CN106258495A - A kind of technique utilizing dreg to produce monolithic Pleurotus ulmarius( Bullex Franch) Quel - Google Patents
A kind of technique utilizing dreg to produce monolithic Pleurotus ulmarius( Bullex Franch) Quel Download PDFInfo
- Publication number
- CN106258495A CN106258495A CN201610703429.6A CN201610703429A CN106258495A CN 106258495 A CN106258495 A CN 106258495A CN 201610703429 A CN201610703429 A CN 201610703429A CN 106258495 A CN106258495 A CN 106258495A
- Authority
- CN
- China
- Prior art keywords
- dreg
- quel
- monolithic
- pleurotus ulmarius
- bullex franch
- 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C05—FERTILISERS; MANUFACTURE THEREOF
- C05G—MIXTURES 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
- C05G3/00—Mixtures of one or more fertilisers with additives not having a specially fertilising activity
-
- C—CHEMISTRY; METALLURGY
- C05—FERTILISERS; MANUFACTURE THEREOF
- C05B—PHOSPHATIC FERTILISERS
- C05B1/00—Superphosphates, i.e. fertilisers produced by reacting rock or bone phosphates with sulfuric or phosphoric acid in such amounts and concentrations as to yield solid products directly
- C05B1/02—Superphosphates
-
- C—CHEMISTRY; METALLURGY
- C05—FERTILISERS; MANUFACTURE THEREOF
- C05G—MIXTURES 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
- C05G3/00—Mixtures of one or more fertilisers with additives not having a specially fertilising activity
- C05G3/60—Biocides or preservatives, e.g. disinfectants, pesticides or herbicides; Pest repellants or attractants
Abstract
The present invention relates to a kind of technique utilizing dreg to produce monolithic Pleurotus ulmarius( Bullex Franch) Quel, with antibiotic bacterium dregs, straw, Pedicellus et Pericarpium Trapae rattan, Pericarpium Musae, purple sweet potato powder and winter folium mori as compost, antibiotic bacterium dregs, straw etc., rich in nitrogen, phosphorus, potassium, calcium, magnesium and organic matter etc., crude fiber content is up to 30 40%;Antibiotic bacterium dregs after pretreatment, inactivates degeneration, is completely removed titer of antibodies, make full use of its high protein, high-octane while, also there is the most disease-resistant and insect resistace, and solve a medicine residual problem difficult problem to human injury, it is achieved that the recycling treatment of antibiotic bacterium dregs.Culture material formula is reasonable, and balanced in nutrition, pest and disease damage incidence rate is low, be conducive to the growth of monolithic Pleurotus ulmarius( Bullex Franch) Quel, the monolithic Pleurotus ulmarius( Bullex Franch) Quel piece cultivated is big, and color is red and uniform and stable, and monolithic is many, monolithic sheet is grown thickly, meat is plump, and fresh goods diameter is all at more than 15cm, dry product diameter more than 8 centimetres, without material root, superior product quality, delicious in taste.
Description
Technical field
The invention belongs to fungus growing technique field, be specifically related to a kind of work utilizing dreg to produce powder monolithic Pleurotus ulmarius( Bullex Franch) Quel
Skill.
Background technology
Pleurotus ulmarius( Bullex Franch) Quel like Auricularia also known as Pleurotus citrinopileatus Sing (Pleurotus ulmarius (Bull. Ex Fr.) Quel.), form, in pink brown, high resilience, delicious flavour, has drug effect concurrently, enjoys
The laudatory title of " king of Forest food ".Pleurotus ulmarius( Bullex Franch) Quel sporophore contains rich in protein, and thick protein (including water soluble protein) accounts for
23.65%, crude fat accounts for 0.34%, and carbohydrate accounts for 65.71%, and coarse ash accounts for 10.3%(and wherein contains calcium, phosphorus, ferrum).Albumen
Matter contains the whole required ammonia that must absorb that 21 kinds of aminoacid that abundant species is complete, particularly human body can not synthesize from the external world
Base acid, accounts for the 42.9% of total amino acids content.Containing various saccharides in Pleurotus ulmarius( Bullex Franch) Quel sporophore carbohydrate, and containing some
Vitamin, such as vitamin B, vitamin B z, vitamin B3, vitamin W vitamin E, these vitamin have regulation human body
Metabolism, coarse ash Mineral Elements is higher with content of calcium and magnesium, the most a certain amount of zinc.In a word, Pleurotus ulmarius( Bullex Franch) Quel nutrition is rich
Richness, often this bacterium edible can health invigorating, can use as health food.
