Bacillus subtilis 2012SYX04 for preventing and treating rice blast
A 2012SYX04, Bacillus subtilis technology, applied in the field of microorganisms, to achieve the effects of good rice blast control effect, high control efficiency, and broad-spectrum control effect
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Embodiment 1
[0027] Example 1: Screening and fermentation of Bacillus subtilis 2012SYX04 strain
[0028] (1) Sample collection: The samples were collected from the leaves of late-maturing rice varieties at Ciyun Town, Jiangjin District, Chongqing City. Pull out together with the root system of rice, pack it in a polyethylene plastic bag, and bring it back to the laboratory for isolation.
[0029] (2) Isolation of Bacillus subtilis: cut the healthy leaves of rice and put them in a 75% alcohol triangular flask, shake and wash them for 2 times, pour off the alcohol, add sterile water to soak, then draw the diluted solution and apply it on the NA medium plate. After drying, they were incubated upside down in a constant temperature incubator at 30°C for 48 hours. A single colony was picked, and the picked single colony was purified by gradient streak separation, and the purified strain was stored in NA slant medium for future use.
[0030] Broth medium (NA): peptone 10g, beef powder 3g, sodiu...
Embodiment 2
[0035] The inventor has deposited this strain in the General Microorganism Center (CGMCC) of the China Committee for the Collection of Microorganisms, with the preservation date being May 21, 2014, and the preservation number being CGMCC No.9189. Embodiment 2: The biological activity assay of Bacillus subtilis 2012SYX04 bacterial strain:
[0036] (1) Determination of the inhibition of Bacillus subtilis 2012SYX04 strain on Magnaporthe grisea P131: Place the rice blast fungus cake in the center of the tomato oat plate medium, and inoculate the prepared 2012SYX04 at a distance of 2cm from both sides of the cake with a toothpick. The rice blast fungus cake was used for confrontation culture, and sterile water was used as a control, and it was placed in an incubator at 28°C for dark culture, and each treatment was repeated 3 times. After 12 days, the diameter of the pathogenic bacteria colony and the zone of inhibition were measured, and the results are shown in Table 1.
[0037] (2...
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