Algicidal Shewanella and application thereof in controlling blue algae water bloom
A technology of Shewanella and cyanobacteria blooms, applied in the field of environmental microorganisms, can solve the problems of limited processing capacity, secondary pollution, etc., and achieve the effects of short preparation cycle, good lethal effect, and good algae-dissolving effect
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Embodiment 1
[0036] The screening of embodiment 1 algae-lytic bacteria
[0037] Add 10mL of natural water samples collected from the Meiliang Bay waters of Taihu Lake to 90mL of algae liquid of Microcystis aeruginosa 9110 in the logarithmic phase, take the yellow algae liquid two days later, apply the gradient dilution method to the beef extract peptone medium agar plate, and cultivate at 28°C After 24 hours, take a plate with a moderate colony density, and select different strains according to the different colony shapes.
[0038] The screened strains were inoculated into 10 mL of beef extract peptone medium, cultured at 28°C and 200 rpm for 24 hours, and 10 mL of cultured bacterial liquid was added to 90 mL of algae liquid of Microcystis aeruginosa in logarithmic phase. In addition, 10 mL of sterilized beef extract peptone medium was also added to 90 mL of algae liquid as a control. All the algae fluids of the experimental group and the control group were cultured in the light incubator...
Embodiment 2
[0042] The identification of embodiment 2 Shewanella Lzh-2 bacterial strains
[0043] Lzh-2, which has the strongest algicidal effect, was identified by morphological observation, staining, physiological and biochemical reactions, and 16srRNA gene sequence analysis. μm ~ 1.0μm × 1.0μm ~ 4.0μm, after 24 hours of shaker culture in liquid medium, individual cells up to 7μm. After being cultured on nutrient agar solid medium plate for 24 hours, the colony shape is round, the surface is smooth and flat, the edges are neat, colorless to light flesh red, transparent, and the size of the colony is 2mm to 3mm. After 16srRNA gene sequence analysis and homology comparison, it was known that it had 99% homology with a certain Shewanella strain in GenBank, so it was identified as Shewanella sp. and named Shewanella Lzh- 2. The strain has been preserved in the General Microbiology Center of the China Committee for the Collection of Microbial Strains, the preservation number is CGMCC No.65...
Embodiment 3
[0044] Embodiment 3 Shewanella Lzh-2 fermented liquid and the preparation method of ethyl acetate extract thereof
[0045] Shewanella Lzh-2 was inoculated in sterilized beef extract peptone medium according to the inoculum amount of 1%, and cultured on a shaker at 200 rpm at 28°C for 48 hours to obtain a fermentation broth containing Shewanella Lzh-2. Add ethyl acetate into the fermentation broth at a ratio of 1:1, put it into a shaker and vibrate for 24 hours, and separate the upper layer solution, that is, the ethyl acetate extract. The ethyl acetate was evaporated to dryness, dissolved in water, and filtered through a microporous membrane with a pore size of 0.22 μm for further purification of metabolites.
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