Theses and Dissertations at Montana State University (MSU)
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Item An omics-based interrogation of disparate microbial systems: multi-omics analysis of a bio-mining archaeon and the effects of arsenic on the E. coli Lipidome(Montana State University - Bozeman, College of Letters & Science, 2023) Fausset, Hunter Lee; Chairperson, Graduate Committee: Brian Bothner; This is a manuscript style paper that includes co-authored chapters.Systems biology represents the next frontier in the elucidation of biochemical mechanisms, disease states, and microorganisms. Rather than approaching individual parts of an organism, such as a specific protein, molecule, or mRNA, a systems biology or "omics" investigation seeks to characterize all proteins, molecules, or RNA simultaneously. This is crucial, because all macromolecules in a lifeform exist in dynamic equilibria with those around them; no one biological process occurs in a vacuum. Omics investigations have ballooned in usage over the last decades due to scientists realizing their power in characterizing complex biological phenomena. This has also been spurred on by advances in technologies enabling the robust elucidation of thousands of molecules at once, particularly benefitting from the modernization of mass spectrometry. This technique can be used to study any number of biological problems including those presented here; a multi-omics investigation into a mineral- eating methanogen and a lipidomic characterization of arsenic exposure in a key member of the gut microbiome, E.coli. Methanosarcina barkeri, a widespread methanogen found in marine sediments, is able to reductively dissolve minerals such as pyrite (FeS2) to satisfy their iron and sulfur requirements. Presented here are two investigations containing transcriptomic, proteomic, metabolomic, and lipidomic analyses, performed in parallel on the same biomass. Together, these experiments suggest that the organism undergoes a significant phenotypic shift in response to changes in just two elements, Fe and S. Overall inferences are echoed in the small molecule analyses; the metabolomes and lipidome of the organism change similarly in to the proteome. Key sulfur equilibria are implied in the process, as are specific lipids, choline, and dethiobiotin. A similar approach was applied to E.coli treated with arsenic, as a proxy for understanding the detoxifcation that takes place in the gut microbiome after ingestion. Marked lipidomic changes were observed in E.coli resulting from treatment, which were dependent both on species of arsenic as well as presence of the Ars operon. As a foundational study, this work answered some and generated many more hypotheses on the biochemical fate of As in microorganisms in the gut microbiome.Item Proteomics analysis of the metabolic transition between aerobic and anaerobic conditions in Escherichia coli(Montana State University - Bozeman, College of Letters & Science, 2019) Refai, Mohammed Yahya; Chairperson, Graduate Committee: Brian Bothner; Nina Paris, Hunter Fausset, Monika Tokmina Lukaszewska were co-authors of the article, 'Proteomics analysis of the transition between aerobic and anaerobic growth conditions in Escherichia coli' submitted to the journal 'Biochimica et biophysica acta' which is contained within this dissertation.As a facultative anaerobe, Escherichia coli has the ability to grow in anaerobic and aerobic environments. Despite detailed characterizations of this model organism in the presence and absence of oxygen, an in-depth understanding of changes to the proteome during transitions from aerobic to anaerobic growth is lacking. This thesis work focuses on elucidating how protein thiol oxidation and reduction change during a facultative anaerobe's transition from aerobic to anaerobic growth conditions, and pathways of thiol-mediated cell signaling. Redox driven changes in cysteine oxidation involved in signaling are referred to as 'thiol switches'. These modulate diverse biological activities ranging from gene expression and protein synthesis to environmental stress response. Surprisingly, little is known about the role of thiol switches during microbial transitions from aerobic and anaerobic growth conditions. To explore this uncharted territory, a mass-spectrometry (MS)-based proteomics workflow was developed and refined. Following extensive protocol optimization for high-throughput MS data processing, normalization, and pattern matching, the analytical pipeline was fine-tuned for the specific proteome-wide analysis of cysteine chemical modifications in E. coli. The approach was based on open-source software and publicly accessible databases, creating a transparent, reproducible, and easily sharable proteomics approach. Herein, the redox state and chemical forms of protein-based thiol switches in E. coli were characterized over time as the bacterium reversibly transitioned between aerobic and anaerobic growth conditions. Unexpectedly, differential alkylation analysis of cysteine-containing E. coli proteins revealed a higher degree of protein thiol oxidation under anaerobic growth conditions, a result not reported for E. coli or any other facultative anaerobe. Our proteome-wide analysis also revealed that cysteine redox potentials vary widely, and several specific E. coli proteins contain highly reactive thiols. These findings provide strong evidence for thiol-based signaling in E. coli in response to environmental changes such as aerobic to anaerobic growth transitions. Characterization of specific redox switches underlying metabolic changes associated with oxygen availability has uncovered a previously unknown E. coli cell signaling mechanism. Since transitioning between aerobic and anaerobic environments is associated with bacterial virulence, this work opens new avenues to target pathogenic facultative anaerobes and to develop novel thiol-based antibacterial therapies.