Pleurotus ulmarius( Bullex Franch) Quel sporophore divides monolithic raw or storied 2 kinds of imbricate, and monolithic Pleurotus ulmarius( Bullex Franch) Quel quality is higher, the most more by joyous
Meet.In recent years, having tame Pleurotus ulmarius( Bullex Franch) Quel, color and luster, shape are preferable, but nutritive value to be worth wilder Pleurotus ulmarius( Bullex Franch) Quel poor.And Pleurotus ulmarius( Bullex Franch) Quel training
During educating environmentally sensitive, if working condition control improper, sporophore can growth arrest, deformity the most withered, and culture medium
When arranging in pairs or groups unreasonable, Pleurotus ulmarius( Bullex Franch) Quel product colour, profile, yield all effected, may finally be difficult to obtain the thick big monolithic elm of sheet
Ear.
Dreg typically refers to the compost after culturing edible fungus, remains substantial amounts of mycelium rich in aminoacid and fiber
Element, Hydrocarbon and trace element, can be as the good fertilizer of vegetable growing.Antibiotic bacterium dregs is due to containing residual medicine
Thing, and antibiosis dreg is wide in variety, mass discrepancy is relatively big, and particularly drug residue, pH is too low, is unsuitable for being directly used in crops etc.
Production, be often taken as offal treatment to fall, the most both wasted resource, caused again environmental pollution. and burn or landfill
Processing cost is the highest, and enterprise's pressure is big.Actually containing the rich in protein (Organic substance such as albumen in butt in antibiotic bacterium dregs
Content is up to more than 90%), if recycling after mycelia waste residue is inactivated, it is achieved recycling treatment, will be that antibiotic bacterium dregs is practical
Feasible processing method.
Summary of the invention
The present invention is directed to above-mentioned deficiency present in prior art, have developed a kind of work utilizing dreg to produce monolithic Pleurotus ulmarius( Bullex Franch) Quel
Skill, cultivates the Pleurotus ulmarius( Bullex Franch) Quel obtained, and monolithic is many, and Pleurotus ulmarius( Bullex Franch) Quel piece is big, and color is red, and monolithic sheet is grown thickly.
Technical solution of the present invention is as follows:
A kind of technique utilizing dreg to produce monolithic Pleurotus ulmarius( Bullex Franch) Quel, comprises the following steps:
1) take the antibiotic bacterium dregs of 80-120 weight portion, be heated to 50-60 DEG C of insulation 2h, be down to room temperature, atomizing spray same volume
The hydrogen peroxide that concentration is 95%, stir, seal compacting and stand 1h, regulation water content is injection of ozone stirring after 60%
30min, makes ozone be sufficiently mixed with antibiotic bacterium dregs, and whipping process ozone concentration keeps 1.5g/m3, ventilates and places 10-15 days
After, regulation water content, to 40%, adds proteolytic enzyme, and addition concentration is 0.8-1.0g/m3, and 28-32 DEG C ferments 7 days, again add
Heat is to 50-60 DEG C of insulation 2h, and sterilize dry for standby;
2) straw 100-120 weight portion, Pedicellus et Pericarpium Trapae rattan 60-80 weight portion, Pericarpium Musae 20-30 weight portion are taken respectively, by straw, Pedicellus et Pericarpium Trapae
Rattan and Pericarpium Musae are smashed by pulverizer, and length, at 1-3cm, mixes to obtain compound, layering spray account for compound weight 1% mistake
Calcium phosphate aqueous solution, compresses layer by layer, seals, and 37 DEG C of anaerobic fermentations 30-40 days, when PH is reduced to 5.5-6.0, surface sprinkling accounts for mixed
Close the yeast fermentation liquor of material weight 5%, seal, 35-37 DEG C of anaerobic fermentation 15-20 days, the steam normal-pressure sterilization of 100 DEG C, dries
Dry, standby;
3) take purple sweet potato powder 20-30 weight portion and winter folium mori 60-80 weight portion, become thoroughly decomposed respectively, then with above-mentioned steps 1), 2) material
Mixing, the stirring that adds water reaches 60-65% to water content, obtains fermentation culture material, loads in culture bottle, after tying, pasteurize;
4) material temperature 20-25 DEG C is controlled, inoculation, postvaccinal cultivation, ventilation, cultivate 5-10 days in 26-29 DEG C of lucifuge, mycelia
After covering with culture bottle abundant maturation, keep relative air humidity more than 90%, temperature 15-18 DEG C, illuminance 300-450 Le gram
This, when diameter 15cm, gather.
