Microbial preparation for aquaculture water environment ammonia-nitrogen degradation and application thereof
A microbial preparation, aquaculture water technology, applied in the field of microbial preparations for ammonia nitrogen degradation in aquaculture water environment, can solve problems such as limited emergency degradation effect
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preparation example Construction
[0023] In the present invention, the preparation method of Rhodopseudomonas palustris PSB20 bacterial agent preferably comprises the following steps:
[0024] (1) Inoculate the basal medium with Rhodopseudomonas palustris strain PSB20, and culture it under light at 2500-3500Lx for 72-144 hours at 25-35°C to obtain the seed liquid;
[0025] (2) inoculate the seed liquid into the propagation medium according to the inoculum amount of 5%-20% of the volume concentration, and cultivate under light at 30-35° C. for 3-5 days at 2500-3500 Lx to obtain the bacterial liquid;
[0026] (3) adding a flocculant to the bacterial liquid, and removing the supernatant after flocculation to obtain a thick bacterial paste;
[0027] (4) Adding a protective agent to the thick bacterial paste to obtain the Rhodopseudomonas palustris PSB20 microbial agent.
[0028] In the present invention, the PSB20 bacterial strain of Rhodopseudomonas palustris is first inoculated into the basic medium for light c...
Embodiment 1
[0038] (1) Cultivation of bacterial strain PSB20:
[0039] Take bacterial strain PSB20 and inoculate it into basal medium (sodium acetate 3.3g, potassium dihydrogen phosphate 0.6g, ammonium chloride 1.0g, magnesium sulfate 0.3g, calcium chloride 0.05g, sodium chloride 1.0g, yeast extract 1.0 g, manganese sulfate 0.023g, ferrous sulfate 0.005g, water 1000mL, pH 7.5~8.5), 27°C, 2500Lx light culture for 72h, when the OD of the culture solution 660 When it reached 1.5, the seed liquid was obtained.
[0040] Inoculate the seed liquid to the transparent plastic agricultural film (containing propagation medium: 1.0 g of ammonium chloride, 3.5 g of sodium acetate, 2.0 g of magnesium chloride, 0.1 g of calcium chloride, potassium dihydrogen phosphate, etc. 0.6g, 0.4g of dipotassium hydrogen phosphate, 0.1g of yeast extract, 1000mL of water, pH 7.2), 30~35°C (when the temperature is too high, use water spray to cool down), and use sunlight to cultivate for 3 days (cloudy and At night,...
Embodiment 2
[0044] Determination of the components of the product prepared in Example 1: After gradient dilution of the product prepared in Example 1 with physiological saline, each dilution was coated by the double-layer plate method and incubated at 35°C. The technical results showed that the product in Example 1 1 The number of viable PSB20 bacteria in the prepared product was 5.82×10 9 CFU / mL.
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