Difference between revisions of "Part:BBa K4579000"

 
 
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<partinfo>BBa_K4579000 short</partinfo>
 
<partinfo>BBa_K4579000 short</partinfo>
  
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<h1>Introduction</h1>
 +
The 2023 UT Austin iGEM Team’s modular microcin expression parts collection includes parts necessary for engineering a bacterial chassis to secrete microcins, a type of small antimicrobial peptide. Our team has specifically designed parts to engineer a modular two-plasmid system that facilitates extracellular secretion of microcins by the chassis. One plasmid contains the microcin with a signal peptide sequence that indicates to the cell that the microcin is to be secreted. The other plasmid (pSK01) is from the literature (Kim et al., 2023) and contains genes for the proteins CvaA and CvaB, which are necessary to secrete small peptides using the <i>E. coli</i> microcin V (MccV) type I secretion system (T1SS) shown in Figure 2 of our <html><a href="https://2023.igem.wiki/austin-utexas/description">Project Description.</a></html>
  
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<!-- Add more about the biology of this part here
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Our parts collection includes a a selection of promoter (Type 2), coding sequence (Type 3), and terminator/regulatory gene (Type 4) parts that can be easily assembled to express microcins either constitutively or under inducible control. This allows for the modular engineering of microcin expression plasmids containing various microcins that can undergo extracellular secretion when used in conjunction with the secretion system plasmid pSK01.
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===Usage and Biology===
+
 
 +
<html><center><img src=https://static.igem.wiki/teams/4579/wiki/parts-collection-by-type.jpeg style="width:900px;height:auto;"></center></html>
 +
<center><b>Figure 1.</b> <i>Basic parts categorized by their BTK/YTK part type. Type 3p and 3q parts assemble as if they were a single Type 3 part.</i> </center>
 +
 
 +
Our basic and composite parts follow the Bee Toolkit/Yeast Toolkit standard of Golden Gate assembly (Lee et al., 2015; Leonard et al., 2018). Our assembly method involves the use of BsmBI digestion-ligation to create basic parts which can then be further digested with BsaI and ligated to form composite parts. The BTK/YTK standard includes part type-specific prefix and suffix overhangs generated by BsaI for each part, and these overhangs are NOT included in their sequences in the registry. For reference, our standard’s part type-specific overhangs are listed in Figure 2 on our <html><a href=" https://2023.igem.wiki/austin-utexas/parts">Parts page</a></html>.
 +
 
 +
<h1>Categorization</h1>
 +
 
 +
===Basic parts===
 +
<ul>
 +
<li><b>Promoters (Type 2)</b> – Seven inducible promoters selected due to their relatively high dynamic range (Meyer et al., 2019) and apparent functionality in a variety of Proteobacteria (Schuster & Reisch, 2021), and one constitutive CP25 promoter (Leonard et al., 2018).</li>
 +
 
 +
<li><b>Coding Sequences (Type 3)</b> – Signal peptide + microcin fusion coding sequences, a green fluorescent protein gene, and secretion system genes <i>cvaA</i> and <i>cvaB</i> which are together referred to as CvaAB.</li>
 +
 
 +
<li><b>Terminators/Regulatory Genes (Type 4)</b> – An <i>rpoC</i> terminator plus a collection of seven regulatory genes, each associated with one of our seven inducible promoters.</li>
 +
</ul>
 +
 
 +
===Composite parts===
 +
<ul>
 +
<li><b>Constitutive Microcin Expression Assemblies</b> - Assemblies of microcins (some with immunity proteins) with a constitutive CP25 promoter and <i>rpoC</i> terminator. These function alongside pSK01 in a two-plasmid secretion system, and we use these two-plasmid systems to assess if our novel microcins are effective inhibitors of pathogenic targets.</li>
 +
 
 +
<li><b>Inducible GFP Expression Assemblies</b> – Assemblies of GFP under the control of various inducible promoter systems. These were used to assess the dynamic range of our inducible promoter systems.</li>
 +
 
 +
<li><b>Inducible Microcin Expression Assemblies</b> – Assemblies of select microcins under the control of an inducible promoter system.</li>
 +
</ul>
 +
 
