Team:USTC-China/Project/results

From 2011.igem.org

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(Verification of the modified Toggle-switch (protocol))
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[[File:Rs14.jpg|550px|center ]]
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<p align=center>Figure4. The conlonies of the bacteria with the modified Toggle Switch exhibit two different states or just one state(4X Objective)</p>
<p align=center>Figure4. The conlonies of the bacteria with the modified Toggle Switch exhibit two different states or just one state(4X Objective)</p>
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<p>By calculating with the help of the fluorescence microscope, the ratio between the numbers of colonies with RFP and colonies with GFP ≈ 6:1. It is useful to our project design.</p>
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<p>&nbsp;&nbsp;&nbsp;&nbsp;By calculating with the help of the fluorescence microscope, the ratio between the numbers of colonies with RFP and colonies with GFP ≈ 6:1. It is useful to our project design.</p>
==Test of Incorporated Riboswitch into one side of Toggle-switch  <html><a  href= "https://2011.igem.org/Team:USTC-China/Protocol#Toggle Switch"><font size="4"><u>(protocol)</u></font></a> </html>==
==Test of Incorporated Riboswitch into one side of Toggle-switch  <html><a  href= "https://2011.igem.org/Team:USTC-China/Protocol#Toggle Switch"><font size="4"><u>(protocol)</u></font></a> </html>==

Revision as of 17:34, 5 October 2011

Contents

Experimental Results of the Basic Parts

Verification of ΔcheZ strain (protocol)

    The size of colonies of E.coli strain RP1616 was much smaller than that E.coli steain RP437 under the same circumstance and after same period of incubation time(about 10h), and the result is shown in Figure1. In colony PCR using the primers of cheZ gene following , RP437 absolutely has much more outcomes than RP1616 and we conclude that RP1616 is actually a ΔcheZ strain.

Figure1.

Figure1.The result of colony PCR(From left to right, the first lane is the marker, the third and the forth lane is the PCR outcome of strain RP437 and strain RP1616, the sixth and the seventh lane is the PCR outcome of strain RP437 and strain RP1616.)

Verification of the function of the constructed Aptamer-cheZ part(protocol)

    From the results shown in Figure2. We can be sure that the Aptamer-cheZ part actually works effectively, especially on 0.3% Semi-solid medium.

X().jpg

Figure2. The growing state of the reprogrammed bacteria with Aptamer-cheZ part(Left:0.3%agar with 0mM Thephylline, Right:0.3%agar with 0.25mM Thephylline)

Verification of the original Toggle-switch from PKU(protocol)

Res14.jpg

Figure3.A conlony of the bacteria with the original Toggle Switch exhibit two different states(4X Objective)

    By calculating with the help of the fluorescence microscope, the ratio between the numbers of colonies with RFP and colonies with GFP ≈ 8:25. It means the original Toggle Switch is not fit for our purpose, so we modify the original by luxPR-cI device.

Verification of the modified Toggle-switch (protocol)

Rs14.jpg

Figure4. The conlonies of the bacteria with the modified Toggle Switch exhibit two different states or just one state(4X Objective)

    By calculating with the help of the fluorescence microscope, the ratio between the numbers of colonies with RFP and colonies with GFP ≈ 6:1. It is useful to our project design.

Test of Incorporated Riboswitch into one side of Toggle-switch (protocol)

                    Results18.jpg   Results9.jpg

Verification of the constructed system’s function (protocol)

Results110.jpg
  • 6 tubes of constructed monoclonal RP1616
Results111.jpg
  • Results of the sixth tube

                    Results12.jpg          Results113.jpg