No description available.

Dans un monde changeant et incertain, pouvoir moduler sa réponse phénotypique selon les conditions locales représente un avantage adaptatif majeur. Cette aptitude passe par la récolte d’informations, et plus précisément, dans le cadre de la plasticité du comportement, par la combinaison d’informations passées et présentes. Ceci est rendu possible par l’apprentissage et la mémoire, qui permettent aux animaux de stocker l’information en vue d’une utilisation ultérieure. Cette thèse a pour vocation de renforcer les liens entre écologie comportementale et cognition. Tout d’abord, nous nous sommes penchés sur deux questions propres à l’utilisation d’information passée. (i) Quelle importance est accordée aux informations anciennes face aux récentes ? (ii) En cas de redondance, toutes les informations récoltées sont-elles conservées ? Nous avons montré que (i) l’hyménoptère parasitoïde Venturia canescens accorde un poids égal à l’information issue de l’exploitation de parcelles successives d’hôtes. (ii) Parmi trois sources possibles d’information passée, une seule est utilisée. Dans un second temps, nous avons testé l’hypothèse selon laquelle apprentissage et mémoire ont évolué en réponse au milieu de vie. Nous avons mené une étude comparative sur des V. canescens arrhénotoques et thélytoques vivant dans des habitats contrastés. Les résultats obtenus lors d’un conditionnement olfactif concordent en partie avec nos prédictions, renforçant l’idée d’un lien entre distribution de la ressource et apprentissage. Du point de vue théorique, la question de la valeur adaptative de la durée des différentes phases de mémoire n’a jusqu’ici pas été traitée. Un modèle de simulation est proposé pour commencer à combler cette lacune / In an uncertain and changing world, being able to shape its phenotype according to the current environmental conditions should provide individuals with a major fitness benefit. This depends on information gathering. In the context of behavioural plasticity, it more specifically implies to combine past and current information pieces. Past information use happens through learning and memory, that enables animals to store information in memory for a subsequent decision making. This thesis aims at strengthen the links between behavioural ecology and cognition. First, we tackled two questions specific to past information use. (i) Which weight is given to an older information piece in front of a more recent one? (ii) If several redundant information pieces are gathered, are they all stored? We showed that (i) the parasitoid wasp Venturia canescens seems, at the time scaled we worked with, to weight equally information pieces coming from older and more recent host patches successively foraged. (ii) Among three possible past information sources, only one is stored for a later use. Second, we tested the hypothesis that learning and memory evolved in response to ecological constraints. We conducted a comparative study with arrhenotokous and thelytokous V. canescens thriving in different habitats. Results obtained through olfactory conditioning partially matched our initial predictions; this support the idea of a link between resource distribution and learning features. From the theoretical point of view, the question of the adaptive significance of the length of memory phases has not been tackled yet. Here is shown a model, as a first attempt to fill this gap

No description available.

This study evaluated the early establishment phase of various monocultures and mixed species plantings of Agropyron desertorum (AGDE), Medicago sativa (MESA), and Atriplex canescens (ATCA). The study was conducted under both greenhouse and field conditions. In the green-house, the experimental design was a split-plot, randomized-block design in time, using transplanted seedlings. The treatments were exposed to three water levels to determine species response to varying moisture availability. Plastic pots of 15.4 cm (diameter) by 17.9 cm (depth) were filled with 2,800 g of sandy-loam soil and brought to field capacity. The pots were weighted twice weekly and the water lost to evapotranspiration was replaced. The plants were measured for plant height on six occasions at two week intervals. On the last measurement date, plants were harvested for above-and-below ground biomass. The field used the species treatment as in the greenhouse study and these were hand sown in 1 m2 plots. Using a line-source sprinkler system, species responses at four water levels were examined. Soil water content in the various field plots was determined at various depths via access tubes and a neutron soil moisture probe. The experimental design was a split-plot design in time. Seedling emergence was recorded daily for the first 35 days after seeding. Plant height was measured six times during the growing season. All the species were clipped, oven-dried, and weighed at the end of the experimental period in 1982. In the greenhouse, AGDE was the dominant species, yet produced more in the MESA combination. MESA exhibited a marked decrease in production when grown with AGDE. ATCA showed a remarkable ability to survive under high water stress. Variable soil water content created in the field resulted in significant differences in germination, emergence, and establishment among planting treatments. MESA germinated and emerged faster than AGDE and ATCA, allowing it to utilize water and nutrient resources earlier than the competing species. The greatest shoot production occurred when MESA grew alone. In the AGDE-MESA combination, shading apparently reduced AGDE growth and shoot production at the two most favorable water levels. ATCA exhibited poor germination and emergence in treatments with low soil water availability.

