Mycolicibacteriumneworleansense WCJ and application thereof in degradation of organic pollutants
A technology for organic pollutants and mycobacteria, applied in water pollutants, microorganism-based methods, bacteria, etc., can solve the problems of high-efficiency degradation of mycobacteria not found, and achieve the effect of high-efficiency degradation ability and broad application prospects.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0031] Example 1: Isolation, purification and identification of strain WCJ.
[0032] 1. Isolation and purification of strain WCJ.
[0033] Strain WCJ is a Gram-positive bacterium domesticated and isolated from activated sludge. The specific steps are as follows:
[0034]Add 50mL of inorganic salt culture solution to a 300mL shake flask, add 10mL of activated sludge collected from a sewage treatment plant and n-hexane with a final concentration of 30mg / L, and carry out enrichment culture at 30°C until the concentration of n-hexane is the initial addition When the concentration is 50%, take out 5mL of the enrichment solution and put it into 50mL of fresh inorganic salt culture solution, add the same amount of n-hexane (to make the concentration 30mg / L), repeat the above enrichment process 5 times, and then add the enrichment solution for the last time. Dilute the collected solution 1500 times with sterile water, then streak LB solid medium, culture at 30°C, select a single colo...
Embodiment 2
[0049] Embodiment 2, the acquisition of mycobacterium new orleans WCJ resting cell
[0050] 1. Incline cultivation:
[0051] Inoculate Mycobacterium New Orleans WCJ into LB liquid medium, culture at 30°C, 160rpm for 24-36 hours, then line the activated bacteria on a solid LB plate in a 30°C incubator, take a single colony and continue to line the plate In order to detect the purity of the bacteria, the LB test tubes were stored on the inclined plane (4°C) routinely.
[0052] 2. Expand training
[0053] Inoculate the slanted bacteria in step 1 into LB liquid medium, culture at 30°C and 160rpm for 24-36 hours, obtain the expanded culture medium, centrifuge, collect the wet bacteria, wash with inorganic salt culture medium, and obtain Mycobacterium new orleans WCJ resting cells.
Embodiment 3
[0054] Example 3: Detection of the degradation performance of Mycobacterium new orleans WCJ on different concentrations of n-hexane.
[0055] Divide the inorganic salt culture solution into 300mL shake flasks each with a volume of 50mL, and sterilize at 110°C for 40min. After the sterilization, it was placed at room temperature for 2 days to confirm that there was no growth of miscellaneous bacteria. Add the quiescent cells that the final concentration reaches 50mg / L (with cell dry weight) embodiment 2 method acquisition, then add n-hexane as the only carbon source to make the final concentration respectively 85, 195, 230, 335, 405mg / L, After the shaker flask was sealed, culture it on a shaker at 30°C and 160 rpm, and make a blank control without adding bacteria. Regularly measure the concentration of n-hexane remaining in the shake flask, and draw the removal rate curve of different initial concentrations of n-hexane over time for the strains, the results are shown in Figu...
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