Method for evaluating influence on energy metabolism of living body caused by electromagnetic radiation by using MFC
A technology of energy metabolism and electromagnetic radiation, applied in microorganism-based methods, biochemical equipment and methods, and the determination/inspection of microorganisms, which can solve the problems of low experimental reproducibility, inconsistent experimental methods and experimental standards, and reliable experimental results. questions such as reliability and credibility, to achieve the effect of good repeatability, simple operation, and extended application
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Embodiment 1
[0029] The embodiments described below are exemplary and are intended to explain the present invention, but should not be construed as limiting the present invention.
[0030] Example 1:
[0031] (1) Strain cultivation: the electrogenic microorganism Shewanella Oneida ( Shewane1la oneidensis MR-1, ATCC700550) were streaked and inoculated in solid LB medium (tryptone 10 g / L, yeast extract 5 g / L, NaCl 10 g / L, agar powder 15 g, pH adjusted to 7.0), cultured at 30°C After 24 hours, a single colony was picked and placed in liquid LB medium, 30°C, 180 rpm, and cultured for 12 hours.
[0032] (2) Preparation of MFC inoculum solution: Centrifuge the bacterial solution in (1) at 6000 r / min at 4°C for 2 min, remove the supernatant under anaerobic conditions, and obtain bacterial cells, use PBS buffer solution, the composition is ( / L): Na 2 HPO 4 12H 2 O 22.2 g; NaH 2 PO 4 2H 2 O5.93 g; KCl 0.13 g, pH7.0, washed three times, and resuspended in 0.5 mL to obtain MFC inoculum.
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Embodiment 2
[0039] (1) Strain cultivation: the electrogenic microorganism Geobacter sulfur-reducing ( Geobacter sulfur reducers PCA, DSMZ12127) were inoculated in liquid NBAF medium (fumaric acid 4.64 g / L, NaHCO 3 2.50 g / L, NH 4 Cl0.25 g / L, NaH 2 PO 4 2H 2 O 0.68 g / L, KCl 0.10 g / L, vitamin mother solution 10 ml / L, trace element mother solution 10 ml / L, sodium acetate 0.85 g / L, pH adjusted to 7.0), the inoculation amount of the bacterial solution was 10% of the inoculation medium amount %, cultured at 30°C for 18 h.
[0040] (2) Preparation of MFC inoculum solution: centrifuge the bacterial solution in (1) at 6000 r / min at 4°C for 2 min, remove the supernatant under anaerobic conditions, and obtain bacterial cells, use PBS buffer solution, the composition is ( / L): Na 2 HPO 4 12H 2 O 22.2 g; NaH 2 PO 4 2H 2 O5.93 g; KCl 0.13 g, washed three times, and resuspended in 0.5 mL to obtain the MFC inoculum.
[0041] (3) Preparation of MFC electrode solution: MFC catholyte is PBS buf...
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