Screening method of aspergillus versicolor HY12
A technology of Aspergillus versicolor and a screening method, which is applied in the field of screening of Aspergillus versicolor HY12, can solve the problems of low efficiency of pathogenic strains, low pertinence, and difficult to repeat, and achieves inhibition of the growth of various bacteria, high lethality and pathogenicity. Distortion rate, not easy to repeat the effect
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Embodiment 1
[0033] Screening of Aspergillus versicolor HY12 strain
[0034] Collect the larvae of susceptible Spodoptera litura that died naturally from the infested area of Spodoptera litura, screen the susceptible larvae of Spodoptera litura without mold layer on the surface, immerse them in 75% alcohol for 2 seconds, disinfect the body surface, and peel off under aseptic conditions The rotted viscera in the larvae were removed, and the rotted viscera were homogenized. The homogenate was diluted with sterile water into 10-fold, 100-fold, and 1000-fold gradients, and spread on the surface of a screening medium plate, and cultured at 25.6°C for 5 days. Wherein the screening medium is HECK medium, comprising the following components in parts by weight: 4 parts of glucose, 2 parts of peptone, 0.025 part of potassium permanganate, 0.5 part of cycloheximide, 0.2 part of gentamicin, 0.048 part of ampicillin , 2 parts of agar and 100 parts of water.
[0035] Pick a single colony in the HECK m...
Embodiment 2
[0053] Identification of Aspergillus versicolor HY12 strain
[0054] Inoculate the Aspergillus strain (HY12) obtained in Example 1 onto the SDAY medium, cultivate it in a constant temperature incubator at 25.6°C, observe its colony character and color, and pick mycelium from the colony to make a microscopic examination, observe The color and properties of the mycelia, conidiophores and sporulation axes; after the colony produced sporulation, the conidia were picked up for microscopic examination to observe the conidia’s properties, color, size, and photograph. The results were as follows: figure 1 shown. Depend on figure 1 It can be seen that after culturing on SDAY medium for 14 days, the diameter of the colony reaches 66.3mm, the colony is round, white cotton-like mycelia, the colony is thicker, and the texture is dense and soft; a large number of conidia are produced in the later stage, and the spores are brown powdery, and the powder layer Thick, with concentric ridges. ...
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