A strain of Burkholderia for aerobic degradation of indole and its application
A technology of Burkholderia and indole, applied in the field of microorganisms, to achieve the effect of good temperature and pH tolerance and strong degradation ability
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Embodiment 1
[0025] Example 1: Screening of Burkholderia bacterial strains
[0026] The activated sludge from the reactor was repeatedly diluted and plated on the inorganic salt solid medium plate, and cultured at 30°C. Finally, a well-growing single colony was picked and cultivated in a liquid inorganic salt medium, and the bacterial liquid was obtained at 30°C and 150 rpm.
Embodiment 2
[0027] Embodiment 2: 16S rRNA molecular identification of bacterial strain
[0028] Pick a single colony grown on an inorganic salt solid medium plate and dissolve it in 10 µL of sterilized water, denature at 99°C and centrifuge to take the supernatant as a template for PCR amplification reaction. Use TaKaRa 16S rDNA Bacterial IdentificationPCR Kit with Forward primer / Reverse primer as primers to amplify the target fragment. The total volume of the PCR reaction system is 50 µL: PCR Premix 25 µL, Forward Primer 0.5 µL, Reverse Primer 0.5 µL, template DNA 5 µL, sterile ultrapure water 19 µL. The PCR reaction conditions were: pre-denaturation at 94°C for 5 min, after 30 cycles, including denaturation at 94°C for 1 min, annealing at 55°C for 1 min, extension at 72°C for 1.5 min, after 30 cycles, extension at 72°C for 5 min, 5 μL of PCR products were subjected to 1% agarose gel electrophoresis, and UV detection after EB staining. Use TaKaRa Agarose Gel DNAPurification Kit Ver. 2....
Embodiment 3
[0031] Embodiment 3: the broad-spectrum determination of the substrate of Burkholderia IDO3
[0032] Utilize the bacterium liquid in embodiment 1, adopt the inorganic salt culture medium ((NH 4 ) 2 SO 4 2.0 g / L, KH 2 PO 4 2.0 g / L, Na 2 HPO 4 •12H 2 O 3.28 g / L, FeCl 3 0.00025 g / L) culture, 5% inoculum, specifically investigated the growth of strain IDO3 with a variety of compounds as the sole carbon source, including benzoic acid, tryptophan, phenol, catechol, salicylic acid, indole, etc. The concentration of each compound is 50 mg / L.
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