Prodigiosin

Prodigiosin
Names
IUPAC name
4-methoxy-5-[(Z)-(5-methyl-4-pentyl-2H-pyrrol-2-ylidene)methyl]-1H,1′H-2,2′-bipyrrole
Identifiers
82-89-3 N
3D model (Jmol) Interactive image
ChEBI CHEBI:82758 N
ChEMBL ChEMBL275787 N
ChemSpider 10577755 YesY
MeSH Prodigiosin
PubChem 5351169
Properties
C20H25N3O
Molar mass 323.432 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Prodigiosin is the red pigment produced by many strains of the bacterium Serratia marcescens,[1] other Gram-negative, gamma proteobacteria such as Vibrio psychroerythrus and Hahella chejuensis[2] It is in a family of compounds termed "prodiginines", which are produced in some Gram-negative gamma proteobacteria, as well as select Gram-positive Actinobacteria (e.g. Streptomyces coelicolor).[2] The name "prodigiosin" is derived from "prodigious" (i.e. something marvelous).

Secondary metabolite

Prodigiosin is a secondary metabolite of Serratia marcescens. Because it is easy to detect, it has been used as a model system to study secondary metabolism. Prodigiosin production has long been known to be enhanced by phosphate limitation. In low phosphate conditions, pigmented strains have been shown to grow to a higher density than unpigmented strains.[3]

Religious function

The ability of pigmented strains of Serratia marcescens to grow on bread has led to a possible explanation of Medieval transubstantiation miracles, in which Eucharistic bread is converted into the Body of Christ. Such miracles led to Pope Urban IV instituting the Feast of Corpus Christi in 1264. This followed celebration of a Mass at Bolsena in 1263, led by a Bohemian priest who had doubts concerning transubstantiation. During the Mass, the eucharist appeared to bleed and each time the priest wiped away the blood, more would appear. This event is celebrated in a fresco in the Pontifical Palace in the Vatican City, painted by Raphael.[4]

Biological activity

Prodigiosin has recently received renewed attention[2][5] for its wide range of biological activities, including activities as antimalarial,[6] antifungal,[7] immunosuppressant,[8] and antibiotic agents.[9] It is perhaps best known for its capacity to trigger apoptosis of malignant cancer cells. The exact mechanism of this inhibition is highly complex and not entirely elucidated, but could involve multiple processes, including phosphatase inhibition, copper mediated cleavage of double stranded DNA, or disrupting the pH gradient through transmembrane transport of H+ and Cl- ions.[10] As a result, Prodigiosin is a highly promising drug lead, and is currently in preclinical phase study for pancreatic cancer treatment.[11] Prodigiosin has recently been found to have excellent activity against stationary phase Borrelia burgdorferi, the causative agent of Lyme Disease.[12]

Biosynthesis

Figure 1: Structure of Prodigiosin 1 highlighting the A, B, and C pyrrole rings

The biosynthesis of Prodigiosin[13] [14] involves the convergent coupling of three pyrrole type rings (labeled A, B, and C in figure 1) from L-proline, L-Serine, L-methionine, pyruvate, and 2-octenal.

Ring A is synthesized from L-proline through the nonribosomal peptide synthase (NRPS) pathway (figure 2), wherein the pyrrolidine ring of proline is oxidized twice through FAD+ to yield pyrrole ring A.

Ring A is then expanded via the polyketide synthase pathway to incorporate L-serine into ring B (figure 3). Ring A fragment is transferred from the peptidyl carrier protein (PCP) to the Acyl Carrier Protein (ACP) by a KS domain, followed by transfer to malonyl-ACP via decarboxylative Claisen condensation. This fragment is then able to react with the masked carbanion formed from the PLP mediated decarboxylation of L-Serine, which cyclizes in a dehydration reaction to yield the second pyrrole ring. This intermediate is then modified by methylation (which incorporates a methyl group from L-methionine onto the alcohol at the 6 position) and oxidation of the primary alcohol to the aldehyde to yield the core A-B ring structure.

Ring C is formed from the TPP mediated decarboxylative addition of pyruvate to 2-octenal, followed by reaction with PLP to generate an amine for intramolecular condensation. Oxidation of the resulting ring yields the final pyrrole ring C.

Finally, these two pieces are stitched together in a dehydration reaction driven forward by the establishment of a conjugated system across all three rings. This completes the convergent synthesis of the natural product.

See also

Project SHAD

References

  1. ↑ Bennett JW, Bentley R (2000). "Seeing red: The story of prodigiosin". Adv Appl Microbiol. 47: 1–32. doi:10.1016/S0065-2164(00)47000-0. PMID 12876793.
  2. 1 2 3 Williamson NR, Fineran PC, Gristwood T, Leeper FJ, Salmond GP (2006). "The biosynthesis and regulation of bacterial prodiginines". Nature Reviews Microbiology. 4 (12): 887–899. doi:10.1038/nrmicro1531. PMID 17109029.
  3. ↑ M. Todd-Guay and P.H. Demchick. 1995. Role of prodigiosin in phosphate-starved Serratia marcescens. Abstract of the Annual Meeting, American Society for Microbiology.
  4. ↑ "The Mass at Bolsena by Raphael". Vatican Museums. Retrieved 2006-05-03.
  5. ↑ Williamson NR, Fineran PC, Gristwood T, Chawrai SR, Leeper FJ, Salmond GP (2007). "Anticancer and immunosuppressive properties of bacterial prodiginines". Future Microbiol. 2 (6): 605–618. doi:10.2217/17460913.2.6.605. PMID 18041902.
  6. ↑ Castro, A. J. Antimalarial Activity of Prodigiosin. Nature 213, 903–904 (1967).
  7. ↑ Berg, G. Diversity of antifungal and plant-associated Serratia plymuthica strains. J. Appl. Microbiol. 88, 952–960 (2000).
  8. ↑ Magae, J., Miller, M. W., Nagai, K. & Shearer, G. M. Effect of metacycloprodigiosin, an inhibitor of killer T cells on murine skin and heart transplants. J. Antibiot. (Tokyo) 49, 86–90 (1996).
  9. ↑ Kataoka, T. et al. Prodigiosin 25-C uncouples vacuolar type H+-ATPase, inhibits vacuolar acidification and affects glycoprotein processing. FEBS Lett. 359, 53–59 (1995)
  10. ↑ Rastogi, S. et al. Synthetic prodigiosenes and the influence of C-ring substitution on DNA cleavage, transmembrane chloride transport and basicity. Org. Biomol. Chem. 11, 3834–3845 (2013).
  11. ↑ Perez-Tomas, R. & Vinas, M. New Insights on the Antitumoral Properties of Prodiginines. Curr. Med. Chem. 17, 2222–2231 (2010).
  12. ↑ Feng, Jie; Shi, Wanliang; Zhang, Shuo; Zhang, Ying (3 June 2015). "Identification of new compounds with high activity against stationary phase Borrelia burgdorferi from the NCI compound collection". Emerging Microbes & Infections. 4 (5): e31. doi:10.1038/emi.2015.31.
  13. ↑ Walsh, C. T., Garneau-Tsodikova, S. & Howard-Jones, A. R. Biological formation of pyrroles: Nature’s logic and enzymatic machinery. Nat. Prod. Rep. 23, 517–531 (2006).
  14. ↑ Structure, Chemical Synthesis, and Biosynthesis of Prodiginine Natural Products Dennis X. Hu, David M. Withall, Gregory L. Challis, and Regan J. Thomson Chemical Reviews Article ASAP doi:10.1021/acs.chemrev.6b00024
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