Difference between revisions of "Part:BBa K1045017:Design"

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===Design Notes===
 
===Design Notes===
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DarR fused to the terminator were cut out from [[Part:BBa_K1045016|BBa_K1045016]] and ligated in a pre-fixing composition into [[Part:BBa_K1045015|BBa_K1045015]].
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The insert [[Part:BBa_K1045015|BBa_K1045015]] was cut out from its plasmid and ligated in a post-fixing composition into the vector [[Part:BBa_K1045016|BBa_K1045016]].
  
 
===Source===
 
===Source===
  
−
This composite part was constructed using parts which were either obtained via hybridization oligos ([[Part:BBa_K1045011|BBa_1045011]];[[Part:BBa_K1045012|BBa_1045012]])or by amplification of plasmid DNA ([[Part:BBa_K1045009|BBa_1045009]]) or ''M. smegmatis'' chromosomal DNA ([[Part:BBa_K1045001|BBa_1045001]]). Part [[Part:BBa_E0240|BBa_E0240]] derived from the plasmid in the distribution kit.
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This composite part was constructed using hybridization oligos for [[Part:BBa_K1045010|BBa_1045010]], [[Part:BBa_K1045011|BBa_1045011]] and [[Part:BBa_K1045012|BBa_1045012]]. The hybridization oligos were ordered from Sigma-Aldrich. Sequence information derived from the Parts Registry and Zhang ''et al.'', 2013. In addition, parts that were obtained either by amplification of plasmid DNA from the distribution kit 2013 (inverse terminator [[Part:BBa_K1045009|BBa_1045009]]) or ''Mycobacterium smegmatis'' chromosomal DNA (DarR ORF, [[Part:BBa_K1045001|BBa_1045001]]) were employed. The chromosomal DNA of ''M. smegmatis'' was purchased from DSMZ, Braunschweig, Germany ([http://www.dsmz.de/catalogues/details/culture/DSM-43756.html?tx_dsmzresources_pi5%5BreturnPid%5D=304 DSM No. 43756]). Part [[Part:BBa_E0240|BBa_E0240]] derived from the plasmid in the distribution kit 2013.
  
 
===References===
 
===References===
 +
Lei Zhang, Weihui Li, and Zheng-Guo He (2013) “DarR, a TetR-like Transcriptional Factor, Is a Cyclic Di-AMP-responsive Repressor in ''Mycobacterium smegmatis''”, THE JOURNAL OF BIOLOGICAL CHEMISTRY VOL. 288, NO. 5, pp. 3085–3096

Latest revision as of 20:06, 28 October 2013

DarR reporter system


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 806
    Illegal NheI site found at 829
    Illegal NheI site found at 909
    Illegal NheI site found at 932
    Illegal NotI site found at 718
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 731
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 860
    Illegal AgeI site found at 168
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 1630


Design Notes

The insert BBa_K1045015 was cut out from its plasmid and ligated in a post-fixing composition into the vector BBa_K1045016.

Source

This composite part was constructed using hybridization oligos for BBa_1045010, BBa_1045011 and BBa_1045012. The hybridization oligos were ordered from Sigma-Aldrich. Sequence information derived from the Parts Registry and Zhang et al., 2013. In addition, parts that were obtained either by amplification of plasmid DNA from the distribution kit 2013 (inverse terminator BBa_1045009) or Mycobacterium smegmatis chromosomal DNA (DarR ORF, BBa_1045001) were employed. The chromosomal DNA of M. smegmatis was purchased from DSMZ, Braunschweig, Germany ([http://www.dsmz.de/catalogues/details/culture/DSM-43756.html?tx_dsmzresources_pi5%5BreturnPid%5D=304 DSM No. 43756]). Part BBa_E0240 derived from the plasmid in the distribution kit 2013.

References

Lei Zhang, Weihui Li, and Zheng-Guo He (2013) “DarR, a TetR-like Transcriptional Factor, Is a Cyclic Di-AMP-responsive Repressor in Mycobacterium smegmatis”, THE JOURNAL OF BIOLOGICAL CHEMISTRY VOL. 288, NO. 5, pp. 3085–3096