Difference between revisions of "Part:BBa K3174008"

 
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For more information on how this part was conceived and designed, please visit the [[Part:BBa_K3174008:Design|design page]].<br><br>
 
For more information on how this part was conceived and designed, please visit the [[Part:BBa_K3174008:Design|design page]].<br><br>
This is a redesigned version of the Super Yellow Fluorescent Protein 2 (BBa_K864100) that has had a region that was prone to IS10 insertion element mutations altered. This removal of a mutation hotspot resulted in the expression of SYFP2 in TOP10 <I>E. Coli</I> cells being maintained for a longer period of time than the original sequence.
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This is a redesigned version of the Super Yellow Fluorescent Protein 2 ([[Part:BBa_K864100]]) that has had a region that was prone to IS10 insertion element mutations altered. This removal of a mutation hotspot resulted in the expression of SYFP2 in TOP10 <I>E. coli</I> cells being maintained for a longer period of time than the original sequence.
  
  
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===Testing and Measurement===
 
===Testing and Measurement===
  
Cultures of TOP10 E. coli were transformed with either the original SYFP2 plasmid or the redesign and propogated over four days. Each day a new culture was created using a 1:1000 dilution of the previous day's culture and allowed to grow for 24 hours at 37 C. Fluorescence was measured daily using flow cytometry. The data showed that while the original plasmid stopped expressing fluorescence after one day, the redesigned plasmid retained expression for up to four days.   
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Cultures of TOP10 <I>E. coli</I> were transformed with either the original SYFP2 plasmid or the redesign and propogated over four days. Each day a new culture was created using a 1:1000 dilution of the previous day's culture and allowed to grow for 24 hours at 37 C. Fluorescence was measured daily using flow cytometry. The data showed that while the original plasmid stopped expressing fluorescence after one day, the redesigned plasmid retained expression for up to four days.   
 
[[File:SYFP2redesignFigure1.png|430px|left|thumb|<b>Figure 1: Fluorescence histograms for TOP10 cells with the original SYFP2 plasmid.</b> The x-axis shows the intensity of  
 
[[File:SYFP2redesignFigure1.png|430px|left|thumb|<b>Figure 1: Fluorescence histograms for TOP10 cells with the original SYFP2 plasmid.</b> The x-axis shows the intensity of  
 
fluorescence on a logarithmic scale, and the y-axis displays the number of cells. Each line represents  
 
fluorescence on a logarithmic scale, and the y-axis displays the number of cells. Each line represents  
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This data indicated of functional improvement of the redesigned SYFP2 sequence over the original. While the original sequence mutated out of culture within a day, the redesign lasted up to four days of propagation in TOP10 cells. This improvement is particularly useful as TOP10 is a common competent cell strain used in synthetic biology research. By making the SYFP2 sequence more resilient to IS10 mutations, it can be used more effectively in TOP10 cells which are known to carry IS elements in their genomes. 
  
  

Latest revision as of 21:27, 21 October 2019


SYFP2 coding sequence with IS hotspot removed

For more information on how this part was conceived and designed, please visit the design page.

This is a redesigned version of the Super Yellow Fluorescent Protein 2 (Part:BBa_K864100) that has had a region that was prone to IS10 insertion element mutations altered. This removal of a mutation hotspot resulted in the expression of SYFP2 in TOP10 E. coli cells being maintained for a longer period of time than the original sequence.


Usage and Biology

This part codes for the bright yellow fluorescent protein SYFP2, which has an excitation peak of 515 nm and an emission peak of 527 nm.

Testing and Measurement

Cultures of TOP10 E. coli were transformed with either the original SYFP2 plasmid or the redesign and propogated over four days. Each day a new culture was created using a 1:1000 dilution of the previous day's culture and allowed to grow for 24 hours at 37 C. Fluorescence was measured daily using flow cytometry. The data showed that while the original plasmid stopped expressing fluorescence after one day, the redesigned plasmid retained expression for up to four days.

Figure 1: Fluorescence histograms for TOP10 cells with the original SYFP2 plasmid. The x-axis shows the intensity of fluorescence on a logarithmic scale, and the y-axis displays the number of cells. Each line represents a different day of propagation, and the shaded gray curve is a blank. Peaks to the right of the blank represent fluorescent cells while peaks on or to the left of the blank represent cells that have ceased to be fluorescent. All replicates were grown under the same conditions.
Figure 2: Fluorescence histograms for TOP10 cells with the redesigned SYFP2 plasmid. The x-axis shows the intensity of fluorescence on a logarithmic scale, and the y-axis displays the number of cells. Each line represents a different day of propagation, and the shaded gray curve is a blank. Peaks to the right of the blank represent fluorescent cells while peaks on or to the left of the blank represent cells that have ceased to be fluorescent. All replicates were grown under the same conditions. No data could be collected for Day 3 of Replicate 4.


This data indicated of functional improvement of the redesigned SYFP2 sequence over the original. While the original sequence mutated out of culture within a day, the redesign lasted up to four days of propagation in TOP10 cells. This improvement is particularly useful as TOP10 is a common competent cell strain used in synthetic biology research. By making the SYFP2 sequence more resilient to IS10 mutations, it can be used more effectively in TOP10 cells which are known to carry IS elements in their genomes.


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]