Preparation and application of continuous cropping peanut resistant complex bacteria
A compound inoculant and continuous cropping technology of peanuts, applied in the application, biocide, fungicide and other directions, can solve problems such as serious disease occurrence and environmental pollution, and achieve the effects of preventing and controlling plant diseases, simple use and good stability.
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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. The soil sample of the peanut root of the sample is brushed into a ziplock bag, and the soil within 2mm around the root system is collected, total The collected soil weighs about 500g, and it is used for the screening and determination of microorganisms and the isolation and identification of allelochemical substances in cold storage.
[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...
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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