Regular morphology of fusarium oxysporum laboratory material and preparation and application method thereof
The invention discloses a laboratory technology of banana fusarium wilt, which is applied to the standing form of laboratory materials of banana fusarium wilt and its preparation and application method. It can solve the problems of not being able to carry out in time and delay, and achieve the effects of standardization, convenient and fast work, and accurate and quantitative access
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Embodiment 1
[0037] Apply the present invention's standing form of laboratory materials of Fusarium wilt of banana and its preparation and application method, cultivate and prepare the laboratory standing form material of Fusarium wilt of banana bacterial strain Fo-1 with conidia as the thallus; preparation and application of bacterial strain Fo-1 The standing form of the material is operated according to the following steps:
[0038] 1. Preparation and culture of conidia
[0039] Use a triangular flask as a culture device, and fill the potato glucose medium as a spore-producing medium. The composition ratio of the medium is: 200g of potatoes, 20g of glucose, 20g of agar, and 1000mL of water; The filaments were transplanted into the spore-forming medium in the Erlenmeyer flask, and after culturing at 28° C. for 5 days, the colonies on the surface of the medium formed a large number of conidia.
[0040] 2. Preparation of standing form of banana Fusarium wilt material
[0041]Inject steril...
Embodiment 2
[0051] Apply the present invention's standing form of laboratory materials of Fusarium wilt of banana and its preparation and application method, cultivate and prepare the laboratory standing form material of Fusarium wilt of banana strain Fo-2 with conidia as thallus; preparation and application of bacterial strain Fo-2 The standing form of the material is carried out according to step 1 to step 5 of embodiment 1, the difference is that the bacterial strain used in step 1 is Fo-2, and step 2 obtains the standing spore liquid of Fusarium wilt bacterial strain Fo-2.
[0052] Use a pipette to quantitatively draw 5 μL of the calibrated standing spore solution, transplant it to the middle of the potato glucose culture plate, and culture it at 28°C for 2 days, and it can grow into a typical small colony.
[0053] Take 10 μL of the calibrated standing spore spore liquid, transplant it into the potato glucose culture medium, shake it at 28°C for 5 days, and form a large number of new ...
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