CN107750813A - A kind of implantation methods of pleurotus eryngii - Google Patents
A kind of implantation methods of pleurotus eryngii Download PDFInfo
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- CN107750813A CN107750813A CN201711016370.4A CN201711016370A CN107750813A CN 107750813 A CN107750813 A CN 107750813A CN 201711016370 A CN201711016370 A CN 201711016370A CN 107750813 A CN107750813 A CN 107750813A
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- pleurotus eryngii
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- mushroom
- culture medium
- implantation methods
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Abstract
The present invention relates to planting edible mushroom technical field, a kind of more particularly to implantation methods of pleurotus eryngii, specific steps include preparing culture medium, pack, sterilizing cooling, inoculated and cultured, fruiting, harvesting management, the present invention is when preparing culture medium, using cotton seed hulls, weed tree sawdust, cotton seed hulls contains the nutriments such as abundant protein and trace element for primary raw material, makes the pleurotus eryngii of plantation nutritious, the raw material is easy to get simultaneously, and cost is low；Corn mixed powder is added in culture medium of the present invention, both supplements trace element, improves the nutritional ingredient of pleurotus eryngii again；In planting process of the present invention, first lucifuge culture, then illumination cultivation, in incubation, reed time controll temperature and humidity and illumination, the pleurotus eryngii yield of production is high, and pleurotus eryngii is not limited by natural environmental condition, stay in grade, and yield is high.
Description
Technical field
The present invention relates to planting edible mushroom technical field, more particularly to a kind of implantation methods of pleurotus eryngii.
Background technology
Pleurotus eryngii, also known as pleurotus eryngii, gained the name because it has the fragrance of almond and the plump such as mouthfeel of abalone of bacterial context.It is
Exploitation in recent years cultivates successful and edible, medicinal, dietotherapy in the Rare edible fungus new varieties of one.In the market pleurotus eryngii product
Compare it is more, it is common such as hundred mountain ancestral's mushroom pickles -- pleurotus eryngii, pleurotus eryngii extract, instant pleurotus eryngii inner wrapping, also have it is independent
Parcel pleurotus eryngii of packaging etc..The yield of pleurotus eryngii is not universal high at present, fruiting time length, management inconvenience, pleurotus eryngii waste material
It can not use.Growth of Pleurotus eryngii development needs the nutriments such as carbon source, nitrogen source, mineral matter, vitamin, traditional planting almond abalone mushroom
It is the natural environment using winter, is planted in vinyl house, the pleurotus eryngii that this mode is planted, which exists, yields poorly, and quality is unstable
It is fixed, it is big by effect of natural conditions, while the pleurotus eryngii nutritive value planted is low, it is difficult to meet the needs in market.
The content of the invention
In order to solve the above problems, the invention provides a kind of implantation methods of pleurotus eryngii, concrete technical scheme are as follows：
A kind of implantation methods of pleurotus eryngii comprise the following steps：
（1）Prepare culture medium：The formula and its mass fraction of culture medium be：Cotton seed hulls 50-55%, weed tree sawdust 25-30%, corn mix
Close powder 15-20%, lime 1-2%, land plaster l-2%；Each raw material is weighed by mass fraction, each raw material is mixed evenly, then
Add water, culture medium moisture content is maintained at 60%-65%, then mixed material is sent into fermenting cellar, fermented at 50-70 DEG C
25-35 hours；
（2）Pack：Knuckle Polythene Bag or Polypropylene Bag charging, per packed 500-600 grams of siccative, 1100-1300 grams of weight in wet base is right
The direct insertion sealing of angle reflexed, is made cultivating bag；
