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Eucaryotic cells systems and their biotechnologycal applications
Porubiaková, Otília ; Obruča, Stanislav (referee) ; Vorlíčková, Michaela (referee) ; Brázda, Václav (advisor)
The submitted dissertation is divided into several parts. The first part deals with the interactions of the p53 protein and its isoforms with different potential DNA substrates under different experimental conditions. These are predominantly DNA and its non-canonical structural motifs, such as G-quadruplexes or cruciform structures, whose interactions have been studied in yeast isogenic systems or by in vitro methods. The seconds part deals with the bioinformatic analysis of the mentioned secondary DNA structures in different organismal groups, and the result is a set of publications that show their non-random distribution in the genome and their relationship with regulation. The last part of the work contains unpublished results, including the results of testing the effect of natural and synthetic substances on aging in model human cells.
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Analyses of inverted repeats localization in bacterial genomes
Šedý, Michal ; Zemanová, Jana (referee) ; Brázda, Václav (advisor)
Inverted repeats (IR) are common part of DNA of all living prokaryotic and eukaryotic organisms. Inverted repeats plays an important role in the regulation of basics cells processes. They are responsible for formation of cruciform structures. Inverted repeats also cause genomic instability and can be a source of numerous mutations. Cruciform structures can be recognized by DNA-binding proteins and can also act as a transcriptional regulators. Using the Palindrome Analyser tool, the frequency of IR and localization of inverted repeats in bacterial genomes was analyzed. The frequency of IR across the bacterial genome is variable. The frequency of short inverted repeats shows an approximately quadratic dependence on the %GC content in the genome with a minimum of about 50% of GC content. The localization of inverted repeats with respect to “annotated features” show a non-random distribution. The frequency of IR for most features is higher “outside” than “inside”.
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Analysis of local structures in DNA molecules
Nyczová, Adéla ; Smetana, Jan (referee) ; Brázda, Václav (advisor)
Local DNA structures are alternative DNA conformations which can be formed aside from typical B-DNA conformation. These structures often play pivotal roles in regulation of basic biological processes, such as DNA replication, transcription or binding of specific ligands. This biological significance makes alternative DNA secondary structures a potential drug target. In this diploma thesis, local structures in genomes of viruses from Flaviviridae and Retroviridae families are analysed using bioinformatics tools. Furthermore, these structures are visualised using atomic force microscopy.
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Impact of temperature and drought on gliadins content in two varieties of wheat
Seidlová, Kateřina ; Brázda, Václav (referee) ; Hrstka, Miroslav (advisor)
This bachelor’s thesis focuses on the effect of high temperature and drought on protein content of gliadin fraction on two varieties of wheat. Chosen varieties were Hyfi and Julie, cultivated at 26, 29, 32, 35 and 38 °C during flowering in watering controlled conditions. The condition for ‘wet’ samples was at least 70 % soil moisture and for ‘dry’ samples less than 30 % soil moisture. After harvesting, the seeds were milled into flour from which the gliadins were extracted with 2-chlorethanol. A-PAGE method was used for gliadin separation, quantification was carried out through computer densitometry. A significant genotype effect was discovered. Whilst temperature ranging from 26-38 °C with simultaneous drought stress had no significant effect on gliadin content of Hyfi variation, gliadin content of Julie variation shown obvious maximum at 32 °C. Therefore, Hyfi variation shown better resistance to heat stress than Julie variation. Both variations had higher gliadin content under drought stress than under good watering conditions.
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Sequences forming G-quadruplexes in the amyloid beta precursor human gene and its homologues
Stránská, Anna ; Šedrlová, Zuzana (referee) ; Brázda, Václav (advisor)
The APP gene encodes the transmembrane protein amyloid beta precursor, which is expressed in many cell types, including neurons. Its functions have not yet been fully described, but it is clear that it is being cleaved before being exported to the extracellular space. It is degraded by various degradation pathways also undergoes homodimerization, which can produce particles with protective neuronal function as well as fragments that are toxic and cause nerve cell death. The formation of harmful amyloid beta plaques and their accumulation among neurons in the brain is closely linked to the onset and progression of Alzheimer's disease, a neurodegenerative brain disease manifested by death and loss of neurons, which leads to dementia, i.e. loss of cognitive functions. There is currently a lot of research that deals with the links between neurodegenerative diseases and the occurrence of G-quadruplexes in genes that are involved in disease manifestations. G-quadruplexes are non-canonical DNA and RNA nucleic acid secondary structures that arise in guanine-rich regions. They are important mainly in terms of their connection with biological processes such as the regulation of gene expression in genes and mainly in oncogenes because they occur in important regions of the gene such as the promoter. It is possible to stabilize them with small molecules, and it is this ability that is used in research into the therapeutic treatment of various diseases. A bioinformatics analysis of both the human gene and 346 other gene homologs was performed to determine the importance of G-quadruplexes localization and conservation in the human APP gene. For this purpose, the G4Hunter program was used, which provided information about the found sequences with the potential to form a G-quadruplex, such as their location or G4Hunter score. In vitro analysis was performed using thioflavin T reagent, which tested the ability of the found sequences to form G-quadruplexes under physiological conditions. The results confirmed the presence and evolutionary importance of G-quadruplexes found in the APP gene of Homo sapiens and their ability to assemble into quadruplex structures in the presence of salts such as sodium and potassium.
