Difference between revisions of "Part:BBa K3598022"
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<partinfo>BBa_K3598022 short</partinfo> | <partinfo>BBa_K3598022 short</partinfo> | ||
| − | [[Part: mTyr-CNK tyrosinase(BBa_K3089006)|BBa_K3089006]] | + | [[Part:mTyr-CNK tyrosinase(BBa_K3089006)|BBa_K3089006]] |
This is the RBS lib construction system for mTyr-CNK expression. The T7 promoter is regulated by lacI repressor through lacO operator to control the expression of mTyr-CNK. The system is used to produce mTyr-CNK, so we construct a RBS library to improve the yield of mTyr-CNK. | This is the RBS lib construction system for mTyr-CNK expression. The T7 promoter is regulated by lacI repressor through lacO operator to control the expression of mTyr-CNK. The system is used to produce mTyr-CNK, so we construct a RBS library to improve the yield of mTyr-CNK. | ||
Revision as of 05:09, 26 October 2020
LacI_LacI promoter_T7 promoter_lac operator_RBS lib_mTyr-CNK_T7 terminator
This is the RBS lib construction system for mTyr-CNK expression. The T7 promoter is regulated by lacI repressor through lacO operator to control the expression of mTyr-CNK. The system is used to produce mTyr-CNK, so we construct a RBS library to improve the yield of mTyr-CNK.
Experiments and Results
We have improved the previous part BBa_K3089006 by using a series of new RBSs that differ in their expression efficiencies in expressing tyrosinase mTyr-CNK.
We began with randomly arranging six pairs in the system's RBS sequence TAAGTATAAGNNNNNNATAT, and verifying the resulting RBSs' strengths with RBS calculator. 15 of the strongest RBSs from verification are taken into our RBS library.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal XhoI site found at 2233
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 1280
Illegal BsaI.rc site found at 1270