Lead and cadmium tolerant bacteria and method for plants renovation of soil pollution by heavy metal
A heavy metal and cadmium resistance technology, applied in the fields of agriculture and environmental pollution control, can solve the problems of low biomass, complex equipment, inability to absorb and enrich, etc., to achieve the goal of promoting plant growth, improving repair efficiency, and improving plant stress resistance Effect
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Embodiment 1
[0018] Insoluble heavy metal lead and cadmium in the activation solution of embodiment 1 bacterial strain J62
[0019] Fill 100ml of PbCO into a 250ml Erlenmeyer flask 3 0.064g and CdCO 3 0.077g 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. The strain J62 was inoculated, cultured on a shaker at 30°C and 150r / min, and samples were taken and analyzed at different time points. Measure the number of bacterial strains by dilution coating method; measure the pH value in the culture solution with a pH meter; centrifuge the culture solution, take the supernatant and use the atomic absorption method to determine Pb 2+ and Cd 2+ concentration. The results are shown in Table 1. Effect of strain J62 on PbCO in culture medium 3 and CdCO 3 The activation efficiency can reach 1.5-6 times and 2.7-17.2 times.
Embodiment 2
[0020] Example 2 Bacterial strain J62 activates soil heavy metal lead and cadmium
[0021] Accurately weigh 10.00 g of a soil sample containing lead carbonate (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. Bacteria strain J62 was cultured on a shaker at 28°C for 20 hours, the bacteria were collected by centrifugation, and the bacteria suspension was made with deionized water. Inoculate 3ml of bacterial suspension into the soil sample, take the same amount of deionized water and inactivated bacteria as the control, set 3 repetitions 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 metals Pb and Cd. Weigh...
Embodiment 3
[0022] Embodiment 3 liquid preparation
[0023] The slant bacteria were inoculated in the nitrogen medium, cultured for 18 hours and then transferred to the seed tank. The seed tank is 0.5 tons, the feeding amount is 0.4 tons, and the medium composition is 2.0kg 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 be sterilized by steam and cooled to 28-30°C, the volume ratio of the inoculation volume is 5%, the cultivation temperature of the seed tank is controlled at 28-32°C, the stirring speed is 220 rpm, and the amount of sterile air is 1 : 0.8, after 20 hours of cultivation, the seed liquid was connected 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, KH 2 PO 4 9.0kg, MgSO 4 2.3kg, NaCl 0.9kg, CaCO 3 4.5kg, yeast paste 0.9kg. The production t...
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