Copper activation bacterium and method for plants renovation of soil pollution by heavy metal
A heavy metal and bioremediation technology, applied in the field of agriculture and environmental pollution control, can solve the problems of low biomass, difficult preservation and control, secondary pollution of chelating agents, etc., to promote plant growth, improve restoration efficiency, and no secondary pollution. Effect
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Embodiment 1
[0019] Insoluble copper carbonate in the activation solution of embodiment 1 bacterial strain JYC17
[0020] Fill 100ml of CuCO into a 250ml Erlenmeyer flask 3 0.100g nitrogen medium (sucrose 10g, (NH 4 ) 2 SO 4 1g, KH 2 PO 4 2g, MgSO 4 0.5g, NaCl 0.1g, CaCO 3 0.5g, yeast extract 0.5g), sterilized at 121°C for 30min. Inoculate strain JYC17, shake culture at 30°C and 150r / min on a shaker, take samples at 0, 18, 36, 54, and 72 hours, and measure OD 600 ; Measure the pH value in the culture solution with a pH meter; The culture solution is centrifuged, and the supernatant is taken to measure Cu by atomic absorption method 2+ concentration. The results are shown in Table 1. In the initial growth stage of the bacteria, the effective copper concentration in the culture solution decreases with the increase of the density of the bacteria. In the later stage, the metabolism of the bacteria is the main factor, and the acid production of the bacteria makes the pH of the c...
Embodiment 2
[0021] Precipitated copper hydroxide in soil activated by bacterial strain JYC17 in embodiment 2
[0022] Accurately weigh 10.00 g of a soil sample containing copper hydroxide (Pb 500 mg / kg) and cadmium carbonate (Cd 500 mg. / kg), add it to a 50 ml centrifuge tube, wrap the mouth with gauze, and sterilize under high pressure. Strain JYC17 was cultured on a shaker at 28°C for 20 hours, the bacteria were collected by centrifugation, and the bacterial suspension was made with deionized water. Inoculate 3ml of bacterial suspension into the soil sample, take the same amount of deionized water as the control, set 3 replicates for each treatment, and replenish water regularly. The centrifuge tubes were placed in an incubator at 28°C for 3d, 7d, 13d and 21d and then taken out. Weigh 2g of soil into a 7ml centrifuge tube, add 4ml of water, shake and mix for 2h, centrifuge to take the supernatant to measure the concentration of water-soluble heavy metal Cu. Weigh 1g of soil into a 7ml ...
Embodiment 3
[0023] Embodiment 3 liquid preparation
[0024] The slants were inoculated on a nitrogenous medium (sucrose 10 g, (NH 4 ) 2 SO 4 1g, KH 2 PO 4 2g, MgSO 4 0.5g, NaCl 0.1g, CaCO 3 0.5g, yeast extract 0.5g), cultured for 18 hours and then inserted into the seed tank. The seed tank is 0.5 tons, the feeding amount is 0.4 tons, and the medium composition of the seed tank is 2.0 kg of sucrose, (NH 4 ) 2 SO 4 0.25kg, KH 2 PO 4 0.7kg, MgSO 4 0.17kg, NaCl 0.07kg, CaCO 3 0.4kg, yeast paste 0.2kg. The seed tank must first be sterilized by steam and cooled to 28-30°C, the inoculation volume is 5% by volume, the seed tank culture temperature is controlled at 28-32°C, the stirring speed is 220 rpm, and the sterile air intake is 1:0.8, after 20 hours of cultivation, the seed solution was transferred to the production tank. The production tank is 7 tons, the feeding amount is 4.5 tons, and the medium composition is 8kg of sucrose, 18kg of starch, (NH 4 ) 2 SO 4 4.5kg,...
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