Difference between revisions of "Part:BBa K1031014"

 
Line 1: Line 1:
 
__NOTOC__
 
__NOTOC__
 
<partinfo>BBa_K1031014 short</partinfo>
 
<partinfo>BBa_K1031014 short</partinfo>
 +
<html>
 +
<p>For detailed information concerning Band-pass Filter, please visit <a href="http://2013.igem.org/Team:Peking/Project/BandpassFilter">2013 Peking iGEM Band-pass Filter</a></p>
 +
 +
<img src="https://static.igem.org/mediawiki/igem.org/c/c9/Peking_Logo.jpg" style="width:960px;"/>
 +
</html>
 +
  
  
 
== '''Components and Characterization''' ==
 
== '''Components and Characterization''' ==
  
K1031014 consists of NahR[https://parts.igem.org/Part:BBa_J61051], Psal promoter, RBS B0031[https://parts.igem.org/Part:BBa_B0031] and transcription factor CƖ. CƖ functions as a repressor of hybrid promoter[https://parts.igem.org/Part:BBa_K1031021]. It is the repression branch of the Band-pass Filter circuit ('''Fig 1'''). In order to fine-tune the expression level of transcriptional repressor, we adjusted the RBS (Ribosome Binding Site) intensity in front of CƖ. K1031014 adopts RBS B0031.   
+
K1031014 consists of NahR[https://parts.igem.org/Part:BBa_J61051], Psal promoter, RBS B0031[https://parts.igem.org/Part:BBa_B0031] and transcription factor CƖ. CƖ functions as a repressor of <html><a href="https://parts.igem.org/Part:BBa_K1031021">hybrid promoter</a></html>. It is the repression node of the Band-pass Filter circuit ('''Fig 1'''). In order to fine-tune the expression level of transcriptional repressor, we adjusted the RBS (Ribosome Binding Site) intensity in front of CƖ. K1031014 adopts RBS <html><a href="https://parts.igem.org/Part:BBa_B0031">B0031</a></html>.   
  
 
<html>
 
<html>
<img src="https://static.igem.org/mediawiki/igem.org/thumb/9/9e/Peking2013_part_K1031014.png/800px-Peking2013_part_K1031014.png", width=700px; />
+
<img src="https://static.igem.org/mediawiki/igem.org/thumb/9/9e/Peking2013_part_K1031014.png/800px-Peking2013_part_K1031014.png" style="width:750px; margin-left:100px" />
 +
<p style="text-align:center"><b>Fig 1</b> Repression circuit of Band-pass Filter. The orange square represents transcription factor NahR activating Psal promoter shown in light blue. Once Psal promoter is initiated, CƖ repressor, which is shown as square in dark blue, is expressed, inhibit hybrid promoter marked with two colors, thus inhibit expression of sfGFP. The RBS B0031 is shown in light green, regulating the expression level of CƖ protein. 
 
</html>
 
</html>
 
'''Fig 1''' Repression circuit of Band-pass Filter. The orange square represents transcription factor NahR activating Psal promoter shown in light blue. Once Psal promoter is initiated, CƖ repressor, which is shown as square in dark blue, is expressed, inhibit hybrid promoter marked with two colors, thus inhibit expression of sfGFP. The RBS B0031 is shown in light green, regulating the expression level of CƖ protein. 
 
 
   
 
   
  

Latest revision as of 21:03, 27 September 2013

NahR-Psal-B0031-RiboJ-CI

For detailed information concerning Band-pass Filter, please visit 2013 Peking iGEM Band-pass Filter


Components and Characterization

K1031014 consists of NahR[1], Psal promoter, RBS B0031[2] and transcription factor CƖ. CƖ functions as a repressor of hybrid promoter. It is the repression node of the Band-pass Filter circuit (Fig 1). In order to fine-tune the expression level of transcriptional repressor, we adjusted the RBS (Ribosome Binding Site) intensity in front of CƖ. K1031014 adopts RBS B0031.

Fig 1 Repression circuit of Band-pass Filter. The orange square represents transcription factor NahR activating Psal promoter shown in light blue. Once Psal promoter is initiated, CƖ repressor, which is shown as square in dark blue, is expressed, inhibit hybrid promoter marked with two colors, thus inhibit expression of sfGFP. The RBS B0031 is shown in light green, regulating the expression level of CƖ protein.


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 576
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 408
  • 1000
    COMPATIBLE WITH RFC[1000]