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Analysis of Thick Film Amperometrical Sensors Signal and Its Usage for Measurement and Characterization of Enzymes
Ondruch, Vít ; Kizek, René (referee) ; Masojídek,, Jiří (referee) ; Vrba, Radimír (advisor)
V práci je popsán princip synchronní detekce (SD), který byl uplatněn při měření s biosenzory. Metoda SD umožňuje dosažení výrazně lepšího poměru signálu k šumu, vyššího limitu detekce a celkové zlepšení robustnosti měření. Uplatnění SD při měření s biosenzory umožní zlepšit analýzu jeho odezvy a umožní odstranění nežádoucích interferencí nebo šumů, které mohou být způsobeny například mícháním roztoku, elektromagnetickými vlivy nebo parazitními proudy. SD také umožňuje rozložit získaný signál na odezvu stimulace a na dlouhodobý signál jiného procesu, a dále také identifikovat jevy druhého řádu. Pro identifikaci stimulačního signálu ve výstupním signálu měření byl na základě lineárního statistického modelu vyvinut specializovaný software. SD byla ověřena na modelovém případu výstupního signálu biosenzoru s aplikovaným komplexem fotosystému II (PSII) a jeho odezvě na stimulaci světlem. Odezva PSII se řídí kinetikou prvního řádu a může být také ovlivněna inhibitory. Kinetické konstanty vazby herbicidu na PSII závisí lineárně na koncentraci herbicidu. To umožňuje jejich měření také při nízkých koncentracích herbicidu.
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Characterisation of Arabidopsis thaliana mutants psbo1 and psbo2
Nykles, Ondřej ; Duchoslav, Miloš (advisor) ; Hála, Michal (referee)
The PsbO protein is necessary for the function of the electron-transport chain of the thylakoid membrane in higher plants. In most of the angiosperms, including Arabidopsis thaliana, this protein has two isoforms termed as PsbO1 and PsbO2. Many authors tried to reveal the fundamental difference between the PsbO1 and PsbO2 with the help of the mutant lines which lack one of the isoforms. The problem is that the mutants in psbO isoforms do not possess the same level of PsbO as WT does. So we made psbo1isoL mutants. These lines contain only one isoform but their level of the whole PsbO is comparable to the level of the whole PsbO of WT. Results from these experiments suggest that if a psbo1isoL plant has the same amount of PsbO as WT does, there is no observable phenotype difference. Thus we were not able to identify, in the usual cultivation conditions, if there are any functional differences between PsbO1 and PsbO2 Following the above mentioned results, we would like to know conditions (if there are any) in which T-DNA insertion mutants psbo2 (respectively psbo2cr which are made with the use of the CRISPR/Cas9), which have only PsbO1 isoform, could be phenotypically distinguished from WT. With the use of usual cultivation conditions, we are unable to tell apart the psbo2 and psbo2cr from WT by the...
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Function of PsbO isoforms
Duchoslav, Miloš ; Fischer, Lukáš (advisor) ; Špunda, Vladimír (referee) ; Sobotka, Roman (referee)
(English version) Oxygenic photosynthesis is crucial for most forms of the life on the Earth. The splitting of water and evolution of oxygen is conducted by photosystem II (PSII), a multi-subunit pigment- protein complex embedded in the thylakoid membrane. PsbO is an indispensable subunit of PSII, bound to its transmembrane subunits from the luminal side. The main function of PsbO is to stabilise and protect Mn4CaO5 cluster where the water splitting occurs. However, it has probably also some auxiliary functions. These additional functions might be different for isoforms of PsbO proteins, as suggested for Arabidopsis thaliana, which expresses two genes encoding protein isoforms PsbO1 and PsbO2. This thesis studies auxiliary functions of PsbO with a focus on functional differences between PsbO isoforms. We found that besides Arabidopsis thaliana, also many other plant species express two psbO genes. Interestingly, the duplication of psbO gene occurred many times independently, generally at the roots of modern angiosperm families. In spite of this, the PsbO isoforms differ at similar sites in the protein structure, suggesting that similar subfunctionalisation of PsbO isoforms occurred parallelly in various lineages. Biochemical characterisation of PsbO from green alga Chlamydomonas reinhardtii and...
