Die einzellige Grünalge Chlamydomonas reinhardtii ist ein vielseitiger Modellorganismus sowohl in der Grundlagenforschung als auch für biotechnologische Anwendung. Für die genetische Veränderung wurden verschiedene Methoden entwickelt, jedoch ist die gezielte Modifikation kerncodierter Gene immernoch sehr schwierig. In dieser Arbeit wird eine Strategie vorgestellt, die es ermöglicht, kerncodierte Gene in Chlamydomonas gezielt mit sequenzspezifischen Zinkfinger-Nukleasen zu verändern. Das COP3-Gen, welches den lichtaktivierbaren Ionenkanal Kanalrhodopsin-1 codiert, diente hierbei als Zielsequenz der für die Deletion hergestellten Zinkfinger-Nukleasen. Um eine Charakterisierung der ZFNs zu ermöglichen, wurde ein Modelstamm generiert, der ein inaktiviertes Markergen enthält. Die Inaktiverung erfolgte hierbei durch Insertion der COP3-ZFN Zielsequenz. Die Transformation dieses Modellstamms mit ZFN codierender Plasmid-DNA und einem Reparatur-Template ermöglichte die Wiederherstellung der Markeraktivität und eine Selektion Antibiotika-resistenter Kolonien. Wenn in diesen Experimenten zusätzlich ein COP3 veränderndes Template benutzt wurde, enthielt 1% der analysierten Klone ein mutiertes COP3-Gen. Der Chlamydomonas Augenfleck ist ein lichtsensitives Organell mit entscheidender Funktion für die phototaktische Orientierung der Alge. Eine Deletionsmutante des Blaulicht-Photorezeptors Phototropin zeigte in Experimenten eine veränderte Regulation der lichtabhängigen Augenfleckgröße. Durch Komplementierung der Phototropin-Dysfunktion konnte der lichtabhängige Regulationsprozess wiederhergestellt werden. Die Expression der Phototropin-Kinasedomäne führte zu einer lichtunabhängigen Reduktion der Augenfleckfläche. Interessanterweise führte auch die Expression der N-terminalen LOV-Domänen zu einer geänderten Regulation des Augenflecks und der Phototaxis. Dies deutet, zusätzlich zur Lichtregulation der Kinasedomäne, auf eine zelluläre Signalfunktion der LOV-Domänen hin. / The unicellular green alga Chlamydomonas reinhardtii is a versatile model for fundamental and biotechnological research. A wide toolset for genetic manipulation has been developed for this alga, but specific modification of nuclear genes is still not routinely possible. Here we present a nuclear gene targeting strategy for Chlamydomonas that is based on the application of zinc-finger nucleases (ZFNs). Initially, we designed a set of ZFNs for targeting the COP3 gene that encodes the light-activated ion channel channelrhodopsin-1. To evaluate the designed ZFNs, we constructed a model strain by inserting a non-functional selection marker interspaced with a short COP3 target sequence into the nuclear genome. Upon co-transformation of this recipient strain with the engineered ZFNs and a DNA repair template, we were able to restore marker activity and select antibiotic resistant clones with active nucleases. In cases where cells were co-transformed with a modified COP3 template, 1% of these clones contained a modified COP3 locus as well. The eyespot of Chlamydomonas is a light-sensitive organelle important for phototactic orientation of the alga. Here we found that eyespot size is downregulated in light. In a strain in which the blue light photoreceptor phototropin was deleted, the light regulation of the eyespot size was affected. We restored this dysfunction in different phototropin complementation experiments. Complementation with the phototropin kinase fragment reduced the eyespot size, independent of light. Interestingly, overexpression of the N-terminal LOV-domains alone also affected eyespot size and phototaxis, suggesting that aside from activation of the kinase domain, they fulfill an independent signaling function in the cell. We propose that phototropin is a light regulator of phototaxis that desensitizes the eyespot when blue light intensities increase.

