、あるいはオカラーオガ屑だけでは欠
落する栄養源がフスマ等によって供給される結果である
と考えられる。The tree species for sawdust vary depending on the type of inoculum, etc., but in the case of shimeji, by using the method of the present invention, it is possible to use red pine, cedar, chestnut, zelkova, oak, cypress, beech, etc.
You will be able to use a wide variety of trees, including Spanish mackerel, Japanese larch, oak, horse chestnut, fir, maple, and cherry tree. This point is a major feature of the present invention, and by combining okara with auxiliary additives such as bran, it is possible to use a wide variety of tree species. Furthermore, the reason why the growth characteristics of mushrooms in the Okara sawdust mixed medium is significantly improved by the use of supplementary additives is that the growth-inhibiting substances for mushrooms caused by sawdust are blocked by the substances contained in the supplementary additives. It is thought that this is due to the fact that the nutrients that are missing from only Okara sawdust are supplied by wheat bran and the like.
培地を栽培瓶に詰込んだ後は、従来法と同様に瓶中央部
に直径1.5cm程度の穴をあけ、更に瓶の口にキャッ
プを取付ける。滅菌、種菌の接種作業、更に培養、菌掻
、発芽、生育の操作を従来法と同様に行うことによって
キノコを収穫する。After filling the cultivation bottle with the culture medium, a hole with a diameter of about 1.5 cm is made in the center of the bottle, and a cap is attached to the mouth of the bottle, as in the conventional method. Mushrooms are harvested by performing sterilization, seed inoculation, culturing, scratching, germination, and growth in the same manner as in conventional methods.
次に、具体的実施例を用い本発明の方法を更に詳しく説
明するが、本発明の方法はここで取り上げたシメジや大
ヒラタケに限定されるものではな(、エノキタケ、ナメ
コ、シロタモギタケ、タモギタケ、クリタケ、マイタケ
、ヅイタケ等種々のキノコ類に対しても適用可である。Next, the method of the present invention will be explained in more detail using specific examples, but the method of the present invention is not limited to Shimeji mushrooms and large oyster mushrooms (Enoki mushrooms, Nameko mushrooms, Shirotamogitake mushrooms, Tamogitake mushrooms). It can also be applied to various mushrooms such as , Kuritake, Maitake, and Tsuitake.
また、補助添加物としてもフスマ、米糠、トウモロコシ
粕等に限定されるものではなく、酵母、小麦胚芽、魚粉
、油粕、肉汁、ペプトン、マイロ胚芽、牛乳、卵白、活
性炭など各種の物質をフスマと同一の目的で使用するこ
とができる。また、補助添加物としてこれらの1種又は
2種以上を培地中に混合して使用することもできる。In addition, auxiliary additives are not limited to bran, rice bran, corn meal, etc., but various substances such as yeast, wheat germ, fishmeal, oil cake, meat juice, peptone, milogerm, milk, egg white, and activated carbon can be added to bran. It can be used for the same purpose. Furthermore, one or more of these may be used as a mixture in the medium as an auxiliary additive.
実施例1
フスマ:オカラの混合比率が乾物重量基準で0%=30
%、2.5%: 27.5%、5%:25%、10%:
20%、15%:15%および30%:0%(残部70
%はブナオガ屑)とし、一連の混合物に水を添加し、水
分含有率65%の培地を調製した。これらを内容積85
0mA!のポリプロピレン製栽培瓶各3本に450〜5
20gずつ詰め込み、次に培地中央部に瓶底部まで到達
する直径1.5cmの穴をあけた。瓶の口にキャップを
した後に120℃の飽和水蒸気圧下で1時間加熱滅菌し
た。Example 1 Mixing ratio of bran: okara is 0% on dry weight basis = 30
%, 2.5%: 27.5%, 5%: 25%, 10%:
20%, 15%: 15% and 30%: 0% (remaining 70%
% of beech sawdust) and water was added to a series of mixtures to prepare a medium with a water content of 65%. These have an internal volume of 85
0mA! 450-5 for each 3 polypropylene cultivation bottles
20 g each was packed, and then a hole with a diameter of 1.5 cm was made in the center of the medium, reaching the bottom of the bottle. After capping the mouth of the bottle, it was heat sterilized at 120° C. under saturated steam pressure for 1 hour.
