A strain of Paenibacillus jemira, its fermentation product, preparation method and application
A technology of Bacillus and fermentation products, applied in the field of microorganisms, can solve the problems of affecting the quality of citrus, withering of branches, and reducing production of citrus, achieving good application prospects, inhibiting growth and colonization, and good stability
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Embodiment 1
[0041] Example 1 Screening of X. citri antagonistic strain WAC199
[0042] 1. Preparation of LB solid medium containing Xac jx-6
[0043] Xanthomonas axonopodis pv.citrijx-6 strain, referred to as Xac jx-6, (the full-length sequence of the strain has been published in NCBI, the sequence number is CP011827.2), provided by the Laboratory of Population Microbiology Center, College of Agriculture, South China Agricultural University .
[0044] The activation medium of Xac jx-6 of citrus canker sores Xac jx-6 is LB solid medium, and a single colony was picked and inoculated in LB liquid medium, and cultured with shaking at 30°C.
[0045]Mix LB solid medium and Xac jx-6 bacterial suspension (OD600 about 1) at a temperature of 40-50°C at a ratio of 500 μL of bacterial suspension per 50 mL of LB solid medium, pour about 12 mL into each dish The medium after mixing is LB solid medium containing Xac jx-6.
[0046] 2. Screening of antagonistic strains against citrus canker
[0047] (...
Embodiment 2
[0050] Example 2 Identification of X. citri antagonistic strain WAC199
[0051] 1. Observation of the morphological characteristics of the strain
[0052] The preserved antagonistic strain WAC199 was inoculated on LB plates, cultured at 30°C for 24h-36h, and the characteristics of the colonies were observed. WAC199 grows well in LB medium, the colonies are off-white, raised, opaque, with irregular edges, Gram staining is positive, spores are middle or apical, spores are oval, and the cells are arranged singly or in pairs. The growth morphology and the morphology observed by microscope after Gram staining are as follows: figure 2 , image 3 shown.
[0053] 2.16S rDNA sequence analysis
[0054] Inoculate the preserved antagonistic strain WAC199 on an LB plate, culture at 30°C for 24h to 36h, and use the method of direct PCR amplification of a single bacterial colony, using 16S rDNA universal primers F27: 5'-AGAGTTTGATCATGGCTCAG-3', R1492: 5'- TACGGTTACCTTGTTACGACTT-3' was ...
Embodiment 3
[0062] Example 3 Media Screening for Optimal Production of Metabolic Active Substances of X. citri Antagonistic Strain WAC199
[0063] Prepare the following liquid media respectively:
[0064] (1) NYD liquid medium: beef extract 8g, yeast extract 3g, glucose 1g, distilled water 1000mL;
[0065] (2) YPG liquid medium: yeast extract 10g, peptone 20g, glucose 20g, distilled water 1 000mL;
[0066] (3) YPD liquid medium: yeast extract 10g, tryptone 20g, glucose 20g, distilled water 1 000mL;
[0067] (4) LB liquid medium: yeast extract 5g, peptone 20g, NaCl 20g, distilled water 1 000mL,
[0068] (5) LB broth liquid medium: LB broth medium (Haibo Biotechnology Co., Ltd., product number: HB0128) 30g, distilled water 1000mL;
[0069] (6) Corn flour liquid medium: 30 g of corn powder (Haibo Biotechnology Co., Ltd., product number: HBYL004), 1 000 mL of distilled water;
[0070] (7) Tryptone soy liquid medium: Tryptone soy liquid medium, Haibo Biotechnology Co., Ltd., product number...
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