In der vorliegenden Arbeit wurden Experimente zur pflanzlichen Eisenassimilation durchgeführt. Zwei cDNAs aus Tomatenwurzeln (LeIRT1 und LeIRT2, GenBank Acc-Nr. AF176579 und AF176580) wurden isoliert. Sie komplementierten Fe-aufnahmedefiziente Hefestämme in Bezug auf das Wachstum auf Fe-limitierendem Medium. Die durch die LeIRT-Proteine vermittelte Fe-Aufnahme wurde in Hefezellen charakterisiert. Sie war temperaturabhängig, sättigbar und Fe2+, nicht Fe3+ wurde transportiert. Kompetitions- und Komplementationsexperimente mit metall-aufnahmedefizienten Hefemutanten legten die Vermutung nahe, daß die beiden cDNAs für Kationentransporter codieren, die eine breite Substratspezifität für Übergangsmetalle aufweisen. Die Transkripte der LeIRT-Gene konnten fast ausschließlich in Wurzeln nachgewiesen werden, wobei LeIRT1 durch Fe-Mangel induziert war, während für LeIRT2 keine Regulation durch die Fe-Ernährung der Pflanzen erkennbar war. Die Genstruktur wurde aufgeklärt (GenBank Acc-Nr. AF246266). Schwierigkeiten in der Analyse der Fe-Assimilation höherer Pflanzen machten es notwendig, einen neuen Modellorganismus zu suchen. Dabei wurde die einzellige Alge Chlamydomonas reinhardtii ausgewählt. Physiologische Studien zeigten, daß diese Alge ähnliche Fe-Mangelreaktionen wie die meisten höheren Pflanzen aufweist. Insbesondere die starke Induktion einer Fe3+-Chelatreduktase und die parallele Induktion der Fe-Transportkapazität unter Fe-Mangel waren deutlich. Mindestens zwei Fe-Transportsysteme wurden postuliert, von denen das höheraffine durch Cu-Ionen gehemmt wurde. / In the present study, experiments were conducted to analyze the iron assimilation in plants. Two cDNAs from tomato roots (LeIRT1 and LeIRT2, GenBank Acc-Nr. AF176579 and AF176580) were isolated that complemented the growth defect of Fe uptake-deficient yeast mutants. The Fe uptake mediated by the LeIRT proteins was characterized in yeast. It was temperature-dependent, saturable and Fe2+ rather than Fe3+ was transported. Competition and complementation experiments with metal uptake-deficient yeast mutants suggested that both cDNAs code for cation transporters exhibiting broad substrate specificity for transition metals. The transcripts of both genes were predominantly detected in roots, LeIRT1 being induced by Fe deficiency whereas LeIRT2 was unaffected by the Fe status of the plants. The gene structure was determined (GenBank Acc-Nr. AF246266). Problems in the analysis of Fe assimilation in higher plants made it necessary to establish a new model organism. The unicellular eucaryotic alga, Chlamydomonas reinhardtii, was chosen. Physiological studies indicated that this alga reacted to Fe deficiency similar to most higher plants. Particularly the strong induction of an Fe3+-chelate reductase paralleled by the induction of Fe transport capacitiy under Fe deficiency were evident. At least two Fe transporters were postulated, one of which was inhibited by Cu ions.

No description available.

Les suspensions d'objets microscopiques ayant la faculté de se déplacer par eux-mêmes dans le fluide qui les entoure sont des systèmes qui présentent un intérêt croissant dans la communauté scientifique. Du fait de leur dynamique intrinsèquement hors-équilibre au sens de la physique statistique, ils génèrent des effets particulièrement complexes. Parmi les micro-objets autopropulsés existants, les micro-algues vertes représentent une part importante de la biomasse de la Terre et participent activement au retraitement du CO2 par leur activité photosynthétique. Elles présentent de plus un remarquable potentiel dans les domaines de la production de bio-carburants, du retraitement des déchets, de la fabrication de cosmétiques et de compléments alimentaires. La compréhension de la dynamique de nage de ce type de microorganisme est d'un intérêt primordial d'un point de vue industriel. Cet ouvrage présente l'étude de la dynamique de la micro-algue Chlamydomonas Reinhardtii. En utilisant un système de suivi de particules en imagerie optique que nous avons développé, nous analysons ici le mécanisme fondamental de nage utilisé par cette algue jusqu'à ses implications en terme d'effets collectifs sur la dynamique de nage d'une suspension semi-diluée. / The suspensions of microscopic objects with the ability to propel themselves into the surrounding fluid are systems of growing interest in the scientific community. Due to their intrinsic out-of-equilibrium dynamics in the sense of statistical physics, they generate complex effects. Among the existing self-propelled micro-objects, green micro-algae are an important part of the biomass of Earth and they actively participate to the recycling of CO2 by their photosynthetic activity. Moreover they have remarkable potential for the production of bio-fuels, waste reprocessing, cosmetics and dietary supplements production. From an industrial point of view, understanding the dynamics of this type of swimming microorganism is of primary interest. This work presents the study of the dynamics of microalgae Chlamydomonas Reinhardtii. Using a system of particle tracking with optical imaging that we have developed, we analyze the mechanism of stroke used by the algae up to its implications in terms of collective effects on the dynamics of swimming in a semi-dilute suspension.

