Pseudomonas PR1 as well as preparation method and application thereof
A technology of Pseudomonas and culture method, applied in the field of Pseudomonas PR1 and its preparation, can solve problems such as difficulty in balancing flocculation efficiency and secondary pollution
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0046] Screening of bacteria
[0047] (1) Preparation of medium:
[0048] (A) Separation medium
[0049] Beef extract peptone (g / L): beef extract 3.0, peptone 10.0, sodium chloride 5.0 and agar 20.0, pH=7.0;
[0050] LB medium (g / L): peptone 10.0, yeast extract 5.0, sodium chloride 6.0 and agar 20.0, pH=7.0.
[0051] (B) Fermentation medium (g / L): glucose 10.0, potassium dihydrogen phosphate 0.5, dipotassium hydrogen phosphate 5.0, ammonium sulfate 0.2, sodium chloride 0.1, urea 0.5, yeast extract 0.5 and magnesium sulfate 0.2, pH=7 .
[0052] (C) Seed medium (g / L): glucose 10.0, potassium dihydrogen phosphate 0.5, dipotassium hydrogen phosphate 5.0, ammonium sulfate 0.2, sodium chloride 0.1, urea 0.5, yeast extract 0.5 and magnesium sulfate 0.2, pH=7 .
[0053] The above-mentioned culture medium was sterilized at 120°C for 30 minutes and left for 24 hours before use if there is no contamination.
[0054] (2) Bacterial source preparation: The soil was collected from lead...
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