Difference between revisions of "Part:BBa K4239003"
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<partinfo>BBa_K4239003 short</partinfo> | <partinfo>BBa_K4239003 short</partinfo> | ||
− | + | fiatluxA is made to be used with fiatluxB. It codes for a subpart of the luciferase protein. With the subpart coding from fiatluxD, they form the luciferase protein. | |
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+ | Luciferase has as substrats FMNH2, O2 and Fatty aldehydes, and produces H20, Fatty Acids and FMN and emits luminescence. | ||
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+ | The systeme fiatluxA/fiatluxB is made to be used with fiatluxC, fiatluxD and fiatluxE, gathered in the fiatluxCDABE operon. | ||
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+ | Fiatlux genes come from ilux genes (C, D, A, B, E). They were modified to remove every Igem restriction site (EcoR1, Xba1, Spe1 and Pst1) included in genes. They were also adapted to include the biobrick format. | ||
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+ | The ilux operon was born from a mutated natural luminescence operon present in the bacteria P.luminescens: the lux operon. These mutations were error-prone PCR induced according to Gregor et al.’s study in 2018 (Gregor et al. 2018). The aim was to create a system of genes that produced more light. | ||
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===Usage and Biology=== | ===Usage and Biology=== | ||
Revision as of 19:20, 6 October 2022
Enhanced luciferase substrate forming units fiatluxA
fiatluxA is made to be used with fiatluxB. It codes for a subpart of the luciferase protein. With the subpart coding from fiatluxD, they form the luciferase protein.
Luciferase has as substrats FMNH2, O2 and Fatty aldehydes, and produces H20, Fatty Acids and FMN and emits luminescence.
The systeme fiatluxA/fiatluxB is made to be used with fiatluxC, fiatluxD and fiatluxE, gathered in the fiatluxCDABE operon.
Fiatlux genes come from ilux genes (C, D, A, B, E). They were modified to remove every Igem restriction site (EcoR1, Xba1, Spe1 and Pst1) included in genes. They were also adapted to include the biobrick format.
The ilux operon was born from a mutated natural luminescence operon present in the bacteria P.luminescens: the lux operon. These mutations were error-prone PCR induced according to Gregor et al.’s study in 2018 (Gregor et al. 2018). The aim was to create a system of genes that produced more light.
Usage and Biology
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 504
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI site found at 1023