Difference between revisions of "Part:BBa K1976051"
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+ | table, td, th { border: 0px solid black; } | ||
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+ | <h1>Colicin E2 DNase trypsin fragment and immunity protein Im2 generator with anderson promoters</h1> | ||
− | + | The DNase trypsin fragment (part <a href="https://parts.igem.org/Part:BBa_K197604">BBa_K1976049</a>) can be obtained by trypsin digestion of colicin E2. In this part the gene is fusioned to the strong ribosomal binding site B0034. | |
− | < | + | |
− | + | <br> | |
+ | <br> | ||
+ | <div align="center"> | ||
+ | <img style="width: 40%; height: 40%; margin-left: 15px; margin-right: 15px;" alt="" src="https://static.igem.org/mediawiki/parts/8/8b/Immuno_colicine2.png"> | ||
− | The | + | <p align="left" style="width: 650px; margin-left: 15px; margin-right: 15px;" alt=""> |
+ | <b>Figure 1:</b> The structure of the Im2 immunity protein and Colicin E2 in a complex. | ||
+ | </p> | ||
+ | </div> | ||
+ | <br> | ||
− | < | + | </body> |
− | ===Usage | + | </html> |
− | This part can be used for assembly of generators. In combination with the immunity protein Im2 (part | + | ===<h2>Usage</h2>=== |
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+ | <html> | ||
+ | <body> | ||
+ | |||
+ | This part can be used for assembly of generators. In combination with the immunity protein Im2 (part <a href="https://parts.igem.org/Part:BBa_K197604">BBa_K1976026</a>) it serves as a safety mechanism (see part <a href="https://parts.igem.org/Part:BBa_K197604">BBa_K1976053</a>). | ||
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+ | <body> | ||
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+ | </html> | ||
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+ | ===<h2>Characteristics</h2>=== | ||
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+ | <html> | ||
+ | <body> | ||
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+ | The DNase trypsin fragment of colicin E2 consists of 137 residues what conforms to about one third to colicin. We used only one of the three domains of colicin since the metabolic burdon would be significant smaller. This fragment differs to the part 50 in 5 additional amino acids since a trypsin digestion described in the literature leaded to this fragment. So we wanted to check out any difference in the activities between the DNase fragment with and without theese additional amino acids. The activity tests showed that the so called miniColicin has functional DNase activity. | ||
+ | <br> | ||
+ | <center> | ||
+ | |||
+ | |||
+ | </html> | ||
+ | |||
+ | ===<h2>Characteristics</h2>=== | ||
+ | |||
+ | </body> | ||
+ | </html> | ||
+ | |||
+ | |||
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+ | Fragment of Colicin E2 as if treated with trypsin with B0034 as a ribosomal binding site. | ||
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<span class='h3bb'>Sequence and Features</span> | <span class='h3bb'>Sequence and Features</span> | ||
<partinfo>BBa_K1976051 SequenceAndFeatures</partinfo> | <partinfo>BBa_K1976051 SequenceAndFeatures</partinfo> | ||
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<partinfo>BBa_K1976051 parameters</partinfo> | <partinfo>BBa_K1976051 parameters</partinfo> | ||
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Revision as of 03:05, 28 October 2016
Colicin E2 DNase trypsin fragment and immunity protein Im2 generator with anderson promoters
The DNase trypsin fragment (part BBa_K1976049) can be obtained by trypsin digestion of colicin E2. In this part the gene is fusioned to the strong ribosomal binding site B0034.Figure 1: The structure of the Im2 immunity protein and Colicin E2 in a complex.
Usage
This part can be used for assembly of generators. In combination with the immunity protein Im2 (part BBa_K1976026) it serves as a safety mechanism (see part BBa_K1976053).
Characteristics
The DNase trypsin fragment of colicin E2 consists of 137 residues what conforms to about one third to colicin. We used only one of the three domains of colicin since the metabolic burdon would be significant smaller. This fragment differs to the part 50 in 5 additional amino acids since a trypsin digestion described in the literature leaded to this fragment. So we wanted to check out any difference in the activities between the DNase fragment with and without theese additional amino acids. The activity tests showed that the so called miniColicin has functional DNase activity.
Characteristics
</body> </html>
Fragment of Colicin E2 as if treated with trypsin with B0034 as a ribosomal binding site. Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 64
- 1000COMPATIBLE WITH RFC[1000]