CN106613336A - Lucid ganoderma planting method - Google Patents

Lucid ganoderma planting method Download PDF

Info

Publication number
CN106613336A
CN106613336A CN201611052200.7A CN201611052200A CN106613336A CN 106613336 A CN106613336 A CN 106613336A CN 201611052200 A CN201611052200 A CN 201611052200A CN 106613336 A CN106613336 A CN 106613336A
Authority
CN
China
Prior art keywords
bacterium rod
grams
mycelia
bacterium
culture
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
Application number
CN201611052200.7A
Other languages
Chinese (zh)
Inventor
邓小坤
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to CN201611052200.7A priority Critical patent/CN106613336A/en
Publication of CN106613336A publication Critical patent/CN106613336A/en
Pending legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01GHORTICULTURE; CULTIVATION OF VEGETABLES, FLOWERS, RICE, FRUIT, VINES, HOPS OR SEAWEED; FORESTRY; WATERING
    • A01G18/00Cultivation of mushrooms
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N1/00Microorganisms, e.g. protozoa; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor
    • C12N1/14Fungi; Culture media therefor

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Organic Chemistry (AREA)
  • Biotechnology (AREA)
  • Zoology (AREA)
  • Mycology (AREA)
  • Genetics & Genomics (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Biomedical Technology (AREA)
  • Virology (AREA)
  • Microbiology (AREA)
  • Botany (AREA)
  • Medicinal Chemistry (AREA)
  • Biochemistry (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Environmental Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Mushroom Cultivation (AREA)

Abstract

The invention relates to a lucid ganoderma planting method. The lucid ganoderma planting method comprises the steps of culture medium preparing, strain making, fungus stick material making, inoculating, hypha culturing, underwood planting and fungus bud removing. The best raw material is prepared for the next step by conducting careful operation in every step, high-quality fungus sticks which are most suitable for large-scale planting are obtained through stepped optimization and scale expansion, and then lucid ganoderma is high in quality and yield.