冷却後、米糠−オガ屑培地で生育させた種菌(KR−1
)約7gを瓶中央の穴と培地上面に添加した0種菌接種
15〜20日後に培地全体に菌糸が伸長したが、25日
後に菌掻きを行い、栽培瓶の蓋を除去した状態で温度1
3°C1湿度90〜95%、照度150尼uxの条件下
においたところ、菌掻き11〜14日後にキノコを収穫
することができた。フスマ/オカラ混合比とキノコ収量
の関係を第2図に示す。第2図において、培地中のフス
マの量が乾物重量基準で5〜15%でキノコ収量が高く
、特に8〜12%のときにキノコ収量が高いことを示し
ている。なお、キノコ収量はフスマ添加量(培地中の乾
物重量基準)10%の場合に最大値97.0g/瓶を示
した。After cooling, the inoculum (KR-1) grown in rice bran-sawdust medium
) Approximately 7 g was added to the hole in the center of the bottle and the top surface of the culture medium.After 15 to 20 days of inoculation, mycelia grew throughout the culture medium, but after 25 days, the fungus was scraped, and the culture bottle was heated to temperature 1 with the lid removed.
When the mushrooms were placed under the conditions of 3° C., humidity of 90 to 95%, and illuminance of 150 ux, mushrooms could be harvested 11 to 14 days after the mushrooms were scraped. Figure 2 shows the relationship between the bran/okara mixture ratio and mushroom yield. FIG. 2 shows that the mushroom yield is high when the amount of bran in the medium is 5 to 15% on a dry weight basis, especially when it is 8 to 12%. The maximum mushroom yield was 97.0 g/bottle when the amount of bran added was 10% (based on the weight of dry matter in the medium).
また、培地組成が乾物重量基準でブナオガ屑70%、オ
カラ15%、フスマ15%の場合、菌掻14日後に3本
の栽培瓶からキノコをそれぞれ81g、78gおよび8
5g収穫すること誹(できた。In addition, when the medium composition was 70% beech sawdust, 15% okara, and 15% bran on a dry weight basis, 81g, 78g, and 8g of mushrooms were grown from the three cultivation bottles after 14 days of fungal scraping, respectively.
Harvesting 5g (I was able to do it.)
実施例2
種菌KR−1をKR−2に変更した以外は実施例1と同
様に栽培テストを行ったところ、キノコの平均収量は8
3gであった。Example 2 A cultivation test was conducted in the same manner as in Example 1 except that the seed fungus KR-1 was changed to KR-2, and the average yield of mushrooms was 8.
It was 3g.
実施例3
オガ屑の樹種をブナから杉に変更し、その混合比率を乾
物重量基準でオガ屑64%、オカラ24%、フスマ12
%、培地水分含有率を65%、培地詰込量を380gと
した。その他の操作は実施例1と同様に行ったところ、
キノコの平均収量は81gであった。Example 3 The wood species of sawdust was changed from beech to cedar, and the mixing ratio was 64% sawdust, 24% Japanese porridge, and 12% wheat bran on a dry weight basis.
%, the medium moisture content was 65%, and the medium packed amount was 380 g. Other operations were performed in the same manner as in Example 1.
The average yield of mushrooms was 81 g.
実施例4
実施例1と同一の培地に大ヒラタケの種菌を接種し、2
2°Cにおいて25日間培養した後に菌掻した。温度1
8℃、湿度90〜95%の条件に置いたところ、11日
後にキノコを収穫でき、収量85gが得られた。Example 4 The same medium as in Example 1 was inoculated with Oyster mushroom inoculum, and 2
After culturing at 2°C for 25 days, the bacteria were scratched. temperature 1
When placed under conditions of 8° C. and 90-95% humidity, mushrooms could be harvested 11 days later with a yield of 85 g.
実施例5
フスマを米糠に変更した以外は実施例1と同様にシメジ
の栽培テストを実施したところ、菌掻16日後にキノコ
を収穫でき、平均収量78gが得られた。Example 5 A shimeji mushroom cultivation test was carried out in the same manner as in Example 1 except that rice bran was used instead of bran. Mushrooms could be harvested 16 days after the mushrooms were scraped, and an average yield of 78 g was obtained.
比較例1〜4
実施例1.2.3および4におけるフスマあるいは米糠
を等量のオカラに置き替え、従って培地材料をオガ屑お
よびオカラのみに変更してシメジあるいは大ヒラタケの
栽培地試験を行ったところ、キノコの平均収量はそれぞ
れ34g、23g、20gおよび43gに過ぎなかった
。Comparative Examples 1 to 4 The bran or rice bran in Examples 1.2.3 and 4 was replaced with an equal amount of okara, and therefore the culture medium materials were changed to only sawdust and okara, and a cultivation site test for shimeji mushrooms or large oyster mushrooms was conducted. The average mushroom yields were only 34g, 23g, 20g and 43g, respectively.
