Atromentin

Atromentin
2,5-Dihydroxy-3,6-bis(4-hydroxyphenyl)-1,4-benzoquinone
Structural formula of atromentin
Names
Preferred IUPAC name
14,23,26,34-Tetrahydroxy[11,21:24,31-terphenyl]-22,25-dione
Other names
2,5-Dihydroxy-3,6-bis(4-hydroxyphenyl)-1,4-benzoquinone
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
UNII
  • InChI=1S/C18H12O6/c19-11-5-1-9(2-6-11)13-15(21)17(23)14(18(24)16(13)22)10-3-7-12(20)8-4-10/h1-8,19-21,24H checkY
    Key: FKQQKMGWCJGUCS-UHFFFAOYSA-N checkY
  • InChI=1S/C18H12O6/c19-11-5-1-9(2-6-11)13-15(21)17(23)14(18(24)16(13)22)10-3-7-12(20)8-4-10/h1-8,19-21,24H
    Key: FKQQKMGWCJGUCS-UHFFFAOYSA-N
  • C1=CC(=CC=C1C2=C(C(=O)C(=C(C2=O)O)C3=CC=C(C=C3)O)O)O
Properties
C18H12O6
Molar mass 324.288 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N (what is checkY☒N ?)

Atromentin is a natural chemical compound found in Agaricomycetes fungi in the orders Agaricales and Thelephorales. It can also be prepared by laboratory synthesis.[1] Chemically, it is a polyphenol and a benzoquinone.[2]

Occurrences

Atromentin has been found in cultures of Clitocybe subilludens[3] and in extracts of Hydnellum peckii. The first enzymes in its biosynthesis have been characterized in Tapinella panuoides.[4] One of those is called atromentin synthetase.[5]

Biological activities

A number of potential biological activities of atromentin have been studied in vitro. Atromentin possesses in vitro antibacterial activity, inhibiting the enzyme enoyl-acyl carrier protein reductase (essential for the biosynthesis of fatty acids) in the bacteria Streptococcus pneumoniae.[6] Atromentin has been shown to be a smooth muscle stimulant.[7] It also induces apoptosis in isolated human leukemia U937 cells.[8] It is also an anticoagulant.[9]

Genetic and enzymatic basis of atromentin

Atromentin is biosynthesized from two units of 4-hydroxyphenylpyruvic acid (4-HPP) via a nonribosomal peptide synthetase-like enzyme (atromentin synthetase), containing the domain architecture adenylation-thiolation-thioesterase (A-T-TE). 4-HPP is produced from a deamination via an aminotransferase. The genetic basis of these two genes is clustered (i.e., adjacent to one another). These enzymes were first characterized in Tapinella panuoides by overexpressing the respective genes (AtrA and AtrD) in E. coli and incubating the holo-enzyme with 4-HPP to observe the formation of atromentin.[4] This was followed by characterization of the enzyme GreA in Suillus grevillei,[10] six (InvA1-6, of which InvA1, 2 and 5 were functional) in Paxillus involutus,[11] and NPS3 from Serpula lacrymans.[12][13] In addition, there is another adjacent and conserved gene encoding for an alcohol dehydrogenase/oxidoreductase whose function is unclear. In most cases the clustered biosynthetic genes are found orthologous in basidiomycetes. A common promoter motif was found shared between the atromentin synthetase and aminotransferase of 23 different atromentin-producing basidiomycetes that was in almost all cases absent from the alcohol dehydrogenase, indicating co-regulation of the two essential genes that ensure atromentin production by a common transcription factor.[12][14] Additional promoter motifs were identified preceding the atromentin genes for ectomycorrihzae that were absent from brown rotters, indicating dissimilar genetic regulation of atromentin.[14] The genes for the atromentin synthetase and aminotransferase from S. lacrymans were up-regulated during co-incubation with bacteria.[14]

