CN104557211A - Special strain culture medium for mushroom liquefaction and corresponding culture method - Google Patents
Special strain culture medium for mushroom liquefaction and corresponding culture method Download PDFInfo
- Publication number
- CN104557211A CN104557211A CN201510028938.9A CN201510028938A CN104557211A CN 104557211 A CN104557211 A CN 104557211A CN 201510028938 A CN201510028938 A CN 201510028938A CN 104557211 A CN104557211 A CN 104557211A
- Authority
- CN
- China
- Prior art keywords
- mushroom
- liquefaction
- parts
- bacterial classification
- special
- 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.)
- Granted
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C05—FERTILISERS; MANUFACTURE THEREOF
- C05B—PHOSPHATIC FERTILISERS
- C05B7/00—Fertilisers based essentially on alkali or ammonium orthophosphates
-
- 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
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Mycology (AREA)
- Environmental Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Mushroom Cultivation (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Abstract
The invention discloses a special strain culture medium for mushroom liquefaction. The special strain culture medium is prepared from the following components in parts by weight: 40-50 parts of corn starch, 1-2 parts of glucose, 15-20 parts of wheat cellulose, 15-23 parts of fine bran, 1-1. 5 parts of a yeast extract, 1-1.5 parts of beef peptone, 2-3 parts of potassium dihydrogen phosphate, 1-1.5 parts of magnesium sulfate, 2 parts of gypsum and 100 parts of water. The invention further discloses a strain culture method for carrying out mushroom liquefaction by employing the culture medium. The culture method sequentially comprises the following steps: carrying out high-temperature and high-pressure sterilization on a special strain culture medium for mushroom liquefaction; inoculating into a mushroom mother strain in the sterilized culture medium under a sterile condition, and carrying out darkness culture at 22-24 DEG C for 25-26 days; and carrying out dilution treatment on the obtained special solid strain for liquefaction so as to obtain the liquefied mushroom strain.
Description
Technical field
The present invention relates to a kind of mushroom liquefaction special bacteria formula and cultivation.
Background technology
Edible mushroom is one of strong industry of Chinese most modern agricultural development feature.This is not only because China is Edible Fungi the biggest in the world and country of consumption, and Edible Fungi has a large capacity and a wide range, and the more important thing is the good carrier of mushroom industry in biotechnology industry and agricultural sustainable development and prominent position.The mushroom industry system of current China, there is the key element being much not suitable with world market economy, wherein intensive, the low degree of specialized division of labor of most importantly Industry Management, production factors fall behind, production technology is perfect not to the utmost, lack the support of key technology, wherein most is representational is the intensive efficient raising technology of bacterial classification, has become the Main Bottleneck that industry faces.The tradition three grades of solid spawns generally adopted at present breed technique, production efficiency is low, cultivation cycle is long, bacterial classification microbiological contamination rate is high, manualization, workshop-based poor efficiency production model cannot be broken through, make Large-scale enterprises and casual household's production of hybrid seeds be in same competition platform, this be cause current Edible Fungi safety, main contributor that quality accident takes place frequently, be also the not good enough main cause of the edible mushroom performance of enterprises.External as generally adopted liquid spawn technology at present in Japan, Korea S's edible fungus industrial production; and China lacks the successful experience of large-scale production and technology in this field; so the research and development that reinforcement bacterial classification is applied in large-scale production; utilize modern biotechnology science and technology and biotechnology, realize efficiently breeding of bacterial classification (bacterium bag) extremely urgent.
