CN102550296A - Indoor cultivation method for Ganoderma lucidum - Google Patents
Indoor cultivation method for Ganoderma lucidum Download PDFInfo
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Abstract
The invention discloses an indoor cultivation method for Ganoderma lucidum, and aims to provide an indoor cultivation technique of Ganoderma lucidum high in yield, high in quality and pollution-free. The cultivation method is technically characterized by including the steps: firstly, breeding a strain, namely mother culture breeding, stock breeding and cultivar breeding; secondly, fruiting body cultivating, namely when mushroom bags are substantially full of white mycelia, reserving a cross-shaped hole 1cm wide beside an opening of each culture bag, and performing management according to requirements of fruiting bodies; and thirdly, collecting spore powder of Ganoderma lucidum, namely erecting an elastic frame at the constant temperature above 20 DEG C, and collecting spore powder. The indoor cultivation method for Ganoderma lucidum belongs to the technical field of edible fungus cultivation.
Description
Technical field
The present invention relates to the red ganoderma cultivation, specifically, is the indoor cultivation method of red ganoderma, belongs to the fungus growing technique field.
Background technology
In short supply day by day in resources such as soil, grains; Ecotope constantly worsens; Today that human health care's consciousness strengthens gradually; Can raw fiber is converted into the high-quality mycoprotein, have the food of fungi of unique health care to be favored day by day to human body, mushroom industry have become the model of green, environmental protection, efficient, circular agriculture.
Modern study proves that glossy ganoderma has many-sided pharmacological action, as many-sides such as central nervous system, respiratory system, cardiovascular system and liver, smooth muscle, internal secretion and immune system being had treatment or regulatory function.Glossy ganoderma is used also very extensive clinically; Be used to treat diseases such as chronic bronchitis, coronary heart disease, hyperlipemia, leukocyte minimizing, alpastic anemia, hepatitis, Keshan disease, muscular dystrophy, alopecia areata, neurasthenia, cancer; All obtained curative effect preferably; General obvious effective rate is about 39%, and total effective rate is 70%～90%.Glossy ganoderma mainly is that the enhances human body resistance against diseases reaches through the function of raising body immune system to the therapeutic action of various diseases.Because Wild ganoderma seldom, and artificial cultivation is limited to summer, autumn more, so present glossy ganoderma output has the gesture that supply falls short of demand, therefore, the method for research raising glossy ganoderma output is necessary.Utilize artificial infection; Under manually operated indoor environment; Make glossy ganoderma better the condition of being grown be surplus in the of nearly 40 year the culture technique that just grows up, mainly contain: (1) indoors artificial bottle is planted technology: this method is generalized to all parts of the country at the initial stage seventies, so far still in application.(2) the indoors artificial bag is planted technology: be to utilize special high temperature resistant, high pressure and nontoxic plastic sack to replace the cultivation method of vial, start from the end of the seventies, still using so far.Yet traditional ganoderma lucidum cultivation method yields poorly; Though the critical technical parameter of artificial cultivation glossy ganoderma has a lot of reports in the relative chamber on all kinds of books and periodicals; But the critical technical parameter of its demonstration is inconsistent; And all be single factor comparative test to the test of various technical parameters, not systematically, all sidedly the method for cultivation of glossy ganoderma, the process of glossy ganoderma growth and the critical technical parameter of glossy ganoderma vegetative stage are made an experiment.
Summary of the invention
The purpose of this invention is to provide a kind of high yield, high-quality, non-harmful red ganoderma indoor growing method.
