|
| Status |
Public on Apr 18, 2013 |
| Title |
Pool for sample 28 |
| Sample type |
genomic |
| |
|
| Source name |
Initial pool for competition 28
|
| Organism |
Saccharomyces cerevisiae |
| Characteristics |
yeast collection: Whole genome homozygous deletion collection
phase or medium: Preculture
number of generations: 0
|
| Growth protocol |
Bioreactors containing 200 mL of the previously described synthetic must were inoculated to an initial OD600 of 0.2. Cultures were grown in batch mode during about 12 h prior to triggering the continuous cultures. According to the data obtained from batch characterization, dilution rate was set to 0.23 h-1 for competitions mimicking Phase I and to 0.04 h-1 for those mimicking Phase II. Competition experiments using the heterozygous collection were run for 20 generations (corresponding to 60 h for Phase I or 347 h for Phase II) while those performed with the homozygous collection were run for 10 generations (30 h for Phase I or 174 h for Phase II). Yeast cell samples were taken at the onset of the continuous cultures, and after the indicated numbers of generations, in order to compare pool compositions at the beginning and the end of the competition experiments. Additional triplicate competition experiments, using YPD broth (D=0.23 h-1), were performed in order to differentiate deletions unspecifically affecting yeast growth from those specific for Phase I or Phase II fermentation conditions.
|
| Extracted molecule |
genomic DNA |
| Extraction protocol |
Genomic DNA was extracted bu using the YeaStarTM Genomic DNA Kit (Zymo Research).
|
| Label |
biotin
|
| Label protocol |
Amplification of the barcodes (uptags and downtags), with simoultaneous labelling using biotinilated primers was performed according to [Pierce SE, Davis RW, Nislow C, Giaever G (2007) Genome-wide analysis of barcoded Saccharomyces cerevisiae gene-deletion mutants in pooled cultures. Nat Protocols 2: 2958-2974]
|
| |
|
| Hybridization protocol |
Reactions hybridized overnight to custom-built TAG4 microarrays (Affymetrix). GeneChips were washed and stained in the Affymetrix Fluidics Station 450 according to [Pierce SE, Davis RW, Nislow C, Giaever G (2007) Genome-wide analysis of barcoded Saccharomyces cerevisiae gene-deletion mutants in pooled cultures. Nat Protocols 2: 2958-2974]
|
| Scan protocol |
GeneChips were scanned at an emission wavelength of 560 nm using a GeneChip scanner (Affymetrix).
|
| Description |
HOP 3 t=0 F2
Control for competition 28
|
| Data processing |
Data procesing was performed according to [Pierce SE, Davis RW, Nislow C, Giaever G (2007) Genome-wide analysis of barcoded Saccharomyces cerevisiae gene-deletion mutants in pooled cultures. Nat Protocols 2: 2958-2974]. Perl scripts were downloaded from the supplementary web [Pierce, S.E. et al. A unique and universal molecular barcode array. Nat. Methods 3, 601-603 (2006)]. Data were normalized by quantile. Extracted data are in natural scale, but Ratios used for discussion in the associated manuscript are expressed in log2.
|
| |
|
| Submission date |
Apr 17, 2013 |
| Last update date |
Apr 18, 2013 |
| Contact name |
Ramon Gonzalez |
| E-mail(s) |
rgonzalez@icvv.es
|
| Phone |
+34 941299684
|
| Organization name |
Consejo Superior de Investigaciones Científicas
|
| Department |
Instituto de Ciencias de la Vid y del Vino
|
| Lab |
Enología
|
| Street address |
C. Madre de Dios, 51
|
| City |
Logroño |
| ZIP/Postal code |
E-26006 |
| Country |
Spain |
| |
|
| Platform ID |
GPL17030 |
| Series (1) |
| GSE46145 |
Genome-wide study of the adaptation of Saccharomyces cerevisiae to the proliferative stages of wine fermentation |
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