Team:TU Darmstadt/result

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<img alt="Problem" src="/wiki/images/6/66/Darmstadt_green_Problem.jpg" width="100" height="30"></a>
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<a href="https://2013.igem.org/Team:TU_Darmstadt/solution">
 
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<a href="https://2013.igem.org/Team:TU_Darmstadt/result">
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<img alt="result" src="/wiki/images/2/2c/Darmstadt_green_Result.jpg" width="80" height="30"></a>
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<img alt="result" src="/wiki/images/c/ca/04._Result_(angewählt).jpg" width="80" height="30"></a>
<a href="https://2013.igem.org/Team:TU_Darmstadt/safety">
<a href="https://2013.igem.org/Team:TU_Darmstadt/safety">
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<h1 align="center"><font size="6" color="#F0F8FF" face="Arial regular">Our results</font></h1>
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<b>LSSmOrange:</b><br>
 
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LSSmOrange is an orange fluorescent protein that we want to use for FRET, we us it as a donor. In an
 
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actual paper Daria M. Shcherbakova<sup>[1]</sup> showed that LSSmOrange has an excitation maximum by
 
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437 nm and an emission maximum by 572 nm.
 
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In the following diagram (graph 1) one can see our results with our own expressed LSSmOrange. The
 
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colored dots show the different maximums. The excitation maximum is at 415 nm, another at 453 nm
 
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and our measured emission maximum is at 564 nm. This aberration changes nothing
 
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on the FRET system. The excitation maximum is big enough to stimulate mKate, the other fluorescent
 
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protein. Of course, we checked also the emission and excitation of our Bl21DE3 cells (data
 
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not shown) and we can eliminate the theories that these cells disturb this florescence measurement.
 
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Graph 1 "Bl21DE3pLys[pBR-IBA2-Lssmorange]"<br>
 
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Caption: Excitation Spectrum (dashed line) and emission spectrum (solid line) from
 
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LssmOrange with marked maximums.<br><br>
 
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<b>mKate:</b><br>
 
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mKate2 is a red fluorescent protein that we want to use as a acceptor for FRET. According to Evrogen<sup>[2]</sup>
 
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mKate2 has an excitation maximum at 588 nm and an emission maximum at 633 nm. The
 
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diagram below (graph 2, colored dots) shows that the excitation maximum is at 579 nm and the
 
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emission maximum is 611 nm. The first peak does not look exactly like a single peak, but we can see a
 
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clear maximum. The problem for our FRET system is the very low intensity which results
 
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in the next diagram (graph 3) in a huge difference of intensity of the two fluorescence
 
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proteins.<br><br>
 
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Graph 2 "Bl21DE3pLys[pBR-IBA2-mKate]"
 
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Caption:Excitation Spectrum (dashed line) and emission spectrum (solid line) of
 
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mKate with marked maximums.<br><br>
 
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<b>FRET:</b><br>
 
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Both diagrams in an overlay shows us the FRET system. LSSmOrange is the donor and mKate is the
 
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acceptor. For an optimum in FRET, it should display a stronger overlap between the emission maximum of LssmOrange and the excitation maximum of mKate.<br><br>
 
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Graph 3 "FRET pair LSSmOrange-mKate"<br>
 
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Caption:Overlay of figure 1 and figure 2.
 
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The next figure is from the paper of M. Shcherbakova. In this figure one can
 
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clearly see the overlap between donor and acceptor in an optimal FRET system. <br><br>
 
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<center><img alt="Spectra" src="/wiki/images/6/6c/ShcherbakovaSpectra.png" width="400" height="349"></center> <br>
 
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<center>Excitation and emission spectra overlay of donor LSSmOrange and acceptor mKate2<sup>[1]</sup><br>
 
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(dashed line = excitation spectrum, solid line = emission spectrum)</center><br><br>
 
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<b>Growth curves:</b>
 
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To determine the influence of the induced constructs mKate and LssmOrange on the BL21DE3, growth curves were used. During a time period of 8 h the OD of the samples was measured at a wavelength of 600 nm in time steps of 15 min. The measurement was started at an OD600nm  value of 0.3.  With the help of the following formulas the growth rate k and the doubling time g were calculated:
 
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<a href="https://2013.igem.org/Team:TU_Darmstadt/result/molecular_engineering">
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<font size="8" color="#F0F8FF" face="Arial regular">Molecular engineering |</font>
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<a href="https://2013.igem.org/Team:TU_Darmstadt/result/electrical_engineering">
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<font size="8" color="#F0F8FF" face="Arial regular">Electrical engineering </font>
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The calculated values of k and td of the competent cells BL21DE3 containing the mKate or LssmOrange construct were compared to the level of the wild type strain, to reveal possible toxicity of the constructs. In the following diagrams the OD600, respectively the ln OD600, values are plotted against the time and in the table below the resulting values of the growth rates k and the doubling times td are listed. <br><br>
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Graph!<br>
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Caption:Growth curves of BL21DE3 WT, BL21DE3 mKate and BL21DE3 LSSmOrange. The OD600 values are plotted against the time [min].  
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Graph!
 
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Caption: Semi-logarithmic growth curves of BL21DE3 WT, BL21DE3 mKate and BL21DE3 LSSmOrange. The ln (OD600 values) are plotted against the time [min].
 
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Table: The growth rate k and the doubling time t<sub>d</sub> of BL21DE3 WT, BL21DE3 mKate and BL21DE3LSSmOrange.
 
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TABLE
 
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As can be seen in the two diagrams the course of the growth curves are rather similar. The growth rate as well as the doubling time of the wild type BL21DE3 and the one including the LSSmOrange construct are almost identical. The growth rate of the strain including the mKate construct is slightly lower and therefore the doubling time is around 5 min higher. All in all, the differences of the samples including the constructs compared to the wild type BL21DE2 are neglectably low. Therefore it can be assumed that the construct mKate as well as LSSmOrange are not toxic for the BL21DE3 cells and have no or a neglectably low influence on the growth of the cells.
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<h2><font size="6" color="#F0F8FF" face="Arial regular">References</font></h2>
 
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[1] J Am Chem Soc. 2012 May 9; 134(18): 7913–7923. doi:10.1021/ja3018972
 
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Daria M. Shcherbakova, An orange fluorescent protein with a large Stokes shift for
 
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single-excitation multicolor FCCS and FRET imaging.<br>
 
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[2] http://www.evrogen.com/products/basicFPs.shtml
 
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Latest revision as of 03:32, 5 October 2013







Molecular engineering | Electrical engineering




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Labbookdetection Visit our lab book for the detection construct

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Labbookdetection Visit our lab book for the cutinase

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