Compound bacterium preparation capable of efficiently adsorbing mercury and application of compound bacterium preparation
A technology for composite bacteria and mercury adsorption, which is applied in the application, restoration of contaminated soil, bacteria, etc., can solve the problems of mercury resistance performance to be improved, and the number of mercury resistant bacteria is small, so as to achieve the advantage of adsorption efficiency, strong mercury adsorption capacity, adaptable effect
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[0039] The preparation of composite bacteria preparation of the present invention may further comprise the steps:
[0040] (1) Klebsiella N-type strain and Bacillus tokyo K-type strain were obtained by isolation and purification from mercury-contaminated soil; Bacillus subtilis W-type strain was obtained by isolation and purification from microbial selenium-enriched bacterial agents; the isolation, Purification is carried out with mercury-containing media.
[0041] The above-mentioned separation and purification adopt the plate marking method, and repeated operations are performed. During the repeated operations, the Hg in the mercury-containing medium 2+ Concentrations increased sequentially; for Klebsiella type N strains, Bacillus tokyo K type strains, the initial Hg in the mercury-containing medium 2+ The concentration is 5mg / L, the highest Hg 2+ Concentration of 30-35 mg / L (eg 30 mg / L, 31 mg / L, 32 mg / L, 33 mg / L, 34 mg / L, 35 mg / L); for Bacillus subtilis type W strains, in...
Embodiment 1
[0054] The preparation method of the composite bacteria of the present embodiment may further comprise the steps:
[0055] (1) Isolation and domestication, isolation and purification of N-type bacteria, K-type bacteria and W-type bacteria
[0056] N-type strains and K-type strains were isolated from mercury-contaminated soil, and W-type strains were isolated from microbial selenium-enriched bacterial agents. The specific process is as follows:
[0057] ① Take 10g of soil with low, medium and high mercury pollution levels and place them in 250mL Erlenmeyer flasks, dilute with 100mL ultrapure water to make bacterial suspension, shake at 140r / min for 30min, let stand, and take 1mL supernatant;
[0058] Microbial selenium-enriched bacterial agent directly takes 1mL of bacterial liquid for subsequent processing.
[0059] ② Inoculate the obtained 3 supernatants into Hg-containing 2+ Streak culture was carried out in a solid plate medium with a concentration of 5 mg / L, and after st...
Embodiment 2
[0088] The difference between the preparation method of the composite bacterial preparation of this example and that of Example 1 lies in step (3), and the other steps are the same as those of Example 1, and will not be repeated here. Step (3) is as follows:
[0089] Pick one of the obtained N-type bacteria, K-type bacteria, and W-type bacteria for enrichment culture in TSB medium respectively, and obtain three kinds of enrichment solutions with OD values between 0.5 and 0.6. The solution was mixed at a mass ratio of 0.8:1.0:1.2 to obtain a composite strain, and 5 mL of the composite strain was inoculated in TSB medium for cultivation. The initial pH of the cultivation was 7.08, the cultivation temperature was 30°C, and the cultivation time was 18 hours. During cultivation, the culture medium is shaken at a speed of 140 r / min. When the OD value is between 0.5 and 0.6, the cultivation ends, and the obtained composite bacteria solution is the composite bacteria preparation of ...
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