Part:BBa_K1893016
Arabinose inducible gp2 (pBAD+gp2)
The T7 phage gene Gp2 under control of the pBAD promoter. This part allows for robust growth inhibition in E. coli within half an hour upon addition of arabinose to the culture. Addition of glucose switches off the production of Gp2, and allows recovery of normal growth rates after several hours.
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.
Characterisation data
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 1342
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 1281
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 1116
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 1473
Illegal SapI site found at 1098
None |