CN105027978A - Mushroom cultivation method - Google Patents

Mushroom cultivation method Download PDF

Info

Publication number
CN105027978A
CN105027978A CN201510461970.6A CN201510461970A CN105027978A CN 105027978 A CN105027978 A CN 105027978A CN 201510461970 A CN201510461970 A CN 201510461970A CN 105027978 A CN105027978 A CN 105027978A
Authority
CN
China
Prior art keywords
wood fragments
mushroom
bacterium bag
bacterium
carry out
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
Application number
CN201510461970.6A
Other languages
Chinese (zh)
Inventor
李睿坚
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.)
Chengdu Shengling Biotechnology Co Ltd
Original Assignee
Chengdu Shengling Biotechnology Co Ltd
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 Chengdu Shengling Biotechnology Co Ltd filed Critical Chengdu Shengling Biotechnology Co Ltd
Priority to CN201510461970.6A priority Critical patent/CN105027978A/en
Publication of CN105027978A publication Critical patent/CN105027978A/en
Pending 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
    • CCHEMISTRY; METALLURGY
    • C05FERTILISERS; MANUFACTURE THEREOF
    • C05DINORGANIC FERTILISERS NOT COVERED BY SUBCLASSES C05B, C05C; FERTILISERS PRODUCING CARBON DIOXIDE
    • C05D3/00Calcareous fertilisers
    • CCHEMISTRY; METALLURGY
    • C05FERTILISERS; MANUFACTURE THEREOF
    • C05GMIXTURES OF FERTILISERS COVERED INDIVIDUALLY BY DIFFERENT SUBCLASSES OF CLASS C05; MIXTURES OF ONE OR MORE FERTILISERS WITH MATERIALS NOT HAVING A SPECIFIC FERTILISING ACTIVITY, e.g. PESTICIDES, SOIL-CONDITIONERS, WETTING AGENTS; FERTILISERS CHARACTERISED BY THEIR FORM
    • C05G3/00Mixtures of one or more fertilisers with additives not having a specially fertilising activity

Abstract

The invention discloses a mushroom cultivation method, and the method comprises the steps of mixing 30-60% wood chip, 20-40% secondary chopped straw hydrolyzed by cellulose, 10%-15% secondary wood chip hydrolyzed by laccase, 5%-10% white sugar and 1%-5% gesso to get the cultivation matrix; performing mushroom inoculation in the cultivation matrix for growing to get the mushroom that has large petal and small straw and tastes crisp.

