Corynebacterium sp strain and application thereof
A technology of Corynebacterium and bacterial strains, applied in Corynebacterium strains and its application fields, can solve the problem of difficult wastewater discharge up to standard, and achieve the effects of protecting human health, low production and use costs, and wide degradation spectrum
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Embodiment 1
[0025] Embodiment 1, the acquisition and identification of bacterial strain SG-20
[0026] 1. Obtaining of strain SG-20
[0027] In August 2008, 2 g of activated sludge from coking wastewater was taken from Shaoguan, Guangdong, and added to phenol-containing basal salt medium for 7 days of cultivation. After dilution, it was spread on a phenol-containing basal salt medium plate. After 7 days of cultivation, a single Colonies were preserved after streaking and purification.
[0028] 2. Identification of strain SG-20
[0029] Morphological characteristics: The bacteria are rod-shaped.
[0030] Physiological and biochemical characteristics: the main biological characteristics are G + , Gram-positive bacteria; catalase reaction and glucose fermentation acid production are positive; nitrate reduction, gelatin hydrolysis, nitrite reduction reaction, methyl red reaction, oxidase, V.P. reaction, indole reaction are negative; use Citric acid and propionate, which cannot utilize tar...
Embodiment 2
[0034] Embodiment 2, the degradation rate of bacterial strain SG-20 to different compounds in basic salt liquid medium
[0035] Embodiment 2, bacterial strain are to the degradation rate of different compounds in basal salt liquid medium
[0036] Basal salt liquid medium: mix 1.0g NaCl, 1.0g NH 4 NO 3 , 1.5g K 2 HPO 4 , 0.5g KH 2 PO 4 and 0.2g MgSO 4 ·7H 2 O was made up to 1L with water.
[0037] Pick a single colony of SG-20 and put it in 3ml LB liquid medium, shake it at 30°C and 165 rpm for 24 hours to obtain fresh bacterial liquid. Into 100ml of solution A (or solution B or solution C), insert 5ml of fresh bacterial solution, culture on a shaker at 30°C (165 rpm), and take a sample after 3 days (72 hours) to determine the degradation rate of the compound. The results are shown in Table 1.
[0038] The preparation method of solution A: add phenol and chromium (VI) into the basal salt liquid medium, the final concentration of phenol is 100 mg / L, and the final conce...
Embodiment 3
[0044] Embodiment 3, the degradation rate of bacterial strain SG-20 to phenol and the removal rate to chromium (VI) in tannery wastewater
[0045] Pick a single colony of SG-20 and put it in 3ml LB liquid medium, shake it at 30°C and 165 rpm for 24 hours to obtain fresh bacterial liquid. Measure 100ml of tannery wastewater, and detect the concentration (initial concentration) of chromium (VI) therein. The initial concentration of chromium is about 2mg / L. Add phenol to the tannery wastewater to make the final concentration 100mg / L; add 4ml of fresh bacterial solution, mix well, place it on a shaker at 30°C and 165rpm for cultivation, and take a sample after 3 days (72 hours) to determine the degradation rate of the compound . The results are shown in Table 2.
[0046] Table 2 Degradation rate of phenol and removal rate of chromium (VI) in tannery wastewater by strain SG-20 (3 days)
[0047] substrate
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