Difference between revisions of "Part:BBa K3482017"

(Characterization)
(Characterization)
Line 17: Line 17:
 
[[File:BBa K3482017 killswitchresults2.png|800px]]
 
[[File:BBa K3482017 killswitchresults2.png|800px]]
  
Quantitative assessment of viability of <i>E. coli Nissle 1917</i> containing the plasmids pAND (red), pKC1 (green), and pKC3 (blue) under permissive and non-permissive conditions, 37 °C (dashed line) and 25 °C (solid line), respectively. Both conditions were tested without addition of aTc or IPTG. Viability is measured by the OD of the samples on the y-axis, as a function of time in hours on the x-axis. The lines denote the mean and the shade the standard deviation.
+
Dose-response growth curve of <i>E. coli Nissle 1917 ΔclbA</i> harboring kill switch plasmids pKC1 and pKC3 at 37 and 25°C.  E. coli Nissle with pAND (red line), E. coli Nissle with pKC1 (green line), and <i>E. coli Nissle</i> with pKC3 (blue line), at 37°C (dashed line) and 25°C (solid line). The lines and shade represent the mean ± standard error. Each plot shows the absorbance at 600 nm measured every 10 min for a period of 10 hours at different aTc and IPTG concentrations.
  
  

Revision as of 03:07, 28 October 2020


aTc and heat-inducible IM2 antitoxin

IM2 immunity protein fused with an aTc sensible promoter and a heat-inducible ARN thermosensor.

Usage and Biology

Colicin E2 is an endonuclease that cuts on both single and double-stranded DNA. It has no specific cutting site. Colicins are toxins that can be produced by E. coli and closely related bacteria. The IM2 molecule gives an immunity to the Colicin E2 toxin

Characterization

We tested this part with the heat-repressible miniColicin toxin (BBa_K3482018) inserted on a plasmid. We inserted the heat-inducible RNA thermosensor upstream of the IM2 antitoxin genes in the plasmid pKC3. In order to demonstrate that the heat-inducible RNA thermosensor promotes the antitoxin synthesis and thus allows cells to grow in permissive conditions, we grew them at different temperatures and observed their growth curves. The backbone of the plasmid (pAND) and the plasmid pKC1 containing the toxin and the antitoxin, but no thermosensors were used as controls. Two different temperatures were chosen in order to test the permissive and non-permissive conditions, i.e. inside (37°C) and outside (≤25°C) the body, respectively. For this assessment no aTc or IPTG were used for induction.

BBa K3482017 killswitchresults2.png

Dose-response growth curve of E. coli Nissle 1917 ΔclbA harboring kill switch plasmids pKC1 and pKC3 at 37 and 25°C. E. coli Nissle with pAND (red line), E. coli Nissle with pKC1 (green line), and E. coli Nissle with pKC3 (blue line), at 37°C (dashed line) and 25°C (solid line). The lines and shade represent the mean ± standard error. Each plot shows the absorbance at 600 nm measured every 10 min for a period of 10 hours at different aTc and IPTG concentrations.


At permissive temperature (37°C) the pKC3 containing cells grew a bit slower than the two controls, but their viability was not impaired. Indeed, after 10 hours the cells containing either pAND or pKC1 seemed to reach a plateau where the pKC3 cells were still growing. At lower temperature (25°C), the viability of pAND and pKC1 cells remains unchanged while pKC3 growth was significantly impaired. Thus we showed that the plasmid pKC3 containing the part BBa_K3482017 is able to control the viability of its host depending on the temperature.



Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal SpeI site found at 90
    Illegal PstI site found at 96
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal SpeI site found at 90
    Illegal PstI site found at 96
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 265
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal SpeI site found at 90
    Illegal PstI site found at 96
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal SpeI site found at 90
    Illegal PstI site found at 96
  • 1000
    COMPATIBLE WITH RFC[1000]