Difference between revisions of "Part:BBa K5152000"
 
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__NOTOC__
 
__NOTOC__
 
<partinfo>BBa_K5152000 short</partinfo>
 
<partinfo>BBa_K5152000 short</partinfo>
  
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Our team designed a composite part to verify and compare the expression of chromoprotein reporters. Our project aims to develop biosensors for heavy metals that don't require specialized equipment for measurement. Therefore, we chose chromoproteins instead of fluorescence or luciferase.
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Our team designed this composite part to verify and compare the expression of chromoprotein reporters. Our project aims to develop biosensors for heavy metals that don't require specialized equipment for measurement. Therefore, we chose chromoproteins instead of fluorescence or luciferase.
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This composite part includes: A constitutive strong promoter (<partinfo>BBa_J23100</partinfo>), a strong ribosome binding site (<partinfo>BBa_B0034</partinfo>), the tsPurple coding sequence (<partinfo>BBa_K1033906</partinfo>), and a strong double terminator (<partinfo>BBa_B0015</partinfo>). Additionally, the 5' and 3' ends feature a 20 base pair overlap sequence for NEBuilder HiFi assembly using the pUC19 PstI and EcoRI restriction sites. The graphical illustration of this construct design is shown below:
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<html>
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<center>
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<img src="https://static.igem.wiki/teams/5152/part-registry/img-0669.png" width="800">
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</center>
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</html>
  
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This composite part includes: A constitutive strong promoter (<partinfo>BBa_J23100</partinfo>), a strong ribosome binding site (<partinfo>BBa_B0034</partinfo>), The tsPurple coding sequence (<partinfo>BBa_K1033906</partinfo>), and a strong double terminator (<partinfo>BBa_B0015</partinfo>). Additionally, the 5' and 3' ends feature a 20 base pair overlap sequence for NEBuilder HiFi assembly using the pUC19 PstI and EcoRI restriction sites.
 
  
 
The purpose of this part in our project includes:
 
The purpose of this part in our project includes:
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1. Ensuring successful protein expression in our E. coli strain under lab conditions.
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<ol>
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2. Verifying that the expressed protein colors match expected results.
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<li>Ensuring successful protein expression in our <i>E. coli</i> strain under lab conditions.</li>
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3. Using these constructs to validate our cloning process and experimental setup.
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<li>Verifying that the expressed protein colours match expected results.</li>
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4. Employing these constructs as positive controls for future experiments.
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<li>Using these constructs to validate our cloning process and experimental setup.</li>
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<li>Employing these constructs as positive controls for future experiments.</li>
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</ol>
  
 
===Usage and Biology===
 
===Usage and Biology===
 
<b>Successful Expression of Chromoproteins</b>
 
<b>Successful Expression of Chromoproteins</b>
  
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We selected five chromoproteins as potential biosensor candidates: tsPurple (<partinfo>BBa_K1033906</partinfo>), eforRed (<partinfo>BBa_K592012</partinfo>), cjBlue (<partinfo>BBa_K592011</partinfo>), amilCP (<partinfo>BBa_K592009</partinfo>), and dTomato (<partinfo>BBa_K4813000</partinfo>). Our 2023 team constructed dTomato, which showed promising coloration and stable expression.
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We selected five chromoproteins as potential biosensor candidates: tsPurple (<partinfo>BBa_K1033906</partinfo>), eforRed (<partinfo>BBa_K592012</partinfo>), cjBlue (<partinfo>BBa_K592011</partinfo>), amilCP (<partinfo>BBa_K592009</partinfo>), and dTomato (<partinfo>BBa_K4813000</partinfo>). Our 2023 team constructed dTomato, which showed promising colouration and stable expression. The expression constructs of the above chromoproteins are tsPurple (<partinfo>BBa_K5152000</partinfo>), eforRed (<partinfo>BBa_K5152003</partinfo>), cjBlue (<partinfo>BBa_K5152001</partinfo>), amilCP (<partinfo>BBa_K5152002</partinfo>), and dTomato (<partinfo>BBa_K4813005</partinfo>).
  
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Successful expression was observed for most proteins after 12 hours of incubation, except cjBlue, which displayed color after 24 hours, making it less ideal for our project.
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To simplify observation, we centrifuged 1 mL of the culture at 8000g for 2 minutes to form a pellet and then observed the colour.
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<html>
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<center>
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<img src="https://static.igem.wiki/teams/5152/part-registry/4-pellet-of-chromoproteins.webp" alt="Pellets of chromorproteins" width="500">
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<figcaption><u>Fig. 1 The pellets we obtained from our <i>E. coli</i> cells expressing chromoproteins.</u> </figcaption>
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</center>
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</html>
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Successful expression was observed for most proteins after 12 hours of incubation, except cjBlue, which displayed colour after 24 hours, making it less ideal for our project.
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<html>
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<center>
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<img src="https://static.igem.wiki/teams/5152/part-registry/3-cjblue-weak.webp" alt="Weak cjBlue" width="500">
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<figcaption><u>Fig. 2 After 12 hours of incubation, most of the cjBlue expressing cells did not display the expected colour.</u> </figcaption>
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</center>
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</html>
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<html>
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<center>
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<img src="https://static.igem.wiki/teams/5152/part-registry/chromoprotein-plates.webp" alt="chromoproteins" width="500">
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<figcaption><u>Fig. 3 After incubating for at least 24 hours, the cjBlue plates have finally displayed the expected colouration.</u> </figcaption>
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</center>
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</html>
  
 
<b>Expression Properties</b>
 
<b>Expression Properties</b>
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Diagrams below show results from the 12-hour and 18-hour time points for reference.
 
