Diversity and bioactivity of Armillaria sesquiterpene aryl ester natural products

[1]  B. Thongbai,et al.  Biological and chemical diversity go hand in hand: Basidiomycota as source of new pharmaceuticals and agrochemicals. , 2019, Biotechnology advances.

[2]  O. Werz,et al.  Melleolides impact fungal translation via elongation factor 2. , 2019, Organic & biomolecular chemistry.

[3]  O. Werz,et al.  Melleolides from Honey Mushroom Inhibit 5-Lipoxygenase via Cys159. , 2019, Cell chemical biology.

[4]  K. Scheidt,et al.  A Carbene Catalysis Strategy for the Synthesis of Protoilludane Natural Products. , 2017, Angewandte Chemie.

[5]  Andrew W. Wilson,et al.  Resolved phylogeny and biogeography of the root pathogen Armillaria and its gasteroid relative, Guyanagaster , 2017, BMC Evolutionary Biology.

[6]  D. Hoffmeister,et al.  Biochemical and genetic basis of orsellinic acid biosynthesis and prenylation in a stereaceous basidiomycete. , 2017, Fungal genetics and biology : FG & B.

[7]  Y. Bao,et al.  Structure, cytotoxic activity and mechanism of protoilludane sesquiterpene aryl esters from the mycelium of Armillaria mellea. , 2016, Journal of ethnopharmacology.

[8]  D. Hoffmeister,et al.  A Fivefold Parallelized Biosynthetic Process Secures Chlorination of Armillaria mellea (Honey Mushroom) Toxins , 2015, Applied and Environmental Microbiology.

[9]  Y. Kuo,et al.  Three New Sesquiterpene Aryl Esters from the Mycelium of Armillaria mellea , 2015, Molecules.

[10]  Hirofumi Hirai,et al.  Bioactive sesquiterpene aryl esters from the culture broth of Armillaria sp. , 2015, Journal of natural products.

[11]  Hans-Wilhelm Nützmann,et al.  Cytotoxic and antifungal activities of melleolide antibiotics follow dissimilar structure-activity relationships. , 2014, Phytochemistry.

[12]  O. Werz,et al.  Melleolides induce rapid cell death in human primary monocytes and cancer cells. , 2014, Bioorganic & medicinal chemistry.

[13]  D. Hoffmeister,et al.  Assembly of melleolide antibiotics involves a polyketide synthase with cross-coupling activity. , 2013, Chemistry & biology.

[14]  Thomas M. Keane,et al.  Genomic and Proteomic Dissection of the Ubiquitous Plant Pathogen, Armillaria mellea: Toward a New Infection Model System , 2013, Journal of proteome research.

[15]  R. Fischer,et al.  Untersuchungen zur Biosynthese sesquiterpenoider Naturstoffe, der Melleolide, in Armillaria gallica , 2013 .

[16]  D. Lindner,et al.  Armillaria altimontana, a new species from the western interior of North America , 2012, Mycologia.

[17]  D. Hoffmeister,et al.  Characterisation of the ArmA adenylation domain implies a more diverse secondary metabolism in the genus Armillaria. , 2011, Fungal biology.

[18]  M. Coetzee,et al.  Secrets of the subterranean pathosystem of Armillaria. , 2011, Molecular plant pathology.

[19]  D. Hoffmeister,et al.  In vitro cytotoxicity of melleolide antibiotics: structural and mechanistic aspects. , 2011, Bioorganic & medicinal chemistry letters.

[20]  Jikai Liu,et al.  N-containing compounds of macromycetes. , 2011, Natural product reports.

[21]  M. Stadler,et al.  Cloning and Characterization of an Armillaria gallica cDNA Encoding Protoilludene Synthase, Which Catalyzes the First Committed Step in the Synthesis of Antimicrobial Melleolides , 2010, The Journal of Biological Chemistry.

[22]  D. Hoffmeister,et al.  Sesquiterpene aryl ester natural products in North American Armillaria species , 2010, Mycological Progress.

[23]  Jikai Liu,et al.  Pigments of fungi (macromycetes). , 2010, Natural product reports.

[24]  I. Merfort,et al.  Structure and cytotoxicity of arnamial and related fungal sesquiterpene aryl esters. , 2009, Journal of natural products.

[25]  Wolfgang Schmidt-Heck,et al.  Intimate bacterial–fungal interaction triggers biosynthesis of archetypal polyketides in Aspergillus nidulans , 2009, Proceedings of the National Academy of Sciences.

[26]  C. Jones,et al.  A Darwinian view of metabolism: molecular properties determine fitness. , 2009, Journal of experimental botany.

[27]  J. Zjawiony Biologically active compounds from Aphyllophorales (polypore) fungi. , 2004, Journal of natural products.

[28]  A. Oppermann Das antibiotische Verhalten einiger holzzersetzender Basidiomyceten zueinander und zu Bakterien , 1951, Archiv für Mikrobiologie.

[29]  R. Firn,et al.  Natural products--a simple model to explain chemical diversity. , 2003, Natural product reports.

