Literature DB >> 15654124

Neutral glycolipids of the filamentous fungus Neurospora crassa: altered expression in plant defensin-resistant mutants.

Chaeho Park1, Beau Bennion, Isabelle E J A François, Kathelijne K A Ferket, Bruno P A Cammue, Karin Thevissen, Steven B Levery.   

Abstract

To defend themselves against fungal pathogens, plants produce numerous antifungal proteins and peptides, including defensins, some of which have been proposed to interact with fungal cell surface glycosphingolipid components. Although not known as a phytopathogen, the filamentous fungus Neurospora crassa possesses numerous genes similar to those required for plant pathogenesis identified in fungal pathogens (Galagan, J. E., et al. 2003. Nature 422: 859-868), and it has been used as a model for studying plant-phytopathogen interactions targeting fungal membrane components (Thevissen, K., et al. 2003. Peptides. 24: 1705-1712). For this study, neutral glycolipid components were extracted from wild-type and plant defensin-resistant mutant strains of N. crassa. The structures of purified components were elucidated by NMR spectroscopy and mass spectrometry. Neutral glycosphingolipids of both wild-type and mutant strains were characterized as beta-glucopyranosylceramides, but those of the mutants were found with structurally altered ceramides. Although the wild type expressed a preponderance of N-2'-hydroxy-(E)-Delta3-octadecenoate as the fatty-N-acyl component attached to the long-chain base (4E,8E)-9-methyl-4,8-sphingadienine, the mutant ceramides were found with mainly N-2'-hydroxyhexadecanoate instead. In addition, the mutant strains expressed highly increased levels of a sterol glucoside identified as ergosterol-beta-glucoside. The potential implications of these findings with respect to defensin resistance in the N. crassa mutants are discussed.

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Year:  2005        PMID: 15654124     DOI: 10.1194/jlr.M400457-JLR200

Source DB:  PubMed          Journal:  J Lipid Res        ISSN: 0022-2275            Impact factor:   5.922


  5 in total

1.  The plant defensin RsAFP2 induces cell wall stress, septin mislocalization and accumulation of ceramides in Candida albicans.

Authors:  Karin Thevissen; Patricia de Mello Tavares; Deming Xu; Jill Blankenship; Davy Vandenbosch; Jolanta Idkowiak-Baldys; Gilmer Govaert; Anna Bink; Sonia Rozental; Piet W J de Groot; Talya R Davis; Carol A Kumamoto; Gabriele Vargas; Leonardo Nimrichter; Tom Coenye; Aaron Mitchell; Terry Roemer; Yusuf A Hannun; Bruno P A Cammue
Journal:  Mol Microbiol       Date:  2012-03-05       Impact factor: 3.501

2.  Structural determination and tryptophan fluorescence of heterokaryon incompatibility C2 protein (HET-C2), a fungal glycolipid transfer protein (GLTP), provide novel insights into glycolipid specificity and membrane interaction by the GLTP fold.

Authors:  Roopa Kenoth; Dhirendra K Simanshu; Ravi Kanth Kamlekar; Helen M Pike; Julian G Molotkovsky; Linda M Benson; H Robert Bergen; Franklyn G Prendergast; Lucy Malinina; Sergei Y Venyaminov; Dinshaw J Patel; Rhoderick E Brown
Journal:  J Biol Chem       Date:  2010-02-17       Impact factor: 5.157

3.  Stress-induced cell death is mediated by ceramide synthesis in Neurospora crassa.

Authors:  Nora S Plesofsky; Steven B Levery; Sherry A Castle; Robert Brambl
Journal:  Eukaryot Cell       Date:  2008-10-24

4.  Structural analysis of fungal cerebrosides.

Authors:  Eliana Barreto-Bergter; Guilherme L Sassaki; Lauro M de Souza
Journal:  Front Microbiol       Date:  2011-12-05       Impact factor: 5.640

5.  Membrane Sphingolipids Regulate the Fitness and Antifungal Protein Susceptibility of Neurospora crassa.

Authors:  Anna Huber; Gregor Oemer; Nermina Malanovic; Karl Lohner; Laura Kovács; Willi Salvenmoser; Johannes Zschocke; Markus A Keller; Florentine Marx
Journal:  Front Microbiol       Date:  2019-04-11       Impact factor: 5.640

  5 in total

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