What is flagellar swimming? Cilia and flagella are whip-like cell appendages that can exhibit regular bending waves. This active process emerges from the non-equilibrium dynamics of molecular motors distributed along the length of cilia and flagella. Eukaryotic cells can possess many cilia and flagella that beat in a coordinated fashion, thus transporting fluids, as in mammalian airways or the ventricular system inside the brain. Many unicellular organisms posses just one or two flagella, rendering them microswimmers that are propelled through fluids by the flagellar beat including sperm cells and the biflagellate green alga Chlamydomonas. Objectives. In this thesis in theoretical biological physics, we seek to understand the nonlinear dynamics of flagellar swimming and synchronization. We investigate the flow fields induced by beating flagella and how in turn external hydrodynamic flows change speed and shape of the flagellar beat. This flagellar load-response is a prerequisite for flagellar synchronization. We want to find the physical principals underlying stable synchronization of the two flagella of Chlamydomonas cells. Results. First, we employed realistic hydrodynamic simulations of flagellar swimming based on experimentally measured beat patterns. For this, we developed analysis tools to extract flagellar shapes from high-speed videoscopy data. Flow-signatures of flagellated swimmers are analysed and their effect on a neighboring swimmer is compared to the effect of active noise of the flagellar beat. We were able to estimate a chemomechanical energy efficiency of the flagellar beat and determine its waveform compliance by comparing findings from experiments, in which a clamped Chlamydomonas is exposed to external flow, to predictions from an effective theory that we designed. These mechanical properties have interesting consequences for the synchronization dynamics of Chlamydomonas, which are revealed by computer simulations. We propose that direct elastic coupling between the two flagella of Chlamydomonas, as suggested by recent experiments, in combination with waveform compliance is crucial to facilitate in-phase synchronization of the two flagella of Chlamydomonas.

When microalgae are exposed to changing environmental conditions, e.g., light-dark cycles or oscillations in nutrient availability (CO2, nitrogen, phosphate or silicate) they respond with metabolic changes in the carbon allocation pattern. Short time regulations in the time range of few seconds to minutes can be mirrored best by mass spectroscopy based metabolomics. However, these snap shots do not reflect the alterations in the carbon flow to the cellular macromolecules like protein, carbohydrate or lipid. In this review it is shown how the combination of FTIR spectroscopy and Chla-in-vivo-fluorescence based electron transport rates can reveal changes in the metabolic flux rates of carbon during a shift of the environmental conditions. The review will demonstrate in which time range FTIR spectroscopy can deliver significant information and how FTIR spectroscopy data can synergistically support metabolome analysis by mass-spectroscopy.

What is flagellar swimming? Cilia and flagella are whip-like cell appendages that can exhibit regular bending waves. This active process emerges from the non-equilibrium dynamics of molecular motors distributed along the length of cilia and flagella. Eukaryotic cells can possess many cilia and flagella that beat in a coordinated fashion, thus transporting fluids, as in mammalian airways or the ventricular system inside the brain. Many unicellular organisms posses just one or two flagella, rendering them microswimmers that are propelled through fluids by the flagellar beat including sperm cells and the biflagellate green alga Chlamydomonas. Objectives. In this thesis in theoretical biological physics, we seek to understand the nonlinear dynamics of flagellar swimming and synchronization. We investigate the flow fields induced by beating flagella and how in turn external hydrodynamic flows change speed and shape of the flagellar beat. This flagellar load-response is a prerequisite for flagellar synchronization. We want to find the physical principals underlying stable synchronization of the two flagella of Chlamydomonas cells. Results. First, we employed realistic hydrodynamic simulations of flagellar swimming based on experimentally measured