Sphingomonas strain and application thereof in water treatment
A sphingomonas and strain technology, applied in the fields of environmental engineering and bioengineering, can solve problems such as harsh control conditions and limited application, and achieve the effects of high biosafety, broad application potential and strong degradation ability.
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Embodiment 1
[0038] Embodiment 1 The screening steps of the Sphingomonas bacterial strain provided by the present invention:
[0039] Use a pre-sterilized layered water sample collector to collect 0.25 L of water samples at different depths above the sediment interface of Taihu Lake, and pack them in pre-sterilized brown glass bottles; use a pre-sterilized Peterson mud sampler (1 / 16m 2 ) to collect the surface sediments of Taihu Lake (thickness is about 10cm), put them into a sterilized stainless steel container; Brown glass bottles, sealed immediately after sampling the above samples, used as bacteria source for isolation and enrichment culture. Under sterile conditions, add the water sample to the ammonia oxidizing bacteria enrichment medium (the composition of the ammonia oxidizing bacteria medium is (NH 4 ) 2 SO 4 0.2g, K 2 HPO 4 0.1g, MgSO 4 0.05g, NaCl 0.2g, FeSO 4 0.04g, CaCO 3 0.5g, H 2 O 100ml, pH value 7.2, wherein the culture medium was used after sterilizing wit...
Embodiment 2
[0048] The application of the present invention to the research on the degradation of ammonia nitrogen in the rich nutrient medium, its steps are as follows:
[0049] [1] Add 50ml of rich nutrient medium (ammonia nitrogen concentration is 100mg / L) into a 250ml Erlenmeyer flask.
[0050] [2] Add the cell liquid culture of the Sphingomonas strain prepared in Example 1 into the Erlenmeyer flask of the above [1], and cultivate it aerobically at 28°C and 80r / min. Samples were taken every 2 hours. figure 1 Degradation of ammonia nitrogen by Sphingomonas strains in enriched medium. from figure 1 It can be seen that a small amount of bacterial growth is enough to degrade ammonia nitrogen, and the removal rate of ammonia nitrogen is close to 100% after 6 hours of inoculation.
Embodiment 3
[0052] The present invention uses glucose and CO 2 For the application of nitrite degradation research in mixed carbon source and nitrite as nitrogen source medium, the steps are as follows:
[0053] [1] The medium in Example 1 was replaced with glucose and CO 2 It is a mixed carbon source, nitrite is the basal medium of nitrogen source (nitrite concentration is 100mg / L)
[0054] [2] Add the cell liquid culture of the Sphingomonas strain prepared in Example 1 into the Erlenmeyer flask of the above [1], and culture it anaerobically at 28°C, 80r / min. Samples were taken every 2 hours. figure 2 Degradation of nitrite by Sphingomonas strains in enriched medium. from figure 2 It can be seen that a small amount of bacterial growth is enough to degrade nitrite, and after 12 hours of inoculation, the removal rate of nitrite is close to 100%.
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