A strain of Bacillus subtilis and its application in fermentative production of adenosine
A technology of Bacillus subtilis and adenosine, which is applied in the field of Bacillus subtilis and its application in the fermentation and production of adenosine, which can solve the problem that adenosine cannot meet the market demand, the fermentation yield and conversion rate are low, and the raw materials and energy consumption are large and other problems, to achieve the effect of good industrial application prospects, high yield and conversion rate, and improved strain stability
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0025] Example 1: A strain of Bacillus subtilis and its application in fermentative production of adenosine
[0026] A strain of Bacillus subtilis ACA301, which is classified as Bacillus subtilis, was preserved in the China General Microorganism Culture Collection Center (CGMCC) on November 19, 2018, and the culture preservation number is CGMCC No. .16753.
[0027] The Bacillus subtilis ACA301 and its application in fermentative production of adenosine comprise the following steps:
[0028] (1) Strain culture, inoculate the preserved Bacillus subtilis ACA301 strain in a sterile activation medium, cultivate at 34°C for 21 hours until fresh bacteria grow, sterilize the seed medium, cool to 40°C, The pH was adjusted to 7, and the activated Bacillus subtilis ACA301 strain was inoculated into the seed medium for cultivation until the logarithmic growth phase. Strain culture conditions: temperature 34°C, pH value 7, dissolved oxygen 12%, tank pressure 0.035MPa.
[0029] (2) Ferme...
Embodiment 2
[0038] Example 2: A strain of Bacillus subtilis and its application in fermentative production of adenosine
[0039] The Bacillus subtilis ACA301 and its application in fermentative production of adenosine comprise the following steps:
[0040] (1) Strain cultivation, inoculate the preserved Bacillus subtilis ACA301 strain in a sterile activation medium, cultivate at 28°C for 18 hours until fresh bacteria grow, sterilize the seed medium, cool to 40°C, The pH was adjusted to 6.5, and the activated Bacillus subtilis ACA301 strain was inoculated into the seed medium for cultivation until the logarithmic growth phase. Strain culture conditions: temperature 28°C, pH 6.5, dissolved oxygen 10%, tank pressure 0.02MPa.
[0041] (2) Fermentation culture, the fermentation medium is sterilized, cooled to 40 DEG C, and the pH is adjusted to 6.5, the logarithmic growth phase bacterial classification obtained in step (1) is inserted into the fermentation medium for fermentation and cultivat...
Embodiment 3
[0050] Example 3: A strain of Bacillus subtilis and its application in fermentative production of adenosine
[0051] The mutagenesis screening method of Bacillus subtilis ACA301 described in the present invention is as follows:
[0052] Using Bacillus subtilis CICC10082 as the starting strain, through multiple times of diethyl sulfate (DES) chemical mutagenesis, ultraviolet mutagenesis, and then separation and purification, the adenosine high-yielding strain with substrate resistance and genetic markers was screened.
[0053] Starting bacteria: Bacillus subtilis CICC10082
[0054] Starting bacteria characteristics: G+, irregular bacteria, movement. The colony is round, with smooth surface, low convex surface, notched edge, off-white, translucent. Liquid cultures are cloudy. Gelatin liquefies. V.P positive, M.R. positive, H2S positive, urease negative, catalase positive, aerobic. The optimum growth temperature is 28-32°C, and the maximum growth temperature is 50°C. Litmus ...
PUM
Property | Measurement | Unit |
---|---|---|
pore size | aaaaa | aaaaa |
pore size | aaaaa | aaaaa |
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