beat patterns. For this, we developed analysis tools to extract flagellar shapes from high-speed videoscopy data. Flow-signatures of flagellated swimmers are analysed and their effect on a neighboring swimmer is compared to the effect of active noise of the flagellar beat. We were able to estimate a chemomechanical energy efficiency of the flagellar beat and determine its waveform compliance by comparing findings from experiments, in which a clamped Chlamydomonas is exposed to external flow, to predictions from an effective theory that we designed. These mechanical properties have interesting consequences for the synchronization dynamics of Chlamydomonas, which are revealed by computer simulations. We propose that direct elastic coupling between the two flagella of Chlamydomonas, as suggested by recent experiments, in combination with waveform compliance is crucial to facilitate in-phase synchronization of the two flagella of Chlamydomonas.:1 Introduction 1.1 Physics of cell motility: flagellated swimmers as model system 2 1.1.1 Tissue cells and unicellular eukaryotic organisms have cilia and flagella 2 1.1.2 The conserved architecture of flagella 3 1.1.3 Synchronization in collections of flagella 5 1.2 Hydrodynamics at the microscale 9 1.2.1 Navier-Stokes equation 10 1.2.2 The limit of low Reynolds number 10 1.2.3 Multipole expansion of flow fields 11 1.3 Self-propulsion by viscous forces 13 1.3.1 Self propulsion requires broken symmetries 13 1.3.2 Signatures of flowfields: pusher & puller 15 1.4 Overview of the thesis 16 2 Flow signatures of flagellar swimming 2.1 Self-propulsion of flagellated swimmers 20 2.1.1 Representation of flagellar shapes 20 2.1.2 Computation of hydrodynamic friction forces 21 2.1.3 Material frame and rigid-body transformations 22 2.1.4 The grand friction matrix 23 2.1.5 Dynamics of swimming 23 2.2 The hydrodynamic far field: pusher and puller 26 2.2.1 The flow generated by a swimmer 26 2.2.2 Force dipole characterization 27 2.2.3 Flagellated swimmers alternate between pusher and puller 29 2.2.4 Implications for two interacting Chlamydomonas cells 31 2.3 Inertial screening of oscillatory flows 32 2.3.1 Convection and oscillatory acceleration 33 2.3.2 The oscilet: fundamental solution of unsteady flow 35 2.3.3 Screening length of oscillatory flows 35 2.4 Energetics of flagellar self-propulsion 36 2.4.1 Impact of inertial screening on hydrodynamic dissipation 37 2.4.2 Case study: the green alga Chlamydomonas 38 2.4.3 Discussion: evolutionary optimization and the number of molecular motors 38 2.5 Summary 39 3 The load-response of the flagellar beat 3.1 Experimental collaboration: flagellated swimmers exposed to flows 41 3.1.1 Description of the experimental setup 42 3.1.2 Computed flow profile in the micro-fluidic device 43 3.1.3 Image processing and flagellar tracking 43 3.1.4 Mode decomposition and limit-cycle reconstruction 47 3.1.5 Changes of limit-cycle dynamics: deformation, translation, acceleration 49 3.2 An effective theory of flagellar oscillations 50 3.2.1 A balance of generalized forces 50 3.2.2 Hydrodynamic friction in generalized coordinates 51 3.2.3 Intra-flagellar friction 52 3.2.4 Calibration of active flagellar driving forces 52 3.2.5 Stability of the limit cycle of the flagellar beat 53 3.2.6 Equations of motion 55 3.3 Comparison of theory and experiment 56 3.3.1 Flagellar mean curvature 57 3.3.2 Susceptibilities of phase speed and amplitude 57 3.3.3 Higher modes and stalling of the flagellar beat at high external load 59 3.3.4 Non-isochrony of flagellar oscillations 63 3.4 Summary 63 4 Flagellar load-response facilitates synchronization 4.1 Synchronization to external driving 65 4.2 Inter-flagellar synchronization in the green alga Chlamydomonas 67 4.2.1 Equations of motion for inter-flagellar synchronization 68 4.2.2 Synchronization strength for free-swimming and clamped cells 70 4.2.3 The synchronization strength depends on energy efficiency and waveform compliance 73 4.2.4 The case of an elastically clamped cell 74 4.2.5 Basal body coupling facilitates in-phase synchronization 75 4.2.6 Predictions for experiments 78 4.3 Summary 80 5 Active flagellar fluctuations 5.1 Effective description of flagellar oscillations 84 5.2 Measuring flagellar noise 84 5.2.1 Active phase fluctuations are much larger than thermal noise 84 5.2.2 Amplitude fluctuations are correlated 85 5.3 Active flagellar fluctuations result