Difference between revisions of "Part:BBa K4129108"
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Magnus Haahr (Talk | contribs) |
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<partinfo>BBa_K4129108 short</partinfo> | <partinfo>BBa_K4129108 short</partinfo> | ||
− | FunsTF58 is a synthetic transcription factor (sTF). FunsTF58 should initiate the transcription through the 6xLexO minimal promoter. This sTF is the sensing part of the biosensor. | + | FunsTF58 is a synthetic transcription factor (sTF). FunsTF58 should initiate the transcription through the 6xLexO minimal promoter. This sTF is the sensing part of the biosensor. |
− | FunsTF58 is a fusion protein consisting of the DNA-binding domain | + | |
− | LexA is a repressor that regulates the SOS response in E. coli (Radman. 1975). LexA binds to a specific DNA motif, | + | FunsTF58 is a fusion protein consisting of the DNA-binding domain LexA, the ligand sensing domain HbaR4, transactivation domain VP16 and the nuclear localization signal (NLS) SV40. The linker between LexA and HbaR4 is a longer version linker (Ottoz et. al (2014) compared to sBAD, which was the reference sTF (Castaño-Cerezo et. al (2020)). FunsTF58 was codon optimised to <i>A. Niger </i>. |
+ | |||
+ | LexA is a repressor that regulates the SOS response in <i>E. coli</i> (Radman. 1975). LexA binds to a specific DNA motif, namely LexO sites (Erill. et al (2003)). HbaR is a transcription factor from <i>Rhodopseudomonas palustris</i> that initiates transcription in the presence of benzoic acid (Egland. et al (2000) or in the presence of benzoic acid derivatives (Castaño-Cerezo et. al (2020)). We created 16 mutants of HbaR and FunsTF58 carried mutant 4 of HbaR, which had the following mutations: A45V, L69A, G71K, E77W, F85G, A86G, E87G, A88G, A89P, Y96A, L97Y, A98M, N99T, A100V, and V142Q. | ||
Viral Protein 16 (VP16) from herpes simplex virus type 1 is a transcription factor that uses a transactivation domain to recruit the RNA polymerase II.The NLS SV40 is a small peptide sequence of PKKKRKV that enables transport of the protein to the nucleus (Garcia-Bustos et. al (1991)). | Viral Protein 16 (VP16) from herpes simplex virus type 1 is a transcription factor that uses a transactivation domain to recruit the RNA polymerase II.The NLS SV40 is a small peptide sequence of PKKKRKV that enables transport of the protein to the nucleus (Garcia-Bustos et. al (1991)). | ||
+ | |||
+ | FunsTF58 did not show functionality. | ||
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Revision as of 12:38, 11 October 2022
The fungal synthetic transcription factor, FunsTF58 (LexA-LL-HbaR4-VP16-SV40)
FunsTF58 is a synthetic transcription factor (sTF). FunsTF58 should initiate the transcription through the 6xLexO minimal promoter. This sTF is the sensing part of the biosensor.
FunsTF58 is a fusion protein consisting of the DNA-binding domain LexA, the ligand sensing domain HbaR4, transactivation domain VP16 and the nuclear localization signal (NLS) SV40. The linker between LexA and HbaR4 is a longer version linker (Ottoz et. al (2014) compared to sBAD, which was the reference sTF (Castaño-Cerezo et. al (2020)). FunsTF58 was codon optimised to A. Niger .
LexA is a repressor that regulates the SOS response in E. coli (Radman. 1975). LexA binds to a specific DNA motif, namely LexO sites (Erill. et al (2003)). HbaR is a transcription factor from Rhodopseudomonas palustris that initiates transcription in the presence of benzoic acid (Egland. et al (2000) or in the presence of benzoic acid derivatives (Castaño-Cerezo et. al (2020)). We created 16 mutants of HbaR and FunsTF58 carried mutant 4 of HbaR, which had the following mutations: A45V, L69A, G71K, E77W, F85G, A86G, E87G, A88G, A89P, Y96A, L97Y, A98M, N99T, A100V, and V142Q. Viral Protein 16 (VP16) from herpes simplex virus type 1 is a transcription factor that uses a transactivation domain to recruit the RNA polymerase II.The NLS SV40 is a small peptide sequence of PKKKRKV that enables transport of the protein to the nucleus (Garcia-Bustos et. al (1991)).
FunsTF58 did not show functionality.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 673
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 607
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 765
- 1000COMPATIBLE WITH RFC[1000]