Difference between revisions of "Part:BBa K2918009"

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(References)
 
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<partinfo>BBa_K2918009 short</partinfo>
 
<partinfo>BBa_K2918009 short</partinfo>
  
A T7 promoter variant with strength that should give 50% expression compared to T7 promoter. The T7 promoter variant contains a binding site for TALE protein
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T7 promoter variant with about 50% strength relative to wild type T7 promoter and has been engineered to contain a binding site for TALE repressor.
  
 
<span class='h3bb'>Sequence and Features</span>
 
<span class='h3bb'>Sequence and Features</span>
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===Usage and Biology===
 
===Usage and Biology===
The <html> <a target=”_blank” href=”https://parts.igem.org/Part:BBa_K2918006”>0.5 T7 promoter variant</a> </html> was engineered to contain a binding site for a Transcriptional Activator like Effector protein (TALE). TALE proteins consist of repeats where 12th and 13th amino acids can vary, the repeats are called the repeat variable diresidue (RVD) <html><a href="#Segall2018">(Segall-Shapiro et al., 2018)</a></html>. These RVDs have been shown to bind to DNA in a simple one-to-one binding code. A unique 18bp binding site was incorporated into the promoter, this binding site recruits a specific TALE protein called TALEsp1 that acts as a repressor <html><a href="#Segall2018">(Segall-Shapiro et al., 2018)</a></html>. The TALEsp1 protein was designed to bind protein specifically at the binding site and are predicted not be bind anywhere in the <i> E.coli </i> genome. The position of the binding site can be readjusted to alter the extent of repression by the TALE protein.
+
The <html> <a href="https://parts.igem.org/Part:BBa_K2918006">medium T7 promoter variant</a> </html> was engineered to contain a binding site for a Transcriptional Activator like Effector protein (TALE). TALE proteins consist of repeats where 12th and 13th amino acids can vary, the repeats are called the repeat variable diresidue (RVD) <html><a href="#Segall2018">(Segall-Shapiro et al., 2018)</a></html>. These RVDs have been shown to bind to DNA in a simple one-to-one binding code. A unique 18bp binding site was incorporated into the promoter, this binding site recruits a specific TALE protein called <html> <a href="https://parts.igem.org/Part:BBa_K2918008">TALEsp1</a> </html> that acts as a repressor <html><a href="#Segall2018">(Segall-Shapiro et al., 2018)</a></html>. The TALEsp1 protein was designed to bind protein specifically at the binding site and are predicted not to bind anywhere in the <i> E. coli </i> genome. The position of the binding site can be readjusted to alter the extent of repression by the TALE protein.
 +
<div><ul>
 +
<center>
 +
  <li style="display: inline-block;"> [[File:T--TUDelft--T7.png|thumb|none|550px|<b>Figure 1: Design of TALEsp1-regulated version of T7 promoter variants was done by annexing the operator sequence directly downstream of the 23 base pair promoter.  </b>]] </li>
 +
</center>
 +
    </ul></div>
  
 
===Strain Construction===
 
===Strain Construction===
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===Modular Cloning===
 
===Modular Cloning===
Modular Cloning (MoClo) is a system which allows for efficient one pot assembly of multiple DNA fragments. The MoClo system consists of Type IIS restriction enzymes that cleave DNA 4 to 8 base pairs away from the recognition sites. Cleavage outside of the recognition site allows for customization of the overhangs generated. The MoClo system is hierarchical. First, basic parts (promoters, UTRs, CDS and terminators) are assembled in level 0 plasmids in the kit. In a single reaction, the individual parts can be assembled into vectors containing transcriptional units (level 1). Furthermore, MoClo allows for directional assembly of multiple transcriptional units. Successful assembly of constructs using MoClo can be confirmed by visual readouts (blue/white or red/white screening).
+
Modular Cloning (MoClo) is a system which allows for efficient one pot assembly of multiple DNA fragments <html><a href="#Weber2011">(Weber et al., 2011)</a></html>. The MoClo system consists of Type IIS restriction enzymes that cleave DNA 4 to 8 base pairs away from the recognition sites. Cleavage outside of the recognition site allows for customization of the overhangs generated. The MoClo system is hierarchical. First, basic parts (promoters, UTRs, CDS and terminators) are assembled in level 0 plasmids in the kit. In a single reaction, the individual parts can be assembled into vectors containing transcriptional units (level 1). Furthermore, MoClo allows for directional assembly of multiple transcriptional units. Successful assembly of constructs using MoClo can be confirmed by visual readouts (blue/white or red/white screening).
 