Tradition three grades of solid spawns breed technique 3 steps (test tube stock-bottled original seed-bottled cultivated species): the 1st grade is test tube stock, fill a prescription as PDA is main (peeling fresh potato 200 grams, glucose 20 grams, agar 20, water 1000ml), incubation time 7-15 days (different according to mushroom kind, mushroom is generally 12-15 days), 1 female kind switching, 5 bottles of original seeds.2nd grade is bottled original seed (750ml), formula is based on wood chip, bran mass (wood chip 78% as thin in mushroom original seed formula, wheat bran 20%, white sugar 1%, gypsum 1%, water content 60%), incubation time 45-60 days (different according to mushroom kind), 1 bottle of switchable 50 bottles of cultivated species of original seed.3rd level is bottled cultivated species (750ml), fill a prescription based on wood chip, bran mass (with original seed formula, incubation time 35-45 days (different according to mushroom kind), 1 bottle of switchable 20 fruiting bag of cultivated species (weight in wet base 600 grams of composts or fertilisers of cultivating), every bag of fruiting bag needs solid spawn 30 grams.The omnidistance cultivation cycle 87-120 days of above-mentioned 3 grades of kind techniques.When the bacterial classification inoculation fruiting bag method conveniently of the method gained cultivates fresh mushroom, microbiological contamination rate is generally 5-10%.Remarks illustrate: above-mentioned solid spawn original seed (the 2nd grade), cultivated species (3rd level) stage due to incubation time long, culture environment is poor, add that sealing is lack of standardization, the finished product bacterial classification stealthy microbiological contamination in surface of full mycelia can sent out, after the bacterial classification of this subclinical infection is vaccinated, dominant pollution (now miscellaneous bacteria is faster than hypha of edible fungus growth) can be become.So existing solid spawn is very risky, and be difficult to avoid.
The technological process of current existing edible fungus liquid fermented bacterium (also claiming submerged fermentation) is 3 steps (test tube stock-triangular flask shaker fermentation liquid original seed-fermentation tank submerged fermentation liquid cultivation seeds): plant for female for the 1st grade, (facture is the same) incubation time 7-15 days is (different according to mushroom kind, mushroom is generally 12-15 days), 1 female kind switching 2-3 bottle triangular flask shaker fermentation liquid original seed (200ml).2nd grade is triangular flask shaker fermentation liquid original seed (putting into 200ml culture fluid in 500ml triangular flask), formula is to remove the peel fresh potato, glucose, yeast extract, peptone etc., shaking table incubation time 7-10 days (different according to mushroom kind), 3 grades of fermentation tank culture liquid (10% inoculum concentration) of 1 bottle of switchable 2000ml of liquid original seed.3rd level is fermentation tank submerged fermentation liquid cultivation seed, formula is with triangular flask shaking table liquid pedigree seed culture medium, fermentation needs special submerged fermentation tank or fermentation system, incubation time 3-5 days (different according to mushroom kind), 1 liter of switchable 100 fruiting bag of liquid spawn.Aforesaid liquid bacterial classification breeds the omnidistance cultivation cycle 22-30 days of technique.When the bacterial classification inoculation fruiting bag method conveniently of the method gained cultivates fresh mushroom, microbiological contamination rate is generally 2-5%.Remarks illustrate: on liquid fermentation bacterial classification technology theory, bacterial classification purity is high, the microbiological contamination rate (in 3 grades of fermentation tanks) between 1%-5% that large scale fermentation is produced, add microbiological contamination (bacillary is main) often phase after fermentation, conventional in the very difficult discovery of X-ray inspection X, cause the production accident producing fruiting bag in enormous quantities pollution by liquid fermentation strain inoculation, lesson is painful.In addition, liquid spawn need by nutrient components such as the organic nitrogen of high concentration and sugared sources owing to cultivating, these component residue are access in fruiting bag in bacterium liquid, miscellaneous bacteria is unavoidably had to bring into due to during operation, so residual nutrition just becomes the hotbed of miscellaneous bacteria, add the postvaccinal pollution risk of fruiting bag.This be liquid fermentation bacterial classification can not large-scale application in the subject matter of Edible Fungi.
Summary of the invention
The technical problem to be solved in the present invention is to provide the mushroom liquefaction special bacteria medium and corresponding cultivation that a kind of cultivation cycle is short, strain quality is high.
