Surface waters subject to algal blooms have a high rate of fouling water treatment filtration membrane. These waters typically contain high concentrations of hydrophilic organic carbon compounds such as proteins and polysaccharides. These compounds have been found to contribute greatly to membrane fouling. In this study the fouling propensity, and the components of the fouling layer, for microfiltration (MF) and ultrafiltration (UF) membranes, were characterised for samples taken from a wastewater treatment plant with lagoons prone to algal blooms and a blue-green algae culture (Anabaena circinalis). It was found that the organic carbon compounds released during the growth phase (EOM) of Anabaena circinalis have a similar fouling propensity for UF than those released during the lysis phase (AOM), and a slightly higher fouling propensity for MF. However, due to the presence of higher UV-absorbing hydrophilic compounds, higher concentration of intracellular proteins and/or humic acid-like matter in the AOM, irreversible fouling was significantly higher during the lysis phase.

This study investigates the operation of dual media filter DMF during ambient and simulated algal bloom conditions, and the role of coagulation and dissolved air flotation (DAF) in mitigating the adverse effects of algal blooms on DMF performance. The study also highlights which AOM concentration as a function of biopolymer is critical to organic fouling in DMF pretreatment for Red Sea water desalination with RO. On the other hand, the present study has carried out another experiment on AOM fouling in comparison with bacterial organic matter (BOM) and humic organic matter (HOM) using two different pore sizes of UF ceramic membranes, 5 and 50 kDa. The main aim of this comparison is to examine fouling behavior and mechanism and removal efficiency. The study revealed that AOM can induce organic fouling in DMF during simulated algal bloom conditions at biopolymer concentrations as low as 0.2 mg C/L. DMF performance was strongly affected by AOM concentration as observed by flow rate decline through time. Liquid chromatography – organic carbon detection (LC-OCD) analysis showed higher removal rates of biopolymers than lower molecular weight fractions (i.e., humic substances, building blocks and low molecular weight neutrals) for all pretreatment scenarios. The study also indicated that while DMF performance was enhanced with coagulation and sedimentation, the most significant improvement in performance was observed for DMF operation preceded by coagulation and DAF. Hydraulic performance of DMF correlated well with biopolymers removal, with removal rates of 72%, 53% and 39%, for coagulation/DAF, coagulation/sedimentation, and no coagulation, respectively. For UF ceramic membranes, results showed that more TEP/organics were removed by the 5 kDa membranes compared to the 50 kDa membrane, which is accounted for lower MWCO. The UF 5 kDa membrane also showed low fouling formation than 50 kDa membrane for all of three types of organic matter tested. Analysis of the fouled membranes by SEM images showed that fouling was dominated by cake layer formation for the 5 kDa membrane while pore blockage followed by cake layer formation is apparent for the 50 kDa membrane.

No description available.

