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metabolite quantification via enzymatic analysis
Creators: Theresa Kouril, Jacky Snoep
Submitter: Theresa Kouril
Creators: Theresa Kouril, Jacky Snoep
Submitter: Theresa Kouril
PGK yeast without recycling of ATP
Creators: Jacky Snoep, Theresa Kouril
Submitter: Jacky Snoep
PGK yeast with recycling of ATP
Creator: Jacky Snoep
Submitter: Jacky Snoep
Creators: Trond Ellingsen, Øyvind Jakobsen, Per Bruheim, Håvard Sletta, Anders Øverby, Sven Even Borgos, Sunniva Hoel, Alexander Wentzel
Submitter: Jay Moore
Creators: David Rand, R Jansen, Maria Elena Merlo, Morris Swertz, Preben Krabben, Kay Nieselt, Wolfgang Wohlleben, Jens Reuther, David Hodgson, Anthony Palathingal, David Wild, Elizabeth Wellington, Gregory Challis, Nigel Burroughs, Walid Omara, William Gaze, Brent Kiernan, Roxane Legaie, Sunniva Hoel, Juan-Francisco Martin, Antonio Rodríguez-García, Trond Ellingsen, Øyvind Jakobsen, Per Bruheim, Håvard Sletta, Anders Øverby, Sven Even Borgos, Jay Moore, Alexander Wentzel, Maggie Smith, Louise Thomas, Eriko Takano, Lubbert Dijkhuizen, Rainer Breitling, M. Tauqeer Alam
Submitter: Jay Moore
Creator: Jan-Willem Veening
Submitter: Jan-Willem Veening
Creator: Jan-Willem Veening
Submitter: Jan-Willem Veening
Creator: Jan-Willem Veening
Submitter: Jan-Willem Veening
Strain MK423 was grown under the same conditions as used when growing cells for microscopy analysis; cells of OD600 = 0.4 were diluted 100-fold in C+Y medium with 0.1 mM ZnCl2 and incubated for 2.5 hours until OD600 = 0.15. Cells were then harvested by centrifugation for 5 min at 6500 x g at 4°C. Genomic DNA was isolated using the Wizard® Genomic DNA Purification Kit (Promega) as described previously (Slager et al. 2014 Cell). Fragmentation was performed using Covaris instrument, and libraries ...
Creator: Jan-Willem Veening
Submitter: Jan-Willem Veening
Strain MK422 was grown under the same conditions as used when growing cells for microscopy analysis; cells of OD600 = 0.4 were diluted 100-fold in C+Y medium with 0.1 mM ZnCl2 and incubated for 2.5 hours until OD600 = 0.15. Cells were then harvested by centrifugation for 5 min at 6500 x g at 4°C. Genomic DNA was isolated using the Wizard® Genomic DNA Purification Kit (Promega) as described previously (Slager et al. 2014 Cell). Fragmentation was performed using Covaris instrument, and libraries ...
Creator: Jan-Willem Veening
Submitter: Jan-Willem Veening
Strain MK350 was grown under the same conditions as used when growing cells for microscopy analysis; cells of OD600 = 0.4 were diluted 100-fold in C+Y medium with 0.1 mM ZnCl2 and incubated for 2.5 hours until OD600 = 0.15. Cells were then harvested by centrifugation for 5 min at 6500 x g at 4°C. Genomic DNA was isolated using the Wizard® Genomic DNA Purification Kit (Promega) as described previously (Slager et al. 2014 Cell). Fragmentation was performed using Covaris instrument, and libraries ...
Creator: Jan-Willem Veening
Submitter: Jan-Willem Veening
L. lactis was grown in rich THY medium, strongly concentrated and glucose-pulsed in a MES buffer. Intracellular metabolite concentration is followed in time.
Creator: Martijn Bekker
Submitter: Martijn Bekker
Lactobacillus plantarum JDM1 differentially expressed proteins, comparison between low and high growth rates
Creator: Anette McLeod
Submitter: Anette McLeod
Lactobacillus plantarum ATCC 14917 differentially expressed proteins, comparison between low and high growth rates
Creator: Anette McLeod
Submitter: Anette McLeod
Lactobacillus plantarum strains WCFS1, NC8, JDM1 and ATCC 14917 amino acid concentrations mM supernatant, high (D=0.4) and low (D=0.05) growth rates
Creator: Anette McLeod
Submitter: Anette McLeod
Heterologous Expression of LDH from L.actis (MG1363) in E. coli DH5α. Assessment of kinetic parameters of LDH to include in a catabolic model
Creator: Wayne Aubrey
Submitter: Wayne Aubrey
Lactobacillus plantarum, 4 strains (WCFS1, NC8, ATCC 14917, JDM1) chemostat experiments low and high growth rates, OD and DW measurements
Creator: Anette McLeod
Submitter: Anette McLeod
Lactobacillus plantarum strains WCFS1, NC8, ATCC14917, JDM1. HPLC end products mM measurements (CDM subtracted) and flux calculations, high and low growth rates.
Creator: Anette McLeod
Submitter: Anette McLeod
Creator: Margrete Solheim
Submitter: Margrete Solheim
amino acid auxotrophies as determined for S. pyogenes, E. faecalis, L. lactis and L. plantarum (ATCC, NC8, JDM1 and WCFS1) subsequent inoculation (3x) in CDM
Creator: Koen van Grinsven
Submitter: Koen van Grinsven
Vmaxes E. faecalis from chemostat cultures, D0.05, D0.15 en D0.4 triplicates for every growthrate, measured in in-vivo-like assay (Goel, Teusink, AEM, 2012) glycolytic enzymes + LDH + acetate/EtOH branch
Creator: Koen van Grinsven
Submitter: Koen van Grinsven
raw data OD600 of amino acid auxotrophy exps S. pyogenes
Creator: Koen van Grinsven
Submitter: Koen van Grinsven
raw data OD600
Creator: Koen van Grinsven
Submitter: Koen van Grinsven
Lactobacillus plantarum WCFS1 differentially expressed proteins, comparison between low and high growth rates
Creator: Anette McLeod
Submitter: Anette McLeod
Lactobacillus plantarum NC8 differentially expressed proteins, comparison between low and high growth rates
Creator: Anette McLeod
Submitter: Anette McLeod
Creator: Margrete Solheim
Submitter: Margrete Solheim
Creator: Margrete Solheim
Submitter: Margrete Solheim
Creator: Margrete Solheim
Submitter: Margrete Solheim
Creator: Margrete Solheim
Submitter: Margrete Solheim