Difference between revisions of "Part:BBa K2904013"
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==<strong>Result</strong>==
 
==<strong>Result</strong>==
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We did three kinds of experiments to help us confirm the function of modular Adda riboswitch containing Tuner D.
 
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===The result by confocal microscopy===
 
  
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===Modular Adda riboswitch===
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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 adenine riboswitch had sfGFP introduced directly. The direct fusion of sfGFP to Stabilizer yielded very clear inclusion bodies, manifested as distinct spots present at one pole of the cell which are formed by misfolded insoluble proteins. By comparison, the modular Adda riboswitch yielded soluble working protein since Tuner has the ability to insulation the target gene from Stabilizer.  
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In order to validate the effect of Tuner D, we utilized Adda riboswitch, which can regulate the expression of <i>adenosine deaminase</i> by binding 2-aminopurine in <i>Vibrio vulnificus</i>. The first 150bp of <i>adenosine deaminase</i> was chosen as Stabilizer of Adda riboswitch because our docking matrix suggested that a normal riboswitch structure would be observed when using this length of Stabilizer. We used Tuner D to construct [https://parts.igem.org/Part:BBa_K2904011 modular Adda riboswitch] and [https://parts.igem.org/Part:BBa_K2904110 sfGFP]as the reporter gene to reflect output of our system.
 
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===The result by microplate reader===
 
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The qualitative experiment is not enough to analyze the modular Adda 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 Adda riboswitch can restore the structure of riboswitch and control the downstream gene expression during the whole cultivation period.
 
 
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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 Tuner D can enhance the function of riboswitch and help riboswitch control the downstream gene expression during the whole cultivation period.
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[[Image:T--OUC-China--053microplateduizho.jpg|left|thumb|400px|'''Fig.1  The results of the original Adda riboswitch by microplate reader.''']] [[Image:T--OUC-China--053microplate.jpg|right|thumb|400px|'''Fig.2  The results of modular Adda riboswitch containing Tuner D by microplate reader.''']]
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[[Image:T--OUC-China--004micro.png|center|thumb|800px|'''Figure1: The results of modular Adda riboswitch containing Tuner D by microplate reader.''']]  
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The above results demonstrate that Tuner D can help achieve tunable and efficient gene regulation. Besides, we also designed Tuner A to E.[http://2019.igem.org/Team:OUC-China/Model The design process about Tuners is on this page!]
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<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Latest revision as of 14:36, 21 October 2019


Modular Adda riboswitch containing Tuner D

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 activating Adda riboswitch, which can regulate the expression of adenosine deaminase by binding 2-aminopurine in Vibrio vulnificus.The first 150bp of adenosine deaminase was chosen as Stabilizer of Adda riboswitch because our docking matrix suggested that a normal riboswitch structure would be observed when using this length of Stabilizer. This part was modular Adda riboswitch containing the original riboswitch, Stabilizer and Tuner D.


Result

Modular Adda riboswitch

In order to validate the effect of Tuner D, we utilized Adda riboswitch, which can regulate the expression of adenosine deaminase by binding 2-aminopurine in Vibrio vulnificus. The first 150bp of adenosine deaminase was chosen as Stabilizer of Adda riboswitch because our docking matrix suggested that a normal riboswitch structure would be observed when using this length of Stabilizer. We used Tuner D to construct modular Adda riboswitch and sfGFPas the reporter gene to reflect output of our system.

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 Tuner D can enhance the function of riboswitch and help riboswitch control the downstream gene expression during the whole cultivation period.

Figure1: The results of modular Adda riboswitch containing Tuner D by microplate reader.




The above results demonstrate that Tuner D can help achieve tunable and efficient gene regulation. Besides, we also designed Tuner A to E.[http://2019.igem.org/Team:OUC-China/Model The design process about Tuners is on this page!]

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 257
    Illegal NgoMIV site found at 269
  • 1000
    COMPATIBLE WITH RFC[1000]