CN106852255A - A kind of cultural method of pleurotus eryngii - Google Patents
A kind of cultural method of pleurotus eryngii Download PDFInfo
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- CN106852255A CN106852255A CN201611254896.1A CN201611254896A CN106852255A CN 106852255 A CN106852255 A CN 106852255A CN 201611254896 A CN201611254896 A CN 201611254896A CN 106852255 A CN106852255 A CN 106852255A
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- blake bottle
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01G—HORTICULTURE; CULTIVATION OF VEGETABLES, FLOWERS, RICE, FRUIT, VINES, HOPS OR SEAWEED; FORESTRY; WATERING
- A01G18/00—Cultivation of mushrooms
- A01G18/60—Cultivation rooms; Equipment therefor
- A01G18/64—Cultivation containers; Lids therefor
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Abstract
The invention provides a kind of cultural method of pleurotus eryngii, including carry out successively prepare culture base-material, culture base-material bottling, blake bottle sterilizing, blake bottle cooling, inoculation strain, cultural hypha and management of producing mushroom.The present invention is by improved blake bottle and coordinates improved high-temperature sterilization tank, by way of the gas in blake bottle is drawn twice, it is ensured that high-temperature steam can enter in blake bottle, culture base-material thoroughly be sterilized, and accelerate sterilizing process.Sterilization process substantially reduces sterilization time only more than 2 hour, shortens cultivation period.Enter the mode of Base top contact by blake bottle bottom in high-temperature steam, certain antigravity has been carried out to culture base-material and has been broken up, it is ensured that culture base-material will not be collapsed, it is ensured that gas permeability, be conducive to the uniform inoculation of strain, cell age uniformity is good, and fruiting is neat.The two-port of improved blake bottle can be inoculated with strain, i.e., in same cultivation period, fruiting amount increased one times, improve economic benefit.
Description
Technical field
The present invention relates to fungus growing technique field, more particularly to a kind of cultural method of pleurotus eryngii.
Background technology
Pleurotus eryngii also known as pleurotus eryngii, are south of europe, African the north, Central Asia's high mountain, grassland, the one of desert region
Plant large-scale agaric best in quality.Pleurotus eryngii nutrition very abundant, the protein content of dry product is up to 25%, containing 18 kinds of amino
Acid, and rich in polysaccharide and oligosaccharide.Pleurotus eryngii meat is plump, quality is tender and crisp, and particularly stem color and luster is snow-white, thick length, and tissue is caused
It is close, solid, it is one of mushroom class for having a very delicious taste.So, current China, Japan, South Korea, Thailand and TaiWan, China etc. it is national and
Area all has started to enter industrialized production.
The cultivation technique of pleurotus eryngii is one of important technology of industrialized production.In the cultivation of existing pleurotus eryngii,
Sterilization time is long, causes cultivation period long.And occur because sterilizing is not thorough, cause during culture mycelia and fruiting
There is pollution bag, reduce fruiting yield.And the high-temp steam sterilizing mode for generally using at present, cause culture base-material in sterilizing
During easily collapse, lump, cause gas permeability to be deteriorated, influence the uniform inoculation of follow-up strain, and then influence the uniform of fruiting
Property and uniformity etc., cause pleurotus eryngii quality uneven, influence economic benefit.
The content of the invention
For the drawbacks described above and problem of prior art, it is an object of the invention to provide a kind of cultural method of pleurotus eryngii,
Sterilizing and the cool time for solving culture base-material in the cultivation of existing pleurotus eryngii are long, cause cultivation period long；And culture base-material
Easily collapsed during high-temp steam sterilizing, the technical problem of poor air permeability.