 +
 
 +
 
 +
<h1>Usage and Biology</h1>
 +
This part consists of the P<sub>tet*</sub> promoter upstream of a ribosome binding site, with a hammerhead ribozyme (HHRz) sequence included in the intervening 5' untranslated region to insulate gene expression levels from coding sequence effects on mRNA structure. This promoter can be bound by TetR (<html><a href="https://parts.igem.org/Part:BBa_K4579026">BBa_K4579026</a></html>), a transcriptional repressor that can be removed from the promoter when bound by anhydrotetracycline (aTc), allowing for the selective induction of transcription in cells containing both P<sub>tet*</sub> and the <i>tetR</i> gene. This part can be used as a Type 2 part in the BTK/YTK standard.
 +
 
 +
==Composite Parts==
 +
<html><center><img src=https://static.igem.wiki/teams/4579/wiki/part-inducible-promoter.jpeg style="width:700px;height:auto;"></center></html>
 +
<center><b>Figure 2.</b> <i>The general schematic for our inducible microcin and GFP expression assemblies with emphasis on the inducible promoter. Although this example contains an immunity protein sequence, not all of our inducible microcin expression parts include an immunity protein.</i></center>
 +
 
 +
 
 +
<ul>
 +
<li>TetR regulated Mcc04 + IP expression plasmid (<html><a href="https://parts.igem.org/Part:BBa_K4579056">BBa_K4579056</a></html>)</li>
 +
<li>TetR regulated Mcc04 expression plasmid (<html><a href="https://parts.igem.org/Part:BBa_K4579057">BBa_K4579057</a></html>)</li>
 +
<li>TetR regulated GFP expression plasmid (<html><a href="https://parts.igem.org/Part:BBa_K4579061">BBa_K4579061</a></html>)</li>
 +
</ul>
 +
 
 +
<h1>Design Notes</h1>
 +
When creating our inducible promoter parts, we used the YFP-expressing individual sensor plasmids from the <i>E. coli</i> ‘Marionette’ paper as PCR templates (Meyer et al., 2019), as these include inducible promoters and their regulatory transcription factors on a standardized backbone. Due to the homology of the backbone between these plasmids, we created universal primers that allowed us to amplify the promoter from any one of the sensor plasmids. One big design complication in this process was the fact that the YFP-expressing sensor plasmids all contained a BsaI site in the region just upstream of the promoter where one of the universal primers would bind. We designed our primers to create a single point mutation in order to mutate out this illegal BsaI site.
 +
 
 +
<h1>Characterization</h1>
 +
​​Below is the fluorescence characterization data for the four inducible promoter-regulator systems that we tested in composite parts using a GFP reporter gene (<html><a href="https://parts.igem.org/Part:BBa_K4579035">BBa_K4579035</a></html>). The table below lists the inducible promoters within our parts collection, their basic part numbers, and their composite part numbers with the GFP reporter.  Below that, the first figure shows fluorescence/OD600 data for the characterization of our inducible GFP assemblies in <i>E. coli</i> DH5α. This first experiment was done as a proof of concept to test whether our inducible GFP assemblies were functional. After confirming functionality of the assemblies by measuring levels of fluorescence under induced and non-induced conditions, we moved on to testing the assemblies in <i>Pantoea agglomerans</i> PNG92-11 in order to determine whether these inducible promoter systems are functional in <i>Pantoea</i>. This data confirms the functionality of our inducible promoter systems in <i>Pantoea</i>.
 +
<center>
 +
 
