EP0504142A1 - Substrate and method for culture of fungi, including shiitake (lentinus edodes) - Google Patents

Substrate and method for culture of fungi, including shiitake (lentinus edodes)

Info

Publication number
EP0504142A1
EP0504142A1 EP90911078A EP90911078A EP0504142A1 EP 0504142 A1 EP0504142 A1 EP 0504142A1 EP 90911078 A EP90911078 A EP 90911078A EP 90911078 A EP90911078 A EP 90911078A EP 0504142 A1 EP0504142 A1 EP 0504142A1
Authority
EP
European Patent Office
Prior art keywords
grain
approximately
mixture
grain mixture
sterilizing
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.)
Withdrawn
Application number
EP90911078A
Other languages
German (de)
English (en)
French (fr)
Other versions
EP0504142A4 (en
Inventor
Bryan Tokuichi Hiromoto
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.)
MAUI SHIITAKE TRADING COMPANY Inc
Original Assignee
MAUI SHIITAKE TRADING COMPANY Inc
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 MAUI SHIITAKE TRADING COMPANY Inc filed Critical MAUI SHIITAKE TRADING COMPANY Inc
Publication of EP0504142A4 publication Critical patent/EP0504142A4/en
Publication of EP0504142A1 publication Critical patent/EP0504142A1/en
Withdrawn legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01GHORTICULTURE; CULTIVATION OF VEGETABLES, FLOWERS, RICE, FRUIT, VINES, HOPS OR SEAWEED; FORESTRY; WATERING
    • A01G18/00Cultivation of mushrooms
    • A01G18/60Cultivation rooms; Equipment therefor
    • A01G18/64Cultivation containers; Lids therefor
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01GHORTICULTURE; CULTIVATION OF VEGETABLES, FLOWERS, RICE, FRUIT, VINES, HOPS OR SEAWEED; FORESTRY; WATERING
    • A01G18/00Cultivation of mushrooms
    • A01G18/20Culture media, e.g. compost
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01GHORTICULTURE; CULTIVATION OF VEGETABLES, FLOWERS, RICE, FRUIT, VINES, HOPS OR SEAWEED; FORESTRY; WATERING
    • A01G18/00Cultivation of mushrooms
    • A01G18/40Cultivation of spawn
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01GHORTICULTURE; CULTIVATION OF VEGETABLES, FLOWERS, RICE, FRUIT, VINES, HOPS OR SEAWEED; FORESTRY; WATERING
    • A01G18/00Cultivation of mushrooms
    • A01G18/50Inoculation of spawn

