Microbial strain capable of remedying heavy metal-contaminated soil and application of microbial strain
A technology that pollutes soil and heavy metals, applied in the field of microorganisms, can solve the problems of soil destruction, high implementation cost, pollution, etc., and achieve the effect of small soil disturbance, high implementation cost and good effect
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Embodiment 1
[0028] Embodiment 1: the screening of microbial strain of the present invention
[0029] Liquid-phase enrichment method: Weigh an appropriate amount of cadmium-contaminated soil sample and add it to a conical flask filled with LB liquid medium, and add an appropriate amount of glass beads. Shake the triangular flask at 28-30° C., 150-170 rpm; transfer the soil mixture into a centrifuge tube, and take the supernatant after centrifugation as the source of cadmium-inactivated microorganisms. The above supernatant was inoculated into cadmium-containing LB liquid medium, and cultured with shaking at 28-30° C. and 150-170 rpm. Draw 1-2mL with a sterile pipette and transfer to another enrichment culture Erlenmeyer flask. After three transfers in this way, streak the plate on LB solid medium and inorganic salt solid medium respectively to isolate single colonies.
[0030] The supernatants were diluted 10 -1 、10 -2 、10 -3 、10 -4 、10 -5 、10 -6 、10 -7 、10 -8 , absorb an appropria...
Embodiment 2
[0031] Embodiment 2: the identification of microbial strain of the present invention
[0032] The DNA of the strain was extracted according to the steps of the Tiangen bacteria genomic DNA extraction kit (TIANampbacteriaDNAkit) for identification of strains. Among the results with the highest matching degree, the measured 16SrDNA sequence of the strain has 100% homology with the 16SrDNA sequence of Burkholderia cepacia (Burkholderiacepacia), and it can be determined that the strain is Burkholderia cepacia. Burkholderia cepacia.
Embodiment 3
[0033] Embodiment 3: the cadmium passivation characteristic of bacterial strain of the present invention
[0034] The isolated pure culture strains were inoculated in LB liquid medium, and cultured by shaking at 28-30°C and 160-170rpm for 18-20h, in which a group of bacterial cells were first inactivated at 121°C for 15min, and then 6000- Centrifuge at 8000rpm at low temperature for 15-20min to collect dead bacteria as a dead cell inactivator; another group of bacteria cells are directly centrifuged at 3000-5000rpm at low temperature for 20-30min to collect live bacteria and wash them with sterile water 2-3 times. Acts as a passivating agent for living cells. Two groups of bacteria were added to cadmium-containing (50-300mg / LCd 2+ ) in an aqueous solution for adsorption experiments, the results are as follows figure 1 shown. according to figure 1 It can be seen from the results that both of them have strong ability to remove cadmium ions, but the adsorption capacity of liv...
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