（3）Sterilizing cooling：By cultivating bag cotton beyond the Great Wall, moisture-proofing film is covered, sterilizing chamber is moved on to and stacks, be warming up to 125-128 DEG C,
Insulation 15-17 hours sterilize, and sterilizing makes the temperature in sterilizing chamber near 20-25 DEG C within 48-72 hours after terminating；
（4）Inoculated and cultured：Cultivation sack access strain is opened, the training of 40-60 bag cultivatings bag is connect per 750-800 grams of planting almond abalone mushroom kind
Support base-material；The indoor bacterium germination culture of rearmounted sanitation and hygiene is inoculated with, is maintained the temperature between 20 DEG C~25 DEG C, relative air humidity
More than 70%；Ventilation 1-2 times daily, keep air fresh, about 30 days or so mycelia pursefuls；
（5）Fruiting：The bacterium bag for covering with mycelia is uprightly emitted on fruiting Ground and forms bacterium bed, opens sack, sack surface is covered
1 layer of blotting paper of lid, twice daily spraying water smoke moistens blotting paper, 15 DEG C~18 DEG C of regulating and controlling temperature, relative air humidity 80%,
Promote its fruiting；Pleurotus eryngii is formed to fructification from former base after 13~15 days, and every other day spraying water smoke moistens blotting paper, water smoke
In include 0.03% dipotassium hydrogen phosphate and 0.2% glucose；The young mushroom phase grows in bacterium bag, when mushroom body is in the bacterium bag of closing
It is interior to remove blotting paper when growing to 2-3 centimetres away from bacterium bag mouth upwards, allow mushroom body to receive scattering light and stretched to space, increase water spray by
Gradually improve relative humidity and reach 85%-90%, promote mushroom body constantly to grow up, form normal fructification；
（6）Harvesting management：When pleurotus eryngii fructification length is to 4-6 centimetres, the cap of pleurotus eryngii fructification is open and flat, middle recessed, table
Face slightly fine hair, should be harvested in time when spore not yet launches, and hold stem during harvesting, whole pulls up；Charge level is cleared up after harvesting,
Stop water spray, the bacteria that lives can go out the 2nd damp mushroom in 7-10 days；It is small that the pleurotus eryngii harvested is put into precooling 4-6 in 2-5 DEG C of freezer
When, mushroom shape is then arranged under the conditions of 18-20 DEG C, is finally dispensed with polypropylene knuckle polybag, is vacuumized and tighten sack
And it is moved into 0 DEG C of freezer and preserves.
Further, the step（1）The middle raw material of culture medium is put into mixer is stirred.
Further, the step（4）Middle inoculation uses aseptic inoculating apparatus for mushroom.
Further, the step（5）The water smoke sprayed water before middle fruiting includes micro-amounts of liquids filler and solid is micro fills out
Fill agent；The ratio of the micro filler of the micro-amounts of liquids filler and solid is 7：3.
Further, the micro filler of the solid is potassium chloride and the mixture with zinc sulfate；The potassium chloride and sulfuric acid
The weight ratio of zinc is 1：1.
Further, every gram of micro-amounts of liquids filler includes 30mg selenium element and 75mg vitamin B compound, its
Remaining is deionized water.
Compared with the prior art, beneficial effects of the present invention are as follows：
（1）The implantation methods of the pleurotus eryngii of the present invention, when preparing culture medium, use cotton seed hulls, weed tree sawdust as primary raw material, cotton
Seed shell contains the nutriments such as abundant protein and trace element, makes the pleurotus eryngii of plantation nutritious, while the raw material is easy
, cost is low；
（2）Corn mixed powder is added in culture medium of the present invention, both supplemented with trace element, improve again the nutrition of pleurotus eryngii into
Point；
（3）In planting process of the present invention, first lucifuge culture, then illumination cultivation, in incubation, reed time controll temperature and humidity with
And illumination, the pleurotus eryngii yield of production is high, and pleurotus eryngii is not limited by natural environmental condition, stay in grade, and yield is high.
