Scytonemin

Last updated
Scytonemin
Scytonemin.png
Names
Preferred IUPAC name
(3E,3′E)-3,3′-Bis[(4-hydroxyphenyl)methylidene][1,1′-bi(cyclopropa[b]indole)]-2,2′(3H,3′H)-dione
Other names
Scytonemin
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
PubChem CID
UNII
  • InChI=1S/C36H20N2O4/c39-21-13-9-19(10-14-21)17-25-33-29(23-5-1-3-7-27(23)37-33)31(35(25)41)32-30-24-6-2-4-8-28(24)38-34(30)26(36(32)42)18-20-11-15-22(40)16-12-20/h1-18,39-40H/b25-17+,26-18+ X mark.svgN
    Key: CGZKSPLDUIRCIO-RPCRKUJJSA-N X mark.svgN
  • InChI=1/C36H20N2O4/c39-21-13-9-19(10-14-21)17-25-33-29(23-5-1-3-7-27(23)37-33)31(35(25)41)32-30-24-6-2-4-8-28(24)38-34(30)26(36(32)42)18-20-11-15-22(40)16-12-20/h1-18,39-40H/b25-17+,26-18+
    Key: CGZKSPLDUIRCIO-RPCRKUJJBK
  • C1=CC=C2N=C\3C(=C(C(=O)/C3=C/C4=CC=C(C=C4)O)C5=C6C(=NC7=CC=CC=C67)/C(=C\C8=CC=C(C=C8)O)/C5=O)C2=C1
Properties
C36H20N2O4
Molar mass 544.6 g/mol
Appearancebrown solid
Solubility 25mg/ml DMSO
UV-vismax)370nm
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Scytonemin is a secondary metabolite and an extracellular matrix (sheath) pigment synthesized by many strains of cyanobacteria, including Nostoc , Scytonema , Calothrix, Lyngbya , Rivularia, Chlorogloeopsis , and Hyella. [1] Scytonemin-synthesizing cyanobacteria often inhabit highly insolated terrestrial, freshwater and coastal environments such as deserts, semideserts, rocks, cliffs, marine intertidal flats, and hot springs. [2]

The pigment was originally discovered in 1849 by Swiss botanist Carl Nägeli, [3] although the structure remained unsolved until 1993. [4] It is an aromatic indole alkaloid built from two identical condensation products of tryptophan yl- and tyrosy l-derived subunits linked through a carbon-carbon bond. [4] Depending on the redox conditions it can exist in two inter-convertible forms: a more common oxidized yellow-brown form which is insoluble in water and only slightly soluble in organic solvents, such as pyridine, and a reduced form with bright red color that is more soluble in organic solvents. [5] Scytonemin absorbs very strongly and very broadly across the UV-C-UV-B-UV-A-violet-blue spectral region, with an in vivo maximum absorption at 370 nm and an in vitro maximum absorption at 386 and 252 nm, and with smaller peaks at 212, 278 and 300 nm. [6]

It is believed that scytonemin acts as a highly efficient protective biomolecule (sunscreen) that filters out damaging high frequency UV rays while at the same time allowing the transmittance of wavelengths necessary for photosynthesis. [7] Its biosynthesis in cyanobacteria is mostly triggered by exposure to UV-A and UV-B wavelengths. [8] [9]

Recently, Couradeau and coworkers found that cyanobacterial soil crusts warm the soil surface by as much as 10 °C through the production and accumulation of scytonemin pigments. [10] This effect is due to the dissipation of the absorbed photons by the scytonemin molecules into heat.

Biosynthesis

The biosynthesis in Lyngbya aestuarii was recently explored by Balskus, Case, and Walsh. It proceeds by the conversion of L-tryptophan to 3-indole pyruvic acid, followed by coupling to p-hydroxyphenylpyruvic acid. Cyclization of the resultant β-ketoacid yields a tricyclic ketone. Oxidation and dimerization yields the completed natural product. Three scytonemin biosynthetic enzymes are necessary, denoted as ScyA-C. [11]

Scytonemin biosynthesis in Lyngbya aestuarii. Scytonemin biosynthesis.png
Scytonemin biosynthesis in Lyngbya aestuarii.