Description

Glossy ganoderma implantation methods
Technical field
The present invention relates to a kind of implantation methods, particularly glossy ganoderma implantation methods.
Background technology
Glossy ganoderma is rare Chinese medicine, needs the implantation methods of the constantly good quality and high output of exploration glossy ganoderma.
The content of the invention
In order to solve the above problems, it is an object of the invention to provide a kind of glossy ganoderma implantation methods.
Specifically, the technical scheme of present invention offer is:A kind of glossy ganoderma implantation methods, including step:
A, culture medium are prepared, and every 200 g potato matches somebody with somebody 20 grams of glucose, 4 grams of dusty yeast, 2 grams of potassium dihydrogen phosphate, magnesium sulfate 0.5 Gram, 20 grams of agar;Weigh peeling, section 200 grams of potato, be placed in pot, add 1000 milliliters of water, boil to potato chips it is soft and not It is rotten;With 4-6 layer filtered through gauze, filtrate is taken;20 grams of agar is added in filtrate, is continued to boil to fat and is melted completely, add grape 20 grams of sugar, moisturizing is to 1000 milliliters;It is sub-packed in while hot in test tube, is filled to 1/ 5-1/ 4 of test tube length, cleans the mouth of pipe, beyond the Great Wall Lid, keeps sealing;Then sterilize 30 minutes under hot conditions;Sterilizing is retreaded and puts test tube, is cultivated 3 days under being placed in 30 degrees Celsius, If occurring without miscellaneous bacteria, show that sterilizing is thorough, be available for inoculation to use, if miscellaneous bacteria occur and should again sterilize or reconfigure;
B, bacterial classification make, and are divided into ripe fresh sesame and are done lucidum seed from the 6-7 of no disease and pests harm, and lucidum seed surface Jing ultraviolet irradiations disappear Poison, alcohol wipe sterilization, then cap is torn, it is divided into two;Select on cap yellow-white vitellarium meat bacteria organization or stem Meat bacteria organization in the middle part of square cap is to take kind of a position;First meat bacteria organization is carefully cut with aseptic operation knife when taking kind, then with connecing The fritter meat bacteria organization that pin takes 5 millimeters × 5 millimeters is planted, Tube propagation base middle and upper part surface is inoculated into;Bacterial context group is put into by above-mentioned The culture medium knitted is placed in biochemical cultivation case and cultivates, and to 28-30 degree Celsius, lucifuge culture 2-3 days, meat bacteria organization starts to sprout for temperature adjustment Send out, macroscopic mycelium occur, and gradually spread in media surface, 7-10 days mycelium cover with test tube slant, mycelia Body is pure white, very thin, flat, fine and close, uniform, obtains the healthy Ganoderma lucidum mycelium without miscellaneous bacteria, with the growth of mycelia, the expansion of bacterium colony Exhibition, the mycelia at inoculation is gradually aging to form tough and tensile mycoderma, and as mycoderma is aging, at this time selects Ganoderma lucidum mycelium bulk-growth Neatly, long speed is normal, mycelia outward appearance is full, growing way is vigorous, and aerial hyphae is pure white, very thin, flat, fine and close, uniform part is made For bacterial classification;
C, bacterium rod make of material, select the seeds for being adapted to cultivation basswood, sawed-off for length 14-15 centimetre in 10 to 20 days after felling Or 28-30 centimetre, a diameter of 3-16 centimetre, the short linden that section is smooth, length is consistent is used as bacterium rod material;From high temperature resistant, The packed bacterium rod material of polyethylene cylinder of stretching resistance, slip-knot is pricked respectively at two after pack, is handled with care, prevents breakage;Will be packed Bacterium rod material is put into high-temperature sterilization in pot, and very hot oven onslaught, makes kettle temperature be rapidly reached 100 degrees Celsius after being put in pot, works as pot To maintain do not lower the temperature after 100 degrees Celsius of Nei Wenduda within 12 hours, taking the dish out of the pot after truce is cooled to 28-30 degree Celsius;
D, inoculation, transfer room can select good doors and windows sealing, place drying, 10-15 square metre of room of cleaning, interior to use plastic foil system Into equal inoculation account, 4-8 hours are carried out disinfection per cubic metre of account is inoculated with disinfectant before inoculation, and bacterial classification is filled into bacterium Rod with bacterium rod is obtained after the section of material two, wrap and tying is stacked by bacterium rod plastic foil;
E, cultural hypha, select the cob wall room of good heat insulating as between culture, and room temperature is controlled at 20-30 degree Celsius;Culture Between want lucifuge, illumination is suitably increased when mycelia covers with full bag, promotes mycelial growth, 60-70 days mycelia of culture are ripe, bacterium rod table Layer mycelia is pure white sturdy, is close between bacterium wood and is difficult to break into two with one's hands, and minority bacterium wood section has the big former base of beans to occur, you can carry out sylvan life kind Plant;
F, underwood planting, selected from right pavilion leaf woods, it is desirable to seven parts of the moon of sylvan life, three parts of sun, can grow be used for where wild weeds on the ground Glossy ganoderma underwood planting, 4-5 hole of often row digging, cheats away from 20 centimeters, and bacterium rod is stood up in hole, equal with ground, upper cover 1-2 public affairs The soil for dividing, the place of cultivating ganoderma keeps weed growth, Planting Grass or mowing capping when weeds are very few;
G, go button, to be unclogged and readjusted when button grows two centimeters high, unnecessary button is removed, go it is weak stay strong, per rod only Retain 1-2 button.
Further technical scheme is the present invention:What the bacterium rod material was selected is the maple for bending many knots.
The present invention obtain beneficial effect be:It is that next step makes best raw material by the carefulness operation to each step And preparation, by step-by-step optimization and expansion scale, obtain the high-quality bacterium rod of optimum implant mass so that glossy ganoderma high-quality is high Produce.
Description of the drawings
Fig. 1 is the plantation flow chart of glossy ganoderma of the present invention.
Specific embodiment
As shown in figure 1, a kind of glossy ganoderma implantation methods, are that next step making is best by the carefulness operation to each step Raw material and preparation, by step-by-step optimization and expansion scale, obtain the high-quality bacterium rod of optimum implant mass so that glossy ganoderma high-quality High yield, concrete scheme includes step:
