CN1685796A - Method of raising cordyceps production stability - Google Patents
Method of raising cordyceps production stability Download PDFInfo
- Publication number
- CN1685796A CN1685796A CN 200510034376 CN200510034376A CN1685796A CN 1685796 A CN1685796 A CN 1685796A CN 200510034376 CN200510034376 CN 200510034376 CN 200510034376 A CN200510034376 A CN 200510034376A CN 1685796 A CN1685796 A CN 1685796A
- Authority
- CN
- China
- Prior art keywords
- days
- suspension
- dark
- inoculated
- sampling
- 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
Landscapes
- Mushroom Cultivation (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Abstract
A method for increasing the production stability of cordyceps includes preculturing in the culture liquid, inoculating from a test tube to 5-8 bottles of suspension, further inoculating from one bottle to 100 bottles, and secondary preculturing. Its advantages are short period and high quality stability.
Description
Technical field
The present invention relates to a kind of method that improves cordyceps production stability.
Background technology
The worm summer in winter, worm was a kind of extremely precious medical, edible fungi, in recent years, along with improving constantly of people's living standard, health care the reach of science and to the continuous expansion in Chinese caterpillar fungus understanding field, the medicine, health food, beverage, the cosmetic development that with the Chinese caterpillar fungus are primary raw material emerge in an endless stream, not only the domestic market enlarges day by day to the demand of grass-and-insect painting, and the demand of international markets such as Southeast Asia, Japan, the U.S. is also in continuous increase.Because the wild Chinese caterpillar fungus resource is very rare, excavate difficultly, usually occur that supply falls short of demand, price rises steadily, soaring, made the multiplication of Chinese caterpillar fungus price, and immoderate excavating both caused the exhaustion that is close to of wild resource, caused the destruction to natural ecological environment again.Therefore, Cordyceps militaris has been subjected to extensive concern both domestic and external as unique substitute that can replace wild worm summer in winter worm.
At present, the artificial culture technology of fruiting bodies of cordyceps militaris is succeedd, the market development promise well, but fruiting bodies of cordyceps militaris is cultivated complex procedures, realizes the restraining factors that also exist some can not be ignored in scale and the industrialization production process.General method of cultivating Cordyceps militaris is: select excellent species for use, scrape the mycelium of getting chamfered surface, be inoculated in the liquid nutrient medium, suspension culture obtained liquid spawn about 4 days.Liquid-spawn inoculation to rice medium, is alternately cultivated through illumination-dark, gathered after the maturation.General cultural method, a test tube strains can only be inoculated 5-8 bottle liquid spawn.And general cultural method is not taken a sample and is planted experimentally, and has both made the increase sampling plant experimentally link, can only take a sample on test tube yet, and effect is relatively poor.General cultural method, Cordyceps militaris spawn on rice medium, the early stage growth be nourish and grow and reproductive growth carry out simultaneously, mycelia needs just can cover with rice medium about 10-15 days, and in the same culture vessel, the growth of fruit body has early to be had late, adds the competition of growing space and nutrition, must cause when gathering some old excessively, some is too tender, be difficult to hold collecting time, the more sturdy hypertrophy of the fruit body that grows earlier, after the fruit body that grows more very thin small and weak.Influence outward appearance and the quality of Cordyceps militaris.
Summary of the invention:
The purpose of this invention is to provide a kind of output and quality stability that can guarantee Cordyceps militaris, can shorten the method for the raising cordyceps production stability of growth cycle again.The present invention introduces secondary and cultivates in advance, cultivates in advance for the first time and carries out in liquid.Because suspension has very strong homogeneity, therefrom sampling has better representativeness.Sampling is planted experimentally, and can further confirm the productivity of bacterial classification, guarantees the stability of producing.Pre-for the second time the cultivation carried out in the dark condition of pre-incubation chamber, when cordyceps species is cultivated in dark surrounds, only to nourish and grow, 3-4 days time can be covered with medium, transfer to subsequently in the culturing room after the continuous illumination 3 days, mycelium changes reproductive growth simultaneously over to, thus the cordyceps militaris sporocarp synchronous growth in the culture vessel, the maturity unanimity, thickness, length homogeneous in appearance, can timely collecting, both shortened the incubation growth cycle of Chinese caterpillar fungus, guarantee the stability of product quality again.
