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
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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.
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