Rhodococcus erythropolis and application in removing sulfur element in surfide thereof
A technology of Rhodococcus erythropolis and compound, applied in application, bacteria, plant genetic improvement and other directions, can solve the problems of no ownership of fungi and impossible industrial production.
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Embodiment 2
[0042] Pick the LSSE8-1 strain cultured on the nutrient slant and add it to 25 ml of basal medium. The composition of the medium: deionized water 1000 ml, KH 2 PO 4 2.44 g; Na 2 HPO 4 12H 2 O 14.03 g; NH 4 Cl2.00g; MgCl 2 ·6H 2 O 0.36 g; CaCl 2 2H 2 O 0.001 g FeCl 3 ·6H 2 O 0.001 g MnCl 2 4H 2 O 0.004 g; Glucose 10 g, Na 2 SO 4 1mmol / L. After culturing at 30°C and 150 rpm for 24-48 hours, it was added to 500 ml of basal medium, and after 48-72 hours, it was centrifuged to obtain bacterial cells. Place the bacterial cells in 50 ml of physiological saline containing 1 mmol / L DBT, mix on a shaker for 2-4 hours, and centrifuge to obtain the bacterial cells again. Example 3: Obtaining LSSE8-1 Active Stem Cells
Embodiment 3
[0043] Pick the LSSE8-1 strain cultured on the nutrient slant and add it to 25 ml of basal medium. The composition of the medium: deionized water 1000 ml, KH 2 PO 4 2.44 g; Na 2 HPO 4 12H 2 O 14.03 g; NH 4 Cl2.00g; MgCl 2 ·6H 2 O 0.36 g; CaCl 2 2H 2 O 0.001 g FeCl 3 ·6H 2 O 0.001 g MnCl 24H 2 O 0.004 g; Glucose 10 g, Na 2 SO 4 1mmol / L. After culturing at 30°C and 150 rpm for 24-48 hours, it was added to 500 ml of basal medium, and after 48-72 hours, it was centrifuged to obtain bacterial cells. Place the bacteria in 50 ml of physiological saline containing 0.1 mmol / L DBT, mix on a shaker for 2-4 hours, and centrifuge to obtain the bacteria again. Freeze and vacuum dry to obtain active stem cells. Example 4: Strain LSSE8-1 removes sulfur in the simulated system DBT.
Embodiment 4
[0044] Add DBT to dodecane to make the concentration reach 0.2mmol / L. Pick the LSSE8-1 strain cultured on the nutrient slant and add it to 25 ml of basal medium. The composition of the medium: deionized water 1000 ml, KH 2 PO 4 2.44 g; Na 2 HPO 4 12H 2 O 14.03 g; NH 4 Cl 2.00 g; MgCl 2 ·6H 2 O 0.36 g; CaCl 2 2H 2 O 0.001 g FeCl 3 ·6H 2 O 0.001 g MnCl 2 4H 2 O 0.004 g; glucose 10 g, DBT concentration 1 mmol / L. After culturing at 30° C. and 150 rpm for 24-48 hours, the simulated oil phase and bacterial culture were mixed at an oil-to-water ratio of 1:3. After culturing at 30° C. and 150 rpm for 24-48 hours, the sulfur is completely removed, and the product is HBP (as shown in FIG. 5 ). Example 5: Bacterial strain LSSE8-1 is used for deep desulfurization of diesel oil after hydrodesulfurization
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