本発明の方法はオガ屑中に含まれると思われるキノコに
対する生育阻害物質を他の物質によって封鎖することを
その基本原理の1つとするが、より直接的にはこの生育
阻害物質を壇地調製前に除去する方法が考えられる。One of the basic principles of the method of the present invention is to sequester growth-inhibiting substances for mushrooms that are thought to be contained in sawdust with other substances, but more directly, this growth-inhibiting substance can be used to prepare mushroom beds. There is a way to remove it beforehand.
事実、実施例1および3に示したブナおよび杉のオガ屑
は生の原木を製材する際に発生したものであるが、これ
に水を加えてスラリー状とし、120°Cの飽和水蒸気
圧下に2時間保った後に水先乾燥して培地調製に用いた
ところ、最終的なキノコ収量としてそれぞれ83gおよ
び76gが得られた。因に生の原木を自然状態で上記の
ような生育阻害物質を除去するために通常、半年〜1年
程度の雨ざらし、その他の工程を要する。In fact, the beech and cedar sawdust shown in Examples 1 and 3 was generated when sawing raw wood, but water was added to it to form a slurry, and the sawdust was heated to 120°C under saturated steam pressure. After keeping for 2 hours, the mushrooms were drained and used for medium preparation, resulting in final mushroom yields of 83 g and 76 g, respectively. Incidentally, in order to remove the above-mentioned growth-inhibiting substances from raw logs in their natural state, it is usually necessary to expose them to the rain for about six months to a year and other processes.
本発明の方法によれば、オガ屑中の生育阻害物質を封鎖
し、またキノコあるいはオガ屑の種類によってはオカラ
だけでは不足する栄養源を補給することによって、オカ
ラを栄養源としてのキノコの高効率栽培が可能となる。According to the method of the present invention, growth inhibiting substances in sawdust are sequestered, and depending on the type of mushroom or sawdust, a nutritional source that is insufficient with okara alone is supplied, thereby increasing mushroom growth using okara as a nutritional source. Efficient cultivation becomes possible.
特に、使用可能なオガ屑の種類が拡大され、また半年〜
1年間程度雨ざらしにして生育阻害物質を除去すると言
った煩雑かつ時間を要する作業からの解放という点で本
発明の効果は大きい。In particular, the types of sawdust that can be used have been expanded, and
The present invention has a great effect in that it frees the plant from the complicated and time-consuming task of removing growth-inhibiting substances by exposing it to the rain for about a year.
第1図は本発明にかかるオカラを栄養源とするキノコの
オガ屑法瓶栽培法の一実施例を示すプロセス図、第2図
は本発明の方法になるフスマーオカラーブナオガ屑系培
地を用いるシメジ栽培におけるフスマ/オカラ混合比と
キノコ収量との関係を示すグラフ、第3図は従来のシメ
ジの代表的オガ屑法瓶栽培のプロセス図である。
代理人 弁理士 西 元 勝 −
第2図
フスlメ木カラ5昆6゛之(%/%)Fig. 1 is a process diagram showing an example of the method for cultivating mushrooms in sawdust bottles using okara as a nutrient source according to the present invention, and Fig. 2 shows a method of cultivating mushrooms using sawdust as a nutrient source according to the present invention. FIG. 3 is a graph showing the relationship between the bran/okara mixture ratio and the mushroom yield in the Shimeji mushroom cultivation method used, and FIG. 3 is a process diagram of a typical conventional sawdust cultivation method for Shimeji mushrooms. Agent Masaru Nishimoto, Patent Attorney - Figure 2 Fusu l Mekikara 5 Kon 6 (%/%)
Claims (4)
るキノコ類の人工栽培方法において、培地材料としてオ
カラおよびオガ屑のほかにフスマ、米糠、トウモロコシ
粕等の大豆以外の穀類粉末のうち少なくとも1種類以上
を培地に添加することを特徴とするキノコ類の人工栽培
方法。(1) In an artificial cultivation method for mushrooms that uses okara, which is a by-product during tofu production, as a nutritional source, in addition to okara and sawdust, at least one of grain powders other than soybeans such as wheat bran, rice bran, and corn meal is used as a medium material. A method for artificially cultivating mushrooms, characterized by adding more than one type of mushroom to a medium.
類粉末がフスマからなり、該フスマが培地中に乾物重量
基準で5〜15%含有されていることを特徴とするキノ
コの人工栽培方法。(2) Artificial cultivation of mushrooms according to claim (1), wherein the grain powder is made of bran, and the bran is contained in the medium in an amount of 5 to 15% on a dry weight basis. Method.
類粉末がフスマからなり、オカラ:フスマ:オガ屑が各
乾物重量基準で10〜40%:5〜40%:60〜80
%の割合で混合されていることを特徴とするキノコの人
工栽培方法。(3) In claim (1), the grain powder is made of bran, and the ratio of okara: bran: sawdust is 10 to 40%: 5 to 40%: 60 to 80% on a dry weight basis.