In order to solve the problems of the technologies described above, the invention provides a kind of mushroom liquefaction special bacteria medium, it is grouped into by the one-tenth of following weight portion:
As the improvement of mushroom liquefaction special bacteria medium of the present invention, it is grouped into by the one-tenth of following weight portion:
The present invention also provides the preparation method of above-mentioned medium simultaneously, comprises the steps:
Corn starch, fine bran (wheat bran), Semen Tritici aestivi fiber element, gypsum are mixed, obtains batching I;
Glucose, yeast extract, beef peptone, potassium dihydrogen phosphate, magnesium sulfate are added to the water, fully stir (glucose, yeast extract, beef peptone, potassium dihydrogen phosphate, magnesium sulfate are dissolved in the water), obtain batching II;
After batching I and batching II fully being mixed, obtain mushroom liquefaction special bacteria medium.
The present invention also provides the mushroom liquefaction Spawn incubation method utilizing above-mentioned medium to carry out simultaneously, mushroom mother is planted and carries out following steps successively:
1), bacterial classification makes:
The special bacteria medium that liquefied by mushroom loads in blake bottle, builds microporous barrier ventilating cover, and autoclave sterilization (namely 121 DEG C, carry out autoclave sterilization 90 minutes under 0.11Mpa), obtains sterilizing wild Oryza species;
Remarks illustrate: optional Shanghai Song Tuo Industrial Co., Ltd. ZP14-200 gas-permeable flasks, it carries microporous barrier ventilating cover.
According to the inoculum concentration that mushroom liquefaction special bacteria medium correspondence 4.8 ~ 5.2g (being preferably 5g) the mushroom mother of every 200g plants, under aseptic condition, access mushroom mother after sterilization in medium plant, 22 ~ 24 DEG C of (being preferably 23 DEG C) dark culturing 25 ~ 26 days (being preferably 25 days), must liquefy special solid bacterial classification; Now mycelia sends out completely full bottle;
Remarks illustrate:
1, mushroom mother plants conveniently technology and can obtain;
2, in order to prove the purity of gained of the present invention liquefaction special bacteria and kind property, can to step 1) the liquefaction special bacteria of gained carries out following inspection:
1., purity check, comprise mould inspection, bacteriologic test, adopt microscopic examination and Conventional bacteria test stone;
The detection kind of mould is: mould, the mould of wood;
The detection kind of bacterium is: bacillus subtilis.
2., vitality test, adopt ttc method;
3., organoleptic examination: comprise form (not having immature mushroom flower bud to be formed) without former base, cultivate bottle cap complete seal, label is correct.
2) prepared by the bacterial classification that, liquefies:
Special solid bacterial classification will be liquefied aseptically first through high speed homogenization (under the rotating speed of 8000 ~ 10000 revs/min homogeneous 1 ~ 1.5 minute), then (that is, in the liquefaction special solid bacterial classification of 1 weight portion, the sterile water of 99 weight portions is added according to the dilution factor of 1:100; Remarks illustrate: belong to secondary dilution) dilution, gains after dilution (pH value is 6.5-7.0 naturally) in thinning tank in temperature be 20-23 DEG C, ventilation ratio liquefies under being the condition of 1:0.4 (v/v/min) 4 ~ 6 minutes (being preferably 5 minutes); Obtain mushroom liquefaction bacterial classification.
The mushroom liquefaction bacterial classification of gained of the present invention, liquefaction bacterial classification mycelia fragment is many, good dispersion degree (detects through 400 power microscopes, there is hyphal cell 100 in each visual field), it is energetic that (TTC-dehydrase reducing process detects: 0.2g testing sample+2ml 0.5%TTC-PBS (PH=8.0), 40 DEG C of water bath with thermostatic control dyeing 2h, add 5ml absolute ethyl alcohol room temperature extraction 1h again, extract light absorption value OD485 value, remarks: 0.50-0.55 is qualified), when inoculum concentration 30ml/ bottle, a satisfied bacterium effect can be obtained.Remarks illustrate: inoculum concentration 30ml/ bottle points to the liquefaction bacterium liquid (that is, the mushroom liquefaction special bacteria of gained of the present invention) accessing 30ml in each mushroom fruiting bag to be seeded, and after cultivating, gained is the fresh mushroom product of mushroom.
