Klebsiella pneumoniae and use thereof
A Klebsiella pneumoniae technology, applied to Klebsiella pneumoniae and its application fields in Fe reduction and humic acid reduction, to achieve the effect of strengthening the original and humic acid reduction capabilities
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Embodiment 1
[0023] Example 1 Enrichment, separation and purification of Klebsiella pneumoniae
[0024] Pipette 5mL or weigh 5g ancient forest soil sample to inoculate the liquid separation medium; fill the culture medium with high-purity mixed gas (N 2 / CO 2 =80 / 20), the aeration time is not less than 30 minutes; after the aeration is completed, place the culture in the anaerobic workstation (N 2 / CO 2 =80 / 20) Cultivate statically at 30°C. Detect the yield of Fe(II) while observing the color change of the culture solution. When Fe(II) production continues to increase, the color of the culture fluid gradually darkens from the original orange-yellow, and finally turns to black. When the output of Fe(II) exceeds 50% of the total iron content, it is transferred to another fresh medium with an inoculum amount of 10%, and the above operation is repeated three times.
[0025] Each liter of liquid separation medium contains: 1.0g glucose, 16g ferric citrate, 2.5g NaHCO 3 , 0.25g NH 4 Cl, 0.678g NaH 2...
Embodiment 2
[0037] Example 2 Klebsiella pneumoniae MFC4 anaerobic reduction of goethite
[0038] Medium A formula: Each liter of deionized water contains 2.25g of goethite, NaHCO 3 2.5g, NH 4 Cl 0.25g, NaH 2 PO 4 ·2H 2 O 0.678g, KCl 0.1g, glucose 1.0g, vitamin solution and trace element solution each 10.0mL (vitamin solution and trace element solution composition is the same as the liquid separation medium described in Example 1), sterilized at 121 ℃ for 20 minutes, glucose Sterilize separately and mix with other ingredients after sterilization.
[0039] Preparation of bacterial suspension: Use an inoculating loop to pick a loop of activated strains in 200mL beef extract peptone liquid medium, and incubate in a shaker (30°C, 180 revolutions / min) for 16 hours to make the number of bacteria reach the exponential growth phase. The bacteria were collected by centrifugation at 8000 rpm, the supernatant was decanted, and the precipitated bacteria were suspended in 200 mL of medium A to prepare a ba...
Embodiment 3
[0044] Example 3 Klebsiella pneumoniae (K. pneumoniae MFC4) anaerobic reduction of ferrihydrite
[0045] Medium B formula: 2.5g hydrous iron ore per liter of deionized water, NaHCO 3 2.5g, NH 4 Cl 0.25g, NaH 2 PO 4 ·2H 2 O 0.678g, KCl 0.1g, glucose 1.0g, vitamin solution and trace element solution each 10.0mL (vitamin solution and trace element solution composition is the same as the liquid separation medium described in Example 1), sterilized at 121 ℃ for 20 minutes, glucose Sterilize separately and mix with other ingredients after sterilization.
[0046] Preparation of bacterial suspension: Use an inoculating loop to pick a loop of activated strains in 200mL beef extract peptone liquid medium, and incubate in a shaker (30°C, 180 revolutions / min) for 16 hours to make the number of bacteria reach the exponential growth phase. The bacteria were collected by centrifugation at 8000 rpm, the supernatant was poured, and the precipitated bacteria were suspended in 200 mL of medium B to ...
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