Technical scheme of the present invention is such: glossy ganoderma indoor growing method, it is characterized in that, comprise the steps: 1) strain improvement; 2) fruit body is cultivated; 3) lucidum spore powder is collected; Wherein: the seed selection of the described bacterial classification of step 1) comprises female three-class strain production processes such as cultivation, breading protospecies, cultivated species cultivation of planting; Step 2) to cultivate be when white hypha covers with the bacterium bag basically for described fruit body, by the cultivation sack, opens an osculum that cross shape 1cm is wide, manages by the fruit body requirement; The described lucidum spore powder of step 3) is collected in temperature when being stabilized in more than 20 ℃, and red ganoderma fruit body cap edge white disappears, and it is red that the edge turns; The consistent bag fruiting of opening with fruit body capping color and luster, the good firing mount frame of frame, upper berth, floor one deck blank sheet of paper is rebasing; Stack above the blank sheet of paper that 2 row's Ganderma lucidum bags, bacterium bag are staggered to be put neatly, every row's 100 bag bacterium bags are not in contact with one another between the cap or run into anything else; Around yoke, reach the top respectively with nankin or 17 gram blank sheet of paper or 40 gram blank sheet of paper sealings; Let conidial powder in sealing close shelf, launch and cultivated one to two months, open blank sheet of paper or nankin, collect conidial powder;
Above-mentioned red ganoderma indoor growing method, used medium comprised following components by part by weight when the described female kind of step 1) was cultivated: 180～220 parts of potatos, 18～22 parts of glucose, 18～22 parts of agar glucose, 3.5～4.5 parts of peptone glucose, water 1000ml.
Above-mentioned red ganoderma indoor growing method is characterized in that, the used medium of the described breading protospecies of step 1) comprises following components by part by weight: corn 99%, gypsum 1%, material-water ratio are 1: 1.2, and the pH value is 8.
Above-mentioned red ganoderma indoor growing method is characterized in that, the described cultivated species of step 1) is cultivated used medium and comprised following components by part by weight: weed tree sawdust 78%, corn flour 6%, wheat bran 15%, land plaster 1%, material-water ratio are 1: 1.2.
Above-mentioned red ganoderma indoor growing method, the described bacterium bag of step 1) are cultivated and sent out bacterium is that the bacterium bag that connects is moved in the culturing room that has disinfected, and the bacterium bag is double to be piled up on the ground, sack outwardly, it highly is 6～8 bags that every row puts, 0.5 meter of array pitch.
Further, the red ganoderma indoor growing method of stating, the relative air humidity of described culturing room is less than 75%.
Further, above-mentioned red ganoderma indoor growing method, the described lucidum spore powder of step 3) is collected 25～28 ℃ of temperature.
Further, above-mentioned red ganoderma indoor growing method, the described encapsulant of step 3) is 17 gram blank sheet of paper.
Compared with prior art, the present invention has has with effect as follows:
1) nuisanceless, except that a small amount of use lime, gypsum, production process is not used any additives, chemicals, and production process does not use the Pesticidal products quality to reach NY5095～2006 " pollution-free food edible mushroom " standard;
2) high-quality, lucidum spore powder each item index is good: crude fat 34.1%, crude protein 8.56%, triterpene (g/100g) 2.26, crude polysaccharides (g/100g) 2.27, adenosine (mg/100g) 5.52/100, selenium (mg/kg) 0.34, germanium (mg/kg)＜0.5;
3) high yield; Equal indoor red ganoderma cultivating ganoderma conidial powder output is 6～7 grams; Ganoderma lucidum fruitbody 15 grams; The Reishi sporule powder yield of technical scheme gained provided by the present invention: 14 gram/bags, ganoderma lucidum fruitbody: 20 gram/bags, than red ganoderma cultivation output difference high 100% and 33.3% in the conventional chamber.
Summary of the invention
Below in conjunction with specific embodiment technical scheme of the present invention is done further to specify; But do not constitute any restriction of the present invention; Anyone unsubstantiality of in claim protection domain of the present invention, being made changes, still in claim protection domain of the present invention.
One, test method
A kind of red ganoderma indoor growing method comprises the steps: 1) strain improvement; 2) bacterium bag cultivating; 3) fruiting
The technological process of production that it is concrete:
Strain improvement → batching → pack → sterilization → inoculation → cultural hypha → go out sesame is managed → puts on the shelf and launches the conidial powder → collection conidial powder → fruit body → drying of gathering → broken wall → packing.
