Repositori institucional URV
Belongs to PC:SerieArticles collection
TITLE:
Seven new cytotoxic and antimicrobial xanthoquinodins from jugulospora vestita - imarina:8787055
Handle:
https://hdl.handle.net/20.500.11797/imarina8787055
URV's Author/s:
MARÍN FÉLIX, YASMINA / Stchigel Glikman, Alberto Miguel
Author, as appears in the article.:
Shao L; Marin-Felix Y; Surup F; Stchigel AM; Stadler M
Author's mail:
albertomiguel.stchigel@urv.cat
Author identifier
:
0000-0003-3987-7996
Journal publication year:
2020
Publication Type:
Journal Publications
APA
:
Shao L; Marin-Felix Y; Surup F; Stchigel AM; Stadler M (2020). Seven new cytotoxic and antimicrobial xanthoquinodins from jugulospora vestita. J Fungi (Basel), 6(4), 1-17. DOI: 10.3390/jof6040188
Papper original source
:
J Fungi (Basel). 6 (4): 1-17
Abstract:
© 2020 by the authors. Licensee MDPI, Basel, Switzerland. During the course of a screening for novel biologically active secondary metabolites produced by the Sordariomycetes (Ascomycota, Fungi), the ex-type strain of Jugulospora vestita was found to produce seven novel xanthone-anthraquinone heterodimers, xanthoquinodin A11 (1) and xanthoquinodins B10–15 (2–7), together with the already known compound xanthoquinodin B4 (8). The structures of the xanthoquinodins were determined by analysis of the nuclear magnetic resonance (NMR) spectroscopic and mass spectrometric data. Moreover, the absolute configurations of these metabolites were established by analysis of the1H−1H coupling constants, nuclear Overhauser effect spectroscopy (NOESY) correlations, and Electronic Circular Dichroism (ECD) spectroscopic data. Antifungal and antibacterial activities as well as cytotoxicity of all compounds were tested. Xanthoquinodin B11 showed fungicidal activities against Mucor hiemalis [minimum inhibitory concentration (MIC) 2.1 µg/mL], Rhodotorula glutinis (MIC 2.1 µg/mL), and Pichia anomala (MIC 8.3 µg/mL). All the compounds 1–8 displayed anti-Gram-positive bacteria activity (MIC 0.2–8.3 µg/mL). In addition, all these eight compounds showed cytotoxicity against KB 3.1, L929, A549, SK-OV-3, PC-3, A431, and MCF-7 mammalian cell lines. The six novel compounds (1–3, 5–7), together with xanthoquinodin B4, were also found in the screening of other strains belonging to Jugulospora rotula, revealing the potential chemotaxonomic significance of the compound class for the genus.
Article's DOI:
10.3390/jof6040188
Link to the original source:
https://www.mdpi.com/2309-608X/6/4/188
Papper version:
info:eu-repo/semantics/publishedVersion
licence for use:
https://creativecommons.org/licenses/by/3.0/es/
Department:
Ciències Mèdiques Bàsiques
Licence document URL:
https://repositori.urv.cat/ca/proteccio-de-dades/
Thematic Areas:
Plant science
Mycology
Microbiology (medical)
Microbiology
Farmacia
Ecology, evolution, behavior and systematics
Ciências biológicas iii
Ciências biológicas ii
Keywords:
Xanthoquinodins
Sordariales
Secondary metabolites
Cytotoxicity
Antimicrobial activity
Entity:
Universitat Rovira i Virgili
Record's date:
2023-02-19
Description:
© 2020 by the authors. Licensee MDPI, Basel, Switzerland. During the course of a screening for novel biologically active secondary metabolites produced by the Sordariomycetes (Ascomycota, Fungi), the ex-type strain of Jugulospora vestita was found to produce seven novel xanthone-anthraquinone heterodimers, xanthoquinodin A11 (1) and xanthoquinodins B10–15 (2–7), together with the already known compound xanthoquinodin B4 (8). The structures of the xanthoquinodins were determined by analysis of the nuclear magnetic resonance (NMR) spectroscopic and mass spectrometric data. Moreover, the absolute configurations of these metabolites were established by analysis of the1H−1H coupling constants, nuclear Overhauser effect spectroscopy (NOESY) correlations, and Electronic Circular Dichroism (ECD) spectroscopic data. Antifungal and antibacterial activities as well as cytotoxicity of all compounds were tested. Xanthoquinodin B11 showed fungicidal activities against Mucor hiemalis [minimum inhibitory concentration (MIC) 2.1 µg/mL], Rhodotorula glutinis (MIC 2.1 µg/mL), and Pichia anomala (MIC 8.3 µg/mL). All the compounds 1–8 displayed anti-Gram-positive bacteria activity (MIC 0.2–8.3 µg/mL). In addition, all these eight compounds showed cytotoxicity against KB 3.1, L929, A549, SK-OV-3, PC-3, A431, and MCF-7 mammalian cell lines. The six novel compounds (1–3, 5–7), together with xanthoquinodin B4, were also found in the screening of other strains belonging to Jugulospora rotula, revealing the potential chemotaxonomic significance of the compound class for the genus.
Type:
Journal Publications
Contributor:
Universitat Rovira i Virgili
Títol:
Seven new cytotoxic and antimicrobial xanthoquinodins from jugulospora vestita
Subject:
Ecology, Evolution, Behavior and Systematics,Microbiology,Microbiology (Medical),Mycology,Plant Science
Xanthoquinodins
Sordariales
Secondary metabolites
Cytotoxicity
Antimicrobial activity
Plant science
Mycology
Microbiology (medical)
Microbiology
Farmacia
Ecology, evolution, behavior and systematics
Ciências biológicas iii
Ciências biológicas ii
Date:
2020
Creator:
Shao L
Marin-Felix Y
Surup F
Stchigel AM
Stadler M
Rights:
info:eu-repo/semantics/openAccess
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