@phdthesis{Zupok2015, author = {Zupok, Arkadiusz}, title = {The psbB-operon is a major locus for plastome-genome incompatibility in Oenothera}, school = {Universit{\"a}t Potsdam}, pages = {108}, year = {2015}, language = {en} } @phdthesis{Zinck2009, author = {Zinck, Richard}, title = {Diversity, criticality and disturbance in wildfire ecosystems}, address = {Potsdam}, pages = {97 S.}, year = {2009}, language = {en} } @phdthesis{Zimmermann2017, author = {Zimmermann, Heike Hildegard}, title = {Vegetation changes and treeline dynamics in northern Siberia since the last interglacial revealed by sedimentary ancient DNA metabarcoding and organelle genome assembly of modern larches}, school = {Universit{\"a}t Potsdam}, pages = {138}, year = {2017}, language = {en} } @phdthesis{Zhu2016, author = {Zhu, Fangjun}, title = {Gene evolution and expression patterns in the all-female fish Amazon molly: Poecilia formosa}, school = {Universit{\"a}t Potsdam}, pages = {113}, year = {2016}, language = {en} } @phdthesis{Zhou2008, author = {Zhou, Fei}, title = {Optimization of foreign gene expression in plastids}, pages = {VIII, 134 S.}, year = {2008}, language = {en} } @phdthesis{Zhao2015, author = {Zhao, Liming}, title = {Characterization genes involved in leaf development and senescence of arabidopsis}, school = {Universit{\"a}t Potsdam}, pages = {137}, year = {2015}, language = {en} } @phdthesis{Zhang2016, author = {Zhang, Youjun}, title = {Investigation of the TCA cycle and glycolytic metabolons and their physiological impacts in plants}, school = {Universit{\"a}t Potsdam}, pages = {175}, year = {2016}, language = {en} } @phdthesis{Zhang2019, author = {Zhang, Xiaorong}, title = {Electrosynthesis and characterization of molecularly imprinted polymers for peptides and proteins}, school = {Universit{\"a}t Potsdam}, pages = {116}, year = {2019}, language = {en} } @phdthesis{Zhang2009, author = {Zhang, Gong}, title = {Transient ribosomal attenuation as a generic mechanism to coordinate protein biosynthesis and biogenesis}, address = {Potsdam}, pages = {114 S.}, year = {2009}, language = {en} } @phdthesis{Zeng2017, author = {Zeng, Ting}, title = {Nanoparticles promoted biocatalysis}, school = {Universit{\"a}t Potsdam}, pages = {99}, year = {2017}, language = {en} } @phdthesis{Zbierzak2009, author = {Zbierzak, Anna Maria}, title = {Isolation and characterization of the chilling sensitive 1 gene from Arabidopsis}, address = {Potsdam}, pages = {iii, 131 Bl. : Ill., graph. Darst.}, year = {2009}, language = {en} } @phdthesis{Zauber2013, author = {Zauber, Henrik}, title = {A systems biology driven approach for analyzing lipid protein interactions in sterol biosynthesis mutants}, address = {Potsdam}, pages = {126 S.}, year = {2013}, language = {en} } @phdthesis{You2024, author = {You, Lili}, title = {Chloroplast engineering for recombinant protein production and stress protection}, school = {Universit{\"a}t Potsdam}, pages = {133}, year = {2024}, language = {en} } @phdthesis{Yishai2019, author = {Yishai, Oren}, title = {Engineering the reductive glycine pathway in Escherichia coli}, school = {Universit{\"a}t Potsdam}, pages = {86}, year = {2019}, language = {en} } @phdthesis{Yazdanbakhsh2009, author = {Yazdanbakhsh, Nima}, title = {Development of a robotized image processing platform to decipher root elongation kinetics in a. thaliana and investigating the role of carbohydrates and the circadian clock genes in detected diurnal patterns}, address = {Potsdam}, pages = {97 S. : Ill., graph. Darst.}, year = {2009}, language = {en} } @phdthesis{Yarman2012, author = {Yarman, Aysu}, title = {Biomimetic sensors for substrates of peroxidases and cytochrome P450s}, address = {Potsdam}, pages = {121 S.}, year = {2012}, language = {en} } @phdthesis{Yang2017, author = {Yang, Lei}, title = {Verification of systemic mRNAs mobility and mobile functions}, school = {Universit{\"a}t Potsdam}, pages = {125}, year = {2017}, language = {en} } @phdthesis{Yadav2009, author = {Yadav, Umesh Prasad}, title = {Sucrose and trehalose-6-phosphate signalling in "Arabidopsis thaliana"}, address = {Potsdam}, pages = {X, 156 S. : zahlr. graph. Darst.}, year = {2009}, language = {en} } @phdthesis{XuanNghiem2008, author = {Xuan Nghiem, Dang}, title = {Functional characterization of candidate Arabidopsis thaliana (L.) LEA proteins and Saccharomyces cerevisiae hydrophilins}, address = {Potsdam}, pages = {VIII, 97 S. : graph. Darst.}, year = {2008}, language = {en} } @phdthesis{Xu2016, author = {Xu, Ke}, title = {Functional characterization of two MYB transcription factors, MYB95 and MYB47, in Arabidopsis thaliana}, school = {Universit{\"a}t Potsdam}, pages = {108}, year = {2016}, language = {en} } @phdthesis{Wutke2016, author = {Wutke, Saskia}, title = {Tracing Changes in Space and Time}, school = {Universit{\"a}t Potsdam}, pages = {x, 84}, year = {2016}, abstract = {The horse is a fascinating animal symbolizing power, beauty, strength and grace. Among all the animal species domesticated the horse had the largest impact on the course of human history due to its importance for warfare and transportation. Studying the process of horse domestication contributes to the knowledge about the history of horses and even of our own species. Research based on molecular methods has increasingly focused on the genetic basis of horse domestication. Mitochondrial DNA (mtDNA) analyses of modern and ancient horses detected immense maternal diversity, probably due to many mares that contributed to the domestic population. However, mtDNA does not provide an informative phylogeographic structure. In contrast, Y chromosome analyses displayed almost complete uniformity in modern stallions but relatively high diversity in a few ancient horses. Further molecular markers that seem to be well suited to infer the domestication history of horses or genetic and phenotypic changes during this process are loci associated with phenotypic traits. This doctoral thesis consists of three different parts for which I analyzed various single nucleotide polymorphisms (SNPs) associated with coat color, locomotion or Y chromosomal variation of horses. These SNPs were genotyped in 350 ancient horses from the Chalcolithic (5,000 BC) to the Middle Ages (11th century). The distribution of the samples ranges from China to the Iberian Peninsula and Iceland. By applying multiplexed next-generation sequencing (NGS) I sequenced short amplicons covering the relevant positions: i) eight coat-color-associated mutations in six genes to deduce the coat color phenotype; ii) the so-called 'Gait-keeper' SNP in the DMRT3 gene to screen for the ability to amble; iii) 16 SNPs previously detected in ancient horses to infer the corresponding haplotype. Based on these data I investigated the occurrence and frequencies of alleles underlying the respective phenotypes as well as Y chromosome haplotypes at different times and regions. Also, selection coefficients for several Y chromosome lineages or phenotypes were estimated. Concerning coat color differences in ancient horses my work constitutes the most comprehensive study to date. I detected an increase of chestnut horses in the Middle Ages as well as differential selection for spotted and solid phenotypes over time which reflects changing human preferences. With regard to ambling horses, the corresponding allele was present in medieval English and Icelandic horses. Based on these results I argue that Norse settlers, who frequently invaded parts of Britain, brought ambling individuals to Iceland from the British Isles which can be regarded the origin of this trait. Moreover, these settlers appear to have selected for ambling in Icelandic horses. Relating to the third trait, the paternal diversity, these findings represent the largest ancient dataset of Y chromosome variation in non-humans. I proved the existence of several Y chromosome haplotypes in early domestic horses. The decline of Y chromosome variation coincides with the movement of nomadic peoples from the Eurasian steppes and later with different breeding practices in the Roman period. In conclusion, positive selection was estimated for several phenotypes/lineages in different regions or times which indicates that these were preferred by humans. Furthermore, I could successfully infer the distribution and dispersal of horses in association with human movements and actions. Thereby, a better understanding of the influence of people on the changing appearance and genetic diversity of domestic horses could be gained. My results also emphasize the close relationship of ancient genetics and archeology or history and that only in combination well-founded conclusions can be reached.