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Sample GSM1281605 Query DataSets for GSM1281605
Status Public on Dec 07, 2013
Title KT2440(pCAR1Dphu)
Sample type RNA
 
Source name cDNA prepared from succinate culture of KT2440(pCAR1Dphu)
Organism Pseudomonas putida
Characteristics strain: KT2440
Growth protocol Each strain was grown in 5 ml of LB at 300 strokes/min for 14-14.5 h (pre-culture) and then washed and transferred into 100-ml of NMM-4 buffer (Miyakoshi et al. Transcriptome analysis of Pseudomonas putida KT2440 harboring the completely sequenced IncP-7 plasmid pCAR1. J Bacteriol 2007 Oct;189(19):6849-60. PMID: 17675379) supplemented with 0.1% succinate adjusting its turbidity (600 nm) at 0.05. The resultant culture was incubated on a rotary shaker at 120 rpm and cell growth was monitored in by measuring its turbidity (600 nm).
Extracted molecule total RNA
Extraction protocol Cells were treated with RNA Protect Bacteria reagent (Qiagen, CA, USA) to stabilize RNA of them.Total RNA was extracted using NucleoSpin RNA II (Macherey-Nagel GmbH & Co. KG, Düren, Germany). The eluted RNA was treated with RQ1 RNase-free DNase (Promega, Madison, WI) at 37˚C for 30 min. After inactivation of DNase by the addition of the provided stop reagent and subsequent incubation at 65˚C for 10 min, total RNA was repurified using NucleoSpin RNA Clean-up (Macherey-Nagel).
Label biotin
Label protocol Single-strand cDNA was synthesized in 60 µl of 1× First Strand Buffer (Invitrogen, Carlsbad, CA) containing 12 µg of total RNA, 360ng of actinomycin D (A1410, SIGMA, St.Louis, USA), 750 ng of random primers (Invitrogen), 1500 units of SuperScript II (Invitrogen), 60 units of RNaseOUT (Invitrogen), 10 mM DTT (Invitrogen), 0.5 mM dATP, 0.5 mM dCTP, 0.5 mM dGTP, 0.4 mM dTTP, and 0.1 mM dUTP (Roche Applied Science, Mannheim, Germany). After the RNA and random primers were denatured at 70˚C for 10 min and annealed at 25˚C for 10 min, the remaining reagents were added, and the reaction mixture was then incubated at 25˚C for 10 min, 37˚C for 60 min, 42˚C for 60 min, and 70˚C for 10 min. After cDNA synthesis, template RNA was degraded with one-third volume of 1N NaOH at 65˚C for 30 min; one-third volume of 1N HCl was added to neutralize the reaction mixture before cleanup. The cDNA was purified using a QIAquick PCR Purification Kit (Qiagen). The cDNA was fragmented and labeled using GeneChip WT Double-Stranded DNA Terminal Labeling Kit (Affymetrix). The purified single-stranded cDNA (~3.3 µg) was fragmented in 48 µl of 1× cDNA Fragmentation Buffer containing 15 units of Uracil DNA Glycosylase (UDG) and 225 units of Apurinic/apyrimidinic Endonuclease 1 (APE1) at 37˚C for 60 min, and incubated at 93˚C for 2 min. The fragmented cDNA was labeled in 60 µl of 1× TdT Buffer containing 60 units of Terminal Deoxynucleotidyl Transferase (TdT) and 0.083 mM GeneChip DNA Labeling Reagent at 37˚C for 60 min, and incubated at 70˚C for 2 min.
 
Hybridization protocol Labeled cDNA was mixed with 50 pM control oligonucleotide B2 (Affymetrix), 1× Hybridization Mix (Affymetrix), and 7% DMSO in a total volume of 200 µl and denatured at 95˚C for 5 min. Per array, 200 µl of the hybridization cocktail was hybridized at 50˚C for 16 h with a rotation rate of 60 rpm using a GeneChip Hybridization Oven 640 (Affymetrix). Chips were washed and stained using a Hybridization, Wash, and Stain Kit (Affymetrix) according to the the modified FleX450-0005 protocol (for chromosomal tiling array, changed temperature of ‘the Post Hyb Wash #2” to 50˚C) of GeneChip Fluidics station 450 (Affymetrix).
Scan protocol Arrays were scanned on an Affymetrix Scanner 3000 7G
Description This is an Affymetrix custom-commercial tiling array that covers the IncP-7 carbazole-degradative plasmid pCAR1 (RefSeq: NC_004444.1) at 9-bp density. BPMAP files are provided as supplementary files. pCAR1_8b520435FR-3.bpmap represents the forward strand of pCAR1, and pCAR1_8b520435FF-3.bpmap represents the reverse strand of pCAR1.
Data processing The CEL files were generated using Affymetrix GCOS. Data was quantile normalized and analyzed with Affymetrix Tiling Analysis Software v1.1, which uses non-parametric quantile normalization and a Hodges-Lehmann estimator for fold enrichment.The intensities were linearly scaled so that the median was 100. Bandwidth: 30, Threshold: 0, MaxGap: 30, MinRun, 30.
 
Submission date Dec 06, 2013
Last update date Dec 07, 2013
Contact name Hideaki Nojiri
E-mail(s) anojiri@mail.ecc.u-tokyo.ac.jp
Phone +81-3-5841-3067
Organization name The University of Tokyo
Department Biotechnology Research Center
Lab Laboratory of Environmental Biochemistry
Street address 1-1-1 Yayoi, Bunkyo-ku
City Tokyo
ZIP/Postal code 113-8657
Country Japan
 
Platform ID GPL6591
Series (2)
GSE53068 Cooperative function of the three different kinds of nucleoid-associated proteins encoded on the IncP-7 plasmid pCAR1 [pCAR1 plasmid chip]
GSE53069 Cooperative function of the three different kinds of nucleoid-associated proteins encoded on the IncP-7 plasmid pCAR1

Supplementary file Size Download File type/resource
GSM1281605_090203_KT2440_pCAR1d95a_2_SUC.CEL.gz 441.2 Kb (ftp)(http) CEL
GSM1281605_090203_KT2440_pCAR1d95a_3_SUC.CEL.gz 452.2 Kb (ftp)(http) CEL
GSM1281605_KTPCd95a_takeda_pCAR1_2F_signal.bar.gz 119.4 Kb (ftp)(http) BAR
GSM1281605_KTPCd95a_takeda_pCAR1_2F_signal.bar.txt.gz 133.3 Kb (ftp)(http) TXT
GSM1281605_KTPCd95a_takeda_pCAR1_2R_signal.bar.gz 111.3 Kb (ftp)(http) BAR
GSM1281605_KTPCd95a_takeda_pCAR1_2R_signal.bar.txt.gz 125.4 Kb (ftp)(http) TXT
GSM1281605_KTPCd95a_takeda_pCAR1_3F_signal.bar.gz 121.2 Kb (ftp)(http) BAR
GSM1281605_KTPCd95a_takeda_pCAR1_3F_signal.bar.txt.gz 135.2 Kb (ftp)(http) TXT
GSM1281605_KTPCd95a_takeda_pCAR1_3R_signal.bar.gz 112.4 Kb (ftp)(http) BAR
GSM1281605_KTPCd95a_takeda_pCAR1_3R_signal.bar.txt.gz 126.8 Kb (ftp)(http) TXT
Processed data provided as supplementary file

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