Enzymes are biological catalysts which greatly accelerate the rates of chemical reactions, oftentimes by many orders of magnitude over the uncatalyzed reaction. The remarkable catalytic rate enhancement afforded by enzymes derives ultimately from the structure and chemical properties of the enzyme active sites, which allow enzymes to selectively bind to their substrates and to stabilize high energy chemical species and unstable intermediates along the reaction coordinate. To enhance their catalytic ability, many enzymes have also evolved to require coenzymes for optimal activity. These coenzymes often provide chemical functionality and reactivity that are not accessible by the twenty canonical amino acids and, hence, coenzymes serve to greatly enhance the diversity of chemical reactions that can be mediated by enzymes. The work described in this dissertation focuses on mechanistic studies of two enzymes that use common coenzymes in unusual ways. In the first section of this work, studies will focus on the type II isopentenyl diphosphate:dimethylallyl diphosphate isomerase (IDI-2), an essential enzyme in isoprenoid biosynthesis that employs a flavin mononucleotide (FMN) coenzyme for catalysis. In most biological systems, flavin coenzymes mediate electron transfer reactions. However, the IDI-2 catalyzed reaction involves no net redox change, raising questions as to the role of the flavin in the chemical mechanism. The chemical mechanism of IDI-2 will be interrogated with a combination of spectroscopic studies and biochemical techniques. Our studies suggest that the flavin coenzyme of IDI-2 may employ a novel mode of flavin-dependent catalysis involving acid/base chemistry. In the second section of this dissertation, attention will be focused on elucidating the chemical mechanism of 1-aminocyclopropane-1-carboxylate deaminase (ACCD), an enzyme that plays a role in regulating the production of the potent plant hormone, ethylene. ACCD is a pyridoxal-5ʹ-phosphate (PLP)-dependent enzyme that catalyzes a C-C bond cleavage event that is unique among the catalytic cycles of PLP-dependent enzymes. Altogether, our mechanistic studies of IDI-2 and ACCD help to illustrate the catalytic diversity of common coenzymes, and demonstrate that some enzymes have evolved to exploit readily available coenzymes for atypical reactions. / text

During the process of domestication and selection reduction of genetic diversity of cultivated crops occurred. Currently the main interest of breeders is to transfer some of crop wild relatives’ genes to cultivated crops. Those genes of interest are related e.g. with desease and pest resistance or drought resistance. Hybridization of wild and cultivated species is prevented by reproductive isolation. The frequent phonomenon in hybrids is called nuclear-cytoplasmic incompatibility, which is manifested by reduced fertility, sterility or lethality. In this phenomenon occurs conflict between nuclear-encoded genes with genes encoded in the organellar genomes. The identified accD candidate gene responsible for nuclear-cytoplasmic incompatibility in pea is highly variable due to insertions and deletions. High variability of the accD gene was also confirmed in the genera Lathyrus and Vicia. Variability was observed in gene sequence lenghts caused by presence of indels and single nucleotide polymorphisms. In comparative analysis with other regions of cpDNA commonly used in phylogenetics, the region of the accD gene had the highest value of parsimonially informative sites. The phylogeny derived from the region of the accD gene corresponds to the phylogeny based on combined chloroplast markers, therefore the accD gene may be suitable for this type of analysis.