The preparation method of each concrete steps:
1, strain improvement
1.1 female making of planting
1) culture medium preparation is following prescription
A: potato 200g, glucose 20g, agar 20g, peptone 4g, water 1000ml is distributed into 80 test tubes.
B: potato 180g, glucose 20g, agar 20g, peptone 4.5g, water 1000ml is distributed into 80 test tubes.
C: potato 220g, glucose 20g, agar 22g, peptone 4g, water 1000ml is distributed into 80 test tubes.
The preparation method: prepare the PDA medium by conventional method, with potato, glucose, agar, peptone, water 1000ml, pH nature meta-acid (5～6) divides in the 18ram * 180mm test tube of packing into, every pipe 10ml, and 121 ℃ of sterilization 0.5h take out pendulum inclined-plane, back.In superclean bench, quantitatively insert dull and stereotyped most advanced and sophisticated mycelia, each bacterial strain connects 20,25 ℃ of constant temperature culture.
Strain separating (generally selecting for use tissue isolation to separate)
Select to grow the glossy ganoderma button of normal, individual healthy and strong, no damage by disease and insect or just carried out soon cap edge white portion (growth is enclosed) as parting material; After 75% alcohol wash three times; Wash repeatedly with sterile water and promptly can be used for for three times separating; With prune button or grow and enclose surface portion of the scalpel of sterilize, picking one little block organization one receives on the slant medium during separation.Cultivate down for 25-28 ℃, select no living contaminants, the bacterial strain of robust growth is female the kind.Select two red ganoderma strain excellent ML that are fit to the cultivation of Meizhou region weather through testing sieve
1, ML
2The ganoderma lucidum fruitbody meat that these two bacterial strains are produced is plump, and bacterium shape is rectified, and produces powder amount height.
The making of 2 original seeds
The pedigree seed culture medium prescription is: corn (not pulverizing) 99%, gypsum 1%, material-water ratio are 1: 1.2 (water content about 60%).The pH value is 8.
Preparation method: iblet cleans, after removal of impurities removes badly, and water logging bubble 12～13h; Poach is not to sticking with paste and be advisable by opening iblet the inside with hand, dries to the surface anhydrously, adds land plaster; Mix pack, every bag heavy 500g, 121 ℃ of sterilization 1.5h; Dull and stereotyped most advanced and sophisticated mycelia is quantitatively inserted in the cooling back in superclean bench, each original seed cultivation bag is inoculated 2 places, 25 ℃ of constant temperature culture.
3, bacterium bag cultivating
3.1 the cultivation place is selected
Select away from industrial and mining enterprises' pollution source as far as possible; Can preserve moisture, insulation, well-ventilated, light is moderate, draining is unobstructed indoor the cultivation; As: old farm house, warehouse, schoolhouse, idle workshop etc.; Must carry out the sterilization of Integratively before using, sterilization method can use formalin (10ml/m3), sulphur, aerial fog disinfectant to fumigate or with the limewash spraying etc.Want uproot weeds all around and clean out a drain, reduce living contaminants source and insect breeding ground as far as possible, production site should carry out 1-2 time mouse killing working every year.
3.2 composts or fertilisers of cultivating preparation, inoculation and cultural hypha test
Experiment in cultivation composts or fertilisers of cultivating prescription: weed tree sawdust 78%, corn flour 6%, wheat bran 15%, land plaster 1%.
