Culture and preparation method for pyricularia oryza conidia
A technology of conidia and rice blast fungus, applied in the field of plant pathology technology and microbiology technology, can solve the problems of high probability of contamination by miscellaneous bacteria, inconvenient practical application, and long time-consuming, etc., and achieve simple operation technology and high spore production The effect of large amount and reduced chance of contamination
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Embodiment 1
[0030] Apply a method for cultivating and preparing spores of Magnaporthe oryzae of the present invention to cultivate and prepare conidia of Magnaporthe oryzae bacterial strain Mg2013-1, and operate as follows:
[0031] 1. Preparation of Sporulation Medium
[0032] Prepare spore-producing medium according to conventional methods, and the composition of this medium is: oat 167g, agar 20g, water 1000ml; Routine high temperature sterilization, pour into 9cm petri dish and make culture plate.
[0033] 2. Equipment for transplanting bacteria from multiple origins
[0034] Under aseptic conditions, wash one dish of the bacterium colony of the rice blast fungus bacterial strain Mg2013-1 that routinely keeps with 10ml sterile water, obtain spore-mycelia broken mixed solution, use this mixed solution as the multiple conidia of preparation new generation The starting point is to transplant the bacteria.
[0035] 3. Implant the multi-point transplanted bacteria into the culture plate ...
Embodiment 2
[0040] Apply a method for cultivating and preparing spores of Magnaporthe grisea of the present invention to cultivate and prepare conidia of Magnaporthe grisea strain Mg2015-7, and implement according to steps 1 to 5 of Example 1, except that the bacterial strain of step 2 is Mg2015-7 ; The result was a new generation of conidia liquid obtained by eluting a dish of culture plate with 15ml of sterile water, and the spore concentration could reach 1.20×10 6 pieces / ml.
Embodiment 3
[0042] Apply a method for cultivating and preparing spores of Magnaporthe oryzae of the present invention to culture and prepare conidia of Magnaporthe grisea strain Mg2015-14, and implement according to steps 1 to 5 of Example 1, except that the bacterial strain in step 2 is Mg2015-14 ; The result was a new generation of conidia liquid obtained by eluting a dish of culture plate with 15ml of sterile water, and the spore concentration could reach 1.38×10 6 pieces / ml.
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