Brevundimonas diminuta and its application
A Brevimonas, defect technology, applied in bacteria, biological water/sewage treatment, microorganisms, etc., can solve problems such as shortage, and achieve the effect of environmental friendliness and strong algae-dissolving effect
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Embodiment 1
[0018] Example 1 Strain isolation
[0019] 1. Screening of algicidal bacteria
[0020] Take the natural soil as the source of bacteria, put the collected soil sample into a beaker, which accounts for about 2 / 3 of the volume of the beaker, add sterile water, stir evenly, let stand for 2 hours, and remove 10ml to 100ml of the supernatant. The sterilized beef extract peptone liquid medium was cultured at 37°C for 48h, and it was used for later use.
[0021] The beef extract peptone medium is composed of: peptone 5.0g, NaCl 5.0g, beef extract 5.0g, distilled water 1000ml, pH is about 7.5, for solid medium, need to add agar powder 2.0% (m / v) , the medium used should be sterilized at 120℃, 0.11Mpa for 30min.
[0022] Adjust the density of the bacterial liquid so that it is about 10 8 CFU / mL, according to the ratio of 1:10 (v / v), the bacterial solution was added to the Microcystis algal solution, and the algal cell density was about 10 9 Pieces / L, after 5-7 days, take the yellowe...
Embodiment 2
[0025] Example 2 Application of strain Brevundimonas diminuta in Microcystis algal lysis
[0026] The strain was inoculated into the sterilized beef extract peptone liquid medium, and cultured at 37°C for 48h, and the density of the bacteria was 1.0×10 9 -1.0×10 10 When CFU / mL, the bacterial liquid is added to the algal liquid according to the bacterial liquid: algal liquid volume percentage 1:10-5:10, and the algal cell density in the processed algal liquid is 10 11 pcs / L or less. It can be concluded that the strain Brevundimonasdiminuta has a high algae-dissolving ability to Microcystis, and the algae-dissolving efficiency can reach more than 98% (with chlorophyll a as the measurement index) after the bacteria and algae are mixed for 10 days. figure 1 , 2 shown).
Embodiment 3
[0028] The present embodiment is to treat Microcystis aeruginosa according to the bacterial solution: the algal solution volume ratio is 3:10. The specific implementation steps are as follows: inoculate Brevimonas deficient in 10ml of sterilized beef extract peptone liquid medium, cultivate at 37°C for 48 hours, and then transfer the bacterial liquid to 100ml of sterilized beef extract peptone liquid medium medium, incubate at 37°C for 48h, and adjust the density of the bacterial solution to about 10 9CFU / mL, and then add the bacterial solution to the algal solution according to the bacterial-algae volume ratio of 3:10. The initial concentration of chlorophyll a in the algal solution is 1531 μg / L. After adding the bacterial solution for 10 days, the chlorophyll concentration is 68.7μg / L, the algae-dissolving efficiency was 95.5%.
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