Allotment is during composts or fertilisers of cultivating, with the weed tree sawdust composting 24h that prewets, more various auxiliary materials fully mixed thoroughly earlier, joins then in the weed tree sawdust, and material-water ratio is 1: 1.2 (water content about 60%), regulates pH value to 8 with limewash at last.Test is the Polypropylene Bag charging of 17cm * 35cm, thick 5dmm with the sized; Every packed composts or fertilisers of cultivating (dry weight basis) 350g; Install the back and sterilize, keep 102 ℃ of following constant temperature 16～18h, after the sterilization bacterium bag is moved into already sterilised transfer room with the normal-pressure sterilization mode; Inoculate after reducing to room temperature, strictness is inoculated by the sterile working rules during inoculation.Transfer room cleans up with thimerosal earlier, puts into transfer room after the bacterium bag is cooked, and fumigates with protecting the bacterium king aerosol of sterilizing, and uses ultra violet lamp in addition 1 hour, treats can inoculate when temperature drops to 30 ℃.Before the inoculation, with 75% alcohol wipe hand and bacterial classification bottleneck, general every bag of bacterial classification can connect about 50 bags; Suitably increase inoculum concentration, help sending out bacterium and invade with the assorted bacterium of minimizing, bacterial classification and composts or fertilisers of cultivating are critical to connect airtight and touch; And in time tie sack, operating technology should be skilled, and it is steady, accurate, fast that action is wanted.
3.3 cultivating, the bacterium bag sends out bacterium
The bacterium bag that connects is moved in the culturing room that has disinfected, and the bacterium bag is double to be piled up on the ground, sack outwardly, it is the 6-8 bag highly that every row puts, 0.5 meter of array pitch is so that job management.The relative air humidity of culturing room surpasses 75%, too wetly is prone to cause living contaminants and suitably ventilation; Do not need illumination, generally in the time of 25-28 ℃, sent out bacterium through one month, mycelia just can be covered with the bacterium bag; When temperature was lower than 20 ℃, growth rate obviously slowed down.General mycelia long to three/just can carry out turning for the moment, inside and outside up and down transposing bacterium bag position to keep temperature and to bear pressure consistent, helps mycelia and evenly grows.
4, fruit body is cultivated
When white hypha covers with the bacterium bag basically; Open an osculum that cross shape 1cm is wide on cultivation sack next door; Open a bag method: 1 centimetre of wide osculum of " a ten " word shape is opened with the pocket knife that disinfects in the next door at sack; The position of opening is consistent to keep mushroom consistent with distance between the mushroom as far as possible, prevents adhesion.Every bag only keeps an original hase, and all the other all will prune away, and nutrient is concentrated, and the fruit body lid that grows is big, abundant.Air humidity remains on 90-95%, and can add water on the ground and keep air humidity this moment, with the better effects if of spraying humidification (ultrasonic humidifier).Before button is launched, directly be not sprayed onto water on the button, otherwise button is mouldy or withered easily.Control illumination well, should avoid the sunlight direct projection, also will avoid indoor too dark.Keep the proper ventilation ventilation; Prevent that simultaneously north wind from directly blowing, when fruiting, when special in the button phase; As receive directly to blow than norta; Be easy to cause the temperature of the withered phenomenon cultivating chamber that contracts deadly of large tracts of land button to remain on 26～30 ℃, every day, water spray kept humidity 85～90%, and the bacterium packet start has ganoderma lucidum fruitbody to form.
5, lucidum spore powder is collected
When temperature is stabilized in more than 20 ℃ (Guangdong generally by the end of April by 5 months at the beginning of), can open a bag fruiting, 25～28 ℃ of optimum temperatures.Red ganoderma fruit body cap edge white disappears, and it is red that the edge turns, consistent with fruit body capping color and luster, with wet cloth the bacterium bag wiped clean, and puts on the shelf and prepares to play powder.
Make the wooden frame of growth 200cm, wide 100cm, high 100cm with 16 China fir sides; (wash clean will be dragged in the floor that plays the powder room) shop one deck blank sheet of paper is rebasing on the interior floor of wooden frame; Stacking 2 row's Ganderma lucidum bags, bacterium bag interlock and put neatly above the blank sheet of paper; Every row 100 bag bacterium bags are not in contact with one another between the cap or run into anything else.
