Brevundimonas diminuta and application thereof
A brevemonas, defect technology, applied in bacteria, water/sludge/sewage treatment, biochemical equipment and methods, etc., can solve problems such as lack, 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 algae-lytic bacteria
[0020] Using the natural soil as the source of bacteria, put the collected soil sample into a beaker, accounting for about 2 / 3 of the volume of the beaker, add sterile water, stir evenly, let it stand for 2 hours, and pipette 10ml to 100ml of the supernatant In the sterilized beef extract peptone liquid medium, culture at 37°C for 48h, and set aside.
[0021] The beef extract peptone medium described therein consists of: peptone 5.0g, NaCl5.0g, 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°C, 0.11Mpa for 30min.
[0022] Adjust the density of the bacterial solution to about 10 8 CFU / mL, according to the ratio of 1:10 (v / v), the bacterial liquid was added to the Microcystis algae liquid, and the algal cell density was about 10 9 pc / L, after 5-7 days, take the yellowed algae liquid as...
Embodiment 2
[0025] Application of embodiment 2 bacterial strain Brevundimonas diminuta in Microcystis algae lysis
[0026] The strain was inoculated into the sterilized beef extract peptone liquid medium, and cultivated at 37°C for 48 hours, until the density of the bacteria was 1.0×10 9 -1.0×10 10 For CFU / mL, add the bacterial liquid to the algal liquid according to the volume percentage of bacterial liquid: algal liquid 1:10-5:10, and the algal cell density in the treated algal liquid is 10 11 A / L or less. It can be drawn that the bacterial strain Brevundimonas diminuta has a higher algicidal ability to Microcystis, and after the mixture of bacteria and algae, it is cultivated for 10 days, and the algalytic efficiency can reach more than 98% (taking chlorophyll a as a measurement index) (such as figure 1 , 2 shown).
Embodiment 3
[0028] In the present embodiment, Microcystis aeruginosa is treated at a bacterium injection volume ratio of 3:10 by bacteria liquid: algae liquid. The specific implementation steps are as follows: inoculate Brevundimonas diminuta in 10 ml of sterilized beef extract peptone liquid medium, culture at 37°C for 48 hours, and then transfer the bacterial solution to 100 ml of sterilized beef extract peptone liquid medium , cultured at 37°C for 48 hours, and adjusted the density of the bacterial solution to about 10 9CFU / mL, then add the bacterial solution to the algal liquid according to the bacterial volume ratio of 3:10, and measure the initial concentration of chlorophyll a in the algal liquid to be 1531 μg / L. After 10 days of adding the bacterial liquid, the chlorophyll concentration is 68.7μg / L, algae-dissolving efficiency is 95.5%.
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