CN104350954A - Lyophyllum decastes cultivation method - Google Patents
Lyophyllum decastes cultivation method Download PDFInfo
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- CN104350954A CN104350954A CN201410700135.9A CN201410700135A CN104350954A CN 104350954 A CN104350954 A CN 104350954A CN 201410700135 A CN201410700135 A CN 201410700135A CN 104350954 A CN104350954 A CN 104350954A
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- 238000012364 cultivation method Methods 0.000 title claims abstract description 8
- 240000005856 Lyophyllum decastes Species 0.000 title abstract description 7
- 235000013194 Lyophyllum decastes Nutrition 0.000 title abstract description 7
- 238000005286 illumination Methods 0.000 claims abstract description 24
- 230000000638 stimulation Effects 0.000 claims abstract description 19
- 238000012258 culturing Methods 0.000 claims abstract description 16
- 239000002994 raw material Substances 0.000 claims abstract description 13
- 230000001954 sterilising effect Effects 0.000 claims abstract description 13
- 238000004659 sterilization and disinfection Methods 0.000 claims abstract description 11
- 241000589220 Acetobacter Species 0.000 claims abstract description 7
- 238000001816 cooling Methods 0.000 claims abstract description 7
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 claims abstract description 6
- 239000001963 growth medium Substances 0.000 claims abstract description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 6
- 235000001674 Agaricus brunnescens Nutrition 0.000 claims description 22
- 210000003056 antler Anatomy 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 11
- 230000008569 process Effects 0.000 claims description 11
- 239000003864 humus Substances 0.000 claims description 6
- 235000008733 Citrus aurantifolia Nutrition 0.000 claims description 5
- 240000007594 Oryza sativa Species 0.000 claims description 5
- 235000007164 Oryza sativa Nutrition 0.000 claims description 5
- 235000011941 Tilia x europaea Nutrition 0.000 claims description 5
- 210000004907 gland Anatomy 0.000 claims description 5
- 239000004571 lime Substances 0.000 claims description 5
- 230000003020 moisturizing effect Effects 0.000 claims description 5
- 235000016709 nutrition Nutrition 0.000 claims description 5
- 230000035764 nutrition Effects 0.000 claims description 5
- 235000009566 rice Nutrition 0.000 claims description 5
- 239000002689 soil Substances 0.000 claims description 5
- 235000015099 wheat brans Nutrition 0.000 claims description 5
- 239000002023 wood Substances 0.000 claims description 5
- 239000000203 mixture Substances 0.000 abstract description 5
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 abstract 4
- 229910002092 carbon dioxide Inorganic materials 0.000 abstract 2
- 239000001569 carbon dioxide Substances 0.000 abstract 2
- QJZYHAIUNVAGQP-UHFFFAOYSA-N 3-nitrobicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid Chemical compound C1C2C=CC1C(C(=O)O)C2(C(O)=O)[N+]([O-])=O QJZYHAIUNVAGQP-UHFFFAOYSA-N 0.000 abstract 1
- 239000004021 humic acid Substances 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 238000003825 pressing Methods 0.000 abstract 1
- 238000007789 sealing Methods 0.000 abstract 1
- 238000005303 weighing Methods 0.000 abstract 1
- 230000001580 bacterial effect Effects 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- 239000007788 liquid Substances 0.000 description 5
- 241000894006 Bacteria Species 0.000 description 4
- PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical compound OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 2
- 230000035784 germination Effects 0.000 description 2
- 238000011081 inoculation Methods 0.000 description 2
- 230000035479 physiological effects, processes and functions Effects 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- FYGDTMLNYKFZSV-URKRLVJHSA-N (2s,3r,4s,5s,6r)-2-[(2r,4r,5r,6s)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(2r,4r,5r,6s)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC1[C@@H](CO)O[C@@H](OC2[C@H](O[C@H](O)[C@H](O)[C@H]2O)CO)[C@H](O)[C@H]1O FYGDTMLNYKFZSV-URKRLVJHSA-N 0.000 description 1