After the bacterium bag is stacked well, around yoke, reach the top and seal with different materials respectively: (1) nankin; (2) 17 gram blank sheet of paper; (3) 40 gram blank sheet of paper; (4) 80 gram blank sheet of paper; (5) plastic film.Every kind of about 200 Ganderma lucidum bags of the interior placement of bullet powder frame that material seal forms let conidial powder in sealing close shelf, launch.Conidial powder is launched the room and is kept clean, shady and cool, and suitably ventilates.Be cultured on June 28th, 2011, open encapsulants such as blank sheet of paper or Bao Bu, collect conidial powder with hairbrush, fruit body is plucked in the back.Record conidial powder and fruit body harvest result see table 1 and table 2.
The collection technique and the requirement of indoor growing red ganoderma conidial powder
When red ganoderma fruit body cap edge white disappears, it is red that the edge turns, when consistent with fruit body capping color and luster, with wet cloth the bacterium bag wiped clean, and the preparation bullet powder of putting on the shelf, bacterium bag interlock and put neatly, can put multilayer, can not be in contact with one another or run into anything else between the cap.Not crowded excessively in the frame, long-pending 1/3 of the frame inner volume that can not surpass of general bacterium bag is advisable, to guarantee that oxygen concentration can be not low excessively in the frame.Available 20 gram blank sheet of paper or thin cloth (nankin) are obturaged the bacterium frame, and are strict to papery or cloth, and papery and cloth is blocked up to be unfavorable for ventilatedly, and the long easily deer horn of glossy ganoderma has a strong impact on the output of powder; Papery is crossed and thin is blown mashedly easily by wind and rain, and cloth is crossed thin conidial powder and can be flown out, and also is unfavorable for preserving moisture.It is clean, shady and cool that conidial powder is launched the room requirement, and suitably ventilate, can be with ultrasonic humidifier timing spraying humidification, to reach the effect of cooling and humidification when temperature is too high.Generally, put 15-25 days on the shelf for playing the powder peak period, should be careful observation this moment, if glossy ganoderma edge president deformity projection (like goat's horn shape projection) is then explained anoxic in the frame, add forced ventilation.As find that indivedual bacterium bags or ganoderma lucidum fruitbody go mouldy, and should in time remove to protect from infection, guarantee the quality of glossy ganoderma and conidial powder.Open blank sheet of paper or thin cloth after 35-45 days, collect conidial powder, pluck fruit body with hairbrush.Conidial powder will in time be dried or dry after collecting, and the back packing of sieving on request, leaves the place in drying, cool place in.
After harvesting powder, if find that the Ganderma lucidum bag is also heavier, fruit body is more moistening in addition, still can neatly put into to play powder frame continuation bullet powder, carries out receiving the second time powder after 20-25 days.
Two, damage by disease and insect and the control thereof in the sesame cultivation
The harm of assorted bacterium and insect also can take place in glossy ganoderma in the course of cultivation, influence output and the quality of glossy ganoderma, can cause the failure of cultivating when serious, therefore, will make great efforts the mix extent of injury of bacterium and insect of handle in process of production and drop to minimum.
Major measure: 1. pollution source such as vegetable plot, herding schoolhouse are avoided in the place addressing as far as possible; 2. fresh, clean, the no worm of planting material, no mould, free from extraneous odour; 3. cultivation house installs fly net additional, reduces the worm source, adopts artificial method for catching when finding glossy ganoderma bridge worm.
Three, result and conclusion
1, the different powder frame encapsulants that play are collected the conidial powder PR
Can find out that from table 1 the different conidial powder that play the collection of powder frame encapsulant have very big difference, what output was the highest is to make encapsulant with 17 gram blank sheet of paper and nankin, and what output was minimum is to make encapsulant with 80 gram blank sheet of paper and plastic film.
