Microbial agent for preventing and controlling brown spot of tobaccos and preparation method of microbial agent
A microbial inoculum and a technology for tobacco brown spot disease, applied in the field of biological pesticides, can solve the problems of weak inhibitory effect on the pathogen of tobacco wildfire disease, and achieve the effects of efficient synergistic disease control, large processing capacity, and avoidance of resource waste.
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Embodiment 1
[0041] A kind of microbial inoculant for preventing and treating tobacco red spot, the microbial inoculant is formulated according to the following volume ratio:
[0042] Achromobacter xylosoxidans 25%;
[0043] Enterobacter sp. 5%;
[0044] Ochrobactrum sp. 15%;
[0045] Stenotrophomonas sp. 40%;
[0046] Bacillus subtilis 15%.
Embodiment 2
[0048] A kind of microbial inoculant for preventing and treating tobacco red spot, the microbial inoculant is formulated according to the following volume ratio:
[0049] Achromobacter xylosoxidans 20%;
[0050] Enterobacter sp. 10%;
[0051] Ochrobactrum sp. 10%;
[0052]Stenotrophomonas sp. 50%;
[0053] Bacillus subtilis 10%.
[0054] A kind of microbial inoculant for preventing and treating tobacco red spot, the microbial inoculant is formulated according to the following volume ratio:
[0055] Achromobacter xylosoxidans 15%;
[0056] Enterobacter sp. 15%;
[0057] Ochrobactrum sp. 5%;
[0058] Stenotrophomonas sp. 60%;
[0059] Bacillus subtilis 5%.
Embodiment 4
[0061] A preparation method of a microbial inoculant for preventing and treating tobacco red spot disease, comprising the steps of:
[0062] S1-Strain preparation: prepare Achromobacter xylosoxidans, Enterobacter sp., Ochrobactrum sp., Stenotrophomonassp., Bacillus subtilis ) each;
[0063] S2-Strain activation: Achromobacter xylosoxidans, Enterobacter sp., Ochrobactrum sp., Stenotrophomonassp., Bacillus subtilis ) are respectively activated into the original species through a solid slope;
[0064] S3-expansion culture: Inoculate the activated strains into liquid medium and cultivate them until the initial bacterial concentration is 1×10 6 Individual / mL, then transfer to aerated culture in new liquid medium, transfer inoculum size is 15% (v / v), the temperature of described aerated culture is 28 ℃, and the aeration rate is 0.20m 3 / min, expand the culture for 24h, when the number of microorganisms is 3×10 9 pcs / ml, use storage tanks to collect the bacterial liquid of each s...
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