A salt-tolerant and growth-promoting bacterium jp-jh that alleviates plant salt damage and its application
A JP-JH, growth-promoting bacteria technology, applied in the field of microorganisms, to achieve the effect of promoting plant growth, solving the cost increase, and alleviating the ability of plant salt damage
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Embodiment 1
[0025] Example 1: Isolation and purification of salt-tolerant growth-promoting bacteria JP-JH
[0026] Sample source: Rhizospheric soil of Suaeda salsa in saline-alkali land in Haixing County, Cangzhou City, Hebei Province, China.
[0027] LB medium (solid): tryptone 10g / L, yeast extract 5g / L, sodium chloride 50g / L, agar 20g / L, use 5M / L NaOH to adjust the pH value, sterilize by high pressure steam at 121℃ for 30min .
[0028] LB medium (liquid): Tryptone 10g / L, yeast extract 5g / L, sodium chloride 50g / L, after adjusting the pH value with 5M / L NaOH, sterilize under high pressure steam at 121°C for 30min.
[0029] Separation and purification steps: 1) collect the root system of Suaeda salsa in Haixing County, Cangzhou City, Hebei Province, China, shake off the surface soil of the root system, put it into a sterile 50mL centrifuge tube, add sterile water and vortex to obtain the rhizosphere soil stock solution ; 2) leave it still, take an appropriate amount of supernatant, and u...
Embodiment 2
[0030] Example 2: Identification of salt-tolerant growth-promoting bacteria JP-JH
[0031] 1) Identification of biological characteristics
[0032] The colony of the salt-tolerant growth-promoting bacteria JP-JH on the LB medium was orange-yellow protruding, and the edge of the colony was slightly transparent ( figure 1 ).
[0033] 2) System classification identification
[0034] The present invention adopts the kit TIANamp Bacteria DNA Kit (Tiangen, Beijing) and extracts the salt-tolerant growth-promoting bacteria JP-JH genome DNA according to its operation steps. The 16S rDNA sequence of strain JP-JH was amplified by primers 27F (5'-AGAGTTTGATCCTGGCTCAG-3') and 1492R (5'-TACGGCTACCTTGTTACGACTT-3'). The PCR reaction system was 50 μL, which contained 10 μL EasyTaq buffer, 5 μL dNTPs, 0.5 μL primer 27F, 0.5 μL primer 1492R, 1.5 μL DNA template, 2 μL Easy Taq DNA polymerase, and finally added sterile ultrapure water to 50 μL. The PCR reaction program was: (i) pre-denaturatio...
Embodiment 3
[0036] Example 3: Evaluation of Salt-tolerant and Alkali-resistant Ability of Salt-tolerant Growth-Promoting Bacteria JP-JH
[0037]Pick a single colony of the strain JP-JH on the solid LB medium, inoculate it in 50mL liquid LB medium, cultivate it at 28°C and 150r / min for 48h, and then inoculate it in NaCl solution containing 1%, 5%, 10%, 15% and 20%, and the LB solid medium combined with the pH value of 7.0, 8.0 and 9.0 for streak culture. Grow in the medium of ~9.0.
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