Difference between revisions of "Part:BBa K4632002:Design"

(Sequence and Features)
Line 1: Line 1:
__NOTOC__
 
 
  
 +
__NOTOC__
 
<br>
 
<br>
  
 
</html>
 
</html>
  
__NOTOC__
+
<h2>Sequence and Features</h2>
<partinfo>BBa K4632002 short</partinfo>
+
 
+
 
<partinfo>BBa K4632002 SequenceAndFeatures</partinfo>
 
<partinfo>BBa K4632002 SequenceAndFeatures</partinfo>
  
===Design Notes===
+
<html>
 +
 
 +
<br>
 +
 
 +
<h2>Design Notes</h2>
  
 
In our design, we aimed to introduce the gene fragment encoding an active Cry3A-like toxin into Escherichia coli using the pET30a vector as a carrier, in order to confer upon it the ability to produce Cry3A-like toxin. To achieve secretion expression, we added a signal peptide sequence, OmpA, to the N-terminus of Cry3A-like toxin. This signal peptide was included to guide the transport of Cry3A-like toxin to the extracellular space. OmpA is a commonly used signal peptide in Escherichia coli that has been verified for the secretion expression of foreign proteins. Additionally, we fused a 6×His tag to the C-terminus of Cry3A-like toxin to facilitate subsequent protein purification and enable specific characterization experiments using Western blot.
 
In our design, we aimed to introduce the gene fragment encoding an active Cry3A-like toxin into Escherichia coli using the pET30a vector as a carrier, in order to confer upon it the ability to produce Cry3A-like toxin. To achieve secretion expression, we added a signal peptide sequence, OmpA, to the N-terminus of Cry3A-like toxin. This signal peptide was included to guide the transport of Cry3A-like toxin to the extracellular space. OmpA is a commonly used signal peptide in Escherichia coli that has been verified for the secretion expression of foreign proteins. Additionally, we fused a 6×His tag to the C-terminus of Cry3A-like toxin to facilitate subsequent protein purification and enable specific characterization experiments using Western blot.
  
  
===Source===
+
<h2>Source</h2>
  
 
We obtained the sequence of the active Cry protoxin of UTD-001 from the original literature. After codon optimization, we entrusted GUANGZHOU IGE BIOTECHNOLOGY LTD to synthesize the gene fragment OmpA-active Cry protoxin of UTD-001.
 
We obtained the sequence of the active Cry protoxin of UTD-001 from the original literature. After codon optimization, we entrusted GUANGZHOU IGE BIOTECHNOLOGY LTD to synthesize the gene fragment OmpA-active Cry protoxin of UTD-001.
===References===
+
<h2>References</h2>
  
 
<html>
 
<html>

Revision as of 17:56, 8 October 2023



</html>

Sequence and Features

No part name specified with partinfo tag.


Design Notes

In our design, we aimed to introduce the gene fragment encoding an active Cry3A-like toxin into Escherichia coli using the pET30a vector as a carrier, in order to confer upon it the ability to produce Cry3A-like toxin. To achieve secretion expression, we added a signal peptide sequence, OmpA, to the N-terminus of Cry3A-like toxin. This signal peptide was included to guide the transport of Cry3A-like toxin to the extracellular space. OmpA is a commonly used signal peptide in Escherichia coli that has been verified for the secretion expression of foreign proteins. Additionally, we fused a 6×His tag to the C-terminus of Cry3A-like toxin to facilitate subsequent protein purification and enable specific characterization experiments using Western blot.

Source

We obtained the sequence of the active Cry protoxin of UTD-001 from the original literature. After codon optimization, we entrusted GUANGZHOU IGE BIOTECHNOLOGY LTD to synthesize the gene fragment OmpA-active Cry protoxin of UTD-001.

References

[1] Lee A. Bulla, Jr.Mehmet Candas Formicidae (ant) control using Bacillus thuringiensis toxin US 6,551,800B1[P]. 2003-04-22.