- 241000222382 Agaricomycotina Species 0.000 description 1
- 241000222518 Agaricus Species 0.000 description 1
- 229920002498 Beta-glucan Polymers 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 235000019750 Crude protein Nutrition 0.000 description 1
- 208000001953 Hypotension Diseases 0.000 description 1
- 240000002853 Nelumbo nucifera Species 0.000 description 1
- 235000006508 Nelumbo nucifera Nutrition 0.000 description 1
- 235000006510 Nelumbo pentapetala Nutrition 0.000 description 1
- 241001494479 Pecora Species 0.000 description 1
- 240000001462 Pleurotus ostreatus Species 0.000 description 1
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 230000003266 anti-allergic effect Effects 0.000 description 1
- 230000003178 anti-diabetic effect Effects 0.000 description 1
- 230000000118 anti-neoplastic effect Effects 0.000 description 1
- 239000003472 antidiabetic agent Substances 0.000 description 1
- 244000144987 brood Species 0.000 description 1
- 235000012000 cholesterol Nutrition 0.000 description 1
- 239000002361 compost Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 208000021822 hypotensive Diseases 0.000 description 1
- 230000001077 hypotensive effect Effects 0.000 description 1
- 230000036039 immunity Effects 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 229960003512 nicotinic acid Drugs 0.000 description 1
- 235000001968 nicotinic acid Nutrition 0.000 description 1
- 239000011664 nicotinic acid Substances 0.000 description 1
- 230000000050 nutritive effect Effects 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 239000011669 selenium Substances 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 235000015961 tonic Nutrition 0.000 description 1
- 230000001256 tonic effect Effects 0.000 description 1
- 229960000716 tonics Drugs 0.000 description 1
- 239000011573 trace mineral Substances 0.000 description 1
- 235000013619 trace mineral Nutrition 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C05—FERTILISERS; MANUFACTURE THEREOF
- C05G—MIXTURES OF FERTILISERS COVERED INDIVIDUALLY BY DIFFERENT SUBCLASSES OF CLASS C05; MIXTURES OF ONE OR MORE FERTILISERS WITH MATERIALS NOT HAVING A SPECIFIC FERTILISING ACTIVITY, e.g. PESTICIDES, SOIL-CONDITIONERS, WETTING AGENTS; FERTILISERS CHARACTERISED BY THEIR FORM
- C05G5/00—Fertilisers characterised by their form
- C05G5/40—Fertilisers incorporated into a matrix
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Mycology (AREA)
- Environmental Sciences (AREA)
- Mushroom Cultivation (AREA)
Abstract
The invention relates to a lyophyllum decastes cultivation method. The lyophyllum decastess cultivation method comprises the following steps: weighing culture medium raw materials in parts by mass; mixing the raw materials; controlling the pH value to be 6-7 and putting the materials into culture bottles, wherein 400-500 parts of the raw materials are put into each bottle; pressing a cap and sealing; conveying the culture bottle into a vacuum sterilization pot; sterilizing with ozone for 1 to hours until the vacuumizing degree is 50KPa-80KPa; sterilizing at 150 DEG C for 100-120 minutes; cooling at 15-20 DEG C and adding 1-4 parts of humic acid; cooling and conveying a mixture into each bottle to be inoculated for 40-50 minutes; culturing in a culture room at 20-25 DEG C for 20-25 days under the conditions that the humidity is 70%-80% and the concentration of carbon dioxide is 1600PPM-3200PPM; carrying out mycelium stimulation: carrying out mycelium stimulation treatment by using a mycelium stimulation machine and supplying water according to 85% of the weight of old mycoderma; carrying out bud promotion and collecting: after the mycelium stimulation, starting to collect after 21 days in the culture room under the conditions that the temperature is 14-15 DEG C, the humidity is 95%-98%, the concentration of the carbon dioxide is under 1200PPM, the illumination intensity of 0-50Lux from day 1 to day 3, the illumination intensity of 50Lux-100Lux from day 4 to day 6, the illumination intensity of 150Lux-200Lux from day 7 to day10 days, and the illumination intensity of 200Lux-300Lux for day 10 to day 20.
