Difference between revisions of "Part:BBa K533009"
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<partinfo>BBa_K533009 short</partinfo> | <partinfo>BBa_K533009 short</partinfo> | ||
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Tar receptor is now under the drive of lacI promoter, a constitutive weak promoter. In addition, the Shine-Dalgarno sequence is removed to lower translation efficiency. Lower expression level ensures more specific chemotaxis and better engineering of movement control. | Tar receptor is now under the drive of lacI promoter, a constitutive weak promoter. In addition, the Shine-Dalgarno sequence is removed to lower translation efficiency. Lower expression level ensures more specific chemotaxis and better engineering of movement control. | ||
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===Usage and Biology=== | ===Usage and Biology=== | ||
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+ | [[Image:mgoulian_tar.jpg]] | ||
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+ | pPD10, the empty vector demonstrated no significant chemotaxis while pPD12 vector demonstrated strong chemotaxis. We thus cloned the expression cassette from pPD12 and use it for our chemotaxis experiments. | ||
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Latest revision as of 16:03, 5 October 2011
Tar receptor weak expression cassette
Tar receptor is now under the drive of lacI promoter, a constitutive weak promoter. In addition, the Shine-Dalgarno sequence is removed to lower translation efficiency. Lower expression level ensures more specific chemotaxis and better engineering of movement control.
Usage and Biology
pPD10, the empty vector demonstrated no significant chemotaxis while pPD12 vector demonstrated strong chemotaxis. We thus cloned the expression cassette from pPD12 and use it for our chemotaxis experiments.
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal XbaI site found at 1074
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23INCOMPATIBLE WITH RFC[23]Illegal XbaI site found at 1074
- 25INCOMPATIBLE WITH RFC[25]Illegal XbaI site found at 1074
Illegal AgeI site found at 1936 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 2514
Illegal BsaI site found at 3582
Illegal SapI.rc site found at 765