In step 1), described antibiotic bacterium dregs preferred beta-lactam dreg, aminoglycosides dreg, Tetracyclines bacterium
One or more mixing in slag, Macrolide dreg, quinolones dreg etc.;
In step 1), described proteolytic enzyme is serine protease, aspartic protease, thiol protease, metal egg
One or more mixing in white enzyme.
Step 2) in, described calcium superphosphate aqueous solution mass concentration is 2%;
Step 2) in, in described yeast fermentation liquor, yeast mass concentration is 0.25-0.45%.
In step 3), described fermentation culture material organoleptic indicator is color dark-brown, gently draws with hands the most disconnected, has a large amount of white
Actinomycetes, without ammonia taste, have bread sweet taste, PH6-7.
In step 4), lucifuge incubation, compost relative humidity controls at 60-65%;Relative humidity of atomsphere is at 85-
95%。
Monolithic Pleurotus ulmarius( Bullex Franch) Quel culture process of the present invention, compost composition collocation rationally, assembles carbon source, fibre for Pleurotus ulmarius( Bullex Franch) Quel growth characteristic
Nutrition, the Pleurotus ulmarius( Bullex Franch) Quel profile cultivated and quality better and the color even such as dimension element and hemicellulose are stable.Employing antibiotic bacterium dregs,
Straws etc. are primary raw material, rich in nitrogen, phosphorus, potassium, calcium, magnesium and organic matter etc., are that one has multiduty reproducible biology
Resource, crude fiber content is up to 30-40%;Antibiotic bacterium dregs after pretreatment, inactivates degeneration, is completely removed titer of antibodies,
Make full use of its high protein, high-octane while, also there is the most disease-resistant and insect resistace, and solve the residual problem of medicine to human body
A difficult problem for injury, it is achieved that the recycling treatment of antibiotic bacterium dregs.
The present invention utilizes dreg to produce the technique of monolithic Pleurotus ulmarius( Bullex Franch) Quel, and it has the beneficial effect that culture material formula is reasonable, and nutrition is equal
Weighing apparatus, pest and disease damage incidence rate is low, and compost has good retentiveness and breathability, the beneficially growth of monolithic Pleurotus ulmarius( Bullex Franch) Quel, sends out bacterium fast,
Pest and disease damage is few, can shorten the production cycle, and yield is high and stable, and economic benefit is obvious, is suitable for factorial praluction, the monolithic cultivated
Pleurotus ulmarius( Bullex Franch) Quel piece is big, and color is red and uniform and stable, and monolithic is many, and monolithic sheet is grown thickly, and meat is plump, and fresh goods diameter is all at more than 15cm, dry
Product diameter more than 8 centimetres, without material root, superior product quality, delicious in taste.
Specific implementation method
In order to be better understood from the present invention, further illustrate below in conjunction with specific embodiment.
