Abstract
Degradation of plant biomass to fermentable sugars is of critical importance for the use of plant materials for biofuels. Filamentous fungi are ubiquitous organisms and major plant biomass degraders. Single colonies of some fungal species can colonize massive areas as large as five soccer stadia. During growth, the mycelium encounters heterogeneous carbon sources. Here we assessed whether substrate heterogeneity is a major determinant of spatial gene expression in colonies of Aspergillus niger. We analyzed whole-genome gene expression in five concentric zones of 5-day-old colonies utilizing sugar beet pulp as a complex carbon source. Growth, protein production and secretion occurred throughout the colony. Genes involved in carbon catabolism were expressed uniformly from the centre to the periphery whereas genes encoding plant biomass degrading enzymes and nitrate utilization were expressed differentially across the colony. A combined adaptive response of carbon-catabolism and enzyme production to locally available monosaccharides was observed. Finally, our results demonstrate that A. niger employs different enzymatic tools to adapt its metabolism as it colonizes complex environments.
Original language | English |
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Article number | 13592 |
Number of pages | 13 |
Journal | Scientific Reports |
Volume | 5 |
DOIs | |
Publication status | Published - 28 Aug 2015 |
Funding
IB was supported by a grant of the Dutch Technology Foundation STW, Applied Science division of NWO and the Technology Program of the Ministry of Economic Affairs UGC 07938 to RPdV. MZ was supported by a grant from the Netherlands Organisation for Scientific Research (NWO) and the Netherlands Genomics Initiative 93511035 to RPdV. The data analysis was partially carried out on the Dutch national e-infrastructure with the support of SURF Foundation. AVD was supported by grants of the Dutch Technology Foundation STW, Applied Science division of NWO and the Technology Program of the Ministry of Economic Affairs UGC 07063 to RPdV. This work is also part of the project Proteins At Work, financed by the Netherlands Organisation for Scientific Research (NWO) as part of the National Roadmap Large-scale Research Facilities of the Netherlands (project number 184.032.201). DJD was supported by the Kansas State University Plant Biotechnology Center and a Kansas NSF EPSCoR First Award EPS-0903806 to RBT. This is contribution number 15-305-J from the Kansas Agricultural Experiment Station.
Keywords
- AMMONIUM PERMEASE GENES
- SIGNAL PEPTIDES
- MICROARRAY DATA
- PROTEOMICS DATA
- NIDULANS
- LOCALIZATION
- CLONING
- PROTEIN
- DEGRADATION
- SUBSTRATE