Spinal cord injury (SCI) leads to axonal damage and limits the ability of the brain to communicate with the rest of the body. Several bioengineered approaches have been developed for the recovery of SCI. Among these techniques, degradable guidance tubes have shown promising results. However, design of nerve guide tubes requires several design considerations and has been a significant challenge. To assess the efficacy of a prototypical implanted nerve guide tubes, it is essential to perform continuous monitoring. In this respect, magnetic resonance imaging (MRI) is one of the most reliable imaging techniques as it offers the ability to achieve extraordinary high temporal and spatial resolution in addition to its non-invasive features. In spite of the excellent image quality of non-enhanced MRI various types of contrast agents have been developed to further enhance the contrast and allow improved visualization. The MRI contrast agents principally work by shortening the T1 or T2 relaxation times of protons located nearby. The presented study was intended to evaluate the in vitro degradation of the nerve guide tubes made of poly (lactic-co-glycolic acid) (PLGA). PLGA tubes incorporated with different concentrations of superparamagnetic iron oxide (SPIO) were scanned by MRI 3T on weekly basis during the degradation period. Spin-echo (SE) sequence with various echo times (TEs) ranged from 13.3 to 314.4 msec was applied. T2 mapping was computed using in-house algorithm developed in Matlab. Least square fit was used to find the slope of the decay curve by plotting log intensity on the y-axis and echo time on the x-axis. The average T2 values were calculated. Mass loss and water uptake of the degrading tubes were also measured weekly. Moreover, the micro-structural changes of the tubes were investigated using the scanning electron microscope (SEM). The MRI results showed that the concentration of SPIO affects the signal intensity of the T2 weighted images reducing the T2 relaxation time value. Accordingly, a linear correlation between SPIO concentration and T2 relaxation time was found. At the beginning of degradation, the SPIO nanoparticles were trapped within the polymeric network. Therefore, water penetration was the predominant factor affecting the T2 relaxation times. At week 5, a significant mass loss was observed. From this stage onwards, the trapped SPIO were released from the polymeric network increasing T2 relaxation time dramatically. According to SEM images, the size of the pores in PLGA guide tubes was increased with the degradation. Approaching the end of degradation, shrinkage of the tubes was observed and the degraded nerve guide tubes were shown to be collapsed. Similar shape variation was observed in T2 weighted MR images. In summary, this study provided an approach to non-invasive monitoring of degradation behavior of nerve guide tubes using contrast enhancement. The developed technique is of great importance since it opened an insight to non-invasive monitoring of tissue engineered scaffolds for in vivo studies.

This thesis describes the characterization of benzene-degrading denitrifying cultures. Four objectives were pursued. The first objective was to identify conditions that promote or inhibit benzene decomposition and thus, to improve the biodegradation capacity of the cultures. FeS, resazurin, and nitrite had a detrimental impact on benzene degradation, whereas addition of supernatant from an active culture improved the benzene degradation activity by reducing the lag times. The second objective was to determine the microbial community composition in enrichment cultures and to identify the bacterial species that mediate benzene mineralization. Five dominant bacterial Operational Taxonomic Units (OTUs) were identified. The most abundant phylotype was related to the gram-positive Peptococcaceae family. Other bacteria present were closely affiliated with Dechloromonas, Azoarcus, Chlorobi and Anammox species. To correlate the growth of these specific microbes with benzene degradation, the abundance of specific 16S rRNA genes was monitored during mineralization process using quantitative polymerase chain reaction (qPCR). Based on the result of qPCR experiments and information about the metabolisms of the above bacteria, a syntrophic mode of benzene degradation was hypothesized to occur under denitrifying conditions. In this process, Peptococcaceae initiate attack on benzene, and ferment benzene to hydrogen and low molecular weight products such as acetate. These products are then consumed by nitrate-respiring Azoarcus and Dechloromonas or phototrophic Chlorobi. Anammox bacteria recycle and detoxify nitrite, and stabilize the culture. The third objective was to isolate and characterize pure cultures with the ability to mineralize benzene anaerobically. Dechloromonas- and Dechlorosoma-like microorganisms were isolated from several benzene-degrading microcosms. Theses bacteria, however, were not able to metabolize benzene anaerobically. The fourth objective was to investigate the key metabolic steps in the anaerobic benzene degradation pathway and to identify enzymes that are involved in this process. Differential transcription during growth of the culture on benzene versus growth on a metabolite of benzene degradation, i.e. benzoate was examined. Carboxylase-related genes were specifically transcribed in the presence of benzene. Furthermore, mRNA sequences corresponding to the genes that encode different enzymes of the benzoyl-CoA degradation pathway were present in the culture. These findings suggest that mineralization of benzene starts by its activation to benzoate through a carboxylation reaction catalyzed by benzene carboxylase. Benzoate is further metabolized through benzoyl-CoA pathway.