In order to achieve the above object, the present invention provides following technical scheme：
A kind of cultural method of pleurotus eryngii, it is characterised in that comprise the following steps：
Step one, prepare pleurotus eryngii culture base-material；
Step 2, culture base-material bottling：(1) prepare blake bottle, the tubular bottle of the blake bottle including both ends open and
Two bottle stoppers of adaptation, a bottle stopper as blake bottle bottom plug, the bottom plug opens up at least one passage, described at least one
Covering connects Ventilate cloth on passage；Another bottle stopper is filled in as lid, and the lid opens up a passage, the passage beyond the Great Wall
Upper connection wireway；By on the Single port of bottom plug plug to tubular bottle, blake bottle is constituted；
(2) bottle：It is 4/5ths of blake bottle volume filling specification with admission space, culture base-material is filled in training
Support in bottle, then by lid plug plug to another port, obtain multiple blake bottles；
Step 3, blake bottle sterilizing：(1) high-temperature sterilization tank is prepared, the high-temperature sterilization tank increased multiple branch air entraining pipes
With total air entraining pipe, the inlet end of multiple branch air entraining pipes stretched into the high-temperature sterilization tank, and outlet side is connected with total air entraining pipe；It is described
Connecting valve and air-introduced machine on total air entraining pipe；There is the rack for placing blake bottle in high-temperature sterilization tank；
(2) multiple blake bottles are placed on rack, then by the inlet end of multiple branch air entraining pipes respectively with the lid of blake bottle
Wireway connection beyond the Great Wall；Then high-temperature sterilization tank is sealed, starts sterilizing；Sterilization process is as follows：It is 100 DEG C, pressure in temperature
It is the 50~60min that in the steam of 0.2~0.3MPa, sterilizes；Then the valve and air-introduced machine on total air entraining pipe are opened, by blake bottle
Interior gas is drawn, and the extraction time is 30~60s；It is then shut off valve and air-introduced machine；Then it is 120 DEG C in temperature, pressure is
In the steam of 0.5~0.8MPa, sterilize 60~80min；Then the valve and air-introduced machine on total air entraining pipe are opened again, by blake bottle
Interior gas is drawn, and the extraction time is 50~80s, completes sterilizing；
Step 4, blake bottle cooling：In gnotobasis, high-temperature sterilization tank is opened, the high-temperature steam in tank is discharged
Come, then open the valve and air-introduced machine on total air entraining pipe, the filtrated air of environment temperature is entered into training by the bottom plug of blake bottle
Support in bottle, drawn by the wireway of lid plug, culture base-material is cooled down, be reduced to room temperature；
Step 5, inoculation strain：The branch air entraining pipe of the wireway of the blake bottle after cooling and high-temperature sterilization tank is disconnected and is connected
Connect；Then the lid plug of blake bottle is removed, by aseptic guidelines by the culture base-material of pleurotus eryngii quel strains implantation culture bottle；
Step 6, cultural hypha：To be moved into culturing room through the postvaccinal blake bottle of step 5, control condition of culture is such as
Under：Half-light, temperature is 22~25 DEG C, and relative air humidity is 55%~60%；Culture 21~24 days, it is long in culture to blake bottle
Full mycelia；
Step 7, management of producing mushroom：To be moved into mushroom room through the blake bottle for covering with mycelia of step 6 culture, control fruiting
The primary condition in room is：20~22 DEG C, relative air humidity is 70%~80%；Then lowered the temperature 1 time at interval of 2~3 days, every time
2~3 DEG C are reduced, l0~12 DEG C are down to, stimulates fruit-body formation；After after fruiting flower bud long；Carry out dredging flower bud, dredge flower bud control 2~3
Piece；During fruiting, the illumination condition is controlled to be：Daily 12 noon to the diffusing scattering light that natural light is carried out during 3 points shines
Penetrate 3 hours；In evening, using daylight light irradiation 8~10 hours, the illumination requirement of fluorescent lamp was 800~900lux；Sooner or later it is each daily
Ventilation once, is once divulged information 5~10 minutes；
Treat that long to more than 4 centimetres of pleurotus eryngii fructification or canopy will be harvested usually；Complete the cultivation of pleurotus eryngii.
