Tylosin degrading bacterium and application thereof
A technology of tylosin and degrading bacteria, which is applied in the direction of bacteria, water/sludge/sewage treatment, biochemical equipment and methods, etc., and can solve the problems of tylosin environmental residues, etc.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0016] The collection of embodiment 1 bacterial strain
[0017] Bacteria sample collection and processing
[0018] Collect the soil, weigh 5g of the soil, add it to a Erlenmeyer flask filled with 95mL of sterilized distilled water (250mL, containing glass beads), shake it on a constant temperature shaker at 30°C, 200r / min for 30min, take it out and let it stand still;
[0019] Strain Isolation
[0020] Take 100uL of soil extract, spread it on the beef extract peptone solid medium plate, and culture it under the condition of 30°C in shade for 2 days. The composition of beef extract-peptone solid medium is: 3g beef extract, 5g peptone, 5g sodium chloride, 18g agar, distilled water to 1000mL, adjust pH to 7.0-7.2 with 1mol / L sodium hydroxide, and then sterilize.
[0021] Strain purification
[0022] Take the single colony isolated on the plate, streak it on the beef extract peptone solid medium plate, further separate and purify; this step can be repeated 2 to 3 times until a ...
Embodiment 2
[0042] Example 2 Degradation Efficiency Determination of Tylosin Degrading Strains
[0043] Add 100 mg / L tylosin to the inorganic salt liquid medium, shake well, inoculate a single colony, and place it at 30°C, 150r / min, and culture in shading. Chromatographic conditions: Sunfire C18 chromatographic column (150mm×4.6mm, 3.5um, Waters, USA); mobile phase is 0.01% formic acid aqueous solution (A) and acetonitrile (B); flow rate is 1.0mL / min; column temperature is 40°C; The injection volume is 10uL; the detection wavelength is 274nm. Elution program: 0~6min, 80%~0%A, 20%~100%B; 6~7min, 0%~80%A, 100%~20%B; 7~10min, 80%A, 20% b. Take 1 mL of the liquid to be tested, add 5 mL of methanol, shake well, centrifuge at 10,000 r / min for 15 min, take the supernatant, filter it with a 0.22 μm syringe filter to obtain the filtrate, and then measure it with a high-performance liquid chromatograph, such as image 3 , according to the linear regression equation to calculate the degradation r...
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