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Staphylococcus aureus subsp. aureus NCTC 8325

ABSTRACT: Effect of TetR family regulator SAOUHSC_02897 deletion in S. aureus NCTC8325

PROVIDER: PRJNA231982 | ENA |

REPOSITORIES: ENA

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Staphylococcus aureus subsp. aureus NCTC 8325

Project description:Effect of SAOUHSC_02810 deletion in S. aureus NCTC8325

| PRJNA242840 | ENA

Staphylococcus aureus subsp. aureus NCTC 8325

Project description:Effect of different Two-component systems system deletion in S. aureus NCTC8325

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Effect of TetR family regulator SAOUHSC_02897 deletion in S. aureus NCTC8325

Project description:To analyze function of TetR family regulator SAOUHSC_02897, we have employed whole genome microarray expression profiling to identify genes transcription changed in respective mutant strains. Target SAOUHSC_02897 was replaced by ermB gene. Bacteria grown in the wells of biofilm formation at 12 hours, and the RNA level of wild type NCTC8325 and SAOUHSC-02897 mutant were compared.

2013-12-18 | E-GEOD-53432 | biostudies-arrayexpress

Predictive characterization of hypothetical proteins in Staphylococcus aureus NCTC 8325.

Project description: Not available

| S-EPMC5267966 | biostudies-literature

Staphylococcus aureus subsp. aureus NCTC 8325

Project description:Staphylococcus aureus subsp. aureus NCTC 8325 Raw sequence reads

| PRJNA279231 | ENA

Effect of TetR family regulator SAOUHSC_02897 deletion in S. aureus NCTC8325

2013-12-18 | GSE53432 | GEO

Analysis of differential gene expression in the Streptococcus sanguinis brpT mutant

Project description:Gene expression profile of the Streptococcus sanguinis TetR family transcriptional regulator, brpT, deletion mutant compared to the wild-type strain SK36

2017-03-08 | GSE89964 | GEO

RNA-seq reveals differential gene expression in Staphylococcus aureus at single-nucleotide resolution

Project description:Staphylococcus aureus is a gram-positive cocci and an important human commensal bacteria and pathogen. S. aureus infections are increasingly difficult to treat because of the emergence of highly resistant MRSA (Methicillin-resistant S. aureus) strains. Here we present a method to study differential gene expression in S. aureus using high-throughput RNA-sequencing (RNA-seq). We use RNA-seq to examine the differential gene expression in S. aureus RN4220 cells containing an exogenously expressed transcription factor and between two S. aureus strains (RN4220 and NCTC8325-4). The information provided by RNA-seq was a significant advance over previously described microarray based techniques. We investigated the sequence and gene expression differences between RN4220 and NCTC8325-4 and used the RNA-seq data to identify S. aureus promoters suitable for in vitro analysis. We used RNA-seq to describe, on a genome wide scale, genes positively and negatively regulated by a phage encoded transcription factor, gp67. RNA-seq offers the ability to study differential gene expression with single-nucleotide resolution, and is a considerable improvement over the predominant genome-wide transcriptome technologies used in S. aureus.

2013-11-07 | GSE48896 | GEO

RNA-seq reveals differential gene expression in Staphylococcus aureus at single-nucleotide resolution

2013-11-07 | E-GEOD-48896 | biostudies-arrayexpress