Description
Technical field
The present invention relates to a kind of pilose antler mushroom cultivation method.
Background technology
Pilose antler mushroom is also known as Lyophyllum decastes (Lyophyllum decastes (Fr.: Fr.) Sing.), and lotus leaf mushroom, is also called cold fragrant bacterium in the Yunnan of China, a brood of sheep, Fungus Pleurotus ostreatus etc., belong to Basidiomycotina, Hymenomycetes, cap order, Bai Mo section, from Agaricus, be called fried chicken mushroom in Europe, bacterial context is plump, fine and smooth, A sweety scent assails the nostrils, delicious flavour, research shows that crude protein in pilose antler massee fruiting bodies, amino acid whose content are higher, and fat content is lower; But also contain useful trace element zinc, copper and the selenium of human body and a large amount of vitamin B1s, B2, B6, B12 and nicotinic acid, there is very high nutritive value.Show according to modern scientific research, the beta glucan that pilose antler mushroom contains, long-term eating has antineoplastic effect, meanwhile, pilose antler mushroom have hypotensive, reduce the pharmacologic action such as cholesterol, anti-diabetic, antiallergy, can strengthening by means of tonics, strengthen the body resistance to consolidate the constitution, strengthen immunity, delay senility.
The domestic research for the cultivation of pilose antler mushroom at present concentrates in the research of biological character mostly, and less to cultivation research, within 2007, Shanghai Finc Bio-tech Inc. reports industrialized cultivation pilose antler mushroom first.This article is pointed out to guarantee that the low stain rate that factory culture brings benefits is that cultivation is successfully crucial simultaneously.The link of Environmental capacity most critical is that bacterial classification can realize surely growing fast on composts or fertilisers of cultivating, and the vigor of bacterial classification is then surely grow most important factor fast.Inner Mongolia Autonomous Region in 2008 Yakeshi City Yi Tuli river State Forestry Administration, P.R. China feels that Lyophyllum decastes (pilose antler mushroom) cultivation method patent has been applied in careless Xun forest farm, adopt solid spawn planting type, solid spawn preparation cost is long, and inoculation efficiency is low, bacterial classification germination physiology is slow, and the pollution rate of blake bottle is high.
Summary of the invention
The invention provides a kind of preparation cost low, inoculation efficiency, bacterial classification germination physiology, reduce the pilose antler mushroom liquid strain preparation method of blake bottle pollution rate.
The technical solution used in the present invention is: a kind of pilose antler mushroom cultivation method, is characterized in that:
(1), by mass fraction culture medium raw material is taken: wood chip 40-60 part, rice bran 10-20 part, wheat bran 5-10 part, continuous seed shell 10-20 part, lime 1-3 part, Nutrition Soil 10-15 part, water 80-110 part;
(2), by step (1) raw material mix, control pH value 6-7, load blake bottle, every bottle of 400-500 part, gland encapsulates;
(3), blake bottle sends into vacreation pot, suction 50-80KPa after ozone sterilization 1-2 hour, sterilization 100-120 minute at 150 DEG C;
(4), at 15-20 DEG C cool, add humus 1-4 part, after cooling, send into every bottle graft original seed 40-50;
(5), 20-25 DEG C of culturing room, humidity 70-80%, between gas concentration lwevel 1600-3200PPM, cultivates 20-25 days;
(6), mycelium stimulation process, utilize mushroom culturing device to carry out mycelium stimulation process and carry out moisturizing by 85% of old mycoderma weight simultaneously;
(7) flower bud process, is urged, in culturing room after mycelium stimulation, temperature 14-15 DEG C, humidity 95-98%, below gas concentration lwevel 1200PPM, 1-3 days intensity of illumination 0-50Lux, 4-6 days intensity of illumination 50-100Lux, 7-10 days intensity of illumination 150-200Lux, 10-20 days intensity of illumination 200-300Lux, started to gather after 21 days.
