Preparation method of tilletia foetida protoplasts
A technology of Tilletia clematis and protoplasts, which is applied in the field of preparation of protoplasts of Tilletia clematis, which can solve the problem of less research on the pathogenic mechanism of pathogenic bacteria
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Embodiment 1
[0052] Embodiment 1: Optimization of Tilletia glabra protoplast preparation method
[0053] Cultivate the teliospores of Tilletia tritici in 2% water agar medium at a temperature of 16°C and a relative humidity of 80%. Select the cells of different culture days and wash them down with sterilized distilled water, collect the bacterial liquid and filter it , centrifuge at 5000r / min for 10min to remove the supernatant, take 1g of mycelium, add 20ml of different types of compound enzyme solution, 28°C, 180r / min oscillating enzymolysis, observe the protoplast yield with a hemocytometer every half hour, and screen out The most suitable bacterial age, enzymatic hydrolysis time, enzymatic hydrolysis system, and osmotic pressure stabilizer for protoplast preparation.
[0054] 1. Bacteria culture time
[0055] Cultivate the teliospores of Tilletia tritici on the water agar medium, the temperature is 16 ℃, and the relative humidity is 80%. After 4 days, the first mycelium begins to germ...
Embodiment 2
[0073] Embodiment 2: Adopt optimized method to prepare Tilletia glabra protoplasts
[0074] 1.2 mol / L potassium chloride was used to prepare a composite enzyme solution with a mass concentration of 1.5% collapsing enzyme, 1.5% lysozyme and 1.5% helicase. Then prepare protoplasts according to the following steps:
[0075] (1) Mycelia culture: Cultivate the teliospores of Tilletia tritici on 2% water agar medium for 7 days, the culture condition is 16 ℃ of temperature, 80% relative humidity, then the teliospores of germination are rinsed with sterilized distilled water After coming down, collect the bacterial liquid.
[0076] (2) Enzymatic hydrolysis of mycelial cell wall: filter the collected bacterial liquid, then centrifuge at 5000r / min for 10min to remove the supernatant, take 1g of mycelium, add 20mL compound enzyme solution, 28°C, 180r / min, oscillating enzymatic hydrolysis for 2h, and Filtrate the enzymatic solution and centrifuge at 5000r / min for 10min to obtain protopl...
Embodiment 3
[0079] Embodiment 3: the regeneration of Tilletia tritici protoplast
[0080] The protoplasts prepared in Examples 1 and 2 were resuspended with 1.2 mol / L potassium chloride, respectively, and spread on PDA and TB3 solid medium respectively, cultured at 16° C. for 4 days, and observed single colony growing.
[0081] The result is as Image 6 Shown, the protoplast of Tilletia tritici grows more single bacterium colony on TB3 medium, and grows without single bacterium colony on PDA medium, therefore, TB3 medium is more suitable for protoplast regeneration than PDA medium, It can be used for regeneration culture of protoplast of Tilletia tritici.
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