The objective of the invention is to realize: select excellent species (test tube kind) for use by following approach, introduce the pre-stability of producing of cultivating of secondary with the raising Cordyceps militaris, concrete steps are: a, scrape the mycelium of getting chamfered surface, be inoculated in the liquid nutrient medium, suspension culture 2~3 days, introduce pre-for the first time the cultivation, when cultivating in advance, 1 test tube strains can be inoculated 5-8 bottle suspension.B, suspension sampled plant experimentally, all the other are put in the 3-5 ℃ of refrigerator and preserve.Must put into refrigerator after the sampling, the time of preserving in refrigerator preferably is no more than 60 days at once.After c, the affirmation bacterial classification productivity, the taking-up sampling is planted experimentally the suspension of acting normally and is inoculated, and eliminates other suspension.Get suspension 1.5-2ml during inoculation and be inoculated in the liquid nutrient medium, suspension culture 4 days obtains liquid spawn.Every bottle of switchable 100 bottles of liquid spawns of suspension.D, with liquid-spawn inoculation to rice medium, under the dark condition of pre-incubation chamber, carry out the second time and pre-cultivate dark culturing 3-4 days.E, transfer in the culturing room continuous illumination 3 days, make daylight every day afterwards, the alternately cultivation of dark each illumination-dark of 12 hours in evening, incubation time 40-45 days.According to routine, culturing room's temperature is 18-20 ℃, and humidity is about 80%, and intensity of illumination is controlled at the 1000-5000 lux.Gather after the maturation.
The present invention not only can strengthen the production capacity of excellent species greatly; reduce production costs; improve the output of cordyceps militaris sporocarp; promote scale and the industrialization production of Chinese caterpillar fungus; and because suspension has very strong homogeneity, therefrom sampling has better representativeness, and sampling is planted experimentally; can further confirm the productivity of bacterial classification, guarantee the stability of producing.In for the second time pre-incubation, cordyceps species is is only nourished and grown in dark surrounds, mycelium changes reproductive growth simultaneously over to subsequently, therefore the fruit body synchronous growth in the culture vessel, the maturity unanimity, thickness, length are even in appearance, but timely collecting, both shorten the grown cultures cycle of Chinese caterpillar fungus, guaranteed the stability of product quality again.Simultaneously in for the second time pre-incubation, culture vessel can be concentrated stacking, takes up room, the place is few, can improve the factory building availability.
Embodiment
The method of raising cordyceps production stability of the present invention is selected excellent species (in the test tube) for use, introduces secondary and cultivates in advance, improves the stability of Cordyceps militaris growth, and its concrete steps are:
A, scrape the mycelium of getting chamfered surface, be inoculated in the liquid nutrient medium, suspension culture 2~3 days is introduced pre-for the first time the cultivation, and 1 test tube strains can be inoculated 5-8 bottle suspension.
B, sampling are planted experimentally, and all the other are put in the 3-5 ℃ of refrigerator and preserve.Must put into refrigerator after the sampling, the time of preserving in refrigerator preferably is no more than 60 days at once.
After c, the affirmation bacterial classification productivity, the taking-up sampling is planted experimentally the suspension of acting normally and is inoculated, and eliminates other suspension.Get suspension 1.5-2ml during inoculation and be inoculated in the liquid nutrient medium, suspension culture 4 days obtains liquid spawn.Every bottle of switchable 100 bottles of liquid spawns of suspension.
D, with liquid-spawn inoculation to rice medium, under the dark condition of pre-incubation chamber, carry out the second time and pre-cultivate dark culturing 3-4 days.
