Detailed Information on Publication Record
2012
Development of capillary electrophoretic method for nucleotide and coenzyme analysis in bacterial and stem cells
MUSILOVÁ, Jindra and Zdeněk GLATZBasic information
Original name
Development of capillary electrophoretic method for nucleotide and coenzyme analysis in bacterial and stem cells
Name in Czech
Vývoj kapilárně elektroforetické metody pro stanovení nukleotidů a koenzymů v bakteriálních a kmenových buňkách
Authors
Edition
CHEMICA 50S, p. 97-98, 2 pp. 2012
Publisher
Faculty of Science, Palacký University Olomouc
Other information
Language
English
Type of outcome
Stať ve sborníku
Field of Study
10600 1.6 Biological sciences
Country of publisher
Czech Republic
Confidentiality degree
není předmětem státního či obchodního tajemství
Organization unit
Faculty of Science
ISBN
978-80-244-3115-4
ISSN
Keywords (in Czech)
kapilární elektroforéza, nukleotidy, koenzymy
Keywords in English
capillary electrophoresis, nucleotides, coenzymes
Změněno: 21/1/2014 15:04, prof. RNDr. Zdeněk Glatz, CSc.
V originále
Metabolite profiling is one of the major approaches for metabolomics studies. It involves the identification and quantitation of a group of metabolites common to a specific pathway or chemical class. Nucleotides and coenzymes represent central energetic metabolites in the complex metabolic network. As a consequence, the quantitative determination of such important compounds is fundamental in many areas of biochemical research. The concentrations of the nucleotides and coenzymes in living cells are in the micromolar concentration range therefore highly sensitive separation techniques are required for their determination. A combination of capillary zone electrophoresis (CZE) with probably the most extensively used on-line preconcentration technique – field enhanced sample stacking – allows their analysis in different cell types. Appropriate conditions for selective separation of 17 energetically important metabolites (purine, pyrimidine nucleotides, adenine coenzymes and Acetyl CoA) were found. The most dominant parameter for the analysis was pH of the background electrolyte. The optimized methodology was applied on the cell-extract of bacterium Paracoccus denitrificans and stem cell extract. The described method is suitable for determination of large group of energetically important metabolites and its utilisation depends on character of real cell samples.
In Czech
Byly nalezeny vhodné podmínky pro separaci purinových a pyrimidinových nukleotidů, adeninových koenzymů a acetylCoA na kapilární elektroforéze. Pro zvýšení koncentrační citlivosti byla CE kombinována s on-line prekoncentrací - field enhanced stacking.Optimalizovaná metoda byla aplikována na bezbuněčné extrakty bakterie P. denitrificans a extrakty kmenových buněk.
Links
CZ.1.07/2.3.00/20.0182, interní kód MU (CEP code: EE2.3.20.0182) |
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GAP206/11/0009, research and development project |
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