A kind of method utilizing heterotrophic microorganism to remove hydrogen sulfide
A microorganism and sulfide technology, applied in the directions of using microorganisms, microorganism-based methods, biochemical equipment and methods, etc., can solve problems such as unfavorable hydrogen sulfide absorption and oxidation, slow growth, and difficulty in forming large biomass, etc. To achieve the effect of convenient cultivation, rapid growth and efficient removal
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[0035] Preparation of polysulfides: 13 mg of sulfur powder and 70 mg of sodium sulfide were added to distilled water pre-deoxygenated with argon, sealed, and the pH value was adjusted to 9.3 with hydrochloric acid.
[0036] Preparation of acetone sulfur: Add excess sulfur powder into acetone, shake to dissolve fully, and the saturated solution contains about 20mM sulfur.
[0037] The detection method of sulfur disulfide is: add 0.55ml 1% boric acid to 1.5ml EP tube, heat in boiling water for 1min, add 0.25ml sample, add 0.2ml 0.1M potassium cyanide and heat for 1min, cool at room temperature, add 0.1ml Ferric nitrate reagent, mix immediately, if there are cells, remove by centrifugation, measure OD 460nm , and the blank control was deionized water.
[0038] Sulfite, sulfate and thiosulfate were detected by ion chromatography (ICS-1100system; Dionex), and the specific conditions were: mobile phase flow rate: 1ml / min, column temperature: 30°C, suppressor type: ASRS_4mm, suppres...
Embodiment 1
[0039] Example 1: Research on the hydrogen sulfide oxidation rate of five heterotrophic bacteria.
[0040] Five strains of heterotrophic bacteria (Gluconobacter oxydans 621H, Pseudomonas putida S16, Pseudomonas aeruginosa PAO1, Ralstonia (Cupriavidus necator) JMP134 , or Burkholderia cepacia (Burkholderia cepacia) ATCC25416) at 30 degrees Celsius and 200rpm shaking culture for more than 20 hours, the bacterial turbidity is greater than OD 600nm When =4, the cells were collected by centrifugation and washed once with pure water, and then the treated heterotrophic cells were dissolved in 4-(2- Hydroxyethyl)-1-piperazineethanesulfonic acid (HEPES:4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid) buffer, and adjust the bacterial turbidity to OD 600 =2. In application, the cultured bacteria solution can also be used to deal with sulfide directly or after dilution.
[0041] Add 10 mL of the adjusted heterotrophic bacterial cell suspension into a 50 mL centrifuge tube, and then ...
Embodiment 2
[0045] Example 2: Research on the induction effect of hydrogen sulfide.
[0046] Ralstonia (Cupriavidus pinatubonensis) JMP134, Pseudomonas aeruginosa (Pseudomonas aeruginosa) PAO1, Burkholderia cepacia (Burkholderia cepacia) ATCC 2541, or Pseudomonas putida (Pseudomonas putida) S16 bacteria When the method in Example 1 was cultivated to the early logarithmic growth period (OD 600 =0.5), the final concentration of 20μM Na was additionally added in the medium 2 S, polysulfide or acetone sulfide, continue to cultivate and induce for 1 hour, then collect the thalline according to the method in Example 1, measure the oxidation rate of hydrogen sulfide, and compare with the control group without induction, the results show that hydrogen sulfide, polysulfide And acetone sulfur can induce bacteria to enhance their ability to oxidize hydrogen sulfide, see image 3 .
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