Phyllobacterium myrsinacearum
A technology of Zijin Bovis and its preservation number, which is applied in the field of microbial compound agent for treating oil field fracturing flowback fluid and its preparation, can solve the problems of difficult degradation and secondary pollution of fracturing flowback fluid, and achieve clear water quality , high degradation rate, and the effect of reducing secondary pollution
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Embodiment 1
[0023] Embodiment 1: Separation and purification of Cladosporium mold and Pyrobacterium bovis
[0024] Taking the oilfield fracturing fluid flowback fluid as the sampling source, the fracturing fluid flowback fluid was diluted to 10 -1 ~10 -10 Dilute it, spread it on a solid medium containing 3% high-molecular organic compound guar gum, and cultivate it at a temperature of 30°C for 5 days.
[0025] A single colony was picked on the above plate and separated and purified by streaking on the plate to obtain two strains EB1 and EB2 with excellent traits.
Embodiment 2
[0026] The sequencing and identification of embodiment 2 bacterial strain EB1
[0027] 1. Genome extraction and electrophoresis detection
[0028] (1) Genome extraction process: Extract according to the method described in the instruction manual of the SK1375 Fungal Genome DNA Extraction Kit of Shanghai Sangon Bioengineering Technology Service Co., Ltd.
[0029] The extraction steps are described as follows:
[0030] 1. Take 50-100mg of fresh fungus or 20mg of dried fruiting bodies or mycelia, and grind them into powder in liquid nitrogen. Add 700 μl of FPCB Solution preheated at 65°C and 7 μl of β-mercaptoethanol in sequence, mix thoroughly, incubate at 65°C for 25 minutes, and mix occasionally.
[0031] 2. Centrifuge at 12,000rpm for 10min, transfer the supernatant to a clean 1.5ml centrifuge tube, add 700μl chloroform, mix well, and centrifuge at 12,000rpm for 5min.
[0032] 3. Pipette the supernatant into a clean 1.5ml centrifuge tube, add 40μl RNase A (20mg / ml), mix we...
Embodiment 3
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