Click <html><a href="http://2019.igem.org/Team:TUDelft/Experiments" target="_blank">here</a> </html> for the protocol.  
 
Click <html><a href="http://2019.igem.org/Team:TUDelft/Experiments" target="_blank">here</a> </html> for the protocol.  
  
  
<b>Note: The basic parts sequences of the Sci-Phi 29 collection in the registry contain only the part sequence and therefore contain no overhangs or restriction sites. For synthesizing MoClo compatible parts, refer to table 2. The complete sequence of our parts including backbone can be found <html><a href="http://2019.igem.org/Team:TUDelft/Experiments" target="_blank">here</a>.</html></b>
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<b>Note: The basic parts sequences of the Sci-Phi 29 collection in the registry contain only the part sequence and therefore contain no overhangs or restriction sites. For synthesizing MoClo compatible parts, refer to table 2. </b>
  
  
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     </body>
 
     </body>
 
</html>
 
</html>
 
  
 
===Characterization===
 
===Characterization===
  <p> The 0.5 T7<sub>sp1</sub> was characterized by comparing it to our <html><body><a href="https://parts.igem.org/Part:BBa_K2918010"> T7<sub>sp1<sub> promoter</a></body></html>, to see the relative strength of the promoter in our constructs. As a reporter, a GFP fluorescence readout was used.  In order to measure fluorescence, we use a flow cytometer.  <br>
 
 
The GFP used as readout was our <html><body><a href="https://parts.igem.org/Part:BBa_K2918037"> harmonized eGFP </a></body></html>. The ribosome binding site was our <html><body><a href="https://parts.igem.org/Part:BBa_K2918014"> Universal RBS </a></body></html>. All of these parts were cloned into a level 1 backbone <html><body><a href="http://www.addgene.org/47761/"> pICH47761 </a></body></html>
 
<br>
 
  
The protocol for preparation of samples for the flow cytometry assay is as follows:
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<p>The strength of the medium T7<sub>sp1</sub> promoter was characterized by comparing it to <html><a href="https://parts.igem.org/Part:BBa_K2918010"> T7<sub>sp1</sub> promoter</a></body></html>. For comparision of the promoter strengths, the two promoters were cloned in the same backbone <html><body><a href="http://www.addgene.org/47761/">(pICH47761)</a></body></html> and were paired with the same RBS <html><body><a href="https://parts.igem.org/Part:BBa_K2918014"> (Universal RBS)</a></body></html>. The strengths were compared by measuring fluorescence readout from <html><body><a href="https://parts.igem.org/Part:BBa_K2918037"> harmonized GFP </a></body></html> by flow cytometry and <i> E. coli </i> BL21 (DE3) cells were used as blank. FCSalyzer v.0.9.18-alpha was used to analyze data from the flow cytometry experiment. Click <html><a href="http://2019.igem.org/Team:TUDelft/Experiments" target="_blank">here</a> </html> for the protocol.
<html>
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<body>
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<ol>
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<li>Samples were grown overnight</li>
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<li>Overnight cultures were diluted to OD = 0.01 into 1 mL, and grow for 2 hours on 37 degrees 250 rpm shaking in 2 mL Eppendorf tubes. </li>
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<li>Overnight cultures were diluted 1:100 into 5 mL, and grow for 4 hours on 37 degrees 250 rpm shaking in 50 mL eppendorf tubes. Induce with 1 mM IPTG where necessary </li>
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<li>Samples were kept at 4 degrees for 1 hour </li>
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</ol>
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</body>
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</html>
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<br>
 
