A strain of Streptomyces albidoflavus Z9, and applications of Streptomyces albidoflavus Z9 in prevention and control of sunflower sclerotium blight
A technology of Streptomyces albicans and sunflower, applied in the field of microorganisms, can solve the problems of limited sclerotia effect, tall sunflower plants, and difficulties in field application
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Embodiment 1
[0024] Screening and identification of embodiment one sclerotinia
[0025] The sclerotinia strain of the present invention is isolated from diseased sunflower stalks in Inner Mongolia field. The diseased sunflower stalks picked back from Inner Mongolia were cut open with a knife, and the sclerotia sclerotia were taken out, disinfected with 75% ethanol, rinsed with sterile water for 2-3 times, and placed in potato dextrose agar medium on Cultivate at a constant temperature of 25°C for 3-5 days until the mycelium grows, and then pick the mycelium to a new potato dextrose agar medium for growth (see figure 1 ), the purified Sclerotinia sclerotiorum (Lib.) de Bary was determined to be Sclerotinia sclerotiorum (Lib.) de Bary by sequencing the sequence of the ITS region.
Embodiment 2
[0026] Primary screening and identification of embodiment two bacterial strain Z9
[0027] The method that the present invention screens and prevents the sunflower sclerotinia bacterial strain is as follows:
[0028] 1. Collection of soil samples
[0029] Five soil samples were randomly collected from Qilian County, Qinghai. Remove the surface soil, collect about 300g of soil samples at a depth of 5-20cm, and bring them back to the laboratory after subpackaging and marking.
[0030] 2. Purification and cultivation of isolated strains
[0031] Isolate bacterial strains by dilution coating plate method, weigh 1g soil sample, mix in 9mL sterile water as 10 -1 Diluent, for gradient dilution; use 10 -2 、10 -3 and 10 -4 The sample dilution was coated on each separation medium plate, and each dilution was coated on 2 plates, and the amount of coating on each plate was 0.2 mL. The surface of the agar plate must be dry so that the inoculum can be absorbed immediately; separate t...
Embodiment 3
[0055] Rescreening and Preliminary Application of Example Three Bacterial Strain Z9
[0056] 1. Sunflower seed husk experiment
[0057] The strain Z9 was inoculated in the seed medium (soluble starch 2g, casein hydrolyzate 0.3g, glucose 0.5g, Bacto-yeast extract 0.2g, Bacto-malt extract 0.5g, Calcium carbonate 0.3g, sterile water 100ml, pH 7.2), placed in a full-temperature shaking incubator at 170rpm / min, 28°C constant temperature activation and constant temperature cultivation for 24h. According to the inoculum size of 5% (that is, the seed medium of 10ml is added in the corresponding medium of 190ml), the bacterial strain Z9 in the seed medium is inoculated to No. agar), and then placed in a full-temperature shaking incubator for cultivation, maintaining a rotation speed of 170 rpm / min, controlling the temperature at 28° C., and culturing for 3-5 days.
[0058] Treatment of strain Z9 fermentation liquid: Take out the strain Z9 fermentation liquid in a constant temperature...
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