Difference between revisions of "Part:BBa K2273108:Design"
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__NOTOC__ | __NOTOC__ | ||
− | <partinfo>BBa_K2273108 short</partinfo> | + | ===<partinfo>BBa_K2273108 short</partinfo>=== |
+ | The <i>blaR1</i> gene is part of the Beta-Lactam Biosensor project of [http://2017.igem.org/Team:TU_Dresden iGEM Team TU Dresden 2017 (EncaBcillus - It's a trap!)].<br><br> | ||
+ | This gene is part of the <i>bla</i> operon found in <i>Staphylococcus aureus</i> and encodes a receptor that localizes in the inner cell membrane and can bind beta-lactam antibiotics, Uniprot [http://www.uniprot.org/uniprot/P18357]).<br><br> | ||
+ | ===DesignNotes=== | ||
+ | This part has been codon optimized for expression in <i>Bacillus subtilis</i> using the online tool provided by IDT DNA. A Ribosome Binding Site (AGGAGG) specific for translation in <i>Bacillus subtilis</i> has been added upstream of the gene. Further the part features the RFC10 prefix and suffix:<br> | ||
+ | <table> | ||
+ | <tr> | ||
+ | <td width="70">Prefix with</td> | ||
+ | <td width="200"><span style="color:blue">EcoRI</span>, <span style="color:green">NotI</span>, <span style="color:red">XbaI</span> and <span style="color:silver">SD</span></td> | ||
+ | <td><span style="color:blue">GAATTC</span><span style="color:green">GCGGCCGC</span>T<span style="color:red">TCTAGA</span>T<span style="color:silver">AAGGAGG</span>TCAAAA</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>Suffix with</td> | ||
+ | <td><span style="color:red">SpeI</span>, <span style="color:green">NotI</span> and <span style="color:blue">PstI</span></td> | ||
+ | <td><u>TAA</u>T<span style="color:red">ACTAGT</span>A<span style="color:green">GCGGCCG</span><span style="color:blue">CTGCAG</span>A</td> | ||
+ | </tr> | ||
+ | </table> | ||
+ | Sites of restriction enzymes generating compatible overhangs are indicated by sharing one color. (<span style="color:blue">EcoRI</span> and <span style="color:blue">PstI</span> are marked in blue, <span style="color:green">NotI</span> in green, <span style="color:red">XbaI</span> and <span style="color:red">SpeI</span> in red | ||
<partinfo>BBa_K2273108 SequenceAndFeatures</partinfo> | <partinfo>BBa_K2273108 SequenceAndFeatures</partinfo> | ||
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===Source=== | ===Source=== | ||
− | + | This part was chemically synthesized as we needed a codon optimized version of the <i>blaR1</i> gene from <i>Staphylococcus aureus</i>. The original sequence was taken from the <i>S. aureus</i> N315 genome sequence found in the NCBI database. | |
− | + | ||
===References=== | ===References=== | ||
+ | Llarrull, L., Prorok, M., Mobashery, S. (2011) |
Revision as of 12:52, 25 September 2017
BlaR1 Beta-Lactam Receptor derived from Staphylococcus aureus N315
The blaR1 gene is part of the Beta-Lactam Biosensor project of [http://2017.igem.org/Team:TU_Dresden iGEM Team TU Dresden 2017 (EncaBcillus - It's a trap!)].
This gene is part of the bla operon found in Staphylococcus aureus and encodes a receptor that localizes in the inner cell membrane and can bind beta-lactam antibiotics, Uniprot [http://www.uniprot.org/uniprot/P18357]).
DesignNotes
This part has been codon optimized for expression in Bacillus subtilis using the online tool provided by IDT DNA. A Ribosome Binding Site (AGGAGG) specific for translation in Bacillus subtilis has been added upstream of the gene. Further the part features the RFC10 prefix and suffix:
Prefix with | EcoRI, NotI, XbaI and SD | GAATTCGCGGCCGCTTCTAGATAAGGAGGTCAAAA |
Suffix with | SpeI, NotI and PstI | TAATACTAGTAGCGGCCGCTGCAGA |
Sites of restriction enzymes generating compatible overhangs are indicated by sharing one color. (EcoRI and PstI are marked in blue, NotI in green, XbaI and SpeI in red
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Source
This part was chemically synthesized as we needed a codon optimized version of the blaR1 gene from Staphylococcus aureus. The original sequence was taken from the S. aureus N315 genome sequence found in the NCBI database.
References
Llarrull, L., Prorok, M., Mobashery, S. (2011)