Further, in step 7, it is necessary to periodically be carried out disinfection to mushroom room, disinfection way is during fruiting：
Ozone generator is installed in the air inlet of mushroom room, periodically ozone generator is being opened, mushroom room is disappeared using ozone
Poison treatment.
Further, every 2~3 days, when operation is aerated to mushroom room, ozone generator is opened, logical
Ozone is carried in the air-flow of wind, completion is disinfected to mushroom room.
Further, in step 5, the lid plug and bottom plug of blake bottle are removed simultaneously, obtains the inoculable training of two-port
Bottle is supported, pleurotus eryngii quel strains are inoculated with two ports of the blake bottle；Correspondingly, in step 6, the blake bottle is moved into and is trained
Support interior and be suspended vacantly placement vertically；And in the management of producing mushroom of step 7, also ensure that blake bottle is suspended vacantly placement vertically,
And in thin flower bud operates, 2~3 are controlled in each port of blake bottle.
Further, in step 5, the vaccination ways of the inoculable blake bottle of two-port, on the ground of mushroom room
It is upper that multiple fluorescent lamps are installed, for the pleurotus eryngii for growing straight down provides illumination condition.
In the cultural method of pleurotus eryngii of the invention, by improved blake bottle and the improved high-temperature sterilization tank of cooperation, lead to
After the mode for twice drawing the gas in blake bottle, it is ensured that high-temperature steam can enter in blake bottle, culture base-material be carried out thorough
Bottom sterilizes, and accelerates sterilizing process.Sterilization process of the invention substantially reduces sterilization time only more than 2 hour, shortens cultivation
The training cycle.And enter the mode of Base top contact by blake bottle bottom in high-temperature steam, culture base-material is carried out certain anti-
Gravity is broken up, it is ensured that culture base-material will not be collapsed, it is ensured that gas permeability and sponginess.Into when strain is accessed, be conducive to bacterium
The uniform inoculation planted, cell age uniformity is good, and fruiting is neat, the pleurotus eryngii quality better of cultivation.
In improved blake bottle of the invention, two-port can be inoculated with strain, i.e., in same cultivation period, fruiting amount increases
Add one times, improve economic benefit.
Brief description of the drawings
In order to illustrate more clearly about the embodiment of the present invention or technical scheme of the prior art, below will be to embodiment or existing
The accompanying drawing to be used needed for having technology description is briefly described, it should be apparent that, drawings in the following description are only this
Some embodiments of invention, for those of ordinary skill in the art, without having to pay creative labor, may be used also
Other accompanying drawings are obtained with according to these accompanying drawings.
Fig. 1 is a kind of FB(flow block) of the cultural method of pleurotus eryngii of the invention；
Fig. 2 be a kind of pleurotus eryngii of the invention cultural method in the blake bottle that uses and high-temperature sterilization tank annexation
Structure structural representation；
Fig. 3 be a kind of pleurotus eryngii of the invention cultural method in the cross-sectional view of blake bottle that uses.
Specific embodiment
Below in conjunction with embodiments of the invention, technical scheme is clearly and completely described, it is clear that
Described embodiment is only a part of embodiment of the invention, rather than whole embodiments.Based on the implementation in the present invention
Example, the every other embodiment that those of ordinary skill in the art are obtained under the premise of creative work is not made is belonged to
The scope of protection of the invention.
According to Fig. 1 to Fig. 3, a kind of cultural method of pleurotus eryngii of the invention is illustrated, comprised the following steps：
Step one, prepare pleurotus eryngii culture base-material.Culture base-material uses existing conventional base-material, can voluntarily match somebody with somebody
Put, also can directly buy.