Embodiment 1
A kind of technique utilizing dreg to produce monolithic Pleurotus ulmarius( Bullex Franch) Quel, comprises the following steps:
1) take 100 weight portions antibiotic mixing dreg (beta-lactam dreg, aminoglycosides dreg, Tetracyclines dreg,
Macrolide dreg, quinolones dreg), it is heated to 50-60 DEG C of insulation 2h, is down to room temperature, atomizing spray same volume dense
Degree is the hydrogen peroxide of 95%, stirs, and seals compacting and stands 1h, and regulation water content is injection of ozone stir 30min after 60%,
Making ozone be sufficiently mixed with antibiotic bacterium dregs, whipping process ozone concentration keeps 1.5g/m3, ventilates after placing 12 days, and regulation contains
The water yield, to 40%, adds proteolytic enzyme (serine protease of mass ratio 1:1:1:1, aspartic protease, sulfydryl albumen
Enzyme, metalloproteases mix), addition concentration is 1.0g/m3, and 28-32 DEG C ferments 7 days, is again heated to 50-60 DEG C of insulation 2h,
Sterilization dry for standby;
2) straw 110 weight portion, Pedicellus et Pericarpium Trapae rattan 70 weight portion, Pericarpium Musae 25 weight portion are taken respectively, by straw, Pedicellus et Pericarpium Trapae rattan and Pericarpium Musae
Being smashed by pulverizer, length, at 1-3cm, mixes to obtain compound, layering spray account for compound weight 1% calcium superphosphate water-soluble
Liquid (mass concentration is 2%), compresses layer by layer, seals, 37 DEG C of anaerobic fermentations 30-40 days, when PH is reduced to 5.5-6.0, and surface sprinkling
Account for the yeast fermentation liquor (yeast mass concentration is 0.3%) of compound weight 5%, seal, 35-37 DEG C of anaerobic fermentation 18 days,
The steam normal-pressure sterilization of 100 DEG C, dries, standby;
3) take purple sweet potato powder 30 weight portion and winter folium mori 70 weight portion, become thoroughly decomposed respectively, then with above-mentioned steps 1), 2) material mixing,
The stirring that adds water reaches 63% to water content, and (fermentation culture material organoleptic indicator is color dark-brown, gently draws with hands to obtain fermentation culture material
The most disconnected, have a large amount of actinomyces albus, without ammonia taste, have bread sweet taste, PH6~7), loading in culture bottle, after tying, Pasteur kills
Bacterium;
4) material temperature 20-25 DEG C is controlled, inoculation, postvaccinal cultivation, ventilation, cultivate 5-10 days in 26-29 DEG C of lucifuge, mycelia
After covering with culture bottle abundant maturation, keeping relative air humidity more than 90%, temperature 15-18 DEG C, illuminance 300-450 is strangled
Ke Si, when diameter 15cm, gathers.
Embodiment 2
A kind of technique utilizing dreg to produce monolithic Pleurotus ulmarius( Bullex Franch) Quel, comprises the following steps:
1) take the antibiotic bacterium dregs (beta-lactam dreg, aminoglycosides dreg) of 80 weight portions, be heated to 50-60 DEG C of insulation
2h, is down to room temperature, and the concentration of atomizing spray same volume is the hydrogen peroxide of 95%, stirs, and seals compacting and stands 1h, and regulation contains
The water yield is injection of ozone stir 30min after 60%, makes ozone and antibiotic bacterium dregs (serine protease, aspartic acid albumen
Enzyme, thiol protease, metalloproteases) it is sufficiently mixed, whipping process ozone concentration keeps 1.5g/m3, ventilates and places 10 days
After, regulation water content, to 40%, adds proteolytic enzyme, and addition concentration is 0.8g/m3, and 28-32 DEG C ferments 7 days, be again heated to
50-60 DEG C of insulation 2h, sterilize dry for standby;
2) straw 100 weight portion, Pedicellus et Pericarpium Trapae rattan 60 weight portion, Pericarpium Musae 20 weight portion are taken respectively, by straw, Pedicellus et Pericarpium Trapae rattan and Pericarpium Musae
Being smashed by pulverizer, length, at 1-3cm, mixes to obtain compound, layering spray account for compound weight 1% calcium superphosphate water-soluble
