CN103340093A - Artificial cultivation method for phellinus linteus - Google Patents
Artificial cultivation method for phellinus linteus Download PDFInfo
- Publication number
- CN103340093A CN103340093A CN2013102522552A CN201310252255A CN103340093A CN 103340093 A CN103340093 A CN 103340093A CN 2013102522552 A CN2013102522552 A CN 2013102522552A CN 201310252255 A CN201310252255 A CN 201310252255A CN 103340093 A CN103340093 A CN 103340093A
- Authority
- CN
- China
- Prior art keywords
- cultivation
- bag
- phellinus
- yellow
- phellinus linteus
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Landscapes
- Mushroom Cultivation (AREA)
- Cultivation Of Plants (AREA)
Abstract
The invention relates to an artificial cultivation method for phellinus linteus. Artificial domestication cultivation research of the phellinus linteus newly starts in China, a few exploration tests are conducted in parts of areas, and the problems such as sporocarp is low in productivity and poor in quality (unshaped) exist mainly due to the fact that cultivation techniques are immature. The artificial cultivation method for the phellinus linteus comprises the steps that phellinus linteus strains are activated, 0.3 square centimeter stain blocks are taken on the aseptic condition to be inoculated to phellinus linteus cultivation culture media in cultivation bags, the stain blocks are cultivated at constant temperature being 28 DEG C without light until mycelia grow all over the cultivation bags, and cultispecies are obtained; when the mycelia in the cultivation bags are yellow or have protuberant nodular primordia, the cultivation bags are moved out of yellow areas, and semi-bag-off soil-cast yellow-out cultivation is conducted. According to the artificial cultivation method for the phellinus linteus, mulberry fields are used for phellinus linteus cultivation, and growing conditions of generation, differentiation and development of wild phellinus linteus sporocarps are imitated in nature. The phellinus linteus is high in productivity, good in quality (similar to wild phellinus linteus in shape), short in growth cycle, simple in cultivation mode, and capable of being cultivated in large scale.
Description
Technical field
The invention belongs to medicinal fungi artificial cultivation technique field, be specifically related to a kind of method of artificial cultivation Phellinus.
Background technology
Phellinus [
Phellinus igniarius(L.ex. Fr.) Quel]; have another name called Sang Chen, mulberry ear, white heart-rot fungus, Phellinus mushroom etc.; belong to Basidiomycotina (Basidiomycotina), Hymenomycetes (Hymenomycetes), Aphyllophorales (Aphyllophorales), Polyporaceae (Polyporaceae), shelf fungus genus [Fomes (Fr.) Fr.]; be a kind of large-scale medicinal fungi of preciousness, the laudatory title of " forest gold " is arranged." Chinese medicine voluminous dictionary " record, gynecological diseases such as it can control under metrorrhagia, blood pouring, the band, amenorrhoea.Modern medicine study shows that Phellinus has antitumor, antibiotic, anti-fibrosis, anti-oxidant and improve remarkable result such as body immunity; be the rare medicinal fungi of present internationally recognized biological antitumous effect first, be widely used in industries such as medicine, food, daily-use chemical industry, health products.
In recent years; because domestic and international market increases the Phellinus demand; cause the excessive exploitation of wild Phellinus to stop; be subjected to the restriction of particularity and complexity and the external condition of its physiological ecological again, it is very rare to cause natural world to form fruit body, wild natural Phellinus scarcity of resources; face exhaustion; the artificial domesticating cultivation difficulty of adding Phellinus is bigger, is difficult to form stable medical industry rule of origin, has limited the development of Phellinus industry greatly.
At present; domestic research to Phellinus mainly concentrates on the aspects such as extraction of relevant its protection of resources, chemical composition, medical mechanism, strain improvement, liquid fermentation technology, effective ingredient; and it is at the early-stage to artificial domesticating cultivation research; there is groping property test on a small quantity some areas; also have and cultivate successfully; but all because culture technique is not mature enough, exist fruiting body yield low, problems such as (shapeless) of poor quality mostly.
Summary of the invention
The method that the purpose of this invention is to provide a kind of artificial cultivation Phellinus, it is low to overcome in the existing Phellinus culture technique ubiquitous fruiting body yield, problems such as (shapeless) of poor quality.
The technical solution adopted in the present invention is:
A kind of method of artificial cultivation Phellinus is characterized in that:
Realized by following steps:
Step 1: after the Phellinus bacterial classification activated, under aseptic condition, get 0.3 cm
2The bacterial classification piece is inoculated on the interior Phellinus culture medium for cultivating of cultivation bag, and 28 ℃ of lucifuges of constant temperature are cultured to mycelia and cover with bacterium bag acquisition cultivated species;
Step 2: when treating warty original hase that mycelia in the cultivation bag begins to present yellow or projection occurs, the bacterium bag is moved to out yellow place, partly take off a bag earthing and go out yellow the cultivation: 22 ℃~28 ℃ of cultivation temperature, relative air humidity 85~98%, soil moisture 45~70%, intensity of illumination 100~300lex, 1~7 time/d of ventilation rate, each time 5~25min.
