38 results on '"Teleki, Attila"'
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2. Systemic intracellular analysis for balancing complex biosynthesis in a transcriptionally deregulated Escherichia colil‐Methionine producer
3. Characterization of Agrobacterium tumefaciens PPKs reveals the formation of oligophosphorylated products up to nucleoside nona-phosphates
4. A universal polyphosphate kinase: PPK2c of Ralstonia eutropha accepts purine and pyrimidine nucleotides including uridine diphosphate
5. From nutritional wealth to autophagy: In vivo metabolic dynamics in the cytosol, mitochondrion and shuttles of IgG producing CHO cells
6. Quantitative Profiling of Endogenous Metabolites Using Hydrophilic Interaction Liquid Chromatography–Tandem Mass Spectrometry (HILIC-MS/MS)
7. A Two-Compartment Fermentation System to Quantify Strain-Specific Interactions in Microbial Co-Cultures
8. Polyphosphate Kinases Phosphorylate Thiamine Phosphates
9. Electron availability in CO2, CO and H2 mixtures constrains flux distribution, energy management and product formation in Clostridium ljungdahlii
10. Monitoring Intracellular Metabolite Dynamics in Saccharomyces cerevisiae during Industrially Relevant Famine Stimuli
11. Polyphosphate Kinases Phosphorylate Thiamine Phosphates.
12. Comparison of l‐tyrosine containing dipeptides reveals maximum ATP availability for l‐prolyl‐l‐tyrosine in CHO cells
13. Compartment‐specific 13 C metabolic flux analysis reveals boosted NADPH availability coinciding with increased cell‐specific productivity for IgG1 producing CHO cells after MTA treatment
14. Compartment-specific metabolome labeling enables the identification of subcellular fluxes that may serve as promising metabolic engineering targets in CHO cells
15. Identifying and Engineering Bottlenecks of Autotrophic Isobutanol Formation in Recombinant
16. Micro‐aerobic production of isobutanol with engineered Pseudomonas putida
17. Micro‐aerobic production of isobutanol with engineered Pseudomonas putida
18. Identifying and Engineering Bottlenecks of Autotrophic Isobutanol Formation in Recombinant C. ljungdahlii by Systemic Analysis
19. Revisiting the Growth Modulon of Corynebacterium glutamicum Under Glucose Limited Chemostat Conditions
20. Streamlining the Analysis of Dynamic 13C-Labeling Patterns for the Metabolic Engineering of Corynebacterium glutamicum as l-Histidine Production Host
21. Revisiting the Growth Modulon of Corynebacterium glutamicum Under Glucose Limited Chemostat Conditions
22. S ‐adenosylmethionine and methylthioadenosine boost cellular productivities of antibody forming Chinese hamster ovary cells
23. Electron availability in CO 2 , CO and H 2 mixtures constrains flux distribution, energy management and product formation in Clostridium ljungdahlii
24. Comparison ofl‐tyrosine containing dipeptides reveals maximum ATP availability forl‐prolyl‐l‐tyrosine in CHO cells
25. Compartment‐specific 13C metabolic flux analysis reveals boosted NADPH availability coinciding with increased cell‐specific productivity for IgG1 producing CHO cells after MTA treatment.
26. HILIC-Enabled 13C Metabolomics Strategies: Comparing Quantitative Precision and Spectral Accuracy of QTOF High- and QQQ Low-Resolution Mass Spectrometry
27. In vivo quantification of mitochondrial shuttle activities via 13C flux analysis in mAB producing CHO cells
28. The Less the Better: How Suppressed Base Addition Boosts Production of Monoclonal Antibodies With Chinese Hamster Ovary Cells
29. Perfusion cultures require optimum respiratory ATP supply to maximize cell‐specific and volumetric productivities
30. Electron availability in CO2, CO and H2 mixtures constrains flux distribution, energy management and product formation in Clostridium ljungdahlii.
31. Robust Identification of Metabolic Engineering Targets via Pool Efflux Capacities (PECs)
32. LC–MS-based compartment-specific metabolome analysis in CHO
33. Hyperosmotic stimulus study discloses benefits in ATP supply and reveals miRNA/mRNA targets to improve recombinant protein production of CHO cells
34. Compartment-specific metabolomics for CHO reveals that ATP pools in mitochondria are much lower than in cytosol
35. Alkaline conditions in hydrophilic interaction liquid chromatography for intracellular metabolite quantification using tandem mass spectrometry
36. Streamlining the Analysis of Dynamic 13 C-Labeling Patterns for the Metabolic Engineering of Corynebacterium glutamicum as l-Histidine Production Host.
37. Systemic intracellular analysis for balancing complex biosynthesis in a transcriptionally deregulated Escherichia coli l-Methionine producer.
38. Quantitative Profiling of Endogenous Metabolites Using Hydrophilic Interaction Liquid Chromatography-Tandem Mass Spectrometry (HILIC-MS/MS).
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