Bacillus mojavensis for preventing and treating root rot of cotton in seedling stage and application of Bacillus mojavensis
A Bacillus, Mohaiwei technology, applied in the application, bacteria, fungicides and other directions, can solve the problem of not finding root rot diseases of Bacillus Mohaiwei, and achieve difficult drug resistance, high efficacy and long-lasting effect. long effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0029] Example 1 Isolation and screening of Bacillus mohewei HWt34
[0030] (1) Isolation of strain HWt34
[0031] Strain HWt34 was isolated from the cotton field soil in Shihezi by the Institute of Plant Protection, Xinjiang Academy of Agricultural Sciences. Soil samples from cotton fields in Shihezi were collected and brought back to the laboratory for separation and purification using the soil dilution method. Taking cotton blight as the target, the biocontrol bacteria were screened through plate confrontation method, pot test method and field plot test. A strain with obvious control effect on cotton blight was screened out and named as HWt34.
[0032] (2) Taxonomic identification of strain HWt34
[0033] ① Identification and classification by 16S rDNA sequence
[0034] Using the genomic DNA of HWt34 as a template, PCR amplification was carried out with bacterial universal primers 27F and 1492R to obtain PCR amplification products, wherein the primer sequences are:
[...
Embodiment 2
[0045] The preparation of embodiment 2HWt34 wettable powder
[0046] (1) Strain activation: put the preserved bacterial strain HWt34 on the LB plate medium (its composition and weight ratio are: yeast extract 5g, peptone 10g, NaCl 5g, agar powder 15g, water 1000ml, pH7.4~7.6 ), activated at 30°C, picked a single colony and cultured it on LB slant medium at 30°C for 24 hours to obtain the activated strain;
[0047] (2) Preparation of seed liquid: make LB liquid medium according to conventional methods (its composition and weight ratio are: tryptone 10g, yeast extract 5g, sodium chloride 5g, water 1000ml), and put it in a 250ml Erlenmeyer flask Add 100ml of LB culture solution, and sterilize with high-pressure damp heat. After the temperature drops to room temperature, insert an inoculation loop in each bottle into the above-mentioned activated strain in step (1), and oscillate at 30°C and shaker speed 150rpm Cultivate for 24 hours to obtain seed liquid;
[0048] (3) Preparati...
Embodiment 3
[0052] Embodiment 3 Mohaiwei bacillus HWt34 is to the inhibition of R. solani mycelia growth of cotton
[0053] In March 2019, the plant disease laboratory of the Institute of Plant Protection, Xinjiang Academy of Agricultural Sciences conducted an inhibition test of Bacillus mohaiwei HWt34 on the mycelial growth of R. solani.
[0054] Rhizoctonia solani for testing: The strain of Rhizoctonia solani was collected from a cotton field in Xinjiang. It was isolated and purified in the laboratory and identified as Rhizoctoni solani (Rhizoctoni asolani). The pathogenicity test showed strong pathogenicity.
[0055] Tablet standoff test:
[0056] Rhizoctonia solani is activated in the PDA substratum, cultivates after 3 days in the colony edge area, punches with the hole puncher (0=6mm) and makes the bacterium cake, the bacterium cake adopts cross method to be inoculated to the PDA medium center, Then the Bacillus mohewei HWt34 activated in the step (1) of Example 2 was inoculated wit...
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