Enterobacter gergoviae and its use in bioflocculation
A microbial flocculant, enterobacteriaceae technology, applied in the field of microorganisms, can solve the problem of no enterobacteriaceae and achieve good pH stability, short flocculation time and high efficiency
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Embodiment example 1
[0043]The flocculation bacterial strain is screened from activated sludge, landfill leachate, and each bacterial strain that is separated is connected respectively in the 250ml wide-mouth Erlenmeyer flask that 50ml seed culture medium (below referring to embodiment 3) is housed, is placed in the shaker at 30 Cultivate at 200rpm for 24 hours, and take the culture solution to measure the flocculation rate. A strain of Enterobacter diazoae with the highest flocculation activity was obtained, its biological deposit number was CCTCC M2013042 strain, and it was named eth-2. and use it as the target for subsequent experiments.
[0044] Identification method: eth-2 such as figure 1 As shown, by 16S rRNA sequencing (the sequencing result is shown in SEQ ID NO: 1) and compared in NCBI, the similarity with Enterobacter.Gergoviae (AB682278.1) reaches 99%.
[0045] The preparation of embodiment 2 culture medium
Embodiment 2
[0046] 1. Culture medium preparation
[0047] 1. Solid plate medium: tryptone, 10.0g; yeast powder, 5.0g; NaCl, 10.0g; agar powder, 20.0g; distilled water, 1L.
[0048] 2. Seed medium: glucose, 10.0g; K 2 HPO 4 , 5.0g; MgSO 4 ·7H 2 O, 0.2g; KH 2 PO 4 , 2.0g; NaCl, 0.1g; urea, 0.5g; yeast powder, 0.5g; distilled water 1L.
[0049] 3. Fermentation medium: glucose, 10.0g; K 2 HPO 4 , 5.0g; MgSO 4 ·7H 2 O, 0.2g; KH 2 PO 4 , 2.0g; NaCl, 0.1g; sodium nitrate, 1.0g; distilled water 1L.
[0050] Second, the culture and fermentation conditions of microorganisms:
[0051] The culture condition of the solid plate medium: the eth-2 strain was inoculated in the solid medium and cultured at 30° C. for 1 day, and stored in a refrigerator at 4° C. after being matured.
[0052] The cultivation conditions of the seed culture medium: the seed culture medium was sterilized at 115° C. for 20 minutes, and then inserted into the strains of the seed plate culture medium after sterilizat...
Embodiment example 3e
[0057] 1. Centrifuge a certain volume of culture medium at 8000rpm and 5minl to collect the supernatant and precipitate respectively, and wash the precipitate with distilled water for 3 times and then resuspend it in a considerable volume of distilled water. Compare the supernatant, the precipitate suspension and the fermentation broth respectively The flocculation effect on kaolin to determine the distribution of flocculation activity. The result is as figure 2 As shown, the flocculation rates of the fermentation broth, bacterial suspension and supernatant were 90.45%, 94.36% and 63.20%, respectively, indicating that the flocculation activity of eth-2 was mainly distributed in the bacterial sediment, so the following experiments were used After repeated washing with distilled water for 3 times, the bacterial pellet resuspended in distilled water was used as a microbial flocculant.
[0058] 2. The effect of carbon source on the activity of microbial flocculant: select glucos...
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