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Creeping bentgrass (Agrostis stolonifera L.) is a major low-cut cool-season turfgrass used worldwide. The objectives of this research were to: 1) to gain insight into the diurnal fluctuation of N metabolism and effects of cytokinin (CK) and nitrate; 2) to characterize the impacts of N and CK on creeping bentgrass under heat stress; 3) to investigate the simultaneous effects of CK and N on the antioxidant responses of heat stressed creeping bentgrass; and 4) to examine the expression pattern of the major heat shock proteins (HSPs) in creeping bentgrass during different heat stress periods, and then to study the influence of N on the expression pattern of HSPs. The transcript abundance of nitrate reductase (NR), nitrite reductase (NIR), plastidic glutamine synthetase (GS2), ferredoxin-dependent glutamate synthase (Fd-GOGAT), and glutamate dehydrogenase (GDH) and N metabolites in shoots were monitored during the day/night cycle (14/8 h). All the measured parameters exhibited clear diurnal changes, except GS2 expression and total protein. Both NR expression and nitrate content in shoots showed a peak after 8.5 h in dark, indicating a coordinated oscillation. Nitrate nutrition increased diurnal variation of nitrate content compared to control and CKHowever, CK shifted the diurnal in vivo NR activity pattern during this period. Grass grown at high N had better turf quality (TQ), higher Fv/Fm, normalized difference vegetation index (NDVI), and chlorophyll concentration at both 15 d and 28 d of heat stress than at low N, except for TQ at 15 d. Shoot NO3-, NH4+, and amino acids increased due to the high N treatment, but not water soluble proteins. High N also induced maximum shoot nitrate reductase activity (NRmax) at 1 d. CK increased NDVI at 15 d and Fv/Fm at 28 d. In addition, grass under 100 µM CK had greatest NRmax at both 1 d and 28 d. Under high N with 100 µM CK, root tZR and iPA were 160% and 97% higher than under low N without CK, respectively. Higher O2- production, H2O2 concentration, and higher malonydialdehyde (MDA) content in roots were observed in grass grown at high N. The activities of superoxide dismutase (SOD), ascorbate peroxidase (APX), and guaiacol peroxidase (POD) in roots were enhanced by high N at 19, 22, and 24% levels, respectively, relative to low N. Twenty-eight days of heat stress resulted in either the development of new isoforms or enhanced isoform intensities of SOD, APX, and POD in roots compared to the grass responses prior to heat stress. However, no apparent differences were observed among treatments. No CK effects on these antioxidant parameters were found in this experiment. At week seven, grass at medium N had better TQ, NDVI, and Fv/Fm accompanied by lower shoot electrolyte leakage (ShEL) and higher root viability (RV), suggesting better heat resistance. All the investigated HSPs (HSP101, HSP90, HSP70, and sHSPs) were up-regulated by heat stress. Their expression patterns indicated cooperation between different HSPs and that their roles in creeping bentgrass thermotolerance were affected by N level. / Ph. D.

Ruminant animals consuming low N-diet have been reported to have increased urea reabsorption with the Nguni being categorized as N-recycling ruminant. The enzymes associated with N-cycling are hypothesized to contribute to survival of the Nguni in harsh conditions. Enzymes responsible for such a function needed to be characterized in order to determine their effect in the functioning of the Nguni as opposed to Hereford breed. Crude enzymes from both breeds were separated from most or some contaminants by sephadex G-25, DEAE sephacel, and different affinity column chromatography. CPS and GDH were successfully purified and characterized by LC-MS/MS and further analysed by ProteinPilot™, blasted and matched >95% with those of Bos Taurus. Comparison of characterized enzymes and those which failed to ionise such as ARG, GS and GA was done using kinetics and graphs annotating specific activities. Partial purification and characterization was in part achieved. / Life & Consumer Sciences / M. Sc. (Life Sciences)

Os modelos de evolução de vias metabólicas estão baseados em técnicas moleculares e bioinformática e nem sempre levam em consideração o contextos fisiológico e ecológico do organismo. Assim, tomando como plataforma o metabolismo de nitrogênio, procurou-se estabelecer uma hipótese evolutiva para o uso de α-aminoácidos por metazoários como fonte de nitrogênio. O objetivo é traçar essa história evolutiva, contextualizando fisiológica e ecologicamente as alterações que ocorreram no perfil de utilização desses compostos. Para traçar essa história evolutiva, recorreu-se a dados disponíveis na literatura partindo-se dos elementos moleculares/metabólicos que compõem o ciclo do nitrogênio e em qual contexto geológico e evolutivo se deu tal história. Os dados obtidos, reorganizados e reestruturados