Compared with mushroom liquefaction Spawn incubation method of the present invention breeds technique with tradition three grades of solid spawns, there is following technical advantage:
Technique of the present invention is 2 walk (test tube stock-bottled liquefaction Special seed) greatly, and the 1st step be female kind (facture is with above-mentioned prior art); 2nd step is liquefaction special bacteria (200ml), and incubation time about 25 days, then only need carry out dilution liquefaction about 5 minutes.Therefore, the omnidistance cultivation cycle 37-40 days of technique.Every bottle of liquefaction special bacteria (200 grams) is through liquefaction, and become 20 liters of bacterium liquid, switchable more than 600 fruiting bags (every bag connects 30ml bacterium liquid), every bag of fruiting bag needs solid spawn 0.3 gram.Inoculation efficiency is 100 times of conventional solid bacterial classification.
The maximum difference of mushroom liquefaction Spawn incubation method of the present invention and existing liquid fermentation is: adopt 2 step provenance cultivations, the cycle is short, technique is simple; Simultaneously because sowing quantity is 1/100 of solid spawn, so bacterial classification can carry out the inspection of purity, vigor and kind to every bottle of provenance before using, thus the quality of standard bacteria provenance (liquid spawn is not accomplished at X-ray inspection X before using, dangerous); 3rd when being liquefaction strain inoculation fruiting bag of the present invention without the need to cultivating (liquid spawn needs 3-5 days fermented and cultured), use simple, low equipment investment, more crucially bacterium liquid is only containing pure mycelia, there is no medium (only having sterile water), all stopped to inoculate after bacterium liquid band abundant nutrition and the secondary contact scar that causes, improve the purity (this does not accomplish in solid three-class strain and liquid fermentation bacterial classification) of inoculation yield rate and fruiting bag.
The liquefaction special solid bacterial classification of gained of the present invention can preserve 30 days under 5 DEG C of environment (clean dry refrigerator), and aforesaid liquid fermented bacterium can not be preserved, and will use immediately after having fermented.
Beneficial effect of the present invention is as follows:
Mushroom of the present invention liquefaction special bacteria and liquefaction inoculation technique, due to good dispersion, mycelia is energetic, can send out cultivation bag sooner full, the dark culturing time of liquefaction bacterial classification purseful time (that is, step 1)) shorten about 1/3 than solid spawn; And pollution rate is low, after purseful, bacterium bag weight-loss ratio is low, and mycelia is energetic.Yield and quality is than using the with the obvious advantage of solid spawn inoculation.Both the cultivation of provenance had been solved, simplify technique, decrease inoculation consumption, what is more important, it efficiently solves the mycelia problem that size is uneven in liquefaction medium, improve the quality and viability of bacterium liquid, and met the requirement of quick inoculation, overall minimizing inoculates link cost more than 50%.
In sum, inventor is to mushroom strain quality responses key technology, bacterium bottle (bag) scale is efficiently bred and has been carried out new industrial research, a kind of mushroom liquefaction special bacteria medium and corresponding culture technique are invented, the special bacteria cycle of producing with this invention is short, mycelial growth is vigorous, energetic, production cost is low, culture bottle or cultivation bag is used for through post liquefaction, after inoculation, multiple spot sends out bacterium, mycelial growth is rapid, yield rate is high, inoculation efficiency is 50 times-100 times of conventional solid bacterial classification, a kind of efficient, stable, reliable bacterial classification pattern, suitable especially mushroom plant intensive production mode pattern.
