Difference between revisions of "Part:BBa K4239001"
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<partinfo>BBa_K4239001 short</partinfo> | <partinfo>BBa_K4239001 short</partinfo> | ||
− | fiatluxC is made to be used with fiatluxD. It codes for a subpart | + | fiatluxC is made to be used with fiatluxD and fiatluxE. It codes for a subpart fatty acid reductase. With the subparts coding from fiatluxD and fiatluxE, they form a complex that recycles fatty acids to fatty aldehydes. |
Luciferase has as substrats FMNH2, O2 and Fatty aldehydes, and produces H20, Fatty Acids and FMN and emits luminescence. | Luciferase has as substrats FMNH2, O2 and Fatty aldehydes, and produces H20, Fatty Acids and FMN and emits luminescence. |
Revision as of 19:29, 6 October 2022
Enhanced luciferase subunits fiatluxC
fiatluxC is made to be used with fiatluxD and fiatluxE. It codes for a subpart fatty acid reductase. With the subparts coding from fiatluxD and fiatluxE, they form a complex that recycles fatty acids to fatty aldehydes.
Luciferase has as substrats FMNH2, O2 and Fatty aldehydes, and produces H20, Fatty Acids and FMN and emits luminescence.
The systeme fiatluxC/fiatluxD is made to be used with fiatluxA, fiatluxB 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.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 1311