Biological surfactant functional modification method for deinococcus radiodurans (DR) and application thereof
A technology of Deinococcus radioresistant and biological surface, which is applied in the field of bioremediation of uranium-contaminated water bodies, can solve problems such as difficult separation, influence on the actual effect of repairing uranium-contaminated water bodies, small difference in density between bacteria and water, and achieve mechanical strength High, overcoming the problem of radiation resistance resistance, the effect of easy heating conditions
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Embodiment 1
[0037] (1) Deinococcus radiodurans DR Preparation of bacteria
[0038] Deinococcus radiodurans to be kept in the laboratory DR Streak inoculation on the pre-prepared solid TGY medium, use the inoculation loop to pick a single strain of Deinococcus radiodurans DR Inoculate in Erlenmeyer flasks and shake the flasks until early logarithmic growth, then inoculate at 0.5% inoculum and transfer to medium in large flasks, and continue to cultivate at 25°C for 20 hours. Deinococcus radiodurans DR After the cell culture is stabilized, collect Deinococcus radiodurans by centrifugation DR Bacteria were centrifuged at 7000r / min for 10min to collect fresh Deinococcus radiodurans DR bacteria. Then use a phosphate buffer solution with a pH value of 7 to resuspend the bacteria, shake it well, and centrifuge again to collect Deinococcus radiodurans DR Bacteria were centrifuged at 8000r / min for 15min, and then the collected Deinococcus radiodurans DR The bacteria were placed in a vacuum ...
Embodiment 2
[0047] (1) Deinococcus radiodurans DR Preparation of bacteria
[0048] Deinococcus radiodurans to be kept in the laboratory DR Streak inoculation on the pre-prepared solid TGY medium, use the inoculation loop to pick a single strain of Deinococcus radiodurans DR Inoculate in the Erlenmeyer flask and shake the flask to culture to the early logarithmic growth stage, then inoculate and transfer to the medium in the large bottle according to the inoculum amount of 0.5%, and continue to cultivate at 30°C for 25h. Deinococcus radiodurans DR After the cell culture is stabilized, collect Deinococcus radiodurans by centrifugation DR Bacteria were centrifuged at 7000r / min for 10min to collect fresh Deinococcus radiodurans DR bacteria. Then use a phosphate buffer solution with a pH value of 7 to resuspend the bacteria, shake it well, and centrifuge again to collect Deinococcus radiodurans DR Bacteria were centrifuged at 8000r / min for 15min, and then the collected Deinococcus radiod...
Embodiment 3
[0057] (1) Deinococcus radiodurans DR Preparation of bacteria
[0058] Deinococcus radiodurans to be kept in the laboratory DR Streak inoculation on the pre-prepared solid TGY medium, use the inoculation loop to pick a single strain of Deinococcus radiodurans DR Inoculate in Erlenmeyer flasks and shake the flasks until early logarithmic growth, then inoculate at 1% inoculum and transfer to medium in large flasks, and continue to cultivate at 35°C for 30h. Deinococcus radiodurans DR After the cell culture is stabilized, collect Deinococcus radiodurans by centrifugation DR Bacteria were centrifuged at 7000r / min for 10min to collect fresh Deinococcus radiodurans DR bacteria. Then use a phosphate buffer solution with a pH value of 7 to resuspend the bacteria, shake it well, and centrifuge again to collect Deinococcus radiodurans DR Bacteria were centrifuged at 8000r / min for 15min, and then the collected Deinococcus radiodurans DR The bacteria were placed in a vacuum freezer...
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