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Lignin Degradation and Its Use in Signaling Development by the Coprophilous Ascomycete Podospora anserina.


ABSTRACT: The filamentous fungus Podospora anserina is a good model to study the breakdown of lignocellulose, owing to its ease of culture and genetical analysis. Here, we show that the fungus is able to use a wide range of lignocellulosic materials as food sources. Using color assays, spectroscopy and pyrolysis-gas chromatography mass spectrometry, we confirm that this ascomycete is able to degrade lignin, primarily by hydrolyzing ?-O-4 linkages, which facilitates its nutrient uptake. We show that the limited weight loss that is promoted when attacking Miscanthus giganteus is due to a developmental blockage rather than an inefficiency of its enzymes. Finally, we show that lignin, and, more generally, phenolics, including degradation products of lignin, greatly stimulate the growth and fertility of the fungus in liquid cultures. Analyses of the CAT????? mutant lacking all its catalases, pro-oxidants and antioxidants indicate that improved growth and fertility of the fungus is likely caused by augmented reactive oxygen species levels triggered by the presence of phenolics.

SUBMITTER: Dicko M 

PROVIDER: S-EPMC7712204 | biostudies-literature | 2020 Nov

REPOSITORIES: biostudies-literature

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Lignin Degradation and Its Use in Signaling Development by the Coprophilous Ascomycete <i>Podospora anserina</i>.

Dicko Moussa M   Ferrari Roselyne R   Tangthirasunun Narumon N   Gautier Valérie V   Lalanne Christophe C   Lamari Farida F   Silar Philippe P  

Journal of fungi (Basel, Switzerland) 20201111 4


The filamentous fungus <i>Podospora anserina</i> is a good model to study the breakdown of lignocellulose, owing to its ease of culture and genetical analysis. Here, we show that the fungus is able to use a wide range of lignocellulosic materials as food sources. Using color assays, spectroscopy and pyrolysis-gas chromatography mass spectrometry, we confirm that this ascomycete is able to degrade lignin, primarily by hydrolyzing β-O-4 linkages, which facilitates its nutrient uptake. We show that  ...[more]

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