La cycline A2 est un régulateur essentiel du cycle cellulaire qui, en association avec des kinases dépendantes des cyclines (CDK) régule la réplication de l'ADN et l’entré des cellules en mitose. Dans de nombreux types de cancers humains, la cycline A2 a été considérée comme un facteur de prolifération contribuant à la cancérogenèse de par ses fonctions dans la régulation du cycle cellulaire. Récemment, la complexité des fonctions de cycline A2 a été révélée. Certaines études in vitro ont démontré que l'inactivation de la cycline A2 induit une augmentation de la motilité cellulaire et de l'invasion dans les fibroblastes consécutive à une activation défective de RhoA. De plus, il a été montré que l'inactivation de la cycline A2 induit la EMT par l’intermédiaire d’une augmentation de l'activité transcriptionnelle de la β-caténine, mais aussi via la voie TGFβ/Prefoldin. Ces études suggèrent que des niveaux réduits de cycline A2 sont liés à une invasion accrue et à l’apparition de métastases dans certains types de cancer. A l’aide d’un modèle de souris mutante pour la cycline A2, une étude récente a établi une fonction de cette dernière, indépendante des CDK, dans la réparation des cassures double brin de l'ADN et a montré que la perte de la cycline A2 favorise l’apparition de cancers de la peau et du poumon. L’ensemble de ces études met en évidence l’existence de multiples fonctions pour la cycline A2. Mon travail de thèse a consisté à explorer le rôle de la cycline A2 dans l'homéostasie du colon et le développement du Le cancer colorectal.Pour évaluer la valeur pronostique de la cycline A2 dans le CCR, nous avons analysé l'expression de la cycline A2 par IHC sur un grand nombre d'échantillons tumoraux dérivés de patients atteints de CCR de différents stades. Nous avons trouvé que les niveaux élevés de la cycline A2 sont corrélés avec un mauvais pronostic et une survie plus faible chez les patients atteints de CCR de stade I et II. Cependant, une diminution de l'expression de la cycline A2 a été détectée aux stades III et IV par comparaison aux biopsies de CCR de stade I et II. Il est tentant de proposer que le profil d'expression de la cycline A2 reflète ses rôles distincts au cours de la cancérogenèse du côlon, comme la prolifération cellulaire au stade précoce, lorsqu'elle est fortement exprimée, mais favorise l'invasion et l'agressivité à des stades plus avancés, lorsque ses niveaux d’expression sont réduits.En complément de cette étude clinique, nous avons généré des modèles murins porteurs d’une mutation constitutive ou inductible de la cycline A2 dans l’épithélium intestinal. Nous avons montré que la déplétion de la cycline A2 dans l'épithélium intestinal de la souris provoque une rupture de la crypte colique, une inflammation, une augmentation de la prolifération des cellules épithéliales et l’apparition de dysplasies de bas et haut grade, reconnues comme lésions précancéreuses dans le CCR. Ces observations suggèrent un rôle majeur pour la cycline A2 dans la régulation de l'homéostasie du côlon et l'initiation de la tumorigénèse. Une analyse plus poussée a révélé une proportion accrue de lésions au niveau de l'ADN et une activation aberrante de la β-caténine, anomalies couramment détectées chez les patients humains atteints de CCR et considérées comme les premières altérations de cette pathologie. En outre, nous avons détecté une expression élevée de NFkB et YAP1 chez les souris mutantes pour la cycline A2, voies qui jouent un rôle critique dans la régénération tissulaire et peuvent conduire la dédifférenciation des cellules épithéliales du côlon contribuant ainsi à la tumorigenèse. Finalement, les souris mutantes cycline A2 ont été soumises à un protocole de colite associé au cancer et ont développé une proportion accrue d'inflammation, mais aussi de dysplasies et d'adénocarcinomes, en taille et en nombre, suggérant que la perte de la cycline A2 participe à la carcinogenèse colorectale chez la souris. / Cyclin A2 is an essential cell cycle regulator required for accurate DNA replication and mitotic entry in association with cyclin-dependent kinases (CDKs). In multiple types of human cancers, cyclin A2 was considered as a proliferation driver contributing to carcinogenesis based on its function to promote cell cycle.Recently, the complexity of cyclin A2 functions has been revealed. Some in vitro studies demonstrated that cyclin A2 inactivation induces increased cell motility and invasiveness of mouse fibroblasts due to defective RhoA activation. Moreover, cyclin A2 inactivation has been shown to induce EMT through the upregulation of β-catenin transcriptional activity, but also via the TGFβ/Prefoldin pathway. These studies suggest that reduced levels of cyclin A2 are linked to increased invasiveness and metastasis in some cancer types. Using a cyclin A2 mutant mouse model, a recent study established the CDK-independent function of cyclin A2 in the repair of double-stranded DNA breaks and showed that loss of cyclin A2 promotes tumorigenesis in skin and lung due to deficient DSBs repair.Altogether, these studies highlight the multiple functions cyclin A2 can execute. The aim of my thesis was to explore the role of cyclin A2 in colon homeostasis and colorectal cancer development.To evaluate the prognostic value of cyclin A2 in CRC, we analyzed cyclin A2 expression by IHC on tumor samples derived from CRC patients of different stages. We found that high levels of cyclin A2 correlate with bad prognosis and lower survival in patients with stage I and II CRC. However, decreased cyclin A2 expression was detected in stage III and IV by comparison to stage I and II CRC biopsies. Complementary to the clinical study, we generated tissue-specific mutant mouse models bearing either a constitutive or inducible cyclin A2 deletion in the intestinal epithelium. We showed that depletion of cyclin A2 in mouse intestinal epithelium causes colonic crypt disruption, inflammation, increased proliferation of epithelial cells and occurrence of low- and high-grade dysplasia, recognized as precancerous lesions of CRC. These observations suggest a major role for cyclin A2 in the regulation of normal colon homeostasis and tumor initiation. Further analysis revealed an increased proportion of DNA damage and aberrant activation of β-catenin, commonly detected in human patients with CRC and which are considered as the first occurring alterations in this pathology. Furthermore, we detected elevated expression of NFkB and YAP1 in the colons of cyclin A2 mutant mice, pathways that have been previously shown to play critical roles for tissue regeneration after tissue damage and to drive dedifferentiation of colonic epithelial cells thus contributing to tumorigenesis. Finally, cyclin A2 mutant mice were subjected to a modified colitis-associated CRC model and developed increased proportion of inflammation, but also dysplasia and adenocarcinomas, in size and numbers, suggesting that loss of cyclin A2 contributes to inflammation-associated colorectal carcinogenesis in mice.

