Bacillus licheniformis strain BL06 and application thereof
A technology of Bacillus licheniformis and strains, applied in the field of agricultural microorganisms, to achieve the effect of reducing residue problems and improving quality
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0025] Screening method: Bacillus licheniformis BL06 (CGMCC NO.13462) was isolated from the cucumber rhizosphere in Dingji Town, Huaian City, Jiangsu Province. Cut the cucumber root tissue into small pieces of 1 cm, soak in 1% sodium hypochlorite for 5 minutes, soak in 70% alcohol for 1-2 minutes, and wash with sterile water for 3 times (take the last cleaning solution 100 μl and apply it to R 2 A solid culture medium, if sterile growth after 48h, it is considered that the surface is clean and sterile). Take 3g of the sterilized sample and place it in a sterile mortar, add 27ml of sterile 0.85% NaCl, macerate the tissue, grind it, and dilute with sterile 0.85% NaCl gradient. take 10 -1 、10 -2 、10 -3 100 μl each of the three gradient dilutions were applied to R 2 On A, culture at 28°C for 48h. Pick the largest single colony to inoculate into fresh R 2 A solid medium, through repeated transfer to obtain purified strains. The purified strains were stored in -70°C ultra-low...
Embodiment 2
[0032] The preparation of embodiment 2BL06 biocontrol agent
[0033] Inoculate the Bacillus licheniformis BL06 (CGMCC NO.13462) strain into the LB culture medium for 16 hours at 28°C with shaking at 200rpm, then take a sample every 2 hours in the ultra-clean workbench to measure its OD value at 600nm, when the OD value is 0.8 When the culture is over, this bacterial solution is used as the seed bacterial solution. Inoculate the seed bacteria solution into LB fermentation medium at a volume ratio of 1:500 for fermentation and culture, culture at 28°C and 200 rpm for 48 hours, then centrifuge at 6000 rpm for 10 minutes, and collect the precipitate to obtain the biocontrol agent HS10. The total concentration of viable bacteria in the resulting biocontrol agent was 1×10 9 ~1×10 10 CFU / mL.
Embodiment 3
[0034] Example 3 Greenhouse Experiment Determination of BL06's Growth-promoting Effect on Cucumber
[0035] The biocontrol bacteria treatment group used 30ml concentration of 10 for each seedling 8 The bacterial solution of CFU / ml was treated, and the control group was treated with clear water. Each treatment had 12 seedlings, and each treatment was repeated 3 times. 25 days after inoculation, the cucumber plant height, leaf area, fresh weight and dry weight were measured. Biomass increase (%)=(fresh weight of plants in treatment group-fresh weight of control plants) / fresh weight of control plants×100%.
[0036] The growth promotion data in the greenhouse showed (Table 2) that the cucumber plants treated with BL06 were higher than the control in terms of plant height, leaf area, and fresh weight, and the plant biomass increment was 15.62%. The dry weight of the melon seedlings treated with BL06 was 4.89g / plant, which was significantly smaller than that of the control group, ...
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