Compared with prior art, advantage of the present invention is: medium is easy to make, cost is low, and when making for liquid spawn, it is fast that bacterial classification sends out bacterium speed, pollution-free, without old mycoderma, is conducive to improving and sends out bacterium effect and output.Add humus, effectively improve rate of buddingging, guarantee bacterium mushroom output.
Embodiment
Below in conjunction with embodiment, the invention will be further described.
Embodiment one
A kind of pilose antler mushroom liquid strain preparation method:
(1), by mass fraction culture medium raw material is taken: wood chip 40 parts, 10 parts, rice bran, 5 parts, wheat bran, 10 parts, continuous seed shell, 1 part, lime, Nutrition Soil 10 parts, 80 parts, water;
(2), by step (1) raw material mix, control pH value 6, load blake bottle, 400 parts every bottle, gland encapsulates;
(3), blake bottle sends into vacreation pot, and ozone sterilization is suction 50KPa after 1 hour, sterilization 100 minutes at 150 DEG C;
(4), at 15 DEG C cool, add humus 1 part, after cooling, send into every bottle graft original seed 40;
(5), 20 DEG C of culturing room, humidity 70%, between gas concentration lwevel 1600PPM, cultivates 20 days;
(6), mycelium stimulation process, utilize mushroom culturing device to carry out mycelium stimulation process and carry out moisturizing by 85% of old mycoderma weight simultaneously;
(7), flower bud is urged to gather, in culturing room after mycelium stimulation, temperature 14 DEG C, humidity 95%, below gas concentration lwevel 1200PPM, 1-3 days intensity of illumination 0-50Lux, 4-6 days intensity of illumination 50-100Lux, 7-10 days intensity of illumination 150-200Lux, 10-20 days intensity of illumination 200-300Lux, started to gather after 21 days.
Embodiment two
A kind of pilose antler mushroom liquid strain preparation method:
(1), by mass fraction culture medium raw material is taken: wood chip 60 parts, 20 parts, rice bran, 10 parts, wheat bran, 20 parts, continuous seed shell, 3 parts, lime, Nutrition Soil 15 parts, 110 parts, water;
(2), by step (1) raw material mix, control pH value 7, load blake bottle, 500 parts every bottle, gland encapsulates;
(3), blake bottle sends into vacreation pot, and ozone sterilization is suction 80KPa after 2 hours, sterilization 120 minutes at 150 DEG C;
(4), at 20 DEG C cool, add humus 2 parts, after cooling, send into every bottle graft original seed 50;
(5), 25 DEG C of culturing room, humidity 80%, between gas concentration lwevel 3200PPM, cultivates 25 days;
(6), mycelium stimulation process, utilize mushroom culturing device to carry out mycelium stimulation process and carry out moisturizing by 85% of old mycoderma weight simultaneously;
(7), flower bud is urged to gather, in culturing room after mycelium stimulation, temperature 15 DEG C, humidity 98%, below gas concentration lwevel 1200PPM, 1-3 days intensity of illumination 0-50Lux, 4-6 days intensity of illumination 50-100Lux, 7-10 days intensity of illumination 150-200Lux, 10-20 days intensity of illumination 200-300Lux, started to gather after 21 days.