in noisy swimming paths 86 5.3.1 Effective diffusion of swimming circles of sperm cell 86 5.3.2 Comparison of the effect of noise and hydrodynamic interactions 87 5.4 Summary 88 6 Summary and outlook 6.1 Summary of our results 89 6.2 Outlook on future work 90 A Solving the Stokes equation A.1 Multipole expansion 95 A.2 Resistive-force theory 96 A.3 Fast multipole boundary element method 97 B Linearized Navier-Stokes equation B.1 Linearized Navier-Stokes equation 101 B.2 The case of an oscillating sphere 102 B.3 The small radius limit 103 B.4 Greens function 104 C Hydrodynamic friction C.1 A passive particle 107 C.2 Multiple Particles 107 C.3 Generalized coordinates 108 D Data analysis methods D.1 Nematic filter 111 D.1.1 Nemat 111 D.1.2 Nematic correlation 111 D.2 Principal-component analysis 112 D.3 The quality of the limit-cycle projections of experimental data 113 E Adler equation F Sensitivity analysis for computational results F.1 The distance function of basal coupling 117 F.2 Computed synchronization strength for alternative waveform 118 F.3 Insensitivity of computed load-response to amplitude correlation time 118 List of Symbols List of Figures Bibliography

Actuellement, plus de 70% des biomédicaments commercialisés sont des glycoprotéines recombinantes. Les coûts élevés de production de ces biomédicaments ont poussé les scientifiques à développer des organismes de production alternatifs. Récemment, les microalgues ont été proposées en tant que potentiel système de production compte-tenu de leur rapidité de croissance et de leurs faibles coûts de production. Cependant, avant de produire des biomédicaments industriels chez les microalgues, il est impératif de s’assurer que les modifications post-traductionnelles, comme la N-glycosylation, soit conservées et compatibles avec une utilisation thérapeutique. Dans ce contexte, l’étude de la Nglycosylation de deux microalgues modèles, Chlamydomonas reinhardtii (microalgue verte) et Phaeodactylum tricornutum (diatomée) a été réalisée. Dans un premier temps, l’ingénierie de la N-glycosylation de C. reinhardtii a été initiée en exprimant une Nacétylglucosaminyltransférase I (GnT I) hétérologue. Les résultats obtenus ont permis de réévaluer les voies de N-glycosylation de C. reinhardtii et de montrer que cette microalgue synthétise une structure glycannique linéaire qui n’est pas substrat de la GnT I. Dans un second temps, un protocole d’extraction et de caractérisation des précurseurs glycanniques de C. reinhardtii et P. tricornutum a été développé et appliqué pour déterminer la structure des précurseurs glycanniques dans ces espèces. Enfin, la caractérisation de deuxxylosyltransférases potentielles (XTA et XTB) de C. reinhardtii a été menée en utilisant des mutants d’insertion et des analyses des N-glycannes par spectrométrie de masse. Cette étude a confirmé les rôles spécifiques de XTA et XTB dans la voie de N-glycosylation de C. reinhardtii. / Currently, more than 70% of the commercialized biopharmaceuticals are glycoproteins. The high production costs lead scientists to develop alternative organisms suitable for such production. Recently, microalgae emerged as a potential interesting production system thanks to their quick growth rate and low production costs. However, prior to start industrial glycoproteins production in microalgae, protein post-translational modifications like Nglycosylation, must be carefully controlled. This PhD thesis focused on the analysis of the Nglycosylation pathway of two different microalgae, Chlamydomonas reinhardtii (greenmicroalgae) and Phaeodactylum tricornutum (diatom). In order to start N-glycan engineering, heterologous N-acetylglucosaminyltransferase I (GnT I) sequences were expressed in C.reinhardtii. This study demonstrated that C. reinhardtii synthetize a linear N-glycan unsuitable for GnT I activity and allows the reinvestigation of the C. reinhardtii N-glycosylation pathway. A second chapter of this work focus on the optimization of a protocol suitable for analyzing the structure of the Dolichol N-linked precursors of C. reinhardtii and P. tricornutum. Lastly, two potential xylosyltransferases (XTA and XTB) from C. reinhardtii were characterized using insertional mutants and N-glycomic analyses by mass spectrometry approaches. This work allows us to propose specific involvement of XTA and XTB in the xylosylation processing of C.reinhardtii N-glycans.

