Difference between revisions of "Part:BBa K1976055"

Line 1: Line 1:
 +
<!--
 +
<!DOCTYPE html>
 +
-->
 +
<html>
 +
    <head>
 +
        <style>
 +
            table, td, th { border: 0px solid black; }
 +
        </style>
 +
    </head>
 +
    <body>
 +
        <h1>trypsin fragment of Colicin E2 with B0034 and T7 promoter</h1>
 +
Generator for the Colicin DNase domain <a href="https://parts.igem.org/Part:BBa_K1976048">BBa_K1976048</a>.
 +
<br>
 +
<br>
 +
        <div align="center">
 +
<img style="width: 40%; height: 40%; margin-left: 15px; margin-right: 15px;" alt="" src="https://static.igem.org/mediawiki/2016/e/ed/T--TU_Darmstadt--minicolgrowth.png">
  
__NOTOC__
+
<p align="left" style="width: 650px; margin-left: 15px; margin-right: 15px;" alt="">
<partinfo>BBa_K1976055 short</partinfo>
+
<b>Figure 1:</b>Figure 5: growth of BL21 E. coli transformed with a): BBa_K1976054 and b): BBa_K1976055.
 +
</p>
 +
</div>
 +
<br>
  
T7 generator of the trypsin fragment of the Colicin E2 DNase
+
</body>
<!-- Add more about the biology of this part here
+
</html>
===Usage and Biology===
+
===<h2>Usage</h2>===
  
<!-- -->
+
<html>
<span class='h3bb'>Sequence and Features</span>
+
<body>
<partinfo>BBa_K1976055 SequenceAndFeatures</partinfo>
+
    <p>
 +
This part exhibited signs of leakage, that can kill the host if cells are transformed with it, that have a T7 promoter system, due to the endonuclease activity of the Colicin E2 DNase domain.
 +
</p>
  
 +
<body>
 +
 +
</html>
  
<!-- Uncomment this to enable Functional Parameter display
+
===<h2>Characteristics</h2>===
===Functional Parameters===
+
 
<partinfo>BBa_K1976055 parameters</partinfo>
+
<h2>Sequence and Features</h2>
<!-- -->
+
<partinfo>BBA_K1976055 SequenceAndFeatures</partinfo>
 +
<br>
 +
<html>
 +
<body>
 +
<b>References</b>
 +
<br>
 +
[1] Cascales et al, Colicin Biology, Microbiology and Molecular Biology Reviews, vol. 71, pp. 158-229, 2007<br>
 +
</body>
 +
</html>

Revision as of 15:09, 25 October 2016

trypsin fragment of Colicin E2 with B0034 and T7 promoter

Generator for the Colicin DNase domain BBa_K1976048.

Figure 1:Figure 5: growth of BL21 E. coli transformed with a): BBa_K1976054 and b): BBa_K1976055.


Usage

This part exhibited signs of leakage, that can kill the host if cells are transformed with it, that have a T7 promoter system, due to the endonuclease activity of the Colicin E2 DNase domain.

Characteristics

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 84
  • 1000
    COMPATIBLE WITH RFC[1000]


References
[1] Cascales et al, Colicin Biology, Microbiology and Molecular Biology Reviews, vol. 71, pp. 158-229, 2007