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Sample GSM859600 Query DataSets for GSM859600
Status Public on Jan 11, 2012
Title 1.2_2
Sample type RNA
 
Source name nitrogen-limited cultures sparged with 1% oxygen, with 0.8 micromolar dissolved oxygen
Organism Saccharomyces cerevisiae EC1118
Characteristics condition: nitrogen-limited cultures sparged with 1% oxygen, with 0.8 micromolar dissolved oxygen
Treatment protocol cultures were sparged with different oxygen/nitrogen mixtures to achieve different dissolved oxygen concentration. When reached the culture steady state for each level, samples were taken and inmediately placed on crushed ice. Afterwards, they were centrifuged at max. speed, eliminated the supernatant and the cell pellet frozen in liquid nitrogen and stored at -80ºC until analysis
Growth protocol cells were grown in chemostats with a syntethic must medium (MS300), custom modified to achieve nitrogen limitation with d=0.1 h-1, pH=3.5
Extracted molecule total RNA
Extraction protocol RNA was extracted from frozen cell pellets using the AxyPrep Multisource RNA kit (Axygen Biosciences, USA), modified for the use with glass beads for cell lysis. Briefly, we resuspended the cell pellet in the R-I kit buffer, added it to a screw-cap tube containing 250 µl of 500 µm acid-washed glass beads (Sigma, USA). We stirred the tubes in three cycles of 45 s in a Mini Bead BeaterTM (Biospec), standing an equivalent time in ice between cycles. Later, the lysate was centrifuged at 10.000 x g and supernatant was transferred to a tube with 250 µl of isopropanol. After this point, we followed the kit manufacturer instructions.
Label biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 500 ng total RNA (Expression Analysis Technical Manual, 2009, Affymetrix).
 
Hybridization protocol Following fragmentation, 15 ug of cRNA were hybridized for 16 hr at 45C on Yeast Genome 2,0 Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
Scan protocol GeneChips were scanned using the Hewlett-Packard GeneChip Scanner 3000 7G.
Data processing The data were analyzed in R with the affy, affyQCReport and simpleaffy packages from Bioconductor. Data was normalized using the RMA algorithm.
 
Submission date Jan 10, 2012
Last update date Oct 01, 2012
Contact name Felipe F Aceituno
E-mail(s) [email protected]
Organization name PUC
Department Chemical Engineering and Bioprocesses
Lab Biotechnology
Street address Vicuña Mackena 4860
City Santiago
ZIP/Postal code 45647687
Country Chile
 
Platform ID GPL2529
Series (1)
GSE34964 Transcriptomic analysis of the oxygen response in Saccharomyces cerevisiae EC1118 under wine fermentation conditions

Data table header descriptions
ID_REF
VALUE log2 RMA-normalized signal intensity

Data table
ID_REF VALUE
1769308_at 6.66738661
1769311_at 8.672390635
1769312_at 6.831599818
1769313_at 6.716882563
1769314_at 8.794664274
1769317_at 4.910638075
1769319_at 9.30226284
1769320_at 5.879563215
1769321_at 6.484074265
1769322_s_at 6.614327072
1769323_at 5.94457405
1769324_at 6.082414035
1769325_at 4.792173671
1769329_at 6.783363779
1769331_at 5.301559794
1769333_at 7.069166394
1769335_at 8.412317678
1769336_at 5.733194379
1769338_at 3.880109411
1769339_at 7.099409006

Total number of rows: 5716

Table truncated, full table size 128 Kbytes.




Supplementary file Size Download File type/resource
GSM859600_6_FA_Yeast_2_2.CEL.gz 631.9 Kb (ftp)(http) CEL
Processed data included within Sample table

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