Step 2, culture base-material bottling：(1) present invention is improved the mechanism of blake bottle, as shown in Figures 2 and 3,
The blake bottle 10 includes the tubular bottle 11 of both ends open and two bottle stoppers of adaptation.One bottle stopper as blake bottle bottom plug
12, the bottom plug 12 opens up at least one passage 121, and covering connects Ventilate cloth 15 at least one passage 121,
It is preferred that opening up multiple passages 121, the effect of Ventilate cloth 15 is to prevent from the culture base-material in bottle from dissipating to spill.Another bottle stopper
As lid plug 13, a passage 131 is opened up on the lid plug 13, wireway 14 is connected on the passage 131；By bottom plug 12 fill in
On the Single port of tubular bottle 11, blake bottle is constituted.
(2) bottle：It is 4/5ths of the volume of blake bottle 10 filling specification with admission space, culture base-material is filled in
In blake bottle 10, then by plug to the another port of lid plug 13, multiple blake bottles are obtained.
Step 3, blake bottle 10 are sterilized：(1) high-temperature sterilization tank 20 is prepared, the high-temperature sterilization tank 20 increased multiple branch
Air entraining pipe 31 and total air entraining pipe 32, the inlet end of multiple branch air entraining pipes 31 are stretched into the high-temperature sterilization tank 20, outlet side with it is total
Air entraining pipe 32 is connected, and multiple branch air entraining pipes 31 can use multiple-pass joint with the connection of total air entraining pipe 32.Total air entraining pipe 32
Upper connecting valve 33 and air-introduced machine 34.There is the rack 21 for placing blake bottle 10, rack 21 is using stainless in high-temperature sterilization tank 20
The resistant to elevated temperatures waffle slab of steel mesh or plastic material.
(2) multiple blake bottles 10 are placed on rack 21, then by the inlet end of multiple branch air entraining pipes 31 respectively with culture
Wireway 14 on the lid plug 13 of bottle 10 is connected, and can ensure the reliability of connection by using pagoda joint 22.Then seal
High-temperature sterilization tank 20, starts sterilizing；Sterilization process is as follows：It is 100 DEG C in temperature, during pressure is the steam of 0.2~0.3MPa, goes out
50~60min of bacterium；Then the valve 33 and air-introduced machine 34 on total air entraining pipe 32 are opened, the gas in blake bottle 10 is drawn, drawn
Go out the time for 30~60s；It is then shut off valve 33 and air-introduced machine 34；Then it is 120 DEG C in temperature, pressure is 0.5~0.8MPa
Steam in, sterilize 60~80min；Then the valve 33 and air-introduced machine 34 on total air entraining pipe 32 are opened again, by blake bottle 10
Gas draw, the extractions time be 50~80s, complete sterilize.
In the sterilization process of step 3, by improved blake bottle 10 and the improved high-temperature sterilization tank 20 of cooperation, first
When secondary Open valve 33 and air-introduced machine 34, the cold air that cannot be excluded in blake bottle 10 can will be caused due to steam pressure
(for high-temperature steam) discharge, high-temperature steam is introduced inside culture base-material, accelerates sterilizing process.Second opening valve
Door 33 and air-introduced machine 34, accelerate sterilizing speed again, it is ensured that the sterilizing of culture base-material inside is thorough, prevents going out for subsequent contamination bottle
It is existing.Sterilization process of the invention substantially reduces sterilization time only more than 2 hour, shortens cultivation period.
Step 4, blake bottle 10 are cooled down：In gnotobasis, high-temperature sterilization tank 20 is opened, the high-temperature steam in tank is released
Release, the valve 33 and air-introduced machine 34 on total air entraining pipe 32 are then opened, by the filtrated air of environment temperature by blake bottle 10
Bottom plug 12 enter blake bottle 10 in, by lid plug 13 wireway 14 draw, culture base-material is cooled down, be reduced to room
Temperature.Cold air is continued to flow through inside culture base-material, accelerates shedding for internal heat, accelerates cooling procedure, shortens cooling drop
The warm time, and then shorten cultivation period.
Step 5, inoculation strain：By the wireway 14 of the blake bottle 10 after cooling and the branch air entraining pipe of high-temperature sterilization tank 20
31 disconnect.Then the lid plug 13 of blake bottle 10 is removed, pleurotus eryngii quel strains is implanted into blake bottle 10 by aseptic guidelines
Culture base-material in.
