Ganoderma lucidum cultivation method capable of increasing content of ganoderma lucidum polysaccharide
A cultivation method and technology of Ganoderma lucidum polysaccharide are applied in the field of cultivation of Ganoderma lucidum, can solve the problems of long production cycle of fruit body cultivation, low content of biologically active substances, hindering mass production of Ganoderma lucidum, etc., so as to promote the growth of Ganoderma lucidum, improve the activity and shorten the full bag effect of time
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0016] 1) Selection of strains: use the tissue separation method to obtain the pure mother seed, and use 75v% alcohol to disinfect a part of the wild or artificially cultivated fresh Hanzhi fruiting body, and then cut it into 3~ For small pieces of 5mm, take 5 pieces and place them on the plate culture medium, or take one piece and place them on the test tube slope culture medium. Cultivate for 3 to 4 days at 25~28℃. When white hyphae grow around the small tissues, select pure white hyphae and transplant them to a new slant medium. Continue to cultivate for about 5 days to obtain Ganoderma lucidum mother Species, and then expand into the original species and cultivated species.
[0017] 2) Preparation of culture medium: the following parts by weight of raw materials: 30 parts of sawdust, 10 parts of corn cob, 5 parts of rice bran, 1 part of Grifola frondosa, and 2 parts of burdock; the above raw materials are mixed and crushed, and water is added to a moisture content of 60 %, r...
Embodiment 2
[0022] 1) Selection of strains: use the tissue separation method to obtain the pure mother seed, and use 75v% alcohol to disinfect a part of the wild or artificially cultivated fresh Ganoderma lucidum fruit body, and then cut it into 3 by aseptic operation ~5mm small pieces, take about 5 pieces and place them on the plate culture medium, or take one piece and place them on the test tube slope culture medium. Cultivate for 3 to 4 days at 25~28℃. When white hyphae grow around the small tissues, select pure white hyphae and transplant them to a new slant medium. Continue to cultivate for about 5 days to obtain Ganoderma lucidum mother Species, and then expand into the original species and cultivated species.
[0023] 2) The following parts by weight of raw materials: 35 parts of sawdust, 20 parts of corn cob, 10 parts of rice bran, 3 parts of Grifola frondosa, and 4 parts of burdock; mix and pulverize the above raw materials, add water to 65% of water content. Bagging. Each bag of...
Embodiment 3
[0028] 1) Selection of strains: use the tissue separation method to obtain the pure mother seed, and use 75v% alcohol to disinfect a part of the wild or artificially cultivated fresh sweet mushroom fruit bodies, and then cut them into aseptic methods For small pieces of 3 to 5 mm, take 5 pieces and place them on the plate culture medium, or take one piece and place them on the test tube slope culture medium. Cultivate for 3 to 4 days at 25~28℃. When white hyphae grow around the small tissues, select pure white hyphae and transplant them to a new slant medium. Continue to cultivate for about 5 days to obtain Ganoderma lucidum mother Species, and then expand into the original species and cultivated species.
[0029] 2) The following parts by weight of raw materials: 32 parts of sawdust, 15 parts of corn cob, 8 parts of rice bran, 2 parts of Grifola frondosa and 3 parts of burdock; mix and crush the above raw materials, add water to 62% water, and then bag . Each bag of dry materi...
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