 +
{| class="wikitable"
 +
|+ This table summarizes which of the basic type 2 promoter parts we created and characterized by assembling into a level 1 composite part and running the following fluorescence experiments on.
 +
|-
 +
! Short Description
 +
! Basic Part ID
 +
! Composite Part (with GFP, Regulator and Terminator)
 +
|-
 +
| PTet* promoter + RBS
 +
| <html><a href="https://parts.igem.org/Part:BBa_K4579000">BBa_K4579000</a></html>
 +
| <html><a href="https://parts.igem.org/Part:BBa_K4579061">BBa_K4579061</a></html>
 +
|-
 +
| PTac promoter + RBS
 +
| <html><a href="https://parts.igem.org/Part:BBa_K4579001">BBa_K4579001</a></html>
 +
| <html><a href="https://parts.igem.org/Part:BBa_K4579056">BBa_K4579058</a></html>
 +
|-
 +
| PLuxB promoter + RBS
 +
| <html><a href="https://parts.igem.org/Part:BBa_K4579002">BBa_K4579002</a></html>
 +
| None
 +
|-
 +
| PCymRC promoter + RBS
 +
| <html><a href="https://parts.igem.org/Part:BBa_K4579003">BBa_K4579003</a></html>
 +
| None
 +
|-
 +
| PBAD promoter + RBS
 +
| <html><a href="https://parts.igem.org/Part:BBa_K4579004">BBa_K4579004</a></html>
 +
| None
 +
|-
 +
| PVanCC promoter + RBS
 +
| <html><a href="https://parts.igem.org/Part:BBa_K4579005">BBa_K4579005</a></html>
 +
| <html><a href="https://parts.igem.org/Part:BBa_K4579059">BBa_K4579059</a></html>
 +
|-
 +
| PCin promoter + RBS
 +
| <html><a href="https://parts.igem.org/Part:BBa_K4579056">BBa_K4579006</a></html>
 +
| <html><a href="https://parts.igem.org/Part:BBa_K4579056">BBa_K4579060</a></html>
 +
|}
 +
</center>
 +
 
 +
<center>
 +
===Characterization Assays===
 +
</center>
 +
 
 +
<html><center><img src=https://static.igem.wiki/teams/4579/wiki/dh5afluorescenceassayforreal.png style="width:600px;height:auto;"></center></html>
 +
<p>
 +
<center><b>Figure 3.</b> <i> This displays the dynamic range of all the inducible promoters we were able to characterize in E. Coli DH5α. + indicates the presence of inducer in the overnight culture and – indicates a lack of inducer in the overnight culture. A mean of all three fluorescence readings divided by mean OD600 were plotted on a bar graph. Standard deviation of readings was used to create error bars. </i></center>
 +
</p>
 +
<p>
 +
To test each of the inducible promoter systems we incorporated them with GFP into composite parts (BBa_K4579058, BBa_K4579059, BBa_K4579060, BBa_K4579061). The parts were sequence confirmed and subsequently transformed into DH5α. Inducers were added using the following volumes (LacI: 50 µL of 0.1 M IPTG, VanR: 5 µL of 100 mM vanillic acid, CinR: 5 uL of 10 mM OHC14, TetR: 18 µL of a ~54 µM stock). These cultures were then loaded into a clear backed 96 well plate (in triplicate) and into a plate reader. A single fluorescence reading was taken using Ex: 485, Em: 535 (Elston et al., 2023). 
 +
</p>
 +
 
 +
<html><center><img src=https://static.igem.wiki/teams/4579/wiki/1597fluorescenceassay.png style="width:600px;height:auto;"></center></html>
 +
<p>
 +
<center><b>Figure 4.</b> <i>This displays the dynamic range of all the inducible promoters we were able to characterize in P. Agglomerans with the T1SS. + indicates the presence of inducer in the overnight culture and – indicates a lack of inducer in the overnight culture. A mean of all three fluorescence readings divided by mean OD600 were plotted on a bar graph. Standard deviation of readings was used to create error bars.</i></center>
 +
</p>
 +
<p>
 +
In order to test our inducible promoters in a chassis organism with a secretion system we transformed our inducible GFP expression plasmids into a <i>P. Agglomerans </i>  strain with a native T1SS. We opted to not use the LacI regulatory system (BBa_K4579058) since it had high levels of expression in the absence of inducer. 5 ml induced and uninduced overnight cultures were created per each strain. Inducers were added using the following volumes (VanR: 5 uL of 100 mM vanillic acid, CinR: 5 uL of 10 mM OHC14, TetR: 18 uL of a ~54 uM stock). These cultures were then loaded into a clear backed 96 well plate (in triplicate) and into a plate reader. A single fluorescence reading was taken using Ex: 485, Em: 535 (Elston et al., 2023).
 +
</p>
 +
<h1>Source</h1>
 +
This promoter part was amplified from <html><a href="http://www.addgene.org/108529/">pAJM.011</a></html> using PCR before being integrated into a basic part plasmid for use in our assemblies. pAJM.011 contains YFP under inducible control by P<sub>tet*</sub> and TetR.
 +
 
