Difference between revisions of "Part:BBa K3187028"
Line 3: | Line 3: | ||
<partinfo>BBa_K3187028 short</partinfo> | <partinfo>BBa_K3187028 short</partinfo> | ||
− | < | + | <html> |
+ | <div class="container"> | ||
+ | <div class="row"> | ||
+ | <div class="col mx-2"> | ||
+ | |||
+ | <h3>Profile</h3> | ||
+ | <table style=“width:80%“> | ||
+ | <tr> | ||
+ | <td><b>Name</b></td> | ||
+ | <td>Sortase A7M </td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td><b>Base pairs</b></td> | ||
+ | <td>470</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td><b>Molecular weigth</b></td> | ||
+ | <td>17.85 kDa</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td><b>Origin</b></td> | ||
+ | <td><i>Staphylococcus aureus</i>, synthetic</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td><b>Parts</b></td> | ||
+ | <td>Basic part</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td><b>Properties</b></td> | ||
+ | <td> calcium-independent, transpeptidase, linking sorting motif LPXTG to poly-glycine Tag </td> | ||
+ | </tr> | ||
+ | </table> | ||
+ | <h3> Usage and Biology</h3> | ||
+ | <p> Sortase A7M (SrtA7M) is a calcium-independent transpeptidase derived from the enzyme Sortase A from Staphylococcus aureus.<sup id="cite_ref-1" class="reference"> | ||
+ | <a href="#cite_note-1">[1]</a> | ||
+ | </sup> Similar to Sortase A, SrtA7M connects two peptides covalently, one with a poly-glycine (poly-G) at the N-terminus and one with LPXTG motif at the C-terminus. It acts by cleaving between Gly and Thr of the LPXTG motif and catalyzing the formation of an amide bond to the poly-G sequence.<sup id="cite_ref-2" class="reference"> | ||
+ | <a href="#cite_note-2">[2] </a> | ||
+ | </sup> | ||
+ | |||
+ | <h3>Methods</h3> | ||
+ | <p>The basic part Sortase A7M is produced and purified as the composite part <a href="https://parts.igem.org/Part:BBa_K3187005"target="_blank">BBa_K3187005</a>(Sortase A7M). | ||
+ | For the expression and purification of SrtA7M, a part containing T7 promoter, a lac operator and a ribosomal binding site <a href="https://parts.igem.org/Part:BBa_K3187029MMM"target="_blank">BBa_K3187029</a> N-terminal and a 6xHis-Tag with a TGA stop codon <a href="https://parts.igem.org/Part:BBa_K3187024"target="_blank">(BBa_K3187024)</a> C-terminal of the coding sequence were added. | ||
+ | The production was performed in the <i>E. Coli</i> strain BL21 (DE3). The purification was done with the <a href="#"target="_blank">GE Healthcare ÄTKA Pure machine</a> which is a machine for FPLC. </p> | ||
+ | |||
+ | <h3>Results</h3> | ||
+ | |||
+ | |||
+ | </div> | ||
+ | </div> | ||
+ | |||
+ | </div> | ||
+ | </html> | ||
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Revision as of 12:33, 16 October 2019
Sortase A7M (Ca2+-independent variant)
Profile
Name | Sortase A7M |
Base pairs | 470 |
Molecular weigth | 17.85 kDa |
Origin | Staphylococcus aureus, synthetic |
Parts | Basic part |
Properties | calcium-independent, transpeptidase, linking sorting motif LPXTG to poly-glycine Tag |
Usage and Biology
Sortase A7M (SrtA7M) is a calcium-independent transpeptidase derived from the enzyme Sortase A from Staphylococcus aureus. [1] Similar to Sortase A, SrtA7M connects two peptides covalently, one with a poly-glycine (poly-G) at the N-terminus and one with LPXTG motif at the C-terminus. It acts by cleaving between Gly and Thr of the LPXTG motif and catalyzing the formation of an amide bond to the poly-G sequence. [2]
Methods
The basic part Sortase A7M is produced and purified as the composite part BBa_K3187005(Sortase A7M). For the expression and purification of SrtA7M, a part containing T7 promoter, a lac operator and a ribosomal binding site BBa_K3187029 N-terminal and a 6xHis-Tag with a TGA stop codon (BBa_K3187024) C-terminal of the coding sequence were added. The production was performed in the E. Coli strain BL21 (DE3). The purification was done with the GE Healthcare ÄTKA Pure machine which is a machine for FPLC.
Results
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal XhoI site found at 445
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]