NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM955169 Query DataSets for GSM955169
Status Public on Aug 07, 2012
Title T1 during hacA MT triplicate 2/3
Sample type RNA
 
Source name Mycelial biomass, exponential growth, glucose-limited bioreactor batch cultures of hacA mt
Organism Aspergillus niger
Characteristics strain: MA70.15 (DkusA::amdS+ in AB4.1 pyrG-)
genotype/variation: hacA mutant
phase: T1 exponential growth
Biomaterial provider Arthur Ram: Molecular Microbiology and Biotechnology group at the Institute Biology at Universiteit Leiden
Treatment protocol Mid-exponential growth phase from bioreactor batch culture with carbon-limited (glucose) minimal medium
Growth protocol Conidia for inoculation of bioreactor cultures were harvested from solidified CM with a sterile detergent solution containing 0.05% (w/v) Tween80 and 0.9% (w/v) NaCl. Batch cultivation of HacAWT and HacACA was initiated by inoculating 5L MM with conidial suspension to give 109 conidia L-1. Glucose was sterilized separately and added to sterile MM to give a final concentration of 0.75% (w/v). During cultivation at 30 °C, pH 3 was maintained by computer-controlled addition of 2 M NaOH or 1 M HCl. Sterile air was supplied at 1 L min-1 through a ring-sparger. Dissolved oxygen tension was above 40% of air saturation at any time, ensuring sufficient oxygen for growth. After spore germination 0.01% (v/v) polypropyleneglycol P2000 was added as antifoam agent. Submerged cultivation was performed with 6.6 L BioFlo3000 bioreactors (New Brunswick Scientific, NJ, USA).
Extracted molecule total RNA
Extraction protocol Total RNA was isolated from homogenized mycelial samples using TRIzol reagent (Invitrogen).
Label Biotin
Label protocol The Affymetrix One-Cycle Target Labeling Kit and Control Reagents (#900493) are used to synthesize Biotin-labeled cRNA. From each RNA sample 2 μg is used for the labeling experiments.
 
Hybridization protocol The GeneChip Hybridization, Wash and Stain Kit (#900720) is used for the for the hybridizations, washing, staining and scanning of the chips. The Affymetrixprotocols are strictly followed. The Affymetrix custom Aspergilus niger Genome Arrays are used for hybridization. To the 270 μl hybridization cocktail, 30 μl labeled material is added according the manual of the Affymetrix One Cycle Target Labeling Kit.
Scan protocol Standard Affymetrix protocol
Description strain nc2.1: homologous recombination of the wild-type hacA locus in strain MA70.15 (DkusA::amdS+ in AB4.1 pyrG-) with a construct carying the constitutively active hacA locus and the AopyrG gene as selection marker
Data processing The RMA Bioconductor package was used for data processing
 
Submission date Jul 03, 2012
Last update date Aug 07, 2012
Contact name Benjamin M. Nitsche
E-mail(s) bmnitsche@gmail.com
Organization name Leiden University
Department Institute of Biology
Lab Molecular Microbiology and Biotechnology
Street address Sylviusweg 72
City Leiden
State/province The Netherlands
ZIP/Postal code 2333 BE
Country Netherlands
 
Platform ID GPL6758
Series (1)
GSE39070 Genome-wide expression analysis upon constitutive activation of the HacA bZIP transcription factor in Aspergillus niger

Data table header descriptions
ID_REF
VALUE RMA expression data (log2 scale)

Data table
ID_REF VALUE
An00g00001_at 6.44
An00g00002_at 5.29
An00g00003_at 4.65
An00g00004_at 4.52
An00g00005_at 6.37
An00g00006_at 5.40
An00g00007_at 6.78
An00g00008_at 5.01
An00g00009_at 9.46
An00g00010_at 4.57
An00g00010_x_at 6.24
An00g00011_at 4.52
An00g00012_at 5.19
An00g00013_at 5.81
An00g00014_at 4.64
An00g00015_at 3.83
An00g00016_at 5.83
An00g00017_at 5.24
An00g00018_at 5.00
An00g00019_at 4.83

Total number of rows: 14489

Table truncated, full table size 270 Kbytes.




Supplementary file Size Download File type/resource
GSM955169_080807MJA_ANIGERa_100480_12.CEL.gz 1.9 Mb (ftp)(http) CEL
Processed data included within Sample table

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