Strain 1LN2 for preventing and treating rice sheath blight disease and application of strain 1LN2
A rice sheath blight, 1LN2 technology, applied in the direction of application, bacteria, fungicides, etc., to achieve the effect of improving the control effect, saving expenses, and increasing income
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0023] Screening and Identification of Example 1 Bacterial Strains
[0024] In October 2011, samples were collected in Donglin Village, Chengxiang Town, Taicang City, Jiangsu Province, and the plots in the Science and Education New City with severe disease. The five-point sampling method is adopted, and the interval between each point is at least 10m. Three healthy plants per point were collected together with severely diseased plants together with rhizosphere soil. The collected samples were quickly put into numbered plastic bags and brought back to the laboratory for separation.
[0025] Strain 1LN2 was isolated from the stems of diseased plants. The separation method is as follows: respectively cut off 3 g of roots, stems and leaves, soak in 1 mL of 1% sodium hypochlorite for 5 minutes, soak in 70% alcohol for 2 minutes, and wash with sterile water for 3 times. (Take 0.1 mL of the last cleaning solution and apply it to the R2A plate, or take 0.1 mL of the last cleaning s...
Embodiment 2
[0032] Embodiment 2: the preparation of biocontrol agent
[0033] Streak the strain 1LN2 on the LB plate, and culture it in a biochemical incubator at 28°C for 14-16h. After a single colony grows, pick a single colony and put it into a test tube containing 5mL of LB culture medium, and place it at 28°C, 200r Cultivate in a shaker / min to make a seed solution; inoculate the seed solution with 1% inoculum in a conical flask containing 500mL of LB culture solution, and culture it in a shaker at 28°C and 200r / min for 48h , when the bacterial concentration reached 10 9 When CFU / mL is diluted for use, it is the prepared 1LN2 biocontrol agent.
Embodiment 3
[0034] Example 3: Greenhouse Control Effect Experiment and Greenhouse Growth Promotion Test
[0035] 1. Greenhouse control effect experiment:
[0036] Disinfect the rice seeds with 2% sodium hypochlorite solution for 15 minutes, rinse them with clean water for 3-4 times, soak them in a 30°C incubator for 48 hours, take them out, rinse them with clean water, and place the seeds that have absorbed enough water at 35 Cover the room at -38°C with gauze for high-temperature moisturizing and germination acceleration until the chest is broken. After the chest is broken, spread the buds in a cool place for 4h-8h. After the seeds are wet inside and dry outside, they can be sown and raised. Using the method of raising seedlings and transplanting, first sow the seeds in a seedling tray equipped with a sterilized substrate, and then place them in a room with a humidity of 85% or more at 30°C-35°C for darkening and emergence, and place them at 28°C- Cultivate in a greenhouse at 30°C, 16 / 8...
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