Difference between revisions of "Part:BBa K300002:Experience"

(Applications of BBa_K300002)
m (Applications of BBa_K300002)
 
(8 intermediate revisions by 2 users not shown)
Line 4: Line 4:
  
 
===Applications of BBa_K300002===
 
===Applications of BBa_K300002===
===Applications of BBa_K300097===
+
This part was tested through <partinfo>BBa_K300086</partinfo>.
====Methods====
+
{{Template:UNIPV-Pavia/2010/pTETtag}}
Inoculum (into 5 ml LB+Amp) from glycerol stock of:
+
*<partinfo>BBa_K300086</partinfo>
+
*<partinfo>BBa_K300088</partinfo>
+
*<partinfo>BBa_K300090</partinfo>
+
*<partinfo>BBa_K300099</partinfo>
+
*<partinfo>BBa_K173000</partinfo> (positive control)
+
*<partinfo>BBa_B0031</partinfo> (negative control)
+
They were let grow ON at +37°C, 220 rpm.
+
 
+
The following day cultures were diluted 1:100 and let grow again for about five hours at +37°C, 220 rpm.
+
 
+
Optical density (O.D.) of each cell culture was than measured with TECAN Infinte F200. Samples were diluted in order to obtain the same O.D. equal to 0,02.
+
 
+
Than we performed a 21 hours' experiment with measurements of absorbance and green fluorescence every five minutes with TECAN Infinite F200. Each value shown is the mean of three measurements, from GFP data that of a non-fluorescent culture (negative control) was subtracted; cultures were shaken for 15 seconds every five minutes.
+
====Results====
+
<div align="center">
+
<table border="0">
+
<tr>
+
<td>[[Image:UNIPV10_pTET_c_ASB.png|thumb|300px|Raw growth curve]]</td>
+
<td>[[Image:UNIPV10_pTET_c_GFP.png|thumb|300px|Raw GFP curve]]</td>
+
</tr>
+
</table>
+
<table>
+
<tr>
+
<td>[[Image:UNIPV10_pTET_c_BAR.png|thumb|300px|Mean (dGFP/dt)/O.D. over the exponential phase (under the hypothesis that GFP half-life in fusion contructs is similar to the original one -<partinfo>BBa_E0040</partinfo>)]]</td>
+
</tr>
+
</table>
+
 
+
<table border="1">
+
<tr align="center">
+
<th>Culture</th><th>Doubling time [min.]</th>
+
</tr>
+
<tr align="center">
+
<td><partinfo>BBa_K173000</partinfo></td><td>77</td>
+
</tr>
+
<tr align="center">
+
<td><partinfo>BBa_K300086</partinfo></td><td>74</td>
+
</tr>
+
<tr align="center">
+
<td><partinfo>BBa_K300088</partinfo></td><td>75</td>
+
</tr>
+
<tr align="center">
+
<td><partinfo>BBa_K300090</partinfo></td><td>76</td>
+
</tr>
+
<tr align="center">
+
<td><partinfo>BBa_K300099</partinfo></td><td>76</td>
+
</tr>
+
<tr align="center">
+
<td><partinfo>BBa_B0031</partinfo></td><td>69</td>
+
</tr>
+
</table>
+
</div>
+
====Discussion====
+
All cell cultures showed a similar growth curve and doubling time was computed as described [http://2010.igem.org/Team:UNIPV-Pavia/Parts/Characterization#Doubling_time_evaluation here] in order to have informations about the burden due to synthesis of such fusion proteins. It's possible to see that all doubling time are very similar; it's possible to assert that the expression of these BioBrick parts doesn't cause abnormal stress to the cells.
+
 
+
In GFP curve it's possible to appreciate that in <partinfo>BBa_K300086</partinfo>, <partinfo>BBa_K300088</partinfo>, <partinfo>BBa_K300090</partinfo>, <partinfo>BBa_K300099</partinfo> GFP accumulation it's very similar and it's significantly different from that of negative control <partinfo>BBa_B0031</partinfo>. These results show the right folding of the green fluorescent protein assembled downstream of the genetic circuit.
+
 
+
The mean protein synthesis rate was also computed over the growth exponential phase, showing again an appreciable GFP production rate that is about a half of the positive control.
+
  
 
===User Reviews===
 
===User Reviews===

Latest revision as of 21:46, 27 October 2010

This experience page is provided so that any user may enter their experience using this part.
Please enter how you used this part and how it worked out.

Applications of BBa_K300002

This part was tested through BBa_K300086.

Methods

Inoculum (into 5 ml LB+Amp) from glycerol stock of:

Cultures were grown ON at 37°C, 220 rpm.

The following day cultures were diluted 1:100 and let grow again for about five hours at 37°C, 220 rpm.

The optical density (O.D.) of each culture was than measured with TECAN Infinte F200. Samples were diluted in order to obtain the same O.D. equal to 0.02.

Then we performed a 21-hour experiment with measurements of absorbance and green fluorescence every five minutes with TECAN Infinite F200; cultures were shaken for 15 seconds every five minutes. Acquired data were blanked by subtracting the media absorbance (for absorbance measurements) and the BBa_B0031 fluorescence (for fluorescence measurements). Then, the relative GFP synthesis rate per cell was evaluated by computing (1/O.D.600)*dGFP/dt, where O.D.600 is the blanked absorbance of the culture of interest and GFP is its blanked fluorescence. Each value shown below is the mean of three measurements in exponential phase and error bars represent the 95% confidence interval of the mean.

Results

Raw growth curve
Raw GFP curve
Mean (dGFP/dt)/O.D. over the exponential phase (under the hypothesis that GFP half-life in fusion contructs is similar to the original one - BBa_E0040)
CultureDoubling time [min.] ± std error
BBa_K17300076.3336 ± 1.4362
BBa_K30008673.6685 ± 1.6245
BBa_K30008874.8806 ± 2.7699
BBa_K30009075.9433 ± 3.6808
BBa_K30009978.4634 ± 2.5622
BBa_B003170.8421 ± 2.2181

Discussion

All the cultures showed a similar growth curve; doubling time was computed as described [http://2010.igem.org/Team:UNIPV-Pavia/Parts/Characterization#Doubling_time_evaluation here] in order to obtain information about the metabolic burden due to the synthesis of the studied fusion proteins. It is possible to see that all doubling times are comparable; it is possible to assert that the expression of these BioBrick parts doesn't cause abnormal stress to the cells.

From GFP curve it is possible to appreciate that in BBa_K300086, BBa_K300088, BBa_K300090, BBa_K300099 GFP accumulation is very similar and it is significantly different from the one of the negative control BBa_B0031. These results show that the green fluorescent protein assembled downstream of the genetic circuit is correctly folded.

The mean protein synthesis rate was also computed over the exponential growth phase, showing again an appreciable GFP production rate that is about half of the positive control GFP.

User Reviews

UNIQ813066ffeda0e41c-partinfo-00000014-QINU

••

UNIPV-Pavia iGEM 2010

This part was used as a head domain alone and to construct the following synthetic composite affinity tags:


UNIQ813066ffeda0e41c-partinfo-0000001B-QINU