Difference between revisions of "Part:BBa K228004"
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|Maximum Output<br>
 
|Maximum Output<br>
 
(Output tested in a time sequence)
 
(Output tested in a time sequence)
−
|Click here(链接到transfer function最下面的表格）
+
|[https://parts.igem.org/Part:BBa_K228004:Transfer#data Click here]
 
|-
 
|-
 
|Hill coefficient<br>
 
|Hill coefficient<br>
 
(Output tested in a time sequence)
 
(Output tested in a time sequence)
−
|Click here(链接到transfer function最下面的表格
+
|[https://parts.igem.org/Part:BBa_K228004:Transfer#data Click here]
 
|-
 
|-
−
|[[ |Switch Point]]<br>
+
|[[Part:BBa_K228004:Transfer|Switch Point]]<br>
 
(Output tested in a time sequence)
 
(Output tested in a time sequence)
−
|Click here(链接到transfer function最下面的表格
+
|[https://parts.igem.org/Part:BBa_K228004:Transfer#data Click here]
 
|-
 
|-
 
|Demand
 
|Demand
−
|[[ |Decrease on Growth Rate]]<br>
+
|[[Part:BBa_K228004:Growth|Decrease on Growth Rate]]<br>
 
(Input at a gradient of concentration)
 
(Input at a gradient of concentration)
 
|The decrease level has significantly positive correlation with the input, the concentration of salicylate.  
 
|The decrease level has significantly positive correlation with the input, the concentration of salicylate.  

Revision as of 00:29, 18 October 2009

NahR( reverse) - salicylate promoter

Designed by Lin Min Group: iGEM09_PKU_Beijing (2009-09-18)
Input: Salicylate molecules
Output: GFP fluorescence


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]
Part Main Page Transfer Function Growth Rate

Description

This is a salicylate inducible promoter part constructed by Lin Min. The activator protein (NahR) gene is in the upstream but in an opposite direction of the regulated promoter. In the presence of salicylate, the promoter can be activated. If we place a generator on its downstream, the transcription of the coding sequence will be triggered by the salicylate-binded positive transcriptional activator protein which is encoded by NahR.

It is necessary to notice that there is no terminator downstream of the NahR coding sequence, but it has no effect son parts that are in the same direction as the pSal promoter. However, if coding gene is placed upstream of this part and in the same direction as NahR, it may cause unexpected expression.

For the purpose of characterization, we connected BBa_E0840 downstream of the salicylate promoter to make the composite part, BBa_K228850. This report system allowed us to test the salicylate inducible promoter indirectly via the fluorescence output of BBa_E0840, while the input is salicylate solution at a gradient of concentration.

Performance

Experiment* Characteristics* Value & Result*
Transfer Function Maximum Output

(Output tested in a time sequence)

Click here
Hill coefficient

(Output tested in a time sequence)

Click here
Switch Point

(Output tested in a time sequence)

Click here
Demand Decrease on Growth Rate

(Input at a gradient of concentration)

The decrease level has significantly positive correlation with the input, the concentration of salicylate.

Measured by Haoqian Zhang & Chengzhe Tian, 2009

Compatibility

Chassis: Device has been shown to work in DH5α. Plasmids: Device has been shown to work on pSB1A2 and pSB1A3, pSB4K5 Devices: Device has been shown to work with BBa_K228013, BBa_K228227 - BBa_K228235, BBa_K228255 - BBa_K228263, BBa_K228851, BBa_K228852 - BBa_K228860, BBa_K228870 - BBa_K228878.