Regulatory

Part:BBa_K3034005

Designed by: Jiayi Lu 、Yubing Zhou   Group: iGEM19_UESTC-China   (2019-10-02)
Revision as of 05:55, 14 October 2019 by BINGO (Talk | contribs)

PtisAB PtisAB is a promoter which can be induced by ciprofloxacin(CIP) through SOS response, and the expression of it varies with different concentrations of CIP. This part is responsible for starting to express subsequent genes once it sensed CIP.

PtisAB gene was derived from Escherichia coli K12 MG1655 and has been codon optimized.（GenBank：AE000445.1）


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]

Contribution

  • Group: [http://2019.igem.org/Team:UESTC-China iGEM Team UESTC-China 2019]
  • Author: Yubing Zhou, Jiayi Lu

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Characterization from iGEM19-UESTC-China

The Mechanism of PtisAB

Ciprofloxacin can cause the SOS reaction of the bacteria, and the SOS reaction activates the RecA enzyme. When the RecA enzyme is activated, the lexA repressor is cleared, whereby the promoter starts to start and express the downstream gene.

Fig. 1Schematic diagram of CIP-induced PtisAB principle

As the schematic of the piGEM2019-01 shown above(Fig.1), when PtisAB senses ciprofloxacin, subsequent genes will express, one of them is eGFP. By detecting the fluorescence intensity of eGFP, the expression of PtisAB can be reflected.

Detection of Green fluorescence intensity—Methods

Fixed strain: The experimental group used E.coli DH5α carrying piGEM2019-01. The control group used wild-type Ⅰ E.coli DH5α.

1. A blank vector and a single clone of E.coli DH5α carrying piGEM2019-01 and wild-type E.coli DH5α were taken from the crossed plates, and 5 ml of LB and 5 μl of ampicillin were added to a 12 ml BD tube, and shaken for 11 hours.

2. Take 800μl from yesterday's bacteria and prepare a 15ml system (100ml small conical flask), cultivate the bacteria to the logarithmic growth phase（1.5h）.

3. separately add CIP to prepare a system having a CIP concentration of 0, 0.1, 1, 6, 10 μg/ml.

4. Detect OD600 and green fluorescence after 0h, 2h,4h,6h by a multi-function microplate reader.

• OD600 detection method: in 96-well plate, 3 duplicate holes, minus LB blank.

• Green fluorescence intensity detection method: At each time point, 1.5ml of bacterial liquid was taken in a light-proof tube,centrifuged at 12000rpm for 20 minutes, washed once with distilled water, and resuspended once. Add 96-well plate 200μl, excitation wavelength at 475nm, emission wavelength520nm.

Detection of Green fluorescence intensity—Result

Fig. 2 Fluorescence in unit OD for E.coli DH5α carrying piGEM2019-01 and wild-type Ⅰ E.coli DH5α. wild-type E.coli DH5αcarries a plasmid which only have AmpR. Cells were exposed to 0 0.1 1 6 10ug/ml CIP in exponential phase.Fold induction is GFP unit fluorescence after 2/4/6 h of exposure normalized to initial unit fluorescence.（Unit fluorescence=green fluorescence of 1.5ml bacteria/OD600 of 0.2ml bacteria）This graph is a representative of two independent experiments with similar results; error bars indicate the standard error.


Compared E.coli DH5α carrying piGEM2019-01 with wild-type E.coli Ⅰ DH5α, we can see that the the fluorescence intensity in E.coli DH5α carrying piGEM2019-01 is significantly stronger than wild-type Ⅰ E.coli DH5α.

To determine that our green fluorescence is produced by ciprofloxacin-induced promoter expression, we performed the same experimental procedure on WTII (with an arabinose-inducible promoter) and narrowed the range of concentration gradients to find the most appropriate The concentration of ciprofloxacin and the linear relationship between green fluorescence intensity and CIP concentration.

Fig. 3 Fluorescence in unit OD for E.coli DH5α carrying piGEM2019-001 and wild-type Ⅱ E.coli DH5α 2. Wild-type Ⅱ E.coli DH5α 2 carries a plasmid which has AmpR and GFP, and GFP is initiated by the IPTG-induced promoter. Cells were exposed to 0 0.2 0.4 0.6 0.8 1.0 ug/ml CIP in exponential phase. Fold means GFP unit fluorescence after 2h of exposure normalized to initial unit fluorescence.（Unit fluorescence=green fluorescence of 1.5ml bacteria/OD600 of 0.2ml bacteria）This graph is a representative of three independent experiments with similar results; error bars indicate the standard error.


Conclusion

For E.coli DH5α carrying piGEM2019-01, we can see PtisAB responds differently to CIP at different concentrations, among them, 1ug/ml is the most appropriate response concentration for PtisAB.

Besides, We can infer the concentration of ciprofloxacin based on the green fluorescence intensity. At a concentration of 0-1 μg/ml of ciprofloxacin, its relationship with green fluorescence intensity is basically in accordance with y = 0.3698x + 0.5477. R2 = 0.9721. Where y is the green fluorescence intensity and x is the ciprofloxacin concentration.

References

[1]Vogel J, Argaman L, Wagner EG, Altuvia S: The small RNA IstR inhibits synthesis of an SOS-induced toxic peptide. Current biology : CB 2004, 14(24):2271-2276.


[2]Dörr T, Vulić M, Lewis K: Ciprofloxacin causes persister formation by inducing the TisB toxin in Escherichia coli. PLoS Biol 2010, 8(2):e1000317-e1000317.



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