Difference between revisions of "Part:BBa K1893016"

Revision as of 14:08, 23 October 2016

Arabinose inducible gp2 (pBAD+gp2)

The T7 phage gene Gp2 under control of the pBAD promoter. This part allows for robust and reversible growth inhibition in E. coli by adding arabinose to the culture.

Usage and Biology

The T7 phage is a bacteriophage that infects Escherichia coli and leads to cell lysis of the host. It is known in synthetic biology as the source of the T7 promoter, which allows for tight control of gene expression in the presence of T7 RNA polymerase. The T7 phage infection mechanism is facilitated by a number of viral genes encoded in the 40kb T7 phage genome, including gene product 2.

Gene product 2 (gp2) is a small 7 kDA protein that plays a key role in the late stages of T7 phage infection. It binds to the β’ subunit of RNA polymerase (RNAP) in the E. coli host, which inhibits host transcription by preventing formation of the active RNAP holoenzyme. This allows the phage-encoded RNAP to transcribe the phage proteins required for successful infection without interference from the host transcriptional machinery. One effect of inhibited host transcription is a decrease in the growth rate of the host.

This part can arrest the growth of E. coli within half an hour of induction by arabinose. Once the pBAD promoter is switched off with glucose, the cells can recover back to normal growth rate within approximately 50 minutes. We have submitted this part as our best composite, because it represents an effective an novel way to control the size of a bacterial population, and has several advantages over existing population control methods.

1. Controlling cells in this way doesn’t require the usage of supplemented or minimal media, as in the case of antibiotics and auxotrophy. 2. The system can easily be induced by L-arabinose, and switched off by D-glucose, both of which are non-toxic. 3. Gp2 is particularly good for regulating population size in co-cultures, as it only affects the size of one population.

Characterisation data

Sequence and Features