Method for producing exopolysaccharides by promoting fermentation of lucid ganoderma liquid
A technology for liquid fermentation and extracellular polysaccharide, applied in the field of microbial fermentation, can solve the problems of labor consumption, long cycle, small solid fermentation yield, etc., and achieve the effects of reducing equipment and production costs, facilitating industrial production, and increasing polysaccharide yield
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0022] Static culture compared with shaker culture: add 150ml (liquid level about 2cm) culture medium into 500ml Erlenmeyer flask, inoculate seed culture medium with a wet weight of 0.5g per 100ml fermentation broth, and culture at 30°C for 6 days; The shaker culture under the conditions was used as the control, and the shaker speed was 150r·min -1 . At the end of fermentation, the bacterial biomass and exopolysaccharide content were measured. When cultured statically, the exopolysaccharide produced per gram of bacteria was 0.179g; the exopolysaccharide produced per gram of bacteria in the control group was 0.086g.
Embodiment 2
[0024] Fermentation of Ganoderma lucidum with different liquid levels: Add appropriate amount of medium into a 500ml Erlenmeyer flask to control the liquid level at 0.1, 0.5, 1, 2, and 5 cm respectively, and inoculate seed liquid with a wet weight of 0.5 g per 100 ml of fermentation liquid. Cultured at 30°C for 6 days. At the end of fermentation, the bacterial biomass and exopolysaccharide content were measured. When the height of the liquid level is 0.1cm, the exopolysaccharide produced by each gram of bacteria is 0.104g; when the height of the liquid level is 0.5cm, the extracellular polysaccharide produced by each gram of bacteria is 0.148g; At 1cm, the exopolysaccharide produced per gram of bacteria is 0.166g; when the liquid level is 2cm, the exopolysaccharide produced per gram of bacteria is 0.179g; The exopolysaccharide produced was 0.242g.
Embodiment 3
[0026] Culture medium and culture method are the same as embodiment 1. The height of the liquid level in the experimental group was 0.5cm, and it was placed on a shaking table at 30°C and 150r min at intervals of 6, 12, 24, and 48 hours respectively. -1 Cultured for 10 min, and the control group was cultured statically throughout. The fermentation time is 6 days. At the end of fermentation, the bacterial biomass and exopolysaccharide content were measured. When the interval time is 6h, the extracellular polysaccharide produced by each gram of bacteria can reach 0.127g; when the interval time is 12h, the extracellular polysaccharide produced by each gram of bacteria can reach 0.136g; The extracellular polysaccharide produced by one gram of bacteria can reach 0.145g; when the interval time is 48h, the extracellular polysaccharide produced per gram of bacteria can reach 0.157g; Up to 0.148g.
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