<br>
  
In the measurement, <i>E. coli Top 10</i> cells without a plasmid were used as a reference. The gating for flow cytometry was determined by eye by selecting the densest region of the blank. Furthermore, the fluorescence histogram was gated to discern between cells that were 'on' and 'off', as in expressing fluorescence or not. Only cells of similar forward and side scatter were compared.  The median fluorescence intensity of the blank is subtracted from the fluorescence intensity of the samples to correct for autofluorescence. In figure 1 we plot the corrected fluorescence of the samples. Figure 2 shows the gating based on size and figure 3 shows the fluorescence histogram of each sample. </p>
 
  
<html><body><img src = "https://2019.igem.org/wiki/images/0/00/T--TUDelft--T7characterisation.svg" alt="Modeling" style="width:60%";></body></html>
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The scatter plot in figure 2 was used to gate the most dense cell regions of the blank and the same gating was considered to obtain the fluorescence values depicted in figure 3. Cells of similar forward and side scatter were compared.</p>  
<html><body><figcaption><br><b>Figure 1: Fluorescence values of T7, T7sp1 with median fluorescence of <i>E. coli Top 10</i> cells without a plasmid substracted. </b></figcaption></body></html>
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<br>
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<p>Figure 1 shows that the strength of T7<sub>sp1</sub> in <i>E. coli</i> is very similar to T7 promoter. We can thus conclude that adding the binding site for TALEsp1 does not influence the strength of the promoter.
 
<br> <br>
 
  
<html><body><img src = "https://2019.igem.org/wiki/images/e/eb/T--TUDelft--0.5T7sp1charsscatter.png" alt="Modeling" style="width:60%";></body></html>
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<div><ul>  
<html><body><figcaption><br><b>Figure 2: Scatter plot of forward and side scatter of <i>E. coli Top 10</i> cells without a plasmid. The region selected is the gating we considered to obtain the values depicted in figure 1. </b></figcaption></body></html>
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<center>
<br>
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  <li style="display: inline-block;"> [[File:T--TUDelft--0.5T7sp1charsscatter.png|thumb|none|550px|<b>Figure 2: Scatter plot of forward and side scatter of <i>E. coli</i> BL21 (DE3) cells. </b>]] </li>
 +
</center>
 +
    </ul></div>
  
<html><body><img src = "https://2019.igem.org/wiki/images/0/07/T--TUDelft--0.5T7sp1charsfluorescence.png" alt="Modeling" style="width:60%";></body></html>
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<html><body><figcaption><br><b>Figure 3: Raw fluorescence values. Black is <i>E. coli Top 10</i> cells without a plasmid. Red is T7<sub>sp1</sub> and blue is 0.5 T7<sub>sp1<sub> </b></figcaption></body></html>
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<p>Gating was performed on the data in the fluorescence histogram (figure 3) to discern between fluorescent and non-fluorescent cells. </p>
<br>
+
 
 +
<div><ul>
 +
<center>
 +
  <li style="display: inline-block;"> [[File:T--TUDelft--0.5T7sp1charsfluorescence.png|thumb|none|550px|<b>Figure 3 Raw fluorescence data. The curves represent fluorscenece values of <i>E. coli</i> BL21 (DE3) cells (black), clones with GFP expressed from T7<sub>sp1</sub> (red) and clones with GFP expressed from T7<sub>sp1</sub> (blue).</b>]] </li>
 +
</center>
 +
    </ul></div>
 +
 
 +
<p> From figure 3 the median fluorescence intensity of the two samples was obtained and corrected by the fluorescence of <i>E. coli</i> BL21 (DE3). Figure 4 depicts the fluorescence of GFP expression controlled by T7<sub>sp1</sub> and medium T7<sub>sp1</sub>.
 +
</p>
 +
 
 +
<div><ul>
 +
<center>
 +
  <li style="display: inline-block;"> [[File:T--TUDelft--T7characterisation.png|thumb|none|550px|<b>Figure 4: Fluorescence values of medium T7sp1 and T7sp1. For correction of background fluorescence, <i>E. coli </i> BL21 (DE3) cells without a plasmid were used. </b>]] </li>
 +
</center>
 +
    </ul></div>
 +
 