The different powder frame encapsulants that play of table 1 are collected conidial powder harvest table as a result
2, the different powder frame encapsulant fruiting body yields that play compare
Can find out from table 2, different play powder frame encapsulants and collect conidial powder after, the fruiting body yield difference of each bacterium bag is little, but the trend of output is consistent, i.e. the high encapsulant that is adopted of conidial powder output, its fruiting body yield is also corresponding higher.
The different powder frame encapsulants that play of table 2 are collected fruit body harvest table as a result
Can find out from result of the test, the bullet powder frame that different sealed material is processed, the conidial powder output of collecting has than big-difference; Fruiting body yield is little relatively, but the face shaping of fruit body has obvious differentiation, and the shelf growth normal shape of nankin, 17 gram blank sheet of paper is good; Fruit body is abundant; Deformity, long deer horn appear in the fruit body of 80 gram blank sheet of paper, plastic film, and economic worth is poor, and 40 restrain falling between of blank sheet of paper.The late growing stage that launches with fruit body of lucidum spore powder requires enough oxygen, and suitable temperature, humidity, daylighting are so it is very main to play the encapsulant that the powder frame uses.Papery or cloth are blocked up in production practices is unfavorable for ventilatedly, and the long easily deer horn of glossy ganoderma has a strong impact on the output of powder, and the probability that mould pollutes occurring obviously increases; Papery is crossed and thin is blown mashedly easily by wind and rain, and cloth is crossed thin conidial powder and can be flown out, and material is crossed and also is unfavorable for preserving moisture when thin.
Can draw as drawing a conclusion through this test; Under the consistent situation of bacterial classification, culture medium prescription and prophase management; The bullet powder frame encapsulant that uses when lucidum spore powder and fruiting body yield, quality and conidial powder are collected has very big relation, and best encapsulant is the nankin of 17 gram blank sheet of paper or middle density.
2, according to above-mentioned two groups of lucidum spore powders and the ganoderma lucidum fruitbody cultivated, concrete mass number is referring to table 3
Table 3
Through test, the Reishi sporule powder yield reaches 14 grams, and the output of ganoderma lucidum fruitbody reaches 20 grams, obvious effect of increasing production.In cultivating process, should note following problem:
1, must seed selection in producing cultivation, use improved seeds;
2, the selection of planting environment, cultivation place, raw material are wanted complete monitoring, guarantee that ganoderma lucidum product reaches nuisanceless gold standard;
3, medium scientific formula, major ingredient and auxiliary material rational proportion are with the yield and quality of the effective ingredient that influences ganoderma lucidum product and glossy ganoderma, lucidum spore powder;
4, control temperature, humidity, light, the oxygen concentration of production environment through means such as artificial regulatories, to reach aim of high yield.Cultivation season, preserve moisture, place, bullet powder frame encapsulant, to play aspects such as stacking bacterium bag quantity in the powder frame particularly important.Specific practice is: the general grasp at the beginning of mid-April to 5 in every year month opened a bag fruiting, can make full use of southern area typhoon rain season in 6～July like this, makes that planting environment humidity increases, temperature reduces; Applying of ultrasonic humidifier has fairly obvious effect to temperature, the humidity regulation of planting environment, and effect is obvious especially when running into short of rain, high temperature and drought weather; The blank sheet of paper (or nankin) that uses 17 grams plays and stacks suitable bacterium bag quantity, obvious effect of increasing production in the powder frame as playing powder frame encapsulant.
