Part:BBa_K562005:Experience

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••• iGEM Dundee 2011

This part was seen work in practice. Synthesis of the single encoded polypeptide in a very small scale culture (1 ml) was observed by 35-S-Methionine labelling (Figure 1).

Results

E. coli was transformed with BBa_K562005 expressed from pT7.5, and the plasmid pGP1-2 encoding T7 polymerase, and grown aerobically for 3 hours in LB medium. T7 polymerase synthesis was induced by heat shock before all native transcription in E. coli was halted by the addition of rifampicin. 10 minutes later 1 ml of cells was then collected and spiked with 35-S-labelled Methionine. Following a 10 minute incubation the cell pellet was harvested and resuspended in Laemmli disaggregation buffer. Protein labelling was analysed by SDS-PAGE and autoradiography.

This very small scale and sensitive technique reveals all polypeptides being expressed from the plasmid.

Figure 1: Transcription and translation of gene products produced from BBa_K562005. Radiolabelled revealed a band of the corresponding size to the PduN protein. The RED ARROW points to the lane producing polypeptides from BBa_K562005.

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