This thesis describes the characterization of benzene-degrading denitrifying cultures. Four objectives were pursued. The first objective was to identify conditions that promote or inhibit benzene decomposition and thus, to improve the biodegradation capacity of the cultures. FeS, resazurin, and nitrite had a detrimental impact on benzene degradation, whereas addition of supernatant from an active culture improved the benzene degradation activity by reducing the lag times. The second objective was to determine the microbial community composition in enrichment cultures and to identify the bacterial species that mediate benzene mineralization. Five dominant bacterial Operational Taxonomic Units (OTUs) were identified. The most abundant phylotype was related to the gram-positive Peptococcaceae family. Other bacteria present were closely affiliated with Dechloromonas, Azoarcus, Chlorobi and Anammox species. To correlate the growth of these specific microbes with benzene degradation, the abundance of specific 16S rRNA genes was monitored during mineralization process using quantitative polymerase chain reaction (qPCR). Based on the result of qPCR experiments and information about the metabolisms of the above bacteria, a syntrophic mode of benzene degradation was hypothesized to occur under denitrifying conditions. In this process, Peptococcaceae initiate attack on benzene, and ferment benzene to hydrogen and low molecular weight products such as acetate. These products are then consumed by nitrate-respiring Azoarcus and Dechloromonas or phototrophic Chlorobi. Anammox bacteria recycle and detoxify nitrite, and stabilize the culture. The third objective was to isolate and characterize pure cultures with the ability to mineralize benzene anaerobically. Dechloromonas- and Dechlorosoma-like microorganisms were isolated from several benzene-degrading microcosms. Theses bacteria, however, were not able to metabolize benzene anaerobically. The fourth objective was to investigate the key metabolic steps in the anaerobic benzene degradation pathway and to identify enzymes that are involved in this process. Differential transcription during growth of the culture on benzene versus growth on a metabolite of benzene degradation, i.e. benzoate was examined. Carboxylase-related genes were specifically transcribed in the presence of benzene. Furthermore, mRNA sequences corresponding to the genes that encode different enzymes of the benzoyl-CoA degradation pathway were present in the culture. These findings suggest that mineralization of benzene starts by its activation to benzoate through a carboxylation reaction catalyzed by benzene carboxylase. Benzoate is further metabolized through benzoyl-CoA pathway.

As the global population continues to increase at an alarming rate, the world, as a whole, now faces the issue of overpopulation. If the world’s natural resource consumption and environmental pollution/destruction continue at their current pace, then the earth will eventually no longer be able to sustain all of its inhabitants. Social change is the only way to prevent this. The world’s religious traditions possess particular motivational qualities with respect to people’s worldviews and behaviors. All of the world’s religious traditions are responding, in some way, to overpopulation. Traditions in isolation, however, do not address the complexities of the current ecological crisis. Overpopulation requires a broader approach that unites the respective responses. This thesis examines the value of responses to overpopulation from certain Buddhist intellectuals in the contemporary religion and ecology discourse concerning overpopulation while also underscoring instances of resonance between those responses and ones from modern Christian thinkers.

Genes involved in purine degradation in Sinorhizobium meliloti to date remain largely uncharacterized. Analysis of the bdhAxdhA2xdhB2 operon established a link between the degradation of purines and the carbon storage compound poly-3-hydroxybutyrate (PHB). This operon contains genes (xdhA2xdhB2) that encode xanthine oxidase / xanthine dehy- drogenase, an enzyme involved in the conversion of hypoxanthine and xanthine to uric acid. The bdhA gene located in the same operon encodes 3-hydroxybutyrate dehydrogenase, an enzyme responsible for catalyzing the second step in PHB degradation. This linkage be- tween the degradation of PHB (a carbon source) and purines (a nitrogen source) suggests a possible means by which Sinorhizobium meliloti obtains sufficient carbon and nitrogen to allow it to successfully colonize a host plant. Purine degradation genes in S. meliloti have also been studied by the phenotypic char- acterization of Tn5 mutants unable to utilize hypoxanthine. Mutations resulting in these phenotypes were found in three different genes, SMc03849 (ccmC), a cytochrome c bio- genesis mutant, SMb20684, a gene coding for a hypothetical protein possibly involved in the utilization of glyoxylate and SMb2192, a gene coding for a membrane spanning protein possibly involved in purine transport. In this study we further characterized these mutants by examining their ability to establish a symbiosis with Medicago sativa (alfalfa) and to fix atmospheric nitrogen. It was demonstrated that in the case of all the mutant strains there was a competitive deficiency in terms of gaining entry to root nodules relative to the wild-type strain. It was shown that this deficiency occurred even in strains capable of fixing atmospheric nitrogen suggesting that the inability to utilize hypoxanthine impairs the ability of S. meliloti to colonize the host plant. Of all of these genes studied thus far only one (SMb21292) is located in the region of the genome containing the greatest number of genes potentially involved in purine degra- dation. In this study we used transcriptional fusions to confirm the activation of genes in this genomic region when grown in media containing purines as carbon and nitrogen sources. These genes include xdhA1, SMb21284 and guaD1. Genes from the genome re- gion containing the mixed function operon including xdhA2 and guaD2 were also studied. In addition we were able to demonstrate the requirement of xdhC in producing a func- tional oxidase / xanthine dehydrogenase as well as the ability to grow on hypoxanthine or xanthine as a carbon and nitrogen source. This work was also able to demonstrate the critical nature of the LysR transcription regulator (SMb21291) in purine degradation in S. meliloti. Mutating this gene resulted in an inability to grow on hypoxanthine or xanthine as well as an alteration in levels of xanthine oxidase / xanthine dehydrogenase activity. By transducing the gene fusions into the LysR mutant background it was demonstrated that the protein coded for by SMb21291 acts to regulate or influence the expression of genes involved in the purine degradation cycle such as SMb21284 and xdhA1. In addition we were able to characterize strains with mutations in purine degradation genes in terms of their growth on different purines.

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