Fragrance generating fungus and application thereof
A fungus and aroma-producing technology, applied in the field of microorganisms, can solve the problems of tomato production and post-harvest preservation threats, fruit rot, hazards during transportation and storage, etc., achieving good biocontrol effects and broadening research ideas.
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Embodiment 1
[0026] 1. Isolation and cultivation of aroma-producing fungi
[0027] The aroma-producing fungus was isolated from dead branches of Broussonetia papyrifera, which were collected from the Yangshan Campus of Xinyang Agriculture and Forestry University. The specific isolation and cultivation steps are as follows:
[0028] a. Take 4-5cm dead branches of the mulberry tree, rinse them with tap water for 3 minutes, then disinfect them with 75% alcohol on a sterile table for 3 minutes, rinse them with sterile water three times, and then use pointed tweezers to pick up the mulberry tree The small black dot-shaped conidia on the dead branch are put on the PDA (the streptomycin of 0.3g is added for every liter of PDA) containing streptomycin made in advance on the plate, and each plate is evenly placed at 5 points;
[0029] b. Put the above PDA plate into a 25°C incubator for cultivation, and regularly record the growth of the isolate on the plate every day;
[0030] c. After 3-4 days,...
Embodiment 2
[0038] 1. The fumigation inhibitory effect of aroma-producing fungus GS-1 strain on plant pathogenic fungi
[0039]This test example is determined by the buckle method. The steps are: use the GS-1 strain that has been cultured for 5 days under the condition of 25°C as the aroma-producing strain to be tested; Bipolarisoryzae, Fusarium graminearum, Alternaria brassicae, and Sclerotinia sclerotiorum were inoculated on PDA plates with the tested aroma-producing fungus GS-1, and cultured at 25°C for 7 days , take a bacterium cake with a diameter of 5mm at the edge of the colony of five kinds of phytopathogenic fungi and the tested aroma fungus GS-1 strain; Butt button; take the petri dish only inoculated with phytopathogenic fungi as a contrast, observe the growth of phytopathogenic fungi every 24 hours, observe for 5 days, and measure the colony diameter of pathogenic fungi by the cross method, the calculation formula is: mycelial growth inhibition rate = (control colony growth d...
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