Paenibacillus kribbensis and preparation and application thereof
A technology of bacillus and microbial preparations, applied in the direction of application, fungicides, bacteria, etc., to achieve the effect of promoting the growth of tobacco plants, increasing yield and output value
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[0027] The invention provides a microbial preparation containing Paenibacillus cribbus, and the preparation method of the microbial preparation comprises the following steps:
[0028] (1) activating the above-mentioned Paenibacillus cribbus with beef extract peptone medium to obtain a single colony or a lawn;
[0029] (2) Inoculate the single bacterial colony or bacterial lawn into the liquid Zaburi medium, shake and culture at 28-32°C, 150-250r / min for 36-48 hours, to obtain the propagation solution;
[0030] (3) Inoculate the multiplication solution into a liquid fermentation medium, and ferment and cultivate at 28-30° C. for 4-5 days to obtain a microbial preparation containing Paenibacillus cribbus.
[0031] In the present invention, the above-mentioned Paenibacillus cribbus is firstly activated with beef extract peptone medium to obtain a single colony or a lawn. The present invention does not specifically limit the source and specific composition of the beef extract pep...
Embodiment 1
[0042] (1) Isolation of Paenibacillus sp.
[0043] Paenibacillus crib was isolated from the rhizosphere soil of tobacco planting in Henan. Methods as below:
[0044] Collect rhizosphere soil samples from tobacco planting areas in Henan, weigh 10.0g of soil, put it into a conical flask with 100mL sterile water, place the conical flask on a shaker at 220r / min for 5min; -1 ~10 -6 Diluted rhizosphere soil suspension; draw 100μL of 10 -4 ~10 -6 Soil suspensions with different dilutions were evenly spread on the beef extract peptone medium plate with aseptic technique, and 3 to 5 parallels were made for each dilution, and then placed in a constant temperature incubator at 28-30°C for 2-2 5d. After the colonies grow out, pick a single colony and transfer it to the beef extract peptone medium for purification to obtain pure culture. Using Phytophthora nicotiana, Fusarium and other pathogenic fungi as indicator bacteria, the primary screening of antagonistic bacteria was carried ...
Embodiment 2
[0062] Determination of the antibacterial activity of Paenibacillus by Cribb: plate confrontation method was used, and the pathogenic fungi tested were Phytophthora nicotiana and Fusarium.
[0063] After activating the antagonistic strains, spread and inoculate them on a plate and cultivate them for 24 hours, use a sterilized hole puncher with a diameter of 6mm to make a bacterial dish under aseptic conditions, then inoculate them around the PDA solid medium, and use sterilized The pathogenic bacteria were also made into a plate with a hole punch with a diameter of 6mm and inoculated in the middle of the PDA medium plate, and the treatment of only receiving the plate of the pathogenic bacteria was used as a control. Cultivate at a constant temperature of 28°C. When the control plate is covered with the whole plate, observe the results of confrontation culture. When the zone of inhibition no longer changes, record the size of the zone of inhibition and calculate the rate of inhi...
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