This dissertation describes a study utilizing bioinformatics to analyze homologues of a molecular chaperone, glucose-regulated protein 78 (grp 78), also known as BiP. The selected homologous proteins originate from organisms of infinitely diverse genera. Comparisons of protein sequence yielded the first clues of a common ancestry among these proteins. Furthermore, protein molecular weights, isoelectric points, N-terminal amino acids and half-lives of a known homolog and a non-homologous protein were examined. Additionally, electroporation, a state-of-the-art plasmid insertion technique, was explored using Chlamydomonas reinhardtii, a green alga, as the recipient of a parent plasmid, pSP124S. Distinctive hypertonic solutions and three separate field strengths were used in the plasmolysis of the cell wall of C. reinhardtii and subsequent electroporation, respectively. The number of transformants was tallied to evaluate which electroporation condition would yield the most transformed colonies. We had two discrete hypotheses: 1) that a structurally and functionally similar protein to glucose-regulated protein 78 exists across a wide spectrum of organisms and 2) that Chlamydomonas reinhardtii could be successfully transformed with pSP124S under certain electroporation conditions. The bioinformatics investigation revealed that analogous proteins to Human GRP 78 existed in Mus musculus (mouse), Rattus norvegicus (rat), Gallus domesticus (chicken), Gallus domesticus (chicken), Mesocricetus auratus (golden hamster), Bos taurus (cow), Xenopus laevis (frog), and Spinacia oleracea (spinach). Moreover, these homologous proteins more likely have a common evolutionary origin.

L’étude qui suit porte sur l’évaluation du risque écotoxicologique du cérium, l’élément le plus exploité de la famille des lanthanides. La présence grandissante de ce métal dans notre quotidien rend possible son relargage dans l’environnement. Il est donc primordial de comprendre l’impact qu’il aura sur les organismes vivant dans un système aquatique. Une approche centrée sur le modèle du ligand biotique a été utilisée pour évaluer adéquatement l’interaction entre le cérium et un ligand biotique à la surface de l’algue unicellulaire Chlamydomonas reinhardtii. Pour mener une étude sur le risque écotoxicologique d’un élément métallique il faut, avant tout, comprendre la spéciation (répartition sous ses différentes formes chimiques) de l’élément en question. Les premières sections du mémoire vont donc traiter des expériences qui ont été menées pour évaluer la spéciation du cérium dans les conditions expérimentales d’exposition à C. reinhardtii. Il sera question de faire la distinction entre la forme particulaire du métal et sa forme dissoute, de caractériser ces changements par spectroscopie ainsi que d’évaluer le pouvoir complexant de la matière organique naturelle. Les résultats montrent une importante déplétion du métal dissout en solution à pH neutre et basique et une forte interaction avec la matière organique naturelle, peu importe le pH de la solution. Ensuite, les expériences de bioaccumulation seront expliquéesen comparant l’effet du pH, de la présence d’un ion compétiteur et de la présence de matière organique naturelle sur les paramètres d’internalisation du cérium. Les résultats indiquent qu’à pH acide, le comportement du cérium est plus prévisible qu’à pH neutre. Néanmoins, en tenant compte de la complexité des milieux naturels, l’interaction du métal avec les molécules complexantes va diminuer son risque d’interaction avec un organisme vivant. / The following study is on the ecotoxicological risk evaluation of cerium, the most widely exploited element of the lanthanide family. The increasing presence of this element in our everyday lives renders possible its release in the environment. It is therefore of primary importance to understand the impact this metal will have on living organisms in aquatic environments. An approach centered on the biotic ligand model was used here to evaluate the interaction between cerium and a biotic ligand at the surface of the unicellular algae Chlamydomonas reinhardtii. To study the ecotoxicological risk of a metallic element one must understand the speciation (partitioning between its multiple chemical species) of the element in question. The first chapters of this thesis will discuss the experiments performed to evaluate cerium speciation under exposure conditions C. reinhardtii. The issue will be to distinguish between the particulate and dissolved species of the metal, to characterise these changes by spectroscopy, as well as to evaluate the complex formation capacity of the metal with natural organic matter. Results indicate an important depletion of dissolved metal in neutral and alkaline solutions as well as a strong interaction with natural organic matter, regardless of solution pH. Bioaccumulation experiments will then be explained and will compare the effects of pH, the presence of competing ions and the presence of natural organic matter on cerium uptake. Results show that cerium’s behaviour is more predictable under acidic pH conditions. Nonetheless, considering the complexity of the natural environment, the interaction of the metal with natural ligands will most likely reduce the risk of cerium’s interaction with living organisms.