}, language = {en} } @phdthesis{Wurzbacher2012, author = {Wurzbacher, Christian}, title = {Ecological function and biodiversity of aquatic fungi in lentic freshwater systems}, address = {Potsdam}, pages = {131 S.}, year = {2012}, language = {en} } @phdthesis{Wu2012, author = {Wu, Xu-Na}, title = {Functional characterization of AtSP1, a nutrient-induced receptor-like kinase}, address = {Potsdam}, pages = {112 S.}, year = {2012}, language = {en} } @phdthesis{Wu2017, author = {Wu, Si}, title = {Exploring the Arabidopsis metabolic landscape by genetic mapping integrated with network analysis}, school = {Universit{\"a}t Potsdam}, pages = {121}, year = {2017}, language = {en} } @phdthesis{Wu2010, author = {Wu, Anhui}, title = {Functional analysis of a H2O2-responsive transcription factor, JUB1, in the model plant Arabidopsis thaliana}, address = {Potsdam}, pages = {XVIII, 258 S.}, year = {2010}, language = {en} } @phdthesis{Wozniak2019, author = {Wozniak, Natalia Joanna}, title = {Convergent evolution of the selfing syndrome in the genus Capsella}, school = {Universit{\"a}t Potsdam}, pages = {229}, year = {2019}, language = {en} } @phdthesis{Wojciechowska2022, author = {Wojciechowska, Izabela}, title = {The journey towards the discovery of new protein-metabolite interactions in Arabidopsis thaliana and further functional characterization of selected binding events}, school = {Universit{\"a}t Potsdam}, pages = {150}, year = {2022}, language = {en} } @phdthesis{Wilczek2005, author = {Wilczek, Sabine}, title = {Spatial and seasonal distribution of extracellular enzyme activities in the River Elbe and their regulation by envirommental variables}, pages = {114 S. : Ill., graph. Darst.}, year = {2005}, language = {en} } @phdthesis{Wiemann2009, author = {Wiemann, Annika}, title = {Population genetics and social dynamics in harbour porpoises and bottlenose dolphins (Cetacea) : posibble implications for nature conservation}, address = {Potsdam}, pages = {173 S.}, year = {2009}, language = {en} } @phdthesis{Westphal2010, author = {Westphal, Kera}, title = {Analysis of the proteasome inhibitor-induced induction of antioxidative enzymes}, address = {Potsdam}, pages = {V, 103 Bl. : graph. Darst.}, year = {2010}, language = {en} } @phdthesis{Wenk2020, author = {Wenk, Sebastian}, title = {Engineering formatotrophic growth in Escherichia coli}, school = {Universit{\"a}t Potsdam}, pages = {V, 107}, year = {2020}, abstract = {To meet the demands of a growing world population while reducing carbon dioxide (CO2) emissions, it is necessary to capture CO2 and convert it into value-added compounds. In recent years, metabolic engineering of microbes has gained strong momentum as a strategy for the production of valuable chemicals. As common microbial feedstocks like glucose directly compete with human consumption, the one carbon (C1) compound formate was suggested as an alternative feedstock. Formate can be easily produced by various means including electrochemical reduction of CO2 and could serve as a feedstock for microbial production, hence presenting a novel entry point for CO2 to the biosphere and a storage option for excess electricity. Compared to the gaseous molecule CO2, formate is a highly soluble compound that can be easily handled and stored. It can serve as a carbon and energy source for natural formatotrophs, but these microbes are difficult to cultivate and engineer. In this work, I present the results of several projects that aim to establish efficient formatotrophic growth of E. coli - which cannot naturally grow on formate - via synthetic formate assimilation pathways. In the first study, I establish a workflow for growth-coupled metabolic engineering of E. coli. I demonstrate this approach by presenting an engineering scheme for the PFL-threonine cycle, a synthetic pathway for anaerobic formate assimilation in E. coli. The described methods are intended to create a standardized toolbox for engineers that aim to establish novel metabolic routes in E. coli and related organisms. The second chapter presents a study on the catalytic efficiency of C1-oxidizing enzymes in vivo. As formatotrophic growth requires generation of both energy and biomass from formate, the engineered E. coli strains need to be equipped with a highly efficient formate dehydrogenase, which provides reduction equivalents and ATP for formate assimilation. I engineered a strain that cannot generate reducing power and energy for cellular growth, when fed on acetate. Under this condition, the strain depends on the introduction of an enzymatic system for NADH regeneration, which could further produce ATP via oxidative phosphorylation. I show that the strain presents a valuable testing platform for C1-oxidizing enzymes by testing different NAD-dependent formate and methanol dehydrogenases in the energy auxotroph strain. Using this platform, several candidate enzymes with high in vivo activity, were identified and characterized as potential energy-generating systems for synthetic formatotrophic or methylotrophic growth in E. coli.   In the third chapter, I present the establishment of the serine threonine cycle (STC) - a synthetic formate assimilation pathway - in E. coli. In this pathway, formate is assimilated via formate tetrahydrofolate ligase (FtfL) from Methylobacterium extorquens (M. extorquens). The carbon from formate is attached to glycine to produce serine, which is converted into pyruvate entering central metabolism. Via the natural threonine synthesis and cleavage route, glycine is regenerated and acetyl-CoA is produced as the pathway product. I engineered several selection strains that depend on different STC modules for growth and determined key enzymes that enable high flux through threonine synthesis and cleavage. I could show that expression of an auxiliary formate dehydrogenase was required to achieve growth via threonine synthesis and cleavage on pyruvate. By overexpressing most of the pathway enzymes from the genome, and applying adaptive laboratory evolution, growth on glycine and formate was achieved, indicating the activity of the complete cycle. The fourth chapter shows the establishment of the reductive glycine pathway (rGP) - a short, linear formate assimilation route - in E. coli. As in the STC, formate is assimilated via M. extorquens FtfL. The C1 from formate is condensed with CO2 via the reverse reaction of the glycine cleavage system to produce glycine. Another carbon from formate is attached to glycine to form serine, which is assimilated into central metabolism via pyruvate. The engineered E. coli strain, expressing most of the pathway genes from the genome, can grow via the rGP with formate or methanol as a sole carbon and energy source.}, language = {en} } @phdthesis{Weiss2017, author = {Weiß, Lina}, title = {Understanding the emergence and maintenance of biodiversity in grasslands}, school = {Universit{\"a}t Potsdam}, pages = {153}, year = {2017}, language = {en} } @phdthesis{Weiss2011, author = {Weiß, Julia}, title = {Computer assisted proteomics in a systems biology context}, address = {Potsdam}, pages = {VIII, 138, XVII S.}, year = {2011}, language = {en} } @phdthesis{Weits2015, author = {Weits, Daniel}, title = {Regulation of the molecular response to low oxygen in plants}, school = {Universit{\"a}t Potsdam}, pages = {113}, year = {2015}, language = {en} } @phdthesis{Weckwerth2006, author = {Weckwerth, Wolfram}, title = {Development and applications of mass spectrometric techniques in plant physiology, biochemistry and systems biology : quantifying the molecular phenotype}, address = {Potsdam}, pages = {75, 50 S. : graph. Darst.