A Phomopsis strain and its application in the biotransformation of tripterine
A technology of tripterine and Phomopsis, applied in the biological field, can solve the problems of low water solubility, high myocardial toxicity, and affecting application
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0042] Embodiment 1, acquisition, identification and preservation of bacterial strains
[0043] 1. Acquisition of strains
[0044] 1. Get the disease-free fresh leaves of Tripterygium wilfordii plant in Yao County, Dali, Yunnan Province, and carry out surface disinfection. Surface disinfection method: rinse with clean water, rinse 4 times with clean water, rinse with 75% alcohol for 30s, then soak in 5% sodium hypochlorite for 2s, rinse with sterile water 10 times.
[0045] 2. Sterile filter paper absorbs the moisture on the surface, cuts off the liquid-contact side with a sterilized blade, then cuts the inside into small pieces and transplants it into the modified Martin solid medium containing 150mg / L penicillin and 120mg / L streptomycin , and then pick the growing single colonies for culture.
[0046] 3. Further carry out continuous purification to obtain a purely cultured strain, which is named LGT-5 strain.
[0047] 2. Identification of strains
[0048] 1. Colony morph...
Embodiment 2
[0063] Embodiment 2, application Phomopsis LGT-5 prepares 16-OH-Celastrol
[0064] 1. Application of Phomopsis LGT-5 for tripterine transformation
[0065] 1. Inoculate Phomopsis LGT-5 into a Erlenmeyer flask containing 150mL of modified Martin liquid medium, and cultivate it with shaking at 28°C and 180rpm until the logarithmic growth phase (usually the culture time is 1 day), at this time Phomopsis The concentration of mold LGT-5 was 5 g dry weight / L culture system. Dry weight measurement method: sample the culture system, collect the bacteria by centrifugation, wash thoroughly with sterile water, and then dry to dry weight.
[0066] 2. After completing step 1, add 2 mL of tripterine solution (containing 50 mg of tripterine, the solvent is DMSO) to the culture system, and culture with shaking at 28° C. and 180 rpm for 5 days. That is, the ratio of Phomopsis LGT-5 and tripterine is: 0.75 g dry weight of Phomopsis LGT-5: 50 mg tripterine.
[0067] 3. After completing step 2...
Embodiment 3、1
[0077] Example 3, Functional Verification of 16-OH-Celastrol
[0078] Test compound: Celastrol or 16-OH-Celastrol prepared in Example 2.
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