A kind of preparation method of solid bacterial agent for biological degumming of hemp
A technology of biological degumming and solid inoculum, which is applied in the direction of bacteria and bacterial retting, can solve the problems of difficult preparation technology of bacteria, easy degradation of bacteria and expansion of application of variation, etc. It has great theoretical and practical significance and is easy to popularize and apply. , the effect of saving energy
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0031] Embodiment 1 A kind of preparation method of solid bacterial agent for biological degumming of hemp
[0032] like figure 1 As shown, a ring of DCE-01 bacterial strains was picked from the slant original seed lawn preserved by the research group of Professor Peng Yuande, Chinese Academy of Agricultural Sciences, and inoculated into 5 mL of improved broth culture medium (GR culture medium), fully suspended, and 35 Incubate at ℃ for 6 hours; spread it on YQ nutrient agar plate after dilution, incubate at 35℃ for 20 hours, and isolate a single colony; select a typical colony and streak it on a fresh slope, incubate at 35℃ for 20 hours, vacuum pack, and store at room temperature; put 1mL of sterilized improved Pour the broth culture solution (GR culture solution) into one tube of the above-mentioned slanted bacteria, and gently scrape the bacterial lawn on the surface with an inoculation loop to ensure that the bacterial lawn is completely mixed into the culture solution.
...
Embodiment 2
[0042] Embodiment 2 A kind of preparation method of solid bacterial agent for biological degumming of hemp
[0043] Pick a ring of DCE-01 strains from the slant original species preserved by the research group of Professor Peng Yuande of the Institute of Hemp, Chinese Academy of Agricultural Sciences, and inoculate it into 5mL of improved broth culture medium (GR culture medium), suspend well, and incubate at 35°C for 6h After dilution, spread on YQ nutrient agar plate, culture at 35°C for 18 hours, and isolate a single colony; select typical colonies and streak on a fresh slope, culture at 35°C for 18 hours, vacuum pack, and store at room temperature; culture 1 mL of sterilized improved broth Liquid (GR culture medium) was poured into 1 tube of the above-mentioned slant strains, and the bacterial lawn on the surface was gently scraped with an inoculation loop to ensure that the bacterial lawn was completely mixed into the culture medium.
[0044] Specifically, the mass ratio ...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 
