Team:Chiba/Assay/store

Storage実験方法

Experiment:
We constructed two plasmids as shown in Fig. 1. Human ferritin genes (fth1 and ftl) are placed on the high-copy plasmid under the control of BAD promoter. By adding arabinose into the media, Human ferritin proteins are induced.E. coli strain BL21 and SHuffle® (要link) were transformed with above plasmids. The resultant “ferritin generators” were cultured in the presence of iron citrate (Fe3+) or iron ascorbate (Fe2+), and checked final cell density and colony forming efficiency. As a control, we conducted the same experiment with “sfgfp generator”.

Detailed procedure

1.E. coli strain BL21 and SHuffle® were transformed with the plasmids shown in Fig. 1.
2.All transformants were inoculated into small (2 mL) culture and was shaken for 12h (at 37°C).
3.Inoculated into flesh media (2 mL), shaken for 3 hours.
4.We added L-arabinose into each sample (final conc. 0.2%). Then cultured for another 9 hours (at 37°C).
5.After 9 hours, we measured cell density (OD600) of every sample, and put 10^7 cell of E.coli to fresh medium containing various concentration of iron citrate or iron ascorbate.
6.Then we shaking cultured E.coli for 12 hours.
7.We got 1 mL aliquot from each sample and centrifuged with 7,000 rpm, at 25℃ for 2 minutes.
8.We wasted supernatant and resuspended with 1 mL saline solution (0.9% NaClaq), and we measured cell density (OD600).
9.5 μL of the diluted cell suspension was spotted on the LB agar medium and incubated for 12 hours. Approximately 107, 106, 105, 104, 103, and 102 cells were contained in the spots.

絵とかあるといいよね！！