Definitions

  • Shiitake and other mushrooms are usually cultivated on logs or in cellulose based substrates.
  • a cellulose based substrate is those described in U.S. Patent No. 4,127,965 to
  • U.S. Patent No. 4,674,228 issued to Murata removal of the mycelium from such containers often causes damage that reduces productivity.
  • U.S. Patent No. 4,735,014 to Weber teaches the use of hemp stalks
  • U.S. Patent No. 4,741,122 to Becsy teaches the use of agricultural wastes.
  • the invention is a new substrate for the growth of fungi, especially shiitake, created using a new method of sterilizing the substrate to allow cultivation of the desired fungi without contamination by competing organisms.
  • the new substrate is grain that is essentially cellulose free and that has been sterilized in accordance with the process described herein.
  • the prior art in the growth of mushrooms and other fungi requires growth on logs, sawdust or other substrates containing a major portion of cellulose.
  • cellulose is not necessary for the cultivation of shiitake.
  • Shiitake mushrooms have the ability to break down cellulose for essential nutrients, but can be more efficiently grown in a substrate containing these materials in an already usable form.
  • shiitake can break down lignin, which is a constituent of wood, but again shiitake can be cultivated more efficiently by providing the breakdown products instead of the lignin.
  • the substrate is boiled to kill the bacteria that are present.
  • the substrate is then cooled to induce any heat resistant spores to germinate.
  • the substrate then is steam sterilized after such germination, but before the bacteria have matured sufficiently to form heat-resistant spores.
  • non-heating methods of sterilizing the grain substrate also can be used, such as irradiation.
  • irradiation of the substrate would require greater governmental regulation and may affect marketability of the resulting mushrooms.
  • Other non-heating methods of sterilization could include, for example, chemical sterilization (in which chemical agents in solid, liquid or gaseous form are used for sterilization) or pressure sterilization (in which the substrate is subjected to extremes of high or low pressure (including vacuum), or both).
  • the invention can be practiced with the listed sterilization methods and all other sterilization methods that kill bacteria or other spore-forming microorganisms, but that normally leave surviving spores.
  • a second sterilization that kills the bacteria or other microorganisms will completely sterilize the substrate, if the second sterilization takes place before the bacteria or other microorganisms have matured sufficiently to form new spores.
  • the particular methods of initial and secondary sterilization are not critical, as long as the spores are allowed to germinate after initial sterilization and the substrate is secondarily sterilized before the spores mature sufficiently to form new spores.
  • the substrate of the invention thus provides a more efficient medium for cultivation of mushrooms, including shiitake, because the nutrients required by the mushrooms are furnished directly, rather than being furnished in the form of cellulose and lignin that must be enzymatically broken down by the mushrooms.
  • the invention also provides a more efficient method of cultivating mushrooms because ⁇ i competing microorganisms, including bacteria, are eliminated from the substrate.
  • An advantage of the invention is the shortening of incubation times for the shiitake.
  • a further advantage of the invention is the increase in yield per pound of substrate.
  • One hundred pounds of the substrate of the invention yields approximately 300 pounds of shiitake within 5 months.
  • 100 pounds of logs yields 25 approximately 10 to 15 pounds of shiitake over more than 3 years
  • 100 pounds of sawdust based substrate yields approximately 80 pounds of shiitake over 8 months.
  • a further advantage of the invention is that no 20 special spawn material is necessary.
  • the same material used for fruiting can be used as a spawn material to start new production units, so that production can be increased immediately instead of waiting for new spawn to be grown. Similarly, no
  • a still further advantage of the invention is that production units may be kept in incubation beyond the 21 day period for up to 6 months if, for example, market conditions are unfavorable. This Q also allows stockpiling of colonized units for large seasonal production outputs.
  • the grain for the substrate is then added and boiled for approximately one hour in order to kill the bacteria present and cause the absorption of the dispersed nutritional supplements into the grain.
  • the grain is then allowed to cool to induce germination of any heat-resistant spores. While the grain is cooling, it is mixed with permeability enhancing powders to prevent caking and packed into microorganism impermeable sterilizable containers, such as polypropylene bags. The bags are then steam sterilized in accordance with conventional practice before the germinated bacteria have matured sufficiently to form spores.
  • colonization of the bags is accomplished by introducing either pure spawn of the desired fungi or by introducing previously colonized grain.
  • the bags are then shaken to mix the spawn or previously colonized grain with the grain in order to decrease the incubation time.
  • the bags are then incubated for approximately three weeks at approximately 80 degrees Fahrenheit. During this time, the spawn will digest most, if not all, of the substrate to form a mycelium.
  • the mycelium can then be induced to fruit by subjecting the bags to a cold shock of 40 to 65 degrees Fahrenheit for 5 to 15 days under cool white fluorescent lighting. After the cold shock, fruiting to maturation is accomplished by removing the mycelium from the containers and exposing them to an intermittent chilled water mist, or otherwise placing the mycelium in a high humidity environment.
  • fruiting can be induced using only a cold water spray under lighted conditions Brief Description of Drawing.
  • Figure 1 is a flow chart of a preferred method of preparing the substrate of the invention. Best Mode for Carrying Out Invention.
  • Figure 1 of the drawings sets forth generally a preferred method of preparing the substrate of the invention.
  • the ingredients in the substrate are preferably chosen to provide optimum nutrition for the fungi to be grown without requiring additional artificial supplements. This use of all-natural materials therefore makes sale and marketing of the cultivated fungi easier because fewer regulatory requirements are imposed.
  • the preferred ingredients, their ranges and the optimum amounts are set forth below for preparing batches of the substrate.
  • the maple pea sprouts are preferably grown for 6 to 12 days under a mist system. Commercial bean sprouts may also be used, but more roots and larger cotyledons are available with maple pea sprouts.
  • Sorghum provides vitamins, carbohydrates, starches, protein and minerals such as Copper, Iron, Manganese, Zinc and Selenium.
  • Oats provide vitamins, minerals, carbohydrates, starches, proteins and salicylic acid.
  • Salicylic acid promotes shiitake fruiting.
  • Rolled barley grain provides vitamins and carbohydrates and absorbs excess water.