Step 6, cultural hypha：To be moved into culturing room through the postvaccinal blake bottle 10 of step 5, control condition of culture is such as
Under：Half-light, temperature is 22~25 DEG C, and relative air humidity is 55%~60%；Culture 21~24 days, it is long in culture to blake bottle
Full mycelia.Preferably, control condition of culture is as follows：Half-light, temperature is 22~23 DEG C, and relative air humidity is 58%~60%；
Culture 21~22 days, mycelia is covered with culture to blake bottle.
Step 7, management of producing mushroom：To be moved into mushroom room through the blake bottle 10 for covering with mycelia of step 6 culture, controlled out
The primary condition of mushroom house is：20~22 DEG C, relative air humidity is 70%~80%；Then lowered the temperature 1 time at interval of 2~3 days, often
It is secondary to reduce by 2~3 DEG C, l0~12 DEG C are down to, stimulate fruit-body formation；After after fruiting flower bud long；Carry out dredging flower bud, dredge flower bud control 2~3
Piece；During fruiting, the illumination condition is controlled to be：Daily 12 noon to the diffusing scattering light that natural light is carried out during 3 points shines
Penetrate 3 hours；In evening, using daylight light irradiation 8~10 hours, the illumination requirement of fluorescent lamp was 800~900lux；Sooner or later it is each daily
Ventilation once, is once divulged information 5~10 minutes.In order to realize carrying out the diffusing scattering light irradiation of natural light, by the roof of mushroom room
It is upper that the ridge-roof type skylight of outwardly convex is installed, and shutter is installed on window.
Treat that long to more than 4 centimetres of pleurotus eryngii fructification or canopy will be harvested usually；Complete the cultivation of pleurotus eryngii.
In the cultural method of pleurotus eryngii of the invention, it is necessary to periodically be carried out to mushroom room during the fruiting of step 7
Sterilize, disinfection way is：Ozone generator is installed in the air inlet of mushroom room, periodically ozone generator is being opened, using smelly
Oxygen carries out disinfection treatment to mushroom room.Preferably, every 2~3 days, (e.g., carried out when operation is aerated to mushroom room
When night operates), ozone generator is opened, ozone is carried in the air-flow of ventilation, completion is disinfected to mushroom room.This kind
Disinfection way, can control the concentration of ozone in air, and will not in mushroom room prolonged stay, it is smelly with the circulation of air-flow
Oxygen is carried out mushroom room in the lump, while completing sterilization, also ensure that the personal safety into the administrative staff of mushroom room.
In the cultural method of pleurotus eryngii of the invention, in order to ensure sterilizing quickly and completely, cooling velocity is fast, gives and changes
The blake bottle and the structure of the high-temperature sterilization tank for coordinating for entering.For so improved blake bottle, the strain of step 5 of the invention
In seeded process, the lid plug and bottom plug of blake bottle are removed simultaneously, the inoculable blake bottle of two-port is obtained, in the blake bottle
Two ports in be inoculated with pleurotus eryngii quel strains, increased inoculum concentration, i.e., in same cultivation period, fruiting amount increased one
Times, improve economic benefit.Then, it is necessary to blake bottle to be suspended vacantly placement vertically during the cultural hypha of step 6.
And during the management of producing mushroom of step 7, also ensure that blake bottle is suspended vacantly placement vertically, and in thin flower bud operates, culture
2~3 are controlled in each port of bottle.In culturing room and mushroom room, it is ensured that blake bottle is suspended vacantly the reality of placement vertically
Existing mode is a lot, e.g., on the basis of the support in existing culturing room and mushroom room, transform rest stand as corresponding multiple ring
Shape snap ring, blake bottle is put into the circumferential clasp fixed.
