CN104591899A - Production method for abalone mushroom cultivation material - Google Patents
Production method for abalone mushroom cultivation material Download PDFInfo
- Publication number
- CN104591899A CN104591899A CN201510044215.8A CN201510044215A CN104591899A CN 104591899 A CN104591899 A CN 104591899A CN 201510044215 A CN201510044215 A CN 201510044215A CN 104591899 A CN104591899 A CN 104591899A
- Authority
- CN
- China
- Prior art keywords
- turning
- cultivation material
- fermentation
- mushroom
- particle
- 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
Landscapes
- Mushroom Cultivation (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Abstract
The invention a production method for an abalone mushroom cultivation material, which is a technique applying lentinus edodes stem bases to abalone mushroom cultivation. Compared with the prior art, the production method has the advantages that: 1, lentinus edodes stem base leachate is a pure natural nutrient solution and contains a rich variety of bioactive substances, and a lentinus edodes stem base soaking material and a cultivation material are mixed and piled for fermentation so as to promote the reproduction of beneficial microbes, improve microbial communities in the materials and quicken the catalytic decomposition of the cultivation material; 2, the fermented cultivation material contains high-activity beneficial bacteria and active metabolites thereof, and has a promoting effect on the growth of abalone mushroom mycelia, which is embodied in vigorous growth of mycelia and high infectious microbe resistance; and 3, resources such as labor and coal are saved, environmental pollution is reduced, and the method conforms to a low-carbon environmental protection concept.
Description
Technical field
The making method of a kind of Pleurotus abalonus planting material of the present invention, is mushroom tang is applied to the technology in Pleurotus abalonus cultivation, belongs to fungus growing technique field.
Background technology
Pleurotus abalonus is the rare mushroom kind that a kind of high temperature season occurs.Pleurotus abalonus bacterial context is plump, stem is sturdy, tender and crisp good to eat, rich in proteins, amino acid, polysaccharide etc., wherein Pleurotus abalonus polysaccharide is the important biologically active substance of a class, be called as " biological response modifier (BRMs) " or immunostimulant in the world, there is higher edibleness and commercial value.
The traditional cultivating method of Pleurotus abalonus is cured material bag-cultured, and planting material carries out inoculation culture after high pressure or normal-pressure sterilization, and the miscellaneous bacteria now in material is killed, and therefore, when planting material sends out bacterium, mycelial growth is fast, and living contaminants is few.But along with the significantly rise of the price of labour power and fuel price, grog cultivation cost increases severely, and high-temperature sterilization also causes the loss of planting material nutritive substance, causes planting material transformation efficiency to reduce simultaneously.
Mushroom is famous and precious edible one of the medicinal fungus of holding concurrently in the world, and current China mushroom production accounts for 70% of world's mushroom ultimate production, has the equal mushroom culture in the province of more than 70% in China.Because champignon stems stiffness of foot in children, content of cellulose are higher, palatability is poor, and therefore, mushroom is being eaten raw or in the course of processing, the tang of mushroom can remove as tankage by the producer, causes the mushroom tang accounting for mushroom weight about 30% to become waste.
Summary of the invention
For the deficiencies in the prior art, the present invention adds the immersion of mushroom tang and expects to mix and stir to carry out banking up with planting material to ferment, and do not add sterilant, sterilant during windrow, the planting material after fermentation directly packs inoculation, bacterium bag living contaminants is few, and the Pleurotus abalonus quality of producing is good, output is high.
The technical solution adopted in the present invention is:
A making method for Pleurotus abalonus planting material, comprises batching, fermentation, turning, pack, inoculation, sends out bacterium, concrete operation step:
(1) prepare burden: bagasse 46-54%, wood chip 22-28%, wheat bran 18%, mushroom tang 3-4%, lime 2.4%, potassium primary phosphate 0.1%, calcium carbonate 1%, be all the quality of dry-matter, proportioning sum is 100%; Described bagasse powder is broken into the particle of particle diameter 4mm-5mm; Described wood chip is the deciduous tree weed tree sawdust of particle diameter 3mm-5mm; Described mushroom tang is the tankage in the Lentnus edodes course of processing, is ground into the particle of 2mm-3mm after drying;
(2) ferment: mushroom tang particle is added clear water by 20-30 weight ratio doubly, soak 18h-24h at normal temperatures, then leach liquor is admixed in bagasse, wood chip compound uniformly together with champignon stems slag, stockpile is become high 1.0m-1.2m, wide 2m-3m, the trapezoidal heap that length is not limit, the culture material often piled controls at dry weight 300kg-500kg, after carrying out heap, surrounding is patted, on heap, insert some vertical pores with the wooden stick of diameter 10cm-15cm again, at the bottom of straight through reactor, stomatal frequency is 1/m
3, finally cover straw mat by its spontaneous fermentation;
(3) turning: after material temperature reaches 60 DEG C, keep 24h, then carry out turning, and turning every day later once, during first time turning, add lime, calcium carbonate, potassium primary phosphate is added during second time turning, wheat bran is added, altogether turning 3-4 time, time remaining 5d-6d during last turning, when stopping fermentation, the water content of planting material is 63%-65%;
(4) pack, inoculate, send out bacterium: the planting material fermented is after heat radiation, load the polypropylene plastics pocket of 17cm × 35cm × 0.004cm, stamp and plant bacterium hole, during pack, bag two ends and plant in bacterium hole and put into bacterial classification, then cultivating bag is emitted in dark bacteria room, temperature controls at 20 DEG C-22 DEG C, humid control at 60%-75%, through the cultivation of 24-26d, mycelia covers with pocket, enters management of producing mushroom routinely.