Embodiment three
A kind of pilose antler mushroom liquid strain preparation method:
(1), by mass fraction culture medium raw material is taken: wood chip 50 parts, 15 parts, rice bran, 8 parts, wheat bran, 15 parts, continuous seed shell, 2 parts, lime, Nutrition Soil 13 parts, 90 parts, water;
(2), by step (1) raw material mix, control pH value 6, load blake bottle, 450 parts every bottle, gland encapsulates;
(3), blake bottle sends into vacreation pot, and ozone sterilization is suction 60KPa after 1.5 hours, sterilization 110 minutes at 150 DEG C;
(4), at 18 DEG C cool, add humus 4 parts, after cooling, send into every bottle graft original seed 46;
(5), 22 DEG C of culturing room, humidity 78%, between gas concentration lwevel 2200PPM, cultivates 22 days;
(6), mycelium stimulation process, utilize mushroom culturing device to carry out mycelium stimulation process and carry out moisturizing by 85% of old mycoderma weight simultaneously;
(7), flower bud is urged to gather, in culturing room after mycelium stimulation, temperature 14 DEG C, humidity 98%, below gas concentration lwevel 1200PPM, 1-3 days intensity of illumination 0-50Lux, 4-6 days intensity of illumination 50-100Lux, 7-10 days intensity of illumination 150-200Lux, 10-20 days intensity of illumination 200-300Lux, started to gather after 21 days.
Claims (1)
1. a pilose antler mushroom cultivation method, is characterized in that:
(1), by mass fraction culture medium raw material is taken: wood chip 40-60 part, rice bran 10-20 part, wheat bran 5-10 part, continuous seed shell 10-20 part, lime 1-3 part, Nutrition Soil 10-15 part, water 80-110 part;
(2), by step (1) raw material mix, control pH value 6-7, load blake bottle, every bottle of 400-500 part, gland encapsulates;
(3), blake bottle sends into vacreation pot, suction 50-80KPa after ozone sterilization 1-2 hour, sterilization 100-120 minute at 150 DEG C;
(4), at 15-20 DEG C cool, add humus 1-4 part, after cooling, send into every bottle graft original seed 40-50;
(5), 20-25 DEG C of culturing room, humidity 70-80%, between gas concentration lwevel 1600-3200PPM, cultivates 20-25 days;
(6), mycelium stimulation process, utilize mushroom culturing device to carry out mycelium stimulation process and carry out moisturizing by 85% of old mycoderma weight simultaneously;
(7), flower bud is urged to gather, in culturing room after mycelium stimulation, temperature 14-15 DEG C, humidity 95-98%, below gas concentration lwevel 1200PPM, 1-3 days intensity of illumination 0-50Lux, 4-6 days intensity of illumination 50-100Lux, 7-10 days intensity of illumination 150-200Lux, 10-20 days intensity of illumination 200-300Lux, started to gather after 21 days.
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| CN201410700135.9A CN104350954B (en) | 2014-02-22 | 2014-11-28 | Cornu Cervi Pantotrichum mushroom cultivation method |
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| CN201410064367X | 2014-02-22 | ||
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| CN201410700135.9A CN104350954B (en) | 2014-02-22 | 2014-11-28 | Cornu Cervi Pantotrichum mushroom cultivation method |
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| CN104350954B CN104350954B (en) | 2016-08-31 |
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Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105218197A (en) * | 2015-11-02 | 2016-01-06 | 江苏农牧科技职业学院 | A kind of pilose antler mushroom cultivation medium formula and preparation method thereof |
| CN109548561A (en) * | 2018-12-25 | 2019-04-02 | 昆山青禾食用菌科技有限公司 | A kind of pilose antler mushroom culture method |