In the step 1, the water content of Phellinus culture medium for cultivating is 60~65%, and the solid phase prescription is:
Mulberry branch wood chips 30~60 weight portions, cotton seed hulls 30~60 weight portions, wheat bran 15~25 weight portions, white sugar 0.5~2 weight portion, gypsum 0.5~2 weight portion;
The concrete configuration method is: mulberry branch is pulverized with timber be machined to the wood chip that granularity is 0.5~2mm earlier; Again by culture medium prescription take by weighing white sugar, the gypsum water dissolves; Continue to take by weighing mulberry branch wood chips, cotton seed hulls, wheat bran, add and dissolve the good abundant mixing of white sugar, gypsum, and keep the skin wet, make the composts or fertilisers of cultivating water content reach 60~65%; With the packed bag of the polyethylene bacterium of 17cm * 33cm * 0.05cm, every packed wet feed 1kg, sack sleeving plastic ring seals with two-layer newspaper, layer of polyethylene plastic paper, puts into the high-pressure sterilizing pot sterilization, at pressure 1.0~1.5kg/cm
2, 121~126 ℃ of temperature, time 120min takes out and is cooled to room temperature, moves into and prepares inoculation between inoculation.
In the step 2, go out be chosen in the age of tree 3~5 years, tree spacing 2m, physical features, yellow place lower, not ponding, ventilates, the mulberry field at close water source; The cleaning ground weeds in mulberry field and fallen leaves are organized into the furrow that width is 1m before the cultivation; When outdoor minimum temperature exceeds 20 ℃, enter out yellow management, select to go out at the beginning of 6 months by the end of May yellow row's bag.
Described row's bag method is: move to out yellow place after the bacterium bag mycelia maturation, the 4.5cm place opens a meniscate osculum with scalpel, opening length 8cm from bacterium bag bottom; With sack plastic foil girdling to 1/3 place, take off the bag end following, earthing is to leaving a mouthful 6cm place; The bacterium bag discharges at interval, and bag spacing 10cm fills up soil between bag and the bag; Build the little shed that 1.2m is wide, 1m is high at furrow, covered with plastic film on the shed covers one deck grass felt again; The shed both sides are real with soil pressure, and air regulator is opened at the canopy two ends, is beneficial to the control of temp. and humidity; Ditch is opened on the canopy both sides, is used for pouring water and draining.
The present invention has the following advantages:
The present invention plants Phellinus with adopting the mulberry field; simulate the growth conditions that wild Phellinus fruit body takes place, breaks up and grow at occurring in nature; compare that the Phellinus fruit body that traditional Phellinus cultivation method produces has output height, quality good (the wild Phellinus of shape approximation), growth cycle is short and advantage such as cultivation mode is simple, but large-scale planting.
Embodiment
The present invention will be described in detail below in conjunction with embodiment.
The method of a kind of artificial cultivation Phellinus of the present invention, realized by following steps:
Step 1: after the Phellinus bacterial classification activated, under aseptic condition, get 0.3cm
2The bacterial classification piece is inoculated on the interior Phellinus culture medium for cultivating of cultivation bag, and 28 ℃ of lucifuges of constant temperature are cultured to mycelia and cover with bacterium bag acquisition cultivated species.
The water content of Phellinus culture medium for cultivating is 60~65%, and the solid phase prescription is: mulberry branch wood chips 30~60 weight portions, cotton seed hulls 30~60 weight portions, wheat bran 15~25 weight portions, white sugar 0.5~2 weight portion, gypsum 0.5~2 weight portion.The concrete configuration method is: mulberry branch is pulverized with timber be machined to the wood chip that granularity is 0.5~2mm earlier; Again by culture medium prescription take by weighing white sugar, the gypsum water dissolves; Continue to take by weighing mulberry branch wood chips, cotton seed hulls, wheat bran, add and dissolve the good abundant mixing of white sugar, gypsum, and keep the skin wet; With the packed bag of the polyethylene bacterium of 17cm * 33cm * 0.05cm, every packed wet feed 1kg, sack sleeving plastic ring seals with two-layer newspaper, layer of polyethylene plastic paper, puts into the high-pressure sterilizing pot sterilization, at pressure 1.0~1.5kg/cm
2, 121~126 ℃ of temperature, time 120min takes out and is cooled to room temperature, moves into and prepares inoculation between inoculation.
Step 2: when treating warty original hase that mycelia in the cultivation bag begins to present yellow or projection occurs, the bacterium bag is moved to out yellow place, partly take off a bag earthing and go out yellow the cultivation: 22 ℃~28 ℃ of cultivation temperature, relative air humidity 85~98%, soil moisture 45~70%, intensity of illumination 100~300lex, 1~7 time/d of ventilation rate, each time 5~25min.
