Pestalotiopsis crassipes
A technology for the control of Polychaeta pseudodiscoides and bio-control fungi, applied in the direction of fungi, microorganisms, biocides, etc., to achieve strong pathogenic control effects, potential commercial development and application value, and good control effects
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Embodiment 1
[0025] Example 1: Isolation, Purification and Screening of Herbicidal Fungi
[0026] 1. Isolation and purification of water hyacinth pathogenic bacteria
[0027]1.1. Isolation of strains: Select leaves or stems with typical lesions, wash them with clean water, cut out 2 mm × 2 mm tissue pieces at the junction of disease and health, and place them on the ultra-clean workbench at 70% Alcohol, 0.1% mercury liter disinfection, and then rinse in sterilized water for 3 consecutive times, after taking out, use sterilized absorbent paper to absorb excess water, put it on a PDA plate, and cultivate it in a constant temperature incubator at 25 ℃.
[0028] When the colony on the PDA plate medium grows to a certain size, it is separated and purified, and after being tested for pathogenicity, it is transferred to the slant of the PDA test tube and stored in the refrigerator at 4 °C for later use.
[0029] 1.2. Source and cultivation of host plants: Collect relatively healthy plants wi...
Embodiment 2
[0038] Embodiment 2: Biological characteristics of Polychaete pseudodiscoides of water hyacinth
[0039] 1. Effect of culture medium on bacterial colony growth and sporulation
[0040] On the colonies cultured at a constant temperature of 25 ℃ for 5 days, the bacteria cakes with a diameter of 5.0 mm were punched along the edge of the colonies with a puncher and inoculated on PDA, PSA, CAA, WA, WLA, OSA, WS and WD medium plates (9 cm) central. Incubate at a constant temperature of 25°C and observe continuously. After the 5th day, use the vertical cross method to measure and record the diameter of the colony daily; after the 18th day, measure the amount of sporulation, add sterilized distilled water, gently scrape the surface of the colony with a sterilized glass slide, then elute, filter, and add a certain volume of 0.1 % Tween-80 was made into a suspension, and the spore suspension was sucked up with a pipette gun and dropped on a Neubauer hemocytometer, counted under a ...
Embodiment 3
[0051] Embodiment 3: pathogenic bacteria crude toxin extraction
[0052] Toxicity-producing culture of Polychaete pseudodiscoides in water hyacinth
[0053] On the ultra-clean workbench, take out the cultivated water hyacinth plate of Polychaeta pseudodiscoides strain, use a puncher with a diameter of 5 mm to punch out the fungus cake, and put it into the potato sucrose (PS) culture solution respectively, 4 for each bottle. Truffle Pie. They were placed in a shaker for shaking culture, the temperature was set at 25 °C, the rotation speed was 110 r / min, and the darkness was alternated for 12 h, and the culture was continued for 7 days.
[0054] Crude toxin extraction
[0055] The obtained fermentation broth was filtered once with four layers of gauze, and the obtained filtrate was filtered with double-layer chromatography filter paper, and then the filtrate was centrifuged for 20 min at a speed of 10,000 r / min, and the obtained supernatant was the crude extract of the t...
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