}, year = {2006}, language = {en} } @phdthesis{Wasiolka2007, author = {Wasiolka, Bernd}, title = {The impact of overgrazing on reptile diversity and population dynamics of Pedioplanis l. lineoocellata in the southern Kalahari}, publisher = {Univ.-Verl.}, address = {Potsdam}, pages = {v, 101 BL. : Ill., graph. Darst.}, year = {2007}, language = {en} } @phdthesis{Wanner2000, author = {Wanner, Susanne C.}, title = {Transport, retention, and turnover of particulate organic matter (POM) in the lowland River Spree (Germany)}, pages = {101 S.}, year = {2000}, language = {en} } @phdthesis{Wang2022, author = {Wang, Yang}, title = {Role of the actin cytoskeleton in cellular morphogenesis at the shoot apical meristem of Arabidopsis thaliana}, doi = {10.25932/publishup-55908}, school = {Universit{\"a}t Potsdam}, pages = {130}, year = {2022}, abstract = {The morphogenesis of sessile plants is mainly driven by directional cell growth and cell division. The organization of their cytoskeleton and the mechanical properties of the cell wall greatly influence morphogenetic events in plants. It is well known that cortical microtubules (CMTs) contribute to directional growth by regulating the deposition of the cellulose microfibrils, as major cell wall fortifying elements. More recent findings demonstrate that mechanical stresses existing in cells and tissues influence microtubule organization. Also, in dividing cells, mechanical stress directions contribute to the orientation of the new cell wall. In comparison to the microtubule cytoskeleton, the role of the actin cytoskeleton in regulating shoot meristem morphogenesis has not been extensively studied. This thesis focuses on the functional relevance of the actin cytoskeleton during cell and tissue scale morphogenesis in the shoot apical meristem (SAM) of Arabidopsis thaliana. Visualization of transcriptional reporters indicates that ACTIN2 and ACTIN7 are two highly expressed actin genes in the SAM. A link between the actin cytoskeleton and SAM development derives from the observation that the act2-1 act7-1 double mutant has abnormal cell shape and perturbed phyllotactic patterns. Live-cell imaging of the actin cytoskeleton further shows that its organization correlates with cell shape, which indicates a potential role of actin in influencing cellular morphogenesis. In this thesis, a detailed characterization of the act2-1 act7-1 mutant reveals that perturbation of actin leads to more rectangular cellular geometries with more 90° cell internal angles, and higher incidences of four-way junctions (four cell boundaries intersecting together). This observation deviates from the conventional tricellular junctions found in epidermal cells. Quantitative cellular-level growth data indicates that such differences in the act2-1 act7-1 mutant arise due to the reduced accuracy in the placement of the new cell wall, as well as its mechanical maturation. Changes in cellular morphology observed in the act2-1 act7-1 mutant result in cell packing defects that subsequently compromise the flow of information among cells in the SAM.}, language = {en} } @phdthesis{Wang2013, author = {Wang, Ting}, title = {A novel R2R3 MYB-like transcription factor regulates ABA mediated stress response and leaf growth in Arabidopsis}, address = {Potsdam}, pages = {102 S.}, year = {2013}, language = {en} } @phdthesis{Wandrey2003, author = {Wandrey, Maren}, title = {Molecular and cell biological characterisaton of voltage dependent anion channels and symbiosome membrane proteome analysis in lotus japonicus and Glycine max}, pages = {107 S.}, year = {2003}, language = {en} } @phdthesis{Walther2012, author = {Walther, Dirk}, title = {Bioinformatics studies of biological systems across multiple levels of molecular organization}, address = {Potsdam}, pages = {124 S.}, year = {2012}, language = {en} } @phdthesis{Wagner2007, author = {Wagner, Kerstin}, title = {The regulation of phopholipase activity by lipid membrane structure}, address = {Potsdam}, pages = {105 S. :graph. Darst.}, year = {2007}, language = {en} } @phdthesis{Vyse2022, author = {Vyse, Kora}, title = {Elucidating molecular determinants of the loss of freezing tolerance during deacclimation after cold priming and low temperature memory after triggering}, school = {Universit{\"a}t Potsdam}, pages = {vii, 147}, year = {2022}, abstract = {W{\"a}hrend ihrer Entwicklung m{\"u}ssen sich Pflanzen an Temperaturschwankungen anpassen. Niedrige Temperaturen {\"u}ber dem Gefrierpunkt induzieren in Pflanzen eine K{\"a}lteakklimatisierung und h{\"o}here Frosttoleranz, die sich bei w{\"a}rmeren Temperaturen durch Deakklimatisierung wieder zur{\"u}ckbildet. Der Wechsel zwischen diesen beiden Prozessen ist f{\"u}r Pflanzen unerl{\"a}sslich, um als Reaktion auf unterschiedliche Temperaturbedingungen eine optimale Fitness zu erreichen. Die K{\"a}lteakklimatisierung ist umfassend untersucht worden,{\"u}ber die Regulierung der Deakklimatisierung ist jedoch wenig bekannt. In dieser Arbeit wird der Prozess der Deakklimatisierung auf physiologischer und molekularer Ebene in Arabidopsis thaliana untersucht. Messungen des Elektrolytverlustes w{\"a}hrend der K{\"a}lteakklimatisierung und bis zu vier Tagen nach Deakklimatisierung erm{\"o}glichten die Identifizierung von vier Knockout-Mutanten (hra1, lbd41, mbf1c und jub1), die im Vergleich zum Wildtyp eine langsamere Deakklimatisierungsrate aufwiesen. Eine transkriptomische Studie mit Hilfe von RNA-Sequenzierung von A. thaliana Col-0, jub1 und mbf1c zeigte die Bedeutung der Hemmung von stressreaktiven und Jasmonat-ZIM-Dom{\"a}nen-Genen sowie die Regulierung von Zellwandmodifikationen w{\"a}hrend der Deakklimatisierung. Dar{\"u}ber hinaus zeigten Messungen der Alkoholdehydrogenase Aktivit{\"a}t und der Genexpressions{\"a}nderungen von Hypoxiemarkern w{\"a}hrend der ersten vier Tagen der Deakklimatisierung, dass eine Hypoxie-Reaktion w{\"a}hrend der Deakklimatisierung aktiviert wird. Es wurde gezeigt, dass die epigenetische Regulierung w{\"a}hrend der K{\"a}lteakklimatisierung und der 24-st{\"u}ndigen Deakklimatisierung in A. thaliana eine große Rolle spielt. Dar{\"u}ber hinaus zeigten beide Deakklimatisierungsstudien, dass die fr{\"u}here Hypothese, dass Hitzestress eine Rolle bei der fr{\"u}hen Deakklimatisierung spielen k{\"o}nnte, unwahrscheinlich ist. Eine Reihe von DNA- und Histondemethylasen sowie Histonvarianten wurden w{\"a}hrend der Deakklimatisierung hochreguliert, was auf eine Rolle im pflanzlichen Ged{\"a}chtnis schließen l{\"a}sst. In j{\"u}ngster Zeit haben mehrere Studien gezeigt, dass Pflanzen in der Lage sind, die Erinnerung an einen vorangegangenen K{\"a}ltestress auch nach einer Woche Deakklimatisierung zu bewahren. In dieser Arbeit ergaben Transkriptom- und Metabolomanalysen von Arabidopsis w{\"a}hrend 24 Stunden Priming (K{\"a}lteakklimatisierung) und Triggering (wiederkehrender K{\"a}ltestress nach Deakklimatisierung) eine unikale signifikante und vor{\"u}bergehende Induktion der Transkriptionsfaktoren DREB1D, DREB1E und DREB1F w{\"a}hrend des Triggerings, die zur Feinabstimmung der zweiten K{\"a}ltestressreaktion beitr{\"a}gt. Dar{\"u}ber hinaus wurden Gene, die f{\"u}r Late Embryogenesis Abundant (LEA) und Frostschutzproteine kodieren, sowie Proteine, die reaktive Sauerstoffspezies entgiften, w{\"a}hrend des sp{\"a}ten Triggerings (24 Stunden) st{\"a}rker induziert als nach dem ersten K{\"a}lteimpuls, w{\"a}hrend Xyloglucan- Endotransglucosylase/Hydrolase Gene, deren Produkte f{\"u}r eine Restrukturierung der Zellwand verantwortlich sind, fr{\"u}h auf das Triggering reagierten. Die starke Induktion dieser Gene, sowohl bei der Deakklimatisierung als auch beim Triggering, l{\"a}sst vermuten, dass sie eine wesentliche Rolle bei der Stabilisierung der Zellen w{\"a}hrend des Wachstums und bei der Reaktion auf wiederkehrende Stressbedingungen spielen. Zusammenfassend gibt diese Arbeit neue Einblicke in die Regulierung der Deakklimatisierung und des K{\"a}ltestress-Ged{\"a}chtnisses in A. thaliana und er{\"o}ffnet neue M{\"o}glichkeiten f{\"u}r k{\"u}nftige, gezielte Studien von essentiellen Genen in diesem Prozess.