A, culture medium are prepared, and every 200 g potato matches somebody with somebody 20 grams of glucose, 4 grams of dusty yeast, 2 grams of potassium dihydrogen phosphate, magnesium sulfate 0.5 Gram, 20 grams of agar;Weigh peeling, section 200 grams of potato, be placed in pot, add 1000 milliliters of water, boil to potato chips it is soft and not It is rotten;With 4-6 layer filtered through gauze, filtrate is taken;20 grams of agar is added in filtrate, is continued to boil to fat and is melted completely, add grape 20 grams of sugar, moisturizing is to 1000 milliliters;It is sub-packed in while hot in test tube, is filled to 1/ 5-1/ 4 of test tube length, cleans the mouth of pipe, beyond the Great Wall Lid, keeps sealing;Then sterilize 30 minutes under hot conditions;Sterilizing is retreaded and puts test tube, is cultivated 3 days under being placed in 30 degrees Celsius, If occurring without miscellaneous bacteria, show that sterilizing is thorough, be available for inoculation to use, if miscellaneous bacteria occur and should again sterilize or reconfigure.
B, bacterial classification make, and are divided into ripe fresh sesame and are done lucidum seed, the ultraviolet photographs of lucidum seed surface Jing from the 6-7 of no disease and pests harm Sterilization, alcohol wipe sterilization are penetrated, then cap is torn, be divided into two;Select cap yellow-white vitellarium meat bacteria organization or bacterium Meat bacteria organization in the middle part of the cap of handle top is to take kind of a position;First meat bacteria organization is carefully cut with aseptic operation knife when taking kind, then 5 millimeters × 5 millimeters of fritter meat bacteria organization is taken with transfer needle, Tube propagation base middle and upper part surface is inoculated into;Bacterium is put into by above-mentioned The culture medium of meat tissue is placed in biochemical cultivation case and cultivates, temperature adjustment to 28-30 degree Celsius, lucifuge culture 2-3 days, meat bacteria organization opens Begin to sprout, macroscopic mycelium occur, and gradually spread in media surface, mycelium covers with test tube slant within 7-10 days, Mycelium is pure white, very thin, flat, fine and close, uniform, obtains the healthy Ganoderma lucidum mycelium without miscellaneous bacteria, the growth, bacterium colony with mycelia Extension, the mycelia at inoculation is gradually aging to form tough and tensile mycoderma, and as mycoderma is aging, at this time selects ganoderma lucidum mycelium Growth is neat, long speed is normal, mycelia outward appearance is full, growing way is vigorous, and aerial hyphae is pure white, very thin, flat, fine and close, uniform portion It is allocated as bacterial classification.If separator(Meat bacteria organization)Macroscopic mycelium, eventful miscellaneous bacteria were occurred as soon as less than 2 days.If point From thing(Meat bacteria organization)Culture is still the macroscopic mycelium of appearance in 4 days, it may be possible to cut the scalpel of glossy ganoderma meat bacteria organization Or transfer needle is no sufficiently cool after calcination above Alcohol Flame, or other reasons cause separator(Meat bacteria organization)Lose Deactivation and mycelium can not be sprouted.
C, bacterium rod make of material, select the seeds for being adapted to cultivation basswood, sawed-off for length 14-15 in 10 to 20 days after felling Centimetre or 28-30 centimetre, a diameter of 3-16 centimetre, the short linden that section is smooth, length is consistent is used as bacterium rod material;From resistance to height Temperature, the packed bacterium rod material of polyethylene cylinder of stretching resistance, slip-knot is pricked respectively at two after pack, is handled with care, prevents breakage;Will be packed Bacterium rod material be put into high-temperature sterilization in pot, be put in pot after very hot oven onslaught, make kettle temperature be rapidly reached 100 degrees Celsius, when Kettle temperature will maintain do not lower the temperature for 12 hours up to after 100 degrees Celsius, and taking the dish out of the pot after truce is cooled to 28-30 degree Celsius;Preferably, institute State the selection of bacterium rod material is the maple for bending many knots.
D, inoculation, transfer room can select good doors and windows sealing, place drying, 10-15 square metre of room of cleaning, inside use plastics Film makes equal inoculation account, and 4-8 hours are carried out disinfection per cubic metre of account is inoculated with disinfectant before inoculation, and bacterial classification is filled To bacterium rod with bacterium rod is obtained after the section of material two, bacterium rod plastic foil is wrapped and tying is stacked.
E, cultural hypha, select the cob wall room of good heat insulating as between culture, and room temperature is controlled at 20-30 degree Celsius; Lucifuge is wanted between culture, illumination is suitably increased when mycelia covers with full bag, is promoted mycelial growth, 60-70 days mycelia of culture are ripe, bacterium Mycelia is pure white sturdy on rod top layer, is close between bacterium wood and is difficult to break into two with one's hands, and minority bacterium wood section has the big former base of beans to occur, you can carry out woods Lower plantation.
F, underwood planting, selected from right pavilion leaf woods, it is desirable to seven parts of the moon of sylvan life, three parts of sun, where wild weeds can be grown on the ground For glossy ganoderma underwood planting, 4-5 hole of often row digging, cheat away from 20 centimeters, bacterium rod is stood up in hole, upper cover equal with ground The soil of 1-2 centimetres, the place of cultivating ganoderma keeps weed growth, Planting Grass or mowing capping when weeds are very few;Allow spirit Sesame grows out the glossy ganoderma shape that just keep from grass, can just keep Ganoderma Lucidum pin height, and can prevent rain from beating mud damage Glossy ganoderma bottom surface, if speckling with mud on Ganoderma Lucidum, bottom just has pit, will affect quality.
G, go button, to be unclogged and readjusted when button grows two centimeters high, unnecessary button is removed, go it is weak stay strong, often Rod only retains 1-2 button.Because glossy ganoderma can not draw nutrient from soil, for its growth, it can only draw wood from timber Quality is supplying growth, that is to say, that its nutrient source of Ganoderma Lucidum is limited, so reservation is more such as on same bacterium rod Little is reformed into if individual glossy ganoderma, commodity value can be thus affected.
Specific embodiment be it is exemplary present invention is described, be not intended to limit the present invention be included in right will Seek interior other embodiment.