nesse novo contexto, permitiram conclusões originais no presente trabalho, a saber: (1) a capacidade de fixação de nitrogênio atmosférico foi um fator de seleção natural positiva na transição da atmosfera redutora para oxidante; (2) os organismos fixadores de nitrogênio são bem mais disseminados do que o admitido classicamente; (3) o produto final da fixação biológica de nitrogênio in vivo são α- aminoácidos, e foram um fator de pressão seletiva para os organismos incapazes de fixar nitrogênio; (4) os metazoários evoluíram posteriormente a esse cenário e seu aparato metabólico está mais adaptado para o aproveitamento líquido do nitrogênio obtido apenas na forma de α-aminoácidos. / Metabolic pathway evolution models are molecular and computational based, and do not take account the physiological and ecological contexts in which organisms are inserted. Thus using the nitrogen metabolism as a platform, an evolutionary hypothesis on the α-amino acids utilization by metazoans was proposed. The objective of the present work is to trace an evolutionary history of the nitrogen usage by metazoans taking account the profile changes on a physiological and ecological basis. In order to trace this evolutionary history, a scrutiny were performed in the specialized literature aiming at data about the molecular and metabolic elements which perform the nitrogen cycle and in which geologic and evolutive context has passed such history. The reorganization of obtained data in a new context allowed original conclusions in the present work as follows: (1) the capability of fixing the atmospheric nitrogen was a positive selection factor in the atmospheric condition transition from reductive to oxidant; (2) nitrogen fixing organisms are far most wide spread than classically admitted; (3) α-amino acids are the biological nitrogen fixation end product in vivo, and are a selective factor for non-fixing organisms; (4) metazoans evolved afterwards in these scenario and their metabolic apparatus is adapted to the nitrogen net utilization obtained in the α-amino acid form.

Os modelos de evolução de vias metabólicas estão baseados em técnicas moleculares e bioinformática e nem sempre levam em consideração o contextos fisiológico e ecológico do organismo. Assim, tomando como plataforma o metabolismo de nitrogênio, procurou-se estabelecer uma hipótese evolutiva para o uso de α-aminoácidos por metazoários como fonte de nitrogênio. O objetivo é traçar essa história evolutiva, contextualizando fisiológica e ecologicamente as alterações que ocorreram no perfil de utilização desses compostos. Para traçar essa história evolutiva, recorreu-se a dados disponíveis na literatura partindo-se dos elementos moleculares/metabólicos que compõem o ciclo do nitrogênio e em qual contexto geológico e evolutivo se deu tal história. Os dados obtidos, reorganizados e reestruturados nesse novo contexto, permitiram conclusões originais no presente trabalho, a saber: (1) a capacidade de fixação de nitrogênio atmosférico foi um fator de seleção natural positiva na transição da atmosfera redutora para oxidante; (2) os organismos fixadores de nitrogênio são bem mais disseminados do que o admitido classicamente; (3) o produto final da fixação biológica de nitrogênio in vivo são α- aminoácidos, e foram um fator de pressão seletiva para os organismos incapazes de fixar nitrogênio; (4) os metazoários evoluíram posteriormente a esse cenário e seu aparato metabólico está mais adaptado para o aproveitamento líquido do nitrogênio obtido apenas na forma de α-aminoácidos. / Metabolic pathway evolution models are molecular and computational based, and do not take account the physiological and ecological contexts in which organisms are inserted. Thus using the nitrogen metabolism as a platform, an evolutionary hypothesis on the α-amino acids utilization by metazoans was proposed. The objective of the present work is to trace an evolutionary history of the nitrogen usage by metazoans taking account the profile changes on a physiological and ecological basis. In order to trace this evolutionary history, a scrutiny were performed in the specialized literature aiming at data about the molecular and metabolic elements which perform the nitrogen cycle and in which geologic and evolutive context has passed such history. The reorganization of obtained data in a new context allowed original conclusions in the present work as follows: (1) the capability of fixing the atmospheric nitrogen was a positive selection factor in the atmospheric condition transition from reductive to oxidant; (2) nitrogen fixing organisms are far most wide spread than classically admitted; (3) α-amino acids are the biological nitrogen fixation end product in vivo, and are a selective factor for non-fixing organisms; (4) metazoans evolved afterwards in these scenario and their metabolic apparatus is adapted to the nitrogen net utilization obtained in the α-amino acid form.

