Bacillus amyloliquefaciens and application thereof to preparation of microbial agent for controlling radix rehmanniae root rot and spot blight
A technology for dissolving starch spores and microbial strains is applied in the field of microbial control of plant diseases, and can solve problems such as increasing the hidden danger of Rehmannia glutinosa, infection of Rehmannia glutinosa, and environmental pollution.
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Embodiment 1
[0015] Embodiment 1 (antagonistic rehmannia root rot)
[0016] Adopt plate confrontation method, will cultivate the rehmannia root rot pathogen of 4-5 days on the PDA plate Fusarium solani Break into a bacterium cake with a diameter of 6mm, inoculate it in another PDA medium with a pore size of 6 mm, and then inoculate the purified Bacillus amyloliquefaciens ZSY-1 activated for 36 hours on the LB medium at a distance of 2 cm from the bacterium cake. Each PDA plate was symmetrically inoculated with 4 points, repeated 3 groups, and the point was connected with sterile water as a blank control, and placed in a 28 ° C incubator. After the pathogenic bacteria in the control grew for 4 days, the radius of the pathogenic bacteria colony was measured. According to the inhibition rate = ( Blank control pathogenic bacteria colony radius - ZSY-1 confrontation pathogenic bacteria radius) / blank control pathogenic bacteria colony radius * 100% to calculate the antibacterial effect. The ...
Embodiment 2
[0017] Embodiment 2 (antagonistic macular blight)
[0018] Using the flat plate confrontation method, the ground yellow spot blight bacteria that will be cultivated on the PDA plate for 4-5 days Septoria digitalis pass Break into a bacterium cake with a diameter of 6mm, inoculate it in another PDA medium with a pore size of 6 mm, and then inoculate the purified Bacillus amyloliquefaciens ZSY-1 activated for 36 hours on the LB medium at a distance of 2 cm from the bacterium cake. Each PDA plate was symmetrically inoculated with 4 points, repeated 3 groups, and the point was inoculated with sterile water as a blank control, placed in a 28°C incubator, and after the pathogenic bacteria in the control grew for 4 days, according to the inhibition rate = (blank control pathogenic bacteria Colony radius - ZSY-1 confrontation pathogenic bacteria radius) / blank control pathogenic bacteria colony radius * 100% to calculate the antibacterial effect. The results showed that Bacillus ...
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