Mushroom tang is applied to the method for Pleurotus abalonus cultivation by the present invention, and apart from outside explanation, other operation steps is all undertaken by this area routine techniques.
The present invention's advantage is compared with prior art:
1. mushroom tang leach liquor is full-natural nutritive liquid, containing glucide, amino acid, peptide class, nucleic acid and trace element, bio-hormone also containing abundant species, also the biologically active substance do not leached in a large number is had in champignon stems slag, add and expect to mix and stir to carry out banking up with culturing raw material to ferment with the immersion of mushroom tang, promote beneficial microorganism breeding, improve the microorganism species in material, accelerate the catalytic decomposition of planting material;
2. the planting material after fermentation has high reactivity probiotics and active metabolite thereof, has accelerating effect, show as prosperous, the anti-miscellaneous bacteria ability of mycelium growth vigor strong to the growth of Pleurotus abalonus mycelia;
3. save the resource such as manpower, coal, decrease environmental pollution, meet low-carbon environment-friendly theory.
Embodiment
Below in conjunction with embodiment, the invention will be further described, and what do not illustrate in detail in embodiment is all state of the art.
Embodiment 1: a kind of making method of Pleurotus abalonus planting material, comprises batching, fermentation, turning, pack, inoculation, sends out bacterium, concrete operation step:
1. prepare burden: bagasse 50%, wood chip 25%, wheat bran 18%, mushroom tang 3.5%, lime 2.4%, potassium primary phosphate 0.1%, calcium carbonate 1%, be all the quality of dry-matter, proportioning sum is 100%;
2. ferment: mushroom tang particle is added clear water by 20-30 weight ratio doubly, soak 18h-24h at normal temperatures, then leach liquor is admixed in bagasse, wood chip compound uniformly together with champignon stems slag, stockpile is become high 1.0m-1.2m, wide 2m-3m, the trapezoidal heap that length is not limit, the culture material often piled controls at dry weight 300kg-500kg, after carrying out heap, surrounding is patted, on heap, insert some vertical pores with the wooden stick of diameter 10cm-15cm again, at the bottom of straight through reactor, stomatal frequency is 1/m
3, finally cover straw mat by its spontaneous fermentation;
3. turning: after material temperature reaches 60 DEG C, keep 24h, then carry out turning, and turning every day later once, during first time turning, add lime, calcium carbonate, potassium primary phosphate is added during second time turning, wheat bran is added, altogether turning 3 times, time remaining 5d during third time turning, when stopping fermentation, the water content of planting material is 63%-65%;
4. pack, inoculate, send out bacterium: the planting material fermented is after heat radiation, load the polypropylene plastics pocket of 17cm × 35cm × 0.004cm, stamp and plant bacterium hole, during pack, bag two ends and plant in bacterium hole and put into bacterial classification, then cultivating bag is emitted in dark bacteria room, temperature controls at 20 DEG C-22 DEG C, humid control at 60%-75%, through the cultivation of 25d, mycelia covers with pocket, enters management of producing mushroom routinely.