L'intensification des activités industrielles et les besoins en énergie font des hydrocarbures pétroliers (HP) un enjeu majeur mondial mais augmentent aussi considérablement les risques environnementaux dans divers écosystèmes. La phytoremédiation est une phytotechnologie qui a fait ses preuves en tant que solution verte pour faire face aux contaminations des sols par des HP. La phytoremédiation des sols contaminés par les HP repose principalement sur l’activité des communautés microbiennes associées aux racines des plantes au niveau de la rhizosphère, qui peuvent non seulement favoriser la croissance des plantes hôtes mais aussi augmenter leur tolérance à divers stress biotiques et abiotiques. Parmi les défis majeurs de la phytoremédiation des sols contaminés par les HP, on compte la forte toxicité de certains composés des HP qui entravent la croissance des plantes et par conséquent l’efficacité de la phytoremédiation. Cependant, la croissance des plantes peut être positivement stimulée par la présence de rhizobactéries favorisant leur croissance (PGPR) qui sont capables d'atténuer le stress des plantes par divers mécanismes. Dans cette thèse, un total de 438 bactéries PGPR dégradant les hydrocarbures pétroliers, ont été isolées de la rhizosphère et du sol de deux espèces de plantes, Salix purpurea et Eleocharis obusta, dans un site d'une ancienne raffinerie pétrochimique à Varennes, QC, Canada. Les isolats bactériens ont été classés en 62 genres, appartenant aux phylums Actinobacteria, Bacteroidetes, Firmicutes et aux sous-groupes Alpha-, Beta- et Gamma-Proteobacteria. De plus, cette collection de cultures contient 438 isolats bactériens avec de multiples caractéristiques de dégradation et de stimulation de croissance (PGPR), représentant une diversité fonctionnelle de dégradation des HP et de caractéristiques PGPR qui pourraient être utilisées dans la phytoremédiation assistée par les bactéries, des sols contaminés par les HP. Parmi ces 438 isolats bactériens, 50 isolats représentant une large diversité taxonomique, ont été sélectionnées pour une caractérisation approfondie supplémentaire concernant leur capacité à favoriser la croissance des plantes en présence de différentes concentrations de n-hexadécane (0%, 1%, 2%, 3%) dans des conditions contrôlées. Les résultats ont indiqué que les isolats bactériens Nocardia sp. (WB46), Pseudomonas plecoglossicida (ET27), Stenotrophomonas pavanii (EB31), Bacillus megaterium (WT10) et Gordonia amicalis (WT12) ont significativement augmenté la croissance des plantes cultivées dans 3% de n-hexadécane par rapport au traitement témoin. De plus, ces isolats possèdent plusieurs traits favorisant la croissance des plantes (PGPR) tels que l'activité 1-aminocyclopropane-1-carboxylate (ACC) désaminase (ACCD), la production d'acide indole-3-acétique (IAA) et la fixation de l'azote. De plus, ces isolats étaient capables d'utiliser le n-hexadécane comme seule source de carbone et possédaient des gènes cataboliques liés à la dégradation des hydrocarbures tels que le gène de l'alcane monooxygénase (alkB), le cytochrome P450 hydroxylase (CYP153) et le gène de la naphtalène dioxygénase (nah1). Nocardia sp. isolate WB46, a été sélectionné pour le séquençage de son génome afin de déterminer sa diversité génétique et fonctionnelle relatives à la dégradation des HP et les potentiels PGPR. Les résultats ont indiqué que, sur la base des analyses du gène de l'ARNr 16S, l'hybridation ADN-ADN in silico (DDH) et l'identité moyenne des nucléotides (ANI), Nocardia sp. isolate WB46 représente une nouvelle espèce bactérienne. De plus, l'annotation fonctionnelle de son génome révèle que celui-ci contient de nombreux gènes responsables de la dégradation des hydrocarbures pétroliers tels que l'alcane 1-monooxygénase (alkB) et la naphtalène dioxygénase (ndo) ainsi que d'autres gènes liés à ses potentiels PGPR. En conclusion, la rhizosphère des espèces S. purpurea et E. obusta poussant dans un site fortement pollué par les HP représente un biotope diversifié et comprenant des bactéries PGPR avec de multiples potentiels de dégradation des HP. De plus, plusieurs isolats bactériens tels que Nocardia sp. (WB46), Pseudomonas plecoglossicida (ET27) et Stenotrophomonas pavanii (EB31) démontrent un potentiel d'utilisation comme bioinoculants pour de futures études de phytoremédiation à grande échelle. / Petroleum hydrocarbons (PHCs), as a result of intensification of industrial activities, are a global environmental issue especially in soil environments. Phytoremediation represents an ideal solution to tackle this global crisis. Phytoremediation of PHC-contaminated soils proceeds mainly through the activities of microbial communities that colonize the plant rhizosphere which might promote host plants growth and increase its tolerance to various biotic and abiotic stresses. A main challenge in phytoremediation of PHC-contaminated soils is the high toxicity of PHCs which hinder plant growth and reduce the efficiency of phytoremediation. However, plant growth may be positively stimulated by the presence of plant growth-promoting rhizobacteria (PGPR) that are able to alleviate stresses in plants through various mechanisms. In this thesis, a total of 438 petroleum hydrocarbons degrading-PGPR bacterial isolates were recovered from the rhizosphere and the surrounding bulk soil of Salix purpurea and Eleocharis obusta plants from the site of a former petrochemical plant in Varennes, QC, Canada. Bacterial isolates were classified into 62 genera, belonging to the phyla Actinobacteria, Bacteroidetes, Firmicutes and the Alpha, Beta and Gamma-subgroups of Proteobacteria. Additionally, this culture collection holds 438 bacterial isolates with multiple degradative and PGP features, representing a rich reservoir of metabolically versatile PGPR-PHC degraders that could be used in holistic, bacterial-aided phytomanagement of PHC-contaminated soils. Among the above 438 bacterial isolates, 50 bacterial strains representing a wide phylogenetic range were selected for an additional in-depth characterization regarding their ability to promote plant growth under the presence of different concentrations of n-hexadecane (0%, 1%, 2%, 3%) under gnotobiotic conditions. Results indicated that bacterial isolates Nocardia sp. (WB46), Pseudomonas plecoglossicida (ET27), Stenotrophomonas pavanii (EB31), Bacillus megaterium (WT10) and Gordonia amicalis (WT12) significantly increased the growth of plants grown in 3% n-hexadecane compared with the control treatment. Additionally, these isolates possess several plant-growth-promoting (PGP) traits such as 1-aminocyclopropane-1-carboxylate (ACC) deaminase (ACCD) activity, indole-3-acetic acid (IAA) production and nitrogen fixation. Also, these isolates were able to use n-hexadecane as sole source of carbon and have catabolic genes related to hydrocarbon degradation such alkane monooxygenase (alkB) gene, the cytochrome P450 hydroxylase (CYP153) and the naphthalene dioxygenase (nah1) gene. The isolate that showed the highest growth stimulation of plants grown in 3% n-hexadecane under gnotobiotic conditions, Nocardia sp. isolate WB46, was selected for de novo genome sequencing to unveil its genetic versatility and the mechanisms of PHCs biodegradation and PGP potentials. Results indicated that based on the 16S rRNA gene analyses, in silico DNA-DNA hybridization (DDH) and average nucleotide identity (ANI) Nocardia sp. isolate WB46 is a new species. Additionally, the functional annotation of the genome of Nocardia sp. isolate WB46 reveals that its genome contains many genes responsible for petroleum hydrocarbon degradation such as alkane 1-monooxygenase (alkB) and naphthalene dioxygenase (ndo) as well as other genes related to its PGP potentials. In conclusion, S. purpurea and E. obusta growing in a site highly polluted with PHCs are rich reservoir of diverse PGPR with multiple PHC-degradation and PGP potentials. In addition, several bacterial isolates such as Nocardia sp. (WB46), Pseudomonas plecoglossicida (ET27) and Stenotrophomonas pavanii (EB31) demonstrate potential for use as bioinoculants in future large-scale phytoremediation studies.

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