 +
<p>Figure 4 shows that the strength of medium T7<sub>sp1</sub> is approximately 64% relative to T7<sub>sp1</sub> promoter. We can thus conclude that the binding site for TALEsp1 does not influence the strength of the promoter as the strength of medium T7 promoter has been shown to be 50% of wild type T7 promoter <html><a href="#Komura2018">(Komura et al., 2018)</a></html>
 +
<br> <br>
  
 
===References===
 
===References===
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<a id="Segall2018" href="https://www.nature.com/articles/nbt.4111" target="_blank">
 
<a id="Segall2018" href="https://www.nature.com/articles/nbt.4111" target="_blank">
 
Segall-Shapiro, T. H., Sontag, E. D., & Voigt, C. A. (2018). Engineered promoters enable constant gene expression at any copy number in bacteria. <i>Nature Biotechnology</i>, 36(4), 352–358.</a>
 
Segall-Shapiro, T. H., Sontag, E. D., & Voigt, C. A. (2018). Engineered promoters enable constant gene expression at any copy number in bacteria. <i>Nature Biotechnology</i>, 36(4), 352–358.</a>
 +
</li>
 +
<li>
 +
<a id="Weber2011" href="https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0016765" target="_blank">
 +
Weber, E., Engler, C., Gruetzner, R., Werner, S., & Marillonnet, S. (2011). A Modular Cloning System for Standardized Assembly of Multigene Constructs. Plos ONE, 6(2), e16765. doi: 10.1371/journal.pone.0016765 </a>
 +
<li>
 +
<a id="Segall2018" href="https://www.nature.com/articles/nbt.4111" target="_blank">
 +
Segall-Shapiro, T. H., Sontag, E. D., & Voigt, C. A. (2018). Engineered promoters enable constant gene expression at any copy number in bacteria. <i>Nature Biotechnology</i>, 36(4), 352–358.</a>
 +
</li>
 +
<li>
 +
<a id="Komura2018" href="https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0196905" target="_blank">
 +
Komura, R., Aoki, W., Motone, K., Satomura, A., & Ueda, M. (2018). High-throughput evaluation of T7 promoter variants using biased randomization and DNA barcoding. PLOS ONE, 13(5), e0196905. doi: 10.1371/journal.pone.0196905 </a>
 
</li>
 
</li>
 
</ul>
 
</ul>
 
 
</html>
 
</html>
 +
 +
  
  

Latest revision as of 17:46, 6 December 2019

Medium T7sp1 promoter

T7 promoter variant with about 50% strength relative to wild type T7 promoter and has been engineered to contain a binding site for TALE repressor.

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]

This part has been confirmed by sequencing and has no mutations.

Usage and Biology

The medium T7 promoter variant was engineered to contain a binding site for a Transcriptional Activator like Effector protein (TALE). TALE proteins consist of repeats where 12th and 13th amino acids can vary, the repeats are called the repeat variable diresidue (RVD) (Segall-Shapiro et al., 2018). These RVDs have been shown to bind to DNA in a simple one-to-one binding code. A unique 18bp binding site was incorporated into the promoter, this binding site recruits a specific TALE protein called TALEsp1 that acts as a repressor (Segall-Shapiro et al., 2018). The TALEsp1 protein was designed to bind protein specifically at the binding site and are predicted not to bind anywhere in the E. coli genome. The position of the binding site can be readjusted to alter the extent of repression by the TALE protein.

  • Figure 1: Design of TALEsp1-regulated version of T7 promoter variants was done by annexing the operator sequence directly downstream of the 23 base pair promoter.

Strain Construction

The DNA sequence of the part was synthesized by IDT with flanking BpiI sites and respective MoClo compatible coding sequence overhangs. The part was then cloned in a level 0 MoClo backbone pICH41233 and the sequence was confirmed by sequencing. The cloning protocol can be found in the MoClo section below.

