Rhodococcus ruber and application thereof in degradation of phenol pollutants
A technology of rhodococcus and pollutants, which is applied in the field of rhodococcus and its application in the degradation of phenol pollutants, and can solve the problems that have not yet been applied to rhodococcus
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Embodiment 1
[0014] Embodiment 1: as figure 1 Shown, the degradation performance of phenol of Rhodococcus rubrum SD3;
[0015] Cultivate the preserved Rhodococcus rhodococcus SD3 strain with LB medium, take 10ml of the bacterial solution in the logarithmic phase, centrifuge and separate the bacterial cells, add an equal volume of sterile water to prepare a bacterial suspension, take 1ml of the above bacterial suspension and add 100ml of In the phenol inorganic salt medium (phenol concentration: 1.0 g / L), shake culture at 35° C. and 200 r / min for 72 hours. The degradation rate of phenol was measured by 4-aminoantipyrine spectrophotometry to be 99.73%.
Embodiment 2
[0016] Embodiment 2: as figure 2 Shown, the culture status of Rhodococcus rubella SD3 when different common pollutants were used as the sole carbon source.
[0017] The SD3 strain of Rhodococcus rubrum was picked from the preserved slant, inoculated in LB culture medium, and activated for 28 hours at 35°C and 200 rpm on a shaking table. Take the activated bacterial liquid and inoculate it in the culture medium with isooctane, cyclohexane, benzene, n-heptane, toluene, acetonitrile, chlorobenzene, naphthalene, n-hexane, and 1-naphthol as the only carbon source according to the inoculation amount of 6%. After 72 hours of shaking culture in inorganic salt medium at 35°C and 200r / min shaking table, the dry weight of bacteria reached 0.0203g, 0.0197g, 0.0181g, 0.0180g, 0.0148g, 0.0147g, 0.0136g, 0.0120g, 0.0145g g, 0.0066g.
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