Saline-alkaline tolerance phosphorus solublizing bacteria strain and application thereof
A technology of phosphorus-dissolving bacteria and salt-alkali tolerance, applied in the field of microorganisms, can solve problems such as difficult colonization, restrictions on the application of phosphorus-dissolving fungal preparations, poor colonization and phosphorus-dissolving effects, etc., to achieve strong adaptability, improve fertility, and grow good effect
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Embodiment 1
[0058] Example 1 Acquisition of Phosphorus-Solubilizing Bacteria Strain RPB03
[0059] The acquisition process of phosphate-soluble bacterial strain RPB03 is as follows:
[0060] 1) Enrichment culture: collect the rhizosphere soil in the saline-alkali land of the Yellow River Delta, and carry out enrichment culture in the alkaline PKO medium with a pH value of 8.2 until the Ca in the medium 3 (PO 4 ) 2 all degraded;
[0061] 2) Qualitative screening of phosphate-dissolving strains: Dilute the culture solution obtained in step 1) with 8% normal saline, and dilute it with 10-fold concentration gradient dilution method, and select a dilution concentration of 10 8 -10 12 For coating, draw 100 μl of the above dilution with a 200 μl sterile pipette gun, and spread it on an alkaline PKO agar plate with a pH value of 8.2; Continuous 20 generations on the alkaline PKO medium; 17 primary screened strains that still have phosphorus-dissolving effect were obtained, and the primary st...
Embodiment 2
[0066] The further research of embodiment 2 phosphate-dissolving bacterial strain RPB03
[0067] 1. Effects of pH on phosphorus conversion of phosphate-soluble bacterial strain RPB03
[0068] The preserved strain RPB03 was activated, and cultured in liquid medium for 24 hours as a liquid strain. 1ml (10 8 cfu / ml) seed solution was transferred into PKO medium, and the initial pH values of PKO medium were 6, 7, 8, 9 and 10, respectively, and each treatment was repeated three times. The initial pH was adjusted with hydrochloric acid or NaOH solution. After cultivating on a shaking table for 48 hours, centrifuge at 10,000 rpm / min for 15 minutes, and take the sterile filtrate to measure the available phosphorus content. The results are as follows: figure 2 shown.
[0069] Depend on figure 2 It can be seen that with the increase of the initial pH value of the solution, the phosphorus-dissolving ability of the RPB03 strain continued to decrease, and there was a significant d...
Embodiment 3
[0112] Influence of Indigenous Microorganisms on Phosphorus-Solubilizing Bacteria Strain RPB03
[0113] The RPB03 strain was activated on beef extract-peptone medium (beef extract 3.0g, peptone 10.0g, NaCl 5.0g, agar 15-25g, water 1000ml, pH7.4-8.0), cultured at 28-30°C for 36-48h, Then put it into a 1000mL Erlenmeyer flask, and incubate for 36h at 30°C and 170rpm / min. Inoculate 5% by volume into a 50L seed tank. The culture conditions are 170rpm / min, pH8.0, ventilation 0.6vvm, and cultured for 2 days. After the fermentation is completed, centrifuge, precipitate and dry to obtain bacterial powder. Suspended with tap water to make a concentration of 4.1×10 8 cfu / ml bacterial solution.
[0114] Take two equal amounts of saline-alkali soil in the Yellow River Delta, and set up an experimental group and a control group. The control group was sterilized by dry heat sterilization at a temperature of 170°C for 2 hours, and the soil samples in the experimental group were not treat...
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