Embodiment 2: a kind of making method of Pleurotus abalonus planting material, comprises batching, fermentation, turning, pack, inoculation, sends out bacterium, concrete operation step:
1. prepare burden: bagasse 50%, wood chip 25%, wheat bran 18%, mushroom tang 3.5%, lime 2.4%, potassium primary phosphate 0.1%, calcium carbonate 1%, be all the quality of dry-matter, proportioning sum is 100%;
2. ferment: mushroom tang particle is added clear water by 20-30 weight ratio doubly, soak 18h-24h at normal temperatures, then the leach liquor after removing slag is admixed in bagasse, wood chip compound uniformly, stockpile is become high 1.0m-1.2m, wide 2m-3m, the trapezoidal heap that length is not limit, the culture material often piled controls at dry weight 300kg-500kg, after carrying out heap, surrounding is patted, on heap, insert some vertical pores with the wooden stick of diameter 10cm-15cm again, at the bottom of straight through reactor, stomatal frequency is 1/m
3, finally cover straw mat by its spontaneous fermentation;
3. turning: after material temperature reaches 60 DEG C, keep 24h, then carry out turning, and turning every day later once, during first time turning, add lime, calcium carbonate, potassium primary phosphate is added during second time turning, wheat bran is added, altogether turning 3 times, time remaining 5d during third time turning, when stopping fermentation, the water content of planting material is 63%-65%;
4. pack, inoculate, send out bacterium: the planting material fermented is after heat radiation, load the polypropylene plastics pocket of 17cm × 35cm × 0.004cm, stamp and plant bacterium hole, during pack, bag two ends and plant in bacterium hole and put into bacterial classification, then cultivating bag is emitted in dark bacteria room, temperature controls at 20 DEG C-22 DEG C, humid control at 60%-75%, through the cultivation of 27d, mycelia covers with pocket, enters management of producing mushroom routinely.
Control group: Pleurotus abalonus grog is cultivated, concrete operation step:
1. prepare burden: bagasse 52%, wood chip 28%, wheat bran 18%, lime 0.9%, potassium primary phosphate 0.1%, calcium carbonate 1%, be all the quality of dry-matter, proportioning sum is 100%;
2. prewet: first bagasse, wood chip siccative are mixed thoroughly, then to prewet 2h with 0.9% lime aqueous solution;
3. spice: wheat bran, calcium carbonate, potassium primary phosphate are added in the compound of having prewetted, stir, makes the water content of planting material remain on 63%-65%;
4. pack, sterilizing: employing specification is the high-pressure polypropylene plastics bag charging of 17cm × 35cm × 0.005cm, carries out normal-pressure sterilization after pack, when kettle temperature reaches 100 DEG C, keeps 10h-12h;
5. cool, inoculate: naturally cool to less than 25 DEG C and access bacterial classification, then cultivating bag is emitted in dark bacteria room, temperature controls at 20 DEG C-22 DEG C, and humid control is at 60%-75%, and through the cultivation of 28d, mycelia covers with pocket, enters management of producing mushroom routinely.
Table one Pleurotus abalonus biological efficiency compares
As can be seen from Table I: the ferment effect utilizing mushroom tang leach liquor to add than single leach liquor together with the ferment effect that champignon stems slag adds is good, mycelial growth rate is fast, and bacterium bag pollution rate is low, and biological efficiency is high; Compared with control group, embodiment 1 all has obvious advantage in mycelial growth rate, anti-living contaminants and output.
Claims (1)
1. a making method for Pleurotus abalonus planting material, comprises batching, fermentation, turning, pack, inoculation, sends out bacterium, it is characterized in that:
(1) prepare burden: bagasse 46-54%, wood chip 22-28%, wheat bran 18%, mushroom tang 3-4%, lime 2.4%, potassium primary phosphate 0.1%, calcium carbonate 1%, be all the quality of dry-matter, proportioning sum is 100%; Described bagasse powder is broken into the particle of particle diameter 4mm-5mm; Described wood chip is the deciduous tree weed tree sawdust of particle diameter 3mm-5mm; Described mushroom tang is the tankage in the Lentnus edodes course of processing, is ground into the particle of 2mm-3mm after drying;
(2) ferment: mushroom tang particle is added clear water by 20-30 weight ratio doubly, soak 18h-24h at normal temperatures, then leach liquor is admixed in bagasse, wood chip compound uniformly together with champignon stems slag, stockpile is become high 1.0m-1.2m, wide 2m-3m, the trapezoidal heap that length is not limit, the culture material often piled controls at dry weight 300kg-500kg, after carrying out heap, surrounding is patted, on heap, insert some vertical pores with the wooden stick of diameter 10cm-15cm again, at the bottom of straight through reactor, stomatal frequency is 1/m
3, finally cover straw mat by its spontaneous fermentation;
