Chromium-removing rhodobacterium and application thereof
A red bacteria and chromium removal technology, applied in the field of microorganisms, can solve the problems of harsh culture conditions, less industrial application, and low reduction of Cr, and achieve the effects of low cost, avoiding pollution, and reducing the concentration of total chromium
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Embodiment 1
[0037] Embodiment 1, dechroming rhodobacter CGMCC No.3512 ( Pannonibacter phragmitetus LSSE-09) strain screening
[0038] Soil samples were collected from the Cr(VI)-contaminated soil next to the chromium salt pile. Suspend 5g of soil sample in 25ml of normal saline, put it in a shaker and mix it for 30-60min, let it stand still, absorb the supernatant, and put it in 100ml of selective medium (the supernatant can be directly added to the selection medium for the water sample) culture medium). The composition of the selective medium is: deionized water 1000ml, tryptone 10g / L, yeast extract 5g / L, sodium chloride 10g / L, and K 2 Cr 2 o 7 (Cr(VI) concentration is 300mg / l) as the chromium source, adjust pH 8.0-10.0, place on a shaker at 150rpm, culture at 37°C for three days, dilute the bacterial suspension, and spread it on a selective solid medium plate. The isolated single colonies were respectively inoculated in selective medium with a Cr(VI) concentration of 300 mg / l,...
Embodiment 2
[0045] Embodiment 2, dechroming rhodobacter CGMCC No.3512 ( Pannonibacter phragmitetus LSSE-09) Obtaining resting bacteria
[0046] Pick the Rhodobacter dechrome bacteria CGMCC No.3512 (Pannonibacter phragmitetus LSSE-09) cultured on the nutrient slant, and add it to 40 ml of the basal medium. The ingredients of the culture medium: 1000ml of deionized water, 10g / L of tryptone, 5g / L of yeast extract, and 10gL of sodium chloride. Adjust pH to 7.0, temperature 37°C, 150rpm shaker to activate culture for 12h, then add it to 500ml basal medium according to 1% inoculum amount. After 12 hours, the bacterial cells were obtained by centrifugation, and then washed with 0.9% normal saline, and repeated three times to obtain the bacterial cells.
Embodiment 3
[0047] Embodiment 3, dechroming rhodobacter CGMCC No.3512 ( Pannonibacter phragmitetus LSSE-09) Acquisition of active dried bacteria
[0048] Pick the Rhodobacter dechrome bacteria CGMCC No.3512 (Pannonibacter phragmitetus LSSE-09) cultured on the nutrient slant, and add it to 40 ml of the basal medium. The ingredients of the culture medium: 1000ml of deionized water, 10g / L of tryptone, 5g / L of yeast extract, and 10gL of sodium chloride. Adjust pH to 7.0, temperature 37°C, 150rpm shaker to activate culture for 12h, then add it to 500ml basal medium according to 1% inoculum amount. After 12 hours, the bacterial cells were obtained by centrifugation, and then washed with 0.9% normal saline, and repeated three times to obtain the bacterial cells. Freeze and vacuum dry to obtain active stem cells.
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