Sclerotinia sclerotiorum-antagonizing nitrogen-fixing spore bacterium and its application
A technology of sclerotinia and bacillus, applied in the direction of application, bacteria, fungicides, etc., to achieve strong competitive adaptability, high nitrogenase activity, and good inoculation effect
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Embodiment 1
[0041] Embodiment 1, the separation and identification of nitrogen-fixing bacteria GDSD212
[0042] 1. Enrichment and isolation of nitrogen-fixing bacteria GDSD212
[0043] Take 10g of soil sample (farmland soil with relatively poor nitrogen nutrition in Heilongjiang Province, China) and put it into 90ml of sterile water and shake it for 20min to make a cloudy solution. Take 5ml and put it into 30ml of nitrogen-fixing bacteria enrichment culture medium ACCC55, 100rpm, 28℃ Carry out shaking culture on a shaker, and change fresh culture medium after 72h to continue the culture. The nitrogen-fixing spores were isolated after repeating the culture for 3 times. Draw 1ml of the above-mentioned nitrogen-fixing bacteria enrichment culture and put it into 9ml sterile water to make 10 -1 Dilution, continue to dilute to make 10 -2 、10 -3 、10 -4 、10 -5 Bacterial suspensions of dilutions were heated in boiling water at 100°C for 10 minutes, and after cooling, 0.1ml of each dilution w...
Embodiment 2
[0064] Embodiment 2, determination of nitrogenase activity of Bacillus sp. GDSD212 CGMCC No.5035
[0065] The Bacillus sp. (Bacillus sp.) GDSD212 CGMCC No.5035 gained in Example 1 is carried out nitrogenase activity assay, and concrete operation is as follows: in 15 * 150mm screw-top glass tubes, add 5ml improved nitrogen fixation medium to make inclined-plane, inoculate Bacillus sp. GDSD212 CGMCC No.5035, cultivated at 28°C. Azotobacter chroococcum (Azotobacter chroococcum) ACCC11103, which is commonly used in the production of microbial fertilizers, was used as the positive control, and the blank slant without inoculation was used as the negative control, with 3 replicates. After culturing for 72 hours, replace the rubber stopper, inject acetylene gas to make the final concentration 10%, seal it with medical adhesive tape, continue culturing for 72 hours, take 100 μl of reaction gas, measure the amount of ethylene produced by gas chromatography, and calculate the nitrogenase...
Embodiment 3
[0068] Embodiment 3, Bacillus sp. (Bacillus sp.) GDSD212 CGMCC No.5035 antagonizes pathogenic fungus bacteriostatic rate determination
[0069] The Bacillus sp. GDSD212 CGMCC No.5035 obtained in embodiment 1 is carried out to antagonize pathogenic fungus bacteriostatic rate measurement by two-point confrontation method. The crop pathogenic fungi Sclerotinia sclerotiorum and Bacillus sp. GDSD212 CGMCC No.5035 were inoculated respectively, and each screening treatment was repeated three times. The plate inoculated with only pathogenic fungi but not nitrogen-fixing bacteria was used as a control. Incubate at a constant temperature at 28°C, measure the colony radius r of the pathogenic fungi on the confrontation plate along the direction of the tested Bacillus sp. GDSD212 CGMCC No.5035 with a millimeter scale after 15 days 1 , and the colony radius r of pathogenic fungi on the control plate 0 . Growth inhibition rate of pathogenic fungi (%)=(control radius r 0 - confrontation c...
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