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Strain details
Name | Provider name | Provider's strain ID | Genotypes | Phenotypes | Synonym | Comments | Based on |
---|---|---|---|---|---|---|---|
D39 | Not specified | Not specified | wild-type | wild-type | Not specified | None | Not specified |
Related items
SysMO is a European transnational funding and research initiative on "Systems Biology of Microorganisms".
The goal pursued by SysMO was to record and describe the dynamic molecular processes going on in unicellular microorganisms in a comprehensive way and to present these processes in the form of computerized mathematical models.
Systems biology will raise biomedical and biotechnological research to a new quality level and contribute markedly to progress in understanding. Pooling European research ...
Projects: BaCell-SysMO, COSMIC, SUMO, KOSMOBAC, SysMO-LAB, PSYSMO, SCaRAB, MOSES, TRANSLUCENT, STREAM, SulfoSys, SysMO DB, SysMO Funders, SilicoTryp, Noisy-Strep
Web page: http://sysmo.net/
Bistable switches are the key elements of the regulatory networks governing cell development, differentiation and life-strategy decisions. Transcriptional noise is a main determinant that causes switching between different states in bistable systems. By using the human pathogen Streptococcus pneumoniae as a model bacterium, we will investigate how transcriptional fidelity and processivity influence (noisy) gene expression and participate in bistability. To study this question, we will use both ...
Programme: SysMO
Public web page: http://www.sysmo.net/index.php?index=163
Organisms: Streptococcus pneumoniae
Cells were grown to mid-exponential phase (OD600nm ~0.2) in GM17 medium at 37°C (with 0.15 mM ZnSO4 where relevant) and 84 ml of culture was mixed by inverting with 8.4 ml of fixing solution (50 mM Tris pH 8.0, 100 mM NaCl, 0.5 mM EGTA, 1 mM EDTA, 30% (v/v) formaldehyde) and incubated at room temperature for 30 min. Cells were disrupted and crosslinked DNA was sheared by sonication. Antibodies coupled to magnetic beads were used to pull down cross-linked complexes. DNA was purified, amplified, ...
Submitter: Jan-Willem Veening
Assay type: Transcriptomics
Technology type: ChIP-on-chip
Investigation: Wetlab approach to transcription fidelity
Organisms: Streptococcus pneumoniae : D39 (wild-type / wild-type)
SOPs: No SOPs
Data files: ChIP-chip ParB-GFP
Snapshots: No snapshots
- Preparation of B. subtilis cultures
Inoculate cells from -80°C stocks in 10 ml time-lapse microscopy (TLM) medium (62 mM K2HPO4 , 44mM KH2PO4, 15 mM (NH4)2SO4, 6.5 mM sodium citrate, 0.8 mM MgSO4, 0.02 % casamino acids, 27.8 mM glucose, 0.1 mM L-tryptophan, the pH was set to 7 using a KOH solution) supplemented with antibiotics, if necessary. Grow the cells overnight in a shake flask (30°C, 225 rpm). The following morning, dilute the cells 1:10 in pre-warmed chemically defined medium (CDM) (62 ...
Submitter: Jan-Willem Veening
Assay type: Experimental Assay Type
Technology type: Imaging
Investigation: Wetlab approach to transcription fidelity
Submitter: Jan-Willem Veening
Provider Name: Not specified
Provider's strain ID: Not specified
Organism: Streptococcus pneumoniae
Genotypes: wild-type
Phenotypes: wild-type
Comment: Not specified
Abstract (Expand)
Editor:
Date Published: 4th Oct 2012
Publication Type: Not specified
PubMed ID: 23033921
Citation:
Abstract (Expand)
Authors: Katrin Beilharz, Linda Nováková, Daniela Fadda, Pavel Branny, Orietta Massidda,
Date Published: 21st Mar 2012
Publication Type: Not specified
PubMed ID: 22431591
Citation:
Abstract (Expand)
Date Published: 16th Aug 2011
Publication Type: Not specified
PubMed ID: 21841760
Citation:
Abstract (Expand)
Authors: Anita Minnen, Laetitia Attaiech, Maria Thon, Stephan Gruber,
Date Published: 22nd Jun 2011
Publication Type: Not specified
PubMed ID: 21651626
Citation: