Method for extracting microorganism macrogenome from oil/gas pool environment
A gas reservoir environment and metagenome technology, which is applied in the field of direct extraction of microbial metagenomes to achieve the effects of high repeatability, low cost and a wide range of target microorganisms
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Embodiment 1
[0040] Example 1 Simple method for extracting microbial metagenomics from crude oil
[0041] 1. Take about 100mL of crude oil and put it in a glass beaker, and put it in a water bath at 70°C for 30 minutes.
[0042] 2. Add an equal volume of 30% (V / V) ethanol and half volume of crude oil petroleum ether: n-hexane (V / V=1:1) mixture, shake well.
[0043] 3. Stand still to separate the oil and water phases, and use a rubber hose to extract the lower water phase. Use filter paper to filter out a small amount of crude oil and other impurities in the aqueous phase.
[0044] 4. After filtration, the liquid is vacuum-filtered with a 0.22 μm microporous filter membrane, and the bacteria are enriched on the filter membrane.
[0045] 5. Cut the filter membrane into pieces and put it into a 10mL centrifuge tube, add 360μL lysozyme (10mg / mL dissolved in 10mM Tris-HCl, pH8.0), and bathe in 37℃ water for 1h.
[0046] 6. Add 115 μL of 10% SDS and 25 μL of proteinase K (20 mg / mL), and bathe...
Embodiment 2
[0052] Example 2 Simple method for extracting microbial metagenomics from oil-water mixture
[0053] 1. Take about 100mL of oil-water mixture and put it in a glass beaker, and put it in a water bath at 70°C for 30min.
[0054] 2. Filter the oil-water mixture with filter paper and collect the water phase.
[0055] 3. Mix the crude oil left on the filter paper with twice the volume of sterile PBS, stir well, and collect the aqueous phase by filtering with filter paper, repeat three times.
[0056] 4. Combine and filter the aqueous phase, vacuum filter with a 0.22 μm microporous membrane, and enrich the bacteria on the membrane.
[0057] 5. Cut the filter membrane into pieces and put it into a 10mL centrifuge tube, add 360μL lysozyme (10mg / mL dissolved in 10mM Tris-HCl, pH8.0), and bathe in 37℃ water for 1h.
[0058] 6. Add 115 μL of 10% SDS and 25 μL of proteinase K (20 mg / mL), and bathe in water at 37°C for 2 hours.
[0059] 7. Add 400 μL of 5M NaCl and mix by inversion, add...
Embodiment 3
[0065] Example 3 Simple method for extracting microbial metagenomics from oily soil (sludge)
[0066] 1. Take about 10g of oily soil and put it in a glass beaker, add 100mL of PBS, stir repeatedly, and bathe in 70℃ water for 30min.
[0067] 2. Filter the mixture with filter paper and collect the aqueous phase.
[0068] 3. Dissolve the crude oil and soil left on the filter paper with 100mL sterile PBS, stir well, collect the water phase by filtering with filter paper, and repeat three times.
[0069] 4. Combine and filter the aqueous phase, vacuum filter with a 0.22 μm microporous membrane, and enrich the bacteria on the membrane.
[0070] 5. Cut the filter membrane into pieces and put it into a 10mL centrifuge tube, add 360μL lysozyme (10mg / mL dissolved in 10mM Tris-HCl, pH8.0), and bathe in 37℃ water for 1h.
[0071] 6. Add 115 μL of 10% SDS and 25 μL of proteinase K (20 mg / mL), and bathe in water at 37°C for 2 hours.
[0072] 7. Add 400 μL of 5M NaCl and mix by inversion,...
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