E, transfer in the culturing room after the continuous illumination 3 days, do daylight every day, the alternately cultivation of dark each illumination-dark of 12 hours in evening, incubation time 40-45 days, culturing room's temperature was 18-20 ℃, humidity is about 80%, and intensity of illumination is controlled at the 1000-5000 lux.Gather after the maturation.
The medium of suspension culture and condition of culture are prior art among the present invention.
Wherein the condition of suspension culture among step a, the c is: dark, 18-20 ℃, 120 rev/mins.Its medium is: in every liter of potato glucose liquid nutrient medium, add potassium dihydrogen phosphate 1 gram, and magnesium sulfate 0.5 gram, hairtail peptone 2.5 grams, pH value transfers to 6.2, autoclaving 15 minutes.
Wherein the composition of rice medium is: be made up of Jiangsu rice and nutrient solution, 25 gram rice mixed the back autoclaving 30 minutes with the 35ml nutrient solution.Phosphoric acid potassium dihydrogen 2 grams per liters in the nutrient solution, magnesium sulfate 1 grams per liter, hairtail peptone 3 grams per liters, pH value transfers to 7.0.
Claims (3)
1, a kind of method that improves cordyceps production stability is characterized in that: select excellent species for use, introduce secondary and cultivate in advance, improve the stability that Cordyceps militaris produces, concrete steps are:
A, scrape the mycelium of getting chamfered surface, be inoculated in the liquid nutrient medium suspension culture 2~3 days;
B, suspension sampled plant experimentally, all the other are put into 3-5 ℃ of refrigerator and preserve;
After c, the affirmation bacterial classification productivity, the taking-up sampling is planted experimentally the suspension of acting normally and is inoculated, and eliminates other suspension.Get suspension 1.5-2ml during inoculation and be inoculated in the liquid nutrient medium, suspension culture 4 days obtains liquid spawn;
D, with liquid-spawn inoculation to rice medium, in pre-incubation chamber, cultivated under the dark condition 3-4 days;
E, transferred to culturing room's continuous illumination 3 days, make illumination-dark afterwards and alternately cultivate, gather after the maturation.
2, the method for raising cordyceps production stability according to claim 1 is characterized in that: when sampling is planted experimentally, must put into refrigerator after the sampling, the time of preserving in refrigerator is no more than 60 days at once.
3, the method for raising cordyceps production stability according to claim 1 is characterized in that: illumination-dark alternately cultivate be every day daylight, evening dark culturing each hocketed in 12 hours, incubation time is 40~45 days.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB2005100343765A CN100348713C (en) | 2005-04-29 | 2005-04-29 | Method of raising cordyceps production stability |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB2005100343765A CN100348713C (en) | 2005-04-29 | 2005-04-29 | Method of raising cordyceps production stability |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1685796A true CN1685796A (en) | 2005-10-26 |
CN100348713C CN100348713C (en) | 2007-11-14 |
Family
ID=35303838
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNB2005100343765A Expired - Fee Related CN100348713C (en) | 2005-04-29 | 2005-04-29 | Method of raising cordyceps production stability |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN100348713C (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1944625B (en) * | 2006-10-30 | 2010-05-12 | 刘桢鋆 | Coterpillar fungus hypha cultivating method of rice solid fermenting for caterpillar fungus drink |
CN102870600A (en) * | 2012-10-17 | 2013-01-16 | 山西万海澳生物科技有限责任公司 | Cordyceps militaris fruit body cultivation technology for stabilizing cordycepin content |
CN105875198A (en) * | 2016-04-29 | 2016-08-24 | 安发(福建)生物科技有限公司 | Culture method for improving stability of cordyceps militaris strain |