}, language = {en} } @phdthesis{vonDeuster2010, author = {von Deuster, Carola}, title = {Simulations on several scales: Studies on protein-ligand binding kinetics and on the antimicrobial peptide NK-2}, address = {Potsdam}, pages = {131 S.}, year = {2010}, language = {en} } @phdthesis{vonBismarck2023, author = {von Bismarck, Thekla}, title = {The influence of long-term light acclimation on photosynthesis in dynamic light}, school = {Universit{\"a}t Potsdam}, pages = {x, 163}, year = {2023}, abstract = {Photosynthesis converts light into metabolic energy which fuels plant growth. In nature, many factors influence light availability for photosynthesis on different time scales, from shading by leaves within seconds up to seasonal changes over months. Variability of light energy supply for photosynthesis can limit a plant´s biomass accumulation. Plants have evolved multiple strategies to cope with strongly fluctuation light (FL). These range from long-term optimization of leaf morphology and physiology and levels of pigments and proteins in a process called light acclimation, to rapid changes in protein activity within seconds. Therefore, uncovering how plants deal with FL on different time scales may provide key ideas for improving crop yield. Photosynthesis is not an isolated process but tightly integrates with metabolism through mutual regulatory interactions. We thus require mechanistic understanding of how long-term light acclimation shapes both, dynamic photosynthesis and its interactions with downstream metabolism. To approach this, we analyzed the influence of growth light on i) the function of known rapid photosynthesis regulators KEA3 and VCCN1 in dynamic photosynthesis (Chapter 2-3) and ii) the interconnection of photosynthesis with photorespiration (PR; Chapter 4). We approached topic (i) by quantifying the effect of different growth light regimes on photosynthesis and photoprotection by using kea3 and vccn1 mutants. Firstly, we found that, besides photosynthetic capacity, the activities of VCCN1 and KEA3 during a sudden high light phase also correlated with growth light intensity. This finding suggests regulation of both proteins by the capacity of downstream metabolism. Secondly, we showed that KEA3 accelerated photoprotective non-photochemical quenching (NPQ) kinetics in two ways: Directly via downregulating the lumen proton concentration and thereby de-activating pH-dependent NPQ, and indirectly via suppressing accumulation of the photoprotective pigment zeaxanthin. For topic (ii), we analyzed the role of PR, a process which recycles a toxic byproduct of the carbon fixation reactions, in metabolic flexibility in a dynamically changing light environment. For this we employed the mutants hpr1 and ggt1 with a partial block in PR. We characterized the function of PR during light acclimation by tracking molecular and physiological changes of the two mutants. Our data, in contrast to previous reports, disprove a generally stronger physiological relevance of PR under dynamic light conditions. Additionally, the two different mutants showed pronounced and distinct metabolic changes during acclimation to a condition inducing higher photosynthetic activity. This underlines that PR cannot be regarded purely as a cyclic detoxification pathway for 2PG. Instead, PR is highly interconnected with plant metabolism, with GGT1 and HPR1 representing distinct metabolic modulators. In summary, the presented work provides further insight into how energetic and metabolic flexibility is ensured by short-term regulators and PR during long-term light acclimation.}, language = {en} } @phdthesis{vonBendaBeckmann2008, author = {von Benda-Beckmann, Alexander Michael}, title = {Galaxies and environment from voids to groups}, pages = {139 S.}, year = {2008}, language = {en} } @phdthesis{Vigeolas2004, author = {Vigeolas, Helene}, title = {Regulation of triacylglycerol biosynthesis in developing seeds of Brassica napus L. and Arabidopsis thaliana (L.) Heyn}, pages = {108 S. : graph. Darst.}, year = {2004}, language = {en} } @phdthesis{Verbancic2021, author = {Verbancic, Jana}, title = {Carbon supply and the regulation of primary cell wall synthesis in Arabidopsis thaliana}, school = {Universit{\"a}t Potsdam}, pages = {x, 179}, year = {2021}, abstract = {Cellulose is the most abundant biopolymer on Earth and cell wall (CW) synthesis is one of the major carbon consumers in the plant cell. Structure and several interaction partners of plasma membrane (PM)-bound cellulose synthase (CESA) complexes, CSCs, have been studied extensively, but much less is understood about the signals that activate and translocate CESAs to the PM and how exactly cellulose synthesis is being regulated during the diel cycle. The literature describes CSC regulation possibilities through interactions with accessory proteins upon stress conditions (e.g. CC1), post-translational modifications that regulate CSC speed and their possible anchoring in the PM (e.g. with phosphorylation and S-acylation, respectively). In this thesis, 13CO2 labeling and imaging techniques were employed in the same Arabidopsis seedling growth system to elucidate how and when new carbon is incorporated into cell wall (CW) sugars and UDP-glucose, and to follow CSC behavior during the diel cycle. Additionally, an ubiquitination analysis was performed to investigate a possible mechanism to affect CSC trafficking to and/or from the PM. Carbon is being incorporated into CW glucose at a 3-fold higher rate during the light period in comparison to the night in wild-type seedlings. Furthermore, CSC density at the PM, as an indication of active cellulose synthesizing machinery, is increasing in the light and falling during the night, showing that CW biosynthesis is more active in the light. Therefore, CW synthesis might be regulated by the carbon status of the cell. This regulation is broken in the starchless pgm mutant where light and dark carbon incorporation rates into CW glucose are similar, possibly due to the high soluble sugar content in pgm during the first part of the night. Strikingly, pgm CSC abundance at the PM is constantly low during the whole diel cycle, indicating little or no cellulose synthesis, but can be restored with exogenous sucrose or a longer photoperiod. Ubiquitination was explored as a possible regulating mechanism for translocation of primary CW CSCs from the PM and several potential ubiquitination sites have been identified.. The approach in this thesis enabled to study cellulose/CW synthesis from different angles but in the same growth system, allowing direct comparison of those methodologies, which could help understand the relationship between the amount of available carbon in a plant cell and the cells capacity to synthesize cellulose/CW. Understanding which factors contribute to cellulose synthesis regulation and addressing those fundamental questions can provide essential knowledge to manage the need for increased crop production.}, language = {en} } @phdthesis{Vasilevski2012, author = {Vasilevski, Aleksandar}, title = {Research in pectin synthesis by analysing the seed coat mucilage}, address = {Potsdam}, pages = {134 S.}, year = {2012}, language = {en} } @phdthesis{Vandrich2019, author = {Vandrich, Jasmina}, title = {Metabolic Engineering in Halomonas elongata}, school = {Universit{\"a}t Potsdam}, pages = {80}, year = {2019}, language = {en} } @phdthesis{Vakeel2006, author = {Vakeel, Padmanabhan}, title = {Biochemical and cellular characterization of filamin binding proteins in cross striated muscle}, address = {Potsdam}, pages = {XV, 156 Bl. : graph. Darst.}, year = {2006}, language = {en} } @phdthesis{Uttamchand2012, author = {Uttamchand, Narendra Kumar}, title = {Shape-memory properties of magnetically active compositives based on multiphase polymer networks}, address = {Potsdam}, pages = {XI, 113 S.