Transcriptome and exoproteome analysis of utilization of plant-derived biomass by Myceliophthora thermophila

•Myceliophthora thermophila was grown on a wide range of lignocellulosic biomass.•Transcriptome and exoproteome data on production of CAZymes were collected.•Exoproteome data largely confirmed the transcriptome results.•Despite the range of substrates used, only a core set CAZymes was up-regulated.•...

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Veröffentlicht in:Fungal genetics and biology 2014-11, Vol.72, p.10-20
Hauptverfasser: Kolbusz, Magdalena Anna, Di Falco, Marcos, Ishmael, Nadeeza, Marqueteau, Sandrine, Moisan, Marie-Claude, Baptista, Cassio da Silva, Powlowski, Justin, Tsang, Adrian
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Sprache:eng
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Zusammenfassung:•Myceliophthora thermophila was grown on a wide range of lignocellulosic biomass.•Transcriptome and exoproteome data on production of CAZymes were collected.•Exoproteome data largely confirmed the transcriptome results.•Despite the range of substrates used, only a core set CAZymes was up-regulated.•Enzymes detected reflect substrate composition. Myceliophthora thermophila is a thermophilic fungus whose genome encodes a wide range of carbohydrate-active enzymes (CAZymes) involved in plant biomass degradation. Such enzymes have potential applications in turning different kinds of lignocellulosic feedstock into sugar precursors for biofuels and chemicals. The present study examined and compared the transcriptomes and exoproteomes of M. thermophila during cultivation on different types of complex biomass to gain insight into how its secreted enzymatic machinery varies with different sources of lignocellulose. In the transcriptome analysis three monocot (barley, oat, triticale) and three dicot (alfalfa, canola, flax) plants were used whereas in the proteome analysis additional substrates, i.e. wood and corn stover pulps, were included. A core set of 59 genes encoding CAZymes was up-regulated in response to both monocot and dicot straws, including nine polysaccharide monooxygenases and GH10, but not GH11, xylanases. Genes encoding additional xylanolytic enzymes were up-regulated during growth on monocot straws, while genes encoding additional pectinolytic enzymes were up-regulated in response to dicot biomass. Exoproteome analysis was generally consistent with the conclusions drawn from transcriptome analysis, but additional CAZymes that accumulated to high levels were identified. Despite the wide variety of biomass sources tested some CAZy family members were not expressed under any condition. The results of this study provide a comprehensive view from both transcriptome and exoproteome levels, of how M. thermophila responds to a wide range of biomass sources using its genomic resources.
ISSN:1087-1845
1096-0937
DOI:10.1016/j.fgb.2014.05.006