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S. pneumoniae HPUra 1 DNA PE2
Creator: Jan-Willem Veening
Submitter: Jan-Willem Veening
S. pneumoniae HPUra 1 DNA PE1
Creator: Jan-Willem Veening
Submitter: Jan-Willem Veening
S. pneumoniae Control 2 DNA PE2
Creator: Jan-Willem Veening
Submitter: Jan-Willem Veening
S. pneumoniae Control 2 DNA PE1
Creator: Jan-Willem Veening
Submitter: Jan-Willem Veening
S. pneumoniae Control 1 DNA PE2
Creator: Jan-Willem Veening
Submitter: Jan-Willem Veening
S. pneumoniae Control1 DNA-Seq PE1
Creator: Jan-Willem Veening
Submitter: Jan-Willem Veening
Please fill in thistravel expense reimbursement report and send it together with original receipts to HITS
Creator: Olga Krebs
Submitter: Olga Krebs
Meeting location map
Creator: Olga Krebs
Submitter: Olga Krebs
Monitoring of partial pressure of CO2 in off-gas. Glucose pulse was performed in anaerobically growing yeast Saccharomyces cerevisiae in steady state chemostat (D = 0.1 h-1) and transent concentrations of the extra- and intracellular metabolites from central carbon metabolism (e.g. glycolysis, PPP, glycerol, purines, etc) were measured.
Creator: Maksim Zakhartsev
Submitter: Maksim Zakhartsev
Dynamics of intracellular metabolites (pyr, suc, fum, mal, akg, pep, g3p, 2pg, 3pg, cit, r5p, f6p, g6p, 6pg, ATP, ADP, AMP, UTP, GTP, inosine, NAD+, IMP, UDP, NADP+, CTP, AdenyloSuccinate, NADPH, trehalose) during glucose pulse. Glucose pulse was performed in anaerobically growing yeast Saccharomyces cerevisiae in steady state chemostat (D = 0.1 h-1) and transent concentrations of the extra- and intracellular metabolites from central carbon metabolism (e.g. glycolysis, PPP, glycerol, purines, ...
Creator: Maksim Zakhartsev
Submitter: Maksim Zakhartsev
Dynamics of extracellular metabolites (glc, pyr, suc, lac, gly, ac, etoh, fum, mal, cit, including loss of akg, g3p, 2pg, 3pg, r5p, f6p, g6p, 6pg) during glucose pulse. Glucose pulse was performed in anaerobically growing yeast Saccharomyces cerevisiae in steady state chemostat (D = 0.1 h-1) and transent concentrations of the extra- and intracellular metabolites from central carbon metabolism (e.g. glycolysis, PPP, glycerol, purines, etc) were measured.
Creator: Maksim Zakhartsev
Submitter: Maksim Zakhartsev
Kinetic characterisation of FBPAase. Expermental data for enzyme reaction rates with increasing concentrations of DHAP and GAP.
Creators: Jacky Snoep, Theresa Kouril
Submitter: Jacky Snoep
Kinetic characterisation of TPI. Experimental data for enzyme reaction rates with increasing concentrations of DHAP and GAP, and inhibition with 3PG and PEP.
Creators: Jacky Snoep, Theresa Kouril
Submitter: Jacky Snoep
Kinetic characterisation of GAPDH. Expermental data for enzyme reaction rates with increasing concentrations of BPG, NADPH, NADP, GAP and Pi.
Creators: Jacky Snoep, Theresa Kouril
Submitter: Jacky Snoep
Experimental data for determination of half-life of gluconeogenic intermediates (BPG, GAP and DHAP).
Creators: Jacky Snoep, Theresa Kouril
Submitter: Jacky Snoep
Kinetic characterisation of PGK. Expermental data for enzyme reaction rates with increasing concentrations of ATP, ADP, BPG and 3PG.
Creators: Jacky Snoep, Theresa Kouril
Submitter: Jacky Snoep
Creator: Thomas Rimpf
Submitter: Thomas Rimpf
Creators: Franco du Preez, Jacky Snoep
Submitter: Franco du Preez
Creators: Franco du Preez, Jacky Snoep
Submitter: Franco du Preez
Creators: Franco du Preez, Jacky Snoep
Submitter: Franco du Preez
This document shows the ArcA phosphorylation levels at different aerobiosis units, measured using Phos-tag gels, western immunoblotting. Exposed films were quantitated using ImageJ and the results shown here.
Creator: Matthew Rolfe
Submitter: Matthew Rolfe
Creators: Alexander Ter Beek, Klaas Hellingwerf
Submitter: The JERM Harvester
The data that was published in Alexeeva et al. [1-3] and Alexeeva [4] is an important prerequisite for SUMO. It is used for the development of the models and for the comparison with the SUMO data. By means of the program EasyNPlot [5] the data in the important plots of [1-3] and of the plot of the ArcA activity in [4] was digitalized. The result can be found in the attached files.
[1] Svetlana Alexeeva, Bart de Kort, Gary Sawers, Klaas J. Hellingwerf, and M. Joost Teixeira de Mattos. Effects of ...
Creator: Michael Ederer
Submitter: The JERM Harvester
Measurement of by-product formation rates, substrate consumption rates and extracellular concentrations of cAMP under aerobic batch conditions with glucose as substrate.
Creator: Sonja Steinsiek
Submitter: Sonja Steinsiek
Transcription of glucose uptake transport systems in a mutant background under anaerobic batch conditions.
Creator: Sonja Steinsiek
Submitter: Sonja Steinsiek
Transcription of glucose uptake transport systems in a mutant background under aerobic batch conditions.
Creator: Sonja Steinsiek
Submitter: Sonja Steinsiek
Measurement of by-product formation rates, substrate consumption rates and extracellular concentrations of cAMP under anaerobic batch conditions with glucose as substrate.
Creator: Sonja Steinsiek
Submitter: Sonja Steinsiek
Transcriptional profiles of steady-state chemostat cultures were measured at a range of oxygen levels using microarrays. Oxygen levels were defined by the aerobiosis scale of Alexeeva et al. (2002).
Creator: Matthew Rolfe
Submitter: Matthew Rolfe
Untargeted and targeted metabolic analysis on T. b. brucei 427 grown under oxidative stress with methylene blue has been carried out. This work has been completed with 11 bio-reps and found significant metabolic changes as you can see in the IDEOM file attached. 'Comparison' tab in the data spread sheet shows heat maps and fold change analysis regarding different metabolite levels (T: T brucei, TMB: T. brucei exposed to methylene blue, numbers: time points, 0, 5, 60 & 120min). If you double ...
Creator: Dong-Hyun Kim
Submitter: Dong-Hyun Kim
Metabolic changes of 26 intracellular metabolites extracted from T. b. brucei 427 wild type and arginine kinase knockout cells under high pH stress (pH8.7)
Creator: Dong-Hyun Kim
Submitter: Dong-Hyun Kim