A strain of fritillaria ussuriensis maxim rhizosphere Paenibacillus polymyxa, and applications thereof,
A technology of Paenoid polymyxa and Fritillaria, applied in the direction of bacteria, fungicides, chemicals for biological control, etc., can solve the problems of destroying the soil micro-ecological environment and high residual harmful substances, and improve the soil micro-ecological environment , good control effect
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specific Embodiment approach 1
[0014] Specific embodiment one: present embodiment flat fritillaria rhizosphere Paenibacillus polymyxa is Paenibacillus polymyxa ( Paenibacillus polymyxa ) SBS-SF0105, deposited in the General Microbiology Center (CGMCC) of the China Committee for the Collection of Microbial Cultures (CGMCC), the preservation address is No. 3, No. 1, Beichen West Road, Chaoyang District, Beijing, Institute of Microbiology, Chinese Academy of Sciences, and the preservation date is November 2015 On the 5th, the deposit number is CGMCC No.11586.
[0015] In this embodiment, Paenibacillus polymyxa SBS-SF0105 is cultured at 25° C. for 48 hours on PDA medium, and the colony becomes colorless and transparent without pigmentation. The diameter of the colony is 1.5-2.0 mm, and the colony is moist and sticky with neat edges. The bacterial cell is rod-shaped, the spore is oval, the cyst is enlarged, and the Gram stain is positive.
[0016] Paenibacillus polymyxa (Paenibacillus polymyxa) Paenibacillus...
specific Embodiment approach 2
[0018] Specific embodiment 2: In this embodiment, Paenibacillus polymyxa SBS-SF0105 is isolated from the rhizosphere of Pygnus chinensis. The separation method is carried out as follows:
[0019] 1) Isolation and preservation of rhizosphere bacteria of Fritillaria chinensis: In the cultivation plots of Pingbei, take healthy Pingbei plants, and collect rhizosphere soil samples by shaking off method. First, gently shake off the soil without roots, and then use a brush The rhizosphere soil on the roots and bulbs was brushed down and collected. Take 1g of rhizosphere soil and put it into a 250ml sterilized triangular flask, add 100ml of sterile water, 30-40 sterilized glass beads, shake at 160rpm on a shaker for 30min, let it stand for 30min, take the supernatant, and dilute the concentration by gradient dilution method to 10 -4 、10 -5 、10 -6 For three gradients, draw 0.1ml of liquid from the three gradients and inoculate them on beef extract peptone solid medium, culture at a...
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