Des travaux de recherche en fermentation liquide ont montré que P. canescens est une souche hyperproductrice de xylanases non contaminées par des activités cellulolytiques et amylolytiques. Selon les scientifiques, lintérêt de lutilisation industrielle de ces hémicellulases dans différents secteurs (particulièrement dans la formulation daliments pour le bétail, en industries des jus de fruits et brassicoles, en amidonnerie, en industrie du papier, en pharmacie, dans les textiles et dans la production du bioéthanol) va croître significativement. Mais le développement de ces enzymes est fréquemment limité par le coût de production. Ce travail sest intéressé à loptimisation de la production des xylanases de P. canescens à partir de matières premières peu coûteuses telles les résidus agro-industriels par fermentation solide, une technique traditionnellement utilisée dans la fermentation des aliments en Asie. Létude a démontré que le tourteau de soja est un bon inducteur de la production des xylanases. La teneur initiale en eau, le pH initial, la température de la culture et laération active influencent la synthèse de l'enzyme. Compte tenu des résultats obtenus à léchelle du laboratoire, la transposition à léchelle industrielle serait facilitée naturellement par de fines épaisseurs de cultures statiques, ce qui réduit de moitié le coût de production comparativement à la fermentation liquide. Les expérimentations ont confirmé que la production de xylanases par P. canescens répondait à des phénomènes dinduction et de répression dépendant du substrat et des conditions physico-chimiques de croissance, et non pas à des phénomènes de régulation de type quorum sensing. Lenzyme sous forme liquide concentrée présente une bonne stabilité pendant six mois sans protection préalable (stérilisation, stabilisation ou inhibition de protéases).

La plasticité phénotypique, i.e. la capacité d’un génotype à exprimer plusieurs phénotypes en fonction des conditions environnementales, représente une source de variabilité phénotypique, et tient donc un rôle majeur dans l’évolution. Dans un environnement variable, les stratégies généralistes, capables de maintenir une valeur d’aptitude phénotypique (fitness) stable sur une plus large gamme de conditions environnementales grâce à une plus grande plasticité de traits sous-jacents, devraient être favorisées. L’analyse de normes de réaction, au laboratoire et en conditions naturelles, de traits physiologiques et de traits liés à la fitness en fonction de la température, révèle chez le parasitoïde Venturia canescens, que (i) la variabilité thermique de l’habitat détermine la forme des normes de réaction selon le compromis entre stratégies généraliste et spécialiste, (ii) les différences entre individus généralistes et spécialistes se maintiennent face à des fluctuations de la température mimant les conditions naturelles et (iii) les individus subissant une plus grande variabilité thermique dans leur habitat possèdent une capacité d’acclimatation au froid plus importante. Ces résultats montrent l’existence de deux stratégies chez V. canescens et donc une différenciation de leur niche thermique, autorisant leur coexistence en environnement hétérogène / Phenotypic plasticity, i.e. the ability of a genotype to express several phenotypes depending on environmental conditions, represents an important source of phenotypic variability and so plays a major role in evolution. In a variable environment, generalist strategies, able to maintain a stable value of fitness over a wide range of environmental conditions, thanks to a greater plasticity of underlying traits, should be favored. The analysis of reaction norms of physiological traits and traits related to fitness as a function of temperature reveals in the parasitoid Venturia canescens that (i) thermal variability of the habitat determines the shape of reaction norms, according to the trade-off between generalist and specialist strategies, (ii) differences between generalist and specialist individuals are maintained face to rapid fluctuations in temperature that mimic natural conditions and (iii) individuals experiencing greater variability in their thermal habitat have a greater capacity for cold acclimation. These results indicate the existence of two different strategies in V. canescens and therefore a thermal niche differentiation, allowing their coexistence in a heterogeneous environment

No description available.

