Application of alternaria alternata in preventing and controlling external invasion of weed solanum rostratum
A technology of thorny eggplant and foreign invasion, applied in the direction of application, chemicals for biological control, herbicides and algicides, etc., can solve the problems of single targeting, environmental pollution, time-consuming and labor-intensive, etc., and achieve good control effect , strong toxic lethal effect, strong pathogenic effect
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Embodiment 1
[0043] Isolation, purification and screening of pathogenic bacteria in Solanum japonica:
[0044] Isolation and purification of pathogenic bacteria of Solanum japonica:
[0045] Isolation of bacterial strains: select leaves with typical lesion collected in natural habitat, wash them with clean water, cut out 2mm × 2mm tissue pieces at the junction of disease and health, and wash them in 70% alcohol successively on the ultra-clean workbench, Sterilize in 0.1% mercuric chloride, then rinse continuously in sterilized water for 3 times, take it out, absorb excess water with sterilized absorbent paper, put it on a PDA plate, and cultivate it in a constant temperature incubator at 25°C;
[0046] When the colony on the potato sucrose medium (PDA) plate medium grows to a certain size, it is separated and purified, and after pathogenicity determination, it is transferred to the slant of the potato sucrose medium (PDA) test tube and stored in the refrigerator at 4°C for later use;
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Embodiment 2
[0070] The isolation, purification and screening of the pathogenic bacteria of Solanum japonica are based on Example 1:
[0071] Pathogenicity Test and Preparation of Crude Toxins of Pathogenic Bacteria on Solanum japonica:
[0072] Extraction of crude toxins from pathogenic bacteria:
[0073] Toxin-producing culture of Alternaria chrysalis:
[0074] On the ultra-clean workbench, transplant the Alternaria strains to the test tube potato sucrose medium (PDA) slant medium for activation, and transfer the activated Alternaria strains to the potato sucrose medium (PDA) plate medium for cultivation After 5 days, use a puncher with a diameter of 5mm to take out the fungus cake and put it into the potato dextrose (PDB) culture solution (2 pieces / 100mL), put it into a shaker for shaking culture, set the temperature at 25°C, and rotate at 110r / min , continuously cultivated for 7 days to obtain a fermentation broth;
[0075] Extraction of crude toxins:
[0076] The fermented liquid ...
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