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E. faecalis transcriptional responses to copper stress

ABSTRACT: Transcriptional profiling of Enterococcus faecalis V583 comparing the transcriptome of cells grown in M17 + glucose 0.5% (GM17) with the transcriptome of cells grown in M17 + glucose 0.5% + 0.05 mM CuSO4

ORGANISM(S): Enterococcus faecalis Enterococcus faecalis V583

PROVIDER: GSE30949 | GEO | 2011/08/22

SECONDARY ACCESSION(S): PRJNA146259

REPOSITORIES: GEO

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E. faecalis transcriptional responses to copper stress

Project description:Transcriptional profiling of Enterococcus faecalis V583 comparing the transcriptome of cells grown in M17 + glucose 0.5% (GM17) with the transcriptome of cells grown in M17 + glucose 0.5% + 0.05 mM CuSO4 2 condition experiment: V583 grown in GM17 vs. V583 grown in GM17 + 0.05mM CuSO4. Three biological replicates, one of which is a dye-swap. Three replicates per array.

2011-08-21 | E-GEOD-30949 | biostudies-arrayexpress

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Project description:Transcriptional profiling of Enterococcus faecalis V583 comparing the transcriptome of cells grown in M17 + glucose 0.5% (GM17) with the transcriptome of cells grown in M17 + glucose 0.5% + 4 mM ZnSO4 2 condition experiment: V583 grown in GM17 vs. V583 grown in GM17 + 4mM ZnSO4. Two biological replicates and a dye-swap. Three replicates per array.

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Project description:The aim was to study the transcriptional profiling of the tdc cluster delection mutant E. faecalis V583 Î?tdc (non-tyramine producer) compared to the wild type strain E. faecalis V583 (tyramine producer). We compared the expression profile of the strains grown in M17 medium with glucose as carbon source and suplemented with tyrosine. E. faecalis V583 Î?tdc cells (test) compared with E. faecalis V583 cells (reference). Both strains grown in GM17 medium suplemented 15 mM tyrosine.

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Project description:The aim was to study the transcriptional profiling of the tdc and agdi clusters delection mutant E. faecalis V583 ΔtdcΔagdi (non-tyramine non-putrescine producer) compared to the wild type strain E. faecalis V583 (tyramine producer). We compared the expression profile of the strains grown in M17 medium with glucose as carbon source and suplemented with tyrosine.

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