  • Soybean meal provides a source of minerals, proteins and vitamins. Brewer's yeast powder provides high amounts of vitamins, especially B vitamins that promote mycelial growth.
  • Sunflower seed and sunflower oil provide vitamins, minerals, proteins and saturated and unsaturated oils.
  • the sunflower seed and oil also promote heavier secondary mycelial growth.
  • the pea sprouts promote a heavier amount of fruitings to occur. This allows some control over the size of the mushrooms. More sprouts allow for more mushrooms to form but the mushrooms are smaller in. size. Fewer sprouts allow for fewer mushrooms to form but the mushrooms are larger in size. With no sprouts added, mushrooms with individual weights of from 3/4 lb to 1-1/2 lbs may form on the substrate.
  • Garlic provides natural antibacterial action in order to resist bacterial growth after boiling and sterilization of the substrate.
  • Molasses provides sugars and wheat germ oil provides saturated and unsaturated oils as well as vitamin D.
  • Corn gluten meal provides vitamins, minerals, protein and selenium.
  • Potatoes provide starch. Milk provides cassein and cheese can be substituted instead of milk.
  • the coating ingredients serve additional functions besides increasing permeability of the substrate.
  • Limestone powder adjusts the pH of the substrate to neutral (approximately 7 to 8).
  • the gypsum powder also provides long term pH maintenance and makes the grain substrate loose and powdery.
  • the cottonseed meal provides protein and oil. It should be noted that the prior art teaches that, under certain conditions, calcium inhibits fruiting of mycelium. However, the substrate of this invention contains substantial amounts of calcium from the limestone and gypsum powder.
  • the size and number of mushrooms can be controlled prior to colonization by the amount of substrate that is packed in the bags, with larger bags that contain more substrate producing larger and more mushrooms. For example, eight pound bags will produce 3/4 pound mushrooms for approximately 6 months.
  • Mushroom size and number also can be controlled after colonization by allowing individual colonized units to come into contact with each other.
  • the individual units will form one large continuous unit forming larger and more numerous mushrooms than an individual unit.
  • Fully colonized units can be placed on shelving or strung on rods to maximize production per unit area.
  • the water is boiled in a 60 gallon capacity steam kettle with a bottom spigot.
  • the potatoes are sliced and then added to the boiling water together with the milk, garlic, corn gluten meal, wheat germ oil, sunflower oil, molasses, hulled sunflower seed, brewer's yeast powder and soybean meal.
  • the mixture is then boiled until all components break into small pieces.
  • the mixture is preferably mixed with a portable paint mixer to help break clumps into small pieces.
  • Maple pea sprouts are then added to the boiling mixture, which is stirred with a large paddle until the sprouts are soft.
  • the oat grain, barley grain and sorghum grain are then added, together with sufficient water only to cover the grain.
  • the mixture is then boiled and stirred until the water level falls below the grain level by 3 to 4 inches and the heat source is then turned off. After approximately one hour, any remaining liquid is drawn off from the bottom of the pot. At this point, the grai ⁇ should be half-cooked and semi-hard. The grain is then allowed to cool for approximately 24 hours, at which time it is removed from the pot.
  • the prepared substrate is then packed into double polypropylene plastic bags (1.5 mil.) .
  • Each of these double bag units has a polypropylene collar, a cotton plug and an aluminium foil cover over the plug.
  • the bags from 4 batches of the grain (approximately 2,400 pounds) are then loaded in a steam retort (5 foot diameter, 13 feet long) and steam-sterilized at 250° F, 15 pounds per square inches steam pressure for 7 hours. Each load is then cooled for 24 hours before seeding.
  • the bags of substrate After the bags of substrate have been sterilized, they are preferably seeded under sterile conditions in laminar airflow hoods. Seeding is accomplished by introducing pure spawn or, preferably, colonized grain from previous production runs. Approximately 5 to 10 tablespoons of colonized grain is added into each 2-pound bag. Each of the bags is then shaken to mix the colonized grain throughout the new unit. This thorough mixing of the previously colonized grain with the substrate reduces the normal incubation time considerably. Thus, a 2-pound bag will usually be fully colonized after approximately 3 weeks of incubation at 80° F. Usually 15 new 2-pound units may be started from each colonized 2-pound unit. The preferred size of bag is 8 pounds because of the disproportionately greater number of buds per
  • the grain substrate will be mostly or completely digested, leaving only the mycelium in the bag.
  • the bag can be retained in the mycelial stage for approximately 3 to 4 months for shipment or storage.
  • the bags containing the mycelium are subjected to a cold shock by chilling them at 40 to 65° F for 5 to 15 days under cool white fluorescent lighting of 25 to 100 lux.
  • the preferred cold shock is at a temperature of 45° F for 7 to 9 days, although a cold water bath for 24 to 48 hours also may be used.
  • the bags can be shipped in a refrigerated container during this cold shock stage.
  • the mycelium may be removed from the bags and exposed to an intermittent cold water mist. It is preferred that the misting take place during daylight hours and also during a 2 hour period during the night.
  • the water used for misting is chilled to 50 to 75° F and misting occurs for 2 to 120 seconds at 2 to 10 minute intervals for 6 to 15 hours during the daylight period.
  • shiitake mushrooms may be harvested.
  • Subsequent crops from the bags may occur 20 to 30 days apart.
  • the relative humidity in the misting environment must be at least 80%.
  • the mycelium may be removed from the bags and allowed to fruit using previously known methods. After the substrate has been spent, it may be used for other purposes, such as compost, animal feed, mushroom compost for other mushrooms or insect feed.
  • the mycelium After formation of the mycelium, but before fruiting, the mycelium also may be used as animal feed or for human food. Useful biochemicals also may be extracted from the mycelium.
  • the substrate described herein is suitable for growing many species of mushrooms, including those listed in Mushroom List 1, which is a part of this description and incorporated herein by reference, and many genera of fungi, including those listed in Fungal List 2, which is a part of this description and incorporated herein by reference. Many of these fungi are useful for their biochemical or other properties.
  • the substrate can be used for growing penicillin mold, weed molds, yeasts and medicinal mushrooms. Accordingly, no limitation is to be inferred except as set forth in the claims.
  • Phaeocoriolellus Potebniamyces Phaeolus Preussia Phanerochaete Psathyrella Phellinus Pseudeurotium Phialomyces Pseudofusarium Phialophora Pseudohydnum Phlebia Pseudospiropes Phlogiotis Ptychogaster
  • the invention can be used for the inexpensive and efficient cultivation of fungi, especially shiitake.
  • Other fungi also may be cultivated, including fungi useful for food or medicinal purposes.

