Streptomyces hydrogenans and application thereof in biological control
A technology of Streptomyces hydrangeum and Streptomyces hydrangeum, which is applied in the field of Streptomyces hydrangeum, can solve the problems of lack of biological pesticides, species and quantity cannot meet agricultural production, etc., achieve good social and economic benefits, protect and promote root growth, and enhance resistance effect of ability
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Embodiment 1
[0029] A strain KLBMP-3095 was obtained by collecting eucalyptus rhizosphere soil at Dananshan Forest Farm in Zhaoqing City, Guangdong Province, and was isolated and purified by conventional methods. The strain grows better on Cha's medium, yeast extract powder-malt extract agar medium (ISP2) and glycerol asparagine agar medium. The aerial hyphae and basal hyphae grow luxuriantly, the spore chains formed by mature sporocydia are in the shape of beads, the spores are cylindrical, and the surface is smooth without spines, which has the typical morphological characteristics of Streptomyces ( figure 1 ). Determine the 16S rRNA sequence (SEQ ID No.1) of the strain, compare this sequence with the effective strains in the EzTaxon database, construct a phylogenetic tree with MEGA5.01 software, combine the morphology and culture characteristics, physiological and biochemical characteristics, It was identified as a strain of Streptomyces hydrogenans.
Embodiment 2
[0030] Embodiment 2 Bacterial strain plate face-off experiment
[0031] Pick the Alternaria solani stored in the inclined tube and inoculate it on one side of the PDA plate, and at the same time inoculate the strain KLBMP-3095 on the other side, and culture it in a constant temperature incubator at 28°C. Repeat three times, observe and record the growth status of the two bacteria on the plate. as attached figure 2 shown. It can be seen from the figure that the mycelium of Alternaria solani can not grow close to the strain KLBMP-3095, indicating that the strain KLBMP-3095 can effectively inhibit the growth of Alternaria solani in the plate experiment.
Embodiment 3
[0032] Embodiment 3 Growth Rate Method Measures Fermentation Liquid Inhibits Alternaria Solani Growth Experiment
[0033] In the ultra-clean workbench, pick an appropriate amount of KLBMP-3095 bacteria from the seed tube for activation, and inoculate the activated bacteria into the liquid medium.
[0034] The composition of the liquid fermentation medium is: 4g of sucrose, 10g of malt extract powder, 4g of beef extract, 1000mL of distilled water, and the pH is 8.0.
[0035] 28°C, 150r / min, culture for 5 days, until the bacteria grow to the logarithmic growth phase, stop the fermentation. The fermentation product was centrifuged at 7800 r / min for 10 min, and the supernatant was filtered through a 0.22 μm sterile filter membrane to obtain a sterile fermentation broth. When the PDA medium is autoclaved and cooled to 60°C, mix according to the ratio of medium: sterile fermentation broth = 9:1 and pour onto the plate. The bacterium cake (diameter 4mm) of the pathogenic bacteria c...
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