Efficient phosphate-solubilizing bacterium MQR6 as well as fermentation product and application thereof
A technology of fermentation products and phosphate-dissolving bacteria, which is applied in the field of microbiology to achieve the effects of improving the utilization rate of phosphate fertilizer, promoting plant growth, and promoting root growth
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Embodiment 1
[0057] Embodiment 1, the isolation and identification of phosphate-solubilizing bacteria MQR6
[0058] 1. Isolation of phosphate-solubilizing bacteria MQR6
[0059] Phosphorus-solubilizing bacteria MQR6 was isolated from the rhizosphere soil of Maple indica, and the sampling location was the National Long-term Research Base of Warm Temperate Forest in Jiulongshan, Beijing. The geographical coordinates are 115°59′~116°06′ east longitude, 39°54′~39°57 north latitude '. Nine sampling points were set up in the sample field by the S-shaped sampling method, and the 0-20cm soil was drilled with a soil drill, and the soil was mixed into a sterilization bag and brought back to the laboratory. According to the conventional separation method, apply and separate on the inorganic phosphorus solid medium, culture at 30°C for 48 hours, select the strain with a large clear transparent circle, and perform streak separation and purification on the inorganic phosphorus solid medium to obtain pu...
Embodiment 2
[0081] Embodiment 2, the physiological and biochemical characteristics of phosphate-solubilizing bacteria MQR6
[0082] 1.1 Determination of salt tolerance: Inoculate the same concentration of phosphate-solubilizing bacteria MQR6 bacterial solution (1% inoculum size) in YWA liquid medium containing 0%, 1.0%, 2.0%, 4.0%, 6.0%, 8.0%, 10.0% NaCl , v / v), cultured at 30°C for 7 days with shaking, and measured the absorbance at 600nm with a UV-1800 ultraviolet spectrophotometer. Growth salt concentrations ranged from 0-4.0%.
[0083] 1.2 pH range measurement: prepare phosphate buffer solution (solution A: 8.3ml phosphoric acid, add deionized water and mix to 500ml; solution B: Na 2 HPO 4 14.326g, mixed with deionized water and settled to 500ml; take 72.5ml of solution A and 27.5ml of solution B and mix, pH is about 2.0), acetic acid-sodium acetate buffer system (0.2mol / L acetic acid and 0.2mol / L sodium acetate For preparation, the pH value is about 5.0-6.0), potassium dihydrogen ...
Embodiment 3
[0085] Example 3, Qualitative detection and quantitative analysis of auxin secreted by Phospholyticum MQR6
[0086] According to the reference (Glickmann, E. Dessaux, A. critical examination of the specificity of the salkowski reagent for indolic compounds produced by phytopathogenic bacteria. Applied and environmental microbiology 1995, 61 (2), 793-796) described Salkowski colorimetric assay Phospholytic bacterium MQR6 secretes growth hormone IAA performance. Phosphorus solubilis MQR6 was inoculated in TSB liquid medium, shaken at 30°C and 180 rpm for 4 days to obtain fermentation broth of phosphate solubilizer MQR6. Using the uninoculated TSB liquid medium as a blank control, the OD600nm value of the phospholytic bacteria MQR6 fermentation broth was measured, and the results showed that the OD600nm value of the phospholytic bacteria MQR6 fermentation broth was 1.78 (this value is the OD600nm value of the blank control).
[0087] Qualitative detection is performed as follows...
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