Difference between revisions of "Part:BBa K2319005"

 
 
Line 5: Line 5:
 
This part expresses mCherry-SpyTag under our T7 expression system.
 
This part expresses mCherry-SpyTag under our T7 expression system.
  
<!-- Add more about the biology of this part here
+
<html>
 +
<figure>
 +
<img src="https://static.igem.org/mediawiki/2017/9/91/T--IISc-Bangalore--assembly-C12789-linearized.png" width="100%">
 +
</figure>
 +
</html>
 +
 
 
===Usage and Biology===
 
===Usage and Biology===
  
<!-- -->
+
<html>
 +
<h2>Using this as a T7 expression backbone</h2>
 +
 
 +
<h3>Expressing any protein of interest</h3>
 +
 
 +
<p>This T7 expression backbone can be used to express any protein if its coding sequence (with a start codon) is inserted using the HindIII and NheI sites. These sites can be added to the coding sequence using PCR with primers having 5'-overhangs.</p>
 +
 
 +
<h3>Fusing a protein domain at the N-terminus of an existing protein</h3>
 +
 
 +
<p>By inserting the coding sequence of a protein domain (including the start codon) using the HindIII and AgeI sites into the T7 expression backbone (which already contains a protein coding sequence), an N-terminal fusion can be performed.</p>
 +
 
 +
<h2>Expressing a protein of interest</h2>
 +
 
 +
<p>No system is better for protein expression than E. coli BL21 (DE3) as its lon and ompT protease deficiency yields a huge amount of protein. BL21 (DE3) is a lysogenic strain that has the T7 RNA polymerase gene integrated into its genome under the lac operon; adding IPTG induces expression of T7 RNA polymerase, which recognizes the T7 promoter sequence. Any gene inserted downstream of the T7 promoter can thus be expressed.</p>
 +
 
 +
<p>Transform this part into BL21 (DE3) and induce protein overexpression with IPTG after the culture reaches early-log to mid-log phase (optimize this by inducing at different times).</p>
 +
 
 +
</html>
 +
 
 
<span class='h3bb'>Sequence and Features</span>
 
<span class='h3bb'>Sequence and Features</span>
 
<partinfo>BBa_K2319005 SequenceAndFeatures</partinfo>
 
<partinfo>BBa_K2319005 SequenceAndFeatures</partinfo>

Latest revision as of 10:29, 1 November 2017


mCherry-SpyTag under T7 expression system

This part expresses mCherry-SpyTag under our T7 expression system.

Usage and Biology

Using this as a T7 expression backbone

Expressing any protein of interest

This T7 expression backbone can be used to express any protein if its coding sequence (with a start codon) is inserted using the HindIII and NheI sites. These sites can be added to the coding sequence using PCR with primers having 5'-overhangs.

Fusing a protein domain at the N-terminus of an existing protein

By inserting the coding sequence of a protein domain (including the start codon) using the HindIII and AgeI sites into the T7 expression backbone (which already contains a protein coding sequence), an N-terminal fusion can be performed.

Expressing a protein of interest

No system is better for protein expression than E. coli BL21 (DE3) as its lon and ompT protease deficiency yields a huge amount of protein. BL21 (DE3) is a lysogenic strain that has the T7 RNA polymerase gene integrated into its genome under the lac operon; adding IPTG induces expression of T7 RNA polymerase, which recognizes the T7 promoter sequence. Any gene inserted downstream of the T7 promoter can thus be expressed.

Transform this part into BL21 (DE3) and induce protein overexpression with IPTG after the culture reaches early-log to mid-log phase (optimize this by inducing at different times).

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 828
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 765
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]