Difference between revisions of "Part:BBa K1951009:Design"
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High level flagellin expression: | High level flagellin expression: | ||
This biobrick is composed of two parts: | This biobrick is composed of two parts: | ||
− | * [https://parts.igem.org/Part: | + | * [https://parts.igem.org/Part:BBa_K1951006 BBa_K880006] A strong promoter, strong RBS combination specifically conceived and tested for high expression levels of proteins in <i>E.coli</i> (this part is itself composed of sub-parts [https://parts.igem.org/Part:BBa_J23100 BBa_J23100 ] and [https://parts.igem.org/Part:BBa_B0034 BBa_B0034] |
− | * [https://parts.igem.org/Part:BBa_K1951005 BBa_K1951005] the FliC coding sequence designed by our team for high level expression in <i> | + | * [https://parts.igem.org/Part:BBa_K1951005 BBa_K1951005] the FliC coding sequence designed by our team for high level expression in <i>Desulfovibrio vulgaris</i> with sequence optimization. |
+ | ===Sequence optimization=== | ||
We found the raw sequence from online data base '''QUEL DATA BASE YOANN????'' | We found the raw sequence from online data base '''QUEL DATA BASE YOANN????'' | ||
+ | |||
+ | ===Promoter and RBS selection=== | ||
+ | |||
+ | As the purpose of this part is high level protein expression we selected the part [https://parts.igem.org/Part:BBa_K1951006 BBa_K880006] to drive expression of our coding sequence. We chose this part as: | ||
+ | * it combines a strong promotor and a RBS (so avoiding the separate incorporation of 2 parts). | ||
===Source=== | ===Source=== |
Revision as of 22:12, 15 October 2016
FliC Desulfovibrio producer
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 362
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 461
Design Notes
High level flagellin expression: This biobrick is composed of two parts:
- BBa_K880006 A strong promoter, strong RBS combination specifically conceived and tested for high expression levels of proteins in E.coli (this part is itself composed of sub-parts BBa_J23100 and BBa_B0034
- BBa_K1951005 the FliC coding sequence designed by our team for high level expression in Desulfovibrio vulgaris with sequence optimization.
Sequence optimization
We found the raw sequence from online data base 'QUEL DATA BASE YOANN????
Promoter and RBS selection
As the purpose of this part is high level protein expression we selected the part BBa_K880006 to drive expression of our coding sequence. We chose this part as:
- it combines a strong promotor and a RBS (so avoiding the separate incorporation of 2 parts).
Source
We used previous biobrick :
- BBa_K880005
- BBa_K1951006