Coding
frmA

Part:BBa_K5313015:Design

Designed by: Jinyang Gu   Group: iGEM24_NEFU-China   (2024-09-28)


frmA


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 193
    Illegal AgeI site found at 517
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

When designing the expression system for the frmA gene, we focused on regulating expression levels and managing the effects of toxic substances on the host cells. Since formaldehyde is highly toxic, promoter optimization for frmA was necessary in high-concentration formaldehyde degradation experiments to ensure the gene product effectively handles formaldehyde accumulation. Additionally, frmA protein expression could impose a metabolic burden on the host cells, so we selected a mild expression system to minimize stress. Codon optimization was also considered to enhance the gene's expression efficiency in E. coli.


Source

The frmA gene is derived from the genome of Escherichia coli. This gene is naturally present in wild-type E. coli and is responsible for the metabolism of formaldehyde. The gene sequence can be obtained through genomic sequencing or retrieved from public databases, such as NCBI, which provides detailed information on the frmA gene.

References