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Prodigiosin Production in E. Coli

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Prodigiosin Production in E. Coli Brian Hovey and Stephanie Vondrak What is Prodigiosin? A secondary metabolite of various strains of Serratia, and other Gram ... – PowerPoint PPT presentation

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Title: Prodigiosin Production in E. Coli


1
Prodigiosin Production in E. Coli
  • Brian Hovey and Stephanie Vondrak

2
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)

3
S. marcescens
  • S. marcescens is a species of Gram negative, rod
    shaped bacteria
  • Known to cause many nosocomial infections
  • Thrives in high moisture environments

4
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)

5
pigI Gene
  • We chose pigI because it is involved in one of
    the beginning pathways of MBC(4-methoxy-2,2-bipyr
    role-5-carbaldehyd?)
  • This is a precursor of prodigiosin

6
Prodigiosin Pathway
G.O.I.
7
How
  • We located the gene sequence in NCBI, with the
    accession number AJ833002, and has 1473 base
    pairs.
  • We will amplify the gene by PCR with primers
    (TBD)
  • Amplification will be checked by gel
    electrophoresis
  • Biobrick attachment
  • Using BBa_I732085 Tet repressor generator.
  • We will choose a plasmid with specific antibiotic
    resistances
  • Some strains of S. marcescens are known to be
    resistant to a number of antibiotics naturally
  • The restriction site will be cut by TBD
    restriction enzyme

8
How, continued
  • Hybrid DNA will be inserted into plasmid, then
    ligated.
  • Plasmid will then be inserted into host bacteria
    (E. coli)
  • Detection of pigI product will be determined by
    SDS-PAGE
  • As a backup, we will use the Tetracycline
    repression Biobrick to test for pickup of the
    target gene
  • If resistant to (TBD), then it is assumed that
    the plasmid was successfully picked up, those
    cultures can then be tested for resistance to
    tetracycline if the bacteria die, the Biobrick
    was successful and it is assumed that the gene
    also was.

9
References
  • http//onlinelibrary.wiley.com/store/10.1111/j.136
    5-2958.2005.04602.x/asset/j.1365-2958.2005.04602.x
    .pdf?v1th6od3vl2s343f5137efaeab279766f7fc3f23
    1084b43330f5
  • www.serratiamarcescens.net
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