Difference between revisions of "Part:BBa K3505037"
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===Usage and Biology=== | ===Usage and Biology=== | ||
− | This parts consists of AndersonJ23115:TetR:Double Terminator <bbpart>BBa_K3505033</bbpart> and AndersonJ23115:TetO:RBS-LacI-Double Terminator <bbpart>BBa_K3505034</bbpart>. | + | This parts consists of AndersonJ23115:TetR:Double Terminator <bbpart>BBa_K3505033</bbpart> and AndersonJ23115:TetO:RBS-LacI-Double Terminator <bbpart>BBa_K3505034</bbpart>. AndersonJ23115 is a strong constitutive promoter and TetR is constitutively expressed. TetR binds to tet operator, and inhibits the expression of LacI. |
+ | In the presence of tetracycline or strong chemical repressor as anhydrotetracycline (aTC), TetR inhibition is blocked and the transcription of LacI is allowed. | ||
===Design Notes=== | ===Design Notes=== |
Revision as of 17:44, 27 October 2020
pAndersonJ23115:RBS-TetR-terminator- pAndersonJ23115:tetO:RBS-LacI-terminator
long
Usage and Biology
This parts consists of AndersonJ23115:TetR:Double Terminator BBa_K3505033 and AndersonJ23115:TetO:RBS-LacI-Double Terminator BBa_K3505034. AndersonJ23115 is a strong constitutive promoter and TetR is constitutively expressed. TetR binds to tet operator, and inhibits the expression of LacI.
In the presence of tetracycline or strong chemical repressor as anhydrotetracycline (aTC), TetR inhibition is blocked and the transcription of LacI is allowed.
Design Notes
The coding sequence was domesticated . We removed BsmBI ,BsaI , BtgZI, BpiI sites in order to be compatible with GoldenBraid and MoClo. The sequence is cloned in omega1 vector BBa_K3505010 and has overhangs compatible for Golden Braid cloning.
Verification of Cloning
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal XbaI site found at 76
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 11
Illegal NheI site found at 34
Illegal NheI site found at 838
Illegal NheI site found at 861 - 21COMPATIBLE WITH RFC[21]
- 23INCOMPATIBLE WITH RFC[23]Illegal XbaI site found at 76
- 25INCOMPATIBLE WITH RFC[25]Illegal XbaI site found at 76
- 1000COMPATIBLE WITH RFC[1000]