Embodiment
Embodiment 1, a kind of mushroom liquefaction special bacteria medium, it is grouped into by the one-tenth of following weight portion:
The preparation method of above-mentioned medium is for carry out following steps successively:
In rustless steel container, corn starch, fine bran (wheat bran), Semen Tritici aestivi fiber element, gypsum are mixed in dry conditions, obtains batching I;
Glucose, yeast extract, beef peptone, potassium dihydrogen phosphate, magnesium sulfate are added to the water, fully stir (glucose, yeast extract, beef peptone, potassium dihydrogen phosphate, magnesium sulfate are dissolved in the water), obtain batching II;
After batching I and batching II fully being mixed, obtain mushroom liquefaction special bacteria medium.
Remarks illustrate: this mushroom liquefaction special bacteria medium is now with the current.
Embodiment 2, the mushroom liquefaction Spawn incubation method utilizing the medium of embodiment 1 gained to carry out, mushroom mother is planted and carries out following steps successively:
1), bacterial classification makes:
The mushroom now prepared liquefaction special bacteria medium 200g is dispensed in the special culture bottle of 200ml immediately, build microporous barrier ventilating cover (selecting Shanghai Song Tuo Industrial Co., Ltd. ZP14-200 gas-permeable flasks), 121 DEG C, carry out autoclave sterilization 90 minutes under 0.11Mpa; Obtain sterilizing wild Oryza species;
Under aseptic condition, access mushroom mother in above-mentioned sterilizing wild Oryza species plant 5 grams (solids mother plant), 23 DEG C of dark culturing 25 days, must liquefy special solid bacterial classification; Now mycelia sends out completely full bottle.
Through inspection, purity is 100%;
After testing, the mould such as mould, the mould of wood is not measured;
After testing, the bacterium such as bacillus subtilis is not measured;
The vigor data adopting ttc method to detect gained are OD485 value 0.52;
Organoleptic examination result is: formed without former base, and cultivate bottle cap complete seal, label is correct.
2) prepared by the bacterial classification that, liquefies:
To special solid bacterial classification be liquefied aseptically first through high speed homogenization (homogeneous liquefies 1 minute under the rotating speed of 10,000 revs/min), then according to dilution factor (the belonging to secondary dilution) dilution of 1:100, gains (pH6.5, mycelium) after dilution in thinning tank in temperature be 20 DEG C, ventilation ratio be the condition of 1:0.4 (v/v/min) under liquefaction 5 minutes; Obtain mushroom liquefaction bacterial classification.
Test 1, mushroom liquefaction bacterial classification of the present invention and existing solid spawn, liquid fermentation bacterial classification inoculation fruiting bag method are conveniently cultivated the fresh mushroom of mushroom, acquired results contrast is as follows:
Table 1, mushroom liquefaction bacterial classification and solid spawn, liquid fermentation strain inoculation fruiting bag effectiveness comparison
From the Data Comparison of above-mentioned table 1, known, mushroom liquefaction bacterial classification of the present invention is far superior to solid spawn and the liquid fermentation bacterial classification of prior art gained.
Comparative example 1-1,
The formula of the mushroom liquefaction special bacteria medium in embodiment 1 is done following change:
Cancel the use of Semen Tritici aestivi fiber element 20 parts, and accordingly corn starch is increased to 66 parts by 46 parts; All the other are equal to embodiment 1.
Comparative example 1-2,
The formula of the mushroom liquefaction special bacteria medium in embodiment 1 is done following change:
" Semen Tritici aestivi fiber element 20 parts " is made into " 20 parts, lignin ", and all the other are equal to embodiment 1.
Comparative example 1-3,
The formula of the mushroom liquefaction special bacteria medium in embodiment 1 is done following change:
" Semen Tritici aestivi fiber element 20 parts " is made into " wood chip 20 parts ", and all the other are equal to embodiment 1.
