Difference between revisions of "Part:BBa K2943902:Experience"
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<partinfo>BBa_K2943902</partinfo>
 
<partinfo>BBa_K2943902</partinfo>
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<I>TAU_Israel</I>
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<I>TAU_Israel (year 2019)</I>
 
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<b>Part Characterization:</b><br>
 
<b>Part Characterization:</b><br>
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Using PCR reaction, we amplified part of the plasmid, excluding part of the mRFP and RBS. This enabled us to insert the gblocks into the plasmid which included already the appropriate backbone and overlaps for the assembly.
 
Using PCR reaction, we amplified part of the plasmid, excluding part of the mRFP and RBS. This enabled us to insert the gblocks into the plasmid which included already the appropriate backbone and overlaps for the assembly.
−
The gblock was inserted using Gibson Assembly. Before the assembly, we have done DPN1 to ensure no unwanted DNA template was present and used PCR clean kit to prepare the amplified backbone. Then we proceeded to the Gibson reaction and transformed the resulting plasmid into <em> E. coli</em> DH10beta.  
+
The gblock was inserted using Gibson Assembly. Before the assembly, we have done DPN1 to ensure no unwanted DNA template was present and used PCR clean kit to prepare the amplified backbone. Then we proceeded to the Gibson reaction and transformed the resulting plasmid into <em> E. coli</em> DH10beta. <br>
 +
<b>Fluorescence Experiment:</b><br>
 +
We have used plate reader machine. The plate contained 3 samples of each of the next bacteria:
 +
 
 +
-DH10beta containing non fluorescent plasmid for negative control.
 +
 
 +
-DH10beta containing the original part.
 +
 
 +
-DH10beta containing this part.
 +
 
 +
- We included also 3 samples of pure LB in order to use it as blank.
 +
 
 +
Because RFP can absorb light at 600nm and lead to false measurements, concentration of bacteria was estimated using OD700 as recommended previously by the iGEM committee . For measuring the protein's fluorescence, we used excitation wavelength of 540 nm and emission wavelength of 650 nm.<br>
 +
 
 +
Calculation of the fluorescence intensity:<br> We first measured individual sample intensity as:
 +
 
 +
Individual Intensity= (Florescence of plasmid - florescence of LB) / # Colonies in OD700<br>
 +
 
 +
Then, for each type of bacteria, we calculated the average of the three appropriate samples intensity.<br>
 +
 
 +
 
 +
Results:<br>
 +
We received the following fluorescence intensity (Fig.1):<br>
 +
-Non fluorescence bacteria- Mean: 26,766.72; STDEV: 3423.98.<br>
 +
-Original part bacteria- Mean: 57,853.17; STDEV: 2624.75.<br>
 +
-Variation 1 bacteria- Mean: 154,336.4; STDEV: 8994.96.<br>
 +
-Variation 2 bacteria- Mean: 50,705.19; STDEV: 2436.38.<br>
 +
 
 +
The intensity of  our improvment was almost 3 times stronger than the original part.
 
        
 
        
 
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Revision as of 15:19, 20 October 2019


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Please enter how you used this part and how it worked out.

Applications of BBa_K2943902

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UNIQcd1dc72959bb7e2e-partinfo-00000000-QINU UNIQcd1dc72959bb7e2e-partinfo-00000001-QINU


BBa_K2943902 TAU_Israel (year 2019)

Part Characterization:
This part is an improved version of an existing part (BBa_K608014). The mutations were detected by using bioinformatics softwares, and then the mutated part was ordered as gblock. Next, we proceeded to wet lab work. We started our lab work by transforming BBa_K608014 from the distribution kit to E. coli DH10beta. Then, after growing starters from the transformation plates overnight, we extracted the plasmids using miniprep.

Using PCR reaction, we amplified part of the plasmid, excluding part of the mRFP and RBS. This enabled us to insert the gblocks into the plasmid which included already the appropriate backbone and overlaps for the assembly. The gblock was inserted using Gibson Assembly. Before the assembly, we have done DPN1 to ensure no unwanted DNA template was present and used PCR clean kit to prepare the amplified backbone. Then we proceeded to the Gibson reaction and transformed the resulting plasmid into E. coli DH10beta.
Fluorescence Experiment:
We have used plate reader machine. The plate contained 3 samples of each of the next bacteria:

-DH10beta containing non fluorescent plasmid for negative control.

-DH10beta containing the original part.

-DH10beta containing this part.

- We included also 3 samples of pure LB in order to use it as blank.

Because RFP can absorb light at 600nm and lead to false measurements, concentration of bacteria was estimated using OD700 as recommended previously by the iGEM committee . For measuring the protein's fluorescence, we used excitation wavelength of 540 nm and emission wavelength of 650 nm.

Calculation of the fluorescence intensity:
We first measured individual sample intensity as:

Individual Intensity= (Florescence of plasmid - florescence of LB) / # Colonies in OD700

Then, for each type of bacteria, we calculated the average of the three appropriate samples intensity.


Results:
We received the following fluorescence intensity (Fig.1):
-Non fluorescence bacteria- Mean: 26,766.72; STDEV: 3423.98.
-Original part bacteria- Mean: 57,853.17; STDEV: 2624.75.
-Variation 1 bacteria- Mean: 154,336.4; STDEV: 8994.96.
-Variation 2 bacteria- Mean: 50,705.19; STDEV: 2436.38.

The intensity of our improvment was almost 3 times stronger than the original part.

;