 +
<h1>References</h1>
 +
<ol>
 +
<li>Cole, T. J., Parker, J. K., Feller, A. L., Wilke, C. O., & Davies, B. W. (2022). Evidence for widespread class II microcins in Enterobacterales Genomes. <i>Applied and Environmental Microbiology, 88</i>(23), e01486-22.</li>
 +
 
 +
<li>Kim, S. Y., Parker, J. K., Gonzalez-Magaldi, M., Telford, M. S., Leahy, D. J., & Davies, B. W. (2023). Export of Diverse and Bioactive Small Proteins through a Type I Secretion System. <i>Applied and Environmental Microbiology, 89</i>(5), e00335-23.</li>
 +
 
 +
<li>Lee, M. E., DeLoache, W. C., Cervantes, B., & Dueber, J. E. (2015). A highly characterized yeast toolkit for modular, multipart assembly. <i>ACS Synthetic Biology, 4</i>(9), 975-986.</li>
 +
 
 +
<li>Leonard, S. P., Perutka, J., Powell, J. E., Geng, P., Richhart, D. D., Byrom, M., Kar, S., Davies, B. W., Ellington, D. E., Moran, N. A., & Barrick, J. E. (2018). Genetic engineering of bee gut microbiome bacteria with a toolkit for modular assembly of broad-host-range plasmids. <i>ACS Synthetic Biology, 7</i>(5), 1279-1290.</li>
 +
 
 +
<li>Meyer, A. J., Segall-Shapiro, T. H., Glassey, E., Zhang, J., & Voigt, C. A. (2019). Escherichia coli “Marionette” strains with 12 highly optimized small-molecule sensors. <i>Nature Chemical Biology, 15</i>(2), 196-204.</li>
 +
 
 +
<li>Schuster, L. A., & Reisch, C. R. (2021). A plasmid toolbox for controlled gene expression across the Proteobacteria. <i>Nucleic Acids Research, 49</i>(12), 7189-7202.</li>
 +
</ol>
  
 
<!-- -->
 
<!-- -->
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<span class='h3bb'>Sequence and Features</span>
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<h1>Sequence and Features</h1>  
 
<partinfo>BBa_K4579000 SequenceAndFeatures</partinfo>
 
<partinfo>BBa_K4579000 SequenceAndFeatures</partinfo>
  

Latest revision as of 15:57, 12 October 2023


PTet* promoter + RBS

Introduction

The 2023 UT Austin iGEM Team’s modular microcin expression parts collection includes parts necessary for engineering a bacterial chassis to secrete microcins, a type of small antimicrobial peptide. Our team has specifically designed parts to engineer a modular two-plasmid system that facilitates extracellular secretion of microcins by the chassis. One plasmid contains the microcin with a signal peptide sequence that indicates to the cell that the microcin is to be secreted. The other plasmid (pSK01) is from the literature (Kim et al., 2023) and contains genes for the proteins CvaA and CvaB, which are necessary to secrete small peptides using the E. coli microcin V (MccV) type I secretion system (T1SS) shown in Figure 2 of our Project Description.

Our parts collection includes a a selection of promoter (Type 2), coding sequence (Type 3), and terminator/regulatory gene (Type 4) parts that can be easily assembled to express microcins either constitutively or under inducible control. This allows for the modular engineering of microcin expression plasmids containing various microcins that can undergo extracellular secretion when used in conjunction with the secretion system plasmid pSK01.

Figure 1. Basic parts categorized by their BTK/YTK part type. Type 3p and 3q parts assemble as if they were a single Type 3 part.