Go out be chosen in the age of tree 3~5 years, tree spacing 2m, physical features, yellow place lower, not ponding, ventilates, the mulberry field at close water source; The cleaning ground weeds in mulberry field and fallen leaves are organized into the furrow that width is 1m before the cultivation; When outdoor minimum temperature exceeds 20 ℃, enter out yellow management, select to go out at the beginning of 6 months by the end of May yellow row's bag.Row's bag method is: move to out yellow place after the bacterium bag mycelia maturation, the 4.5cm place opens a meniscate osculum with scalpel, opening length 8cm from bacterium bag bottom; With sack plastic foil girdling to 1/3 place, take off the bag end following, earthing is to leaving a mouthful 6cm place; The bacterium bag discharges at interval, and bag spacing 10cm fills up soil between bag and the bag; Build the little shed that 1.2m is wide, 1m is high at furrow, covered with plastic film on the shed covers one deck grass felt again; The shed both sides are real with soil pressure, and air regulator is opened at the canopy two ends, is beneficial to the control of temp. and humidity; Ditch is opened on the canopy both sides, is used for pouring water and draining.
Embodiment 1:
Step 1: after the Phellinus bacterial classification activated, under aseptic condition, get 0.3cm
2The bacterial classification piece is inoculated on the interior Phellinus culture medium for cultivating of cultivation bag, and 28 ℃ of lucifuges of constant temperature are cultivated, and 50d left and right sides mycelia is covered with the bacterium bag and obtains cultivated species.
The water content of Phellinus culture medium for cultivating is 60%, and the solid phase prescription is: mulberry branch wood chips 30 weight portions, cotton seed hulls 60 weight portions, wheat bran 25 weight portions, white sugar 2 weight portions, gypsum 2 weight portions.The concrete configuration method is: mulberry branch is pulverized with timber be machined to the wood chip that granularity is 0.5~2mm earlier; Again by culture medium prescription take by weighing white sugar, the gypsum water dissolves; Continue to take by weighing mulberry branch wood chips, cotton seed hulls, wheat bran, add and dissolve the good abundant mixing of white sugar, gypsum, and keep the skin wet; With the packed bag of the polyethylene bacterium of 17cm * 33cm * 0.05cm, every packed wet feed 1kg, sack sleeving plastic ring seals with two-layer newspaper, layer of polyethylene plastic paper, puts into the high-pressure sterilizing pot sterilization, at pressure 1.0kg/cm
2, 121 ℃ of temperature, time 120min takes out and is cooled to room temperature, moves into and prepares inoculation between inoculation.
Step 2: when treating warty original hase that mycelia in the cultivation bag begins to present yellow or projection occurs, the bacterium bag is moved to out yellow place, partly take off a bag earthing and go out yellow the cultivation: 22 ℃ of cultivation temperature, relative air humidity 85%, soil moisture 45%, intensity of illumination 100lex, 1 time/d of ventilation rate, each time 25min.
Go out be chosen in the age of tree 3~5 years, tree spacing 2m, physical features, yellow place lower, not ponding, ventilates, the mulberry field at close water source; The cleaning ground weeds in mulberry field and fallen leaves are organized into the furrow that width is 1m before the cultivation; When outdoor minimum temperature exceeds 20 ℃, enter out yellow management, select to go out at the beginning of 6 months by the end of May yellow row's bag.Row's bag method is: move to out yellow place after the bacterium bag mycelia maturation, the 4.5cm place opens a meniscate osculum with scalpel, opening length 8cm from bacterium bag bottom; With sack plastic foil girdling to 1/3 place, take off the bag end following, earthing is to leaving a mouthful 6cm place; The bacterium bag discharges at interval, and bag spacing 10cm fills up soil between bag and the bag; Build the little shed that 1.2m is wide, 1m is high at furrow, covered with plastic film on the shed covers one deck grass felt again; The shed both sides are real with soil pressure, and air regulator is opened at the canopy two ends, is beneficial to the control of temp. and humidity; Ditch is opened on the canopy both sides, is used for pouring water and draining.
The Phellinus sporophore growth is very fast and quality good, approximate wild Phellinus, and the fruit-body color foresythia mostly is the shape of a hoof to yellowish-brown, and quality is hard, and every bag can be produced Phellinus fruit body dry product 35g.
Embodiment 2:
Step 1: after the Phellinus bacterial classification activated, under aseptic condition, get 0.3cm
2The bacterial classification piece is inoculated on the interior Phellinus culture medium for cultivating of cultivation bag, and 28 ℃ of lucifuges of constant temperature are cultivated, and 50d left and right sides mycelia is covered with the bacterium bag and obtains cultivated species.
The water content of Phellinus culture medium for cultivating is 62%, and the solid phase prescription is: mulberry branch wood chips 45 weight portions, cotton seed hulls 45 weight portions, wheat bran 20 weight portions, white sugar 1 weight portion, gypsum 1 weight portion.The concrete configuration method is: mulberry branch is pulverized with timber be machined to the wood chip that granularity is 0.5~2mm earlier; Again by culture medium prescription take by weighing white sugar, the gypsum water dissolves; Continue to take by weighing mulberry branch wood chips, cotton seed hulls, wheat bran, add and dissolve the good abundant mixing of white sugar, gypsum, and keep the skin wet; With the packed bag of the polyethylene bacterium of 17cm * 33cm * 0.05cm, every packed wet feed 1kg, sack sleeving plastic ring seals with two-layer newspaper, layer of polyethylene plastic paper, puts into the high-pressure sterilizing pot sterilization, at pressure 1.0kg/cm
2, 123 ℃ of temperature, time 120min takes out and is cooled to room temperature, moves into and prepares inoculation between inoculation.