[30]  Ben Shen,et al.  Polyketide biosynthesis beyond the type I, II and III polyketide synthase paradigms. , 2003, Current opinion in chemical biology.

[31]  W. Abraham Bioactive sesquiterpenes produced by fungi: are they useful for humans as well? , 2001, Current medicinal chemistry.

[32]  H. Naganawa,et al.  Melleolides K, L and M, new melleolides from Armillariella mellea. , 2000, The Journal of antibiotics.

[33]  J. Wolfender,et al.  A liquid chromatography–thermospray ionisation–mass spectrometry guided isolation of a new sesquiterpene aryl ester from Armillaria novae-zelandiae , 2000 .

[34]  J. Sonnenbichler,et al.  Secondary metabolites from dual cultures of genetically different Armillaria isolates , 1997 .

[35]  T. Konishi,et al.  Sesquiterpene aryl esters from Armillaria tabescens , 1997 .

[36]  J. Wolfender,et al.  Liquid chromatographic-thermospray mass spectrometric analysis of sesquiterpenes of Armillaria (Eumycota: Basidiomycotina) species , 1995 .

[37]  J. Sonnenbichler,et al.  Secondary fungal metabolites and their biological activities, II. Occurrence of antibiotic compounds in cultures of Armillaria ostoyae growing in the presence of an antagonistic fungus or host plant cells. , 1992, Biological chemistry Hoppe-Seyler.

[38]  X. Feng,et al.  Two Novel Protoilludane Norsesquiterpenoid Esters, Armillasin and Armillatin, from Armillaria mellea. , 1991, Planta medica.

[39]  Yang Js,et al.  Chemical constituents of Armillaria mellea mycelium. VII. Isolation and characterization of chemical constituents of the acetone extract , 1991 .

[40]  N. Watanabe,et al.  Armillaric acid, a new antibiotic produced by Armillaria mellea. , 1990, Planta medica.

[41]  Yang Js,et al.  Studies on the chemical constituents of Armillaria mellea mycelium. V. Isolation and characterization of armillarilin and armillarinin , 1990 .

[42]  D. Donnelly,et al.  Sesquiterpene aryl esters from Armillaria mellea , 1990 .

[43]  D. Donnelly,et al.  Armillane, a saturated sesquiterpene ester from Armillaria mellea. , 1990 .

[44]  Q. Zheng,et al.  [Chemical constituents of Armillaria mellea mycelium. VI. Isolation and structure of armillaripin]. , 1990, Yao xue xue bao = Acta pharmaceutica Sinica.

[45]  Q. Zheng,et al.  Isolation and structure elucidation of armillaricin1. , 1989, Planta medica.

[46]  M. Tamai,et al.  Isolation and structures of two new sesquiterpenoid aromatic esters: armillarigin and armillarikin1. , 1989, Planta medica.

[47]  S. V. Meille,et al.  Secondary mould metabolites. Part 19. Structure elucidation and absolute configuration of melledonals B and C, novel antibacterial sesquiterpenoids from Armillaria mellea. X-Ray molecular structure of melledonal C , 1988 .

[48]  D. Donnelly,et al.  Two new sesquiterpene esters from Armillaria mellea , 1987 .

[49]  M. Gill,et al.  Pigments of fungi (Macromycetes). , 1987, Fortschritte der Chemie organischer Naturstoffe = Progress in the chemistry of organic natural products. Progres dans la chimie des substances organiques naturelles.

[50]  A. Arnone,et al.  Structures of melleolides B-D, three antibacterial sesquiterpenoids from Armillaria mellea , 1986 .

[51]  D. Donnelly,et al.  New Sesquiterpene Aryl Esters from Armillaria mellea , 1986 .

[52]  D. Donnelly,et al.  Melledonal and melledonol, sesquiterpene esters from armillaria mellea , 1985 .

[53]  T. Prangé,et al.  Antibacterial sesquiterpene aryl esters from Armillaria mellea. , 1985, Journal of natural products.

[54]  X. Feng,et al.  Chemical constituents of Armillaria mellea mycelium. I. Isolation and characterization of armillarin and armillaridin. , 1984, Planta medica.

[55]  T. Prangé,et al.  The absolute configuration of the orsellinate of armillol; application of the coupled oscillator theory , 1984 .

[56]  T. Prangé,et al.  Isolation and structure (X-ray analysis) of the orsellinate of armillol, a new antibacterial metabolite from Armillaria mellea , 1982 .

[57]  R. M. Wing,et al.  Melleolide, a new antibiotic from , 1982 .

[58]  James J. Sims,et al.  Isolation of antibiotics produced in culture by Armillaria mellea , 1976 .

[59]  T. Mcmorris,et al.  The structure of illudol, a sesquiterpenoid triol from Clitocybe illudens. , 1967, Journal of the American Chemical Society.

[60]  M. Matsuo,et al.  Biosynthesis of lichen depsides, lecanoric acid and atranorin. , 1965, Chemical & pharmaceutical bulletin.