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Mycology (AREA)
  • Environmental Sciences (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Mushroom Cultivation (AREA)
  • Breeding Of Plants And Reproduction By Means Of Culturing (AREA)
EP90911078A 1989-06-29 1990-06-26 Substrate and method for culture of fungi, including shiitake (lentinus edodes) Withdrawn EP0504142A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US37427089A 1989-06-24 1989-06-24
US374270 1989-06-29

Publications (2)

Publication Number Publication Date
EP0504142A4 EP0504142A4 (en) 1992-05-22
EP0504142A1 true EP0504142A1 (en) 1992-09-23

Family

ID=23476031

Family Applications (1)

Application Number Title Priority Date Filing Date
EP90911078A Withdrawn EP0504142A1 (en) 1989-06-29 1990-06-26 Substrate and method for culture of fungi, including shiitake (lentinus edodes)

Country Status (22)

Country Link
EP (1) EP0504142A1 (zh)
JP (1) JPH05500305A (zh)
CN (2) CN1049184A (zh)
AR (1) AR243930A1 (zh)
AU (1) AU6053490A (zh)
BR (1) BR9007483A (zh)
CA (1) CA2059274A1 (zh)
CS (1) CS237990A3 (zh)
DK (1) DK205091A (zh)
FI (1) FI916135A0 (zh)
GB (1) GB2251250B (zh)
HU (1) HUT59277A (zh)
IL (1) IL94900A0 (zh)
NL (1) NL9021178A (zh)
NZ (1) NZ234286A (zh)
OA (1) OA09526A (zh)
PL (1) PL285860A1 (zh)
PT (1) PT94547A (zh)
SE (1) SE9103854L (zh)
TR (1) TR26187A (zh)
WO (1) WO1991000002A1 (zh)
ZA (1) ZA905085B (zh)