Step 2: when treating warty original hase that mycelia in the cultivation bag begins to present yellow or projection occurs, the bacterium bag is moved to out yellow place, partly take off a bag earthing and go out yellow the cultivation: 25 ℃ of cultivation temperature, relative air humidity 91%, soil moisture 57%, intensity of illumination 200lex, 4 times/d of ventilation rate, each time 15min.
Go out be chosen in the age of tree 3~5 years, tree spacing 2m, physical features, yellow place lower, not ponding, ventilates, the mulberry field at close water source; The cleaning ground weeds in mulberry field and fallen leaves are organized into the furrow that width is 1m before the cultivation; When outdoor minimum temperature exceeds 20 ℃, enter out yellow management, select to go out at the beginning of 6 months by the end of May yellow row's bag.Row's bag method is: move to out yellow place after the bacterium bag mycelia maturation, the 4.5cm place opens a meniscate osculum with scalpel, opening length 8cm from bacterium bag bottom; With sack plastic foil girdling to 1/3 place, take off the bag end following, earthing is to leaving a mouthful 6cm place; The bacterium bag discharges at interval, and bag spacing 10cm fills up soil between bag and the bag; Build the little shed that 1.2m is wide, 1m is high at furrow, covered with plastic film on the shed covers one deck grass felt again; The shed both sides are real with soil pressure, and air regulator is opened at the canopy two ends, is beneficial to the control of temp. and humidity; Ditch is opened on the canopy both sides, is used for pouring water and draining.
The Phellinus sporophore growth is very fast and quality good, approximate wild Phellinus, and the fruit-body color foresythia mostly is the shape of a hoof to yellowish-brown, and quality is hard, and every bag can be produced Phellinus fruit body 36.2g.
Embodiment 3:
Step 1: after the Phellinus bacterial classification activated, under aseptic condition, get 0.3cm
2The bacterial classification piece is inoculated on the interior Phellinus culture medium for cultivating of cultivation bag, and 28 ℃ of lucifuges of constant temperature are cultivated, and 50d left and right sides mycelia is covered with the bacterium bag and obtains cultivated species.
The water content of Phellinus culture medium for cultivating is 65%, and the solid phase prescription is: mulberry branch wood chips 60 weight portions, cotton seed hulls 30 weight portions, wheat bran 15 weight portions, white sugar 0.5 weight portion, gypsum 0.5 weight portion.The concrete configuration method is: mulberry branch is pulverized with timber be machined to the wood chip that granularity is 0.5~2mm earlier; Again by culture medium prescription take by weighing white sugar, the gypsum water dissolves; Continue to take by weighing mulberry branch wood chips, cotton seed hulls, wheat bran, add and dissolve the good abundant mixing of white sugar, gypsum, and keep the skin wet; With the packed bag of the polyethylene bacterium of 17cm * 33cm * 0.05cm, every packed wet feed 1kg, sack sleeving plastic ring seals with two-layer newspaper, layer of polyethylene plastic paper, puts into the high-pressure sterilizing pot sterilization, at pressure 1.5kg/cm
2, 126 ℃ of temperature, time 120min takes out and is cooled to room temperature, moves into and prepares inoculation between inoculation.
Step 2: when treating warty original hase that mycelia in the cultivation bag begins to present yellow or projection occurs, the bacterium bag is moved to out yellow place, partly take off a bag earthing and go out yellow the cultivation: 28 ℃ of cultivation temperature, relative air humidity 98%, soil moisture 70%, intensity of illumination 300lex, 7 times/d of ventilation rate, each time 5min.
Go out be chosen in the age of tree 3~5 years, tree spacing 2m, physical features, yellow place lower, not ponding, ventilates, the mulberry field at close water source; The cleaning ground weeds in mulberry field and fallen leaves are organized into the furrow that width is 1m before the cultivation; When outdoor minimum temperature exceeds 20 ℃, enter out yellow management, select to go out at the beginning of 6 months by the end of May yellow row's bag.Row's bag method is: move to out yellow place after the bacterium bag mycelia maturation, the 4.5cm place opens a meniscate osculum with scalpel, opening length 8cm from bacterium bag bottom; With sack plastic foil girdling to 1/3 place, take off the bag end following, earthing is to leaving a mouthful 6cm place; The bacterium bag discharges at interval, and bag spacing 10cm fills up soil between bag and the bag; Build the little shed that 1.2m is wide, 1m is high at furrow, covered with plastic film on the shed covers one deck grass felt again; The shed both sides are real with soil pressure, and air regulator is opened at the canopy two ends, is beneficial to the control of temp. and humidity; Ditch is opened on the canopy both sides, is used for pouring water and draining.
