词条 | Scytonemin |
释义 |
| Verifiedfields = changed | Watchedfields = changed | verifiedrevid = 431787953 | Name = | ImageFile = Scytonemin.png | ImageSize = 200 | ImageAlt = | IUPACName = (3E,3'E)-3,3'-bis(4-hydroxybenzylidene)-[1,1'-bi(cyclopenta[b]indole)]-2,2'(3H,3'H)-dione | OtherNames = Scytonemin | SystematicName = | Section1 = {{Chembox Identifiers | CASNo_Ref = {{cascite|correct|??}} | CASNo = 152075-98-4 | PubChem = | ChEMBL_Ref = {{ebicite|changed|EBI}} | ChEMBL = 505177 | ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}} | ChemSpiderID = 16736974 | ChEBI_Ref = {{ebicite|changed|EBI}} | ChEBI = 90127 | SMILES = 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 | 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+ | InChIKey = CGZKSPLDUIRCIO-RPCRKUJJBK | StdInChI_Ref = {{stdinchicite|changed|chemspider}} | StdInChI = 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+ | StdInChIKey_Ref = {{stdinchicite|changed|chemspider}} | StdInChIKey = CGZKSPLDUIRCIO-RPCRKUJJSA-N}} | Section2 = {{Chembox Properties | Formula = C36H20N2O4 | MolarMass = 544.6 g/mol | MolarMass_notes = | Appearance = brown solid | Density = | MeltingPt = | MeltingPt_notes = | BoilingPt = | BoilingPt_notes = | SublimationConditions = | Solubility = | SolubilityProduct = | SolubilityProductAs = | Solvent = | pKa = | pKb = | IsoelectricPt = | LambdaMax = 370nm | Absorbance = | BandGap = | ElectronMobility = | SpecRotation = | MagSus = | ThermalConductivity = | RefractIndex = | Viscosity = | Dipole = | SolubleOther = 25mg/ml DMSO }} | Section3 = {{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }} | Section4 = | Section5 = | Section6 = }}Scytonemin is a secondary metabolite and an extracellular matrix (sheath) pigment synthesized by many strains of cyanobacteria, including Nostoc, Scytonema, Calothrix, Lyngbya, Rivularia, Chlorogloeopsis, Hyella etc.[1] Scytonemin-synthesizing cyanobacteria often inhabit highly insolated terrestrial, freshwater and coastal environments such as deserts, semideserts, rocks, cliffs, marine intertidal flats, hot springs, etc.[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 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. BiosynthesisThe 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] References1. ^{{Cite journal|last=Sinha, Hader|date=2008-03-01|title=UV-protectants in cyanobacteria|url=https://www.sciencedirect.com/science/article/pii/S0168945207003202|journal=Plant Science|volume=174|issue=3|pages=278–289|doi=10.1016/j.plantsci.2007.12.004|issn=0168-9452|via=}} 2. ^{{Cite book|url=https://www.springer.com/us/book/9789400738546|title=Ecology of Cyanobacteria II - Their Diversity in Space and {{!}} Brian A. Whitton {{!}} Springer|language=en|isbn=9789400738546|publisher=Springer|year=2012}} 3. ^{{Cite book|url=https://archive.org/details/gattungeneinzell00ng|title=Gattungen einzelliger Algen physiologisch und systematisch bearbeitet|last=Nägeli|first=Carl|date=1849|publisher=Zürich, Friedrich Schulthess|others=MBLWHOI Library}} 4. ^1 {{cite journal |pages=825–9 |doi=10.1007/BF01923559 |title=The structure of scytonemin, an ultraviolet sunscreen pigment from the sheaths of cyanobacteria |year=1993 |last1=Proteau |first1=P. J. |last2=Gerwick |first2=W. H. |last3=Garcia-Pichel |first3=F. |last4=Castenholz |first4=R. |journal=Experientia |volume=49 |issue=9 |pmid=8405307}} 5. ^{{Cite journal|last=Garcia-Pichel|first=Ferran|last2=Castenholz|first2=Richard W.