Bacillus amyloliquefaciens y1711, culture method and application thereof
A technology of amylolytic spores and Y1711, which is applied in the field of microorganisms and can solve problems such as inability to promote the growth of beneficial green algae
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Embodiment 1
[0020] Example 1 Isolation and screening of Bacillus amyloliquefaciens Y1711
[0021] Sampling: Select 3 different sampling points in the high-ammonia-nitrogen culture pond to take the sediment, put it into a sterile ziplock bag, seal it, and bring it back.
[0022] Separation: Dilute the bottom mud with sterile water at a ratio of 1g:10mL, and after treatment in a water bath at 80°C for 10min, draw 200μl of bacterial liquid and spread it on a starch medium plate, and cultivate at 37°C.
[0023] Purification: After 24 hours of plate culture, pick the strains that produce hydrolysis circles and streak them on the nutrient agar medium, and then select single bacteria with irregular colony edges and dry and wrinkled surfaces to continue streaking and purifying until a pure culture is obtained.
[0024] Screening: The purified strains were inoculated on the starch medium plate again, and the colony diameter (C) and the hydrolysis circle diameter (H) were measured. The strain with...
Embodiment 2
[0025] Example 2 Identification of Bacillus amyloliquefaciens Y1711
[0026] 1. Morphological identification and detection of physiological and biochemical characteristics
[0027] Bacillus amyloliquefaciens Y1711 was inoculated on a nutrient agar plate, cultured at 37°C for 24 hours, and the colony growth was observed. Physiological and biochemical properties were detected according to Berger's Handbook of Bacteria.
[0028] On the nutrient agar plate, the edges of the strains are irregular, the surface is dry and wrinkled; Gram-positive, the cells are rod-shaped, the spores are mesenchymal, and the cysts are enlarged. The strain nitrate test, contact enzyme test, starch hydrolysis, D mannitol acid production test were all positive.
[0029] 2. Molecular biological identification
[0030] A single colony of Bacillus amyloliquefaciens Y1711 was picked and inoculated into a nutrient broth medium at 37°C and 200rpm for 6h shaking culture, and the bacterial genome was extracte...
Embodiment 3
[0035] Example 3 Determination of laboratory water purification function of Bacillus amyloliquefaciens Y1711
[0036] The simulated aquaculture water is prepared indoors. The simulated aquaculture water is prepared by using shrimp bait soaking solution, ammonium nitrate, dipotassium hydrogen phosphate, and sodium nitrite, and then adjust the salinity to 15 and pH 7.8±0.5 with sea crystal. The total content of ammonia nitrogen in the simulated aquaculture water was 7.79 mg / L, and the total content of nitrite was 1.03 mg / L.
[0037] Add Bacillus amyloliquefaciens Y1711 bacterial liquid to the simulated breeding water, so that the bacterial content in it is 10 6 cfu / mu, before adding the bacteria solution and on the 1st, 2nd, 3rd, 5th, and 7th days after adding the bacteria solution, take water to measure the ammonia nitrogen and nitrite content in the water. The data are shown in Table 1 below.
[0038] The bacterial culture method of Bacillus amyloliquefaciens Y1711 is as foll...
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