(3) turning: after material temperature reaches 60 DEG C, keep 24h, then carry out turning, and turning every day later once, during first time turning, add lime, calcium carbonate, potassium primary phosphate is added during second time turning, wheat bran is added, altogether turning 3-4 time, time remaining 5d-6d during last turning, when stopping fermentation, the water content of planting material is 63%-65%;
(4) pack, inoculate, send out bacterium: the planting material fermented is after heat radiation, load the polypropylene plastics pocket of 17cm × 35cm × 0.004cm, stamp and plant bacterium hole, during pack, bag two ends and plant in bacterium hole and put into bacterial classification, then cultivating bag is emitted in dark bacteria room, temperature controls at 20 DEG C-22 DEG C, humid control at 60%-75%, through the cultivation of 24-26d, mycelia covers with pocket, enters management of producing mushroom routinely.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201510044215.8A CN104591899A (en) | 2015-01-29 | 2015-01-29 | Production method for abalone mushroom cultivation material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201510044215.8A CN104591899A (en) | 2015-01-29 | 2015-01-29 | Production method for abalone mushroom cultivation material |
Publications (1)
Publication Number | Publication Date |
---|---|
CN104591899A true CN104591899A (en) | 2015-05-06 |
Family
ID=53118011
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201510044215.8A Pending CN104591899A (en) | 2015-01-29 | 2015-01-29 | Production method for abalone mushroom cultivation material |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN104591899A (en) |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101570453A (en) * | 2008-05-04 | 2009-11-04 | 孙伟 | Preparation method of abalone mushroom culture material |
CN101597192A (en) * | 2008-06-05 | 2009-12-09 | 姚淑先 | Chinese herb culture medium, its preparation method and culturing edible fungi |
CN102060587A (en) * | 2009-11-18 | 2011-05-18 | 孙伟 | Abalone mushroom culture material |
CN103467203A (en) * | 2013-08-17 | 2013-12-25 | 邬金飞 | Compatibility and production method of abalone mushroom cultivation material |
-
2015
- 2015-01-29 CN CN201510044215.8A patent/CN104591899A/en active Pending
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101570453A (en) * | 2008-05-04 | 2009-11-04 | 孙伟 | Preparation method of abalone mushroom culture material |
CN101597192A (en) * | 2008-06-05 | 2009-12-09 | 姚淑先 | Chinese herb culture medium, its preparation method and culturing edible fungi |
CN102060587A (en) * | 2009-11-18 | 2011-05-18 | 孙伟 | Abalone mushroom culture material |
CN103467203A (en) * | 2013-08-17 | 2013-12-25 | 邬金飞 | Compatibility and production method of abalone mushroom cultivation material |
Non-Patent Citations (1)
Title |
---|
王谦,安雪,刘敏: "以香菇柄为主料固态发酵茯苓菌", 《食品科技》 * |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN104557318A (en) | Preparation method of mushroom cultivation material | |
CN104744143A (en) | Preparation method of lucid ganoderma cultivation material | |
CN104774084A (en) | Manufacturing method of hypsizygus marmoreus cultivation material | |
CN104744138A (en) | Preparation method of black fungus cultivation material | |
CN104774085A (en) | Manufacturing method of hypsizygus marmoreus cultivation material | |
CN104557325A (en) | Method for preparing grifola frondosa cultivation material | |
CN104744123A (en) | Preparation method of grifola frondosa cultivation material | |
CN104744142A (en) | Preparation method of lentinus edodes cultivation material | |
CN104744154A (en) | Method for manufacturing pleurotus geesteranus compost | |
CN104744141A (en) | Preparation method of lentinus edodes cultivation material | |
CN104725126A (en) | Preparation method of pleurotus nebrodensis cultivation material | |
CN104744137A (en) | Preparation method of lentinus edodes cultivation material | |
CN104725120A (en) | Preparation method of hericium erinaceus cultivation material | |
CN104672000A (en) | Manufacturing method of ganoderma lucidum cultivation material | |
CN104744150A (en) | Method for manufacturing pleurotus eryngii compost | |
CN104725115A (en) | Preparation method of flammulina velutipes cultivation material | |
CN104557321A (en) | Preparation method of agrocybe cylindracea cultivation material | |
CN104557319A (en) | Preparation method of black fungus cultivation material | |
CN104725113A (en) | Preparation method of agrocybe aegirit cultivation material | |
CN104557175A (en) | Production method of hericium erinaceus cultivation material | |
CN104591899A (en) | Production method for abalone mushroom cultivation material | |
CN104744147A (en) | Method for manufacturing abalone mushroom compost | |
CN104557320A (en) | Preparation method of pholiota nameko cultivation material | |
CN104744128A (en) | Preparation method of pleurotus nebrodensis cultivation material | |
CN104744148A (en) | Method for manufacturing pleurotus abalone compost |
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: 20150506 |
|
RJ01 | Rejection of invention patent application after publication |