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Role of PsbO isoforms in Arabidopsis thaliana
Svoboda, Václav ; Duchoslav, Miloš (advisor) ; Knoppová, Jana (referee)
Role of PsbO isoforms in Arabidopsis thaliana Abstract Photosystem II (PSII) uses sunlight to catalyze water oxidation and reduce plastoquinone. Water oxidation takes place in oxygen evolving complex (OEC). OEC is stabilized by extrinsic subunits of PSII. The largest and most important of them is PsbO, manganese-stabilizing protein which can be found in all known oxygenic photosynthetic organisms. Model plant Arabidopsis thaliana expresses two isoforms of psbO gene, namely PsbO1and PsbO2.Mutants psbo1 and psbo2 lacking PsbO1 and PsbO2, respectively, recently brought new findings on the particular roles of isoforms in maintaining photosynthesis. PsbO1 is commonly considered as the main isoform facilitating water splitting, whereas PsbO2 is believed to be involved in PSII repair process (replacement of photodamaged D1 subunit). This work focuses on particular roles of Arabidopsis PsbO isoforms in maintaining photosynthesis with special focus on response to light stress. Mutants psbo1, psbo2 and wild type plants Col-0 were used for extensive biochemical investigation. Our aim was to find out what is the impact on overall thylakoid structure and composition in mutants. Furthermore, to investigate response to light stress in wild type regarding to yields of particular subcompartments, changes in photosystem II...
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Proteomic and functional characterization of PsbO isoforms
Duchoslav, Miloš ; Fischer, Lukáš (advisor) ; Hála, Michal (referee)
PsbO (manganese-stabilizing protein) is the largest extrinsic protein of photosystem II, located on the lumen side of photosystem. It is present in all known oxyphototrophic organisms. PsbO facilitates photosynthetic water splitting, which takes place in an oxygen evolving center (Mn4CaO5 cluster) of photosystem II. This work is focused on PsbO of higher plants and its isoforms, particularly their evolution and functions. Bioinformatic analyses revealed that majority of higher plants express exactly two psbO isoforms. A phylogenetic tree of PsbO sequences has an unusual topology. The two paralogous isoforms do not diverge at the base of the phylogenetic tree, as anticipated, but rather at the end of particular branches, at the level of family or lower taxonomic unit. In this work we propose and discuss several hypotheses concerning evolution of PsbO isoforms. The work further includes detailed analysis and identification of protein spots assigned to PsbO on 2D IEF-SDS PAGE gels of potato thylakoid proteins. We identified predominant version of PsbO isoform in most of the spots. We did not succeed to find any posttranslational modification. We optimized a method of psbO expression in E. coli and subsequent purification, which yielded relatively big amount of properly folded recombinant protein. Analysis of...
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The role of manganese-stabilizing protein of photosystem II
Duchoslav, Miloš ; Rothová, Olga (referee) ; Fischer, Lukáš (advisor)
Miloš Duchoslav The role of manganese-stabilizing protein of photosystem II Abstract The appearance of oxygenic photosynthesis was a key event in the evolution of life on the Earth. All molecular oxygen in the atmosphere likely comes from a water-splitting reaction catalysed by the oxygen-evolving center of photosystem II. Photosystem II - a multisubunit protein-cofactor complex with a phylogeneticaly highly conserved structure - is embedded in the thylakoid membrane of chloroplasts and cyanobacteria. The mechanism of the photosynthetic water-splitting reaction, which occurs on the manganese cluster, has been widely investigated; however, it has not yet been fully understood. An essential role in the stabilization of the manganese cluster and in the facilitation of oxygen evolution is played by photosystem II extrinsic proteins that occur in thylakoid lumen. The most important among them is a manganese-stabilizing protein (MSP) that is present in all known oxyphototrophs. This protein is believed to have many functions: besides stabilizing the manganese cluster, it is also carbonic anhydrase activity, GTPase activity and regulation of the turnover of the D1 protein. The functions of the MSP are probably regulated through changes in its dynamic structure. The MSP is likely to take part in the regulation of...