The Phellinus sporophore growth is very fast and quality good, approximate wild Phellinus, and the fruit-body color foresythia mostly is the shape of a hoof to yellowish-brown, and quality is harder, and every bag can be produced Phellinus fruit body 31.6g.
Comparative experimental example 1
This comparative trial is with the difference of embodiment 1:
Making prescription and the proportioning of making the Phellinus culture medium for cultivating are as follows: mulberry branch wood chips 20%, cotton seed hulls 65%, wheat bran 10%, white sugar 2.5%, gypsum 2.5%, moisture content in medium 60%;
In addition, other every contents are all identical with embodiment 1; Indivedual bacterium bags have black warty original hase to form, but do not break up all the time.
Comparative experimental example 2
This comparative trial is with the difference of embodiment 2:
When treating warty original hase that mycelia in the Phellinus cultivation bag begins to present yellow or projection occurs, the bacterium bag is moved to common edible mushroom room, open a crescent osculum about long 8cm apart from sack 4.5cm place with scalpel, the bacterium bag is erect and to be arranged not that earthing directly enters out yellow management;
In addition, other every contents are all identical with embodiment 2; The dehydration of bacterium bag is more serious, and opening part is withered easily, suppresses the differentiation of Phellinus original hase, and indivedual bacterium bags have the Phellinus fruit body to form, but childlike all the time.
Comparative experimental example 3
This comparative trial is with the difference of embodiment 3:
Control out yellow temperature at 30 ℃, relative air humidity 98%, soil moisture 60%, intensity of illumination 100lex, 8 times/d of ventilation, each 30min;
In addition, other every contents are all identical with embodiment 3; The Phellinus fruit body forms behind the 5d, continues to cultivate 45d and can grow up to the finished product size.The Phellinus sporophore growth is fast but fair, and sporophore growth is irregular, and quality is more loose, lighter weight, and indivedual bacterium bags have living contaminants, and every bag can be produced Phellinus fruit body 19.3g.
It is cited that content of the present invention is not limited to embodiment, and the conversion of any equivalence that those of ordinary skills take technical solution of the present invention by reading specification of the present invention is claim of the present invention and contains.
Claims (4)
1. the method for an artificial cultivation Phellinus is characterized in that:
Realized by following steps:
Step 1: after the Phellinus bacterial classification activated, under aseptic condition, get 0.3 cm
2The bacterial classification piece is inoculated on the interior Phellinus culture medium for cultivating of cultivation bag, and 28 ℃ of lucifuges of constant temperature are cultured to mycelia and cover with bacterium bag acquisition cultivated species;
Step 2: when treating warty original hase that mycelia in the cultivation bag begins to present yellow or projection occurs, the bacterium bag is moved to out yellow place, partly take off a bag earthing and go out yellow the cultivation: 22 ℃~28 ℃ of cultivation temperature, relative air humidity 85~98%, soil moisture 45~70%, intensity of illumination 100~300lex, 1~7 time/d of ventilation rate, each time 5~25min.
2. the method for a kind of artificial cultivation Phellinus according to claim 1 is characterized in that:
In the step 1, the water content of Phellinus culture medium for cultivating is 60~65%, and the solid phase prescription is:
Mulberry branch wood chips 30~60 weight portions, cotton seed hulls 30~60 weight portions, wheat bran 15~25 weight portions, white sugar 0.5~2 weight portion, gypsum 0.5~2 weight portion;
The concrete configuration method is: mulberry branch is pulverized with timber be machined to the wood chip that granularity is 0.5~2mm earlier; Again by culture medium prescription take by weighing white sugar, the gypsum water dissolves; Continue to take by weighing mulberry branch wood chips, cotton seed hulls, wheat bran, add and dissolve the good abundant mixing of white sugar, gypsum, and keep the skin wet, make the composts or fertilisers of cultivating water content reach 60~65%; With the packed bag of the polyethylene bacterium of 17cm * 33cm * 0.05cm, every packed wet feed 1kg, sack sleeving plastic ring seals with two-layer newspaper, layer of polyethylene plastic paper, puts into the high-pressure sterilizing pot sterilization, at pressure 1.0~1.5kg/cm
2, 121~126 ℃ of temperature, time 120min takes out and is cooled to room temperature, moves into and prepares inoculation between inoculation.
3. the method for a kind of artificial cultivation Phellinus according to claim 2 is characterized in that:
In the step 2, go out be chosen in the age of tree 3~5 years, tree spacing 2m, physical features, yellow place lower, not ponding, ventilates, the mulberry field at close water source; The cleaning ground weeds in mulberry field and fallen leaves are organized into the furrow that width is 1m before the cultivation; When outdoor minimum temperature exceeds 20 ℃, enter out yellow management, select to go out at the beginning of 6 months by the end of May yellow row's bag.
