Discovery and characterisation of a broderol-like illudin, omphaderol in the mycelial extracts of Omphalotus mexicanus (Omphalotaceae) using UPLC-QTOF-MS and NMR spectroscopy

被引:1
作者
Eckhardt, Paul [1 ]
Reinecke, Silke [2 ,3 ]
Opatz, Till [1 ]
Stadler, Marc [2 ,3 ]
Sandargo, Birthe [2 ,3 ]
机构
[1] Johannes Gutenberg Univ Mainz, Dept Chem, Mainz, Germany
[2] Helmholtz Ctr Infect Res, Microbial Drugs Dept, Inhoffenstr 7, D-38124 Braunschweig, Germany
[3] German Ctr Infect Res DZIF, Partner site Hannover Braunschweig, Braunschweig, Germany
关键词
basidiomycetes; illudins; NMR; Omphalotus mexicanus; structure elucidation; terpenoids; SECONDARY MOLD METABOLITES; STRUCTURE ELUCIDATION; FUNGI;
D O I
10.1002/pca.3301
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Introduction: The genus Omphalotus, in particular the "Jack-O'Lantern mushrooms" Omphalotus illudens and Omphalotus olearius, are famous for the production of the DNA-alkylating illudins. A lesser-known species, Omphalotus mexicanus, native to Central America, also produces cytotoxic illudins S and M, but its minor secondary metabolites are yet to be investigated.Objective: To identify, isolate, and elucidate the structure of novel secondary metabolites of the illudin family in mycelial extracts of O. mexicanus from submerse cultivation.Methodology: A fermentation of the fungus in 15 L stirred tank bioreactors is described. Mycelial extracts were separated using a combination of flash chromatography with preparative RP-C18 high-performance liquid chromatography (HPLC). Analysis of metabolites was done using an ultrahigh-performance liquid chromatography ultraviolet diode array detector (UPLC-UV-DAD) system coupled to an electrospray ionisation quadrupole time-of-flight (ESI-QTOF) mass spectrometer. Structures were elucidated using one-dimensional (1D) and two-dimensional (2D) nuclear magnetic resonance spectroscopy (NMR) techniques followed by comparison of experimental and simulated electronic circular dichroism (ECD) spectra to determine absolute configurations.Results: Two novel illudin derivatives, for which we propose the names omphaderol (1) and illudaneol B (2), as well as illudaneol (3) and the unusual cyclobutylcyclopentane illudosin (4), were isolated from the mycelia and characterised.Conclusion: Particularly the illudaneol derivatives with their high titers may be potential building blocks for an alternative semisynthetic route to new illudin derivatives with improved medical properties. Additionally, the findings improve the knowledge of minor illudin compounds in the mycelial extract of this fungus and may be of significance for future biosynthetic studies of the illudins.
引用
收藏
页码:469 / 475
页数:7
相关论文
共 29 条
  • [1] ANTIBIOTIC SUBSTANCES FROM BASIDIOMYCETES .7. CLITOCYBE ILLUDENS
    ANCHEL, M
    HERVEY, A
    ROBBINS, WJ
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1950, 36 (05) : 300 - 305
  • [2] [Anonymous], 2009, Spartan'10, Version 1.1.0
  • [3] SECONDARY MOLD METABOLITES .34. ISOLATION AND STRUCTURE ELUCIDATION OF ILLUDOSIN, A NOVEL SESQUITERPENE FROM CLITOCYBE-ILLUDENS USING ONE AND 2-DIMENSIONAL NMR TECHNIQUES
    ARNONE, A
    CARDILLO, R
    NASINI, G
    DEPAVA, OV
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1991, (08): : 1787 - 1791
  • [4] SECONDARY MOLD METABOLITES .31. ISOLATION AND STRUCTURE ELUCIDATION OF ILLUDINS-A AND ILLUDINS-B, AND ILLUDALENOL, NEW SESQUITERPENOIDS FROM CLITOCYBE-ILLUDENS
    ARNONE, A
    CARDILLO, R
    NASINI, G
    DEPAVA, OV
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1991, (04): : 733 - 737
  • [5] METABOLITES OF BIRDS NEST FUNGI .15. THE CYBRODINS, A NEW CLASS OF SESQUITERPENES
    AYER, WA
    MCCASKILL, RH
    [J]. CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1981, 59 (14): : 2150 - 2158
  • [6] DENSITY-FUNCTIONAL THERMOCHEMISTRY .3. THE ROLE OF EXACT EXCHANGE
    BECKE, AD
    [J]. JOURNAL OF CHEMICAL PHYSICS, 1993, 98 (07) : 5648 - 5652
  • [7] DENSITY-FUNCTIONAL EXCHANGE-ENERGY APPROXIMATION WITH CORRECT ASYMPTOTIC-BEHAVIOR
    BECKE, AD
    [J]. PHYSICAL REVIEW A, 1988, 38 (06): : 3098 - 3100
  • [8] SpecDis: Quantifying the Comparison of Calculated and Experimental Electronic Circular Dichroism Spectra
    Bruhn, Torsten
    Schaumloeffel, Anu
    Hemberger, Yasmin
    Bringmann, Gerhard
    [J]. CHIRALITY, 2013, 25 (04) : 243 - 249
  • [9] Optimization of the production process for the anticancer lead compound illudin M: downstream processing
    Chaverra-Munoz, Lillibeth
    Briem, Theresa
    Huettel, Stephan
    [J]. MICROBIAL CELL FACTORIES, 2022, 21 (01)
  • [10] Optimization of the production process for the anticancer lead compound illudin M: process development in stirred tank bioreactors
    Chaverra-Munoz, Lillibeth
    Huettel, Stephan
    [J]. MICROBIAL CELL FACTORIES, 2022, 21 (01)