A strain of Raoult ornithinolyticum and its application
A technology of ornithine and bacterial agent, applied in Raoule ornithine solubilization and its application field, can solve the problem that the effect of promoting growth and improving soil is not satisfactory, and the phosphate solubilizing bacteria cannot play a good role and solve the problem. The effect of phosphorus inoculants is getting worse and other problems, so as to achieve the effect of promoting phosphorus utilization, good phosphorus solubilization ability, and improving traits.
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Embodiment 1
[0029] Example 1. Isolation and identification of Raoultella ornithinolytica WN-3
[0030] 1. Isolation of strains
[0031] In April 2012, the activated sludge of Wulongkou Sewage Treatment Plant in Zhengzhou City, Henan Province was collected. On the way, the sample was placed in an ice box below 4°C, and after being brought back to the laboratory, 5g of the sample was weighed and placed in a triangle filled with 45mL of sterile water. Shake the bottle at 28°C and 150rpm for 1h. After the sample is evenly dispersed in sterile water, draw 1mL of the suspension into a test tube filled with 9mL of sterile water, mix well, and make the concentrations of 10 -1 -10 -6 g / mL bacterial suspension, draw 100 μL from each concentration of bacterial suspension and spread it on 1 / 4 Montina solid medium plate, and cultivate it in a constant temperature incubator at 28°C for 5-6 days. Different colonies with transparent circles on the edge of the colonies were streaked and purified, and ma...
Embodiment 2
[0039] Embodiment 2, the phosphorus-solubilizing ability of Raoultella ornithinolytica (Raoultella ornithinolytica) WN-3
[0040]1. Inoculate one loop of WN-3 colony preserved on the slant into 5ml LB liquid medium, and cultivate overnight at 28°C on a 150rpm shaker to obtain bacterial solution 1, and then add 5ml of bacterial solution 1 to 100ml LB liquid medium , cultured on a shaker at 150 rpm at 28°C for 24 hours to obtain bacterial solution 2, take 5ml of bacterial solution 2, centrifuge (8000rpm, 10min), wash twice with sterile water, and resuspend with sterile water to obtain bacterial solution 3.
[0041] 2. Put the bacterial solution 3 into 50ml 1 / 4 Montina liquid medium, culture at 28°C, shaker at 150rpm for 3 days, during which 5ml samples were taken at 0, 0.5, 1, 1.5, 2 and 3 days, and centrifuged at 8000rpm After 10 minutes, the supernatant was taken to measure the concentration of soluble phosphorus, and the phosphorus-solubilizing ability of the strain WN-3 chan...
Embodiment 3
[0044] Embodiment 3, the growth-promoting experiment of Raoultella ornithinolytica (Raoultella ornithinolytica) WN-3 to potted wheat
[0045] 1. The activation of the bacterial strain is the same as step 1 of Example 2, until the bacterial liquid 2 is obtained, and it is centrifuged (6000rpm, 10min) to obtain the bacterium of WN-3 with a wet weight of 0.1g, and 3ml of distilled water is added to resuspend the bacterium to prepare Bacteria.
[0046] 2. Set up the following control group and experimental group:
[0047] Experimental group: Water the flowerpot thoroughly first, then pour the inoculum prepared in step 1 into the center of the flowerpot, and evenly sprinkle 1 gram (about 24 grains) of wheat (Jimai No. 38) on the place where the inoculum is poured. Cover with damp soil.
[0048] Control group: no bacterial agent, other steps are the same as the experimental group.
[0049] Cultivate the experimental group and the control group in the greenhouse at 25°C for 20 day...
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