Description

A kind of cultivation method of mushroom
Technical field
The invention belongs to mushroom cultivation field.
Background technology
In mushroom cultivating process, the main two problems one considered is the level of growth of mushroom itself, another is the control of miscellaneous bacteria and insect pest in mushroom cultivating process, the control of these two aspects and balance are except relying on growth conditions, as outside the regulating and control of temperature, humidity etc., also depend on the selection of culture medium, not only if culture medium is beneficial to the growth of mushroom itself but also pole is beneficial to the breeding of miscellaneous bacteria and insect, then not favourable to the cultivation of mushroom.
Summary of the invention
The object of the present invention is to provide one can both meet mushroom well to grow, obtain a mushroom mushroom that large stem stalk is little, mouthfeel is crisp and refreshing, the method for cultivating mushroom that can effectively suppress varied bacteria growing to be bred again.
Technical scheme of the present invention is as follows: a kind of cultivation method of mushroom, comprises the following steps:
1) by mass content be 20 ~ 40% crushing straw carry out high-temperature sterilization, thereafter use dilute acetic acid solution regulate its pH value to be 4 ~ 6, add at 30 ~ 40 DEG C cellulase reaction 6 ~ 12h, obtain secondary crushing straw, all operations process is all aseptically carried out;
2) by mass content be 10 ~ 15% wood fragments bits carry out high-temperature sterilization, thereafter use dilute acetic acid solution regulate its pH value to be 4 ~ 6, at 30 ~ 40 DEG C, add laccase reactions 5 ~ 8h, obtain secondary wood fragments bits, all operations process is all aseptically carried out;
3) by mass content be 30 ~ 60% wood fragments bits carry out high-temperature sterilization with the white sugar of 5% ~ 10%, the land plaster of 1% ~ 5%, consider to be worth doing with described secondary wood fragments thereafter and described secondary crushing straw mixes mutually, namely obtain culture medium, mixed process is aseptically carried out;
4) culture medium is aseptically packed, and the water sprayed in bag through high-temperature sterilization, reach about 70% to water content of substrate, obtain bacterium bag, inoculate in bacterium bag, place under room temperature, shading, humidity are the environment of 60% ~ 70% after inoculation and within 5 ~ 10 days, carry out sending out bacterium;
5) grow under the bacterium bag after a bacterium being positioned over natural light irradiation and draughty open-air atmosphere, every other day to 1 ~ 2 moisture of sprinkling on bacterium bag, keep bacterium bag water content 60% ~ 70%, can gather after 30 ~ 60 days.
Its preferred embodiment is: described cellulase be selected from circumscribed 1,4 beta-glucanase, Endo-β-glucanase and beta-glucosidase one or more.
Cellulase herein also can select the complex class cellulase of commercial type.
Its another preferred embodiment is: described crushing straw is the crushed material of corn or wheat stalk.
Its another preferred embodiment is: described wood fragments bits are the limb crushed material of fruits trees.
The trees of growth fruit that refer to of said fruits trees herein, as pear tree, Japanese plum, peach, apple tree, apricot etc.
Usefulness of the present invention is:
1) Appropriate application waste straw, is beneficial to circulation and the regeneration of resource;
2) cultivate that the mushroom mushroom that obtains is piece large and stem stalk is little, mouthfeel is crisp and refreshing;
3) this cultivation method can suppress the growth of other miscellaneous bacteria and insect, obtains the mushroom of good quality.
Embodiment
Embodiment 1
1) by mass content be 15% apple tree wood fragments bits carry out high-temperature sterilization after add dilute acetic acid solution and regulate its pH value to be 6, at 35 DEG C, add thereafter quality is obtain secondary wood fragments bits after the laccase reactions 6h of wood fragments bits quality 10%;
2) by mass content be 20% wheat crushing straw carry out high-temperature sterilization after add dilute acetic acid solution and regulate its pH value to be 6, at 30 DEG C, add thereafter quality is obtain secondary crushing straw after the compound cellulose enzyme reaction 7h of crushing straw quality 8%;
3) by mass content be 50% apple tree wood fragments bits, mass content be 10% white sugar, mass content be 5% land plaster carry out high-temperature sterilization, thereafter consider to be worth doing with above-mentioned secondary wood fragments and fully mix with secondary crushing straw, namely obtain culture medium, this process is aseptically carried out;
4) culture medium is aseptically packed, and the water sprayed in bag through high-temperature sterilization, reach about 70% to water content of substrate, obtain bacterium bag, inoculate in bacterium bag, place under room temperature, shading, humidity are the environment of 60% ~ 70% after inoculation and within 5 days, carry out sending out bacterium;
5) grow under the bacterium bag after a bacterium being positioned over natural light irradiation and draughty open-air atmosphere, every other day to 1 moisture of sprinkling on bacterium bag, keep bacterium bag water content 60% ~ 70%, gather after 60 days.
Embodiment 2
1) by mass content be 15% pear tree wood fragments bits carry out high-temperature sterilization after add dilute acetic acid solution and regulate its pH value to be 5, at 40 DEG C, add thereafter quality is obtain secondary wood fragments bits after the laccase reactions 6h of wood fragments bits quality 6%;
2) by mass content be 35% corn crushing straw carry out high-temperature sterilization after add dilute acetic acid solution and regulate its pH value to be 4, at 30 DEG C, add thereafter quality is obtain secondary crushing straw after the circumscribed beta glucan enzyme reaction 8h of crushing straw quality 7%;
3) by mass content be 40% pear tree wood fragments bits, mass content be 5% white sugar, mass content be 5% land plaster carry out high-temperature sterilization, thereafter to consider to be worth doing with above-mentioned secondary wood fragments and secondary crushing straw fully mixes, namely obtain culture medium, said process aseptically carries out;
4) culture medium is aseptically packed, and the water sprayed in bag through high-temperature sterilization, reach about 70% to water content of substrate, obtain bacterium bag, inoculate in bacterium bag, place under room temperature, shading, humidity are the environment of 60% ~ 70% after inoculation and within 10 days, carry out sending out bacterium;
5) grow under the bacterium bag after a bacterium being positioned over natural light irradiation and draughty open-air atmosphere, every other day to 2 moisture of sprinkling on bacterium bag, keep bacterium bag water content 60% ~ 70%, namely gather after 40 days.