Plants are constantly exposed to pathogens and various environmental stresses, such as cold, salinity and drought. Plants normally respond rapidly to these biotic and abiotic stresses. Efficient perception of biotic and abiotic stresses and cell programmed signaling mechanisms for appropriate responses are important for growth and survival of plants. Calcium is an important second messenger in signaling pathways that respond to environmental stresses, pathogen attack as well as hormonal stimuli (For review, see DeFalco et al., 2010; Reddy and Reddy, 2004; Sanders et al., 2002). The transient increase of cytosolic free calcium concentration has been shown in a variety of external signals (Reddy, 2001), which in turn triggers many signal transduction pathways leading to a variety of cellular responses (Bush, 1995). Any calcium mediated signal transduction process involves generation of signal-specific calcium signature in the cytosol (Scrase-Field and Knight, 2003). These changes in cytosolic calcium level or ‘calcium signatures’ are sensed by the specific group of proteins called the ‘calcium sensors’. Different calcium sensors recognize specific calcium signatures and transduce them into downstream effects, including altered protein phosphorylation and gene expression patterns. In plants the protein kinases are a large and differentiated group of calcium sensors. After analyzing 1264 protein kinase sequences, a superfamily of protein kinase called CDPK/SnRK family of protein kinase were defined (Hrabak et al., 2003). CDPK/SnRK family of protein kinases encompasses five subfamilies viz., calcium-dependant protein kinases, (CPKs), calcium/calmodulin dependant protein kinases (CCaMKs), calmodulin-dependant protein kinases (CaMKs), CPKrelated kinases (CRKs), and SnF1 related kinase 3 (SnRK3) and are regulated by calcium directly or indirectly. Among these, in plants, calcium-dependant protein kinases (CPKs) are predominant calcium sensors, which are shown to be involved in myriads of physiological responses. They are Ser/Thr family of protein kinases typically made up of five domains with an Nterminal variable domain followed by catalytic protein kinase domain, an autoinhibitory/ junction domain, a regulatory calmodulin-like domain (CaMLD) and a Cterminal domain of variable length. The CPKs are unique due to the presence of CaMLD which couples the calcium sensor directly to its responder (kinase domain). Although CPKs are highly conserved, there are several features that distinguish different members of the plant CDPK family. In an attempt to investigate the role of a CPK isoform, in the present work we bring out the results and inferences on isolation and characterization of a novel cDNA encoding a calcium-dependant protein kinase isoform ScCPK1 from Swainsonacanescens, a pharmaceutically important Australian herb known to produce an anticancer drug, swainsonine. Initially, we have cloned an 800 bp partial CPK cDNA from S. canescens by reverse transcription polymerase chain reaction (RTPCR) using degenerate oligonucleotide primers designed based on conserved regions of the other known CPKs. A 2.1 kb full length CPK was obtained using 5` and 3` RACE which was designated as ScCPK1. An open reading frame (ORF) of 1659 bp was detected that encodes a protein of 552 amino acids with a calculated molecular mass of 61.8 kDa. Comparison of the deduced amino acid sequence of ScCPK1 with sequences of other CPKs revealed the highest identity (>90%) to Glycine max and Vigna radiate CPKs. As described for other CPKs, ScCPK1 has a long variable domain (88 aa), an auto-inhibitory domain (31 aa) and a C-terminal calmodulin domain (145 aa) containing four EF-hand calcium binding motifs, which is found in many CPKs. Phylogenetic tree analysis showed that ScCPK1 was closely related to StCPK4 , CmCPK1 and CmCPK2. The entire coding region of ScCPK1 was cloned into pRSETA expression vector and expressed as fusion protein in E.coli. The recombinant ScCPK1 protein was purified to homogeneity by NiNTA affinity chromatography. The recombinant purified ScCPK1 was catalytically active in a calcium-dependent manner. The recombinant ScCPK1 phosphorylated itself and histone IIIS as substrate only in the presence of Ca2+. Phosphoaminoacid analyses showed that ScCPK1 phosphorylates serine and threonine residues of histone IIIS and its autophosphorylation also occurs on serine and threonine residues. ScCPK1 has a pH and temperature optima of 7.5 and 37 °C, respectively. It showed high affinity to histone III-S with a Km of 4.8 µM and had a Vmax of 4.700 pmoles of γ32P incorporation/min/mg at saturating substrate concentrations. The ScCPK1 is ~100fold active and showed 10fold higher affinities to histone III-S than CaCPK1 and CaCPK2, CPKs which were characterized from Cicer arietinum previously in our laboratory (Prakash and Jayabaskaran, 2006). From literature it is known that many CPKs are activated or inhibited by metal ions. (PutnamEvans etal., 1990; Anil and Rao, 2001). The influence of Na+ and Mg2+on the in vitro substrate phosphorylation activity of the recombinant ScCPK1 was tested in this work. Addition of NaCl strongly inhibited ScCPK1 activity. The inhibition of substrate phosphorylation activity by salt implies ionic interactions between the positively charged substrate and the enzyme’s active site. The optimum concentration of Mg2+ for ScCPK1 substrate phosphorylation activity was found to be 810 mM, similar to CaCPK1 and CaCPK2 (Prakash and Jayabaskaran, 2006). However, the activity was inhibited above 10 mM Mg2+suggesting the disruption of ionic interactions between the enzyme and the substrate. The kinase and autophosphorylation activities of the recombinant ScCPK1 were calmodulin independent and sensitive to CaM antagonists’ calmidazolium and W7 (N(6aminohexyl)5chloronaphthalene sulphonate). This indicates that the activation was supported by calmodulin-like domain, which is typical of CPK family. Farmer and Choi (1999), showed that DcCPK1 activity was inhibited by polyamines vizspermine and spermidine, and polylysine. We found that substrate phosphorylation activity of ScCPK1 was inhibited by polyLLysine with an IC50 of 8 M but not the polyamines, spermine and spermidine. An interesting aspect that makes CPKs attractive for research is their functional similarity to mammalian PKCs. There are no structural PKC analogues found in plant genomic data. Similar to PKCs, CPKs are regulated by intracellular Ca2+ signals. There is also experimental evidence that some of the CPKs are additionally activated by phospholipids (Farmer and Choi, 1999; Szczegielniak etal., 2000). We investigated the effects of lipid molecules on the activity of ScCPK1. Phosphorylation of histone IIIS by ScCPK1 was stimulated by phosphatidylethanolamine, phosphatidylserine and phosphatidylinositol in the presence of Ca2+, where as lysophosphatidylcholine, phosphatidylcholine and phosphatidic acid did not increase the enzyme activity. Our data that shows interaction of ScCPK1 with phospholipids supports the idea that this protein kinase could be associated with the membrane. The work from Farmer and Choi (1999), with DcCPK1 suggested that some of the PKClike activities observed in plants may be attributed to CPKs. They also demonstrated that DcCPK1 phosphorylated PKC pseudosubstrate peptide and also was sensitive to staurosporine inhibition. However, the protein kinase inhibitor, staurosporine inhibited the substrate phosphorylation activity of ScCPK1 completely with an IC50 value of 700 nM invitro. But PKC inhibitor PMA was less effective, inhibiting the substrate phosphorylation activity of ScCPK1 to a maximum of 50%, but at a very high concentration (200 nM). Our data suggests that ScCPK1 may not have any features attributable to PKC. We investigated subcellular localization of the ScCPK1. To gain a better understanding of the subcellular localization of the ScCPK1, we generated GFP fusion protein of ScCPK1 and transiently expressed it in Agrobacterium-mediated transformed tobacco BY2 cells. Analysis of the GFP expression patterns in transformed tobacco BY2 cells revealed ScCPK1 localization in the plasma membrane of the transformed tobacco BY2 cells despite lacking consensus myristoylation and palmitoylation motifs (as per in silico analyses). Taking together, our data have demonstrated that ScCPK1 is a Ser/Thr protein kinase and its sub-cellular localization studies revealed that it is localized to plasma membrane. We propose that ScCPK1 is a key component of one or more signaling pathways and plays vital roles in plant development, responses to environmental stimuli and/ or in secondary metabolite biosynthetic gene expression. The involvement of the ScCPK1 as a component of signaling pathways warrants further studies.