Claims (8)
1. a red ganoderma indoor growing method is characterized in that, comprises the steps: 1) strain improvement; 2) fruit body is cultivated; 3) lucidum spore powder is collected;
Wherein:
The seed selection of the described bacterial classification of step 1) comprises female three-class strain production processes such as cultivation, breading protospecies, cultivated species cultivation of planting;
Step 2) to cultivate be when white hypha covers with the bacterium bag basically for described fruit body, by the cultivation sack, opens an osculum that cross shape 1cm is wide, manages by the fruit body requirement;
The described lucidum spore powder of step 3) is collected in temperature when being stabilized in more than 20 ℃, and red ganoderma fruit body cap edge white disappears, and it is red that the edge turns; The consistent bag fruiting of opening with fruit body capping color and luster, the good firing mount frame of frame, upper berth, floor one deck blank sheet of paper is rebasing; Stack above the blank sheet of paper that 2 row's Ganderma lucidum bags, bacterium bag are staggered to be put neatly, every row's 100 bag bacterium bags are not in contact with one another between the cap or run into anything else; Around yoke, reach the top respectively with encapsulant nankin or 17 gram blank sheet of paper or 40 gram blank sheet of paper sealings; Let conidial powder in sealing close shelf, launch and cultivated one to two months, open blank sheet of paper or nankin, collect conidial powder.
2. red ganoderma indoor growing method according to claim 1; It is characterized in that used medium comprised following components by part by weight when the described female kind of step 1) was cultivated: 180～220 parts of potatos, 18～22 parts of glucose, 18～22 parts of agar glucose, 3.5～4.5 parts of peptone glucose, water 1000ml.
3. red ganoderma indoor growing method according to claim 1 is characterized in that, the used medium of the described breading protospecies of step 1) comprises following components by part by weight: corn 99%, gypsum 1%, material-water ratio are 1: 1.2, and the pH value is 8.
4. red ganoderma indoor growing method according to claim 1; It is characterized in that; The described cultivated species of step 1) is cultivated used medium and comprised following components by part by weight: weed tree sawdust 78%, corn flour 6%, wheat bran 15%, land plaster 1%, material-water ratio are 1: 1.2.
5. red ganoderma indoor growing method according to claim 1 is characterized in that, the described bacterium bag of step 1) is cultivated and sent out bacterium is that the bacterium bag that connects is moved in the culturing room that has disinfected; The bacterium bag is double to be piled up on the ground; Sack outwardly, it highly is 6～8 bags that every row puts, 0.5 meter of array pitch.
6. red ganoderma indoor growing method according to claim 5 is characterized in that the relative air humidity of described culturing room is less than 75%.
7. red ganoderma indoor growing method according to claim 1 is characterized in that, the described lucidum spore powder of step 3) is collected 25～28 ℃ of temperature.
8. red ganoderma indoor growing method according to claim 1 is characterized in that, the described encapsulant of step 3) is 17 gram blank sheet of paper.
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| CN105660166A (en) * | 2015-12-30 | 2016-06-15 | 桂林大野领御生物科技有限公司 | Method for planting Ganoderma Lucidum |
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| CN112772271A (en) * | 2019-11-11 | 2021-05-11 | 苏州荣世吉自动化设备有限公司 | Edible fungus cultivation method |
