Nitro-reductive pseudomonads and its use
A technology of Pseudomonas and nitro, which is applied in the field of nitroreducing Pseudomonas, can solve the problems of refractory biodegradation and effective degradation of benzothiazoles, etc.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0015] Embodiment 1, the isolation and cultivation of P.nitroreducens S1 bacterial strain
[0016] 1. Isolation of strains
[0017] 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 benzothiazole, 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 LB The culture medium is placed in an incubator at 30° C. for 1 day, and the obtained strain is the strain that degrades benzothiazole.
[0018] Described screening culture medium component is:
[0019] (NH 4 ) 2 SO 4 5g; K 2 HPO 4 1g;
[0020] K H 2 PO 4 4g; NaCl 2g;
[0021] MgSO 4 ·7H 2 O 1g; Agar 15g;
[0022] Water 1000mL; pH 7.0.
[0023] 2. Culture of strains
[0024] Use an inoculation loop to inoculate the isolated strains into shake flasks with a liquid volume of 5...
Embodiment 2
[0031] The cultivation of P.nitroreducens S1 strain is the same as that in Example 1. Take 2 shake flasks, add 50mL sterile water and 0.6mL benzothiazole respectively. One of the shake flasks was taken as a blank control group, and the cultured S1 bacterial agent was added to the other shake flask to make its OD value 4.8. 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.
[0032] initial
Embodiment 3
[0034] The cultivation of P.nitroreducens S1 strain is the same as that in Example 1. Take 2 shake flasks, fill them with 50mL sterile water, and then add 4g of soil contaminated by 0.6mL benzothiazole. Take one shake flask as a blank control group; add S1 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 for analysis, and the results are listed in Table 3.
[0035] initial
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com