No description available.

Dans un monde changeant et incertain, pouvoir moduler sa réponse phénotypique selon les conditions locales représente un avantage adaptatif majeur. Cette aptitude passe par la récolte d'informations, et plus précisément, dans le cadre de la plasticité du comportement, par la combinaison d'informations passées et présentes. Ceci est rendu possible par l'apprentissage et la mémoire, qui permettent aux animaux de stocker l'information en vue d'une utilisation ultérieure. Cette thèse a pour vocation de renforcer les liens entre écologie comportementale et cognition. Tout d'abord, nous nous sommes penchés sur deux questions propres à l'utilisation d'information passée. (i) Quelle importance est accordée aux informations anciennes face aux récentes ? (ii) En cas de redondance, toutes les informations récoltées sont-elles conservées ? Nous avons montré que (i) l'hyménoptère parasitoïde Venturia canescens accorde un poids égal à l'information issue de l'exploitation de parcelles successives d'hôtes. (ii) Parmi trois sources possibles d'information passée, une seule est utilisée. Dans un second temps, nous avons testé l'hypothèse selon laquelle apprentissage et mémoire ont évolué en réponse au milieu de vie. Nous avons mené une étude comparative sur des V. canescens arrhénotoques et thélytoques vivant dans des habitats contrastés. Les résultats obtenus lors d'un conditionnement olfactif concordent en partie avec nos prédictions, renforçant l'idée d'un lien entre distribution de la ressource et apprentissage. Du point de vue théorique, la question de la valeur adaptative de la durée des différentes phases de mémoire n'a jusqu'ici pas été traitée. Un modèle de simulation est proposé pour commencer à combler cette lacune