Chlorpyrifos pesticide degradation strain, inocula and preparation method thereof
A technology for chlorpyrifos pesticides and degrading bacteria, applied in the field of microorganisms, can solve the problems such as no degrading bacterial agents of chlorpyrifos pesticides are found, and achieve the effects of promoting the coordination and unification of pesticides and food safety for pest control, low production cost and good degradation effect.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0033] Embodiment 1 Preparation method and growth status determination of chlorpyrifos pesticide degrading bacteria Hu-01
[0034] Activate the strain of chlorpyrifos pesticide-degrading bacteria Hu-01 on a petri dish, and inoculate it on the slant of the test tube. Prepare Czapek medium according to the following formula: sodium nitrate: 2.0g, potassium chloride: 0.5g, magnesium sulfate: 0.5g, dipotassium hydrogen phosphate: 1.0g, iron sulfate: 0.01g, sucrose: 30.0g , Distilled water: 1000mL. Insert 0.1 g of wet bacteria into the liquid Charpy's medium at pH 7.0, and culture in a shaker at 28°C and 150 r / min for 1-7 days.
[0035] The relationship between the culture time and the growth status of the degrading bacteria Hu-01 is shown in Table 1.
[0036] Table 1 The influence of culture time on the dry weight of mycelia of chlorpyrifos pesticide-degrading bacteria
[0037] Mycelium dry weight (g / 50mL)
[0038] Note: The above results are the average of 3 repetiti...
Embodiment 2
[0040] (1) Activate the strain of chlorpyrifos pesticide-degrading fungus Hu-01 on a petri dish, and measure the degradation performance, and inoculate it on the test tube slope for subsequent use;
[0041] (2) The test tube seeds were inoculated in 1000 mL shake flasks containing 250 mL of Chapit's medium, cultured at a constant temperature and shaken to the logarithmic phase, and prepared to inoculate the seed tank;
[0042] (3) The seed tank is 100 liters, the feeding volume is 80 liters, and the medium formula is: NaNO 3 0.2%, K 2 HPO 4 0.1%, KCl 0.05%, MgSO 4 0.05%, Fe2 (SO 4 ) 3 0.001%, 3% sucrose, 0.5% peptone, 1.1kg / cm after feeding 3 Under high pressure, 121°C high-pressure damp heat sterilization, after cooling to 28°C, inoculate the above-mentioned cultured inoculum strains into 100 liters of seed tanks according to the inoculum amount of 8% to 10%, and cultivate them to the logarithmic growth phase. It is 200-300 rpm, and the sterile air ventilation is 45...
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