}, year = {2012}, language = {en} } @phdthesis{UlbrichtJones2017, author = {Ulbricht-Jones, Elena Sofia}, title = {The virescent and narrow leaf phenotype of a plastome-genome-incompatible Oenothera hybrid is associated with the plastid gene accD and fatty acid synthesis}, school = {Universit{\"a}t Potsdam}, pages = {124}, year = {2017}, language = {en} } @phdthesis{Uflewski2021, author = {Uflewski, Michal}, title = {Characterizing the regulation of proton antiport across the thylakoid membrane}, school = {Universit{\"a}t Potsdam}, pages = {122}, year = {2021}, abstract = {Die Energie, die zum Antrieb photochemischer Reaktionen ben{\"o}tigt wird, stammt aus der Ladungstrennung an der Thylakoidmembran. Aufrgrund des Unterschieds in der Protonenkonzentration zwischen dem Stroma der Chloroplasten und dem Thylakoidlumen wird eine Protonenmotorische Kraft (pmf) erzeugt. Die pmf setzt sich aus dem Protonengradienten (ΔpH) und dem Membranpotential (ΔΨ) zusammen, die gemeinsam die ATP-Synthese antreiben. In der Natur schwankt die Energiemenge, die die Photosynthese antreibt, aufgrund h{\"a}ufiger {\"A}nderungen der Lichtintensit{\"a}t. Der Thylakoid-Ionentransport kann den Energiefluss durch einen Photosyntheseapparat an die Lichtverf{\"u}gbarkeit anpassen, indem er die pmf-Zusammensetzung ver{\"a}ndert. Die Dissipation von ΔΨ verringert die Ladungsrekombination am Photosystem II, so dass ein Anstieg der ΔpH-Komponente eine R{\"u}ckkopplung zur Herabregulierung der Photosynthese ausl{\"o}sen kann. Der durch den K+-Austausch-Antiporter 3 (KEA3) gesteuerte K+/H+-Antiport reduziert den ΔpH-Anteil von pmf und d{\"a}mpft dadurch das nicht-photochemische Quenching (NPQ). Infolgedessen erh{\"o}ht sich die Photosyntheseeffizienz beim {\"U}bergang zu geringerer Lichtintensit{\"a}t. Ziel dieser Arbeit war es, Antworten auf Fragen zur Regulierung der KEA3-Aktivit{\"a}t und ihrer Rolle in der Pflanzenentwicklung zu finden. Die vorgestellten Daten zeigen, dass KEA3 in Pflanzen, denen der Chloroplasten-ATP-Synthase-Assembly-Faktor CGL160 fehlt und die eine verminderte ATP-Synthase-Aktivit{\"a}t aufweisen, eine zentrale Rolle bei der Regulierung der Photosynthese und des Pflanzenwachstums unter station{\"a}ren Bedingungen spielt. Das Fehlen von KEA3 in der cgl160-Mutante f{\"u}hrt zu einer starken Beeintr{\"a}chtigung des Wachstums, da die Photosynthese aufgrund des erh{\"o}hten pH-abh{\"a}ngigen NPQs und des verringerten Elektronenflusses durch den Cytochrom b6f-Komplex eingeschr{\"a}nkt ist. Die {\"U}berexpression von KEA3 in der cgl160-Mutante erh{\"o}ht die Ladungsrekombination im Photosystem II und f{\"o}rdert die Photosynthese. In Zeiten geringer ATP-Synthase-Aktivit{\"a}t profitieren die Pflanzen also von der KEA3-Aktivit{\"a}t. KEA3 unterliegt einer Dimerisierung {\"u}ber seinen regulatorischen C-Terminus (RCT). Der RCT reagiert auf Ver{\"a}nderungen der Lichtintensit{\"a}t, da die Pflanzen, die KEA3 ohne diese Dom{\"a}ne exprimieren, einen reduzierten Lichtschutzmechanismus bei Lichtintensit{\"a}tsschwankungen aufweisen. Allerdings fixieren diese Pflanzen w{\"a}hrend der Photosynthese-Induktionsphase mehr Kohlenstoff als Gegenleistung f{\"u}r einen langfristigen Photoprotektor, was die regulierende Rolle von KEA3 in der Pflanzenentwicklung zeigt. Der KEA3-RCT ist dem Thylakoidstroma zugewandt, so dass seine Regulierung von lichtinduzierten Ver{\"a}nderungen in der Stroma-Umgebung abh{\"a}ngt. Die Regulierung der KEA3-Aktivit{\"a}t {\"u}berschneidet sich mit den pH-{\"A}nderungen im Stroma, die bei Lichtschwankungen auftreten. Es hat sich gezeigt, dass ATP und ADP eine Affinit{\"a}t zum heterolog exprimierten KEA3 RCT haben. Eine solche Wechselwirkung verursacht Konformations{\"a}nderungen in der RCT-Struktur. Die Faltung der RCT-Liganden-Interaktion h{\"a}ngt vom pH-Wert der Umgebung ab. Mit einer Kombination aus Bioinformatik und In-vitro-Ansatz wurde die ATP-Bindungsstelle am RCT lokalisiert. Das Einf{\"u}gen einer Punktmutation in der KEA3-RCT Bindungsstelle in planta f{\"u}hrte zu einer Deregulierung der Antiporteraktivit{\"a}t beim {\"U}bergang zu wenig Licht. Die in dieser Arbeit vorgestellten Daten erm{\"o}glichten es uns, die Rolle von KEA3 bei der Anpassung der Photosynthese umfassender zu bewerten und Modelle zur Regulierung der KEA3-Aktivit{\"a}t w{\"a}hrend des {\"U}bergangs zwischen verschiedenen Lichtintensit{\"a}ten vorzuschlagen.}, language = {en} } @phdthesis{Tung2021, author = {Tung, Wing Tai}, title = {Polymeric fibrous scaffold on macro/microscale towards tissue regeneration}, school = {Universit{\"a}t Potsdam}, year = {2021}, language = {en} } @phdthesis{Tschoep2009, author = {Tschoep, Hendrik}, title = {The response of growth and primary metabolism to a mild but sustained nitrogen limitation in arabidopsis thaliana}, address = {Potsdam}, pages = {176 S.}, year = {2009}, language = {en} } @phdthesis{Tong2019, author = {Tong, Hao}, title = {Dissection of genetic architecture of intermediate phenotypes and predictions in plants}, school = {Universit{\"a}t Potsdam}, pages = {127}, year = {2019}, abstract = {Determining the relationship between genotype and phenotype is the key to understand the plasticity and robustness of phenotypes in nature. While the directly observable plant phenotypes (e.g. agronomic, yield and stress resistance traits) have been well-investigated, there is still a lack in our knowledge about the genetic basis of intermediate phenotypes, such as metabolic phenotypes. Dissecting the links between genotype and phenotype depends on suitable statistical models. The state-of-the-art models are developed for directly observable phenotypes, regardless the characteristics of intermediate phenotypes. This thesis aims to fill the gaps in understanding genetic architecture of intermediate phenotypes, and how they tie to composite traits, namely plant growth. The metabolite levels and reaction fluxes, as two aspects of metabolic phenotypes, are shaped by the interrelated chemical reactions formed in genome-scale metabolic network. Here, I attempt to answer the question: Can the knowledge of underlying genome-scale metabolic network improve the model performance for prediction of metabolic phenotypes and associated plant growth? To this end, two projects are investigated in this thesis. Firstly, we propose an approach that couples genomic selection with genome-scale metabolic network and metabolic profiles in Arabidopsis thaliana to predict growth. This project is the first integration of genomic data with fluxes predicted based on constraint-based modeling framework and data on biomass composition. We demonstrate that our approach leads to a considerable increase of prediction accuracy in comparison to the state-of-the-art methods in both within and across environment predictions. Therefore, our work paves the way for combining knowledge on metabolic mechanisms in the statistical approach underlying genomic selection to increase the efficiency of future plant breeding approaches. Secondly, we investigate how reliable is genomic selection for metabolite levels, and which single nucleotide polymorphisms (SNPs), obtained from different neighborhoods of a given metabolic network, contribute most to the accuracy of prediction. The results show that the local structure of first and second neighborhoods are not sufficient for predicting the genetic basis of metabolite levels in Zea mays. Furthermore, we find that the enzymatic SNPs can capture most the genetic variance and the contribution of non-enzymatic SNPs is in fact small. To comprehensively understand the genetic architecture of metabolic phenotypes, I extend my study to a local Arabidopsis thaliana population and their hybrids. We analyze the genetic architecture in primary and secondary metabolism as well as in growth. In comparison to primary metabolites, compounds from secondary metabolism were more variable and show more non-additive inheritance patterns which could be attributed to epistasis. Therefore, our study demonstrates that heterozygosity in local Arabidopsis thaliana population generates metabolic variation and may impact several tasks directly linked to metabolism. The studies in this thesis improve the knowledge of genetic architecture of metabolic phenotypes in both inbreed and hybrid population. The approaches I proposed to integrate genome-scale metabolic network with genomic data provide the opportunity to obtain mechanistic insights about the determinants of agronomically important polygenic traits.