High salt-resistant phosphate solubilizing bacterial strain and application thereof
A technology of phosphate-solubilizing bacteria and salt tolerance, applied in the direction of bacteria, microbial treatment, organic fertilizers, etc., can solve the problems of poor phosphorus-dissolving performance of phosphate-solving bacteria fertilizer, low activity of phosphate-solving bacteria, and unsuitability for saline-alkali land, etc., to increase the content of available phosphorus , relieve soil compaction, improve the physical and chemical properties of the effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0033] Example 1 Isolation, purification and preservation of highly salt-tolerant phosphate-solubilizing bacteria QDZN-13
[0034] The highly salt-tolerant phosphate-solubilizing bacteria QDZN-13 is isolated through domestication, cultivation, screening and purification, and the specific steps are as follows:
[0035] Acclimatization culture: Add 5g of saline-alkali soil samples from the estuary of the Yellow River in Dongying to 100mg / L inorganic phosphorus-sodium salt medium, shake and cultivate on a shaking table at 28°C and 150r / min for 7 days; then use 5% inoculation amount, In the new inorganic phosphorus-sodium salt medium, the concentration of sodium (Na) was increased in a gradient of 300 mg / L, and transferred 4 times until the sodium ion concentration reached 1200 mg / L.
[0036] Inorganic phosphorus-sodium salt medium is: per liter of inorganic phosphorus-sodium salt medium: glucose 10.0g, (NH4)2SO4 0.5g, NaCl 0.3g, KCl 0.3g, FeSO4 7H2O 0.03g, MgSO4 7H2O 0.3g, MnSO4...
Embodiment 2
[0041] Example 2 Identification of highly salt-tolerant phosphate-solubilizing bacteria QDZN-13.
[0042] Through 16SrDNA sequence analysis and physiological and biochemical experiment identification, it was determined that the strain QDZN-13 belonged to the genus Bacillus subtilis. Specific steps are as follows:
[0043]The DNA of the strain was extracted and purified using a DNA extraction kit (TransGen Biotech Co., Ltd., Beijing), and stored at 4°C. The bacterial 16SrDNA universal primers were synthesized by Huada Gene Company. The primers are as follows:
[0044] The upstream primer is 5'-AGAGTTTGATCMTGGCTCAG-3'
[0045] The downstream primer is 5'-TACGGCTACCTTGTTACGACTT-3'
[0046] Amplification reaction system: 2 μL of 10XBuffer (Mg2+), 2 μL of dNTPs, 1 μL of each primer, 1 μL of bacterial DNA, 0.5 μL of Taq DNA polymerase, and add deionized water to 20 μL.
[0047] The PCR reaction program was set as follows: pre-denaturation at 94°C for 4 min; then denaturation at ...
Embodiment 3
[0050] Example 3 Identification of highly salt-tolerant phosphate-solubilizing bacteria QDZN-13
[0051] Inoculate highly phosphate-tolerant bacterium QDZN-13 on inorganic phosphorus solid medium, culture at 28°C, and observe the characteristics of single colonies after 5 days. The characteristics of the colonies are as follows: the colonies are light milky white, transparent, with neat edges, smooth and moist, and relatively flat.
[0052] Wire-drawing experiment: Take a drop of 4% KOH solvent and drop it on a clean glass slide, and use a sterile toothpick to remove the bacteria to be tested, that is, highly salt-tolerant phosphobacteria QDZN-13. Bacteria toothpick was lifted up, no floc was observed, it can be seen that the highly salt-tolerant phosphate-solubilizing bacteria QDZN-13 is a Gram-positive bacterium.
[0053] Physiological and biochemical measurements were carried out. Through sugar fermentation experiments, it was found that the highly salt-tolerant phosphorus-...
PUM
Property | Measurement | Unit |
---|---|---|
Particle size | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com