Utilize the medium of above-mentioned comparative example 1-1 ~ comparative example 1-3 for mushroom liquefaction special bacteria cultivation described in embodiment 2, in order to make step 1) realize mycelia and send out the completely full time needed for bottle, and the mushroom liquefaction bacterial classification of gained cultivates the fresh mushroom of mushroom according to the inoculation fruiting bag method of the routine of above-mentioned experiment 1, acquired results contrasts as described in Table 2:
Table 2
| Project | Embodiment | Comparative example 1-1 | Comparative example 1-2 | Comparative example 1-3 |
| Strain liquid rate % | 100 | 100 | 90 | 65 |
| Pollution rate % | 0 | 10 | 13 | 15 |
| Mycelia purseful time d | 25 | 35 | 28 | 30 |
| Weight-loss ratio % | 1 | 2 | 2 | 2 |
| Mycelium characteristic | Dense | Generally | Generally | Denseer |
| Damp mushroom formation time (my god) | 75 | 86 | 88 | 91 |
| Per unit area yield g/ bag | 201 | 148 | 159 | 131 |
| Biological efficiency % | 67 | 49 | 53 | 44 |
Comparative example 2-1,
By in embodiment 2 " 2), liquefaction bacterial classification preparation: " do as follows change:
Dilution factor is made into " 1:1 " by " 1:100 "; All the other are equal to embodiment 2.
Result is: bacterial classification cannot carry out follow-up liquefaction, becomes viscose shape.A failure of liquefaction bacterial classification!
Comparative example 2-2,
By in embodiment 2 " 2) liquefaction bacterial classification preparation: " do as follows change:
Dilution factor is made into " 1:200 " by " 1:100 "; All the other are equal to embodiment 2.
Comparative example 2-3, by embodiment 2 " 2) liquefaction bacterial classification preparation: " do as follows change:
Ventilation ratio is made into " 1:0.2 " by " 1:0.4 "; All the other are equal to embodiment 2.
Comparative example 2-4, by embodiment 2 " 2) liquefaction bacterial classification preparation: " do as follows change:
Ventilation ratio is made into " 1:0.6 " by " 1:0.4 "; All the other are equal to embodiment 2.
Comparative example 3-1,
" 1), bacterial classification make " in embodiment 2 is done change as follows:
Cultivation temperature is made into " 25 DEG C " by " 23 DEG C "; All the other are equal to embodiment 2.
Comparative example 3-2,
" 1), bacterial classification make " in embodiment 2 is done change as follows:
Cultivation temperature is made into " 21 DEG C " by " 23 DEG C "; All the other are equal to embodiment 2.
The mushroom of above-mentioned comparative example 2-2 ~ comparative example 3-2 gained liquefaction bacterial classification is cultivated the fresh mushroom of mushroom according to the inoculation fruiting bag method of the routine of above-mentioned experiment 1, and acquired results contrasts as described in Table 3:
Table 3
Remarks illustrate:
By embodiment 2 step 1) the liquefaction special solid bacterial classification of gained preserves 30 days under 5 DEG C of environment (clean dry refrigerator), then proceeds follow-up step 2).
The mushroom liquefaction bacterial classification of gained cultivates the fresh mushroom of mushroom according to the inoculation fruiting bag method of the routine described in above-mentioned experiment 1, and acquired results is substantially with the result (gap is no more than 5%) of " liquefaction bacterial classification (the present invention) " gained in table 1.
Finally, it is also to be noted that what enumerate above is only several specific embodiments of the present invention.Obviously, the invention is not restricted to above embodiment, many distortion can also be had.All distortion that those of ordinary skill in the art can directly derive from content disclosed by the invention or associate, all should think protection scope of the present invention.
