Method for Cultivating Pleurotus eryngii by Solid Fermentation of Burdock
A technology of solid fermentation and king oyster mushroom is applied in cultivation, plant cultivation, mushroom cultivation and other directions, and can solve the problems such as difficulty in meeting the needs of the development of burdock planting industry, low proportion of the total amount of burdock raw materials processed, backward technology, etc. Increased product value, shorter product time and easier operation
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
example 1
[0019] Example 1 The present invention will be described in further detail below in conjunction with embodiment:
[0020] There are many varieties of Pleurotus eryngii, which are highly adaptable to the medium and the environment, but there are still certain differences in the requirements of specific varieties for the environment and the medium, and there are also great differences in the adaptability of the same variety to the medium. Before adjusting the medium, the strains must first be adapted to the new medium, and the strains adapted to the new medium must be screened first;
[0021] Step 1 strain screening:
[0022] The first step, mycelial adaptability screening: select 10 Pleurotus eryngii mushrooms with complete caps, beautiful shapes, strong growth, and no variegation, and select mushrooms 2 cm below the caps and cut them into 0.5*0.5 Centimeter Ding, inoculated on the potato dextrose agar slant medium under sterile conditions, cultured at 20-27°C for 75 hours, se...
example 2
[0031] Step 1 strain screening:
[0032] The first step, mycelial adaptability screening: select 10 Pleurotus eryngii mushrooms with complete caps, beautiful shapes, strong growth, and no variegation, and select mushrooms 2 cm below the caps and cut them into 0.5*0.5 Centimeter Ding, inoculated on potato dextrose agar slant medium under aseptic condition, cultured at 20-22°C for 75 hours, selected the test tubes with strong hyphae growth on the slant medium, eliminated the weak test tubes, and inoculated them on crushed Dried burdock granules, the water content of the granules is 60-62%, cultivated at 22-24°C for 7 to 10 days, and inoculated vigorously growing mycelia on the slant medium of potato dextrose agar, and cultivated at 22-24°C for 75 hour, repeated twice;
[0033] The second step, mycelia mushroom-forming screening: Inoculate the vigorously growing mycelium obtained in the first step of step 1 on the crushed dry burdock granules, the water content of the granules i...
Embodiment 3
[0039] Step 1 strain screening:
[0040] The first step, mycelial adaptability screening: select 10 Pleurotus eryngii mushrooms with complete caps, beautiful shapes, strong growth, and no variegation, and select mushrooms 2 cm below the caps and cut them into 0.5*0.5 Centimeter Ding, inoculated on potato dextrose agar slant medium under sterile conditions, cultured at 25-27°C for 75 hours, selected the test tubes with strong growth of mycelium on the slant medium, eliminated the test tubes with weak growth, and inoculated on crushed Dried burdock granules, the water content of the granules is 64-65%, cultivated at 25-27°C for 7 to 10 days, and inoculated vigorously growing mycelia on the slant medium of potato dextrose agar, cultivated at 25-27°C for 75 Hour;
[0041] The second step, mycelia mushroom-forming screening: Inoculate the vigorously growing mycelium obtained in the first step of step 1 on the crushed dry burdock granules, the water content of the granules is 64-65...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com