Amino acid nonribosomal code for biosynthesis

The nonribosomal peptide synthetase-like enzyme (atromentin synthetase) that symmetrically condenses two monomers of 4-HPP has an adenylation domain that accepts the substrates before catalysis. The acceptor domain contains a 10 amino acid code known as the Nonribosomal Code (NRPS code). Here, the example of the atromentin synthetase from Suills grevillei, GreA, is used. The code is found at amino acid positions 235 (V), 236 (A), 239 (E), 278 (F), 299 (S), 301 (G), 322 (G), 320 (A), 331 (C), 517 (K).[10] The code aligns with atromentin synthetases from S. lacrymans (NPS3), Tapinella panuoides (AtrA), and Paxillus involutus (InvAs). Similarly, the NRPS code for atromentin production supports the universal code for other aromatic alpha-keto acid-derived compounds, such those from L-phenylalanine like ralfuranone B via phenylpyruvic acid, and from L-tryptophane like didemethyl asterriquinone D via indole-3-pyruvic acid (note atromentin is derived from the aromatic alpha-keto acid L-tyrosine via 4-hydroxyphenylpyruvic acid).[citation needed]

For InvAs from Paxillus involutus, a common amino acid motif was also found in the thioesterase domain (last domain) that supported biochemical data of either the enzyme being functional to complete atromentin formation or not.[11]

Biosynthesis of atromentin

The aromatic amino acid L-tyrosine is the precursor to 4-hydroxyphenylpyruvic acid, and 2 units of 4-HPP are condensed to form atromentin. The initial step is deamination via an aminotransferase. The second step is catalyzed by a nonribosomal peptide synthetase-like enzyme (NRPS-like, because it does not have a canonical condensation domain, called the atromentin/quinone synthetase). The adenylation domain of this NRPS-like enzyme accepts 4-HPP as determined by the ATP-PPi-exchange assay. The enzyme, when produced in E. coli, needs to be primed to its holo form via a phosphopantetheinyl transferase (Ppant), although E. coli can in vivo prime the apo-enzyme (e.g. via EntD). Ppants have been successfully used from cDNA derived from A. nidulans (e.g. NpgA), Streptomyces verticillus (Svp), and Paxillus involutus (PptA). A few studies, notably from the bacterium Burkholderia thailandensis by Biggins et al., have shown that the aminotransferase gene may be absent, and this activity can be supplied via its primary metabolism.[citation needed]

Congener pigments

Atromentin is the precursor to various other pigments, including the pulvinic acids such as variegatic acid, xerocomic acid, homoxerocomic acid, isoxerocomic acid, atromentic acid, variegatorubin, xerocomorubin, and other modified derivatives. The main pulvinic acid type pigments were found secreted during co-incubation with bacteria or introduction to high organic nitrogen content (compared to growth on a non-inducing medium containing inorganic nitrogen). Diarylcyclopentenones include involutin, involuton, gyrocycanin, gyroporin (oxidized variant of gyrocyanin), anhydroinvolutin, and chamonixin. Although structurally similar, grevillins (A-D) are derived from 4-HPP, the precursor to atromentin. The grevillins are a chemotaxonomic marker for the genus Suillus. Modifications of atromentin include leucoatromentin, leucomentin-3, leucomentin-4, and cylcoleucomelone. Additionally, thelephoric acid is a derivative that is from the thelephoroid clade. The various enzymes involved in the formation of these pigments aside from the genetic and enzymatic basis for the production of its precursor atromentin is unknown.

Redundant biosynthesis

In Paxillus involutus, six nonribosomal peptide synthetase-like enzymes were identified in the annotated genome that is available via the JGI MycoCosm portal. These genes, termed InvA1,2,3,4,5 and 6, were overexpressed in E. coli and the genes were characterized by co-incubating the apo-enzyme with 4-HPP to determine the formation of atromentin as noted by its characteristic UV-Vis spectrum and monoisotopic mass. Three of the six enzymes were found to be functional. This showed an unprecedented redundancy for atromentin production in a basidiomycete.[11]

