Difference between revisions of "Part:BBa K2560304"

Line 17: Line 17:
 
<li>Can with be combined with a several reporter genes. We had the best results using the LUX operon.</li>
 
<li>Can with be combined with a several reporter genes. We had the best results using the LUX operon.</li>
 
</ul>
 
</ul>
 +
 +
  
 
<div style="width:100%;display:flex;flex-direction:row;flex-wrap: wrap; justify-content:space-evenly; align-items:center;">
 
<div style="width:100%;display:flex;flex-direction:row;flex-wrap: wrap; justify-content:space-evenly; align-items:center;">
Line 22: Line 24:
 
[[File:T--Marburg--3HPA-Sensor.png|600px|thumb|left|'''Figure 1''': <b> HIER TEXT </b> <br>WEITERER TEXT]]
 
[[File:T--Marburg--3HPA-Sensor.png|600px|thumb|left|'''Figure 1''': <b> HIER TEXT </b> <br>WEITERER TEXT]]
  
 
+
</div>
  
 
<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Revision as of 23:37, 17 October 2018


3-HP Sensor. This part is a PhytoBrick variant


This part contains the promoter as well as the coding sequence for the activator HdpR in the 5´region of the part. It also contains the promotor PHdpR which is regulated by HdpR. This promoter is oriented in reverse to the HdpR codon, facing out of the 3`end of the part. When HdpR binds 3-Hydroxypropionate it changes its conformation, enabling it to bind to PHdpR and activate transcription of the gene controlled by it.


Usage and Biology

  • Inducer: 3-Hydroxypropionate
  • 3-Hydroxypropionate is harmless. For induction, a concentration between 1 and 20 mM can be used.
  • The system stems from the S1 safety strain of P. putida KT2440.
  • We designed this biobrick in order to get a system with a usable readout for the intracellular 3-Hydroxypropionate concentration.
  • Can with be combined with a several reporter genes. We had the best results using the LUX operon.


Figure 1: HIER TEXT
WEITERER TEXT

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 1108
    Illegal NotI site found at 279
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal XhoI site found at 263
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]