National Repository of Grey Literature 17 records found  1 - 10next  jump to record: Search took 0.00 seconds. 
Development of a novel method for nucleotide pool analysis in bacterial cells
Zborníková, Eva ; Rejman, Dominik (advisor) ; Pacáková, Věra (referee) ; Kozlík, Petr (referee)
(EN) This thesis deals with the determination of nucleotides in bacterial cells. Nucleotides play crucial role in most of the metabolic pathway. Determining their concentrations could give us important clues about the influence of internal and external conditions on the bacterial metabolism. Previously published papers dealing with the analysis of nucleotides and other intracellular metabolites can be divided into two groups according to the analytical approach: a) metabolomic approach and b) targeted approach dealing with narrow group of target analytes. In the case a) most authors use the state-of-the-art LC-MS/MS technique, whereas in the case b) robust UV detection coupled mainly to IP-LC is widely used. The aim of this study was to combine both approaches to obtain a method for routine analysis that would take advantages of mass detection, such as sensitivity and selectivity, while avoiding the need of demanding optimization of MS/MS transitions and expert service. The main purpose of the newly developed HILIC-MS method is its universal applicability in most biological and biochemical laboratories.
Development of a novel method for nucleotide pool analysis in bacterial cells
Zborníková, Eva ; Rejman, Dominik (advisor) ; Pacáková, Věra (referee) ; Kozlík, Petr (referee)
(EN) This thesis deals with the determination of nucleotides in bacterial cells. Nucleotides play crucial role in most of the metabolic pathway. Determining their concentrations could give us important clues about the influence of internal and external conditions on the bacterial metabolism. Previously published papers dealing with the analysis of nucleotides and other intracellular metabolites can be divided into two groups according to the analytical approach: a) metabolomic approach and b) targeted approach dealing with narrow group of target analytes. In the case a) most authors use the state-of-the-art LC-MS/MS technique, whereas in the case b) robust UV detection coupled mainly to IP-LC is widely used. The aim of this study was to combine both approaches to obtain a method for routine analysis that would take advantages of mass detection, such as sensitivity and selectivity, while avoiding the need of demanding optimization of MS/MS transitions and expert service. The main purpose of the newly developed HILIC-MS method is its universal applicability in most biological and biochemical laboratories.
Conformation analysis of nucleoside analogues containing selenium and tellurium in five-membered pseudosugar ring
Poštová Slavětínská, Lenka ; Pohl, Radek ; Rejman, Dominik
The conformation analysis of synthetized thymine and adenosine nucleoside analogues with selenium and tellurium in five-membered pseudosugar ring has been studied. The experimental NMR measurement was complemented with DFT molecular modeling studies. It was found, that ratio between individual conformers in solution depends on the nature of the heteroatom in the five-membered pseudosugar ring.
Pyrrolidine nucleotides conformationally constrained via hydrogen bonding
Pohl, Radek ; Poštová Slavětínská, Lenka ; Rejman, Dominik
Conformation of pyrroPME nucleotide analogues was studied by means of NMR at different pD values in D2O solutions. Surprisingly, two stable conformers were found at pD > 9 for both cis and trans configurations and their ratio depended on the acid-base properties of nucleobase attached to pyrrolidine ring. The results of conformational analysis suggest that the conformation of the pyrrolidine ring is locked via intramolecular hydrogen bond between negatively charged phosphonate oxygen atom and protonized pyrrolidine nitrogen.
Insights into the mechanism of action of bactericidal lipophosphonoxins
Panova, Natalya ; Zborníková, Eva ; Šimák, Ondřej ; Krásný, Libor ; Kolář, M. ; Látal, T. ; Seydlová, G. ; Rejman, Dominik
The advantages offered by antibiotics in the treatment of infectious diseases are endangered due to the increase in the number of antibiotic-resistant bacterial strains. This reduces the efficiency of antibiotic treatments and poses a serious health and economical problem. Currently, the need for novel antibiotics is becoming increasingly apparent. Recently, we discovered a series of compounds termed lipophosphonoxins exhibiting selective cytotoxicity towards gram-positive bacterial cells. The attempt to elucidate the mode of action of lipophosphonoxins is presented here.
Synthesis of PME derivatives on nucleobases with conformation locked via pyrrolidine ring
Rejman, Dominik ; Pohl, Radek
Among diverse nucleoside phosphonic acids, the acyclic phosphonate derivatives have been earlier shown to involve some exceptionally potent antiviral drugs (e.g., Cidofovir, Adefovir, and Tenofovir). This work presents the synthesis of such acyclic phosphonate nucleotides conformationally locked via pyrrolidine ring.
Piperidine nucleoside phosphonic acid derivatives
Kovačková, Soňa ; Dračínský, Martin ; Rejman, Dominik
A series of novel phosphonic acid derivatives of piperidine nucleosides was prepared, whereby synthesis of both enantiomeric and diastereomeric derivatives was discussed. Preparation of diphosphate analogs of phosphonic acids derivatives is also described. The prepared nucleotide analogs were tested for their potential biological properties.
Konformace pyrrolidinového kruhu v pyrrolidinových analozích nukleotidů
Pohl, Radek ; Buděšínský, Miloš ; Rejman, Dominik ; Kočalka, Petr ; Rosenberg, Ivan
Molecular modeling methods were used for conformation study of pyrrolidine ring in the series of pyrrolidine nucleotide analogues. Theoretical results were compared with experimental ones obtained by NMR conformation analysis.
Pyrrolidinová analoga nukleotidů - konformační studie
Pohl, Radek ; Rejman, Dominik ; Kočalka, Petr ; Rosenberg, Ivan
Conformation analysis of pyrrolidine ring for series of pyrrolidine nucleotide analogue using concept of pseudorotation and experimental 3J(H,H) coupling constants was performed.

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See also: similar author names
3 Rejman, Daniel
3 Rejman, David
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