Ruminant animals consuming low N-diet have been reported to have increased urea reabsorption with the Nguni being categorized as N-recycling ruminant. The enzymes associated with N-cycling are hypothesized to contribute to survival of the Nguni in harsh conditions. Enzymes responsible for such a function needed to be characterized in order to determine their effect in the functioning of the Nguni as opposed to Hereford breed. Crude enzymes from both breeds were separated from most or some contaminants by sephadex G-25, DEAE sephacel, and different affinity column chromatography. CPS and GDH were successfully purified and characterized by LC-MS/MS and further analysed by ProteinPilot™, blasted and matched >95% with those of Bos Taurus. Comparison of characterized enzymes and those which failed to ionise such as ARG, GS and GA was done using kinetics and graphs annotating specific activities. Partial purification and characterization was in part achieved. / Life and Consumer Sciences / M. Sc. (Life Sciences)

Doctor of Philosophy / Department of Plant Pathology / Richard B. Todd / Fungi can be found living in a range of environments, including soil and the ocean, and as pathogens of plants and animals. The ability of fungi to adapt to diverse and changing environments is dependent on their ability to sense and respond to an array of signals, including the presence or absence of nitrogen nutrients. Fungi can utilize a diverse array of nitrogen nutrients and do so in a regulated and preferential manner. When preferred nitrogen nutrients such as ammonium and glutamine are present (nitrogen sufficiency), genes required for the utilization of alternative nitrogen sources are not expressed. In the absence of a preferred nitrogen source (nitrogen limitation) the genes for utilization of alternative nitrogen sources are transcriptionally derepressed and can be induced by the presence of a particular nitrogen nutrient, such as nitrate or proline. In the absence of any nitrogen nutrient (nitrogen starvation) the expression of some genes is further elevated. In filamentous fungi the expression of genes required for the utilization of nitrogen nutrients is coordinated by the orthologs of the conserved Aspergillus nidulans GATA transcription factor AreA, which activates transcription of nitrogen utilization genes. AreA activity is controlled by autogenous transcriptional activation, mRNA transcript stability, regulated nucleo-cytoplasmic distribution, and interactions with NmrA, AreB and TamA. The combined effect of these regulatory mechanisms generally results in AreA being inactive during nitrogen sufficiency and active during nitrogen limitation and nitrogen starvation. However, during nitrogen sufficiency AreA remains active at the promoters of some genes, including gdhA, which encodes the key nitrogen assimilation enzyme NADP-dependent glutamate dehydrogenase. In this work we have used both classical genetics and next generation sequencing approaches to examine regulated gene expression and how AreA activity is modulated, primarily during nitrogen sufficiency. We have studied regulation of gdhA to characterize how AreA evades nitrogen metabolite repression. We identify leucine biosynthesis as being a key regulatory signal involved in gdhA expression and characterize the genes required for leucine biosynthesis. We also show that TamA regulates the gdhA promoter by direct DNA binding, which requires interaction with AreA. We have also characterized repression of AreA to identify a potential mode of NmrA corepressor action. Finally, we have characterized the AreA nuclear export signal and explored mechanisms that control regulated nuclear export of AreA.