Claims (4)
1. mushroom liquefaction special bacteria medium, is characterized in that being grouped into by the one-tenth of following weight portion:
2. mushroom liquefaction special bacteria medium according to claim 1, is characterized in that being grouped into by the one-tenth of following weight portion:
3. the preparation method of the medium described in claim 1 or 2, is characterized in that comprising the steps:
Corn starch, fine bran, Semen Tritici aestivi fiber element, gypsum are mixed, obtains batching I;
Glucose, yeast extract, beef peptone, potassium dihydrogen phosphate, magnesium sulfate are added to the water, fully stir, obtain batching II;
After batching I and batching II fully being mixed, obtain mushroom liquefaction special bacteria medium.
4. the mushroom liquefaction Spawn incubation method utilizing the medium described in claim 1 or 2 to carry out, is characterized in that: mushroom mother planted and carry out following steps successively:
1), bacterial classification makes:
The special bacteria medium that liquefied by mushroom loads in blake bottle, builds microporous barrier ventilating cover, autoclave sterilization, obtains sterilizing wild Oryza species;
According to the inoculum concentration that mushroom liquefaction special bacteria medium correspondence 4.8 ~ 5.2g mushroom mother of every 200g plants, access mushroom mother in medium after sterilization and plant under aseptic condition, 22 ~ 24 DEG C of dark culturing 25 ~ 26 days, must liquefy special solid bacterial classification;
2) prepared by the bacterial classification that, liquefies:
Special solid bacterial classification will be liquefied aseptically first through high speed homogenization, then according to the dilution of 1:100, the gains after dilution in thinning tank in temperature be 20-23 DEG C, ventilation ratio be the condition of 1:0.4 (v/v/min) under liquefaction 4 ~ 6 minutes; Obtain mushroom liquefaction bacterial classification.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201510028938.9A CN104557211B (en) | 2015-01-20 | 2015-01-20 | Mushroom liquefaction special bacteria culture medium and corresponding cultivation |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201510028938.9A CN104557211B (en) | 2015-01-20 | 2015-01-20 | Mushroom liquefaction special bacteria culture medium and corresponding cultivation |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN104557211A true CN104557211A (en) | 2015-04-29 |
| CN104557211B CN104557211B (en) | 2017-11-07 |
Family
ID=53074398
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201510028938.9A Active CN104557211B (en) | 2015-01-20 | 2015-01-20 | Mushroom liquefaction special bacteria culture medium and corresponding cultivation |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN104557211B (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105399470A (en) * | 2015-11-30 | 2016-03-16 | 全椒县香妃农业专业合作社 | Lentinula edodes strain medium and preparing method thereof |
| CN107771614A (en) * | 2017-12-14 | 2018-03-09 | 全椒县香妃农业专业合作社 | A kind of mushroom strain nutrient medium |
| CN108076973A (en) * | 2018-01-15 | 2018-05-29 | 石家庄学院 | A kind of production method of mushroom concentrated strain |
| CN108094051A (en) * | 2018-02-08 | 2018-06-01 | 贵州省生物研究所 | A kind of Coriaria sinica mushroom strain culture medium and preparation method thereof and the method for cultivating Coriaria sinica mushroom |
| CN112655462A (en) * | 2020-12-18 | 2021-04-16 | 廊坊师范学院 | Mushroom reduction strain and preparation and application thereof |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102715014A (en) * | 2012-06-25 | 2012-10-10 | 浙江常山荣昇食用菌有限公司 | Preparation method for liquefied strain of edible mushroom |
| CN102972205A (en) * | 2012-12-10 | 2013-03-20 | 杨凌芝君生物科技有限责任公司 | Liquefying method and use method of solid strains of edible fungi and medicinal fungi |
-
2015
- 2015-01-20 CN CN201510028938.9A patent/CN104557211B/en active Active
