NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM5351983 Query DataSets for GSM5351983
Status Public on Aug 04, 2021
Title submerged growth on sugar beet pulp for 8 hours biological rep2
Sample type RNA
 
Source name Mycelium
Organism Aspergillus niger
Characteristics strain: N402
treatment: during SBP degradation after 8 hour incubation
Treatment protocol One gram (wet weight) of the mycelium was transferred to 250 mL Erlenmeyer flasks containing 50 mL MM supplemented with 1% SBP or PGA (Sigma-Aldrich) and incubated for 8 h and 24 h.
Growth protocol Aspergillus niger N402 was propagated and grown on complete medium (CM) or minimal medium (MM). Liquid cultures were grown in a rotary shaker at 250 rpm and 30C. Transfer experiment was performed by growing the strain for 16 h in 1 L Erlenmeyer flasks that contained 250 mL CM supplemented with 2% D-fructose as carbon source. The mycelium was harvested by filtration and washed with MM without a carbon source.
Extracted molecule total RNA
Extraction protocol RNA was extracted using TRIzol reagent (Invitrogen) and purified using TRIzol® Plus RNA Purification Kit (Sigma-Aldrich) according to the instructions of the manufacturer.
Label biotin
Label protocol Biotin-labeled antisense cRNA was produced from 2 µg of total RNA with the Eukaryotic One-Cycle Target Labeling kit (Affymetrix; www.affymetrix.com)
 
Hybridization protocol Following fragmentation, 10 µg of cRNA was hybridized to Affymetrix A. niger Genome GeneChips (GPL6758). GeneChips were washed and stained in an automated process.
Scan protocol GeneChips were scanned.
Data processing Microarray data was analyzed using the Bioconductor tool package version 2.8 (http://www.bioconductor.org/) together with house-made Perl (version .5.0) and Python (version 3.0) scripts. Probe intensities were normalized for background by the robust multi-array average (RMA) method using the R statistical language and environment. This method makes use of only perfect match (PM) probes. Normalization was processed by the quantiles algorithm. The median polish summary method was used to calculate the gene expression values.
 
Submission date Jun 01, 2021
Last update date Aug 04, 2021
Contact name Ronald de vries
E-mail(s) fungalphysiology@gmail.com
Phone +31(0)30-2122600
Organization name westerdijkinstitute
Street address Uppsalalaan 8
City Utrecht
State/province Utrecht
ZIP/Postal code 3584 CT
Country Netherlands
 
Platform ID GPL6758
Series (1)
GSE175954 Comparative study of gene expression in Aspergillus niger solid and submerged growth during sugar beet pulp utilization

Data table header descriptions
ID_REF
VALUE Normalized and absolute expression value indexes (log2)

Data table
ID_REF VALUE
AFFX-BioB-5_at 97.71993
AFFX-BioB-M_at 106.6176
AFFX-BioB-3_at 43.70713
AFFX-BioC-5_at 144.9662
AFFX-BioC-3_at 270.396
AFFX-BioDn-5_at 326.0951
AFFX-BioDn-3_at 1229.586
AFFX-CreX-5_at 3398.295
AFFX-CreX-3_at 4558.253
AFFX-DapX-5_at 435.025
AFFX-DapX-M_at 720.4197
AFFX-DapX-3_at 1519.185
AFFX-LysX-5_at 21.02338
AFFX-LysX-M_at 60.95041
AFFX-LysX-3_at 165.558
AFFX-PheX-5_at 59.92056
AFFX-PheX-M_at 124.0867
AFFX-PheX-3_at 177.4855
AFFX-ThrX-5_at 156.3067
AFFX-ThrX-M_at 197.0598

Total number of rows: 14554

Table truncated, full table size 326 Kbytes.




Supplementary file Size Download File type/resource
GSM5351983_080813MJA_ANIGERa_100465-02.CEL.gz 1.6 Mb (ftp)(http) CEL
Processed data included within Sample table
Processed data are available on Series record

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap