Production process of bdellophage preparation
A technology for phagocytosis of Bdellovibrio and production methods, applied in the direction of fungicides, botanical equipment and methods, chemicals for biological control, etc., can solve the problems of difficult industrial production of Escherichia coli, environmental pollution, etc., and achieve disease prevention and control Improve the effect, avoid environmental pollution, and prolong the effect of shelf life
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0014] Embodiment 1: 1. Preparation of host bacterium suspension——with the cultured photosynthetic bacterium Rhodopseudomonas suspension (see Chinese Journal of Microecology p.78.1990.3 for the culture method, and the bacterial strains include: Hunqiuhong pseudomonas Monospora P4 or Rhodopseudomonas palustris 101, bacterial classification purchased from Institute of Biotechnology, Shanghai Jiaotong University), let stand for 24 hours, remove the upper layer solution that accounts for 1 / 2 of the total solution volume; add and remove the upper layer solution equal volume Amount of 0.2% NaCl solution, shake well, and then stand still for 24 hours, remove the upper layer solution accounting for 1 / 2 of the total solution volume, then add 0.2% NaCl solution, and make the host bacteria suspension with 2 / 3 of the original total solution volume , the bacterial content is 3 to 30 billion / ml, and the obtained host bacterial suspension is used for future use.
[0015] 2. Preparation of cu...
Embodiment 2
[0017] Example 2: 1. Preparation of the host bacteria suspension - the cultured photosynthetic bacterium Rhodopseudomonas suspension (for the culture method, see China Microecological Impurities p. Monospora P4 or Rhodopseudomonas palustris 101, strains purchased from Shanghai Jiaotong University Biotechnology Institute), let stand for 48 hours, remove the upper layer solution that accounts for 2 / 3 of the total solution volume; add and remove the upper layer solution, etc. 0.75% NaCl solution by volume, shake well, and then let it stand for 48 hours, remove the upper layer solution accounting for 2 / 3 of the total solution volume, and then add 0.3% NaCl solution to make the host bacteria suspension of 1 / 2 of the original total solution volume solution, the bacterial content is 3 to 30 billion / ml, and the obtained host bacterial suspension is used for future use.
[0018] 2. Preparation of culture medium: Dilute PH7.5 phosphate buffer solution (can be PBS) 10 times with water, t...
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