Embodiment
In order to be better understood from the present invention, with reference to specific embodiment, the invention will be further described：
Embodiment 1：
A kind of implantation methods of pleurotus eryngii comprise the following steps：
（1）Prepare culture medium：The formula and its mass fraction of culture medium be：Cotton seed hulls 50%, weed tree sawdust 30%, corn mixed powder
18%th, lime 1%, land plaster l%；Each raw material is weighed by mass fraction, the raw material of culture medium is put into mixer and is stirred
It is even, then add water, culture medium moisture content is maintained at 60%%, then mixed material is sent into fermenting cellar, sent out at 50 DEG C
Ferment 35 hours；
（2）Pack：Knuckle Polythene Bag or Polypropylene Bag charging, per packed 500 grams of siccative, 1100 grams of weight in wet base, diagonal reflexed is straight
The formula of inserting sealing, is made cultivating bag；
（3）Sterilizing cooling：By cultivating bag cotton beyond the Great Wall, moisture-proofing film is covered, sterilizing chamber is moved on to and stacks, be warming up to 125 DEG C, insulation
Sterilize within 17 hours, sterilizing makes the temperature in sterilizing chamber near 20 DEG C in 48 hours after terminating；
（4）Inoculated and cultured：Inoculation uses aseptic inoculating apparatus for mushroom, opens cultivation sack access strain, and every 750 grams of pleurotus eryngiis are planted
Cultivate and connect 40 bag cultivating bag culture medium material；The indoor bacterium germination culture of rearmounted sanitation and hygiene is inoculated with, maintains the temperature at 20 DEG C, air phase
To humidity more than 70%；Ventilation 1-2 times daily, keep air fresh, about 30 days or so mycelia pursefuls；
（5）Fruiting：The bacterium bag for covering with mycelia is uprightly emitted on fruiting Ground and forms bacterium bed, opens sack, sack surface is covered
1 layer of blotting paper of lid, twice daily spraying water smoke moistens blotting paper, and water smoke includes micro-amounts of liquids filler and solid is micro fills out
Fill agent, the ratio of micro-amounts of liquids filler and the micro filler of solid is 7：3, the micro filler of solid is potassium chloride and and sulfuric acid
The weight ratio of the mixture of zinc, potassium chloride and zinc sulfate is 1：1；Every gram of micro-amounts of liquids filler include 30mg selenium element and
75mg vitamin B compound, remaining is deionized water, while 15 DEG C -18 DEG C of regulating and controlling temperature, relative air humidity 80%, promotees it and goes out
Mushroom；Pleurotus eryngii is formed to fructification from former base after 15 days, and every other day spraying water smoke moistens blotting paper, includes in water smoke
0.03% dipotassium hydrogen phosphate and 0.2% glucose；The young mushroom phase grows in bacterium bag, when mushroom body is given birth to upwards in the bacterium bag of closing
Remove blotting paper at long extremely 2 centimetres away from bacterium bag mouth, allow mushroom body to receive scattering light and stretched to space, increase water spray gradually steps up relatively
Humidity reaches 85%-90%, promotes mushroom body constantly to grow up, and forms normal fructification；Blotting paper uses newspaper；
（6）Harvesting management：When pleurotus eryngii fructification length is to 4 centimetres, the cap of pleurotus eryngii fructification is open and flat, middle recessed, surface
It slightly fine hair, should in time be harvested when spore not yet launches, hold stem during harvesting, whole pulls up；Charge level is cleared up after harvesting, is stopped
Only spray water, the bacteria that lives can go out the 2nd damp mushroom in 10 days；The pleurotus eryngii harvested is put into precooling 4 hours, Ran Hou in 5 DEG C of freezers
Mushroom shape is arranged under the conditions of 18 DEG C, is finally dispensed with polypropylene knuckle polybag, is vacuumized and is tightened sack and be moved into 0
Preserved in DEG C freezer.
Embodiment 2：
（1）Prepare culture medium：The formula and its mass fraction of culture medium be：Cotton seed hulls 55%, weed tree sawdust 25%, corn mixed powder
17%th, lime 2%, land plaster 1%；Each raw material is weighed by mass fraction, the raw material of culture medium is put into mixer and is stirred
It is even, then add water, culture medium moisture content is maintained at 65%, then mixed material is sent into fermenting cellar, fermented at 70 DEG C
25 hours；
（2）Pack：Knuckle Polythene Bag or Polypropylene Bag charging, per packed 600 grams of siccative, 1300 grams of weight in wet base, diagonal reflexed is straight
The formula of inserting sealing, is made cultivating bag；