4. the method for a kind of artificial cultivation Phellinus according to claim 3 is characterized in that:
Described row's bag method is: move to out yellow place after the bacterium bag mycelia maturation, the 4.5cm place opens a meniscate osculum with scalpel, opening length 8cm from bacterium bag bottom; With sack plastic foil girdling to 1/3 place, take off the bag end following, earthing is to leaving a mouthful 6cm place; The bacterium bag discharges at interval, and bag spacing 10cm fills up soil between bag and the bag; Build the little shed that 1.2m is wide, 1m is high at furrow, covered with plastic film on the shed covers one deck grass felt again; The shed both sides are real with soil pressure, and air regulator is opened at the canopy two ends, is beneficial to the control of temp. and humidity; Ditch is opened on the canopy both sides, is used for pouring water and draining.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2013102522552A CN103340093A (en) | 2013-06-24 | 2013-06-24 | Artificial cultivation method for phellinus linteus |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2013102522552A CN103340093A (en) | 2013-06-24 | 2013-06-24 | Artificial cultivation method for phellinus linteus |
Publications (1)
Publication Number | Publication Date |
---|---|
CN103340093A true CN103340093A (en) | 2013-10-09 |
Family
ID=49274964
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN2013102522552A Pending CN103340093A (en) | 2013-06-24 | 2013-06-24 | Artificial cultivation method for phellinus linteus |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN103340093A (en) |
Cited By (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103493685A (en) * | 2013-10-14 | 2014-01-08 | 贵州省施秉县民生天麻科技有限公司 | Method for cultivating phellinus igniarius by using wild living tree stumps |
CN103563653A (en) * | 2013-11-14 | 2014-02-12 | 江苏瑞光生物科技有限公司 | Method for bottle cultivation of pleurotus cornucopiae |
CN103598010A (en) * | 2013-11-12 | 2014-02-26 | 淳安县微生物研究所 | Original ecological imitative wild cultivation method for inonotus sanghuang |
CN103749151A (en) * | 2013-12-26 | 2014-04-30 | 广东省微生物研究所 | Artificial cultivation method of Amauroderma rude |
CN103931420A (en) * | 2014-03-20 | 2014-07-23 | 杭州市农业科学研究院 | Method for cultivating phellinus igniarius |
CN104247628A (en) * | 2014-09-26 | 2014-12-31 | 陕西省微生物研究所 | Cultivation medium and cultivation method for artificially-cultivated phellinus igniarius |
CN104381009A (en) * | 2014-09-18 | 2015-03-04 | 杭州千岛湖桑之宝农业开发有限公司 | Artificial bag cultivation process for Phellinus igniarius |
CN104871821A (en) * | 2015-06-01 | 2015-09-02 | 四川省农业科学院土壤肥料研究所 | Phellinus igniarius strain and culturing method for same |
CN105027974A (en) * | 2015-07-22 | 2015-11-11 | 四川晟旦生物科技有限公司 | Large-scale artificial cultivation method for phellinus igniarius |
CN103695322B (en) * | 2013-12-26 | 2016-05-04 | 上林县明山菌业有限责任公司 | Be rich in phellinus igniarius mycelium product and the production method thereof of bioactive ingredients |
CN105660183A (en) * | 2016-01-29 | 2016-06-15 | 吉林省三盛农业开发集团有限公司 | Phellinus igniarius cultivation method |
CN105724049A (en) * | 2016-01-27 | 2016-07-06 | 浙江省农业科学院 | Mulberry parasitical phellinus strain wild environment returning rejuvenation culture method |
CN105993593A (en) * | 2016-05-23 | 2016-10-12 | 浙江省农业科学院 | High-efficiency industrial bag material cultivation process of inonotus linteus with antitumor activity |
CN106941928A (en) * | 2017-03-02 | 2017-07-14 | 江苏道诚生物科技有限公司 | A kind of implantation methods of Phellinus |
CN107094499A (en) * | 2017-06-14 | 2017-08-29 | 成都新柯力化工科技有限公司 | A kind of utilization tanimoto powder is the method for the stable cultivation Phellinus of culture medium |
CN107996288A (en) * | 2017-12-29 | 2018-05-08 | 浙江省林业科学研究院 | A kind of method that hayashishita imitates Wild ecological cultivation Phellinus |
CN108450231A (en) * | 2018-03-16 | 2018-08-28 | 江西省蚕桑茶叶研究所 | A kind of bionical border expanding propagation method of wild Phellinus |
CN109220526A (en) * | 2018-10-12 | 2019-01-18 | 绩溪县徽菜宝生物科技有限公司 | A kind of Phellinus large-scale planting method |
CN109618816A (en) * | 2018-12-08 | 2019-04-16 | 信阳市菌福康生物科技有限公司 | A kind of idle room plantation Phellinus technology in rural area |
CN109832093A (en) * | 2019-03-14 | 2019-06-04 | 湖北省农业科学院经济作物研究所 | A method of Phellinus is cultivated using ramulus mori |