Claims (4)

1. a cultivation method for mushroom, is characterized in that: comprise the following steps:
1) by mass content be 20 ~ 40% crushing straw carry out high-temperature sterilization, thereafter use dilute acetic acid solution regulate its pH value to be 4 ~ 6, add at 30 ~ 40 DEG C cellulase reaction 6 ~ 12h, obtain secondary crushing straw, all operations process is all aseptically carried out;
2) by mass content be 10 ~ 15% wood fragments bits carry out high-temperature sterilization, thereafter use dilute acetic acid solution regulate its pH value to be 4 ~ 6, at 30 ~ 40 DEG C, add laccase reactions 5 ~ 8h, obtain secondary wood fragments bits, all operations process is all aseptically carried out;
3) by mass content be 30 ~ 60% wood fragments bits carry out high-temperature sterilization with the white sugar of 5% ~ 10%, the land plaster of 1% ~ 5%, consider to be worth doing with described secondary wood fragments thereafter and described secondary crushing straw mixes mutually, namely obtain culture medium, mixed process is aseptically carried out;
4) culture medium is aseptically packed, and the water sprayed in bag through high-temperature sterilization, reach about 70% to water content of substrate, obtain bacterium bag, inoculate in bacterium bag, place under room temperature, shading, humidity are the environment of 60% ~ 70% after inoculation and within 5 ~ 10 days, carry out sending out bacterium;
5) grow under the bacterium bag after a bacterium being positioned over natural light irradiation and draughty open-air atmosphere, every other day to 1 ~ 2 moisture of sprinkling on bacterium bag, keep bacterium bag water content 60% ~ 70%, can gather after 30 ~ 60 days.
2. the cultivation method of mushroom according to claim 1, is characterized in that: described cellulase be selected from circumscribed 1,4 beta-glucanase, Endo-β-glucanase and beta-glucosidase one or more.
3. the cultivation method of mushroom according to claim 1, is characterized in that: described crushing straw is the crushed material of corn or wheat stalk.
4. the cultivation method of mushroom according to claim 1, is characterized in that: described wood fragments bits are the limb crushed material of fruits trees.
CN201510461970.6A 2015-07-31 2015-07-31 Mushroom cultivation method Pending CN105027978A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201510461970.6A CN105027978A (en) 2015-07-31 2015-07-31 Mushroom cultivation method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201510461970.6A CN105027978A (en) 2015-07-31 2015-07-31 Mushroom cultivation method

Publications (1)

Publication Number Publication Date
CN105027978A true CN105027978A (en) 2015-11-11

Family

ID=54435472

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201510461970.6A Pending CN105027978A (en) 2015-07-31 2015-07-31 Mushroom cultivation method

Country Status (1)

Country Link
CN (1) CN105027978A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105474993A (en) * 2015-11-30 2016-04-13 全椒县香妃农业专业合作社 Snake butter planting method
CN107602209A (en) * 2017-08-29 2018-01-19 上海雪榕生物科技股份有限公司 A kind of culture medium accelerated compost and decomposed

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01199525A (en) * 1988-02-04 1989-08-10 Koji Miyao Medium for artificial cultivation of edible mushroom
AT395847B (en) * 1989-06-29 1993-03-25 Biochemie Gmbh Use of laccase and laccase/cellulase in the production of edibile mushrooms
US20070227063A1 (en) * 2006-03-30 2007-10-04 Board Of Trustees Of Michigan State University Process for conversion of mushroom lignocellulosic waste to useful byproducts
CN102329171A (en) * 2011-07-15 2012-01-25 安徽省庆元堂徽菊有限公司 Culture base material for cultivating shiitake by using chrysanthemum straws and method for cultivating shiitake by using culture base material
CN102550282A (en) * 2010-12-29 2012-07-11 武汉楚天绿色科技开发有限公司 Method for producing edible fungus with high yield by carrying out enzymolysis on crop straws with enzymatic microorganisms
CN103416177A (en) * 2012-05-24 2013-12-04 韦广荣 Kuding tea cutting propagation method
CN103435397A (en) * 2013-07-16 2013-12-11 龚涛 Practical pholiota nameko culture medium and preparation method thereof
CN104541972A (en) * 2014-12-31 2015-04-29 安徽丰原发酵技术工程研究有限公司 Method for cultivating edible fungi through agricultural straws
CN106455494A (en) * 2014-05-27 2017-02-22 诺维信公司 Methods for mushroom cultivation