（3）Sterilizing cooling：By cultivating bag cotton beyond the Great Wall, moisture-proofing film is covered, sterilizing chamber is moved on to and stacks, be warming up to 128 DEG C, insulation
Sterilize within 15 hours, sterilizing makes the temperature in sterilizing chamber near 25 DEG C in 72 hours after terminating；
（4）Inoculated and cultured：Inoculation uses aseptic inoculating apparatus for mushroom, opens cultivation sack access strain, and every 800 grams of pleurotus eryngiis are planted
Cultivate and connect 60 bag cultivating bag culture medium material；The indoor bacterium germination culture of rearmounted sanitation and hygiene is inoculated with, maintains the temperature at 25 DEG C, air phase
To humidity more than 70%；Ventilation 1-2 times daily, keep air fresh, about 30 days or so mycelia pursefuls；
（5）Fruiting：The bacterium bag for covering with mycelia is uprightly emitted on fruiting Ground and forms bacterium bed, opens sack, sack surface is covered
1 layer of blotting paper of lid, twice daily spraying water smoke moistens blotting paper, and water smoke includes micro-amounts of liquids filler and solid is micro fills out
Fill agent, the ratio of micro-amounts of liquids filler and the micro filler of solid is 7：3, the micro filler of solid is potassium chloride and and sulfuric acid
The weight ratio of the mixture of zinc, potassium chloride and zinc sulfate is 1：1；Every gram of micro-amounts of liquids filler include 30mg selenium element and
75mg vitamin B compound, remaining is deionized water, while 15 DEG C~18 DEG C of regulating and controlling temperature, relative air humidity 80%, promotees it
Fruiting；Pleurotus eryngii is formed to fructification from former base after 13 days, and every other day spraying water smoke moistens blotting paper, includes in water smoke
0.03% dipotassium hydrogen phosphate and 0.2% glucose；The young mushroom phase grows in bacterium bag, when mushroom body is given birth to upwards in the bacterium bag of closing
Remove blotting paper at long extremely 3 centimetres away from bacterium bag mouth, allow mushroom body to receive scattering light and stretched to space, increase water spray gradually steps up relatively
Humidity promotes mushroom body constantly to grow up, forms normal fructification up to 90%；
（6）Harvesting management：When pleurotus eryngii fructification length is to 6 centimetres, the cap of pleurotus eryngii fructification is open and flat, middle recessed, surface
It slightly fine hair, should in time be harvested when spore not yet launches, hold stem during harvesting, whole pulls up.Charge level is cleared up after harvesting, is stopped
Only spray water, the bacteria that lives can go out the 2nd damp mushroom in 7 days, be put into precooling 6 hours in 2 DEG C of freezers, then arrange mushroom under the conditions of 20 DEG C
Shape, finally dispensed with polypropylene knuckle polybag, vacuumize to tighten sack and be moved into 0 DEG C of freezer and preserve.
The present invention is not limited to above-described embodiment, the foregoing is only the preferable case study on implementation of the present invention
, it is not intended to limit the invention, any modification for being made within the spirit and principles of the invention, equivalent substitution and changes
Enter, should be included in the scope of the protection.
Claims (6)
- A kind of 1. implantation methods of pleurotus eryngii, it is characterised in that：Comprise the following steps：（1）Prepare culture medium：The formula and its mass fraction of culture medium be：Cotton seed hulls 50-55%, weed tree sawdust 25-30%, corn mix Close powder 15-20%, lime 1-2%, land plaster l-2%；Each raw material is weighed by mass fraction, each raw material is mixed evenly, then Add water, culture medium moisture content is maintained at 60%-65%, then mixed material is sent into fermenting cellar, fermented at 50-70 DEG C 25-35 hours；（2）Pack：Knuckle Polythene Bag or Polypropylene Bag charging, per packed 500-600 grams of siccative, 1100-1300 grams of weight in wet base is right The direct insertion sealing of angle reflexed, is made cultivating bag；（3）Sterilizing cooling：By cultivating bag cotton beyond the Great Wall, moisture-proofing film is covered, sterilizing chamber is moved on to and stacks, be warming up to 125-128 DEG C, Insulation 15-17 hours sterilize, and sterilizing makes the temperature in sterilizing chamber near 20-25 DEG C within 48-72 hours after terminating；（4）Inoculated and cultured：Cultivation sack access strain is opened, the training of 40-60 bag cultivatings bag is connect per 750-800 grams of planting almond abalone mushroom kind Support base-material；The indoor bacterium germination