A kind of pseudobacillus pallidum strain x21 and its application
A pseudobacillus, X21 technology, applied to Pseudomonas pallidum strain X21 and its application field, can solve the problems of limiting the application range of indole acetic acid and cumbersome application
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Embodiment 1
[0050] 1. Configuration of culture medium
[0051] Prepare the following media:
[0052] (1) PKO liquid medium (inorganic phosphorus bacteria medium)
[0053] Sodium chloride 0.3g, glucose 10g, potassium chloride 0.3g, tricalcium phosphate 5g, ammonium sulfate 0.5g, magnesium sulfate heptahydrate 0.3g, manganese sulfate 0.03g, ferrous sulfate heptahydrate 0.03g, distilled water 1000mL, adjust pH When the value reaches 7.0-7.2, sterilize at 115°C for 30min. Add 15g of agar powder to the culture medium to get PKO solid medium.
[0054] (2) LB liquid medium
[0055] Tryptone 10g, yeast powder 5g, sodium chloride 10g, water 1000mL, adjust pH to 7.0, sterilize at 121°C for 20min. Add 15g of agar powder to the culture medium to get LB solid medium.
[0056] Next, the plant growth-promoting bacteria that can secrete indole acetic acid are screened out through qualitative determination and quantitative determination.
[0057] Table 1 Basic properties of the tested soil
[0058]...
Embodiment 2
[0066] Aerobic test
[0067] Pour the sterilized LB culture medium into 3 sterilized test tubes, at about 2 / 3, on the aseptic operating table, use an inoculation needle to pick up the strain X21 cultured on the slant, and puncture and inoculate it into the above culture medium (must pierce to the bottom of the tube). Cultivate at 30°C, and observe the results in 3 days to 7 days respectively. Those that grow on the surface of the agar column are aerobic bacteria, and those that grow along the puncture line are anaerobic or facultative anaerobic bacteria.
[0068] The test results showed that bacterial strain X21 colonies grew along the surface of the agar column, and colonies also grew in the puncture line, which was facultative anaerobic (see Table 2).
Embodiment 3
[0070] Determination of catalase
[0071] Put 1 drop of 3% HO on a clean slide 2 o 2 , take 1 ring of slant culture of strain X21 LB cultivated for 18~24h, and put it in H 2 o 2 Smear in the middle, if bubbles are produced, it is positive, otherwise it is negative.
[0072] The test results showed that the strain X21 was positive for catalase (see Table 2).
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