Special shewanella and application thereof
A technology of Shewanella and bacterial agents, applied in the field of Isoshewanella, can solve environmental problems such as pollution, waste of resources, etc., and achieve the effects of simple process, improved phosphorus absorption coefficient, and environmental friendliness
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Embodiment 1
[0035] Example 1. Isolation and screening of functional strain GZT-Ali01
[0036] 1) Collection of samples
[0037] (1) Samples were collected from moldy plastered phosphogypsum samples. Select plastered phosphogypsum samples with obvious damp and moldy conditions in the construction site, and put the collected samples into collection bags.
[0038] (2) The collected samples were crushed and sieved, and the 100-mesh samples were collected.
[0039] (3) Store the samples in a refrigerator at 4°C for later use.
[0040] 2) Screening of functional strains
[0041] (1) Accurately weigh 1 g of the sample into a sterilized 250 mL Erlenmeyer flask, and add 99 mL of sterile water.
[0042] (2) Shake for 30 minutes in a constant temperature shaker at 180r / min at about 27°C.
[0043] (3) After shaking for 30 minutes, take the supernatant and dilute to 1.0×10-2, 1.0×10-3, 1.0×10-4, 1.0×10-5, 1.0×10-6, 1.0×10-7 .
[0044] (4) Take 100uL of each concentration and spread on 3 solid m...
Embodiment 2
[0050] Example 2. The drawing of the growth curve of the functional strain
[0051] 1) Preparation of seed solution. The strain was inoculated in LB liquid medium with an inoculation loop, and cultivated to the logarithmic phase at 35°C.
[0052] 2) Vaccination. Take 10 mL of the above seed solution and inoculate it into 200 mL of liquid LB medium, mix well and take 5 mL of the mixed solution and put them in 18 marked sterile test tubes.
[0053] 3) Cultivate. Place the inoculated test tubes at 35°C and incubate in a shaker at 180r / min.
[0054] 4) Measure. Use uninoculated LB liquid culture medium as a blank, and conduct photoelectric turbidimetry with the sample to be tested at a wavelength of 600nm.
[0055] Measurement results such as figure 1 , the strain enters the logarithmic phase after 15h in the culture process of LB liquid medium, enters the stable phase from 17h to 30h, and enters the decay phase after 35h.
Embodiment 3
[0056]Example 3. Identification of functional strains
[0057] 1) Colony appearance
[0058] Such as figure 2 , it can be seen from the figure that the colony morphology of the strain in the solid medium of complete nutrient agar is off-white, opaque, moist, viscous, and the colony morphology is irregular.
[0059] 2) Microscopic morphology of bacteria
[0060] After Gram staining, the microscopic appearance of the bacteria was as follows: image 3 , it can be seen from the figure that the bacterial strain is observed under a microscope, the thalline is granular, a single grain exists, and the thalline has no spores, and it is identified as a Gram-negative bacterium.
[0061] 3) Scanning electron microscope morphology of bacteria
[0062] Such as Figure 4 , the shape of the electron microscope of the bacteria is rod-shaped, which is consistent with the characteristic image of the optical microscope. The length is about 950nm. The surface of the bacteria is shriveled an...
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