The diploma thesis is aimed at adsorption processes during the removal of pesticides onto granular activated carbon (GAC) in the process of drinking water treatment. Adsorption onto GAC represents an efficient method for pesticides removal. High adsorption efficiency can be significantly reduced due to the occurrence of natural organic matter (NOM) in raw water, which involves AOM (Algal Organic Matter) produced by phytoplankton. Analogous to NOM, AOM probably affects adsorption of pesticides by two different mechanisms - a direct site competition and pore blockage effect, in dependence on the different molecular weight of particular AOM fractions. Equilibrium batch and kinetic adsorption experiments were performed using two types of GAC (Norit 1240 and Filtrasorb 400) and two pesticides (terbuthylazine and alachlor). In order to examine the effect of AOM on adsorption of pesticides, raw GAC and GAC preloaded by AOM were used. The effect of pH on the competitive adsorption of AOM was also evaluated. A solid phase extraction (SPE) method and gas chromatography with electron capture detection (GC-ECD) were used to determine pesticides in water samples. AOM was characterized using fractionation onto sorptive resins. The representation of apparent molecular weights of AOM proteins was determined by...

The increasing concern about water quality and energy demand promotes the development of innovative and low-cost processes to improve the nutrient uptake and energy efficiency of existing wastewater treatments (WWT). In this context, the inclusion of a microalgae system (MAS) in the flowsheet of a WWT plant represents a sustainable alternative to conventional technologies, as it combines a low-cost nutrient uptake system with the production of biomass suitable for biofuel production. However, at present, the energy required to cultivate and process the algae cells is often too high to justify their use. The adoption of a low energy harvesting system and an efficient energy conversion process are the sine qua non requirements to guarantee the sustainability of the process. In this thesis, current and innovative harvesting technologies for large scale applications have been reviewed to identify the optimal working conditions of each system and their link to the main characteristics of the algae suspension. In particular, the performance of the Ballasted Dissolved Air Flotation (BDAF) system was investigated using different algae and compared to the conventional Dissolved Air Flotation (DAF). BDAF was demonstrably a very viable harvesting method where the use of floating microspheres as ballasting agents allowed significant coagulant savings, reduced the level of energy dissipation within the flotation chamber, and lowered the overall carbon emissions and the process costs. Cont/d.