}, language = {en} } @phdthesis{Ting2021, author = {Ting, Michael Kien Yin}, title = {Circadian-regulated dynamics of translation in Arabidopsis thaliana}, school = {Universit{\"a}t Potsdam}, pages = {130}, year = {2021}, language = {en} } @phdthesis{Timofeeva2015, author = {Timofeeva, Nadezda}, title = {Effect of ions and amino-acid sequence on collagen structure}, school = {Universit{\"a}t Potsdam}, pages = {121}, year = {2015}, language = {en} } @phdthesis{Tiller2011, author = {Tiller, Nadine}, title = {Plastid translation : functions of plastid-specific ribosomal proteins and identification of a factor mediating plastid-to-nucleus retrograde sifnalling}, address = {Potsdam}, pages = {122 S.}, year = {2011}, language = {en} } @phdthesis{Tietjen2008, author = {Tietjen, Briit-Kristien}, title = {Drylands under climate change : a novel ecohydrological modelling approach}, address = {Potsdam}, pages = {IV, 141 S. : Ill., graph. Darst., Kt.}, year = {2008}, language = {en} } @phdthesis{Thirumalaikumar2019, author = {Thirumalaikumar, Venkatesh P.}, title = {Investigating drought and heat stress regulatory networks in Arabidopsis and tomato}, school = {Universit{\"a}t Potsdam}, pages = {154}, year = {2019}, language = {en} } @phdthesis{Thieme2015, author = {Thieme, Christoph J.}, title = {Sequence and structure determinants of microRNA maturation and the elucidation of RNA transport in plants}, school = {Universit{\"a}t Potsdam}, pages = {137}, year = {2015}, language = {en} } @phdthesis{Thalhammer2012, author = {Thalhammer, Anja}, title = {Physiological, functional and structural characterization of five closely related COR/LEA (COld Regulated/Late Embroygenesis Abundant) proteins from Arabidopsis thaliana (L.)}, address = {Potsdam}, pages = {137 S.}, year = {2012}, language = {en} } @phdthesis{Tews2003, author = {Tews, J{\"o}rg}, title = {The impact of climate change and land use on woody plants in semiarid savanna : modelling shrub population dynamics in the southern kalahari}, pages = {98 S.}, year = {2003}, language = {en} } @phdthesis{Taube2019, author = {Taube, Robert}, title = {Characterisations of Fungal Communities in Temperate Lakes}, school = {Universit{\"a}t Potsdam}, pages = {139}, year = {2019}, language = {en} } @phdthesis{Tartivel2013, author = {Tartivel, Lucile}, title = {Design of hydrogels with inverse shape-memory function for biomedical applications}, address = {Potsdam}, pages = {150 S.}, year = {2013}, language = {en} } @phdthesis{Tabatabaei2017, author = {Tabatabaei, Iman}, title = {Development of new selection systems for organellar genome transformation}, school = {Universit{\"a}t Potsdam}, pages = {II, 152}, year = {2017}, abstract = {Plant cells host two important organelles: mitochondria, known as the cell's 'powerhouse', which act by converting oxygen and nutrients into ATP, and plastids, which perform photosynthesis. These organelles contain their own genomes that encode proteins required for gene expression and energy metabolism. Transformation technologies offer great potential for investigating all aspects of the physiology and gene expression of these organelles in vivo. In addition, organelle transformation can be a valuable tool for biotechnology and molecular plant breeding. Plastid transformation systems are well-developed for a few higher plants, however, mitochondrial transformation has so far only been reported for Saccharomyces cerevisiae and the unicellular alga Chlamydomonas reinhardtii. Development of an efficient new selection marker for plastid transformation is important for several reasons, including facilitating supertransformation of the plastid genome for metabolic engineering purposes and for producing multiple knock-outs or site-directed mutagenesis of two unlinked genes. In this work, we developed a novel selection system for Nicotiana tabacum (tobacco) chloroplast transformation with an alternative marker. The marker gene, aac(6′)-Ie/aph(2′′)-Ia, was cloned into different plastid transformation vectors and several candidate aminoglycoside antibiotics were investigated as selection agents. Generally, the efficiency of selection and the transformation efficiency with aac(6′)-Ie/aph(2′′)-Ia as selectable marker in combination with the aminoglycoside antibiotic tobramycin was similarly high as that with the standard marker gene aadA and spectinomycin selection. Furthermore, our new selection system may be useful for the development of plastid transformation for new species, including cereals, the world's most important food crops, and could also be helpful for the establishment of a selection system for mitochondrial transformation. To date, all attempts to achieve mitochondrial transformation for higher plants have been unsuccessful. A mitochondrial transformation system for higher plants would not only provide a potential for studying mitochondrial physiology but could also provide a method to introduce cytoplasmic male sterility into crops to produce hybrid seeds. Establishing a stable mitochondrial transformation system in higher plants requires several steps including delivery of foreign DNA, stable integration of the foreign sequences into the mitochondrial genome, efficient expression of the transgene, a highly regenerable tissue culture system that allows regeneration of the transformed cells into plants, and finally, a suitable selection system to identify cells with transformed mitochondrial genomes. Among all these requirements, finding a good selection is perhaps the most important obstacle towards the development of a mitochondrial transformation system for higher plants. In this work, two selection systems were tested for mitochondrial transformation: kanamycin as a selection system in combination with the antibiotic-inactivating marker gene nptII, and sulfadiazine as a selection agent that inhibits the folic acid biosynthesis pathway residing in plant mitochondria in combination with the sul gene encoding an enzyme that is insensitive to inhibition by sulfadiazine. Nuclear transformation experiments were considered as proof of the specificity of the sulfadiazine selection system for mitochondria. We showed that an optimized sulfadiazine selection system, with the Sul protein targeted to mitochondria, is much more efficient than the previous sulfadiazine selection system, in which the Sul protein was targeted to the chloroplast. We also showed by systematic experiments that the efficiency of selection and nuclear transformation of the optimized sulfadiazine selection was higher compared to the standard kanamycin selection system. Finally, we also investigated the suitability of this selection system for nuclear transformation of the model alga Chlamydomonas reinhardtii, obtaining promising results. Although we designed several mitochondrial transformation vectors with different expression elements and integration sites in the mitochondrial genome based on the sulfadiazine system, and different tissue culture condition were also considered, we were not able to obtain mitochondrial transformation with this system. Nonetheless, establishing the sul gene as an efficient and specific selection marker for mitochondria addresses one of the major bottlenecks and may pave the way to achieve mitochondrial transformation in higher plants.}, language = {en} } @phdthesis{Szekely2024, author = {Sz{\´e}kely, Andr{\´a}s Csaba}, title = {Long-distance circadian coordination via a phloem-delivered mobile transcript}, school = {Universit{\"a}t Potsdam}, pages = {105}, year = {2024}, language = {en} } @phdthesis{Szymanski2009, author = {Szymanski, Jedrzej}, title = {Integration of correlative relationships in metabolic and transcript data from model organisms : arabidopsis thaliana and escherichia coli}, address = {Potsdam}, pages = {XIII, 137 S. : graph. Darst.