Bacillus subtilis and application thereof for degrading decabromodiphenyl oxide
A technology of Bacillus subtilis and decabromodiphenyl ether, applied in the direction of bacteria, microorganism-based methods, microorganisms, etc., can solve the problems that Bacillus subtilis degrades decabromodiphenyl ether, etc., and achieve high-efficiency secondary pollution, Low cost, no secondary pollution
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Embodiment 1
[0041] Bacillus subtilis DB-2 debromination degradation test of decabromodiphenyl ether with a concentration of 10mg / L:
[0042] Degradation basal medium formula: Each liter of medium contains 1g of peptone, 0.5g of yeast extract, KH 2 PO 4 2.93g, Na 2 HPO 4 8.87g, NH 4 Cl1.0g, NaCl0.5g, MgSO 4 5g, CaCl 2 2H 2 O0.15g, the balance is water.
[0043] 1. Prepare a degradation experiment medium containing 10 mg / L of decabromodiphenyl ether:
[0044] Add 1ml of 300mg / L decabromodiphenyl ether stock solution dissolved in dichloromethane to a 100ml conical flask, avoid light until the dichloromethane volatilizes, then add 30ml of degradation basal medium to the conical flask, shake well to obtain 30ml of degradative Experiment medium.
[0045] That is, the formula of the degradation experiment medium: each liter of medium contains 10 mg of decabromodiphenyl ether, 1 g of peptone, 0.5 g of yeast extract, and KH 2 PO 4 2.93g, Na 2 HPO 4 8.87g, NH 4 Cl1.0g, NaCl0.5g, MgSO ...
Embodiment 2
[0055] Bacillus subtilis DB-2 debromination degradation test of decabromodiphenyl ether with a concentration of 10mg / L:
[0056] 1. Prepare a degradation experiment medium containing 10 mg / L of decabromodiphenyl ether:
[0057] The degradation test medium in this embodiment is the same as the degradation test medium in Example 1.
[0058] 2. Culture the Bacillus subtilis DB-2 pure bacteria of the present invention on LB plate, then pick a single colony from the solid LB plate and inoculate it into 30ml of degradation experiment medium, cultivate it at 30°C, 150 rpm, in the dark, and cultivate for 60h Finally, take the culture solution, utilize ion chromatography to analyze the bromide ion concentration in the culture solution, and do three parallel samples in the experiment.
[0059] 3. Determination of the degradation rate of Bacillus subtilis DB-2:
[0060] Take 2mL of the above-mentioned culture solution from three parallel samples, filter it with a 0.22μm sterile filter ...
Embodiment 3
[0062] Bacillus subtilis DB-2 debromination degradation test of decabromodiphenyl ether with a concentration of 10mg / L:
[0063] 1. Prepare a degradation experiment medium containing 10 mg / L of decabromodiphenyl ether:
[0064] The degradation test medium in this embodiment is the same as the degradation test medium in Example 1.
[0065] 2. Routinely culture the Bacillus subtilis DB-2 pure bacteria of the present invention on an LB plate, then pick a single bacterium from the solid LB plate and inoculate it into a 30ml degradation experiment medium, and cultivate it in the dark at 30°C and 150 rpm for 72 hours , take the culture solution, use ion chromatography to analyze the bromide ion concentration in the culture solution, and do three parallel samples in the experiment.
[0066] 3. Determination of the degradation rate of Bacillus subtilis DB-2:
[0067] Take 2mL of the above-mentioned culture solution from three parallel samples, filter it with a 0.22μm sterile filter ...
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