Preparation and application of an anti-peanut continuous cropping compound bacterial agent
A compound bacterial agent and peanut continuous cropping technology, applied in the direction of application, biocide, fungicide, etc., can solve the problems of serious disease occurrence, environmental pollution, etc., achieve the effects of preventing and controlling plant diseases, easy to use, and improving soil fertility
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Embodiment 1
[0030] (1) Source of bacteria
[0031] The soil was collected in a peanut field in Shandong Province where peanuts have been continuously planted for many years. The soils were soils of 1 year, 2 years, 4 years, and 7 years. No. 16. Brush the soil sample from the peanut root into a ziplock bag with a brush, and collect the soil within 2mm around the root system. The total soil weight is about 500g, and it will be stored in cold storage for the screening of microorganisms and the isolation and identification of allelochemicals.
[0032] (2) Strain screening
[0033] Nutrient agar medium (NA medium): peptone 5.0g; beef extract 3.0g; glucose 2.5g; yeast powder 1.0g; agar powder 16.0-18.0g; distilled water 1000ml; pH7.0-7.2. Prepare NA liquid medium separately. Martin's agar medium: glucose 10g, peptone 5g, KH 2 PO 4 1g, MgSO 4 ·7H 2 O0.5g, 1 / 3000 Bengal Red 100mL, agar 15-20g, pH natural, distilled water 800mL, add 0.03% streptomycin diluent 100mL before use, so that each...
Embodiment 2
[0046] (1) Source of bacteria
[0047] The strain source is with embodiment 1.
[0048] (2) Strain screening
[0049] Culture medium is the same as embodiment 1.
[0050] Screening steps: Take 10 g of fresh soil samples and add them to 100 ml of CM medium containing 2% oleic acid, 1‰ phthalic acid, and 2% hexadecanoic acid respectively, and culture on a shaker at 30°C for 72 hours at 170r / min. Subculture three times, inoculate 100 μl culture solution on NA plate, incubate at 30°C for 24 hours, then randomly pick a single colony according to the different morphology of the colony, purify it for 3 generations, and store it until its degradation efficiency is determined.
[0051] After inoculation in CM medium supplemented with 1 g / L allelochemicals, cultured on a shaker at 170 r / min at 30°C for 7 days, the treatment without inoculation was used as the control, and each treatment was repeated 3 times. Extract 3 times with 1:1 mixed extract of ethanol and ether, combine the ext...
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