Preparation method of TEM (transmission electron microscope) ultrathin section samples of phosphorus-accumulating bacteria
A technique of transmission electron microscopy and ultra-thin sectioning, which is applied in the field of preparation of TEM ultra-thin section samples, can solve the problems of complex sample pretreatment process, difficult to clearly display the ultrastructure of PAOs cells, and strong toxicity of drugs.
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Embodiment 1
[0034] The specific steps of the preparation method of purely cultured phosphorus accumulating bacteria transmission electron microscope ultrathin section samples are as follows:
[0035] (1) Take materials
[0036] The sample was collected from the pure PAOs obtained by isolation, screening and purification, and identified as Pseudomonas putida; the pure culture PAOs sample (volume less than 1mm 3 ) into a 1.5ml centrifuge tube, and an appropriate amount of 0.1M sodium cacodylate (SCB) buffer solution was added dropwise to submerge the purely cultured PAOs sample. The above-mentioned process needs to be completed within 1-2 minutes after the sample is collected. At the same time, in order to prevent the autolysis of purely cultured PAOs cells, the above-mentioned process needs to be operated at a low temperature of 0-4°C.
[0037] (2) cleaning
[0038] Centrifuge the 1.5ml centrifuge tube in the above steps at a speed of 4000-5000r / min, discard the supernatant, and repeat t...
Embodiment 2
[0051] The specific steps of the preparation method of mixed culture phosphorus accumulating bacteria transmission electron microscope ultrathin section sample are as follows:
[0052] (1) Take materials
[0053] The sample was collected from the biofilm in the anaerobic-aerobic alternating biofilter (AABF) with stable laboratory operation, and the mixed culture PAOs sample (volume less than 1mm 3 ) into a 1.5ml centrifuge tube, and an appropriate amount of 0.1M sodium cacodylate (SCB) buffer solution was added dropwise to submerge to mix and culture PAOs samples. The above-mentioned process needs to be completed within 1-2 minutes after the sample is collected, and at the same time, in order to prevent the autolysis of the mixed culture PAOs cells, the above-mentioned process needs to be operated at a low temperature of 0-4°C.
[0054] (2) cleaning
[0055] Centrifuge the 1.5ml centrifuge tube in the above steps at a speed of 4000-5000r / min, discard the supernatant, and rep...
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