Difference between revisions of "Part:BBa K1139110"

 
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This part was designed for a crosstalk circumvention system for two signal molecules ([http://2013.igem.org/Team:Tokyo_Tech/Project/Ninja_State_Switching our wiki]). Our crosstalk circumvention system has a network topology which is composed of two repressor proteins, one repressor and one hybrid promoter (Fig. 2).  Along with the topology, one can just choose any combination of sets of repressor proteins and promoters.  This system can be used for any genetic circuit that has potential crosstalk.  This part is useful to confirm the circumvention because the <i>lux/tet</i> hybrid promoter can be regulated common regulatory protein, TetR and LuxR.  In addition, this part also contains LasR protein which has potential cross talk to luxR-binding sequence. <br>  
 
This part was designed for a crosstalk circumvention system for two signal molecules ([http://2013.igem.org/Team:Tokyo_Tech/Project/Ninja_State_Switching our wiki]). Our crosstalk circumvention system has a network topology which is composed of two repressor proteins, one repressor and one hybrid promoter (Fig. 2).  Along with the topology, one can just choose any combination of sets of repressor proteins and promoters.  This system can be used for any genetic circuit that has potential crosstalk.  This part is useful to confirm the circumvention because the <i>lux/tet</i> hybrid promoter can be regulated common regulatory protein, TetR and LuxR.  In addition, this part also contains LasR protein which has potential cross talk to luxR-binding sequence. <br>  
  
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[[Image:Titech2013 Ninja State Switching 3D.jpg|thumb|right|240px|<b>Fig. 4.</b> Activation of the crosstalk circumvention system circuit]]
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We also screened the concentration of 3OC6HSL and aTc, and examined activation of the crosstalk circumvention system circuit. Then we determined the transfer function of 3OC6HSL-LuxR complex by fitting Hill’s equation and introduced into our [http://2013.igem.org/Team:Tokyo_Tech/Modeling/Crosstalk_Circumvention modeling]
 
We also screened the concentration of 3OC6HSL and aTc, and examined activation of the crosstalk circumvention system circuit. Then we determined the transfer function of 3OC6HSL-LuxR complex by fitting Hill’s equation and introduced into our [http://2013.igem.org/Team:Tokyo_Tech/Modeling/Crosstalk_Circumvention modeling]
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Fig. 4 shows activation of the crosstalk circumvention system circuit. It shows transition of the fluorescence intensity of GFP. It indicates that the concentration of C6 saturates between 10 mM and 30 mM.
  
[[Image:Titech2013 Ninja State Switching 3D.jpg|thumb|right|240px|<b>Fig. 4.</b> Activation of the crosstalk circumvention system circuit]]
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For more information, see [http://2013.igem.org/Team:Tokyo_Tech/Experiment/Crosstalk_Circumvention_Assay our work in Tokyo_Tech 2013 wiki].<br>
  
 
 
For more information, see [http://2013.igem.org/Team:Tokyo_Tech/Experiment/Crosstalk_Circumvention_Assay our work in Tokyo_Tech 2013 wiki].<br>
 
  
 
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Latest revision as of 17:09, 28 October 2013

Pcon-LasR-Plux/tet-GFP

Fig. 1. Signal-dependent state change circuit


On the previous assay we confirmed crosstalk, which 3OC12HSL-LasR complex activates not only las promoter but also lux promoter too (Gray KM et al., 1994). We came up with idea that crosstalk can be suppressed if lux/tet hybrid promoter is inhibited by protein TetR only when 3OC12HSL-LasR complex is around. Our purpose is to check whether lux/tet hybrid promoter would be repressed or not when 3OC12HSL-LasR complex and protein TetR existed. We tried to compare the frequency of crosstalk in the presence or absence of the TetR inhibitor aTc. aTc weakens the bonding of TetR and TetO.

Fig. 2. Gene circuits of "Crosstalk Circumvention Switch"



We made a simple crosstalk circumvention system and named it "Crosstalk Circumvention Switch" (Fig. 2). To construct the circuit in above (Fig. 1), we ligated Pcon-RBS-lasR-TT (BBa_K553003) and Plux/tet-RBS-GFP-TT (BBa_K934025) as a reporter plasmid.
We used Pcon-RBS-luxR-TT-Ptrc-RBS-tetR-TT as the regulator plasmid.

Fig. 3. The result of crosstalk circumvention






This part was designed for a crosstalk circumvention system for two signal molecules ([http://2013.igem.org/Team:Tokyo_Tech/Project/Ninja_State_Switching our wiki]). Our crosstalk circumvention system has a network topology which is composed of two repressor proteins, one repressor and one hybrid promoter (Fig. 2). Along with the topology, one can just choose any combination of sets of repressor proteins and promoters. This system can be used for any genetic circuit that has potential crosstalk. This part is useful to confirm the circumvention because the lux/tet hybrid promoter can be regulated common regulatory protein, TetR and LuxR. In addition, this part also contains LasR protein which has potential cross talk to luxR-binding sequence.











Fig. 4. Activation of the crosstalk circumvention system circuit


We also screened the concentration of 3OC6HSL and aTc, and examined activation of the crosstalk circumvention system circuit. Then we determined the transfer function of 3OC6HSL-LuxR complex by fitting Hill’s equation and introduced into our [http://2013.igem.org/Team:Tokyo_Tech/Modeling/Crosstalk_Circumvention modeling]
Fig. 4 shows activation of the crosstalk circumvention system circuit. It shows transition of the fluorescence intensity of GFP. It indicates that the concentration of C6 saturates between 10 mM and 30 mM.



For more information, see [http://2013.igem.org/Team:Tokyo_Tech/Experiment/Crosstalk_Circumvention_Assay our work in Tokyo_Tech 2013 wiki].














Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 7
    Illegal NheI site found at 30
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 383
    Illegal AgeI site found at 580
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 927
    Illegal BsaI.rc site found at 1675