Xylose staphylocci for degrading 2-picoline and its use
A Staphylococcus xylosus, picoline technology, applied in Staphylococcus xylosus and its application fields, can solve the problems of difficult biodegradation, 2-picoline degradation, no effective methods, etc.
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Embodiment 1
[0014] Embodiment 1, the isolation and cultivation of S.xylous B1 bacterial strain
[0015] 1. Isolation of strains
[0016] Sludge samples were collected at the sewage treatment plant of Fushun Petroleum No. 3 Plant. Take 1 drop of sludge aqueous solution on the screening medium, add 0.1g of 2-picoline, spread it evenly with a spreader, put it in an incubator, and cultivate it at 30°C for 2 days; use an inoculation loop to transfer the screened strains to Connected to LB medium, placed in an incubator at 30°C for 1 day, and the obtained strain was S.xylous B1 strain.
[0017] Wherein said screening medium component is:
[0018] (NH 4 ) 2 SO 4 5g; K 2 HPO 4 1g;
[0019] K H 2 PO 4 4g; NaCl 2g;
[0020] MgSO 4 ·7H 2 O 1g; Agar 15g;
[0021] Water 1000mL; pH 7.0.
[0022] 2. Culture of strains
[0023] Use an inoculation loop to inoculate the strains screened in shake flasks with a liquid volume of 50 ml, and culture them in a shaking incu...
Embodiment 2
[0030] The cultivation of the S.xylous B1 strain was the same as in Example 1. Take 2 shake flasks, add 50mL sterile water and 1mL 2-picoline respectively. One of the shake flasks was taken as a blank control group, and the cultured B1 bacterial agent was added to the other shake flask to make its OD value 4.2. The two shaking flasks were placed on a shaker to shake the 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 listed in Table 2.
[0031] initial
Embodiment 3
[0033] The cultivation of the S.xylous B1 strain was the same as in Example 1. Take 2 shake flasks, fill with 50ml of sterile water respectively, and then add 4g of soil contaminated by 1ml of 2-picoline. Take one shake flask as a blank control group; add B1 bacterial agent to the other shake flask to make its OD value 5.0. Place 2 shake flasks on a shaker to shake the reaction. Shaking table conditions are: temperature 30°C; rotation speed 150 rpm. After 10 hours, samples were taken and analyzed, and the results are shown in Table 3.
[0034] initial
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