Claims (2)

1. a kind of glossy ganoderma implantation methods, it is characterised in that including step:
A, culture medium are prepared, and every 200 g potato matches somebody with somebody 20 grams of glucose, 4 grams of dusty yeast, 2 grams of potassium dihydrogen phosphate, magnesium sulfate 0.5 Gram, 20 grams of agar;Weigh peeling, section 200 grams of potato, be placed in pot, add 1000 milliliters of water, boil to potato chips it is soft and not It is rotten;With 4-6 layer filtered through gauze, filtrate is taken;20 grams of agar is added in filtrate, is continued to boil to fat and is melted completely, add grape 20 grams of sugar, moisturizing is to 1000 milliliters;It is sub-packed in while hot in test tube, is filled to 1/ 5-1/ 4 of test tube length, cleans the mouth of pipe, beyond the Great Wall Lid, keeps sealing;Then sterilize 30 minutes under hot conditions;Sterilizing is retreaded and puts test tube, is cultivated 3 days under being placed in 30 degrees Celsius, If occurring without miscellaneous bacteria, show that sterilizing is thorough, be available for inoculation to use, if miscellaneous bacteria occur and should again sterilize or reconfigure;
B, bacterial classification make, and are divided into ripe fresh sesame and are done lucidum seed from the 6-7 of no disease and pests harm, and lucidum seed surface Jing ultraviolet irradiations disappear Poison, alcohol wipe sterilization, then cap is torn, it is divided into two;Select on cap yellow-white vitellarium meat bacteria organization or stem Meat bacteria organization in the middle part of square cap is to take kind of a position;First meat bacteria organization is carefully cut with aseptic operation knife when taking kind, then with connecing The fritter meat bacteria organization that pin takes 5 millimeters × 5 millimeters is planted, Tube propagation base middle and upper part surface is inoculated into;Bacterial context group is put into by above-mentioned The culture medium knitted is placed in biochemical cultivation case and cultivates, and to 28-30 degree Celsius, lucifuge culture 2-3 days, meat bacteria organization starts to sprout for temperature adjustment Send out, macroscopic mycelium occur, and gradually spread in media surface, 7-10 days mycelium cover with test tube slant, mycelia Body is pure white, very thin, flat, fine and close, uniform, obtains the healthy Ganoderma lucidum mycelium without miscellaneous bacteria, with the growth of mycelia, the expansion of bacterium colony Exhibition, the mycelia at inoculation is gradually aging to form tough and tensile mycoderma, and as mycoderma is aging, at this time selects Ganoderma lucidum mycelium bulk-growth Neatly, long speed is normal, mycelia outward appearance is full, growing way is vigorous, and aerial hyphae is pure white, very thin, flat, fine and close, uniform part is made For bacterial classification;
C, bacterium rod make of material, select the seeds for being adapted to cultivation basswood, sawed-off for length 14-15 centimetre in 10 to 20 days after felling Or 28-30 centimetre, a diameter of 3-16 centimetre, the short linden that section is smooth, length is consistent is used as bacterium rod material;From high temperature resistant, The packed bacterium rod material of polyethylene cylinder of stretching resistance, slip-knot is pricked respectively at two after pack, is handled with care, prevents breakage;Will be packed Bacterium rod material is put into high-temperature sterilization in pot, and very hot oven onslaught, makes kettle temperature be rapidly reached 100 degrees Celsius after being put in pot, works as pot To maintain do not lower the temperature after 100 degrees Celsius of Nei Wenduda within 12 hours, taking the dish out of the pot after truce is cooled to 28-30 degree Celsius;
D, inoculation, transfer room can select good doors and windows sealing, place drying, 10-15 square metre of room of cleaning, interior to use plastic foil system Into equal inoculation account, 4-8 hours are carried out disinfection per cubic metre of account is inoculated with disinfectant before inoculation, and bacterial classification is filled into bacterium Rod with bacterium rod is obtained after the section of material two, wrap and tying is stacked by bacterium rod plastic foil;
E, cultural hypha, select the cob wall room of good heat insulating as between culture, and room temperature is controlled at 20-30 degree Celsius;Culture Between want lucifuge, illumination is suitably increased when mycelia covers with full bag, promotes mycelial growth, 60-70 days mycelia of culture are ripe, bacterium rod table Layer mycelia is pure white sturdy, is close between bacterium wood and is difficult to break into two with one's hands, and minority bacterium wood section has the big former base of beans to occur, you can carry out sylvan life kind Plant;
F, underwood planting, selected from right pavilion leaf woods, it is desirable to seven parts of the moon of sylvan life, three parts of sun, can grow be used for where wild weeds on the ground Glossy ganoderma underwood planting, 4-5 hole of often row digging, cheats away from 20 centimeters, and bacterium rod is stood up in hole, equal with ground, upper cover 1-2 public affairs The soil for dividing, the place of cultivating ganoderma keeps weed growth, Planting Grass or mowing capping when weeds are very few;
G, go button, to be unclogged and readjusted when button grows two centimeters high, unnecessary button is removed, go it is weak stay strong, per rod only Retain 1-2 button.
2. glossy ganoderma implantation methods as claimed in claim 1, it is characterised in that:What the bacterium rod material was selected is many knots of bending Maple.
CN201611052200.7A 2016-11-25 2016-11-25 Lucid ganoderma planting method Pending CN106613336A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201611052200.7A CN106613336A (en) 2016-11-25 2016-11-25 Lucid ganoderma planting method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201611052200.7A CN106613336A (en) 2016-11-25 2016-11-25 Lucid ganoderma planting method