Our basic and composite parts follow the Bee Toolkit/Yeast Toolkit standard of Golden Gate assembly (Lee et al., 2015; Leonard et al., 2018). Our assembly method involves the use of BsmBI digestion-ligation to create basic parts which can then be further digested with BsaI and ligated to form composite parts. The BTK/YTK standard includes part type-specific prefix and suffix overhangs generated by BsaI for each part, and these overhangs are NOT included in their sequences in the registry. For reference, our standard’s part type-specific overhangs are listed in Figure 2 on our Parts page.

Categorization

Basic parts

  • Promoters (Type 2) – Seven inducible promoters selected due to their relatively high dynamic range (Meyer et al., 2019) and apparent functionality in a variety of Proteobacteria (Schuster & Reisch, 2021), and one constitutive CP25 promoter (Leonard et al., 2018).
  • Coding Sequences (Type 3) – Signal peptide + microcin fusion coding sequences, a green fluorescent protein gene, and secretion system genes cvaA and cvaB which are together referred to as CvaAB.
  • Terminators/Regulatory Genes (Type 4) – An rpoC terminator plus a collection of seven regulatory genes, each associated with one of our seven inducible promoters.

Composite parts

  • Constitutive Microcin Expression Assemblies - Assemblies of microcins (some with immunity proteins) with a constitutive CP25 promoter and rpoC terminator. These function alongside pSK01 in a two-plasmid secretion system, and we use these two-plasmid systems to assess if our novel microcins are effective inhibitors of pathogenic targets.
  • Inducible GFP Expression Assemblies – Assemblies of GFP under the control of various inducible promoter systems. These were used to assess the dynamic range of our inducible promoter systems.
  • Inducible Microcin Expression Assemblies – Assemblies of select microcins under the control of an inducible promoter system.


Usage and Biology

This part consists of the Ptet* promoter upstream of a ribosome binding site, with a hammerhead ribozyme (HHRz) sequence included in the intervening 5' untranslated region to insulate gene expression levels from coding sequence effects on mRNA structure. This promoter can be bound by TetR (BBa_K4579026), a transcriptional repressor that can be removed from the promoter when bound by anhydrotetracycline (aTc), allowing for the selective induction of transcription in cells containing both Ptet* and the tetR gene. This part can be used as a Type 2 part in the BTK/YTK standard.

Composite Parts

Figure 2. The general schematic for our inducible microcin and GFP expression assemblies with emphasis on the inducible promoter. Although this example contains an immunity protein sequence, not all of our inducible microcin expression parts include an immunity protein.


Design Notes

When creating our inducible promoter parts, we used the YFP-expressing individual sensor plasmids from the E. coli ‘Marionette’ paper as PCR templates (Meyer et al., 2019), as these include inducible promoters and their regulatory transcription factors on a standardized backbone. Due to the homology of the backbone between these plasmids, we created universal primers that allowed us to amplify the promoter from any one of the sensor plasmids. One big design complication in this process was the fact that the YFP-expressing sensor plasmids all contained a BsaI site in the region just upstream of the promoter where one of the universal primers would bind. We designed our primers to create a single point mutation in order to mutate out this illegal BsaI site.

Characterization

​​Below is the fluorescence characterization data for the four inducible promoter-regulator systems that we tested in composite parts using a GFP reporter gene (BBa_K4579035). The table below lists the inducible promoters within our parts collection, their basic part numbers, and their composite part numbers with the GFP reporter. Below that, the first figure shows fluorescence/OD600 data for the characterization of our inducible GFP assemblies in E. coli DH5α. This first experiment was done as a proof of concept to test whether our inducible GFP assemblies were functional. After confirming functionality of the assemblies by measuring levels of fluorescence under induced and non-induced conditions, we moved on to testing the assemblies in Pantoea agglomerans PNG92-11 in order to determine whether these inducible promoter systems are functional in Pantoea. This data confirms the functionality of our inducible promoter systems in Pantoea.

