NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1111960 Query DataSets for GSM1111960
Status Public on Apr 01, 2013
Title Mono culture type 1_mixed culture type 1 [chemostat cultures]
Sample type RNA
 
Channel 1
Source name Mono
Organism Lactobacillus delbrueckii subsp. bulgaricus
Characteristics culture type: Mono culture
cultivation type: Chemostat
experiment: Co-fermentation experiment
Treatment protocol Sampling for transcriptome analysis from pure and mixed cultures was performed as previously described, using liquid nitrogen for rapid quenching of metabolism (J.Biol.Chem. 283:23524-23532). Samples were stored at -80°C in a mixture of phenol/chloroform and TEA buffer until further processing for total RNA extraction.
Extracted molecule total RNA
Extraction protocol L. bulgaricus total RNA from pure and mixed cultures was isolated as previously described (Appl.Environ.Microbiol. 76:7775-7784). 500 mg of 0.1 mm zirconium beads (Biospec Products Inc., OK, USA) were added to the extraction tubes to ensure efficient mechanical lysis of cells.
Label Cy5
Label protocol Processing of RNA, labeling and hybridization were performed as in Appl.Environ.Microbiol. 76:7775-7784. Each sample was split in two after purification and the halves were labeled with cyanine3 and cyanine 5.
 
Channel 2
Source name Mixed
Organisms Lactobacillus delbrueckii subsp. bulgaricus; Saccharomyces cerevisiae
Characteristics culture type: Mixed culture
cultivation type: Chemostat
experiment: Co-fermentation experiment
Treatment protocol Sampling for transcriptome analysis from pure and mixed cultures was performed as previously described, using liquid nitrogen for rapid quenching of metabolism (J.Biol.Chem. 283:23524-23532). Samples were stored at -80°C in a mixture of phenol/chloroform and TEA buffer until further processing for total RNA extraction.
Extracted molecule total RNA
Extraction protocol L. bulgaricus total RNA from pure and mixed cultures was isolated as previously described (Appl.Environ.Microbiol. 76:7775-7784). 500 mg of 0.1 mm zirconium beads (Biospec Products Inc., OK, USA) were added to the extraction tubes to ensure efficient mechanical lysis of cells.
Label Cy3
Label protocol Processing of RNA, labeling and hybridization were performed as in Appl.Environ.Microbiol. 76:7775-7784. Each sample was split in two after purification and the halves were labeled with cyanine3 and cyanine 5.
 
 
Hybridization protocol For each array, 0.3 µg of cDNA labeled with either Cyanine 3 or Cyanine 5 was hybridized using the solutions and following the protocol delivered by Agilent (version 5.5) for 8x15K slides.
Scan protocol Slides were scanned using an Agilent microarray scanner (G2565BA). Lasers of wavelengths at 532 and 635 nm were used to excite Cyanine3 and Cyanine5 dyes, respectively. Fluorescent images were captured as multi-image-tagged image file format and analyzed with Imagene software (Axon) (BioDiscovery, Marina del Rey, USA).
Description Mono over Mixed
Mono culture L. bulgaricus RNA compared to mixed culture L. bulgaricus + S. cerevisiae RNA (chemostat cultures)
Data processing The extent of hybridization was derived from a median value of pixel-by-pixel ratios. Spots were normalized using Lowess. Differential regulation was determined by false-discovery rate (FDR) from the Cyber-T p-values by means of multiple testing connections. Differential regulation was defined as a two-fold or higher differential expression with a FDR cut-off value of 0.05 or lower. Biological replicates were pooled in the analysis.
 
Submission date Apr 01, 2013
Last update date Apr 01, 2013
Contact name Sander Sieuwerts
Organization name Arla Foods
Department Arla Scientific Innovation Centre
Lab Microbial Cultures and Enzymes
Street address rørdrumvej 2
City Brabrand
ZIP/Postal code 8220
Country Denmark
 
Platform ID GPL16855
Series (1)
GSE45623 Transcriptome-based characterization of the interactions between Saccharomyces cerevisiae and Lactobacillus delbrueckii subsp. bulgaricus in lactose-grown chemostat co-cultures

Data table header descriptions
ID_REF
VALUE Lowess normalized log2 ratio Sample type 1 (channel 1) / Sample type 2 (channel 2), corrected for False discovery rate (fdr), i.e., Mono over Mixed.
fdr Mono over Mixed

Data table
ID_REF VALUE fdr
LBUL_0001_dnaA_357-413 -0.043777181 0.76244675
LBUL_0001_dnaA_888-942 -0.043777181 0.76244675
LBUL_0001_dnaA_1269-1323 -0.043777181 0.76244675
LBUL_0001_dnaA_1132-1187 -0.043777181 0.76244675
LBUL_0001_dnaA_512-566 -0.043777181 0.76244675
LBUL_0002_414-470 0.012120062 0.890555065
LBUL_0002_118-175 0.012120062 0.890555065
LBUL_0002_778-832 0.012120062 0.890555065
LBUL_0002_296-353 0.012120062 0.890555065
LBUL_0002_542-596 0.012120062 0.890555065
LBUL_0003_173-232 -0.14429997 0.511317255
LBUL_0003_68-124 -0.14429997 0.511317255
LBUL_0004_recF_340-395 -0.0286836 0.822010178
LBUL_0004_recF_643-697 -0.0286836 0.822010178
LBUL_0004_recF_2-57 -0.0286836 0.822010178
LBUL_0004_recF_118-172 -0.0286836 0.822010178
LBUL_0004_recF_443-501 -0.0286836 0.822010178
LBUL_0005_423-482 -0.10398694 0.710084281
LBUL_0005_1694-1752 -0.10398694 0.710084281
LBUL_0005_1276-1335 -0.10398694 0.710084281

Total number of rows: 7383

Table truncated, full table size 309 Kbytes.




Supplementary file Size Download File type/resource
GSM1111960_Array_02.txt.gz 364.7 Kb (ftp)(http) TXT
GSM1111960_Array_05.txt.gz 367.3 Kb (ftp)(http) TXT
GSM1111960_Array_07.txt.gz 364.7 Kb (ftp)(http) TXT
GSM1111960_Array_10.txt.gz 372.2 Kb (ftp)(http) TXT
Processed data included within Sample table

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