A stain of Pantoea agglomerans and use thereof
A Pantoea agglomerans, applied technology, applied in the direction of bacteria, microorganisms, biochemical equipment and methods, etc., can solve the undiscovered Pantoea agglomerans and other problems, achieve strong Fe(III) reduction and humic acid reduction capabilities, The screening method is simple and the electron utilization spectrum is wide
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Embodiment 1
[0018] Embodiment 1 Enrichment, separation and purification of Pantoea agglomerans MFC3 of the present invention
[0019] Take 5g ancient forest soil sample in 100mL liquid separation medium. Each liter of liquid separation medium contains 1.0g glucose (as an electron donor), 0.412g AQDS (2,6-anthraquinone disulfonate, as an electron acceptor), 2.5g NaHCO 3 , 0.25g NH 4 Cl, 0.678g NaH 2 PO 4 2H 2 O, 0.1g KCl, 10.0mL vitamin solution, 10.0mL trace element solution. Among them, the vitamin solution contains 2.0mg biotin, 2.0mg folic acid, B610.0mg vitamin, 5.0mg thiamine, 5.0mg riboflavin, 5.0mg niacin, 5.0mg calcium pantothenate and 0.1mg vitamin per liter of deionized water. B12, 5.0mg p-aminobenzoic acid, 5.0mg lipoic acid; the trace element solution contains 1.5g nitrilotriacetic acid, 3.0g MgSO per liter of deionized water 4 ·7H 2 O, 0.5g MnSO 4 ·H 2 O, 1.0g NaCl, 0.1g FeSO 4 ·7H 2 O, 0.1gCoCl 2 ·6H 2 O, 0.1g CaCl 2 , 0.1g ZnSO 4 ·7H 2 O, 0.01g CuSO 4 ·5H ...
Embodiment 2
[0034] Example 2 Reduction activity of Pantoea agglomerans MFC3 on goethite with glucose as electron donor
[0035] Medium A formula: 2.25g of goethite per liter of deionized water, NaHCO 3 2.5g, NH 4 Cl0.25g, NaH 2 PO 4 2H 2 O 0.678g, KCl 0.1g, glucose 1.0g, vitamin solution and trace element solution 10.0mL each, sterilized at 121°C for 20 minutes, glucose was sterilized alone, and mixed with other ingredients after sterilization. Wherein the composition of vitamin solution and trace element solution is the same as that of the separation medium described in Example 1.
[0036] Preparation of bacterial suspension: use an inoculation loop to pick a circle of activated bacterial strains in 200mL beef extract peptone liquid medium, and cultivate it in a shaker (30°C, 180 rpm) for 16 hours, so that the number of bacteria reaches the exponential growth phase, Collect the bacterial cells by centrifugation at 8000 rpm, pour off the supernatant, and suspend the precipitated bact...
Embodiment 3
[0041] Example 3 Reduction activity of Pantoea agglomerans MFC3 on lepidocite with glucose as electron donor
[0042] Medium B formula: per liter of deionized water containing 2.25g lepidocerite, NaHCO 3 2.5g, NH 4 Cl0.25g, NaH 2 PO 4 2H 2 O 0.678g, KCl 0.1g, glucose 1.0g, each 10.0mL of vitamin solution and trace element solution (the components of vitamin solution and trace element solution are the same as the separation medium described in Example 1), sterilized at 121°C for 20 minutes, glucose alone Sterilized, mixed with other ingredients after sterilization.
[0043] Preparation of bacterial suspension: use an inoculation loop to pick a circle of activated bacterial strains in 200mL beef extract peptone liquid medium, and cultivate it in a shaker (30°C, 180 rpm) for 16 hours, so that the number of bacteria reaches the exponential growth phase, Collect the bacterial cells by centrifugation at 8000 rpm, pour off the supernatant, and suspend the precipitated bacterial ...
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