Chryseobacterium and application thereof in preparation of halophyte epiphytic repair and maintenance microbial inoculum
A technology of Chryseobacterium aureus and halophytes, applied in plant growth regulators, plant growth regulators, methods based on microorganisms, etc., can solve the problems of easy diffusion and loss, difficult to multiply and repair, and achieve less bacterial agent consumption , promote growth, promote the effect of plant growth
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Embodiment 1
[0037] Separation and identification of Gold Bacillus
[0038] Separation of strains
[0039] From the coastal wetland, the base is collected from the river, and the mass ratio of 2% is transferred to a sterilized enrichment medium, and after 1-7 days of oscillating, dilution culture is carried out in LB solid medium, and selecting a single colony Separation is carried out on agar solid medium, and the purified strain YTLJ-E-II12 is obtained.
[0040] The enrichment medium is from 0.05 to 0.2% mass (NH) 4 ) SO 4 0.2-1% sodium succinate, 2-5% K 2 HPO 4 1-3% MGSO 4 , 1-3% NaCl, 0.01-0.05% FESO 4 0.01-0.05% MNSO 4 0.001-0.005% (NH 4 ) 2 MOO 4 , 0.001-0.005% CoCl 2 0.1-1% Bacterial population induction inhibitor (specifically chlorozoranone), 0.1-1% bisphenol A and 0.02-0.1% high carbon alcohol fatty acid ester complex.
[0041] 2, identification of strains
[0042] 2.1, morphological identification
[0043] The above step 1 was separated and purified to the obtained strain for analys...
Embodiment 2
[0052] Separation and identification of Obsuscus YTLJ-N-L43
[0053] Separation of strains
[0054] The collection of seaweed with seaweed is transferred to a sterilized enrichment medium by mass ratio of 1%, and after 1-7 days of shocking, dilution culture is carried out in LB solid medium, and single colonies fall in agar solids. The medium is separated on the medium, and the purified strain YTLJ-N-L43 is obtained.
[0055] The enrichment medium is from 0.05 to 0.2% mass (NH) 4 ) SO 4 0.2-1% sodium succinate, 2-5% K 2 HPO 4 1-3% MGSO 4 , 1-3% NaCl, 0.01-0.05% FESO 4 0.01-0.05% MNSO 4 0.001-0.005% (NH 4 ) 2 MOO 4 , 0.001-0.005% CoCl 2 0.1-1% Bacterial population induction inhibitor (specifically phtolinol), 0.1-1% bisphenol A and 0.02-0.1% high carbon alcohol fatty acid ester complex.
[0056] 2, identification of strains
[0057] 2.1, morphological identification
[0058] The above step 1 was separated and purified to the obtained strain for analysis and compared the bacterial s...
Embodiment 3
[0066] 1) Gold pylori YTLJ-E-II12 to the Philipphi Pollution Wastewater Treatment:
[0067] The goldenum paconium YTLJ-E-II12 obtained by the above-described embodiment is added to 1% inoculation amount to a pneryless pollution wastewater, which has a concentration of the waste reaches 20 μg / L. The introduction of goldenumi YTLJ-E-II12 was decreased by 30 ° C for 30 days, and the Philippine removal rate reached 96%.
[0068] 2) Treatment of high-amamine nitrogen breeding wastewater by Cushifa YTLJ-N-N-L43:
[0069] The altoma YTLJ-N-L43 obtained by the above embodiment was added to aquaculture wastewater by 1% inoculation, and the ammonia nitrogen concentration in wastewater reached 10 mg / L. The introduction of the femoraliostel ytlj-N-L43 treatment of aquaculture wastewater at 25 ° C, and the ammonia-removal rate of 7 days can reach 96%.
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