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GB2284429B (en) * 1993-09-28 1997-10-22 House Foods Corp Method for forming fruit bodies of Fistulina hepatica
GB2317898A (en) * 1996-10-02 1998-04-08 Rourke Mel O A system for the manufacture of mushroom spawn
CN1128573C (zh) * 1999-05-20 2003-11-26 江苏理工大学 一种植物育苗和栽培的基质及其制造方法
DE60045095D1 (de) 1999-12-15 2010-11-25 Amino Up Chemical Co Ltd Ahren zur herstellung derselben und deren anwendung
AU2001241774A1 (en) * 2000-03-08 2001-09-17 Hercules Incorporated Control of spore forming bacteria
KR20010098182A (ko) * 2000-04-28 2001-11-08 김춘식 변패 우유를 이용한 버섯 균사체 배양방법
US6405582B1 (en) 2000-06-15 2002-06-18 Hercules Incorporated Biosensor and deposit sensor for monitoring biofilm and other deposits
KR100424608B1 (ko) * 2001-06-13 2004-03-27 주식회사 경기유지 고품질의 버섯을 저비용으로 다수확하기 위한 버섯증수개량제 조성물
DE60234668D1 (de) * 2001-08-01 2010-01-21 Orgaworld B V Verfahren zum Kultivieren von Pilzen
NL1036422C2 (en) * 2009-01-14 2010-07-15 Visser S Gravendeel Holding Container for cultivating agricultural or biological material.
CN101946634A (zh) * 2010-09-13 2011-01-19 云南省农业科学院高山经济植物研究所 一种羊肚菌母种制作方法
CN102978254B (zh) * 2012-12-26 2015-04-08 东华大学 一种脉动培养细菌纤维素的方法
CN103444433B (zh) * 2013-09-02 2015-06-10 辽宁省微生物科学研究院 朱红栓菌的人工栽培方法
MY176220A (en) * 2013-09-30 2020-07-24 Ihi Corp Biomass production method and biomass storage apparatus
CN103667130A (zh) * 2013-12-06 2014-03-26 云南农业大学 一种疫霉培养基及其制备方法
CN103641556B (zh) * 2013-12-08 2015-03-25 邬金梅 一种利用向日葵副产物制作滑菇栽培料的方法
JP6307683B2 (ja) * 2014-03-25 2018-04-11 三重県 オオイチョウタケの屋内人工栽培法
CN104909929A (zh) * 2015-06-19 2015-09-16 桂林健成生物科技开发有限公司 采收芽苗菜后的种皮/胚胎体和根茎在栽培白参菌中的应用
CN104892267A (zh) * 2015-06-19 2015-09-09 桂林健成生物科技开发有限公司 采收芽苗菜后的种皮/胚胎体和根茎在栽培秀珍菇中的应用
CN104926505A (zh) * 2015-06-19 2015-09-23 桂林健成生物科技开发有限公司 采收芽苗菜后的种皮/胚胎体和根茎在栽培鸡腿菇中的应用
CN105110841B (zh) * 2015-07-25 2018-04-13 西峡县食用菌科研中心 利用香菇菌渣栽培羊肚菌的培养基料及其制备方法
CN111990164B (zh) * 2020-09-21 2022-04-01 中华全国供销合作总社昆明食用菌研究所 一种金耳新菌株中菌金耳1号菌株及其栽培方法
CN113475310B (zh) * 2021-08-05 2023-10-27 河南省农业科学院植物营养与资源环境研究所 一种控制白灵菇原基数目形成和原基分化发育的方法
CN114317279A (zh) * 2021-12-20 2022-04-12 贵州省生物研究所 一种分离黑乳菇伴生真菌齿梗孢霉菌的优质培养基配方
CN114568450B (zh) * 2022-02-25 2023-06-20 天津农学院 黄柄曲霉液体发酵代谢物作为生长调节剂的应用和方法
CN114747422B (zh) * 2022-04-06 2023-08-01 赵金亮 北方羊肚菌高产快速出菇方法
CN115039639B (zh) * 2022-08-17 2022-11-22 云南菌视界生物科技有限公司 一种银耳液体菌种短周期生产方法及银耳液体菌种的应用
CN115211322A (zh) * 2022-08-30 2022-10-21 沧州职业技术学院 一种茅窝菌的栽培方法
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Also Published As

Publication number Publication date
HU906030D0 (en) 1992-04-28
OA09526A (en) 1992-11-15
GB9127448D0 (en) 1992-02-19
CS237990A3 (en) 1992-02-19
SE9103854D0 (sv) 1991-12-30
NZ234286A (en) 1992-10-28
HUT59277A (en) 1992-05-28
DK205091A (da) 1992-02-21
JPH05500305A (ja) 1993-01-28
DK205091D0 (da) 1991-12-20
CA2059274A1 (en) 1990-12-30
FI916135A0 (fi) 1991-12-27
CN1090966A (zh) 1994-08-24
CN1049184A (zh) 1991-02-13
GB2251250B (en) 1994-01-19
PL285860A1 (en) 1991-03-11
GB2251250A (en) 1992-07-01
PT94547A (pt) 1991-02-08
NL9021178A (nl) 1992-04-01
IL94900A0 (en) 1991-04-15
AR243930A1 (es) 1993-09-30
WO1991000002A1 (en) 1991-01-10
BR9007483A (pt) 1992-09-01
CN1032567C (zh) 1996-08-21
TR26187A (tr) 1995-02-15
ZA905085B (en) 1992-03-25
SE9103854L (sv) 1991-12-30
AU6053490A (en) 1991-01-17
EP0504142A4 (en) 1992-05-22

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