This table summarizes which of the basic type 2 promoter parts we created and characterized by assembling into a level 1 composite part and running the following fluorescence experiments on.
Short Description Basic Part ID Composite Part (with GFP, Regulator and Terminator)
PTet* promoter + RBS BBa_K4579000 BBa_K4579061
PTac promoter + RBS BBa_K4579001 BBa_K4579058
PLuxB promoter + RBS BBa_K4579002 None
PCymRC promoter + RBS BBa_K4579003 None
PBAD promoter + RBS BBa_K4579004 None
PVanCC promoter + RBS BBa_K4579005 BBa_K4579059
PCin promoter + RBS BBa_K4579006 BBa_K4579060

Characterization Assays

Figure 3. This displays the dynamic range of all the inducible promoters we were able to characterize in E. Coli DH5α. + indicates the presence of inducer in the overnight culture and – indicates a lack of inducer in the overnight culture. A mean of all three fluorescence readings divided by mean OD600 were plotted on a bar graph. Standard deviation of readings was used to create error bars.

To test each of the inducible promoter systems we incorporated them with GFP into composite parts (BBa_K4579058, BBa_K4579059, BBa_K4579060, BBa_K4579061). The parts were sequence confirmed and subsequently transformed into DH5α. Inducers were added using the following volumes (LacI: 50 µL of 0.1 M IPTG, VanR: 5 µL of 100 mM vanillic acid, CinR: 5 uL of 10 mM OHC14, TetR: 18 µL of a ~54 µM stock). These cultures were then loaded into a clear backed 96 well plate (in triplicate) and into a plate reader. A single fluorescence reading was taken using Ex: 485, Em: 535 (Elston et al., 2023).

Figure 4. This displays the dynamic range of all the inducible promoters we were able to characterize in P. Agglomerans with the T1SS. + indicates the presence of inducer in the overnight culture and – indicates a lack of inducer in the overnight culture. A mean of all three fluorescence readings divided by mean OD600 were plotted on a bar graph. Standard deviation of readings was used to create error bars.

In order to test our inducible promoters in a chassis organism with a secretion system we transformed our inducible GFP expression plasmids into a P. Agglomerans strain with a native T1SS. We opted to not use the LacI regulatory system (BBa_K4579058) since it had high levels of expression in the absence of inducer. 5 ml induced and uninduced overnight cultures were created per each strain. Inducers were added using the following volumes (VanR: 5 uL of 100 mM vanillic acid, CinR: 5 uL of 10 mM OHC14, TetR: 18 uL of a ~54 uM stock). These cultures were then loaded into a clear backed 96 well plate (in triplicate) and into a plate reader. A single fluorescence reading was taken using Ex: 485, Em: 535 (Elston et al., 2023).

Source

This promoter part was amplified from pAJM.011 using PCR before being integrated into a basic part plasmid for use in our assemblies. pAJM.011 contains YFP under inducible control by Ptet* and TetR.

References

  1. Cole, T. J., Parker, J. K., Feller, A. L., Wilke, C. O., & Davies, B. W. (2022). Evidence for widespread class II microcins in Enterobacterales Genomes. Applied and Environmental Microbiology, 88(23), e01486-22.
  2. Kim, S. Y., Parker, J. K., Gonzalez-Magaldi, M., Telford, M. S., Leahy, D. J., & Davies, B. W. (2023). Export of Diverse and Bioactive Small Proteins through a Type I Secretion System. Applied and Environmental Microbiology, 89(5), e00335-23.
  3. Lee, M. E., DeLoache, W. C., Cervantes, B., & Dueber, J. E. (2015). A highly characterized yeast toolkit for modular, multipart assembly. ACS Synthetic Biology, 4(9), 975-986.
  4. Leonard, S. P., Perutka, J., Powell, J. E., Geng, P., Richhart, D. D., Byrom, M., Kar, S., Davies, B. W., Ellington, D. E., Moran, N. A., & Barrick, J. E. (2018). Genetic engineering of bee gut microbiome bacteria with a toolkit for modular assembly of broad-host-range plasmids. ACS Synthetic Biology, 7(5), 1279-1290.
  5. Meyer, A. J., Segall-Shapiro, T. H., Glassey, E., Zhang, J., & Voigt, C. A. (2019). Escherichia coli “Marionette” strains with 12 highly optimized small-molecule sensors. Nature Chemical Biology, 15(2), 196-204.
  6. Schuster, L. A., & Reisch, C. R. (2021). A plasmid toolbox for controlled gene expression across the Proteobacteria. Nucleic Acids Research, 49(12), 7189-7202.

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]