Production method of pure protein derivative of tuberculin
A technology of protein derivatives and tuberculin, which is applied in the field of biological protein preparation, can solve the problems that the production conditions cannot meet the production requirements of GMP, the health of production operators is seriously threatened, and the environment is potentially threatened, so as to shorten the preparation time , Improve production efficiency and product quality, and reduce environmental hazards
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0047] A production method of tuberculin pure protein derivatives, comprising the steps of:
[0048] A. Seed Lot Recovery
[0049] Confirm that the attenuated Mycobacterium tuberculosis strain ATCC25177 strain tube has no damage, open the seed batch, dilute the strain with Sutong medium, and mix evenly; use Sutong potato soup solid slant medium, with the inoculation amount of 0.5-5mg / branch , covering the entire slant of the medium; culturing for 3-4 weeks at a temperature of 36-38°C to obtain a seed batch recovery culture;
[0050] B. Seed Lot Expansion
[0051] Take the revived culture of the seed batch, add Sutong medium, elute, grind, centrifuge at 15000g for 5min, centrifuge to discard the supernatant, weigh, and calculate the concentration of the bacterial solution; add Sutong medium, dilute the bacterial solution; Sutong potato soup solid slant medium, the inoculation amount is not less than 0.5mg / branch, and the entire medium slant is covered; cultivated at a tempera...
Embodiment 2
[0074] A production method of tuberculin pure protein derivatives, comprising the steps of:
[0075] A. Seed Lot Recovery
[0076] Confirm that the appearance of the attenuated Mycobacterium tuberculosis strain CMCC93020 strain tube is not damaged, open the seed batch, dilute the strain to a concentration of 10 mg / mL in Sutong medium, and mix evenly; use Sutong potato soup solid slant medium to inoculate the bacteria Amount of 2.5mg / branch, covering the entire slant of the medium; culturing for 3 weeks at a temperature of 38°C to obtain a seed batch of resuscitated culture;
[0077] B. Seed Lot Expansion
[0078] Take the revived culture of the seed batch, add Sutong medium, elute, grind, centrifuge at 15000g for 5min, centrifuge to discard the supernatant, weigh, and calculate the concentration of the bacterial solution; add Sutong medium, and dilute the bacterial solution to 100mg / mL; Sutong Potato Soup solid slant medium was used, and the inoculation amount was 25mg / branch...
Embodiment 3
[0101] Based on Example 1, this example discusses the control conditions in the production process to further illustrate the technical solution.
[0102] (1) Sutong Potato Soup Solid Slant Medium Amplified Inoculum Amount
[0103] Set the inoculated amount of 0.5mg / branch, 1mg / branch, 2.5mg / branch and 5mg / branch. Under the same culture conditions, the results obtained are shown in Table 1 below, and it is known that: with the increase of inoculated bacteria amount, the The yield is increasing; the specific amount of inoculum can be determined according to the production scale, passage times and amplification quality;
[0104] Table 1
[0105] Inoculation amount Bacteria yield (mg) 0.5mg / bottle 118 1mg / bottle 168 2.5mg / bottle 235 5mg / bottle 365
[0106] (2) Sutong potato soup solid slant medium expansion culture time
[0107] Set the culture time for 3 weeks and 4 weeks. Under the same culture conditions, the results obtained are shown ...
PUM
Property | Measurement | Unit |
---|---|---|
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