Difference between revisions of "Part:BBa K2904020"

 
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<partinfo>BBa_K2904020 short</partinfo>
 
<partinfo>BBa_K2904020 short</partinfo>
  
Modular Btub riboswitch containing Tuner A
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==<strong>Design</strong>==
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===Background of 2019 OUC-China's project——RiboLego===
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<p>
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Due to context-dependent performance and limited dynamic range, the widespread application of riboswitches is currently restricted. By replacing its original ORF with a new one, the structure of an aptamer domain can be subtly disrupted, resulting in a loss of ligand response. So riboswitch is still not be considered as a ‘plug and play' device. To tackle these problems, our project focuses on a standardized design principle to be used for modular and  tunable riboswitch. The modular riboswitch we defined consists of the original riboswitch, Stabilizer and Tuner. Stabilizer can protect the structure of riboswitch from damage while Tuner can reduce the expression probability of fusion protein and make improvement of riboswitch function.
 +
</p>
 +
 
 +
===The construction of this part===
 +
To validate our design guideline, we employed a repressing Btub riboswitch, which can regulate the expression of TonB-dependent vitamin B12 receptor BtuB by binding adenosylcobalamin in <i>Escherichia coli</i>.The first 150bp of BtuB was chosen as Stabilizer of Btub riboswitch because our docking matrix suggested that a normal riboswitch structure would be observed when using this length of Stabilizer. This part was modular Btub riboswitch containing the original riboswitch, Stabilizer and Tuner A.
 +
 
 +
<br>
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==<strong>Result</strong>==
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We did three kinds of experiments to help us confirm the function of modular Btub riboswitch containing Tuner A.
 +
</p>
 +
===The result by confocal microscopy===
 +
 
 +
<p>
 +
First, we selected sfGFP as the output of our system. It was under control of the tetracycline promoter, which was induced by aTc. For the sake of functional test, other 2 circuits are set, Adda-sfGFP and Adda-Stabilizer-sfGFP, which also were under control of the same promoter. By Confocal Microscopy Leica TCS SP8, it’s obvious that no fluorescence could be observed when the Btub riboswitch had sfGFP introduced directly. By comparison with Btub fusion, the modular Btub riboswitch demonstrates a greater induction difference since Tuner has the ability to improve the function of riboswitch. 
 +
<br>
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</p>
 +
 
 +
===The result by microplate reader===
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 +
<p>
 +
The qualitative experiment is not enough to analyze the modular Btub riboswitch. So we tested our system by microplate reader, which is used to reflect the intensity of sfGFP changing over time. The following chart shows the dynamic curve measured every two hours. It can prove that the modular Btub riboswitch can restore the structure of riboswitch and control the downstream gene expression during the whole cultivation period.
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<br>
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</p>
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[[Image:T--OUC-China--080microplateg.jpg|center|thumb|400px|'''Figure1: The results of modular Btub riboswitch containing Tuner A by microplate reader.'''  ]]
  
 
<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Revision as of 09:36, 17 October 2019


Modular Btub riboswitch containing Tuner A

Design

Background of 2019 OUC-China's project——RiboLego

Due to context-dependent performance and limited dynamic range, the widespread application of riboswitches is currently restricted. By replacing its original ORF with a new one, the structure of an aptamer domain can be subtly disrupted, resulting in a loss of ligand response. So riboswitch is still not be considered as a ‘plug and play' device. To tackle these problems, our project focuses on a standardized design principle to be used for modular and tunable riboswitch. The modular riboswitch we defined consists of the original riboswitch, Stabilizer and Tuner. Stabilizer can protect the structure of riboswitch from damage while Tuner can reduce the expression probability of fusion protein and make improvement of riboswitch function.

The construction of this part

To validate our design guideline, we employed a repressing Btub riboswitch, which can regulate the expression of TonB-dependent vitamin B12 receptor BtuB by binding adenosylcobalamin in Escherichia coli.The first 150bp of BtuB was chosen as Stabilizer of Btub riboswitch because our docking matrix suggested that a normal riboswitch structure would be observed when using this length of Stabilizer. This part was modular Btub riboswitch containing the original riboswitch, Stabilizer and Tuner A.


Result

We did three kinds of experiments to help us confirm the function of modular Btub riboswitch containing Tuner A. </p>

The result by confocal microscopy

First, we selected sfGFP as the output of our system. It was under control of the tetracycline promoter, which was induced by aTc. For the sake of functional test, other 2 circuits are set, Adda-sfGFP and Adda-Stabilizer-sfGFP, which also were under control of the same promoter. By Confocal Microscopy Leica TCS SP8, it’s obvious that no fluorescence could be observed when the Btub riboswitch had sfGFP introduced directly. By comparison with Btub fusion, the modular Btub riboswitch demonstrates a greater induction difference since Tuner has the ability to improve the function of riboswitch.

The result by microplate reader

The qualitative experiment is not enough to analyze the modular Btub riboswitch. So we tested our system by microplate reader, which is used to reflect the intensity of sfGFP changing over time. The following chart shows the dynamic curve measured every two hours. It can prove that the modular Btub riboswitch can restore the structure of riboswitch and control the downstream gene expression during the whole cultivation period.

Figure1: The results of modular Btub riboswitch containing Tuner A by microplate reader.

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
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 156
  • 1000
    COMPATIBLE WITH RFC[1000]