}, year = {2009}, language = {en} } @phdthesis{Szecowka2011, author = {Szec{\´o}wka, Marek}, title = {Metabolic fluxes in photosynthetic and heterotrophic plant tissues}, address = {Potsdam}, pages = {XII, 145 S.}, year = {2011}, language = {en} } @phdthesis{Swiadek2015, author = {Swiadek, Magdalena Agnieszka}, title = {Hybrid necrosis in local populations of Arabidopsis thaliana}, school = {Universit{\"a}t Potsdam}, pages = {109}, year = {2015}, language = {en} } @phdthesis{Swart2017, author = {Swart, Corn{\´e}}, title = {Managing protein activity in A. thaliana}, school = {Universit{\"a}t Potsdam}, pages = {160}, year = {2017}, language = {en} } @phdthesis{Sviben2016, author = {Sviben, Sanja}, title = {Calcite biomineralization in coccolithophores}, school = {Universit{\"a}t Potsdam}, pages = {119}, year = {2016}, language = {en} } @phdthesis{Sun2011, author = {Sun, Xiaoliang}, title = {Towards understanding the dynamics of biological systems from -Omics data}, address = {Potsdam}, pages = {114 S.}, year = {2011}, language = {en} } @phdthesis{Suchoszek2017, author = {Suchoszek, Monika}, title = {Characterization of inducible galactolipid biosynthesis mutants in tobacco}, school = {Universit{\"a}t Potsdam}, pages = {116}, year = {2017}, abstract = {Chloroplast membranes have a unique composition characterized by very high contents of the galactolipids, MGDG and DGDG. Many studies on constitutive, galactolipid-deficient mutants revealed conflicting results about potential functions of galactolipids in photosynthetic membranes. Likely, this was caused by pleiotropic effects such as starvation artefacts because of impaired photosynthesis from early developmental stages of the plants onward. Therefore, an ethanol inducible RNAi-approach has been taken to suppress two key enzymes of galactolipid biosynthesis in the chloroplast, MGD1 and DGD1. Plants were allowed to develop fully functional source leaves prior to induction, which then could support plant growth. Then, after the ethanol induction, both young and mature leaves were investigated over time. Our studies revealed similar changes in both MGDG- and DGDG-deficient lines, however young and mature leaves of transgenic lines showed a different response to galactolipid deficiency. While no changes of photosynthetic parameters and minor changes in lipid content were observed in mature leaves of transgenic lines, strong reductions in total chlorophyll content and in the accumulation of all photosynthetic complexes and significant changes in contents of various lipid groups occurred in young leaves. Microscopy studies revealed an appearance of lipid droplets in the cytosol of young leaves in all transgenic lines which correlates with significantly higher levels of TAGs. Since in young leaves the production of membrane lipids is lowered, the excess of fatty acids is used for storage lipids production, resulting in the accumulation of TAGs. Our data indicate that both investigated galactolipids serve as structural lipids since changes in photosynthetic parameters were mainly the result of reduced amounts of all photosynthetic constituents. In response to restricted galactolipid synthesis, thylakoid biogenesis is precisely readjusted to keep the proper stoichiometry and functionality of the photosynthetic apparatus. Ultimately, the data revealed that downregulation of one galactolipid triggers changes not only in chloroplasts but also in the nucleus as shown by downregulation of nuclear encoded subunits of the photosynthetic complexes.}, language = {en} } @phdthesis{Stoessel2018, author = {St{\"o}ßel, Daniel}, title = {Biomarker Discovery in Multiple Sclerosis and Parkinson's disease}, school = {Universit{\"a}t Potsdam}, pages = {135}, year = {2018}, abstract = {Neuroinflammatory and neurodegenerative diseases such as Parkinson's (PD) and multiple sclerosis (MS) often result in a severe impairment of the patient´s quality of life. Effective therapies for the treatment are currently not available, which results in a high socio-economic burden. Due to the heterogeneity of the disease subtypes, stratification is particularly difficult in the early phase of the disease and is mainly based on clinical parameters such as neurophysiological tests and central nervous imaging. Due to good accessibility and stability, blood and cerebrospinal fluid metabolite markers could serve as surrogates for neurodegenerative processes. This can lead to an improved mechanistic understanding of these diseases and further be used as "treatment response" biomarkers in preclinical and clinical development programs. Therefore, plasma and CSF metabolite profiles will be identified that allow differentiation of PD from healthy controls, association of PD with dementia (PDD) and differentiation of PD subtypes such as akinetic rigid and tremor dominant PD patients. In addition, plasma metabolites for the diagnosis of primary progressive MS (PPMS) should be investigated and tested for their specificity to relapsing-remitting MS (RRMS) and their development during PPMS progression. By applying untargeted high-resolution metabolomics of PD patient samples and in using random forest and partial least square machine learning algorithms, this study identified 20 plasma metabolites and 14 CSF metabolite biomarkers. These differentiate against healthy individuals with an AUC of 0.8 and 0.9 in PD, respectively. We also identify ten PDD specific serum metabolites, which differentiate against healthy individuals and PD patients without dementia with an AUC of 1.0, respectively. Furthermore, 23 akinetic-rigid specific plasma markers were identified, which differentiate against tremor-dominant PD patients with an AUC of 0.94 and against healthy individuals with an AUC of 0.98. These findings also suggest more severe disease pathology in the akinetic-rigid PD than in tremor dominant PD. In the analysis of MS patient samples a partial least square analysis yielded predictive models for the classification of PPMS and resulted in 20 PPMS specific metabolites. In another MS study unknown changes in human metabolism were identified after administration of the multiple sclerosis drug dimethylfumarate, which is used for the treatment of RRMS. These results allow to describe and understand the hitherto completely unknown mechanism of action of this new drug and to use these findings for the further development of new drugs and targets against RRMS. In conclusion, these results have the potential for improved diagnosis of these diseases and improvement of mechanistic understandings, as multiple deregulated pathways were identified. Moreover, novel Dimethylfumarate targets can be used to aid drug development and treatment efficiency. Overall, metabolite profiling in combination with machine learning identified as a promising approach for biomarker discovery and mode of action elucidation.