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SRX1745058: GSM2144333: T. reesei-glucose media replicate flask-B; Trichoderma reesei; RNA-Seq
8 ILLUMINA (NextSeq 500) runs: 18.3M spots, 2.8G bases, 1,019.7Mb downloads

Submitted by: NCBI (GEO)
Study: Transcriptomic responses of mixed cultures of ascomycete fungi to lignocellulose using dual RNA-seq reveal inter-species antagonism and limited beneficial effects on CAZyme expression
show Abstracthide Abstract
Gaining new knowledge through fungal monoculture responses to lignocellulose is a widely used approach that can lead to better cocktails for lignocellulose saccharification (the enzymatic release of sugars which are subsequently used to make biofuels). However, responses in lignocellulose mixed cultures are rarely studied in the same detail even though in nature fungi often degrade lignocellulose as mixed communities. Using a dual RNA-seq approach, we describe the first study of the transcriptional responses of wild-type strains of Aspergillus niger, Trichoderma reesei and Penicillium chrysogenum in two and three mixed species shake-flask cultures with wheat straw. Based on quantification of species-specific rRNA, a set of conditions was identified where mixed cultures could be sampled so as to obtain sufficient RNA-seq reads for analysis from each species. The number of differentially-expressed genes varied from a couple of thousand to fewer than one hundred. The proportion of carbohydrate active enzyme (CAZy) encoding transcripts was lower in the majority of the mixed cultures compared to the respective straw monocultures. A small subset of P. chrysogenum CAZy genes showed five to ten-fold significantly increased transcript abundance in a two-species mixed culture with T. reesei. However, a substantial number of T. reesei CAZy transcripts showed reduced abundance in mixed cultures. The highly induced genes in mixed cultures indicated that fungal antagonism was a major part of the mixed cultures. In line with this, secondary metabolite producing gene clusters showed increased transcript abundance in mixed cultures and also mixed cultures with T. reesei led to a decrease in the mycelial biomass of A. niger. Significantly higher monomeric sugar release from straw was only measured using a minority of the mixed culture filtrates and there was no overall improvement. This study demonstrates fungal interaction with changes in transcripts, enzyme activities and biomass in the mixed cultures and whilst there were minor beneficial effects for CAZy transcripts and activities, the competitive interaction between T. reesei and the other fungi was the most prominent feature of this study. Overall design: 10 conditions were analysed with three biological replicates (30 RNA samples) which were from monocultures of each of the three fungi analysed (with either glucose or wheat straw as carbon source) or mixed cultures with two or three fungal species (with wheat straw as carbon source).
Sample: T. reesei-glucose media replicate flask-B
SAMN04958162 • SRS1424084 • All experiments • All runs
Library:
Instrument: NextSeq 500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Mycelia were ground under liquid nitrogen using a mortar and pestle, then the RNA was purified using the Plant/Fungi total RNA Purification Kit (Norgen Biotek, Canada) including the on-column DNase treatment step. Total RNA was measured using Qubit RNA BR assay kit (Life technologies, Q10210). 1 µg of Total RNA was used for enrichment of mRNA using NEBNext Poly(A) mRNA Magnetic Isolation Module (NEB, E7490). Illumina stranded whole transcriptome sequencing libraries were prepared using NEBNext Ultra Directional RNA library prep kit for Illumina (NEB, E7420S). Library QC was performed using bioanalyser HS kit (Agilent biotechnologies, 5067-4626). Libraries were quantified using qPCR (Kapa Biosystems, KK4824), pooled at desired concentrations, denatured and loaded for sequencing according to manufacturer's instructions. Sequencing was done on Illumina NextSeq500 sequencing platform using 2 high output runs to generate 2 x 75 bp reads. Sufficient sequencing was done to obtain ~30 M reads from each monoculture replicate and ~ 100 M reads from each mixed culture replicate. Note: For consistency and to avoid bias, all 30 samples were pooled for running on a lane which resulted in a read output for each sample from each of the four lanes from each of the two runs with the exception of sample BP-23 which was only run once. This would generate 480 sequencing files ((read files (total 2) from each sample (total 30) from each lane (total 4) for each run (total 2)) = 2 x 30 x 4 x 2 = 480) except only 472 files were generated as sample BP-23 was only run in run 1.
Experiment attributes:
GEO Accession: GSM2144333
Links:
Runs: 8 runs, 18.3M spots, 2.8G bases, 1,019.7Mb
Run# of Spots# of BasesSizePublished
SRR34793852,405,930363.3M136.8Mb2016-05-09
SRR34793862,393,899361.5M135.6Mb2016-05-09
SRR34793872,415,264364.8M135.9Mb2016-05-09
SRR34793882,385,223360.2M134.1Mb2016-05-09
SRR34793892,179,288329.1M120.3Mb2016-05-09
SRR34793902,154,027325.3M117.7Mb2016-05-09
SRR34793912,200,627332.3M120.9Mb2016-05-09
SRR34793922,171,126327.9M118.3Mb2016-05-09

ID:
2502575

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