| CN110663453A (en) * | 2019-11-15 | 2020-01-10 | 昆山青禾食用菌科技有限公司 | Lyophyllum decastes culture material, preparation method and application |
| CN111296173A (en) * | 2020-03-27 | 2020-06-19 | 江苏华绿生物科技股份有限公司 | Industrialized cultivation medium for velvet antler mushroom and method for cultivating edible fungi |
| CN111512885A (en) * | 2020-04-28 | 2020-08-11 | 江苏华绿生物科技股份有限公司 | Preparation process for industrially cultivating velvet antler mushroom |
| CN111771616A (en) * | 2020-08-18 | 2020-10-16 | 湖南和平生物科技有限公司 | Industrialized cultivation method of velvet antler mushroom |
| CN113412760A (en) * | 2021-06-22 | 2021-09-21 | 江苏华绿生物科技股份有限公司 | Hypsizigus marmoreus culture medium and hypsizigus marmoreus cultivation process |
| CN113796263A (en) * | 2021-09-13 | 2021-12-17 | 贵州大秦农业科技有限公司 | Large-scale cultivation method of velvet antler mushroom |
| CN116171797A (en) * | 2023-04-04 | 2023-05-30 | 福建恒绿生物科技有限公司 | Cultivation method of velvet mushrooms |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| JP2001025320A (en) * | 1990-03-08 | 2001-01-30 | Takara Shuzo Co Ltd | Artificial culture of lyophyllum decastes |
| JP2007054044A (en) * | 2005-07-26 | 2007-03-08 | Yamasa Shoyu Co Ltd | Method for artificially culturing lyophyllum shimeji and culture medium |
| CN103210849A (en) * | 2013-03-04 | 2013-07-24 | 上海丰科生物科技股份有限公司 | Lyophyllum decastes new bacterial strain |
| CN103340156A (en) * | 2013-03-25 | 2013-10-09 | 上海丰科生物科技股份有限公司 | Novel strain of lyophyllum decastes |
-
2014
- 2014-11-28 CN CN201410700135.9A patent/CN104350954B/en active Active
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
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| JP2001025320A (en) * | 1990-03-08 | 2001-01-30 | Takara Shuzo Co Ltd | Artificial culture of lyophyllum decastes |
| JP2007054044A (en) * | 2005-07-26 | 2007-03-08 | Yamasa Shoyu Co Ltd | Method for artificially culturing lyophyllum shimeji and culture medium |
| CN103210849A (en) * | 2013-03-04 | 2013-07-24 | 上海丰科生物科技股份有限公司 | Lyophyllum decastes new bacterial strain |
| CN103340156A (en) * | 2013-03-25 | 2013-10-09 | 上海丰科生物科技股份有限公司 | Novel strain of lyophyllum decastes |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105218197A (en) * | 2015-11-02 | 2016-01-06 | 江苏农牧科技职业学院 | A kind of pilose antler mushroom cultivation medium formula and preparation method thereof |
| CN105218197B (en) * | 2015-11-02 | 2018-07-13 | 江苏农牧科技职业学院 | A kind of pilose antler mushroom cultivation medium formula and preparation method thereof |
| CN109548561A (en) * | 2018-12-25 | 2019-04-02 | 昆山青禾食用菌科技有限公司 | A kind of pilose antler mushroom culture method |
| CN110663453A (en) * | 2019-11-15 | 2020-01-10 | 昆山青禾食用菌科技有限公司 | Lyophyllum decastes culture material, preparation method and application |
| CN111296173A (en) * | 2020-03-27 | 2020-06-19 | 江苏华绿生物科技股份有限公司 | Industrialized cultivation medium for velvet antler mushroom and method for cultivating edible fungi |
| CN111512885A (en) * | 2020-04-28 | 2020-08-11 | 江苏华绿生物科技股份有限公司 | Preparation process for industrially cultivating velvet antler mushroom |
| CN111771616A (en) * | 2020-08-18 | 2020-10-16 | 湖南和平生物科技有限公司 | Industrialized cultivation method of velvet antler mushroom |
| CN113412760A (en) * | 2021-06-22 | 2021-09-21 | 江苏华绿生物科技股份有限公司 | Hypsizigus marmoreus culture medium and hypsizigus marmoreus cultivation process |
| CN113796263A (en) * | 2021-09-13 | 2021-12-17 | 贵州大秦农业科技有限公司 | Large-scale cultivation method of velvet antler mushroom |
| CN116171797A (en) * | 2023-04-04 | 2023-05-30 | 福建恒绿生物科技有限公司 | Cultivation method of velvet mushrooms |
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