Kit and method for rapidly detecting coal geological environment bacteria
A geological environment, kit technology, applied in biochemical equipment and methods, microbial determination/inspection, DNA/RNA fragments, etc. Limited capacity, etc., to achieve the effect of fast experiment speed, reliable results and low price
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Embodiment 1
[0034] 1. A primer set and DNA fragments for the rapid detection of coal geological environment bacteria by chemical synthesis.
[0035] The primer set includes: detection primers for amplifying coal geological environment bacteria, the sequences of which are respectively shown in SEQ ID NO: 1, SEQ ID NO: 2, and SEQ ID NO: 3;
[0036] The DNA fragments are bacterial DNA detection fragments in the coal geological environment, and their sequences are respectively SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9. The sequence shown in SEQ ID NO:10.
[0037] 2. Perform PCR amplification on the chemically synthesized DNA fragments using the primer pair SEQ ID NO: 1 / SEQ ID NO: 3, and the amplified product is used as the standard of the sample to be tested.
[0038] The PCR reaction system is: 10*EasyTaq Buffer: 5 μL, dNTPs (2,5 mM): 4 μL, upstream primer (10 μmol / L): 1 μL, downstream primer (10 μmol / L): 1 μL, EasyTaq DNA Polymerase: 1 μL, template ...
Embodiment 2
[0043] The method for detecting bacteria in a coal mine effluent sample: comprises the following steps:
[0044] 1. Extract the total DNA of the water sample microbial genome
[0045] (1) Suction filter the collected water sample with a 0.22 μm filter membrane, put the filter membrane with microorganisms into an EP tube, wash twice with STE buffer, and then centrifuge at 12000 rpm for 1 minute.
[0046] (2) Add 300 μl of STE buffer solution and 30 μl of lysozyme, wash and mix with a pipette, and place in a constant temperature water bath at 37° C. for 3.5 hours.
[0047](3) Add 35 μl of SDS and 5 μl of Proteinase K, and keep in a constant temperature water bath at 55° C. for 2.5 hours.
[0048] (4) Take it out after completion, cool to room temperature, and add 70 μl of NaCl.
[0049] (5) Add 450 μl DNA extraction phenol reagent, mix for 10 minutes, centrifuge at 12000 rpm for 10 minutes, and take the supernatant.
[0050] (6) Add an equal volume of phenol-chloroform-isoamy...
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