Liquid (mass concentration is 2%), compresses layer by layer, seals, and 37 DEG C of anaerobic fermentations 30 days, when PH is reduced to 5.5-6.0, surface sprinkling accounts for
The yeast fermentation liquor (yeast mass concentration is 0.25%) of compound weight 5%, seals, 35-37 DEG C of anaerobic fermentation 15 days,
The steam normal-pressure sterilization of 100 DEG C, dries, standby;
3) take purple sweet potato powder 20 weight portion and winter folium mori 60 weight portion, become thoroughly decomposed respectively, then with above-mentioned steps 1), 2) material mixing,
The stirring that adds water reaches 60% to water content, and (fermentation culture material organoleptic indicator is color dark-brown, gently draws with hands to obtain fermentation culture material
The most disconnected, have a large amount of actinomyces albus, without ammonia taste, have bread sweet taste, PH6-7), load in culture bottle, after tying, pasteurize;
4) material temperature 20-25 DEG C is controlled, inoculation, postvaccinal cultivation, ventilation, cultivate 5-10 days in 26-29 DEG C of lucifuge, mycelia
After covering with culture bottle abundant maturation, keeping relative air humidity more than 90%, temperature 15-18 DEG C, illuminance 300-450 is strangled
Ke Si, when diameter 15cm, gathers.
Embodiment 3
A kind of technique utilizing dreg to produce monolithic Pleurotus ulmarius( Bullex Franch) Quel, comprises the following steps:
1) take the antibiotic bacterium dregs (beta-lactam dreg, Macrolide dreg, quinolones dreg) of 120 weight portions, add
Heat, to 50-60 DEG C of insulation 2h, is down to room temperature, and the concentration of atomizing spray same volume is the hydrogen peroxide of 95%, stirs, and seals pressure
The real 1h that stands, regulation water content is injection of ozone stir 30min after 60%, makes ozone and antibiotic bacterium dregs (serine stretch protein
Enzyme, aspartic protease, thiol protease, metalloproteases) it is sufficiently mixed, whipping process ozone concentration keeps 1.5g/m3,
Ventilating after placing 15 days, regulation water content, to 40%, adds proteolytic enzyme, and addition concentration is 1.0g/m3,28-32 DEG C of fermentation 7
My god, it is again heated to 50-60 DEG C of insulation 2h, sterilize dry for standby;
2) straw 120 weight portion, Pedicellus et Pericarpium Trapae rattan 80 weight portion, Pericarpium Musae 30 weight portion are taken respectively, by straw, Pedicellus et Pericarpium Trapae rattan and Pericarpium Musae
Being smashed by pulverizer, length, at 1-3cm, mixes to obtain compound, layering spray account for compound weight 1% calcium superphosphate water-soluble
Liquid (mass concentration is 2%), compresses layer by layer, seals, and 37 DEG C of anaerobic fermentations 40 days, when PH is reduced to 5.5-6.0, surface sprinkling accounts for
The yeast fermentation liquor (yeast mass concentration is 0.45%) of compound weight 5%, seals, 35-37 DEG C of anaerobic fermentation 20 days,
The steam normal-pressure sterilization of 100 DEG C, dries, standby;
3) take purple sweet potato powder 30 weight portion and winter folium mori 80 weight portion, become thoroughly decomposed respectively, then with above-mentioned steps 1), 2) material mixing,
The stirring that adds water reaches 65% to water content, and (fermentation culture material organoleptic indicator is color dark-brown, gently draws with hands to obtain fermentation culture material
The most disconnected, have a large amount of actinomyces albus, without ammonia taste, have bread sweet taste, PH6-7), load in culture bottle, after tying, pasteurize;
4) material temperature 20-25 DEG C is controlled, inoculation, postvaccinal cultivation, ventilation, cultivate 5-10 days in 26-29 DEG C of lucifuge, mycelia
After covering with culture bottle abundant maturation, keeping relative air humidity more than 90%, temperature 15-18 DEG C, illuminance 300-450 is strangled
Ke Si, when diameter 15cm, gathers.
