Bacillus subtilis JN005 and application thereof in prevention and control of rice blast
A technology of Bacillus subtilis and rice blast, applied in the direction of application, bacteria, and fungicides, can solve the problems of unsatisfactory effect, poor colonization ability of antagonistic microorganisms, and reduced control effect of antagonistic microorganisms, and achieve both protection and treatment. Tool, avoid adverse effects, good effect of prevention
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Embodiment 1
[0024] Example 1 Isolation of Bacillus subtilis JN005
[0025] Healthy rice plants were selected from the diseased clusters of blast-susceptible rice variety Xiangzaoxian No. 24 in Paixingshang Village (N28°31′49.02″, E111°54′24.86″), Daligang Town, Daligang Town, Taojiang County, Hunan Province, and 871 plants were isolated Strains, the plate confrontation method with Magnaporthe grisea was used to screen out an antagonistic antibacterial JN005 with an inhibition rate of 84% against Magnaporthe oryzae hyphae.
[0026] By cultivating strain JN005 (peptone 5g / L, beef extract 3g / L, glucose 20g / L, agar 17g / L, pH 7.0, prepared with distilled water) on NA solid medium ( figure 2 A and figure 2 B). Observe the morphology of the colony, observe the SEM image of the bacteria, and combine the physiological, biochemical, microbiological test results of the bacteria, and the 16S rDNA sequencing results (see SEQ ID NO. 1) to finally determine the strain JN005 is Bacillus subtilis (Bacillus s...
Embodiment 2
[0028] Example 2 Application of Bacillus subtilis JN005 in the control of rice blast
[0029] After the strain JN005 is activated on the NA solid medium plate, use a punch to punch 2 bacterial cakes with a diameter of 5 mm into 150mL NB liquid medium (peptone 5g / L, beef extract 3g / L, glucose 20g / L, pH 7.0, prepared with distilled water) in a 250 mL Erlenmeyer flask, shake culture in a shaker at 28°C and 180 r / min for 6 days, and filter with a bacterial filter to obtain the metabolites of Bacillus subtilis JN005.
[0030] Add 10 mL of the metabolites of strain JN005 and 0.1 mL of the conidia of Magnaporthe grisea (strain 81) into a sterilized Erlenmeyer flask, mix well, replace the antagonistic culture medium with sterile water as a control, cultivate in the dark at 27°C for 6 hours The germination of spores was checked under microscope, and the experiment was repeated 3 times. The results showed that the inhibition rate of JN005 metabolites on rice blast fungus spore germination ...
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