During this kind of two-port is inoculated with the fruiting of the blake bottle of strain, in order to ensure that thalline receives enough light
According to, in the present invention, the multiple fluorescent lamps of installation on the ground of mushroom room, for the pleurotus eryngii for growing straight down provides illumination bar
Part.The illumination requirement of the fluorescent lamp on control ground is with irradiation time with consistent in step 7.
The above, specific embodiment only of the invention, but protection scope of the present invention is not limited thereto, and it is any
Those familiar with the art the invention discloses technical scope in, change or replacement can be readily occurred in, should all contain
Cover within protection scope of the present invention.Therefore, protection scope of the present invention described should be defined by scope of the claims.
Claims (5)
1. a kind of cultural method of pleurotus eryngii, it is characterised in that comprise the following steps：
Step one, prepare pleurotus eryngii culture base-material；
Step 2, culture base-material bottling：(1) blake bottle is prepared, the blake bottle includes the tubular bottle of both ends open and two
The bottle stopper of adaptation, a bottle stopper as blake bottle bottom plug, the bottom plug opens up at least one passage, at least one ventilation
Kong Shangjun covering connection Ventilate cloths；Another bottle stopper is filled in as lid, and the lid opens up a passage, connects on the passage beyond the Great Wall
Connect wireway；By on the Single port of bottom plug plug to tubular bottle, blake bottle is constituted；
(2) bottle：It is 4/5ths of blake bottle volume filling specification with admission space, culture base-material is filled in blake bottle
It is interior, then by lid plug plug to another port, obtain multiple blake bottles；
Step 3, blake bottle sterilizing：(1) high-temperature sterilization tank is prepared, the high-temperature sterilization tank increased multiple branch air entraining pipes and total
Air entraining pipe, the inlet end of multiple branch air entraining pipes is stretched into the high-temperature sterilization tank, and outlet side is connected with total air entraining pipe；It is described always to draw
Connecting valve and air-introduced machine on tracheae；There is the rack for placing blake bottle in high-temperature sterilization tank；
(2) multiple blake bottles are placed on rack, then by the inlet end of multiple branch air entraining pipes respectively with the lid of blake bottle beyond the Great Wall
Wireway connection；Then high-temperature sterilization tank is sealed, starts sterilizing；Sterilization process is as follows：It it is 100 DEG C in temperature, pressure is 0.2
In the steam of~0.3MPa, sterilize 50~60min；Then the valve and air-introduced machine on total air entraining pipe are opened, by blake bottle
Gas is drawn, and the extraction time is 30~60s；It is then shut off valve and air-introduced machine；Then temperature be 120 DEG C, pressure be 0.5~
In the steam of 0.8MPa, sterilize 60~80min；Then the valve and air-introduced machine on total air entraining pipe are opened again, by blake bottle
Gas is drawn, and the extraction time is 50~80s, completes sterilizing；
Step 4, blake bottle cooling：In gnotobasis, high-temperature sterilization tank is opened, the high-temperature steam in tank is discharged, so
The valve and air-introduced machine on total air entraining pipe are opened afterwards, and the filtrated air of environment temperature is entered into blake bottle by the bottom plug of blake bottle
It is interior, drawn by the wireway of lid plug, culture base-material is cooled down, it is reduced to room temperature；
Step 5, inoculation strain：The wireway of the blake bottle after cooling is disconnected with the branch air entraining pipe of high-temperature sterilization tank；So
The lid plug of blake bottle is removed afterwards, by aseptic guidelines by the culture base-material of pleurotus eryngii quel strains implantation culture bottle；
Step 6, cultural hypha：To be moved into culturing room through the postvaccinal blake bottle of step 5, control condition of culture is as follows：Secretly
Light, temperature is 22~25 DEG C, and relative air humidity is 55%~60%；Culture 21~24 days, bacterium is covered with culture to blake bottle
Silk；
Step 7, management of producing mushroom：To be moved into mushroom room through the blake bottle for covering with mycelia of step 6 culture, control mushroom room
Primary condition is：20~22 DEG C, relative air humidity is 70%~80%；Then lowered the temperature 1 time at interval of 2~3 days, reduce every time
2~3 DEG C, l0~12 DEG C are down to, stimulate fruit-body formation；After after fruiting flower bud long；Carry out dredging flower bud, dredge flower bud and control 2~3；
During fruiting, the illumination condition is controlled to be：Daily 12 noon is small to the diffusing scattering light irradiation 3 that natural light is carried out during 3 points
When；In evening, using daylight light irradiation 8~10 hours, the illumination requirement of fluorescent lamp was 800~900lux；Sooner or later each ventilation daily
Once, once divulge information 5~10 minutes；
Treat that long to more than 4 centimetres of pleurotus eryngii fructification or canopy will be harvested usually；Complete the cultivation of pleurotus eryngii.