L’atmosphère terrestre est très riche en azote (N2). Mais cet azote diatomique est sous une forme très stable, inutilisable par la majorité des êtres vivants malgré qu’il soit indispensable pour la synthèse de matériels organiques. Seuls les procaryotes diazotrophiques sont capables de vivre avec le N2 comme source d’azote. La fixation d’azote est un processus qui permet de produire des substances aminées à partir de l’azote gazeux présent dans l’atmosphère (78%). Cependant, ce processus est très complexe et nécessite la biosynthèse d’une vingtaine de protéines et la consommation de beaucoup d’énergie (16 molécules d’ATP par mole de N2 fixé). C’est la raison pour laquelle ce phénomène est rigoureusement régulé. Les bactéries photosynthétiques pourpres non-sulfureuses sont connues pour leur capacité de faire la fixation de l’azote. Les études faites à la lumière, dans le mode de croissance préféré de ces bactéries (photosynthèse anaérobie), ont montré que la nitrogénase (enzyme responsable de la fixation du diazote) est sujet d’une régulation à trois niveaux: une régulation transcriptionnelle de NifA (protéine activatrice de la transcription des gènes nif), une régulation post-traductionnelle de l’activité de NifA envers l’activation de la transcription des autres gènes nif, et la régulation post-traductionnelle de l’activité de la nitrogénase quand les cellules sont soumises à un choc d’ammoniaque. Le système de régulation déjà décrit fait intervenir essentiellement une protéine membranaire, AmtB, et les deux protéines PII, GlnB et GlnK. Il est connu depuis long temps que la nitrogénase est aussi régulée quand une culture photosynthétique est exposée à la noirceur, mais jusqu’aujourd’hui, on ignore encore la nature des systèmes intervenants dans cette régulation. Ainsi, parmi les questions qui peuvent se poser: quelles sont les protéines qui interviennent dans l’inactivation de la nitrogénase lorsqu’une culture anaérobie est placée à la noirceur? Une analyse de plusieurs souches mutantes, amtB- , glnK- , glnB- et amtY- poussées dans différentes conditions de limitation en azote, serait une façon pour répondre à ces interrogations. Alors, avec le suivi de l’activité de la nitrogénase et le Western Blot, on a montré que le choc de noirceur provoquerait un "Switch-off" de l’activité de la nitrogénase dû à une ADP-ribosylation de la protéine Fe. On a réussit aussi à montrer que ii tout le système déjà impliqué dans la réponse à un choc d’ammoniaque, est également nécessaire pour une réponse à un manque de lumière ou d’énergie (les protéines AmtB, GlnK, GlnB, DraG, DraT et AmtY). Or, Rhodobacter capsulatus est capable de fixer l’azote et de croitre aussi bien dans la micro-aérobie à la noirceur que dans des conditions de photosynthèse anaérobies, mais jusqu'à maintenant sa régulation dans l’obscurité est peu étudiée. L’étude de la fixation d’azote à la noirceur nous a permis de montrer que le complexe membranaire Rnf n’est pas nécessaire à la croissance de R. capsulatus dans de telles conditions. Dans le but de développer une façon d’étudier la régulation de la croissance dans ce mode, on a tout d’abord essayé d’identifier les conditions opératoires (O2, [NH4 + ]) permettant à R. capsulatus de fixer l’azote en microaérobie. L’optimisation de cette croissance a montré que la concentration optimale d’oxygène nécessaire est de 10% mélangé avec de l’azote. / The atmosphere of the Earth is very rich in nitrogen (N2). However, diatomic nitrogen is very stable and therefore unusable by the majority of life forms even though it is necessary for the synthesis of a variety of organic compounds. Only diazotrophic procaryotes are capable of using N2 as nitrogen source. Their nitrogen fixation allows the production of aminated compounds from atmospheric nitrogen (78 %). However, this process is very complex and requires the biosynthesis of about twenty proteins and the consumption of a lot of energy (16 molecules of ATP per molecule of N2 fixed), thus necessitating its tight regulation. The purple non-sulfur photosynthetic bacteria are known for their ability to carry out nitrogen fixation. Studies conducted in the light, the preferred mode of growth of these bacteria (anaerobic photosynthetic), have shown that nitrogenase (the enzyme responsible for dinitrogen fixation) is subject to regulation at three levels: transcriptional regulation of NifA (activator protein for the transcription of nif genes), posttranslational regulation of the activity of NifA to activate nif gene transcription, and posttranslational regulation of nitrogenase activity when cells are subjected to an ammonium shock. The control system already described involves essentially a membrane protein, AmtB and both PII proteins, GlnK and GlnB. It has long been known that nitrogenase is regulated when light is suddenly removed from a culture, but until now it is unclear whether these systems are also involved in the regulation of nitrogen fixation in dark. Thus, one outstanding question is what are the proteins involved in the inactivation of nitrogenase when a light-grown culture is placed in the dark? An analysis of several mutant strains; amtB-, glnK-, glnB-, and amtY- under different conditions of nitrogen deficiency was used to address this question. Using measurements of nitrogenase activity and Fe protein modification by Western blotting, we were able to show that darkness causes a "switch-off” of nitrogenase due to ADP- ribosylation of Fe protein. Thus, the system that has already been described as involved in the response to a lack of ammonia, is also required for a response to a lack of light or energy (AmtB, GlnK, GlnB, DraG, and DraT, and AmtY). However, Rhodobacter capsulatus is also able to fix nitrogen and grow micro-aerobically in the dark as well as photosynthetically under anaerobic conditions, but so far its regulation in the dark has been little studied. The study of nitrogen fixation in the dark allowed us to show that the Rnf membrane complex is not required for growth of R. capsulatus in such conditions. In order to develop a way to study its regulation during this growth mode, we have attempted to identify the operating conditions (O2, [NH4+]), allowing R. capsulatus to fix nitrogen micro-aerobically. The optimization of this conditions has shown that the optimal concentration of oxygen required is 10% mixed with nitrogen.

