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National Repository of Grey Literature 3 records found  Search took 0.00 seconds. 
Light-harvesting like domain of the cyanobacterial ferrochelatase
 PAZDERNÍK, Marek
This thesis is focused on elucidating the function of the C-terminal transmembrane lightharvesting complex like (LHC) domain of the cyanobacterial ferrochelatase (FeCh). Using the model cyanobacterium Synechocystis PCC 6803, I show that the FeCh LHC domain can bind chlorophyll (Chl) and carotenoids; however, this pigment binding occurs only when the biosynthesis of heme and Chl in the cell is misbalanced. Further, I found that point mutation, which prevents the pigment binding to FeCh LHC domain results in a misregulated ratio between heme and Chl during stress conditions due to low heme accumulation. My data also show that the FeCh LHC domain interacts with CurT protein most likely to localize the FeCh into a specialized membrane domain, where the synthesis of photosystem II is proposed to occur. Based on my data I propose that the role of the FeCh LHC domain is to monitor the availability of Chl during photosystem biogenesis and to coordinate Chl availability with the synthesis of heme.
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Identification of Products of Tetrapyrrole Pathway
 HÁJEK, Jan
Cultivation of a model cyanobacterium Synechocystis PCC 6803 under low light conditions in the presence of glucose and TES buffer leads to a change of the medium color from colorless to yellow. The absorption spectrum of the excreted unknown compound indicated a possible relationship to plant chlorophyll degradation products. To confirm this speculation the compound was purified by a combination of solid phase extraction and HPLC. The mass and NMR characteristics excluded its close relationship to modified tetrapyrroles, nevertheless the precise structure could not be determined by these means due to a complicated nature of the compound and its high polarity.
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Evolution of the tetrapyrrole synthesis in eukaryotes
 KOŘENÝ, Luděk
This thesis focuses on the nature of heme metabolism in various eukaryotes. One of the aims was the elucidation of the origin of the unique heme biosynthesis pathway in apicomplexan parasites through a comparative study of their photosynthetic relative Chromera velia combining molecular biology, biochemistry and bioinformatics approach. Using similar strategy, I have also investigated the origin and spatial organization of tetrapyrrole biosynthesis in Euglena gracilis. Based on the phylogenetic data I described the complex evolution of heme metabolism in kinetoplastid flagellates including pathogenic trypanosomes. I revealed that one of them (Phytomonas) does not require heme for viability by the combination of various biochemical and molecular biology experiments and bioinformatic analyses.
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