Part:BBa_K562003:Experience

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••• iGEM Dundee 2011

This part was seen work in practice. Synthesis of the two encoded polypeptides in very small scale cultures (1 ml) was observed by 35-S-Methionine labelling (Figure 1).

Results

E. coli was transformed with BBa_K562003 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_K562003. Radiolabelled revealed bands of the corresponding sizes to the PduA and PduB. PduB can often be expressed as a smaller PduB' variant from an alternative translation start site. The RED ARROW points to the lane producing polypeptides from BBa_K562003.

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