Abstract

BackgroundEnzymatic plant biomass degradation by fungi is a highly complex process and one of the leading challenges in developing a biobased economy. Some industrial fungi (e.g. Aspergillus niger) have a long history of use with respect to plant biomass degradation and for that reason have become ‘model’ species for this topic. A. niger is a major industrial enzyme producer that has a broad ability to degrade plant based polysaccharides. A. niger wild-type, the (hemi-)cellulolytic regulator (xlnR) and xylulokinase (xkiA1) mutant strains were grown on a monocot (corn stover, CS) and dicot (soybean hulls, SBH) substrate. The xkiA1 mutant is unable to utilize the pentoses D-xylose and L-arabinose and the polysaccharide xylan, and was previously shown to accumulate inducers for the (hemi-)cellulolytic transcriptional activator XlnR and the arabinanolytic transcriptional activator AraR in the presence of pentoses, resulting in overexpression of their target genes. The xlnR mutant has reduced growth on xylan and down-regulation of its target genes. The mutants therefore have a similar phenotype on xylan, but an opposite transcriptional effect. D-xylose and L-arabinose are the most abundant monosaccharides after D-glucose in nearly all plant-derived biomass materials. In this study we evaluated the effect of the xlnR and xkiA1 mutation during growth on two pentose-rich substrates by transcriptome analysis.ResultsParticular attention was given to CAZymes, metabolic pathways and transcription factors related to the plant biomass degradation. Genes coding for the main enzymes involved in plant biomass degradation were down-regulated at the beginning of the growth on CS and SBH. However, at a later time point, significant differences were found in the expression profiles of both mutants on CS compared to SBH.ConclusionThis study demonstrates the high complexity of the plant biomass degradation process by fungi, by showing that mutant strains with fairly straightforward phenotypes on pure mono- and polysaccharides, have much less clear-cut phenotypes and transcriptomes on crude plant biomass.

Highlights

  • Enzymatic plant biomass degradation by fungi is a highly complex process and one of the leading challenges in developing a biobased economy

  • In this study we describe a transcriptomic analysis of A. niger wild-type, ΔxlnR and xkiA1 mutant grown on Corn stover (CS) and soybean hulls (SBH)

  • Our results showed an antagonistic effect between ΔxlnR and the xkiA1 mutant after 48 h to CS and SBH, since more genes were up-regulated in the xkiA1 mutant compared to ΔxlnR, while more genes were downregulated in ΔxlnR compared to the xkiA1 mutant

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Summary

Introduction

Enzymatic plant biomass degradation by fungi is a highly complex process and one of the leading challenges in developing a biobased economy. The xkiA1 mutant is unable to utilize the pentoses Dxylose and L-arabinose and the polysaccharide xylan, and was previously shown to accumulate inducers for the (hemi-)cellulolytic transcriptional activator XlnR and the arabinanolytic transcriptional activator AraR in the presence of pentoses, resulting in overexpression of their target genes. Aspergillus niger is a filamentous fungus that degrades plant biomass polysaccharides, such as cellulose, hemicellulose and pectin into monomeric sugars that can serve as a carbon source. A. niger is able to secrete a broad spectrum of enzymes that can hydrolyze polysaccharides into pentoses, hexoses and other monomeric components [1], which can be taken up by the fungus. A. niger uses a variety of catabolic pathways to efficiently convert the monomeric components of plant biomass. The production of D-xylulose-5-phosphate from the PCP enables the fungus to answer efficiently to the increased demands of NADH and NADPH [6]

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