Comparative example 1
The most treated direct use of antibiotic bacterium dregs, other steps are with embodiment 1.
Comparative example 2
Commonsense method cultivation monolithic Pleurotus ulmarius( Bullex Franch) Quel:
Culture medium weight percent form: bagasse 50%~75%, weed tree sawdust 10%~25%, corn cob 5%~20%, Calx 2%~
5%, calcium carbonate 2%, carbamide 1%;Water content reaches inoculation when 60%~68%, and bacterium bag is in the environment of temperature is 22 DEG C~25 DEG C
Bacteria, relative air humidity controls 70%~75%, unglazed photograph, keeps being dried and ventilates;After mycelia is covered with, bacterium bag cuts out
Long mushroom mouth, moves to the long mushroom of booth, and the temperature in booth is 17 DEG C~22 DEG C, and relative air humidity is 70%~80%, and astigmatism is irradiated,
There is the oxygen of abundance simultaneously, within general 7~10 days, former base can be expedited the emergence of out;After growing former base, the temperature in booth be down to 14 DEG C~
16 DEG C, relative air humidity is 85%~95%;When Pleurotus ulmarius( Bullex Franch) Quel growth and maturity can be gathered.
Cultivate monolithic Pleurotus ulmarius( Bullex Franch) Quel comparative result by the embodiment of the present invention and comparative example see table, the most corresponding experimental group 1~3 and
Matched group 1.
From the above results, the monolithic Pleurotus ulmarius( Bullex Franch) Quel that the inventive method cultivates is monolithic sheet and grows thickly, and color even is steady
Fixed, color and luster is red gorgeous vivid, after turning stubble, color is unchanged, and leaf sheet is thick, cap kidney shape, ear or sector, and meat is plump, and size is divided
Cloth is uniform, and pest and disease damage incidence rate is low, sends out bacterium fast, can shorten the production cycle, and yield is high, dry product diameter more than 8 centimetres, without material root,
Economic benefit is obvious, and superior product quality, delicious in taste, and mouthfeel is clear and melodious, flexible.
Above-described embodiment is the present invention preferably embodiment, but embodiments of the present invention are not limited by embodiment
System, the change made, modifies, combines, substitutes, simplifies and all should be under other any spirit without departing from the present invention and principle
Equivalence substitute mode, within being included in protection scope of the present invention.
Claims (7)
1. one kind utilizes the technique that dreg produces monolithic Pleurotus ulmarius( Bullex Franch) Quel, it is characterised in that comprise the following steps:
1) take the antibiotic bacterium dregs of 80-120 weight portion, be heated to 50-60 DEG C of insulation 2h, be down to room temperature, atomizing spray same volume
The hydrogen peroxide that concentration is 95%, stir, seal compacting and stand 1h, regulation water content is injection of ozone stirring after 60%
30min, makes ozone be sufficiently mixed with antibiotic bacterium dregs, and whipping process ozone concentration keeps 1.5g/m3, ventilates and places 10-15 days
After, regulation water content, to 40%, adds proteolytic enzyme, and addition concentration is 0.8-1.0g/m3, and 28-32 DEG C ferments 7 days, again add
Heat is to 50-60 DEG C of insulation 2h, and sterilize dry for standby;
2) straw 100-120 weight portion, Pedicellus et Pericarpium Trapae rattan 60-80 weight portion, Pericarpium Musae 20-30 weight portion are taken respectively, by straw, Pedicellus et Pericarpium Trapae
Rattan and Pericarpium Musae are smashed by pulverizer, and length, at 1-3cm, mixes to obtain compound, layering spray account for compound weight 1% mistake
Calcium phosphate aqueous solution, compresses layer by layer, seals, and 37 DEG C of anaerobic fermentations 30-40 days, when PH is reduced to 5.5-6.0, surface sprinkling accounts for mixed
Close the yeast fermentation liquor of material weight 5%, seal, 35-37 DEG C of anaerobic fermentation 15-20 days, the steam normal-pressure sterilization of 100 DEG C, dries
Dry, standby;
3) take purple sweet potato powder 20-30 weight portion and winter folium mori 60-80 weight portion, become thoroughly decomposed respectively, then with above-mentioned steps 1), 2) material
Mixing, the stirring that adds water reaches 60-65% to water content, obtains fermentation culture material, loads in culture bottle, after tying, pasteurize;
4) material temperature 20-25 DEG C is controlled, inoculation, postvaccinal cultivation, ventilation, cultivate 5-10 days in 26-29 DEG C of lucifuge, mycelia
After covering with culture bottle abundant maturation, keep relative air humidity more than 90%, temperature 15-18 DEG C, illuminance 300-450 Le gram
This, when diameter 15cm, gather.