}, language = {en} } @phdthesis{StoofLeichsenring2011, author = {Stoof-Leichsenring, Kathleen Rosemarie}, title = {Genetic analysis of diatoms and rotifers in tropical Kenyan lake sediments}, address = {Potsdam}, year = {2011}, language = {en} } @phdthesis{Stief2016, author = {Stief, Anna}, title = {Genetics and ecology of plant heat stress memory}, school = {Universit{\"a}t Potsdam}, pages = {175}, year = {2016}, language = {en} } @phdthesis{Stephan2023, author = {Stephan, Mareike Sophia}, title = {A bacterial mimetic system to study bacterial inactivation and infection}, school = {Universit{\"a}t Potsdam}, pages = {150}, year = {2023}, abstract = {The emerging threat of antibiotic-resistant bacteria has become a global challenge in the last decades, leading to a rising demand for alternative treatments for bacterial infections. One approach is to target the bacterial cell envelope, making understanding its biophysical properties crucial. Specifically, bacteriophages use the bacterial envelope as an entry point to initiate infection, and they are considered important building blocks of new antibiotic strategies against drug-resistant bacteria.. Depending on the structure of the cell wall, bacteria are classified as Gram-negative and Gram-positive. Gram-negative bacteria are equipped with a complex cell envelope composed of two lipid membranes enclosing a rigid peptidoglycan layer. The synthesis machinery of the Gram-negative cell envelope is the target of antimicrobial agents, including new physical sanitizing procedures addressing the outer membrane (OM). It is therefore very important to study the biophysical properties of the Gram-negative bacterial cell envelope. The high complexity of the Gram-negative OM sets the demand for a model system in which the contribution of individual components can be evaluated separately. In this respect, giant unilamellar vesicles (GUVs) are promising membrane systems to study membrane properties while controlling parameters such as membrane composition and surrounding medium conditions. The aim of this work was to develop methods and approaches for the preparation and characterization of a GUV-based membrane model that mimics the OM of the Gram-negative cell envelope. A major component of the OM is the lipopolysaccharide (LPS) on the outside of the OM heterobilayer. The vesicle model was designed to contain LPS in the outer leaflet and lipids in the inner leaflet. Furthermore, the interaction of the prepared LPS-GUVs with bacteriophages was tested. LPS containing GUVs were prepared by adapting the inverted emulsion technique to meet the challenging properties of LPS, namely their high self-aggregation rate in aqueous solutions. Notably, an additional emulsification step together with the adaption of solution conditions was employed to asymmetrically incorporate LPS containing long polysaccharide chains into the artificial membranes. GUV membrane asymmetry was verified with a fluorescence quenching assay. Since the necessary precautions for handling the quenching agent sodium dithionite are often underestimated and poorly described, important parameters were tested and identified to obtain a stable and reproducible assay. In the context of varied LPS incorporation, a microscopy-based technique was introduced to determine the LPS content on individual GUVs and to directly compare vesicle properties and LPS coverage. Diffusion coefficient measurements in the obtained GUVs showed that increasing LPS concentrations in the membranes resulted in decreased diffusivity. Employing LPS-GUVs we could demonstrate that a Salmonella bacteriophage bound with high specificity to its LPS receptor when presented at the GUV surface, and that the number of bound bacteriophages scaled with the amount of presented LPS receptor. In addition to binding, the bacteriophages were able to eject their DNA into the vesicle lumen. LPS-GUVs thus provide a starting platform for bottom-up approaches for the generation of more complex membranes, in which the effects of individual components on the membrane properties and the interaction with antimicrobial agents such as bacteriophages could be explored.}, language = {en} } @phdthesis{Steinhauser2009, author = {Steinhauser, Marie-Caroline}, title = {Optimisation and application of enzyme activity assays to characterise carbohydrate metabolism in the fruit of different tomato genotypes}, address = {Potsdam}, pages = {122, XXXVII S. : Ill., graph. Darst.}, year = {2009}, language = {en} } @phdthesis{Stein2008, author = {Stein, Claudia}, title = {Biodiversity and ecosystem functioning : regional and local determinants of plant diversity in montane grasslands}, series = {PhD dissertation / Helmholtz Centre for Environmental Research , UFZ}, volume = {2008, 11}, journal = {PhD dissertation / Helmholtz Centre for Environmental Research , UFZ}, publisher = {UFZ}, address = {Leipzig}, pages = {141 S.}, year = {2008}, language = {en} } @phdthesis{Stech2014, author = {Stech, Marlitt}, title = {Investigations on the cell-free synthesis of single-chain antibody fragments using a cukaryotic translation system}, pages = {ix, 126}, year = {2014}, language = {en} } @phdthesis{Spricigo2009, author = {Spricigo, Roberto}, title = {Investigations of sulfite oxidase and the molybdenum cofactor at surfaces}, address = {Potsdam}, pages = {VIII, 105 S. : Ill., graph. Darst.}, year = {2009}, language = {en} } @phdthesis{Sprenger2014, author = {Sprenger, Heike}, title = {Characterization of drought tolerance in potato cultivars for identification of molecular markers}, pages = {146}, year = {2014}, language = {en} } @phdthesis{Sperfeld2011, author = {Sperfeld, Erik}, title = {Effects of temperature and co-limiting nutritional components on life history traits of Daphnia magna and its biochemical composition}, address = {Potsdam}, pages = {157 S.}, year = {2011}, language = {en} } @phdthesis{Sokolowska2016, author = {Sokolowska, Ewelina Maria}, title = {Implementation of a plasmodesmata gatekeeper system, and its effect on intercellular transport}, school = {Universit{\"a}t Potsdam}, pages = {143}, year = {2016}, language = {en} } @phdthesis{Soja2014, author = {Soja, Aleksandra Maria}, title = {Transcriptomic and metabolomic analysis of Arabidopsis thaliana during abiotic stress}, pages = {134}, year = {2014}, language = {en} } @phdthesis{Smirnova2012, author = {Smirnova, Julia}, title = {Carbohydrate-active enzymes metabolising maltose: kinetic and structural features}, address = {Potsdam}, pages = {162 S.}, year = {2012}, language = {en} } @phdthesis{Sklodowski2015, author = {Sklodowski, Kamil}, title = {Regulation of plant potassium channels}, school = {Universit{\"a}t Potsdam}, pages = {115}, year = {2015}, language = {en} } @phdthesis{SimonRosin2001, author = {Simon-Rosin, Ulrike}, title = {Isolation and characterisation of ammonium transporters from the module legumen : lotus japanicus}, pages = {85 S.}, year = {2001}, language = {en} } @phdthesis{SilvaIturriza2008, author = {Silva Iturriza, Adriana Maria}, title = {Evolutionary relationships between haemosporidian parasites and Philippine birds}, address = {Potsdam}, pages = {130 Bl. : graph. Darst.}, year = {2008}, language = {en} } @phdthesis{Siewert2011, author = {Siewert, Katharina}, title = {Autoaggressive human t cell receptorrs and their antigen specificities}, address = {Potsdam}, pages = {145 S.}, year = {2011}, language = {en} } @phdthesis{Siddiqui2008, author = {Siddiqui, Hamad}, title = {Isolation and functional characterization of novel NAC genes playing a crucial role in leaf senescence in Arabidopsis thaliana (L.) Heynh}, address = {Potsdam}, pages = {VI, 177 S. S. VII-XI : Ill., graph. Darst.}, year = {2008}, language = {en} } @phdthesis{Shivanand2015, author = {Shivanand, Lathe Rahul}, title = {DUF1068 protein family members are involved in cell wall formation in Arabidopsis thaliana}, school = {Universit{\"a}t Potsdam}, pages = {393}, year = {2015}, language = {en} } @phdthesis{Shirokova2005, author = {Shirokova, Elena}, title = {Functional genomics of olfactory and pheromone receptors by reconstitution of their signal transduction in human HeLa cells}, address = {Potsdam}, pages = {83 S. : graph. Darst.}, year = {2005}, language = {en} } @phdthesis{Shen2022, author = {Shen, Yawen}, title = {Functional characterization of the gene regulatory network of C2H2-type zine finger protein ZAT8 in Arabidopsis thaliana}, pages = {124}, year = {2022}, language = {en} } @phdthesis{Sharma2011, author = {Sharma, Tripti}, title = {Regulation of potassium channels in plants : biophysical mechanisms and physiological implacations}, address = {Potsdam}, pages = {104 S.}, year = {2011}, language = {en} } @phdthesis{Sharma2008, author = {Sharma, Reeta}, title = {Molecular genetic analysis of Bengal tiger (Panthera tigris tigres) population and its implication in conservation and wildlife forensics}, address = {Potsdam}, pages = {101 Bl. : gtaph. Darst. Kt.}, year = {2008}, language = {en} } @phdthesis{ShahnejatBushehri2016, author = {Shahnejat-Bushehri, Sara}, title = {Unravelling the role of the Arabidopsis NAC transcription factor JUNGBRUNNEN1 (JUB1) for the regulation of growth and stress responses}, school = {Universit{\"a}t Potsdam}, pages = {155}, year = {2016}, language = {en} }