CN111296172A (en) * | 2020-03-26 | 2020-06-19 | 安徽省森湶谷药业股份有限公司 | Method for cultivating phellinus igniarius in double-bag connected stacked rows |
CN112514734A (en) * | 2020-10-31 | 2021-03-19 | 贵州省农作物品种资源研究所(贵州省现代中药材研究所) | Indoor cultivation method for phellinus igniarius |
CN113575292A (en) * | 2021-07-08 | 2021-11-02 | 六安职业技术学院 | Phellinus igniarius strain growth and cultivation device and cultivation method thereof |
CN113875497A (en) * | 2021-11-18 | 2022-01-04 | 陕西省微生物研究所 | Method for cultivating phellinus linteus |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000236745A (en) * | 1999-02-22 | 2000-09-05 | Shigeo Magara | Cultivation of phellinus linteus |
CN101816256A (en) * | 2009-02-27 | 2010-09-01 | 上海市农业科学院 | Method for cultivating microbial strain of phellinus linteus and planting phellinus linteus |
CN102786333A (en) * | 2012-06-21 | 2012-11-21 | 杭州清正生物科技有限公司 | Phellinus igniarius bag cultivation medium and method for cultivating phellinus igniarius sporophore by same |
-
2013
- 2013-06-24 CN CN2013102522552A patent/CN103340093A/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000236745A (en) * | 1999-02-22 | 2000-09-05 | Shigeo Magara | Cultivation of phellinus linteus |
CN101816256A (en) * | 2009-02-27 | 2010-09-01 | 上海市农业科学院 | Method for cultivating microbial strain of phellinus linteus and planting phellinus linteus |
CN102786333A (en) * | 2012-06-21 | 2012-11-21 | 杭州清正生物科技有限公司 | Phellinus igniarius bag cultivation medium and method for cultivating phellinus igniarius sporophore by same |
Non-Patent Citations (2)
Title |
---|
刘广建等: "江南地区代料栽培桑黄技术初探", 《食用菌》, no. 2, 30 April 2009 (2009-04-30), pages 43 - 44 * |
许一耿: "杉木混交林林冠下桑黄人工栽培技术探析", 《黑龙江生态工程职业学院学报》, no. 5, 30 October 2009 (2009-10-30), pages 34 - 35 * |
Cited By (30)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103493685A (en) * | 2013-10-14 | 2014-01-08 | 贵州省施秉县民生天麻科技有限公司 | Method for cultivating phellinus igniarius by using wild living tree stumps |
CN103598010B (en) * | 2013-11-12 | 2015-04-29 | 淳安县微生物研究所 | Original ecological imitative wild cultivation method for inonotus sanghuang |
CN103598010A (en) * | 2013-11-12 | 2014-02-26 | 淳安县微生物研究所 | Original ecological imitative wild cultivation method for inonotus sanghuang |
CN103563653A (en) * | 2013-11-14 | 2014-02-12 | 江苏瑞光生物科技有限公司 | Method for bottle cultivation of pleurotus cornucopiae |
CN103749151B (en) * | 2013-12-26 | 2015-09-30 | 广东省微生物研究所 | A kind of artificial cultivation method of Amauroderma ruda (Berk) Pat |
CN103695322B (en) * | 2013-12-26 | 2016-05-04 | 上林县明山菌业有限责任公司 | Be rich in phellinus igniarius mycelium product and the production method thereof of bioactive ingredients |
CN103749151A (en) * | 2013-12-26 | 2014-04-30 | 广东省微生物研究所 | Artificial cultivation method of Amauroderma rude |
CN103931420A (en) * | 2014-03-20 | 2014-07-23 | 杭州市农业科学研究院 | Method for cultivating phellinus igniarius |
CN103931420B (en) * | 2014-03-20 | 2016-09-07 | 杭州市农业科学研究院 | A kind of cultural method of Phellinus |
CN104381009A (en) * | 2014-09-18 | 2015-03-04 | 杭州千岛湖桑之宝农业开发有限公司 | Artificial bag cultivation process for Phellinus igniarius |
CN104381009B (en) * | 2014-09-18 | 2016-04-20 | 杭州千岛湖桑之宝农业开发有限公司 | Technique planted by the artificial bag of a kind of Phellinus |
CN104247628A (en) * | 2014-09-26 | 2014-12-31 | 陕西省微生物研究所 | Cultivation medium and cultivation method for artificially-cultivated phellinus igniarius |
CN104871821A (en) * | 2015-06-01 | 2015-09-02 | 四川省农业科学院土壤肥料研究所 | Phellinus igniarius strain and culturing method for same |
CN104871821B (en) * | 2015-06-01 | 2017-10-17 | 四川省农业科学院土壤肥料研究所 | A kind of Phellinus strain and its cultural method |
CN105027974A (en) * | 2015-07-22 | 2015-11-11 | 四川晟旦生物科技有限公司 | Large-scale artificial cultivation method for phellinus igniarius |
CN105724049A (en) * | 2016-01-27 | 2016-07-06 | 浙江省农业科学院 | Mulberry parasitical phellinus strain wild environment returning rejuvenation culture method |
CN105660183A (en) * | 2016-01-29 | 2016-06-15 | 吉林省三盛农业开发集团有限公司 | Phellinus igniarius cultivation method |
CN105993593A (en) * | 2016-05-23 | 2016-10-12 | 浙江省农业科学院 | High-efficiency industrial bag material cultivation process of inonotus linteus with antitumor activity |
CN106941928A (en) * | 2017-03-02 | 2017-07-14 | 江苏道诚生物科技有限公司 | A kind of implantation methods of Phellinus |