CN110663455A (en) * | 2019-10-22 | 2020-01-10 | 安发(福建)生物科技有限公司 | Cordyceps militaris cultivation inoculation method |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1095104A (en) * | 1993-05-13 | 1994-11-16 | 刘文霞 | Cordyccps-militaris-(L.)-link. Sporophore and mycelium batch production production technology |
CN1200403A (en) * | 1997-05-07 | 1998-12-02 | 李春燕 | High yield cultivating method for cordyceps |
-
2005
- 2005-04-29 CN CNB2005100343765A patent/CN100348713C/en not_active Expired - Fee Related
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1944625B (en) * | 2006-10-30 | 2010-05-12 | 刘桢鋆 | Coterpillar fungus hypha cultivating method of rice solid fermenting for caterpillar fungus drink |
CN102870600A (en) * | 2012-10-17 | 2013-01-16 | 山西万海澳生物科技有限责任公司 | Cordyceps militaris fruit body cultivation technology for stabilizing cordycepin content |
CN105875198A (en) * | 2016-04-29 | 2016-08-24 | 安发(福建)生物科技有限公司 | Culture method for improving stability of cordyceps militaris strain |
CN105875198B (en) * | 2016-04-29 | 2019-07-23 | 安发(福建)生物科技有限公司 | A kind of cultural method improving Cordyceps militaris spawn stability |
CN110663455A (en) * | 2019-10-22 | 2020-01-10 | 安发(福建)生物科技有限公司 | Cordyceps militaris cultivation inoculation method |
Also Published As
Publication number | Publication date |
---|---|
CN100348713C (en) | 2007-11-14 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN103125275B (en) | Cultivation method of cordyceps militaris | |
CN110073897A (en) | A kind of hypsizigus marmoreus in factory cultivation strain and its cultural method | |
CN102037856B (en) | Simple cordyceps militaris strain rejuvenation method | |
CN103270887B (en) | Silkworm chrysalis northern Chinese caterpillar Fungus industrial cultivation technique | |
CN108676730A (en) | A kind of fermentation manufacturing technique of Paecilomyces hepiali chen Cs-4 | |
CN101897270A (en) | Production technology of Cordyceps sinensis mycelium | |
CN105543104A (en) | Optimization method of solid culture medium for artificial acclimation and cultivation of wild Isaria cicadae Miquel | |
AU2020103076A4 (en) | Method of preparing Lepista sordida culture spawn with mushroom residue | |
CN115039639B (en) | Tremella liquid strain short-period production method and application of tremella liquid strain | |
CN101045904A (en) | Aweto sporophore culturing process | |
CN110367047A (en) | A kind of Dictyophora rubrovalvata test tube stock culture medium and its application | |
CN110352797A (en) | A kind of fermentation process of high activity pleurotus eryngii liquid strain | |
CN111248026B (en) | Quercus matsutake culture medium and application thereof | |
CN110249912A (en) | A kind of method that Phellinus industrial bottle is planted | |
CN109526552A (en) | A kind of sclerotium industrial planting method of hickory chick | |
CN103571756A (en) | Test tube screening method of isaria cicadae strain and culture medium | |
CN100348713C (en) | Method of raising cordyceps production stability | |
CN106278466B (en) | A kind of agrocybe cultivation matrix and its preparation and cultural method | |
CN106922392A (en) | A kind of compost of selenium-rich pleurotus cornucopiae and the cultural method of selenium-rich pleurotus cornucopiae | |
CN105483014A (en) | Production technology for high-density culture of chlorella by utilizing fermentation method | |
CN110713956B (en) | Lysine bacillus S12 and application thereof | |
CN105296360B (en) | Phellinus parent species tissue detaches tube breeding method | |
CN116472916A (en) | Method for obtaining golden fungus fruiting body by mixed strain | |
CN115725419B (en) | Phosphorus-dissolving blueberry endophytic trichoderma and application thereof | |
CN110218657A (en) | One plant of long shoot trichoderma MD30 and its biological organic fertilizer of development |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20071114 Termination date: 20150429 |
|
EXPY | Termination of patent right or utility model |