Separated streptomyce NBF715 and application thereof in crop disease control
A technology of Streptomyces and Streptomyces brownus, applied in the direction of application, bacteria, microorganisms, etc., can solve problems such as environmental pollution, pesticide residues, and drug resistance of bacteria, and achieve the effect of not polluting the environment and not easily producing drug resistance
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Embodiment 1
[0035] Obtaining and Identification of Streptomyces enissocaesilis NBF715
[0036] An isolated strain of Streptomyces was isolated from the soil of Hefeng County, Enshi, and was identified as Streptomyces enissocaesilis after 16s rDNA combined with physiological and biochemical identification ( figure 1 , Table 1, Table 2), has been sent to the China Center for Type Culture Collection on July 7, 2017 for preservation, classification and name: Streptomycesenissocaesilis (Streptomycesenissocaesilis) NBF715; preservation number is CCTCC NO: M2017414; location: China, Wuhan, Wuhan University.
[0037] In the present invention, Streptomyces enissocaesilis NBF715 may be referred to as NBF715 for short.
[0038] Morphological characteristics: The colony is round, with smooth edges and dense surface. The aerial hyphae are silver-gray, the base mycelium cork is yellow, and the colony is round, without pigment. The spore filaments are distributed in a straight chain, and the spores a...
Embodiment 2
[0049] Fermentation of Streptomyces enissocaesilis NBF715:
[0050]Preparation of Streptomyces enissocaesilis NBF715 seed solution: including activating the slant-preserved bacterial species on the ISP-2 plate, picking and inoculating it into 100 ml of seed medium, at 28°C, on a shaker at 160 rpm Cultivate for 4 days; the seed solution is obtained.
[0051] The formula of the seed medium is: 1L of medium includes 20g of mannitol, 10g of soybean peptone, 0.35g of potassium dihydrogen phosphate, 0.5g of calcium carbonate, 20 μL of soybean oil, and the rest is water.
[0052] Solid fermentation: Inoculate Streptomyces enissocaesilis (Streptomyces enissocaesilis) NBF715 seed liquid into solid medium at 10%, with a sample loading of 20%, and culture at 30°C for 10 days. The bacterial concentration of the culture obtained by this method is 5*10 10 spores / gram.
[0053] The solid fermentation medium is: 83% bran, 3% glucose, 5% potassium nitrate, 3% dipotassium hydrogen phosphate,...
Embodiment 3
[0057] Streptomyces enissocaesilis NBF715 prevents tobacco black shank:
[0058] (1) Antibacterial activity of NBF715 strain against Phytophthora nicotianae in vitro
[0059] The pathogenic bacteria of tobacco black shank tested were isolated from tobacco black shank plants, and stored on V8 slope at 10°C for later use. The slant strain was transferred to the V8 plate for activation, and cultured at 30°C for 6 days for later use. NBF715 was activated from the slant to ISP2 medium for 7 days for later use. Use a 4mm hole puncher to punch out Phytophthora nicotianae bacteria discs and place them in the center of the PDA medium, then use a 4mm hole puncher to punch out NBF715 bacteria discs and place them on both sides of the Phytophthora nicotiana plate with a distance of 25mm. After 8 days, the inhibition zone was observed. Obvious bacteriostatic zone (diameter of bacteriostatic zone is 2cm) can be observed through in vitro confrontation, indicating that NBF715 strain has a ...
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