Difference between revisions of "Part:BBa K1648003"
S1155046866 (Talk | contribs) |
Fatfaatlai (Talk | contribs) |
||
Line 2: | Line 2: | ||
<partinfo>BBa_K1648003 short</partinfo> | <partinfo>BBa_K1648003 short</partinfo> | ||
− | Consist of | + | Consist of a template for recombination of <b> mamXY, mamGC, mms </b> operon([https://parts.igem.org/wiki/index.php?title=Part:BBa_K1648001 K1648001]), a promotor & RBS([https://parts.igem.org/Part:BBa_J13002 J13002]) in front of each template and a double terminator([https://parts.igem.org/Part:BBa_B0015 B0015]) at the back of each template. |
− | + | This part is designed for <b>homologous recombination</b> to introduce the large magnetosome forming operon into <i>Azotobactor vinelandii</i>. | |
− | + | This part is introduced into <i>A. vinelandii</i> genome via <b>random integration</b> before full operon sequences to be transformed into <i>A. vinelandii</i>. | |
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Revision as of 01:39, 19 September 2015
Recombination Template for mamXY,mamGC and mms Operons with Promotor and Terminator
Consist of a template for recombination of mamXY, mamGC, mms operon(K1648001), a promotor & RBS(J13002) in front of each template and a double terminator(B0015) at the back of each template.
This part is designed for homologous recombination to introduce the large magnetosome forming operon into Azotobactor vinelandii.
This part is introduced into A. vinelandii genome via random integration before full operon sequences to be transformed into A. vinelandii.
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 1413
Illegal BamHI site found at 512 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 683
Illegal NgoMIV site found at 865
Illegal NgoMIV site found at 955
Illegal NgoMIV site found at 1363
Illegal AgeI site found at 566 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 550
Illegal BsaI site found at 649
Illegal BsaI site found at 930