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| CN114642169A (en) * | 2022-03-04 | 2022-06-21 | 苏州猫尔科技有限公司 | Method for obtaining hybrid strain with high adenosine content from ganoderma lucidum monospore hybridization breeding and application |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1099217A (en) * | 1994-06-10 | 1995-03-01 | 李茹华 | Method for production of Ganoderma lucidum mycelium |
| WO2006024961A2 (en) * | 2004-09-01 | 2006-03-09 | Peninsular Innovations Limited | Production of artificial hybrid lingzhi and uses thereof |
| CN1883248A (en) * | 2006-06-28 | 2006-12-27 | 中山大学 | Method for improving quality of Ganoderma lucidium spore |
| CN101352144A (en) * | 2008-09-16 | 2009-01-28 | 福建农林大学 | Cross breeding method of Ganoderma lucidum |
| CN102138435A (en) * | 2010-12-29 | 2011-08-03 | 广东侨微生物科技有限公司 | Ecological cultivation method for ganoderma |
-
2012
- 2012-02-15 CN CN201210034440XA patent/CN102550296A/en active Pending
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1099217A (en) * | 1994-06-10 | 1995-03-01 | 李茹华 | Method for production of Ganoderma lucidum mycelium |
| WO2006024961A2 (en) * | 2004-09-01 | 2006-03-09 | Peninsular Innovations Limited | Production of artificial hybrid lingzhi and uses thereof |
| WO2006024961A3 (en) * | 2004-09-01 | 2006-06-22 | Peninsular Innovations Ltd | Production of artificial hybrid lingzhi and uses thereof |
| CN1883248A (en) * | 2006-06-28 | 2006-12-27 | 中山大学 | Method for improving quality of Ganoderma lucidium spore |
| CN101352144A (en) * | 2008-09-16 | 2009-01-28 | 福建农林大学 | Cross breeding method of Ganoderma lucidum |
| CN102138435A (en) * | 2010-12-29 | 2011-08-03 | 广东侨微生物科技有限公司 | Ecological cultivation method for ganoderma |
Non-Patent Citations (4)
| Title |
|---|
| 曾振基等: "赤灵芝高产栽培技术", 《广东农业科学》 * |
| 李忠等: "赤灵芝孢子粉采收与贮存技术", 《现代农业科技》 * |
| 胡景平: "全埋式地下畦栽灵芝菌株优选试验", 《北方园艺》 * |
| 胡景平: "陇东地区全埋式地下畦栽灵芝菌株筛选试验", 《食用菌》 * |
Cited By (13)
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| CN103238464B (en) * | 2013-05-17 | 2014-10-08 | 绍兴儒林生物科技有限公司 | Method of utilizing dendrobium candidum slag for cultivating ganoderma through solid fermentation |
| CN103238464A (en) * | 2013-05-17 | 2013-08-14 | 绍兴儒林生物科技有限公司 | Method of utilizing dendrobium candidum slag for cultivating ganoderma through solid fermentation |
| CN104094773B (en) * | 2014-07-31 | 2017-06-20 | 桂林丰茂源农业技术开发有限公司 | A kind of method by cuboid box cultivating ganoderma |
| CN104094773A (en) * | 2014-07-31 | 2014-10-15 | 桂林丰茂源农业技术开发有限公司 | Method for cultivating glossy ganoderma by rectangular boxes |
| CN105493896A (en) * | 2015-12-30 | 2016-04-20 | 桂林大野领御生物科技有限公司 | Ganoderma lucidum cultivation method capable of increasing content of ganoderma lucidum polysaccharide |
| CN105660166A (en) * | 2015-12-30 | 2016-06-15 | 桂林大野领御生物科技有限公司 | Method for planting Ganoderma Lucidum |
| CN105638238A (en) * | 2015-12-30 | 2016-06-08 | 桂林大野领御生物科技有限公司 | Cultivation method for ganoderma lucidum |
| CN110476710A (en) * | 2016-10-14 | 2019-11-22 | 北京京诚生物科技有限公司 | Improve the cultural method of effective component of glossy ganoderma content |
| CN107637386A (en) * | 2017-10-25 | 2018-01-30 | 翔天农业开发集团股份有限公司 | A kind of method of pleurotus eryngii positioning fruiting |
| CN108101603A (en) * | 2017-11-30 | 2018-06-01 | 山东职业学院 | A kind of ganoderma lucidum pedigree seed culture medium and preparation method thereof |
| CN112772271A (en) * | 2019-11-11 | 2021-05-11 | 苏州荣世吉自动化设备有限公司 | Edible fungus cultivation method |
| CN113317116A (en) * | 2021-06-08 | 2021-08-31 | 广州城建职业学院 | Mushroom cultivation method, device, equipment and medium based on Internet of things |
| CN114642169A (en) * | 2022-03-04 | 2022-06-21 | 苏州猫尔科技有限公司 | Method for obtaining hybrid strain with high adenosine content from ganoderma lucidum monospore hybridization breeding and application |
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