Megacine and its use
A technology of Bacillus megaterium and strains, applied to a strain of Bacillus megaterium and its application fields, can solve the problems of limited degradation ability and inapplicability of high-concentration toluene, and achieve the effect of improving processing efficiency and saving processing time
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Embodiment 1
[0017] Embodiment 1, the isolation and cultivation of B.megaterium J1 bacterial strain
[0018] 1. Isolation of strains
[0019] Sludge samples were collected at the sewage treatment plant of Fushun Petroleum No. 3 Plant. Add 1 drop of sludge aqueous solution to the screening medium, add 0.1g of toluene, spread it evenly with a spreader, place it in an incubator, and cultivate it at 30°C for 2 days; then use an inoculation loop to transfer the screened strains to In the LB medium, culture in an incubator at 30°C for 1 day, and the obtained strain is B. megaterium J1 strain.
[0020] The components of the screening medium are:
[0021] (NH 4 ) 2 SO 4 5g; K 2 HPO 4 1g;
[0022] K H 2 PO 4 4g; NaCl 2g;
[0023] MgSO 4 ·7H 2 O 1g; Agar 15g;
[0024] Water 1000mL; pH 7.0.
[0025] 2. Cultivation of B. megaterium J1 strain
[0026] Use an inoculation loop to inoculate the strains screened in shake flasks with a liquid volume of 50 mL, and culture...
Embodiment 2
[0032] The cultivation of the B. megaterium J1 strain was the same as in Example 1. Take 2 shake flasks, add 50mL sterile water and 1.5mL toluene respectively. One of the shake flasks was taken as a blank control group, and the cultured J1 bacterial agent was added to the other shake flask to make its OD value 5.0. The two shaker flasks were placed on a shaker to vibrate for reaction, and the conditions of the shaker were: temperature 30° C., rotation speed 150 rpm. After 10 hours, samples were taken and analyzed, and the results are shown in Table 2.
[0033] initial
Embodiment 3
[0035] The cultivation of the B. megaterium J1 strain was the same as in Example 1. Take 2 shake flasks, add 50mL sterile water respectively, and then add 4g soil contaminated by 1.5mL toluene. One of the shake flasks was taken as a blank control group; the cultured B. megaterium J1 bacterial agent was added to the other shake flask to make its OD value 5.0. The two shaker flasks were placed on a shaker to vibrate for reaction, and the conditions of the shaker were: temperature 30° C.; rotation speed 150 rpm. After 10 hours, samples were taken for analysis, and the results are listed in Table 3.
[0036] initial
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