Proteus mirabilis capable of eliminating ammonia nitrogen in water environment and application thereof
A technology of Proteus mirabilis and water environment, applied in the field of Proteus mirabilis
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0017] Example 1: Screening of Proteus mirabilis capable of reducing the concentration of ammonia nitrogen in the environment
[0018] Inoculate the Proteus mirabilis seeds stored at -80°C in LB medium, the liquid volume of the shake flask is 30%, the culture temperature is 27-30°C, the culture speed is 150-200rpm / min, and the culture time is 10-16 hours.
[0019] Collect the above-mentioned thalli, and divide the collected Proteus mirabilis V7 into 1.0×10 7 CFU / ml of Proteus mirabilis was inoculated in ammonia nitrogen medium for culture, and the ammonia nitrogen medium without bacteria was used as a control. At different time points, 1ml of the culture solution was taken out, centrifuged at 13,000rpm for 5min, and the supernatant was reserved. The supernatant was semi-quantitatively determined the ammonia nitrogen concentration using the ammonia nitrogen semi-quantitative determination kit (Hangzhou Luheng Biotechnology Co., Ltd.). The yellower the color, the lower the ammo...
Embodiment 2
[0020] Example 2: Changes in ammonia nitrogen content over time after inoculation of Proteus mirabilis V7
[0021] Dilute Proteus mirabilis V7 by 1.0 × 10 7 The initial concentration of CFU / mL was inoculated into the ammonia nitrogen medium, and then loaded into the shake flask, the liquid volume was 30% of the volume of the shake flask, the culture temperature was 28-30°C, and the culture speed was 150-200rpm / min. Take out 1ml of the bacterial culture solution every 24 hours, centrifuge at 12,000rpm for 5min, and analyze the content of ammonia nitrogen in the supernatant by Nessler's reagent colorimetry. See image 3 . After 4 days of inoculation, the removal efficiency of ammonia nitrogen was relatively stable and could reach more than 85%.
Embodiment 3
[0022] Example 3: Effects of Different Initial Concentrations of Ammonia Nitrogen on Ammonia Nitrogen Scavenging Efficiency
[0023] Proteus mirabilis V7 was inoculated into ammonia nitrogen medium containing 20, 50, 100, 200, 500, 1000 and 2000 mg / L, respectively (the initial concentration of bacteria at each concentration was 1.0×10 7 CFU / mL), and then loaded in the shake flask, the volume of the liquid was 30% of the volume of the shake flask, the culture temperature was 28-30°C, and the culture speed was 150-200rpm / min. After 64 hours, 1 ml of bacterial culture solution was taken out, centrifuged at 12,000 rpm for 5 minutes, and the content of ammonia nitrogen in the supernatant of the culture solution was analyzed by Nessler's reagent colorimetric method. The change process of ammonia nitrogen removal efficiency with time after inoculation with Proteus mirabilis V7 is shown in image 3 . When the ammonia nitrogen concentration was 20, 50 and 100mg / L, the efficiency of P...
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