Diagrams below show results from the 12-hour and 18-hour time points for reference.
  
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<html>
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<center>
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<img src="https://static.igem.wiki/teams/5152/part-registry/5-6-chromo-after-12-18-hours.webp" alt="chromoprotein 12 vs 18 hr" width="800">
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<figcaption><u>Fig. 4 Pellets of <i>E. coli</i> cells expressing chromoproteins after 12 and 18 hours of incubation at 37°C, 180 rpm.</u> </figcaption>
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</center>
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</html>
  
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From the result above, we found that at least 12 hours are needed for the cells to develop enough color for clear reading. While waiting around 18 hours gives more noticeable results, we noticed that in cells with metal-sensing constructs, longer incubation can cause unwanted chromoprotein expression, leading to false positives. It's important to set a specific time and threshold for our hardware to ensure accurate detection without extended incubation.
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From the result above, we found that at least 12 hours are needed for the cells to develop enough colour for clear reading. While waiting around 18 hours gives more noticeable results, we noticed that in cells with metal-sensing constructs, longer incubation can cause unwanted chromoprotein expression, leading to false positives. It's important to set a specific time and threshold for our measurement to ensure accurate detection without extended incubation.
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<span class='h3bb'>Sequence and Features</span>
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<span class='h3bb'><b>Sequence and Features</b></span>
 
<partinfo>BBa_K5152000 SequenceAndFeatures</partinfo>
 
<partinfo>BBa_K5152000 SequenceAndFeatures</partinfo>
  

Latest revision as of 11:41, 30 September 2024

Constitutive tsPurple Chromoprotein Expression

Our team designed this composite part to verify and compare the expression of chromoprotein reporters. Our project aims to develop biosensors for heavy metals that don't require specialized equipment for measurement. Therefore, we chose chromoproteins instead of fluorescence or luciferase.

This composite part includes: A constitutive strong promoter (BBa_J23100), a strong ribosome binding site (BBa_B0034), the tsPurple coding sequence (BBa_K1033906), and a strong double terminator (BBa_B0015). Additionally, the 5' and 3' ends feature a 20 base pair overlap sequence for NEBuilder HiFi assembly using the pUC19 PstI and EcoRI restriction sites. The graphical illustration of this construct design is shown below:


The purpose of this part in our project includes:

  1. Ensuring successful protein expression in our E. coli strain under lab conditions.
  2. Verifying that the expressed protein colours match expected results.
  3. Using these constructs to validate our cloning process and experimental setup.
  4. Employing these constructs as positive controls for future experiments.

Usage and Biology

Successful Expression of Chromoproteins

We selected five chromoproteins as potential biosensor candidates: tsPurple (BBa_K1033906), eforRed (BBa_K592012), cjBlue (BBa_K592011), amilCP (BBa_K592009), and dTomato (BBa_K4813000). Our 2023 team constructed dTomato, which showed promising colouration and stable expression. The expression constructs of the above chromoproteins are tsPurple (BBa_K5152000), eforRed (BBa_K5152003), cjBlue (BBa_K5152001), amilCP (BBa_K5152002), and dTomato (BBa_K4813005).

To simplify observation, we centrifuged 1 mL of the culture at 8000g for 2 minutes to form a pellet and then observed the colour.

Pellets of chromorproteins
Fig. 1 The pellets we obtained from our E. coli cells expressing chromoproteins.

Successful expression was observed for most proteins after 12 hours of incubation, except cjBlue, which displayed colour after 24 hours, making it less ideal for our project.

Weak cjBlue
Fig. 2 After 12 hours of incubation, most of the cjBlue expressing cells did not display the expected colour.

chromoproteins
Fig. 3 After incubating for at least 24 hours, the cjBlue plates have finally displayed the expected colouration.

Expression Properties

We characterized the expression properties by focusing on the time required for visible results.

Cells were cultured and harvested at 4, 8, 12, 18, and 24 hours. At each time point, 1 mL of culture was centrifuged at 8,000 g for 2 minutes to obtain cell pellets for observation.

Diagrams below show results from the 12-hour and 18-hour time points for reference.

chromoprotein 12 vs 18 hr
Fig. 4 Pellets of E. coli cells expressing chromoproteins after 12 and 18 hours of incubation at 37°C, 180 rpm.

From the result above, we found that at least 12 hours are needed for the cells to develop enough colour for clear reading. While waiting around 18 hours gives more noticeable results, we noticed that in cells with metal-sensing constructs, longer incubation can cause unwanted chromoprotein expression, leading to false positives. It's important to set a specific time and threshold for our measurement to ensure accurate detection without extended incubation.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 35
    Illegal NheI site found at 58
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]