culture of rearmounted sanitation and hygiene is inoculated with, is maintained the temperature between 20 DEG C~25 DEG C, relative air humidity More than 70%；Ventilation 1-2 times daily, keep air fresh, about 30 days or so mycelia pursefuls；（5）Fruiting：The bacterium bag for covering with mycelia is uprightly emitted on fruiting Ground and forms bacterium bed, opens sack, sack surface is covered 1 layer of blotting paper of lid, twice daily spraying water smoke moistens blotting paper, 15 DEG C~18 DEG C of regulating and controlling temperature, relative air humidity 80%, Promote its fruiting；Pleurotus eryngii is formed to fructification from former base after 13~15 days, and every other day spraying water smoke moistens blotting paper, water smoke In include 0.03% dipotassium hydrogen phosphate and 0.2% glucose；The young mushroom phase grows in bacterium bag, when mushroom body is in the bacterium bag of closing It is interior to remove blotting paper when growing to 2-3 centimetres away from bacterium bag mouth upwards, allow mushroom body to receive scattering light and stretched to space, increase water spray by Gradually improve relative humidity and reach 85%-90%, promote mushroom body constantly to grow up, form normal fructification；（6）Harvesting management：When pleurotus eryngii fructification length is to 4-6 centimetres, the cap of pleurotus eryngii fructification is open and flat, middle recessed, table Face slightly fine hair, should be harvested in time when spore not yet launches, and hold stem during harvesting, whole pulls up；Charge level is cleared up after harvesting, Stop water spray, the bacteria that lives can go out the 2nd damp mushroom in 7-10 days；It is small that the pleurotus eryngii harvested is put into precooling 4-6 in 2-5 DEG C of freezer When, mushroom shape is then arranged under the conditions of 18-20 DEG C, is finally dispensed with polypropylene knuckle polybag, is vacuumized and tighten sack And it is moved into 0 DEG C of freezer and preserves.
- A kind of 2. implantation methods of pleurotus eryngii according to claim 1, it is characterised in that：The step（1）It is middle to cultivate The raw material of base, which is put into mixer, to be stirred.
- A kind of 3. implantation methods of pleurotus eryngii according to claim 1, it is characterised in that：The step（4）Middle inoculation is adopted Use aseptic inoculating apparatus for mushroom.
- A kind of 4. implantation methods of pleurotus eryngii according to claim 1, it is characterised in that：The step（5）Before middle fruiting The water smoke of water spray includes micro-amounts of liquids filler and the micro filler of solid；The micro-amounts of liquids filler and solid is micro fills out The ratio for filling agent is 7：3.
- A kind of 5. implantation methods of pleurotus eryngii according to claim 4, it is characterised in that：The micro filler of solid is Potassium chloride and the mixture with zinc sulfate；The weight ratio of the potassium chloride and zinc sulfate is 1：1.
- A kind of 6. implantation methods of pleurotus eryngii according to claim 4, it is characterised in that：Every gram of micro-amounts of liquids filling Agent includes 30mg selenium element and 75mg vitamin B compound, and remaining is deionized water.
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| CN201711016370.4A CN107750813A (en) | 2017-10-25 | 2017-10-25 | A kind of implantation methods of pleurotus eryngii |
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Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108834751A (en) * | 2018-07-31 | 2018-11-20 | 合肥仙之峰农业科技有限公司 | A kind of implantation methods of Pleurotus eryngii |
| CN109328860A (en) * | 2018-11-06 | 2019-02-15 | 江苏淮香食用菌有限公司 | The industrialization breeding method of Pleurotus eryngii |
| CN110447456A (en) * | 2019-08-20 | 2019-11-15 | 广西壮族自治区农业科学院 | A kind of selenium-enriched edible mushroom production technology |
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| CN105016909A (en) * | 2015-08-20 | 2015-11-04 | 青岛华盛绿能农业科技有限公司 | Oyster mushroom culture medium utilizing Pleurotus eryngii waste and method for cultivating oyster mushrooms with culture medium |
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|---|---|---|---|---|
| CN108834751A (en) * | 2018-07-31 | 2018-11-20 | 合肥仙之峰农业科技有限公司 | A kind of implantation methods of Pleurotus eryngii |
| CN109328860A (en) * | 2018-11-06 | 2019-02-15 | 江苏淮香食用菌有限公司 | The industrialization breeding method of Pleurotus eryngii |
| CN110447456A (en) * | 2019-08-20 | 2019-11-15 | 广西壮族自治区农业科学院 | A kind of selenium-enriched edible mushroom production technology |
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Application publication date: 20180306 |