Publications (1)

Publication Number Publication Date
CN106613336A true CN106613336A (en) 2017-05-10

Family

ID=58811223

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201611052200.7A Pending CN106613336A (en) 2016-11-25 2016-11-25 Lucid ganoderma planting method

Country Status (1)

Country Link
CN (1) CN106613336A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107484548A (en) * 2017-08-07 2017-12-19 霍山县永丰蚕业农民专业合作社 A kind of ganoderma lucidum cultivation method for improving ganoderma polyoses content
CN110122175A (en) * 2019-06-12 2019-08-16 北京葆年堂(菏泽)药业有限公司 A kind of implantation methods of ganoderma lucidum
CN110521488A (en) * 2019-09-24 2019-12-03 广西壮族自治区林业科学研究院 A method of Ganoderma Sinense is cultivated using forest felling stub field original place
CN112088718A (en) * 2019-06-17 2020-12-18 米林县米林镇红太阳科技示范家庭农场 Preparation method of milin ganoderma lucidum strain

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103583210A (en) * 2013-11-13 2014-02-19 福建省农业科学院农业生态研究所 Method for interplanting ganoderma lucidum in tea gardens
CN104488541A (en) * 2013-12-04 2015-04-08 融水苗族自治县怀宝镇富民灵芝专业合作社 Understory wild-imitation ganoderma lucidum cultivation method
CN104798599A (en) * 2015-04-22 2015-07-29 吉林农业大学 Method for planting ganoderma tsugae by imitating wild growth in forest land
CN104823715A (en) * 2015-05-06 2015-08-12 广西壮族自治区农业科学院 Cultivation method of imitated wild ganoderma lucidum in cedar forest
CN104956913A (en) * 2015-06-18 2015-10-07 唐伟 Method for cultivating artificial natural ganoderma lucidum under high-altitude forest
CN105613030A (en) * 2016-03-31 2016-06-01 中国农业科学院特产研究所 Method for intercropping cultivation of acanthopanax sessiliflorus and ganoderma tsugae
CN106069559A (en) * 2016-06-12 2016-11-09 福建省农业科学院农业生态研究所 The stereo circulating cultural method that a kind of Fructus Vitis viniferae couples with Ganoderma