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Analysis of C. necator genome changes after evolutionary adaptation
Kroupa, Štěpán ; Obruča, Stanislav (referee) ; Brázda, Václav (advisor)
This bachelor’s thesis deals with analysis of mutations in bacterial populations of Cupriavidus necator H16 evolved in distinct stress conditions. This analysis was performed by processing data from the genome sequencing method „Next Generation Sequencing“, outsourced through the company DNALink. A list of mutations for each adapted population was constructed through bioinformatic methods. These mutations were then associated with specific areas of the reference Cupriavidus necator H16 genome from NCBI and analysed according to available information. Finally, the effect of these mutations on production of storage polymers polyhydroxyalkanoates was discussed.
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Use of high resolution melting analysis for the study of lactic acid bacteria
Knápková, Monika ; Němcová, Andrea (referee) ; Brázda, Václav (advisor)
Currently, there is a growing interest in the use of probiotic products, and there are many of them in the market. With the growing interest, greater emphasis is placed on the identification of declared probiotic microorganisms. Precise identification of microbial composition is often a difficult task and it requires more advanced methods especially in the field of molecular diagnostics. The diploma thesis was focused on the verification of the presence od declared probiotic microorganisms in probiotic food supplements GS Laktobacily Forte 21, Biopron 9 Premium and Linex® Forte. DNA was isolated from the complex matrices by phenol extraction, commercial kit and magnetic carriers F79/L3-PLL in the quality suitable for PCR. Subsequently, the isolated DNA was amplified by real-time polymerase chain reaction using genus- and species-specific primers. The specific PCR product was subjected to agarose gel electrophoresis, whereas species identification was not always in compliance with the data declared by producers. The next part of the thesis was focused on polymerase chain reaction with high-resolution melting analysis to distinguish bacterial strains belonging to the Lactobacillus group and to identify probiotic microorganisms present in the complex matrices of the probiotic food supplements. Eight primer sets were tested (V1F HRM a V1R-HRM, CHAU-V3F a CHAU-V3R, CHAU-V6F a CHAU-V6R, LAC2 a LAC4, LAC1 a LAC2, P1V1 a P2V1, poxcDNAFw a poxPromRVC, poxcDNAFw a poxPromRVT). Three primer pairs (V1F HRM a V1R-HRM, poxcDNAFw a poxPromRVC, poxcDNAFw a poxPromRVT) were evaluated as the most suitable for distinguishing Lactobacillus bacterial strains.
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Using different methods of DNA isolation of lactic acid bacteria in molecular biological methods
Chvalkovská, Eva ; Skoumalová, Petra (referee) ; Brázda, Václav (advisor)
This thesis focused on the probiotic bacteria, DNA isolated from these bacteria by three different methods and the effect of isolation on DNA identification using molecular biological methods. Probiotic bacteria are an important part of human intestinal tract. They have an important role in the function of the immune system due to adhesion to the mucosa of the intestinal flora. They create a inhostile environment for pathogens. Probiotic bacteria are commonly taken in the food like dairy products or food supplements. However, overuse of antibiotics is at risk of passing on the intrinsic resistance that probiotic bacteria have to the pathogenic bacteria. The intrinsic resistence they have to maintain the natural homeostasis of the intestinal tract. It is important to effectively identify risky probiotic bacteria that have the ability to transmit resistance to eliminate their presence in food and dietary supplements. Three methods of DNA isolation like phenol extraction method, magnetic particle isolation and commercial kit isolation were used in the experimental part. DNA was isolated from three dietary supplements, namely Biopron 9 premium, Linex forte and GS Lactobacily forte 21. The purity and concentration of the isolated DNA was detected spectrophotometrically. The presence of individual DNA strains in dietary supplements was confirmed by real-time polymerase chain reaction. The best method of isolation in terms of purity and concentration of isolated DNA was evaluated by RT-PCR and spectrophotometry using a commercial kit isolation method.