The technique utilizing dreg to produce monolithic Pleurotus ulmarius( Bullex Franch) Quel the most according to claim 1, it is characterised in that: in step 1), described
Antibiotic bacterium dregs preferred beta-lactam dreg, aminoglycosides dreg, Tetracyclines dreg, Macrolide dreg, quinoline
One or more mixing in promise ketone dreg etc..
The technique utilizing dreg to produce monolithic Pleurotus ulmarius( Bullex Franch) Quel the most according to claim 1, it is characterised in that: in step 1), described
Proteolytic enzyme be one or more in serine protease, aspartic protease, thiol protease, metalloproteases
Mixing.
The technique utilizing dreg to produce monolithic Pleurotus ulmarius( Bullex Franch) Quel the most according to claim 1, it is characterised in that: step 2) in, described
Calcium superphosphate aqueous solution mass concentration be 2%.
The technique utilizing dreg to produce monolithic Pleurotus ulmarius( Bullex Franch) Quel the most according to claim 1, it is characterised in that: step 2) in, described
Yeast fermentation liquor in yeast mass concentration be 0.25-0.45%.
The technique utilizing dreg to produce monolithic Pleurotus ulmarius( Bullex Franch) Quel the most according to claim 1, it is characterised in that: in step 3), described
Fermentation culture material organoleptic indicator be color dark-brown, gently draw with hands the most disconnected, have a large amount of actinomyces albus, without ammonia taste, have bread
Sweet taste, PH6-7.
The technique utilizing dreg to produce monolithic Pleurotus ulmarius( Bullex Franch) Quel the most according to claim 1, it is characterised in that: in step 4), lucifuge
Incubation, compost relative humidity controls at 60-65%;Relative humidity of atomsphere is at 85-95%.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201610703429.6A CN106258495A (en) | 2016-08-23 | 2016-08-23 | A kind of technique utilizing dreg to produce monolithic Pleurotus ulmarius( Bullex Franch) Quel |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201610703429.6A CN106258495A (en) | 2016-08-23 | 2016-08-23 | A kind of technique utilizing dreg to produce monolithic Pleurotus ulmarius( Bullex Franch) Quel |
Publications (1)
Publication Number | Publication Date |
---|---|
CN106258495A true CN106258495A (en) | 2017-01-04 |
Family
ID=57661187
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201610703429.6A Pending CN106258495A (en) | 2016-08-23 | 2016-08-23 | A kind of technique utilizing dreg to produce monolithic Pleurotus ulmarius( Bullex Franch) Quel |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN106258495A (en) |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103130548A (en) * | 2013-02-16 | 2013-06-05 | 宁夏中青农业科技有限公司 | Substrate for producing seedling or cultivation with utilization of antibiotic mushroom dregs and preparation method thereof |
CN103651194A (en) * | 2013-11-18 | 2014-03-26 | 苏州依科曼生物农业科技有限公司 | Method for improving quality of aquaculture products |
CN105130661A (en) * | 2015-09-10 | 2015-12-09 | 凤台县绿然农业发展有限公司 | Edible fungus leftover colored agaricus bisporus efficient culture medium and preparation method of culture medium |
CN105478454A (en) * | 2016-01-12 | 2016-04-13 | 宁夏大学 | Method for removing residual high-concentration tetracycline in pharmacy mushroom residues |
-
2016
- 2016-08-23 CN CN201610703429.6A patent/CN106258495A/en active Pending
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103130548A (en) * | 2013-02-16 | 2013-06-05 | 宁夏中青农业科技有限公司 | Substrate for producing seedling or cultivation with utilization of antibiotic mushroom dregs and preparation method thereof |
