Method for quantitating anaerobic ammonia oxidizing bacteria in sediment of aquiculture environment
A technology for anaerobic ammonium oxidation and aquaculture, applied in biochemical equipment and methods, microbial measurement/inspection, fluorescence/phosphorescence, etc., can solve the problems of low specificity and low diversity of 16SrRNA gene detection, and achieve good results Effect of amplification efficiency and regression relationship
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[0029] 1. DNA extraction and quantification
[0030]After collecting aquaculture environmental sediment samples, mix them quickly, put them in dry ice immediately, and transfer them to a -80°C refrigerator for storage. Sediment DNA was extracted using the Fast Prep-24 nucleic acid extractor and the FastDNA Spin kit for soil from MP Biomedicals. The operation method is as follows: add 0.3g of sediment sample (do not exceed 0.3g) to the Lysing MatrixZ tube, and add 1100μl of lysate. Put the above centrifuge tube into the FastPrep-24 nucleic acid extractor, set the speed to 5, and centrifuge for 40s. The centrifuge tube was centrifuged at 14000×g for 10 min at 4°C. Carefully transfer the supernatant to a new 1.5ml centrifuge tube, add 250μl PPS, and gently invert 10 times to mix. Centrifuge the above mixture at 14000×g for 5 min at 4°C, transfer the supernatant into a new centrifuge tube, shake the Binding Matrix Suspension evenly, suspend it, and add 500 μl of Binding Matrix ...
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