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01199525A (en) * 1988-02-04 1989-08-10 Koji Miyao Medium for artificial cultivation of edible mushroom
AT395847B (en) * 1989-06-29 1993-03-25 Biochemie Gmbh Use of laccase and laccase/cellulase in the production of edibile mushrooms
US20070227063A1 (en) * 2006-03-30 2007-10-04 Board Of Trustees Of Michigan State University Process for conversion of mushroom lignocellulosic waste to useful byproducts
CN102550282A (en) * 2010-12-29 2012-07-11 武汉楚天绿色科技开发有限公司 Method for producing edible fungus with high yield by carrying out enzymolysis on crop straws with enzymatic microorganisms
CN102329171A (en) * 2011-07-15 2012-01-25 安徽省庆元堂徽菊有限公司 Culture base material for cultivating shiitake by using chrysanthemum straws and method for cultivating shiitake by using culture base material
CN103416177A (en) * 2012-05-24 2013-12-04 韦广荣 Kuding tea cutting propagation method
CN103435397A (en) * 2013-07-16 2013-12-11 龚涛 Practical pholiota nameko culture medium and preparation method thereof
CN106455494A (en) * 2014-05-27 2017-02-22 诺维信公司 Methods for mushroom cultivation
CN104541972A (en) * 2014-12-31 2015-04-29 安徽丰原发酵技术工程研究有限公司 Method for cultivating edible fungi through agricultural straws

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
周光龙: "漆酶制剂及其在食用菌生产中的应用", 《食用菌》 *
周光龙等: "漆酶与食用菌生产", 《中国生漆》 *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105474993A (en) * 2015-11-30 2016-04-13 全椒县香妃农业专业合作社 Snake butter planting method
CN107602209A (en) * 2017-08-29 2018-01-19 上海雪榕生物科技股份有限公司 A kind of culture medium accelerated compost and decomposed

Similar Documents

Publication Publication Date Title
CN105027981A (en) Black fungus cultivation method
CN106472228B (en) Planting method of selenium-rich camellia oleifera
CN105474956A (en) High-yield planting method for sugarcane
CN104987156B (en) A kind of method of binwang mushroom culture medium and cultivation binwang mushroom using mushroom bran
CN103613455A (en) Preparation method of seedling growing substrate for greenhouse planting
CN103250529B (en) Method of cultivating chrysanthemum by probiotic nutrients
CN105103877A (en) High-yield planting method for eggplants
CN103880521A (en) Flammulina velitupe residue culture medium material and method for culturing agaricus bisporus
CN104429624A (en) Oyster mushroom cultivation method
CN107079711B (en) Cultivation method of morchella
CN112243780B (en) Method for culturing citrus plant cell sap with concentration regulation and control and without girdling
CN102690145A (en) Multifunctional straw soilless nutrient medium and preparation process thereof
CN102487725A (en) Method for culturing hypsizygus marmoreus by using corn byproduct
CN107950315B (en) Interplanting method for pepper and tomato
CN103250638B (en) A kind of chrysanthemum tissue culture method
CN105027978A (en) Mushroom cultivation method
CN105027977A (en) Pleurotus eryngii cultivation method
CN105027980A (en) Hericium erinaceus cultivation method
CN103265363A (en) Preparation method of dwarfing large cherry potting matrix
CN105103841A (en) Method of cultivating seedlings in tomato substrate
CN105027979A (en) Coprinus comatus cultivation method
CN107646591A (en) A kind of bletilla striata direct sowing and seedling matrix and the method cultivated using the matrix
CN105130582A (en) Preparation method of black fungus culture matrix
CN105359838A (en) Planting method for ecological edible fungi
CN105027902A (en) Method for planting tomatoes in matrix

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication

Application publication date: 20151111

RJ01 Rejection of invention patent application after publication