Biological preparation containing plant source component and microorganism source component and application of biological preparation in prevention and treatment of plant nematode diseases
A microbial source, biological preparation technology, applied in plant growth regulators, microorganism-based methods, microorganisms, etc., can solve the problems of unsatisfactory control effect and unstable control effect of single plant-derived preparations
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Embodiment 1
[0045] Screening method and identification method of cold-resistant psesson strain SJ5
[0046] 1. Separation and screening of the biopsy
[0047] Separation and screening of cold sputum strain SJ5 using dilution plate coating method, the specific steps are as follows: Separation of cyclic soil bacteria in the pathogeneous tomato, take 100 μl of dilutions on NA medium, each gradient 3 The repetition was cultured at 30 ° C for 40 hours, and the single colonies different from the form of different morphological characteristics were observed. After purification, it was stored in the 4 ° C refrigerator. Splitting, purified strains were screened in NA medium, and the strain was seeded with Na medium, and after 72 h at 27 ° C, the bacterial morphology was observed, and the SJ5 colony was milky white, circular, bright, micro-transparent (See figure 1 ). Gram-stained results showed that the form of the SJ5 strain was rod, no spores, and the SJ5 strain showed fresh red, which proves that t...
Embodiment 2
[0059] Preparation method of three microbial fermentation fluids
[0060] 1) The LB liquid medium is prepared, 20 min after 121 ° C, to obtain a sterilized LB liquid medium, and after adjusting the pH to 7.4, the LB liquid medium is separated into the shake flask, and 300 ml of medium per bottle. Cooling spare.
[0061] 2) Incoke 1ml to the shake flanet of the hematococcal strain SJ5 strain, inoculated on the shaker after the shaker was placed on the shaker, and 60 h was cultured at 180 rpm, 28 ° C, and the bacterial liquid was collected to obtain a cold pseudomonas strain. Fermentation of SJ5.
[0062] 3) Inoculation of the bond vagobacterium inoculated 1ml to the shake flask, the inoculated shake flask was placed on a shaker, cultured at 200 rpm, 30 ° C for 54 h, and the bacterial liquid was collected, and the fermentation broth of the bonding bunus was obtained.
[0063] 4) Inoculation of the Bacillus strain inoculation, in the shake flask, the inoculated shake flask was placed...
Embodiment 3
[0065] Toxicity assay method of three microbial fermentation fluid on southern roots
[0066] 1) The three microbial fermentation fluids prepared in Example 2 were filtered through a sterile filtration membrane (filtration film pore diameter 0.22 μm), respectively, and the fermentation filtrate of three microorganisms was obtained.
[0067] 2) Set five processes, set 5 petri dishes (35mm diameter) per handle, 20 μl of the roots (J2) suspension (J2) suspension (approximately 100 pieces), each dish add benefit to the final concentration of 100 μg / ml, The addition of mastin to a final concentration of 20 μg / ml, adding streptomycin to a final concentration of 50 μg / ml. Treatment 1 is 3000 μLB liquid medium (control group); 23000 μL strain SJ5 fermentation filtrate; 33000 μL of bispylobacterium fungus fermentation filtrate; 43000 μL of Bacillus fermentation filtrate; 53000 μL of bitter printer inducery oil dilution (1000 times, mother liquor concentration 1%) . 12h was placed in ...
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