A kind of Burkholderia pyrrole and its application in promoting the growth of A.
A technology of Burkholderia pyrrole and Holderia, which is applied in the fields of application, plant growth regulator, plant growth regulator, etc., can solve the problems such as no growth-promoting bacteria of A. Effects of strain resources, promotion of growth and development, and strong auxin secretion
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Embodiment 1
[0026] Example 1: Determination of the ability of LWK2 liquid to dissolve potassium.
[0027] Potassium-solubilizing ability assay medium: sucrose 5g, MgSO 4 ·7H 2 O 0.5g, Na 2 HPO 4 2g, potassium aluminosilicate 2g, FeCl 3 0.005g, pH7.0~7.5, tap water 1000mL, sterilize at 115℃ for 30min.
[0028] Inoculate a single colony of LWK2 after activation in LB (tryptone 10g, yeast extract 5g, sodium chloride 10g, deionized water 1000mL, pH 7.0, sterilize at 121°C for 20min) liquid medium, shake culture at 30°C for 18 ~24h, fully shake to form a uniform bacterial suspension, as the seed liquid. Take 0.5mL and inoculate it into a 300mL Erlenmeyer flask containing 50mL of potassium-dissolving capacity test medium, and inoculate an equal amount of LB liquid medium with the potassium-dissolving capacity test medium as a blank control. Incubate at 28°C with shaking at 200r / min for 5 days. The fermented liquid obtained is placed in a water bath and concentrated to about 10 mL, and 6...
Embodiment 2
[0030] Example 2: Determination of the ability of LWK2 to produce auxin.
[0031] King's B medium: peptone 20g, MgSO 4 ·7H 2 O 1.5g, K 2 HPO 4 1.5g, glycerol 10mL, agar 15g, after adjusting the pH value to 7.0, add to 1000mL.
[0032] S1 colorimetric solution: weigh 12g FeCl 3 Dissolve in 300mL deionized water, slowly add 429.7mL concentrated sulfuric acid, and dilute to 1L after cooling.
[0033] Prepare IAA standard solutions with concentrations of 1, 4, 6, 8, 10, 12, 14, 16, 18, and 20 mg / L, and mix them with S1 reagent at a volume ratio of 1:1, and place them in the dark at room temperature for 30 minutes, then The OD530 values of each concentration were measured respectively (the 1:1 mixture of distilled water and S1 reagent was used as the blank control) value. Taking the IAA concentration as the abscissa and OD530 as the ordinate, the standard curve of IAA is obtained.
[0034] Inoculate a single colony of LWK2 in NB liquid medium and culture for 12h (28°C, 12...
Embodiment 3
[0036] Example 3: Determination of the ability of LWK2 to promote growth of cucumber seeds.
[0037] Cucumber seeds were treated with 10% hydrogen peroxide for 20 minutes, rinsed with sterile water 5-6 times, and dried for later use.
[0038] Inoculate a single colony of the LWK2 strain in NB liquid medium, and culture it on a shaker at 28°C for 24-36 hours, so that the bacterial concentration reaches 10 9 cfu / mL. The bacterial suspension was serially diluted to 10 -7 , divide the bottom of the sterile petri dish into 8 equal areas with a marker pen, mark CK, -1, -2, -3, -4, -5, -6, -7 in turn, place 4 in each area ~6 pieces of sterile filter paper, put sterile absorbent cotton in the middle, put the processed cucumber seeds on the filter paper, drop 100 μl of LWK2 bacterial suspension corresponding to the dilution in the center of the filter paper in each area of the bottom of the dish, and CK area An equal amount of sterile water was added dropwise as a control. 28 ℃, ...
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