Prodigiosin Production in E. Coli Brian Hovey and Stephanie Vondrak

What is Prodigiosin? A secondary metabolite of various strains of Serratia, and other Gram negative gammaproteobacteria. It is responsible for the red pigment produced by Serratia marcescens. Produced under the control of 14 genes(pigA-pigN)

S. marcescens S. marcescens is a species of Gram negative, rod shaped bacteria Grows on TSA Known to cause many nosocomial infections Thrives in high moisture environments Sample graciously donated by Dr. Walter

Significance ? Recently, has gotten attention for its newfound benefits. Such as: antibacterial, antifungal, antiprotozoal, antimalarial, immunosuppressive, and anticancer properties Has no or little toxicity to cell lines (may operate as a cell cycle regulator)

pigI Gene We chose pigI because it is involved in one of the beginning pathways of MBC(4- methoxy-2,2`-bipyrrole-5-carbaldehydе) This is a precursor of prodigiosin

Prodigiosin Pathway G.O.I.

Gene Info We located the gene sequence in NCBI, with the accession number: AJ833002, and has 1473 base pairs. Since from bacteria, no introns

Gene Info Extraction

Primers We will amplify the gene by PCR Amplification will be checked by gel electrophoresis (pigI is kDa) Primers used: Start – 5’ ATG GCA ACC TTC ATT TCA CC 3’ End – 5’ TCA TCG CGC ATT CAC CTC GG 3’

Primers ATG GCA ACC TTC ATT TCA CCG ATA CTG GAG GCC CTG TTC… …AAG GTG GAC AGA GGA CGT TTG TCC GAG GTG AAT GCG CGA TGA ATG GCA ACC TTC ATT TCA CCG ATA GG CTC CAC TTA CGC GCT ACT Primer

Primers Primers altered for Biobrick use: Start – 5’ GAA TTC TCT AGA ATG GCA ACC TTC ATT TCA CC 3’ End – 5’ GAC GTC TGA TCA TCA TCG CGC ATT CAC CTC GG 3’ PS X E

Removal of Internal Restriction Sites There are two PstI restriction sites within the gene

Removal of Internal Restriction Sites 5’ AG CCC GGG AAA GAC GTC CAA CTC GT 3’ 5’ CTC AAG CAG TTC CTG CAG CCC AGG C 3’ 5’ TC GGG CCC TTT CTG GAG GTT GAG CA 3’ 5’ GAG TTC GTC AAG GAG GTC GGG TCC G 3’ Red = Mutated site Light Blue = Complementary strand

Removal of Internal Restriction Sites Mutagenesis Primers: Template for Mut Primer 1 5’ – AGC CCG GGA AAG ACG TCC AAC TCG T 3’ Complimentary for Mut Primer 1 5’ – TCG GGC CCT TTC TGG AGG TTG AGC A 3’

Removal of Internal Restriction Sites Template for Mut Primer 2 5’ – CTC AAG CAG TTC CTG CAG CCC AGG C 3’ Complimentary for Mut Primer 2 5’ – GAG TTC GTC AAG GAG GTC GGG TCC G 3’

Vector and Regulator Vector of choice will be psB2k3

Vector and Regulator Regulator will be Part:BBa_I Inducible pBad/araC promoter (expose to arabinose to activate)

Interface Vector/Gene Cut into vector at SpeI restriction enzyme site on plasmid Cut at XbaI restriction enzyme on biobrick Ligate

Confirmation The gene will be tested for by SDS-PAGE pigI is kDa

References x/pdf f-46 escens