Source:
Generated By: https://synbiohub.org/public/igem/igem2sbol/1
Created by: Monica Victoria Gutierrez Salazar
Date created: 2016-10-02 11:00:00
Date modified: 2016-10-23 08:34:14
SAGTI linker + Luciferase
| Types | DnaRegion |
| Roles | Reporter engineered_region |
| Sequences | BBa_K2017003_sequence (Version 1) |
Description
Firefly luciferase protein. It oxidates its substrate luciferin, emitting light during the process. It can act as a reporter protein when used with a promoter. This part is made to be fused to the 3' with other coding sequence, so it includes the SAGTI linker in order to let the luciferase acquire the correct tertiary structure.The luciferase does not include ATG (Met) to initiate translation, as it needs to be fused to 3' of other coding sequence. The translation must begin in the coding sequence fused to the 3'.
The linker includes a random nucleotide in 5', to change the reading frame of the luciferase. That way, it will not be translated unless an indel is produced in the coding region to which the part is fused.
Notes
This part must be fused to the 3' of other coding sequence. In order to be used in our modular gRNA testing system, it was necessary to remove the ATG (Met codon) to avoid unexpected translation. The translation must begin in the coding sequence fused to the 3'.The linker includes a random nucleotide in 5', to change the reading frame of the luciferase. That way, it will not be translated unless an indel is produced in the coding region to which the part is fused.
Source
Luciferase was obtained from laboratory stock. The linker was fused with a PCR.| Sequence Annotation | Location | Component / Role(s) |
| Luciferase SAGTI Linker Additional nucleotide | 16,1667 2,15 1,1 | CDS feature/protein feature/misc sequence_feature feature/misc sequence_feature |