Difference between revisions of "Part:BBa K1992009"
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__NOTOC__ | __NOTOC__ | ||
− | <partinfo> | + | <partinfo>BBa_K1992009 short</partinfo> |
<span class='h3bb'>Sequence and Features</span> | <span class='h3bb'>Sequence and Features</span> | ||
− | <partinfo> | + | <partinfo>BBa_K1992009 SequenceAndFeatures</partinfo> |
==Introduction== | ==Introduction== | ||
− | A GFP gene was fused to the improved expression system of the Tar chemoreceptor(<partinfo> | + | A GFP gene was fused to the improved expression system of the Tar chemoreceptor(<partinfo>K1992004</partinfo>). The plasmid is comprised of a promoter, a strong RBS, Tar gene, a GFP gene and a terminator. In order to obtain the fusion, a proper linker sequence was introduced between the Tar and the GFP gene. |
==Usage and Biology== | ==Usage and Biology== |
Latest revision as of 22:57, 21 October 2016
Tar GFP tagged expression system (promoter+RBS+coding+terminator)
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 7
Illegal NheI site found at 30 - 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 1343
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 2385
Illegal SapI.rc site found at 172
Introduction
A GFP gene was fused to the improved expression system of the Tar chemoreceptor(BBa_K1992004). The plasmid is comprised of a promoter, a strong RBS, Tar gene, a GFP gene and a terminator. In order to obtain the fusion, a proper linker sequence was introduced between the Tar and the GFP gene.
Usage and Biology
This device was used as a proof of concept in order to verify the migration of the chemoreceptor to the poles of the bacterial membrane.
Experiments and results
Expariments and results of this exprassion system can be seen in the Tar-GFP part (BBa_K1992003) and in our result page [http://2016.igem.org/Team:Technion_Israel/Tar_improvements Tar improvements and characterzation]