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Analysis of Thick Film Amperometrical Sensors Signal and Its Usage for Measurement and Characterization of Enzymes
Ondruch, Vít ; Kizek, René (referee) ; Masojídek,, Jiří (referee) ; Vrba, Radimír (advisor)
V práci je popsán princip synchronní detekce (SD), který byl uplatněn při měření s biosenzory. Metoda SD umožňuje dosažení výrazně lepšího poměru signálu k šumu, vyššího limitu detekce a celkové zlepšení robustnosti měření. Uplatnění SD při měření s biosenzory umožní zlepšit analýzu jeho odezvy a umožní odstranění nežádoucích interferencí nebo šumů, které mohou být způsobeny například mícháním roztoku, elektromagnetickými vlivy nebo parazitními proudy. SD také umožňuje rozložit získaný signál na odezvu stimulace a na dlouhodobý signál jiného procesu, a dále také identifikovat jevy druhého řádu. Pro identifikaci stimulačního signálu ve výstupním signálu měření byl na základě lineárního statistického modelu vyvinut specializovaný software. SD byla ověřena na modelovém případu výstupního signálu biosenzoru s aplikovaným komplexem fotosystému II (PSII) a jeho odezvě na stimulaci světlem. Odezva PSII se řídí kinetikou prvního řádu a může být také ovlivněna inhibitory. Kinetické konstanty vazby herbicidu na PSII závisí lineárně na koncentraci herbicidu. To umožňuje jejich měření také při nízkých koncentracích herbicidu.
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Teoretické studium fotosystemu II, chlorozomů a flavoproteinu WrbA
PALENČÁR, Peter
The power of the current computer clusters allows us to study relatively large biomolecular systems by theoretical computational methods, such as widely used classical molecular dynamics (MD) simulations, at atomic level on the time scale of tens of nanoseconds. The limiting factor for classical MD simulations on most of the physiologically relevant systems is the lack of available force field (FF) parameters. Three biomolecular systems were studied in this thesis, namely membrane protein photosystem II (PSII), green bacteria antennas called chlorosomes and flavoprotein WrbA from E. coli, and all of them contain molecules or molecular fragments for which no FF parameters are available. Therefore, development of new FF parameters for all non-protein molecules was performed by applying quantum-mechanics (QM) methods. Once all FF parameters were available, MD simulations were applied. The computational studies were based on the conditions from wet experiments performed earlier by our research group. For the first time, proposed light-induced conformational changes of the reaction center (RC) of PSII and subsequent changes in arrangement of PSII RC pigments, were confirmed and described at atomic level by series of MD simulations over 20 ns. Optical spectra calculated on equilibrated MD model of PSII RC were in better agreement with experimental analogues when compared with earlier calculations on static model of PSII RC taken from crystal structure. Successful application of classical mechanics, QM and advanced optical spectra calculations on PSII represents one of a few existing computational studies on similar membrane pigment-protein systems. In the case of chlorosomes, equilibrated molecular lamellar models were constructed and critical structural parameters were elucidated by series of MD simulations over 30 ns. The presented models are the first lamellar models of chlorosomes at such scale so far. The equilibrated MD models of flavoprotein WrbA based on recent crystal structure provides starting point for further theoretical studies aimed to elucidate structural details of proposed ping-pong mechanism.
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Structural analysis of extrinsic proteins from the oxygen-evolving complex of photosystem II from higher plants
KOHOUTOVÁ, Jaroslava
All life on earth depends mainly on the presence of oxygen. Largest producers of oxygen are green plants, cyanobacteria and algae. Oxygen is released from the oxygenevolving complex of photosystem II during photosynthesis and it is used in cellular respiration of all life complexes. The oxygen-evolving complex of photosystem II has the same function in each photosynthetic organism, but it has a different composition and organization of extrinsic proteins; only PsbO protein is ubiquitous in all known oxyphototrophs. Until now only low resolution electron microscopy structural models of plant PSII and crystal structures of cyanobacterial PSII are available. Higher plant extrinsic proteins (PsbP, PsbQ and PsbR) are structurally unrelated, non-homologues to the cyanobacterial extrinsic proteins (PsbO, PsbU and PsbV) and this is the reason why it is not possible to predict arrangement of these proteins on the lumenal site of higher plant PSII. Recently, models differ mainly in the structure of the oxygen-evolving complex, which could be resolved by determination of the exact binding sites for extrinsic proteins. An other question evolves: if the difference in the oxygen-evolving complex composition is the result of evolution or adaptation of photosynthetic organisms to their environment. Structural knowledge of extrinsic proteins that could help to resolve the location and subsequently the function of extrinsic proteins is still incomplete. From this case,structural analysis, interactions and probably arrangement of proteins PsbP and PsbQ was studied and is described in detail in this thesis.
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