2. the cultural method of a kind of pleurotus eryngii according to claim 1, it is characterised in that in step 7, in fruiting mistake
, it is necessary to periodically be carried out disinfection to mushroom room, disinfection way is in journey：Ozone generator is installed in the air inlet of mushroom room, it is fixed
Phase is opening ozone generator, mushroom room is carried out disinfection treatment using ozone.
3. the cultural method of a kind of pleurotus eryngii according to claim 3, it is characterised in that every 2~3 days, to fruiting
When room is aerated operation, ozone generator is opened, ozone is carried in the air-flow of ventilation, complete the sterilization to mushroom room
Treatment.
4. the cultural method of a kind of pleurotus eryngii according to claim 1 and 2, it is characterised in that in step 5, by blake bottle
Lid plug and bottom plug simultaneously remove, obtain the inoculable blake bottle of two-port, be inoculated with two ports of the blake bottle
Pleurotus eryngii quel strains；Correspondingly, in step 6, the blake bottle is moved into culturing room and placement is suspended vacantly vertically；And in step
In seven management of producing mushroom, also ensure that blake bottle is suspended vacantly placement vertically, and in thin flower bud operates, in each port of blake bottle
Control 2~3.
5. the cultural method of a kind of pleurotus eryngii according to claim 4, it is characterised in that in step 5, two-port
The vaccination ways of inoculable blake bottle, install multiple fluorescent lamps on the ground of mushroom room, are the apricot for growing straight down
Abalone mushroom provides illumination condition.
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Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN107306670A (en) * | 2017-08-16 | 2017-11-03 | 金寨县聚农种植专业合作社 | A kind of cultural method of pleurotus eryngii |
| CN107726421A (en) * | 2017-11-07 | 2018-02-23 | 江苏久禾生物科技发展有限公司 | A kind of steam-type mushroom room heating system and its application process |
| CN109161483A (en) * | 2018-09-14 | 2019-01-08 | 江苏品品鲜生物科技有限公司 | A kind of pleurotus eryngii quel strains rejuvenation screening technique |
| IT201900024123A1 (en) | 2019-12-16 | 2021-06-16 | Giovanni Pacioni | PROCEDURE FOR THE SYNCHRONOUS AND PROGRAMMED PRODUCTION OF PLEUROTUS ERYNGII |
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| CN107726421A (en) * | 2017-11-07 | 2018-02-23 | 江苏久禾生物科技发展有限公司 | A kind of steam-type mushroom room heating system and its application process |
| CN107726421B (en) * | 2017-11-07 | 2023-07-04 | 江苏久禾生物科技发展有限公司 | Steam type fruiting room heat supply system and application method thereof |
| CN109161483A (en) * | 2018-09-14 | 2019-01-08 | 江苏品品鲜生物科技有限公司 | A kind of pleurotus eryngii quel strains rejuvenation screening technique |
| IT201900024123A1 (en) | 2019-12-16 | 2021-06-16 | Giovanni Pacioni | PROCEDURE FOR THE SYNCHRONOUS AND PROGRAMMED PRODUCTION OF PLEUROTUS ERYNGII |
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