This dissertation investigates harvesting of marine microalgae for bioenergy and production of two recombinant proteins for therapeutic applications in Chlamydomonas reinhardtii. The first study describes harvesting of marine microalgae by flocculation using aluminum chloride (AlCl_3), natural polymer chitosan, and synthetic cationic polymers. Harvesting and concentration process of low concentration microalgae cultures ranging from 1 to 2 g dry weight per liter was affected by algogenic organic matter (AOM), ionic strength, cell concentration, polymer charge density, and media pH. Marine microalgae flocculation was greatly affected by the presence of AOM independently of the flocculant chemistry. Presence of AOM demanded extra flocculant dosage i.e., 3-fold of AlCl3, 7-fold of highly charged synthetic cationic polymer, and 10-fold of chitosan. Flocculant dosage required for > 90 % flocculation efficiency in the presence of AOM was 160 mg/L, 50 mg/L, and 20 mg/L when using AlCl_3, chitosan, and best (more efficient) synthetic polymer respectively. The high-ionic strength of saline water did not have a significant effect on flocculation efficiency when using AlCl_3. However, to achieve efficient algal biomass removal, application of highly-charged synthetic polymers was required to overcome the presence of electrolytes. The best synthetic cationic polymer tested herein, which achieved greater than 90 % flocculation efficiency at 20 mg/L dosage, was a polymer with 99 % cationic charge density. Cell concentration also affected flocculant dosage requirement; low density cultures (10^6 cells/mL) required 6-fold greater dosages than cultures grown until early stationary phase (10^7 cells/mL). The second study addresses cultivation, extraction and purification challenges of two complex recombinant proteins, an immunotoxin molecule (MT51) and malaria vaccine antigen (Pfs25) produced in the chloroplast of C. reinhardtii. Main challenges identified were i) low transgene expression level, ii) proteolytic instability of MT51 immunotoxin, and iii) aggregation of Pfs25 antigen. Optimal expression and accumulation of Pfs25 antigen required growing C. reinhardtii cultures to late exponential phase (10^6 cells/mL) and inducing transgene expression for 24 h at a photon irradiance of 120 µmol/m^2s.

Tens of thousands of migrants headed for the Greece-EU border line immediately after the Turkish Government's decision that it would not prevent third-country nationals wishing to cross into Europe in early spring 2020. This study examines the primary motivations of immigrants and their experiences in encountering Turkish and Greek security forces during the period in question. This study also proceeds from the idea that the immigration institution is autonomous. A total of eleven immigrants were interviewed in nine interviews using in-depth and semi-structured interview techniques. In the light of the data provided by the interviewees, it is understood that they are in an environment of insecurity in all aspects of life in Turkey, that they do not have legal status, employment, income and job security, and that immigrants have become even more vulnerable with the recent economic crisis in the country. The mass migration movement towards Europe in 2015, which is still vividly in the memories of immigrants, positively affects their motivation as an example of a successful border crossing. The Turkish Government faces immigration autonomy as it tries to regulate immigration forward; however, a tacit alliance is formed between the two agents. An irreconcilable conflict is experienced between the immigrants and the Greek border guards. Greek troops employ a strategy designed to create violence and shock, and the immigrants adopt survival against this strategy as the primary method.

