Swamp Rhodopseudomonas of using nitrite nitrogen in high effect, and application
A technology of swamp rhodopseudomonas and nitrous nitrogen, which is applied in the field of photosynthetic bacteria and can solve problems such as effects affecting the application.
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Embodiment 1
[0022] The preparation of embodiment 1 bacterial classification
[0023] Take 100 μl of Rhodopseudomonas palustris 2-8 bacteria solution, spread it on the plate containing medium 2, place it in an anaerobic tank, and cultivate it for 3 days under the condition of light intensity of 2000lux and temperature of 28℃~30℃ , pick 1 inoculation loop strain from the culture medium slant and inoculate it into liquid medium 1, and anaerobically culture it under the same temperature and light conditions for 3 days, then re-amplify twice in liquid medium 1 at an inoculum concentration of 3%, That is, the strain culture fluid that can be used for large-scale production is obtained.
[0024] A, the formula of medium 1 is as follows: ammonium chloride 0.1%, sodium hydrogen phosphate 0.05%, magnesium sulfate or magnesium chloride 0.02%, sodium chloride 0.2%, yeast extract or peptone 0.1~0.2%, the above ingredients are dissolved in water, Steam sterilization at 121°C for 20 minutes. The follo...
Embodiment 2
[0026] The large-scale production culture of embodiment 2 bacterium
[0027] Disinfect culture containers and tap water with sodium hypochlorite solution, and then neutralize with sodium thiosulfate. Then, in the culture container, add reagents according to any culture medium formula described in the content of the invention (2), be prepared into a culture medium, insert 10% of the three-level bacterial classification, and finally neutralize with a neutralizing agent after disinfection Fill the whole container with tap water, place it at 28°C to 30°C, and cultivate it for 5 to 7 days under a light intensity of 2000 lux to obtain the product.
[0028] Disinfection treatment reagents and time are shown in Table 1:
[0029] disinfection pair
Embodiment 3
[0030] The rejuvenation of embodiment 3 bacterial strains
[0031] Collect 200-300g of fertile and fresh sediment from shrimp ponds or fish ponds, put them in a 500ml salt water bottle, and add 10g of Penaeus vannamei feed, then fill up the salt water bottle with water from fish ponds or shrimp ponds, after autoclaving and cooling, press 3% of the inoculum amount is inserted into the strain to be rejuvenated, and anaerobic light culture is carried out for 2 to 6 days to obtain a strain with high activity of reducing nitrite nitrogen. If necessary, the above operation can be repeated more than three times. After the rejuvenation of the strain, the nitrite nitrogen assimilation ability of the rejuvenated strain was measured according to the evaluation method introduced in Example 6.
[0032] After rejuvenating the patent bacterial strain 2-8 according to the above-mentioned method, measure through the evaluation method of embodiment 6, the result is as follows:
[0033] ...
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