Method for preparing alkyl glycoside
A technology of alkyl glycosides and bacterial strains, which is applied in the field of preparation of alkyl glycosides, can solve the problems of shortening, long reaction time, and slow reaction speed, etc., to improve conversion rate and yield, facilitate industrial production, and avoid dehydration condensation Effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
example 1
[0021] First, weigh 10g of glucose, 8g of peptone, 4g of sodium chloride, 8g of agar, and 0.3g of beef extract in turn, add them to a petri dish filled with 700mL of deionized water, stir for 10min, and make a culture medium, divide the culture medium into two parts , one part is culture medium A, and the other is divided into medium B, for later use; inoculate 4 strains of bacillus on the above-mentioned medium A, at 36°C, shake the shaker for 16 hours, and then put the culture solution under 6000r / min Centrifuge for 20 minutes, discard the supernatant to obtain the strain of Bacillus; pipette 10% of the above-mentioned Bacillus into a beaker, place the beaker under ultraviolet light for 10 minutes, and obtain the strain containing Bacillus variabilis; select 3 strains of Bacillus variabilis Bacteria were inoculated onto the medium B prepared in the above steps, cultured on a shaker at 36°C for 16 hours, centrifuged at 6000r / min for 20 minutes, and the supernatant was discarde...
example 2
[0024]First, weigh 15g of glucose, 9g of peptone, 5g of sodium chloride, 9g of agar, and 0.4g of beef extract in turn, add them to a petri dish filled with 750mL of deionized water, stir for 15min, and make a culture medium, divide the culture medium into two parts , one part is culture medium A, the other is divided into medium B, for later use; inoculate 5 strains of bacillus on the above-mentioned medium A, at 37°C, shake the shaker for 17 hours, and then put the culture solution at 7000r / min Centrifuge for 25 minutes, discard the supernatant, and obtain the Bacillus strain; pipette 15% of the above-mentioned Bacillus into a beaker, and place the beaker under ultraviolet light for 15 minutes to obtain the strain containing Bacillus mutator; select 4 strains of Bacillus mutator Bacteria were inoculated onto the medium B prepared in the above steps, and cultured on a shaking table at 37°C for 17 hours, then centrifuged at 7000 r / min for 25 minutes, and the supernatant was disc...
example 3
[0027] First, weigh 20g of glucose, 10g of peptone, 6g of sodium chloride, 10g of agar, and 0.5g of beef extract in sequence, add them to a petri dish filled with 800mL of deionized water, stir for 20min, and make a culture medium, divide the culture medium into two parts , one part is culture medium A, and the other is divided into medium B, for later use; inoculate 6 strains of bacillus on the above-mentioned medium A, at 38°C, shake the shaker for 18 hours, and then put the culture solution at 8000r / min Centrifuge for 30 minutes, discard the supernatant to obtain the strain of Bacillus; pipette 20% of the above-mentioned Bacillus into a beaker, and place the beaker under ultraviolet light for 20 minutes to obtain the strain containing Bacillus mutator; select 5 strains of Bacillus mutator Bacteria were inoculated onto the medium B prepared in the above steps, and cultured on a shaking table at 38°C for 18 hours, then centrifuged at 8000r / min for 30min, and the supernatant wa...
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