Les patients atteints de maladies inflammatoires de l'intestin (MII) ont un risque accru de développer un cancer colorectal dû aux lésions épithéliales secondaires à l’inflammation chronique. La vitamine D (vD) régule NOD2, gène impliqué dans la réponse inflammatoire et dans la susceptibilité aux MII, et induit son expression dans les monocytes et dans l’épithélium intestinal. Dans ce projet, nous avons d’abord induit le cancer colorectal associé à la colite ulcéreuse (CAC) en administrant un traitement combiné d’azoxyméthane (AOM) et de dextran de sulfate de sodium (DSS) aux souris C57BL/6J. Par la suite, nous avons étudié l'effet d’une carence en vD3 sur le développement du CAC et évalué la capacité préventive d’une supplémentation en vD3 sur la tumorigenèse, et vérifié si cet effet est médié par NOD2, en utilisant les souris Nod2-/-. Les C57BL/6J et les Nod2-/-, ayant reçu une diète déficiente en vD3, étaient moins résistantes au CAC par rapport aux souris supplémentées. Le pourcentage de perte de poids, l’indice d’activation de la maladie (DAI), le taux de mortalité et le poids relatif du côlon (mg/cm) chez les souris déficientes en vD3 étaient plus élevés en comparaison avec celles supplémentées en vD3. Une augmentation du score d'inflammation et de la multiplicité tumorale corrélait avec une expression accentuée de l’Il6 dans les colonocytes des souris déficientes en vD3. La vD3 régulait l’expression génétique de Cyp24, Vdr et de gènes pro-inflammatoires chez les C57BL/6, comme chez les Nod2-/-. En conclusion, la supplémentation en vD3 peut prévenir le développement du CAC indépendamment de NOD2. / Patients with inflammatory bowel disease (IBD) have an increased risk of developing colorectal cancer due to continuing epithelial cell injury from the chronic inflammatory process. Vitamin D (vD) regulates NOD2, a gene involved in the inflammatory response and in IBD susceptibility, and induces its expression in monocytes and intestinal epithelial cells. In this project, we first established an azoxymethane (AOM)/dextran sodium sulfate (DSS) murine model of colitis-associated colorectal cancer (CAC) using C57Bl/6J. We then investigated the effect of vD3 deficiency on CAC development, and evaluated the ability of vD3 supplementation to prevent tumorigenesis. Lastly, we assessed whether the preventive benefits of vD3 on colon carcinogenesis are mediated via NOD2 using Nod2 knockout mice (Nod2-/-). vD3 deficient C57Bl/6J and Nod2-/- mice displayed increased severity of AOM/DSS-induced CAC compared to mice given vD3 supplemented diets. In vD3 deficient mice, body weight loss, Disease Activity Index (DAI), mortality rate and the colon weight/length ratio were higher compared to vD3-supplemented mice. An increased inflammation score was observed in the mucosa of vD3 deficient mice along with augmentation in the expression level of IL-6. Higher tumour multiplicity was also observed in vD3 deficient groups compared to vD3-supplemented groups. In both C57Bl/6J and Nod2-/- mice, vD3 regulated Cyp24, Vdr and pro-inflammatory genes. In conclusion, vD3 supplementation can prevent CAC independently of NOD2.

This diploma thesis deals with the efficiency and factors affecting the adsorption of AOM (Algal Organic Matter) amino acids (AAs) arginine (Arg), phenylalanine (Phe) and aspartic acid (Asp) onto granular activated carbon (GAC) Picabiol 12x40 (PIC). The efficiency of AOM AAs removal was studied in laboratory equilibrium and kinetic experiments and it was shown that the adsorption efficiency of the selected AAs is dependent on the structure of the molecule of AAs and the nature of the functional groups of their side chain, and more particularly to solution pH, which determines the nature and size and surface charge of AAs and GAC. In contrast to this, the ionic strength (IS) of solution had relatively low effect on the AAs adsorption. Arg adsorption efficiency increased with increasing pH and reached a maximum at pH 9, where AAs and GAC were oppositely charged, and this leads to attractive electrostatic interactions. In the case of Asp adsorption on PIC practically did not work. The reason is that under all experimental conditions Asp molecules and the surface of the PIC carried identical negative charge. This led to the strong electrostatic repulsion between Asp and PIC which prevented effective adsorption. In the case of Phe the adsorption decreases with increasing pH. Maximum adsorption...