Embedded nano-iron/composite microbial agent and preparation method thereof
A technology of composite microbial bacterial agent and nano-iron, which is applied in the direction of microorganism-based methods, biochemical equipment and methods, microorganisms, etc., can solve the problems of poor stability of nano-zero-valent iron, achieve low microbial toxicity, enhance degradation efficiency, and good The effect of biocompatibility
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0037] (1) Preparation of triclosan-degrading bacterial liquid
[0038]Agrobacterium sp., Enterobactercloacae., Bacillus sp., Gordonia sp., Pseudomonasputida. Pseudomonas (Pseudomonas stutzeri.) 2 rings were transferred to 30mL nutrient solution, the bacteria were cultured at 35°C for 2 days, and inoculated into the proliferation medium container at a volume ratio of 10%, at 35 Cultivate for 2 days under the condition of ℃, centrifuge at a speed of 5000rpm for 15min, and obtain the logarithmic growth phase cells of the above bacteria respectively. The logarithmic growth phase cells of the above-mentioned thalli are taken out, and with phosphate buffer (its main component sodium chloride 9.0g / L, potassium chloride 0.3g / L, dipotassium hydrogen phosphate 1.2g / L and potassium dihydrogen phosphate 0.3g / L, the rest is water) and washed twice. By volume percentage, get 5% Agrobacterium, 5% Bacillus, 10% Enterobacter cloacae, 20% Gordonella, 20% Pseudomonas putida and 40% Pseudomona...
Embodiment 2
[0052] (1) Preparation of triclosan-degrading bacterial liquid
[0053] Agrobacterium sp., Enterobactercloacae., Bacillus sp., Gordonia sp., Pseudomonasputida. Pseudomonas (Pseudomonas stutzeri.) 2 rings were transferred to 30mL nutrient solution, the bacteria were cultured at 35°C for 2 days, and inoculated into the proliferation medium container at a volume ratio of 10%, at 35 Cultivate for 2 days under the condition of ℃, centrifuge at a speed of 5000rpm for 15min, and obtain the logarithmic growth phase cells of the above bacteria respectively.
[0054] The logarithmic growth phase cells of the above-mentioned thalli are taken out, and with phosphate buffer (its main component sodium chloride 9.0g / L, potassium chloride 0.3g / L, dipotassium hydrogen phosphate 1.2g / L and potassium dihydrogen phosphate 0.3g / L, the rest is water) and washed twice. By volume percentage, get 5% Agrobacterium, 5% Bacillus, 10% Enterobacter cloacae, 20% Gordonella, 20% Pseudomonas putida and 40% ...
Embodiment 3
[0068] (1) Preparation of triclosan-degrading bacterial liquid
[0069] Agrobacterium sp., Enterobactercloacae., Bacillus sp., Gordonia sp., Pseudomonasputida. Pseudomonas (Pseudomonas stutzeri.) 2 rings were transferred to 30mL nutrient solution, the bacteria were cultured at 35°C for 2 days, and inoculated into the proliferation medium container at a volume ratio of 10%, at 35 Cultivate for 2 days under the condition of ℃, centrifuge at a speed of 5000rpm for 15min, and obtain the logarithmic growth phase cells of the above bacteria respectively.
[0070]The logarithmic growth phase cells of the above-mentioned thalli are taken out, and with phosphate buffer (its main component sodium chloride 9.0g / L, potassium chloride 0.3g / L, dipotassium hydrogen phosphate 1.2g / L and potassium dihydrogen phosphate 0.3g / L, the rest is water) and washed twice. By volume percentage, get 5% Agrobacterium, 5% Bacillus, 10% Enterobacter cloacae, 20% Gordonella, 20% Pseudomonas putida and 40% P...
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