Rhizobium strain and application thereof
A technology of rhizobia and bacterial strains, applied in the direction of bacteria, water/sludge/sewage treatment, biochemical equipment and methods, etc., can solve the problems of immature application of heterotrophic nitrifying bacteria engineering
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0033] 1. Isolation and screening of rhizobia zb612
[0034] (1) Sludge domestication: Take 5g of activated sludge from a landfill leachate treatment plant and place it in 250ml ammonia nitrogen degradation medium at a temperature of 30°C and a rotating speed of 100 for two days in a continuous shaker. After two days, transfer it to an Erlenmeyer flask Add 5ml of sterilized ammonium sulfate solution (1.5g / L), continue to acclimate it, repeat this step 3 times, take out 5ml of muddy water and place it in a sterilized centrifuge tube.
[0035] (2) Limit dilution separation: Take 1ml of the above supernatant and place it in a centrifuge tube with 10ml of sterile physiological saline, and dilute it to 10 -6, , Do three parallels, from 10 -5 With 10 -6 Take a 0.2ml plate from the section and spread it on the plate, incubate for 48 hours, and observe the colony growth.
[0036] (3) Strain selection and purification: select well-growing strains from the plate for streaking, and when they gr...
Embodiment 2
[0043] Growth of Rhizobium sp.zb612 and determination of ammonia nitrogen degradation
[0044] Rhizobium sp.zb612 was inoculated into 100ml of LB liquid medium (yeast extract 5g / L, peptone 10g / L, NaCl 10g / L), and cultured at 30°C, 100rpm, shaking on a shaker. After culturing for 48 hours, the cells are divided into sterilized preservation tubes, and 0.5 ml bacterial liquid and 0.5 ml 30% glycerol are added to each preservation tube. Store at minus 80°C for later use.
[0045] One loop of the strain was inoculated into 100ml heterotrophic nitrifying bacteria culture medium, 30°C, 100rpm, shaking culture for 24h, used as the active inoculum for the formal degradation experiment, and 5% of the active inoculum was used for 2 groups of experiments, each group separately Connect three cultures containing 100ml of sterilized ammonia nitrogen degradation medium (the concentration of ammonia nitrogen is 150ml / L), shake culture at 30℃, 100rpm, one of them, take samples every few hours to de...
Embodiment 3
[0048] Aerobic denitrification test of Rhizobium sp.zb612
[0049] Add 200ml glucose nitrate medium to a 500ml Erlenmeyer flask, add the cell suspension at 2% volume, and incubate on a shaker for 48 hours to observe the residual nitrate.
[0050] The test results showed that after 48h, the residual nitrate concentration was 48.4mg / L, nitrite was very little accumulated, the nitrate concentration in raw water was 352.7mg / L, and the degradation rate was 86.2%.
[0051] The test results show that under aerobic conditions, Rhizobium zb612 has the function of aerobic denitrification, and there is almost no accumulation of nitrite.
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More - R&D
- Intellectual Property
- Life Sciences
- Materials
- Tech Scout
- Unparalleled Data Quality
- Higher Quality Content
- 60% Fewer Hallucinations
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2025 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com