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102715014A (en) * | 2012-06-25 | 2012-10-10 | 浙江常山荣昇食用菌有限公司 | Preparation method for liquefied strain of edible mushroom |
| CN102972205A (en) * | 2012-12-10 | 2013-03-20 | 杨凌芝君生物科技有限责任公司 | Liquefying method and use method of solid strains of edible fungi and medicinal fungi |
Non-Patent Citations (1)
| Title |
|---|
| 黄伟等: "《菇菌生态栽培新技术》", 31 January 2013, 中国农业出版社 * |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105399470A (en) * | 2015-11-30 | 2016-03-16 | 全椒县香妃农业专业合作社 | Lentinula edodes strain medium and preparing method thereof |
| CN107771614A (en) * | 2017-12-14 | 2018-03-09 | 全椒县香妃农业专业合作社 | A kind of mushroom strain nutrient medium |
| CN108076973A (en) * | 2018-01-15 | 2018-05-29 | 石家庄学院 | A kind of production method of mushroom concentrated strain |
| CN108094051A (en) * | 2018-02-08 | 2018-06-01 | 贵州省生物研究所 | A kind of Coriaria sinica mushroom strain culture medium and preparation method thereof and the method for cultivating Coriaria sinica mushroom |
| CN112655462A (en) * | 2020-12-18 | 2021-04-16 | 廊坊师范学院 | Mushroom reduction strain and preparation and application thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| CN104557211B (en) | 2017-11-07 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN104557211B (en) | Mushroom liquefaction special bacteria culture medium and corresponding cultivation | |
| CN106613355A (en) | Ecological planting method of oyster mushrooms | |
| CN104928202A (en) | Fermentation culture method of bacillus | |
| CN104651239A (en) | Strain for promoting germination and seedling formation of Dendrobium devonianum seed and application thereof | |
| CN102154194B (en) | Preparation method for high-yield chlamydospore liquid fermentation from trichoderma on pilot plant test scale | |
| CN104541975A (en) | Rapid preparation method and use method of hypsizigus marmoreus liquid strains | |
| CN101717309B (en) | Culture medium for straw rotting edible fungi solid strain and method for preparing solid strain | |
| CN104541983B (en) | Seafood mushroom liquefaction special bacteria culture medium and corresponding cultivation | |
| CN104557315B (en) | Elegant precious mushroom liquefaction special bacteria culture medium and corresponding cultivation | |
| CN106676018B (en) | Agaricus bisporus strain breeding method suitable for standardized factory | |
| CN104620852B (en) | Mushroom class liquefaction Spawn incubation method | |
| CN103131652B (en) | Rhizobium japonicum culture medium and method for preparing liquid rhizobium japonicum agent by adopting rhizobium japonicum culture medium | |
| CN103952332A (en) | Bacillus amyloliquefaciens ZH1 and its application | |
| Kuek | Shake-flask culture of Laccaria laccata, an ectomycorrhizal basidiomycete | |
| CN104557209B (en) | Pleurotus eryngii liquefaction special bacteria culture medium and corresponding cultivation | |
| CN1944625B (en) | Coterpillar fungus hypha cultivating method of rice solid fermenting for caterpillar fungus drink | |
| CN105219676A (en) | A kind of cultural method of bacillus laterosporus | |
| CN104557210B (en) | Asparagus liquefaction special bacteria culture medium and corresponding cultivation | |
| CN1952108A (en) | Long term storage method for large-size fungus species | |
| CN104277977B (en) | A kind of preparation method of aspergillus niger spore suspension and the storage method of aspergillus niger spore | |
| CN103340090B (en) | Method for culturing agaricus bisporus kernel microbial strain, namely, kernel cultivated specie, by using white soil as filter layer | |
| CN106399123B (en) | Method for quickly producing seeds of edible fungi | |
| CN105272406A (en) | Microbial fertilizer prepared by bacillus laterosporus and preparation method of microbial fertilizer | |
| CN101099435A (en) | Industrial cultivation method for Gloeostereum incarnatum S. Ito et Imai | |
| CN1952109A (en) | Short term storage method for large-size fungus species |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| GR01 | Patent grant | ||
| GR01 | Patent grant |