Related Research Articles

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References

  1. Sinha, Hader (2008-03-01). "UV-protectants in cyanobacteria". Plant Science. 174 (3): 278–289. doi:10.1016/j.plantsci.2007.12.004. ISSN   0168-9452.
  2. Ecology of Cyanobacteria II - Their Diversity in Space and | Brian A. Whitton | Springer. Springer. 2012. ISBN   9789400738546.
  3. Nägeli, Carl (1849). Gattungen einzelliger Algen physiologisch und systematisch bearbeitet. MBLWHOI Library. Zürich, Friedrich Schulthess.
  4. 1 2 Proteau, P. J.; Gerwick, W. H.; Garcia-Pichel, F.; Castenholz, R. (1993). "The structure of scytonemin, an ultraviolet sunscreen pigment from the sheaths of cyanobacteria". Experientia. 49 (9): 825–9. doi:10.1007/BF01923559. PMID   8405307. S2CID   22975257.
  5. Garcia-Pichel, Ferran; Castenholz, Richard W. (1991-06-01). "Characterization and Biological Implications of Scytonemin, a Cyanobacterial Sheath Pigment1". Journal of Phycology. 27 (3): 395–409. doi:10.1111/j.0022-3646.1991.00395.x. ISSN   1529-8817. S2CID   84058783.
  6. Sinha, Rajeshwar; Klisch, M; Vaishampayan, Akhouri; Häder, Donat (1999-11-01). "Biochemical and spectroscopic characterization of the cyanobacterium Lyngbya sp. inhabiting mango (Mangifera indica) trees: Presence of an ultraviolet-absorbing pigment, scytonemin". Acta Protozoologica. 38: 291–298.
  7. Ekebergh, Andreas; Sandin, Peter; Mårtensson, Jerker (2015-11-25). "On the photostability of scytonemin, analogues thereof and their monomeric counterparts". Photochemical & Photobiological Sciences. 14 (12): 2179–2186. doi:10.1039/C5PP00215J. ISSN   1474-9092. PMID   26452010. S2CID   23558706.
  8. Sorrels, Carla M.; Proteau, Philip J.; Gerwick, William H. (2009-07-15). "Organization, Evolution, and Expression Analysis of the Biosynthetic Gene Cluster for Scytonemin, a Cyanobacterial UV-Absorbing Pigment". Applied and Environmental Microbiology. 75 (14): 4861–4869. doi:10.1128/AEM.02508-08. ISSN   0099-2240. PMC   2708446 . PMID   19482954.
  9. Rastogi, Rajesh P.; Incharoensakdi, Aran (2014-01-01). "Characterization of UV-screening compounds, mycosporine-like amino acids, and scytonemin in the cyanobacteriumLyngbyasp. CU2555". FEMS Microbiology Ecology. 87 (1): 244–256. doi: 10.1111/1574-6941.12220 . ISSN   0168-6496. PMID   24111939.
  10. Couradeau, Estelle; Karaoz, Ulas; Lim, Hsiao Chien; Rocha, Ulisses Nunes da; Northen, Trent; Brodie, Eoin; Garcia-Pichel, Ferran (2016-01-20). "Bacteria increase arid-land soil surface temperature through the production of sunscreens". Nature Communications. 7: 10373. Bibcode:2016NatCo...710373C. doi:10.1038/ncomms10373. PMC   4735820 . PMID   26785770.
  11. 1 2 Balskus, Emily P.; Case, Rebecca J.; Walsh, Christopher T. (2011). "The biosynthesis of cyanobacterial sunscreen scytonemin in intertidal microbial mat communities" (PDF). FEMS Microbiology Ecology. 77 (2): 1–11. doi:10.1111/j.1574-6941.2011.01113.x. PMC   3134115 . PMID   21501195.