CN107094499A (en) * | 2017-06-14 | 2017-08-29 | 成都新柯力化工科技有限公司 | A kind of utilization tanimoto powder is the method for the stable cultivation Phellinus of culture medium |
CN107996288B (en) * | 2017-12-29 | 2020-11-10 | 浙江省林业科学研究院 | Method for ecologically cultivating phellinus igniarius under forest by imitating wild conditions |
CN107996288A (en) * | 2017-12-29 | 2018-05-08 | 浙江省林业科学研究院 | A kind of method that hayashishita imitates Wild ecological cultivation Phellinus |
CN108450231A (en) * | 2018-03-16 | 2018-08-28 | 江西省蚕桑茶叶研究所 | A kind of bionical border expanding propagation method of wild Phellinus |
CN109220526A (en) * | 2018-10-12 | 2019-01-18 | 绩溪县徽菜宝生物科技有限公司 | A kind of Phellinus large-scale planting method |
CN109618816A (en) * | 2018-12-08 | 2019-04-16 | 信阳市菌福康生物科技有限公司 | A kind of idle room plantation Phellinus technology in rural area |
CN109832093A (en) * | 2019-03-14 | 2019-06-04 | 湖北省农业科学院经济作物研究所 | A method of Phellinus is cultivated using ramulus mori |
CN111296172A (en) * | 2020-03-26 | 2020-06-19 | 安徽省森湶谷药业股份有限公司 | Method for cultivating phellinus igniarius in double-bag connected stacked rows |
CN112514734A (en) * | 2020-10-31 | 2021-03-19 | 贵州省农作物品种资源研究所(贵州省现代中药材研究所) | Indoor cultivation method for phellinus igniarius |
CN113575292A (en) * | 2021-07-08 | 2021-11-02 | 六安职业技术学院 | Phellinus igniarius strain growth and cultivation device and cultivation method thereof |
CN113875497A (en) * | 2021-11-18 | 2022-01-04 | 陕西省微生物研究所 | Method for cultivating phellinus linteus |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN103340093A (en) | Artificial cultivation method for phellinus linteus | |
CN102786333B (en) | Phellinus igniarius bag cultivation medium and method for cultivating phellinus igniarius sporophore by same | |
CN104041330B (en) | Ganoderma tsugae imitates wild juggle cultivation method | |
CN102630481B (en) | Cultivation method for oospore oudemansiella mucida | |
CN106472104B (en) | Manufacturing method for phellinus igniarius cultivation | |
CN103598010B (en) | Original ecological imitative wild cultivation method for inonotus sanghuang | |
CN103918475B (en) | The elegant precious method of mushroom bonsai type cultivation and the medium for cultivating elegant precious mushroom | |
CN103891524B (en) | The method of glossy ganoderma dish garden formula cultivation and the medium for cultivating ganoderma | |
CN103387463B (en) | A kind of cultivating method of black fungus and cultivation culture material thereof | |
CN105660191B (en) | A kind of cultural method of crow sesame fructification | |
CN104798601A (en) | Cultivation method for lentinula edodes | |
CN103583225A (en) | Method for cultivating good-quality high-yield pleurotus geesteranus by means of cassava stems | |
CN104557244A (en) | Cultivation medium for hericium erinaceus and cultivation method of hericium erinaceus | |
CN103907478A (en) | Method and medium for cultivating oyster mushrooms in potted landscape manner | |
CN104541938A (en) | Merge-cultivating method of Ganoderma | |
CN103385112A (en) | Production method for cultivating gyrophora through tea garden intercropping | |
CN105237090A (en) | Cultivation method for phellinus igniarius strains from solid culture medium to liquid culture medium | |
CN107736188A (en) | A kind of Bag Material gold ear binary cultural method | |
CN107409743A (en) | A kind of artificial generation material pseudo-wild cultivating method of rainbow conk | |
CN107047068B (en) | Facility greenhouse mushroom yield-increasing cultivation method | |
CN104012303A (en) | Cultivating method of pleurotus geesteranus edible mushroom | |
CN106718027B (en) | The full artificial cultivation technique of umbellate pore furgus | |
CN103493685A (en) | Method for cultivating phellinus igniarius by using wild living tree stumps | |
CN103229664A (en) | Method for planting sweet lucid ganoderma by usage of uncrushed tea seed shells | |
Jeewanthi et al. | Growth and yield of reishi mushroom [Ganoderma lucidum (Curtis) P. Karst] in different sawdust substrates |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C02 | Deemed withdrawal of patent application after publication (patent law 2001) | ||
WD01 | Invention patent application deemed withdrawn after publication |
Application publication date: 20131009 |