Bacillus subtilis jn005 and its application in controlling rice blast
A technology for Bacillus subtilis and rice blast, applied in application, bacteria, fungicides and other directions, can solve the problems of reduced control effect of antagonistic microorganisms, unsatisfactory effect, poor colonization ability of antagonistic microorganisms, etc., and achieves good control effect and protection. Combined with the therapeutic effect, the effect of avoiding adverse effects
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Embodiment 1
[0024] Embodiment 1 The separation and acquisition of Bacillus subtilis JN005
[0025] Healthy rice plants were selected from the diseased clusters of rice blast-susceptible rice variety Xiangzaoxian 24 in Paixingshang Village (N28°31′49.02″, E111°54′24.86″), Daligang Town, Taojiang County, Hunan Province, and a total of 871 plants were isolated For strains, an antagonistic bacteria JN005 with an inhibitory rate of 84% against Magnaporthe oryzae mycelium was screened out by using plate confrontation method with Magnaporthe oryzae.
[0026] Bacterial strain JN005 ( figure 2 A and figure 2 B), observe the colony morphology, observe the scanning electron microscope images of the bacteria, and combine the physiological and biochemical and microbiological detection results of the bacteria, and the 16S rDNA sequencing results (see SEQ ID NO.1), to finally determine the bacterial strain JN005 is Bacillus subtilis.
[0027] In addition, the plate confrontation culture method was ...
Embodiment 2
[0028] Example 2 Application of Bacillus subtilis JN005 in the Control of Rice Blast
[0029] After the bacterial strain JN005 was activated on the NA solid medium plate, two bacterial cakes with a diameter of 5mm were punched out and inserted into 150mL NB liquid medium (peptone 5g / L, beef extract 3g / L, glucose 20g / L L, pH 7.0, prepared with distilled water) in a 250mL Erlenmeyer flask, cultured in a shaking table at 28°C and 180r / min for 6 days, and filtered with a bacterial filter to obtain the metabolite of Bacillus subtilis JN005.
[0030]Add 10mL of metabolites of strain JN005 and 0.1mL of conidium liquid of Magnaporthe grisea (strain No. 81) into a sterilized Erlenmeyer flask, mix well, replace antagonistic bacteria culture solution with sterile water as a control, and incubate in the dark at 27°C for 6h Microscopic examination of spore germination, the experiment was repeated 3 times. The results showed that the inhibition rate of JN005 metabolites on the spore germin...
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