Difference between revisions of "Part:BBa K3885202"

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<partinfo>BBa_K3885202 short</partinfo>
 
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Under the influence of the P70 promoter, the transcription factor &#963;28 is produced and activates expression from the P28 promoter
 
Under the influence of the P70 promoter, the transcription factor &#963;28 is produced and activates expression from the P28 promoter
  
  
 
===Usage===
 
===Usage===
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P70-σ28 is a significant part of genecircuit where P70 can be regulated by the σ70 factor present in Cell-Free system. The rest of the parts in the gene circuit are dependent on the expression of the σ28 factor to initiate expression.<be>
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P70-σ28 is a significant part of genecircuit where P70 can be regulated by the σ70 factor present in Cell-Free system. The rest of the parts in the gene circuit are dependent on the expression of the σ28 factor to initiate expression.
  
 
===Characterization===
 
===Characterization===
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<p style="text-align: center:">Figure 1. Schematic of gene circuits and kinetics of plasmid P70a-σ28(2nM) and P28-tetO-deGFP(5nM). </p>
 
<p style="text-align: center:">Figure 1. Schematic of gene circuits and kinetics of plasmid P70a-σ28(2nM) and P28-tetO-deGFP(5nM). </p>
 
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As seen by the data, high intensity fluorescence was produced, proving that our base part P70-σ28 works as desired.
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As seen by the data, high-intensity fluorescence was produced, proving that our base part P70-σ28 works as desired.
  
 
===Design Page===
 
===Design Page===
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Our goal is to use Cell-Free systems to detect RNA. Therefore, we consider the design of gene lines that are best adapted to Cell-Free systems. Reviewing the literature we obtained that Cell-Free system carries its own σ70 factor, so the promoter of our part should be the promoter P70a regulated by the σ70 factor.[1] And we also intend to use the gene circuit to produce the repressor protein, and we found data demonstrating that the tetR gene expressing the repressor protein can achieve better expression when it is influenced by the P28 promoter. Therefore there should also be a promoter P28 present in the system that is initiated by the σ28 factor. Thus we need to construct a base part that connects the cell-free system to the gene circuit we want to implement. P70a-σ28 part fits perfectly with what we expected.
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Our goal is to use Cell-Free systems to detect RNA. Therefore, we consider the design of gene lines that are best adapted to Cell-Free systems. Reviewing the literature we obtained that Cell-Free system carries its own σ70 factor, so the promoter of our part should be the promoter P70a regulated by the σ70 factor.[1] And we also intend to use the gene circuit to produce the repressor protein, and we found data demonstrating that the tetR gene expressing the repressor protein can achieve better expression when it is influenced by the P28 promoter. Therefore there should also be a promoter P28 present in the system that is initiated by the σ28 factor. Thus we need to construct a base part that connects the Cell-Free system to the gene circuit we want to implement. P70a-σ28 part fits perfectly with what we expected.
  
 
===Biology===
 
===Biology===

Latest revision as of 18:33, 21 October 2021


P70-σ28

Under the influence of the P70 promoter, the transcription factor σ28 is produced and activates expression from the P28 promoter


Usage

P70-σ28 is a significant part of genecircuit where P70 can be regulated by the σ70 factor present in Cell-Free system. The rest of the parts in the gene circuit are dependent on the expression of the σ28 factor to initiate expression.

Characterization

Since P70-σ28 provides σ28 for the remaining gene circuit, this element is the base component for the experimental part. To verify whether our constructed part can achieve the desired effect in Cell-Free system, we bound the P70-σ28 factor to the reporter molecule P28-tetO-deGFP and observed the fluorescent protein intensity.

Figure 1. Schematic of gene circuits and kinetics of plasmid P70a-σ28(2nM) and P28-tetO-deGFP(5nM).

As seen by the data, high-intensity fluorescence was produced, proving that our base part P70-σ28 works as desired.

Design Page

Our goal is to use Cell-Free systems to detect RNA. Therefore, we consider the design of gene lines that are best adapted to Cell-Free systems. Reviewing the literature we obtained that Cell-Free system carries its own σ70 factor, so the promoter of our part should be the promoter P70a regulated by the σ70 factor.[1] And we also intend to use the gene circuit to produce the repressor protein, and we found data demonstrating that the tetR gene expressing the repressor protein can achieve better expression when it is influenced by the P28 promoter. Therefore there should also be a promoter P28 present in the system that is initiated by the σ28 factor. Thus we need to construct a base part that connects the Cell-Free system to the gene circuit we want to implement. P70a-σ28 part fits perfectly with what we expected.

Biology

Recognition sequence from Escherichia coli str. K-12 substr.

References

Sigma Factor-Mediated Tuning of Bacterial Cell-Free Synthetic Genetic Oscillators Maaruthy Yelleswarapu, Ardjan J. van der Linden, Bob van Sluijs, Pascal A. Pieters, Emilien Dubuc, Tom F. A. de Greef, and Wilhelm T. S. Huck ACS Synthetic Biology 2018 7 (12), 2879-2887


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
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI site found at 487
    Illegal SapI.rc site found at 512
    Illegal SapI.rc site found at 668