% artificial cultivation method of mushrooms.
類粉末がフスマからなり、該フスマが培地中に乾物重量
基準で8〜12%含有されていることを特徴とするキノ
コの人工栽培方法。(4) Artificial cultivation of mushrooms according to claim (2), wherein the grain powder is made of bran, and the bran is contained in the medium in an amount of 8 to 12% on a dry weight basis. Method.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62274030A JPH01117724A (en) | 1987-10-29 | 1987-10-29 | Artificial culture of mushroom |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62274030A JPH01117724A (en) | 1987-10-29 | 1987-10-29 | Artificial culture of mushroom |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01117724A true JPH01117724A (en) | 1989-05-10 |
Family
ID=17535980
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62274030A Pending JPH01117724A (en) | 1987-10-29 | 1987-10-29 | Artificial culture of mushroom |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01117724A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20010108876A (en) * | 2000-06-01 | 2001-12-08 | 이수정 | Method for mushroom grow |
KR100399538B1 (en) * | 2002-08-05 | 2003-09-26 | Kea Yeon Cho | Method for growing functional flammulina velutipes using red ginseng extract and herbal extract and culture medium composition for growing the same |
JP2007151444A (en) * | 2005-12-02 | 2007-06-21 | Tottori Prefecture | Mushroom medium, and mushroom cultivating method |
KR100737399B1 (en) * | 2006-03-23 | 2007-07-09 | 대한민국 | The function characteristic shiitake mushroom production method where the calcium is strengthened |
CN111742783A (en) * | 2020-08-14 | 2020-10-09 | 唐湘梅 | Industrial production method of edible fungus sticks |
-
1987
- 1987-10-29 JP JP62274030A patent/JPH01117724A/en active Pending
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20010108876A (en) * | 2000-06-01 | 2001-12-08 | 이수정 | Method for mushroom grow |
KR100399538B1 (en) * | 2002-08-05 | 2003-09-26 | Kea Yeon Cho | Method for growing functional flammulina velutipes using red ginseng extract and herbal extract and culture medium composition for growing the same |
JP2007151444A (en) * | 2005-12-02 | 2007-06-21 | Tottori Prefecture | Mushroom medium, and mushroom cultivating method |
KR100737399B1 (en) * | 2006-03-23 | 2007-07-09 | 대한민국 | The function characteristic shiitake mushroom production method where the calcium is strengthened |
CN111742783A (en) * | 2020-08-14 | 2020-10-09 | 唐湘梅 | Industrial production method of edible fungus sticks |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US5503647A (en) | Mushroom casing spawn | |
US20110143426A1 (en) | Device and process to generate co2 used for indoor crop production and underwater gardening | |
JP3781434B2 (en) | Artificial fungus bed cultivation method of Agaricus persimmon fruiting body | |
Nikšić et al. | Farming of medicinal mushrooms | |
US4987698A (en) | Mushroom cultivation | |
JPH01117724A (en) | Artificial culture of mushroom | |
JPH02156828A (en) | Artificial cultivation of shiitake mushroom | |
KR101687891B1 (en) | Cultivating method of tree ear and the composition of cultur medium | |
KR101687890B1 (en) | Cultivating method of oyster mushroomr and the composition of culture medium | |
CN113396775A (en) | Method for cultivating oyster mushroom by utilizing Maotai-flavor vinasse and formula for cultivating vinasse oyster mushroom | |
Mizuno | Cultivation of the medicinal mushroom royal sun agaricus—Agaricus blazei Murr.(Agaricomycetideae) | |
Saha et al. | Evaluation of various organic substrate for maximization of biological efficiency of Pleurotus species | |
JPH11220946A (en) | Culture of pholiota adiposa | |
JPH0158927B2 (en) | ||
JPH119085A (en) | Culture medium for cultivating mushroom and culture medium for culturing spawn | |
JP4202541B2 (en) | Artificial cultivation method of Honshimeji | |
JPH11196666A (en) | Method of culturing a kind of mushroom (hohenbuehelia serotina) | |
JPS5839485B2 (en) | How to cultivate Maitake mushrooms | |
JPH0436120A (en) | Culture medium for cultivating mushroom and method for artificially cultivating mushroom | |
JPH09308373A (en) | Artificial culture of tricholoma irinum | |
JP2023045617A (en) | Mushroom medium and method for producing mushroom medium, and mushroom production method | |
JPH05153853A (en) | Artificial cultivation of mushroom | |
JPH07298780A (en) | Culture medium for cultivating plant consisting essentially of compressed and milled chaft | |
JPH08291012A (en) | Soil disease injury control for plant | |
WO2001005728A1 (en) | Product and process |