Difference between revisions of "Part:BBa K1893016"
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This part can arrest the growth of <i>E. coli</i> 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.  
 
This part can arrest the growth of <i>E. coli</i> 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.  
  
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<li> 1. Controlling cells in this way doesn’t require the usage of supplemented or minimal media, as in the case of antibiotics and auxotrophy.
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<li> Controlling cells in this way doesn’t require the usage of supplemented or minimal media, as in the case of antibiotics and auxotrophy.
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<li>2. The system can easily be induced by L-arabinose, and switched off by D-glucose, both of which are non-toxic.
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<li>The system can easily be induced by L-arabinose, and switched off by D-glucose, both of which are non-toxic.
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<li> 3. Gp2 is particularly good for regulating population size in co-cultures, as it only affects the size of one population.</li>
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<li> Gp2 is particularly good for regulating population size in co-cultures, as it only affects the size of one population.</li>
  
 
Characterisation data
 
Characterisation data

Revision as of 15:11, 23 October 2016


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.

  • Controlling cells in this way doesn’t require the usage of supplemented or minimal media, as in the case of antibiotics and auxotrophy.
  • The system can easily be induced by L-arabinose, and switched off by D-glucose, both of which are non-toxic.
  • 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


    Assembly Compatibility:
    • 10
      COMPATIBLE WITH RFC[10]
    • 12
      INCOMPATIBLE WITH RFC[12]
      Illegal NheI site found at 1342
    • 21
      INCOMPATIBLE WITH RFC[21]
      Illegal BamHI site found at 1281
    • 23
      COMPATIBLE WITH RFC[23]
    • 25
      INCOMPATIBLE WITH RFC[25]
      Illegal AgeI site found at 1116
    • 1000
      INCOMPATIBLE WITH RFC[1000]
      Illegal BsaI.rc site found at 1473
      Illegal SapI site found at 1098