Actinomycete strain SCAUT009 and application thereof
A technology of actinomycetes and strains, applied in the field of microorganisms, to achieve the effect of promoting growth and good application potential
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Embodiment 1
[0028] The separation and purification of embodiment 1 rhizosphere actinomycete SCAUT009
[0029] 1.1 Isolation of actinomycetes from the rhizosphere of Vitex glabrata in Liangshan
[0030] In 2018, the purple vetch was collected in Huidong County, Liangshan Yi Autonomous Prefecture, Sichuan Province. The excess soil on the root system was shaken off, and the root was placed in a 50mL sterilized centrifuge tube filled with 25mL phosphate buffer solution, and treated with ultrasonic waves (150W) After 10 minutes, the roots were taken out under sterile conditions, and the supernatant was removed by centrifugation at 3000g for 10 minutes. The sediment was rhizosphere soil, and made 10 -1 、10 -2 , 10 -3 For gradient dilution, 100 ul of the suspension was uniformly spread on the modified Gowell's medium for separation, and each dilution concentration was repeated three times, and cultured in a constant temperature incubator at 28°C for 5-7 days. Pick the strains with typical act...
Embodiment 2
[0047] The growth-promoting function screening of embodiment 2 rhizosphere actinomycete SCAUT009
[0048] 2.1 Screening of growth-promoting function
[0049] 2.1.1 Determination of IAA Production Ability
[0050] Take 20 μL of bacterial suspension and insert it into ISP containing 0.5mol / L tryptophan 4 In liquid culture medium, repeated 3 times, set blank control, cultured on a shaker at 28°C at 120r / min for 3d, centrifuged at 8000r / min for 24h, took 1mL of bacterial supernatant, added 2mL of IAA chromogenic solution, reacted in dark at 25°C for 30min, 530nm Colorimetric at the wavelength and record the absorbance value. With the uninoculated liquid culture medium as the control zero adjustment, the indole acetic acid standard solution with the concentration of 0, 5, 20, 40, 60mg / l is the same as above to make the calibration, and calculate the concentration of IAA in the measurement solution.
[0051] 2.1.2 Determination of siderophore production capacity
[0052] Dissolv...
Embodiment 3
[0083] Embodiment 3 hydroponic experiment of purple sweet potato
[0084] 3.1 Hydroponics experiment
[0085] The actinomycete strains to be tested were first connected to the ISP 4 Slope activation, then transfer to ISP 4 The culture solution was cultivated overnight to the logarithmic phase, and the growth of the bacterial strain was detected by the plate method, and the bacterial content was calculated.
[0086] After soaking the seeds of Viola glabrata overnight, carry out surface disinfection, use sterile tweezers to grasp the seeds and implant them into a petri dish equipped with filter paper and sterile vermiculite, plant 10 seeds in each petri dish, and then add sterile water to keep moisture , and maintain air circulation. Sterilize the tweezers, filter paper, petri dishes, plastic cups, vermiculite, quartz sand, and low-nitrogen nutrient solution required for the experiment.
[0087] Low nitrogen nutrient solution formula: KNO 3 10.1g, KH 2 PO 4 2.2g, MnSO ...
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