References

  1. ^ Ye, Y. Q.; Koshino, H.; Abe, N.; Nakamura, T.; Hashizume, D.; Takahashi, S. (2010). "Synthesis of atromentin and its O-alkylated natural products". Bioscience, Biotechnology, and Biochemistry. 74 (11): 2342–2344. doi:10.1271/bbb.100451. PMID 21071857.
  2. ^ Chandra, Sonia; De Mejia Gonzalez, Elvira (2004-06-02). "Polyphenolic compounds, antioxidant capacity, and quinone reductase activity of an aqueous extract of Ardisia compressa in comparison to mate (Ilex paraguariensis) and green (Camellia sinensis) teas". Journal of Agricultural and Food Chemistry. 52 (11): 3583–3589. doi:10.1021/jf0352632. ISSN 0021-8561. PMID 15161234.
  3. ^ Sullivan, G.; Garrett, R. D.; Lenehan, R. F. (1971). "Occurrence of atromentin and thelephoric acid in cultures ofclitocybe subilludens". Journal of Pharmaceutical Sciences. 60 (11): 1727–1729. doi:10.1002/jps.2600601134. PMID 4332377.
  4. ^ a b Schneider, P.; Bouhired, S.; Hoffmeister, D. (2008). "Characterization of the atromentin biosynthesis genes and enzymes in the homobasidiomycete Tapinella panuoides". Fungal Genetics and Biology. 45 (11): 1487–1496. doi:10.1016/j.fgb.2008.08.009. PMID 18805498.
  5. ^ Atromentin synthetase on www.uniprot.org
  6. ^ Zheng CJ, Sohn MJ, Kim WG (2006). "Atromentin and leucomelone, the first inhibitors specific to enoyl-ACP reductase (FabK) of Streptococcus pneumoniae". Journal of Antibiotics. 59 (12): 808–12. doi:10.1038/ja.2006.108. PMID 17323650.
  7. ^ Sullivan, G.; Guess, W. L. (1969). "Atromentin: A smooth muscle stimulant in Clitocybe subilludens". Lloydia. 32 (1): 72–75. PMID 5815216.
  8. ^ Atromentin-Induced Apoptosis in Human Leukemia U937 Cells. Kim Jin Hee and Choong Hwan Lee, Journal of microbiology and biotechnology, 2009, vol. 19, no9, pages 946-950, INIST 21945937
  9. ^ Khanna JM, Malone MH, Euler KL, Brady LR (1965). "Atromentin – anticoagulant from Hydnellum diabolus". Journal of Pharmaceutical Sciences. 54 (7): 1016–20. doi:10.1002/jps.2600540714. PMID 5862512.
  10. ^ a b Wackler, Barbara; Lackner, Gerald; Chooi, Yit Heng; Hoffmeister, Dirk (2012). "Characterization of the Suillus grevillei Quinone Synthetase GreA Supports a Nonribosomal Code for Aromatic α-Keto Acids". ChemBioChem. 13 (12): 1798–804. doi:10.1002/cbic.201200187. PMID 22730234. S2CID 10457901.
  11. ^ a b c Braesel, Jana; Götze, Sebastian; Shah, Firoz; Heine, Daniel; Tauber, James; Hertweck, Christian; Tunlid, Anders; Stallforth, Pierre; Hoffmeister, Dirk (2015). "Three Redundant Synthetases Secure Redox-Active Pigment Production in the Basidiomycete Paxillus involutus". Chemistry & Biology. 22 (10): 1325–1334. doi:10.1016/j.chembiol.2015.08.016. PMID 26496685.
  12. ^ a b Tauber, James P; Schroeckh, Volker; Shelest, Ekaterina; Brakhage, Axel A; Hoffmeister, Dirk (2016). "Bacteria induce pigment formation in the basidiomycete Serpula lacrymans". Environmental Microbiology. 18 (12): 5218–5227. Bibcode:2016EnvMi..18.5218T. doi:10.1111/1462-2920.13558. PMID 27699944.
  13. ^ Eastwood, D. C; Floudas, D; Binder, M; Majcherczyk, A; Schneider, P; Aerts, A; Asiegbu, F. O; Baker, S. E; Barry, K; Bendiksby, M; Blumentritt, M; Coutinho, P. M; Cullen, D; De Vries, R. P; Gathman, A; Goodell, B; Henrissat, B; Ihrmark, K; Kauserud, H; Kohler, A; Labutti, K; Lapidus, A; Lavin, J. L; Lee, Y.-H; Lindquist, E; Lilly, W; Lucas, S; Morin, E; Murat, C; et al. (2011). "The Plant Cell Wall-Decomposing Machinery Underlies the Functional Diversity of Forest Fungi". Science. 333 (6043): 762–5. Bibcode:2011Sci...333..762E. doi:10.1126/science.1205411. PMID 21764756. S2CID 11022844.
  14. ^ a b c Tauber, James P.; Gallegos-Monterrosa, Ramses; Kovács, Ákos T.; Shelest, Ekaterina; Hoffmeister, Dirk (2018). "Dissimilar pigment regulation in Serpula lacrymans and Paxillus involutus during inter-kingdom interactions" (PDF). Microbiology. 164 (1): 65–77. doi:10.1099/mic.0.000582. PMID 29205129.

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