L'achèvement de la fermentation alcoolique est corrélé au niveau de formation de biomasse, qui varie selon les souches de levure S. cerevisiae. La maîtrise de cette fermentation passe par une meilleure compréhension des liens entre métabolisme azoté et formation de biomasse ainsi que des mécanismes contribuant aux variations de formation de biomasse entre souches. L'analyse des cinétiques de consommation de 18 composés azotés a montré que l'ordre de consommation des sources d'azote est similaire pour 14 souches et s'explique principalement par les caractéristiques cinétiques et le mode de régulation des perméases impliquées dans leur transport. Par contre, des variations sont observées dans les profils de consommation de l'azote, qui mettent en jeu des mécanismes différents suivant la disponibilité en azote du milieu. En présence d'un excès d'azote, les souches « faibles productrices » présentent une capacité limitée d'assimilation de l'ammonium ; lorsque l'azote est présent en faible quantité, elles métabolisent plus efficacement l'arginine stockée dans la vacuole pendant la phase de croissance. Afin de déterminer la distribution des flux d'azote dans la cellule, nous avons développé une approche quantitative basée sur la filiation isotopique de sources d'azote marquées 13C ou 15N. Cette étude a révélé une incorporation limitée des acides aminés exogènes dans la biomasse au profit de la synthèse de novo, à l'exception de la leucine majoritairement intégrée dans la biomasse et de l'arginine stockée dans la vacuole. Enfin, cette étude a confirmé expérimentalement que les capacités d'assimilation de l'ammonium et de remobilisation de l'arginine sont des éléments clés des différences de production de biomasse entre souches. Cette étude apporte un nouvel éclairage sur l'efficacité d'utilisation et l'allocation de sources complexes d'azote pendant la fermentation œnologique et sur les mécanismes impliqués dans la variabilité de production de biomasse chez S. cerevisiae. / The completion of alcoholic fermentation is correlated with the level of biomass formation, which varies depending on the S. cerevisiae yeast strain. Achieving a better control of the fermentation requires a better understanding of the relationship between nitrogen metabolism and biomass formation and of the mechanisms contributing to variation in biomass formation between strains. The analysis of the kinetics of consumption of 18 nitrogen compounds showed that the order of consumption of nitrogen sources is similar for 14 strains and is mainly due to the kinetic characteristics and mode of regulation of permeases involved in their transport. By cons, variations are observed in the patterns of nitrogen consumption, which involve different mechanisms depending on the availability of nitrogen in the medium. In the presence of excess nitrogen, "low producing" strains have a limited capacity for assimilation of ammonium; when nitrogen is present in small quantities, they metabolize more efficiently arginine stored in the vacuole during the growth phase. To determine the intracellular distribution of nitrogen fluxes, we developed a quantitative approach based on isotopic filiation of 13C or 15N labeled nitrogen sources. This study revealed a limited incorporation of exogenous amino acids in biomass in favor of de novo synthesis, with the exception of leucine mostly integrated in the biomass and arginine stored in the vacuole. Finally, this study confirmed experimentally that the capacity of ammonium assimilation and remobilization of arginine are key determinant governing the differences of biomass production between strains. This study sheds new light on the efficient use and allocation of complex nitrogen sources during wine fermentation and on the mechanisms involved in the differences in biomass production within the S. cerevisiae species.