Immobilization pseudomonas aeruginosa as well as preparation method and application thereof
A technology of Pseudomonas aeruginosa and live bacteria, which is applied in biochemical equipment and methods, chemical instruments and methods, fixed on or in inorganic carriers, etc. To deal with the problem of high cost, to achieve the effect of good biocompatibility, good compressive strength and aeration resistance, and high activity
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Embodiment 1
[0029] a kind of like figure 1 , figure 2 The shown immobilized Pseudomonas aeruginosa of the present invention includes live Pseudomonas aeruginosa and a mixed carrier for immobilizing the live Pseudomonas aeruginosa, and the mixed carrier is an embedded Pseudomonas aeruginosa The spheres of living bacteria, the mixed carrier is mainly composed of polyvinyl alcohol, calcium alginate and multi-walled carbon nanotubes with a mass ratio of 60:40:4 (although there will be a slight difference in the ratio of the raw materials used, the difference can be can be ignored).
[0030] The above-mentioned immobilized Pseudomonas aeruginosa of the present embodiment is prepared by the following method:
[0031] 1. Preparation of immobilization reagent:
[0032] Mix 6g, 4g, and 0.4g of polyvinyl alcohol, sodium alginate, and multi-walled carbon nanotubes respectively, and dilute to 100mL with water to prepare a mixed solution; then heat the mixed solution to boiling, and stir continuou...
Embodiment 2
[0045] Transfer 20-30 g of the immobilized Pseudomonas aeruginosa prepared in the above-mentioned Example 1 to an Erlenmeyer flask containing 100 mL of the above-mentioned fermentation medium, and activate it at 37°C for two days to fully restore the activity of the immobilized Pseudomonas aeruginosa . Then add hexavalent chromium solutions with different initial concentrations, culture on a shaker at 37°C and 150 rpm, and take samples regularly. After samples are taken at regular intervals and centrifuged at 8000 rpm for 8 minutes (or filtered through a microporous membrane), the supernatant is taken for measurement and the supernatant is used for the determination of hexavalent chromium content. The absorbance was measured at 540 nm by diphenylcarbazide spectrophotometry. All utensils used in the determination were soaked overnight in dilute nitric acid, and then cleaned. In the determination, diphenylcarbazide is prepared with acetone and distilled water with a volume rat...
Embodiment 3
[0050] Using the immobilized Pseudomonas aeruginosa prepared in Example 1 to reduce the hexavalent chromium solution, the operation steps are: first add the immobilized Pseudomonas aeruginosa to 100 mL of fermentation medium for activation, generally for 1 day Above, then the hexavalent chromium solution to be treated is added to the fermentation medium after activating Pseudomonas aeruginosa, so that the concentration of hexavalent chromium is 15mg / L, and the immobilized Pseudomonas aeruginosa is controlled to contain hexavalent chromium The concentration in the fermentation medium was 0.1 g / mL, and the shaking treatment was carried out at 37° C. for 2 days, and the rotational speed during the shaking treatment was 150 rpm. Continue to use the immobilized Pseudomonas aeruginosa for four consecutive times to reduce the hexavalent chromium of 15mg / L. During the reduction process, the continuous use of the immobilized Pseudomonas aeruginosa is to filter the solution after the pre...
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