Coding

Part:BBa_K3944043

Designed by: Olof Dahlman   Group: iGEM21_Chalmers-Gothenburg   (2021-09-30)


FabZ

Bacterial fatty acid synthase (FAS) system enzyme, codon optimized for S.Cerevisiae. Part of the FAS2 system from E.coli, see our wiki for an overview of the system.

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal XbaI site found at 39
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal XbaI site found at 39
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal XbaI site found at 39
  • 1000
    COMPATIBLE WITH RFC[1000]


Usage and Biology

FabZ dehydrates the growing hydroxy-thioester-ACP fatty acid chain, creating a conjugated thioester-ACP system which is then reduced by FabI.

FAS2 Chalms Gu 2021.png

Overview map of FAS2 system (2).

Experimental design

By creating a single genetic fragment with FabZ and FabD and their promoters going in the forward and reverse direction, these two genes are easily inserted using the pCfB2909(XII-5 MarkerFree) plasmid from EasyClone kit (3).

Methodology

Double gene fragment ordered from IDT was cloned using Phusion polymerase according to protocol. Insert was purified following protocol for gel electrophoresis and ThermoFischer gel purification kit, followed by assembly into linearized plasmid backbone. The constructed plasmid was transformed into E.coli, grown overnight, inoculated overnight again, followed by harvesting following protocol for ThermoFischer plasmid miniprep kit. The purified plasmid was digested to yield the linearized insertion fragment and transformed into S.Cerevisiae strain CEN.PK 102-5B along with CAS9 and gRNA plasmids.



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