CN103651194A (en) * | 2013-11-18 | 2014-03-26 | 苏州依科曼生物农业科技有限公司 | Method for improving quality of aquaculture products |
CN105130661A (en) * | 2015-09-10 | 2015-12-09 | 凤台县绿然农业发展有限公司 | Edible fungus leftover colored agaricus bisporus efficient culture medium and preparation method of culture medium |
CN105478454A (en) * | 2016-01-12 | 2016-04-13 | 宁夏大学 | Method for removing residual high-concentration tetracycline in pharmacy mushroom residues |
Non-Patent Citations (6)
Title |
---|
卢晓丽 等: "菌种的细菌抑菌剂研究", 《安徽农业科学》 * |
赵义涛: "榆耳高产栽培技术", 《中国蔬菜》 * |
赵荣艳等: "《榆耳栽培技术》", 31 October 2007 * |
邓德江: "《平菇高效栽培实用新技术》", 31 May 2015, 中国农业大学出版社 * |
韩建东 等: "金针菇菌渣栽培金顶侧耳研究", 《北方园艺》 * |
黄晨翔等: "《甘肃南部资源植物及食用菌栽培技术》", 31 December 2008, 甘肃科学技术出版社 * |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN103355094B (en) | A kind of method utilizing ramulus mori to cultivate white fungus | |
CN106495879B (en) | A kind of preparation method of green peel of walnut residue organic fertilizer | |
CN105110954A (en) | Culture medium for selenium-rich organic edible fungi and culture method thereof | |
CN104478515B (en) | Zymotic fluid, pleurotus eryngii culture medium and preparation method thereof for cultivating pleurotus eryngii matrix | |
CN105850506A (en) | High-quality and high-yield cultivation method of mushrooms | |
CN106187396A (en) | A kind of industrialized cultivation for needle mushroom substrate and cultural method | |
CN104987156B (en) | A kind of method of binwang mushroom culture medium and cultivation binwang mushroom using mushroom bran | |
CN105367171A (en) | Edible fungus cultivation substrate and preparation method therefor | |
CN104291895A (en) | Organic liquid fertilizer special for syzygium samarangense, and preparation technology and application method thereof | |
CN104641942A (en) | Method for cultivating oyster mushroom on mulberry twigs | |
KR20100114619A (en) | Manufacturing method of compound fertilizer and compound fertilizer using animal blood | |
CN108293592A (en) | A method of cultivating needle mushroom using sorghum flour mixture | |
CN108703015A (en) | A kind of mushroom culture medium matter and preparation method thereof | |
CN108064634A (en) | A kind of Primary spawn material of Termitomyces albuminosus with black skin and preparation method thereof | |
CN110419530A (en) | A kind of pesticide made of Chinese medicinal herbs and its production technology | |
CN109511461A (en) | A kind of high yield cultivating in bag method of black fungus | |
CN109526548A (en) | A kind of black fungus bag stuff cultivation method based on cotton seed hulls | |
CN105541494A (en) | Organic fertilizer used for greenhouse strawberries | |
CN105767598A (en) | Phagostimulant preparation method based on edible fungus cultivation waste | |
CN107637396A (en) | A kind of inoculation method of edible mushroom bacterium bag | |
CN107353095A (en) | A kind of golden mushroom plantation method | |
CN106278617A (en) | A kind of Fructus Pruni pseudocerasi growing nursery and culture substrate and preparation method thereof | |
CN103461808A (en) | Grain prepared by decomposing and transforming edible fungi and preparation method of grain | |
CN105917964A (en) | Cultivating method of needle mushroom | |
Iqbal et al. | Optimization of King oyster mushroom (Pleurotus eryngii) production against cotton waste and fenugreek straw. |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
RJ01 | Rejection of invention patent application after publication |
Application publication date: 20170104 |
|
RJ01 | Rejection of invention patent application after publication |