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Use of some molecular techniques to metabolic characterization of industrially significant yeasts
Kostovová, Iveta ; Brázda, Václav (referee) ; Kráčmar, Stanislav (referee) ; Márová, Ivana (advisor)
Karotenoidy, ergosterol a mastné kyseliny jsou velmi žádané látky využívané v krmivářském, potravinářském a kosmetickém průmyslu. Konvenční zdroje mastných kyselin a karotenoidů jsou závislé na sezónních podmínkách, geografické poloze a na dostupnosti zemědělské půdy, což znesnadňuje pokrýt jejich neustále se zvyšující spotřebu. Velmi slibným řešením je mikrobiální produkce výše uvedených látek pomocí karotenogenních kvasinek, které jsou schopny simultánně produkovat karotenoidy, mastné kyseliny i ergosterol. Předložená disertační práce je zaměřená na molekulární a metabolickou charakterizaci karotenogenních kvasinek a na jejich potenciál pro průmyslové aplikace. Proto první experimentální části práce jsou zaměřeny na kvasinky druhu R. mucilaginosa a R. toruloides, jejich produkční vlastnosti, vliv nutričního stresu a různých zdrojů uhlíku, jakými byly xylóza a glycerol. Kromě podrobné charakterizace jejich produkčních vlastností, byly tyto kmeny také charakterizovány molekulárními metodami, zahrnující sekvenční analýzu ITS1, ITS2 a D1/2 ribozomálního operonu a analýzu mini a mikrosatelitních sekvencí M13 a GTG5. Druh R. toruloides je známý jako vynikající producent mastných kyselin, a proto se v poslední době stal cílovou karotenogenní kvasinkou pro vývoj nástrojů pro jeho genetickou manipulaci. V této práci byly úspěšně připraveny geneticky modifikované klony kmene R. toruloides, nesoucí nadměrně exprimované geny pro diacylglycerol acyltransferázu (DGA1) a glycerol-3-fosfát dehydrogenázu (GPD1). Produkce mastných kyselin u modifikovaných klonů nebyla ve srovnání s původním kmenem vyšší. Proto byla další část práce zaměřená na přípravu nadprodukčních mutantních kmenů připravených náhodnou mutagenezí. Kombinace limitace dusíkem a inhibice produkce karotenoidů vedla k úspěšné selekci robustních mutantních kmenů s nadprodukcí karotenoidů vykazující rezistenci vůči difenylaminu. Poslední část práce se zabývá produkčními vlastnostmi méně známých druhů karotenogenních kvasinek náležící do řádů Sporidiobolales a Cystofilobasidales, ve srovnání s relativně dobře prostudovanými karotenogenními druhy R. toruloides a P.rhodozyma. V této studii byly nejlešími producenty mastných kyselin kmeny S.metaroseus CCY 19-6-20 a C. macerans CCY 10-01-02. Nejlepší producent karotenoidů, kmen R. mucilaginosa CCY 19-04-06, navíc produkoval lykopen, který představoval více než 80 % celkového množství karotenoidů produkovaných tímto kmenem.
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Effect of natural substances from tea on G-quadruplexes and binding and transactivation properties of p53 protein
Foltanová, Klára ; Řeháková, Veronika (referee) ; Brázda, Václav (advisor)
The tumor suppressor protein p53 belongs to the most important regulator of the cell cycle in case of DNA damage. Apart from stopping the cell cycle and inducing apoptosis, protein p53 interacts with other proteins and DNA. Mutation of the TP53 gene encoding the protein p53 are a common feature of human cancer. This Bachelor thesis investigates natural substances from tea which could play a positive role in the activation of protein p53 in cancer and be used to support the treatment of these diseases. In the theoretical part of the Bachelor thesis, the secondary structures of DNA were described, specifically the structure and properties of G-quadruplexes, as well as protein p53 and its binding activity to the secondary structure of DNA. Selected natural substances found in tea and food were described – gallic acid and apigenin. The aim of the experimental part of this work was to verify the ability of these substances to interact with G-quadruplexes in vitro and thus to stabilize them in the yeast model and to assess the subsequent effect on measuring the effect of protein p53 transactivation. The interaction of quaternary structures with G4 ligands was verified in vitro by using the ThT fluorescence assay and the luciferase reporter assay. It was found that G4 ligands at 30 M concentration after 20 hours of incubation did not show a significant effect on the tested yeast cultures. At a 60 M concentration of G4 ligands, an increase in protein p53 production was observed due to cellular stress caused by the presence of G4 ligands.
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