Modular Cloning

Modular Cloning (MoClo) is a system which allows for efficient one pot assembly of multiple DNA fragments (Weber et al., 2011). The MoClo system consists of Type IIS restriction enzymes that cleave DNA 4 to 8 base pairs away from the recognition sites. Cleavage outside of the recognition site allows for customization of the overhangs generated. The MoClo system is hierarchical. First, basic parts (promoters, UTRs, CDS and terminators) are assembled in level 0 plasmids in the kit. In a single reaction, the individual parts can be assembled into vectors containing transcriptional units (level 1). Furthermore, MoClo allows for directional assembly of multiple transcriptional units. Successful assembly of constructs using MoClo can be confirmed by visual readouts (blue/white or red/white screening). Click here for the protocol.


Note: The basic parts sequences of the Sci-Phi 29 collection in the registry contain only the part sequence and therefore contain no overhangs or restriction sites. For synthesizing MoClo compatible parts, refer to table 2.


Table 1: Overview of different level in MoClo

Level Basic/Composite Type Enzyme
Level 0 Basic Promoters, 5’ UTR, CDS and terminators BpiI
Level 1 Composite Transcriptional units BsaI
Level 2/M/P Composite Multiple transcriptional units BpiI

For synthesizing basic parts, the part of interest should be flanked by a BpiI site and its specific type overhang. These parts can then be cloned into the respective level 0 MoClo parts. For level 1, where individual transcriptional units are cloned, the overhangs come from the backbone you choose. The restriction sites for level 1 are BsaI. However, any type IIS restriction enzyme could be used.


Table 2: Type specific overhangs and backbones for MoClo. Green indicates the restriction enzyme recognition site. Blue indicates the specific overhangs for the basic parts

Basic Part Sequence 5' End Sequence 3' End Level 0 backbone
Promoter NNNN GAAGAC NN GGAG TACT NN GTCTTC NNNN pICH41233
5’ UTR NNNN GAAGAC NN TACT AATG NN GTCTTC NNNN pICH41246
CDS NNNN GAAGAC NN AATG GCTT NN GTCTTC NNNN pICH41308
Terminator NNNN GAAGAC NN GCTT CGCT NN GTCTTC NNNN pICH41276

Characterization

The strength of the medium T7sp1 promoter was characterized by comparing it to T7sp1 promoter. For comparision of the promoter strengths, the two promoters were cloned in the same backbone (pICH47761) and were paired with the same RBS (Universal RBS). The strengths were compared by measuring fluorescence readout from harmonized GFP by flow cytometry and E. coli BL21 (DE3) cells were used as blank. FCSalyzer v.0.9.18-alpha was used to analyze data from the flow cytometry experiment. Click here for the protocol.
The scatter plot in figure 2 was used to gate the most dense cell regions of the blank and the same gating was considered to obtain the fluorescence values depicted in figure 3. Cells of similar forward and side scatter were compared.


  • Figure 2: Scatter plot of forward and side scatter of E. coli BL21 (DE3) cells.


Gating was performed on the data in the fluorescence histogram (figure 3) to discern between fluorescent and non-fluorescent cells.

  • Figure 3 Raw fluorescence data. The curves represent fluorscenece values of E. coli BL21 (DE3) cells (black), clones with GFP expressed from T7sp1 (red) and clones with GFP expressed from T7sp1 (blue).

From figure 3 the median fluorescence intensity of the two samples was obtained and corrected by the fluorescence of E. coli BL21 (DE3). Figure 4 depicts the fluorescence of GFP expression controlled by T7sp1 and medium T7sp1.

  • Figure 4: Fluorescence values of medium T7sp1 and T7sp1. For correction of background fluorescence, E. coli BL21 (DE3) cells without a plasmid were used.

Figure 4 shows that the strength of medium T7sp1 is approximately 64% relative to T7sp1 promoter. We can thus conclude that the binding site for TALEsp1 does not influence the strength of the promoter as the strength of medium T7 promoter has been shown to be 50% of wild type T7 promoter (Komura et al., 2018)

References