A Salt-resistant Potassium Promoting Microbacterium Oxygenans 41c8, Bacterial Agent and Its Application
A technology of oxidative microbacteria and growth-promoting bacteria, applied in the field of microorganisms, can solve the problems of lack of salt-tolerant growth-promoting microorganisms, lack of high-salt-tolerant growth-promoting microorganisms, etc. The effect of the application foreground
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Embodiment 1
[0048] Example 1 Separation screening of strain 41c8
[0049] Different microorganisms were separated from the soil in Dongying City, and the strains were separated from the solid Lb medium plate from which the strain was isolated from the solid Lb culture plate. The colonies were placed in a liquid LB medium with a concentration of 0.1%, 0.3%, 0.5% and 0.7% different NaCl concentrations for shake flask culture, from 27 ° C to 29 ° C 120R / min culture 2 ~ 3D, the production of strains under different salt concentrations was observed, and the rated plastered strains of the screening were repeatedly paired, and the salt-tolerant strain of five single colonies was obtained, and the single colonies were named strain 41c8.
Embodiment 2
[0050] Example 2 functional qualitative identification of strains 41c8
[0051] The strain 41c8 is cultured, activated and expanded, and formulated with pitcassing, phosphorus and nitrogen solid medium, and prepared a flat plate of the bacteria. After culturing the bacteria, the plate is replaced, Thereafter, 1 μl of the bacteria is supreme onto the plate, and the sealing plate is placed in inverted culture, and the experimental results are observed when the transparent water is unpowered or plaque. Such as figure 2 As shown, the strain 41c8 of the present embodiment can be soluble organophos, difficult soluble potassium and nitrogen. Organic phosphorus medium, inorganic phosphorus medium, pita-potassium medium and nitrogen nitrogen medium are as follows.
[0052] Organophosphorus medium: glucose 10g, NaCl 0.3g, MgSO 4 0.3 g, MNSO 4 0.03 g, Caco 3 5 g, lecithin 2g, agar 18g, (NH 4 ) 2 SO 4 0.5 g, KCl 0.3g, FESO 4 0.03 g, yeast paste 0.4 g, 1000 ml of distilled water, pH 7.0-7.5, 1...
Embodiment 3
[0058] Example 3 Fungi, bacteria and supernatant of bacterial liquid, bacteria and supernatant
[0059] Potassium analysis of 1 strain 41C8
[0060] Different processing Colony diameter (d) / cm Water solution diameter (d) / cm Cosmetic index (D / D) Bacterial liquid 0.9 1.5 1.67 Bacterial 0.8 1 1.25 Supernatant 0.7 0.9 1.29 Sterilizing fluid - - -
[0061] Prepare the potassium solid medium plate, further xylosomic analysis of strain 41C8, the strain 41C8 was cultured, and the bacterial liquid was taken to the centrifuge tube, 5000 r / min for 2 minutes, and the supernatant The liquid is taken into the new centrifuge tube, and the remaining bacteria is added to the sterile water. Then 1 μl of bacterial liquid, supernatant, sterilized bacterial liquid and bacterial suspension to prepared xa-potassium solid medium, placed in a 25 ° C incubator culture, to a plate long out of water, and a plaque statistical experiment .
[0062] Calculatio...
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