Bacillus for antagonizing fusarium wilt and promoting growth and application thereof
A technology of bacillus and fusarium wilt, applied in the field of microorganisms, can solve the problem of poor control effect of plant fusarium wilt
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Embodiment 1
[0027] Example 1 Screening of antagonistic strains
[0028] 1. Soil sample collection and Bacillus isolation and purification
[0029] The grassland soil samples near Bayong, Shenzha County, Tibet were made into soil suspension, which was then properly diluted with sterile water and coated on LB plates (LB: tryptone 10g L -1 , sodium chloride 10g·L -1 , yeast powder 5g·L -1 , agar powder 1.5%, pH 7.0-7.2); cultivated at 30°C for 48 hours, picked a single colony, stored in glycerol, and used it as the strain to be tested. 60 strains were isolated and purified by dilution plate method as the strains to be tested.
[0030] 2. Screening of fusarium wilt biocontrol strains
[0031] (1) Preliminary screening by confrontation method
[0032] The tested strains were activated on LB plates and cultured at 30°C for 48 hours.
[0033] Fusarium oxysporum FJAT-30512 (Chen Qianqian, Liu Bo, Liu Guohong, Che Jianmei, Gong Haiyan. Study on the Diversity of Geobacillus in the Rhizosphere...
Embodiment 2
[0057] Identification of embodiment 2 antagonistic strains
[0058] 1. Morphological characteristics
[0059] The Bacillus sp. FJAT-47158 was activated on the LB plate, and the colony shape, size, color, transparency, protrusion and edge of the strain were observed after 48 hours.
[0060] The colony characteristics of strain FJAT-47158 are as follows figure 1 As shown, round, pale yellow, neat edges, wrinkled surface, opaque, viscous medium-sized colonies.
[0061] 2.16S rRNA gene sequence analysis
[0062] Genomic DNA of strain FJAT-47158 was extracted by Tris-saturated phenol method, PCR amplification was carried out using 16S rRNA gene general primers 27F and 1492R, and the PCR reaction procedure was referred to the literature of Zheng Xuefang et al (Zheng Xuefang, Liu Bo, Zhu Yujing, et al. Screening and identification of biocontrol Bacillus [J]. Chinese Journal of Biological Control, 2016, 32(5): 657-665.), the PCR product was sent to Shanghai Boshang for sequencing, ...
Embodiment 3
[0064] The inhibitory effect of embodiment 3 bacillus to Xanthomonas rugosa
[0065] Inoculate the FJAT-47158 strain on the LB plate, and then pick a single bacterial colony and transfer it to 10mL LB liquid medium, 170r min -1 , cultured at 30°C for 48 hours, and counted by hemocytometer, the colony density of FJAT-47158 reached 2.352×10 8 cfu mL -1 . The FJAT-47158 fermentation broth was centrifuged at 4000rpm for 8min, the supernatant was taken, and the bacterial cells were discarded.
[0066] 1mL of the bacterial suspension of Xanthomonas rugosa FJAT-10151 (preserved in the General Microbiology Center of China Microbiological Culture Collection Management Committee, preservation number CGMCC NO.10271) (colony density 4.224×10 8 cfu mL -1 ) mixed with 200mL of 50°C NA semi-solid medium (3g of beef extract, 5g of peptone, 10g of glucose, 9g of agar, and 1L of water), draw 4mL and pour it into the prepared NA solid medium (3g of beef extract, 5g of peptone, Glucose 10g, ...
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