|date=1991-06-01|title=Characterization and Biological Implications of Scytonemin, a Cyanobacterial Sheath Pigment1|journal=Journal of Phycology|language=en|volume=27|issue=3|pages=395–409|doi=10.1111/j.0022-3646.1991.00395.x|issn=1529-8817}} 6. ^{{Cite journal|last=Sinha|first=Rajeshwar|last2=Klisch|first2=M|last3=Vaishampayan|first3=Akhouri|last4=Häder|first4=Donat|date=1999-11-01|title=Biochemical and spectroscopic characterization of the cyanobacterium Lyngbya sp. inhabiting mango (Mangifera indica) trees: Presence of an ultraviolet-absorbing pigment, scytonemin|url=https://www.researchgate.net/publication/266383468|journal=Acta Protozoologica|volume=38|pages=291–298}} 7. ^{{Cite journal|last=Ekebergh|first=Andreas|last2=Sandin|first2=Peter|last3=Mårtensson|first3=Jerker|date=2015-11-25|title=On the photostability of scytonemin, analogues thereof and their monomeric counterparts|url=http://pubs.rsc.org/en/Content/ArticleLanding/2015/PP/C5PP00215J#!divAbstract|journal=Photochemical & Photobiological Sciences|language=en|volume=14|issue=12|doi=10.1039/C5PP00215J|pmid=26452010|issn=1474-9092|pages=2179–2186}} 8. ^{{Cite journal|last=Sorrels|first=Carla M.|last2=Proteau|first2=Philip J.|last3=Gerwick|first3=William H.|date=2009-07-15|title=Organization, Evolution, and Expression Analysis of the Biosynthetic Gene Cluster for Scytonemin, a Cyanobacterial UV-Absorbing Pigment|url=http://aem.asm.org/content/75/14/4861|journal=Applied and Environmental Microbiology|language=en|volume=75|issue=14|pages=4861–4869|doi=10.1128/AEM.02508-08|issn=0099-2240|pmid=19482954|pmc=2708446}} 9. ^{{Cite journal|last=Rastogi|first=Rajesh P.|last2=Incharoensakdi|first2=Aran|date=2014-01-01|title=Characterization of UV-screening compounds, mycosporine-like amino acids, and scytonemin in the cyanobacteriumLyngbyasp. CU2555|url=https://academic.oup.com/femsec/article/87/1/244/507915|journal=FEMS Microbiology Ecology|language=en|volume=87|issue=1|pages=244–256|doi=10.1111/1574-6941.12220|issn=0168-6496}} 10. ^{{Cite journal|last=Couradeau|first=Estelle|last2=Karaoz|first2=Ulas|last3=Lim|first3=Hsiao Chien|last4=Rocha|first4=Ulisses Nunes da|last5=Northen|first5=Trent|last6=Brodie|first6=Eoin|last7=Garcia-Pichel|first7=Ferran|date=2016-01-20|title=Bacteria increase arid-land soil surface temperature through the production of sunscreens|url=https://www.nature.com/articles/ncomms10373|journal=Nature Communications|language=En|volume=7|pages=10373|doi=10.1038/ncomms10373|pmid=26785770}} 11. ^1 {{cite journal|last1=Balskus|first1=Emily P.|last2=Case|first2=Rebecca J.|last3=Walsh|first3=Christopher T.|year=2011|title=The biosynthesis of cyanobacterial sunscreen scytonemin in intertidal microbial mat communities|journal=FEMS Microbiology Ecology|volume=77|issue=2|pages=1–11|doi=10.1111/j.1574-6941.2011.01113.x|pmid=21501195|url=https://dash.harvard.edu/bitstream/handle/1/12169551/nihms292647.pdf?sequence=1}} 3 : Biological pigments|Secondary metabolites|Cyanobacteria |
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