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Sample GSM5351986 Query DataSets for GSM5351986
Status Public on Aug 04, 2021
Title fungi growth on 1% polygalacturonic acid for 8 hour rep1
Sample type RNA
 
Source name Mycelium
Organism Aspergillus niger
Characteristics strain: N402
treatment: grown on PGA 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) [email protected]
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 105.4643
AFFX-BioB-M_at 87.08093
AFFX-BioB-3_at 38.10606
AFFX-BioC-5_at 141.049
AFFX-BioC-3_at 198.7552
AFFX-BioDn-5_at 247.206
AFFX-BioDn-3_at 1061.29
AFFX-CreX-5_at 2308
AFFX-CreX-3_at 3127.043
AFFX-DapX-5_at 1023.691
AFFX-DapX-M_at 1649.554
AFFX-DapX-3_at 2548.778
AFFX-LysX-5_at 31.45316
AFFX-LysX-M_at 102.1313
AFFX-LysX-3_at 380.0945
AFFX-PheX-5_at 131.5856
AFFX-PheX-M_at 196.4132
AFFX-PheX-3_at 330.6615
AFFX-ThrX-5_at 291.4727
AFFX-ThrX-M_at 400.2512

Total number of rows: 14554

Table truncated, full table size 326 Kbytes.




Supplementary file Size Download File type/resource
GSM5351986_080409MJA_ANIGERa_100122-12.CEL.gz 1.9 Mb (ftp)(http) CEL
Processed data included within Sample table
Processed data are available on Series record

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