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103583210A (en) * 2013-11-13 2014-02-19 福建省农业科学院农业生态研究所 Method for interplanting ganoderma lucidum in tea gardens
CN104488541A (en) * 2013-12-04 2015-04-08 融水苗族自治县怀宝镇富民灵芝专业合作社 Understory wild-imitation ganoderma lucidum cultivation method
CN104798599A (en) * 2015-04-22 2015-07-29 吉林农业大学 Method for planting ganoderma tsugae by imitating wild growth in forest land
CN104823715A (en) * 2015-05-06 2015-08-12 广西壮族自治区农业科学院 Cultivation method of imitated wild ganoderma lucidum in cedar forest
CN104956913A (en) * 2015-06-18 2015-10-07 唐伟 Method for cultivating artificial natural ganoderma lucidum under high-altitude forest
CN105613030A (en) * 2016-03-31 2016-06-01 中国农业科学院特产研究所 Method for intercropping cultivation of acanthopanax sessiliflorus and ganoderma tsugae
CN106069559A (en) * 2016-06-12 2016-11-09 福建省农业科学院农业生态研究所 The stereo circulating cultural method that a kind of Fructus Vitis viniferae couples with Ganoderma

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
无: "灵芝母种的制作", 《中国食用菌商务网,HTTP://JISHU.MUSHROOMMARKET.NET/201607/08/10109.HTML》 *
潘庆松等: "林下仿野生灵芝高产栽培技术", 《农业与技术》 *

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107484548A (en) * 2017-08-07 2017-12-19 霍山县永丰蚕业农民专业合作社 A kind of ganoderma lucidum cultivation method for improving ganoderma polyoses content
CN110122175A (en) * 2019-06-12 2019-08-16 北京葆年堂(菏泽)药业有限公司 A kind of implantation methods of ganoderma lucidum
CN112088718A (en) * 2019-06-17 2020-12-18 米林县米林镇红太阳科技示范家庭农场 Preparation method of milin ganoderma lucidum strain
CN110521488A (en) * 2019-09-24 2019-12-03 广西壮族自治区林业科学研究院 A method of Ganoderma Sinense is cultivated using forest felling stub field original place

Similar Documents

Publication Publication Date Title
CN103918475B (en) The elegant precious method of mushroom bonsai type cultivation and the medium for cultivating elegant precious mushroom
KR20080105001A (en) Mushroom bed cultivation of mushroom
CN106613336A (en) Lucid ganoderma planting method
KR101148759B1 (en) A method for cultivating mushrooms having uniformly grown fruiting-bodies
CN103004469A (en) Tall gastrodia tuber culture method, tall gastrodia tuber liquor and tall gastrodia tuber production process by using small-caliber container
CN103004466A (en) Needle mushroom cultivating method
CN104557244A (en) Cultivation medium for hericium erinaceus and cultivation method of hericium erinaceus
CN102754596A (en) Establishing method of symbiont of cyclobalanopsis glaucoides and bolete
CN107125028A (en) A kind of wild yellow ring squama agaric domestication and artificial culturing method
KR100483333B1 (en) Production method of the cauliflower mushroom using fermented sawdust
CN110140591B (en) Morchella high-yield strain and application thereof
CN108243832A (en) The artificial method for planting of paint face mushroom
CN108887077A (en) A kind of wild red ganoderma cultural method of high-efficient breeding
KR100276842B1 (en) Culture medium composition for snow Cordyceps sinensis and its culture method
KR20100071155A (en) Method for cultivation of fragrant mushroom
CN101690453A (en) Hon-shimeji mushroom-fungal bed culture
CN111019835A (en) Method for separating Armillaria mellea from ambary endophytic fungi
CN105028213A (en) Tissue-culturing rapid propagation method for dendrobium officinale
CN107667776A (en) A kind of Household edible mushroom planting method
JP2676502B2 (en) Artificial cultivation method of fruiting body of Cordyceps sinensis
KR20190040536A (en) Method for cultivation of fragrant mushroom and fragrant mushroom produced by the process
US20060112618A1 (en) Method for cultivating mushroom
JPH07184473A (en) Method for artificially cultivating mushroom of genus pleurotus
KR20060045093A (en) A manufacturing method of mushroom
CN106754402A (en) Lucidum strain preparation method

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication
RJ01 Rejection of invention patent application after publication

Application publication date: 20170510