Bionic culture method for cordyceps sobolifera
A cultivation method and technology of cicadae, which is applied in the direction of fungi, etc., can solve the problems of wild cicadae resource scarcity, seasonality, production cannot meet market demand, etc., and achieve the effect of easy harvesting and good air permeability
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0040] The conidia of Paecilomyces cicadae were collected from natural cicada flowers, the spores were diluted by the dilution method, coated on a potato-sucrose-agar plate, and cultured upside down at 25°C for 7 days to obtain a single colony. Pick the strains with vigorous colony growth, dense spores, and no angular change as monospore strains.
[0041] The monospore strain Paecilomyces cicadae was inoculated on the fruiting body formation medium (rice, water, ratio 40:60), and cultured at 22° C. for 30 days. Pick fast-growing, fruiting bodies that produce abundant, stout strains.
[0042] The bacterial strain obtained by screening was transferred to the sporulation medium (bran, silkworm chrysalis powder, water, ratio 40:10:50), cultivated at 25°C for 15 days, collected conidia, and separated them with 0.05% Tween 80 water. Spores made up to 1×10 6 single / ml concentration of spore fluid.
[0043] Soak tussah silkworm pupae in spore liquid for 3 minutes, pick them up, put...
Embodiment 2
[0046] Paecilomyces cicadae conidia were collected from natural cicada flowers, the spores were diluted by the dilution method, coated on a potato-glucose-agar medium plate, and cultured upside down at 25°C for 7 days to obtain monospore colonies. Pick the bacterial strains with vigorous growth, dense spores, and no angular change, and inoculate them on the fruiting body formation medium (millet, water, ratio 35:65), and cultivate them at 22° C. for 30 days. Will grow fast, producing abundant, stout strains with fruiting bodies.
[0047] The bacterial strain obtained by screening was transferred to the spore-producing medium (bran, silkworm chrysalis powder, water, ratio 45:8:47), cultivated at 26°C for 14 days, collected conidia, and separated them with 0.04% Tween 80 water. Spores made up to 3×10 6 / ml concentration of spore liquid.
[0048] Soak silkworm pupae in spore liquid for 2.5 minutes, pick them up, put them in a sterilized container, keep warm at 24°C, humidity 90...
Embodiment 3
[0051] The conidia of Paecilomyces cicadae were collected from natural cicadae flowers, the spores were diluted by the dilution method, coated on a potato-sucrose-agar plate, and cultivated upside down at 25°C for 7 days to obtain monospore strains. Pick the strains with vigorous growth, dense spores, and no angular transformation, and inoculate them on the fruiting body formation medium (barley, water, ratio 40:60), and cultivate them at 22°C for 30 days. Inoculate the fast-growing, fruiting bodies to produce abundant and strong strains on surface-sterilized grasshopper nymphs to maintain the pathogenicity of insects.
[0052] The bacterial strain obtained by screening was transferred to the spore-producing medium (bran, silkworm chrysalis powder, water, ratio 50:5:45), cultivated at 24°C for 13 days, collected conidia, and separated them with 0.03% Tween 80 water. Spores made up to 1×10 7 single / ml concentration of spore fluid.
[0053] Soak the grasshopper nymphs in the s...
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