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DC Field | Value | Language |
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dc.contributor.advisor | Rabinowitz, Joshua D. | - |
dc.contributor.author | Rubin, Sara Ann | - |
dc.date.accessioned | 2014-07-29T14:13:00Z | - |
dc.date.available | 2015-07-06T16:00:06Z | - |
dc.date.created | 2014-04-21 | - |
dc.date.issued | 2014-07-29 | - |
dc.identifier.uri | http://arks.princeton.edu/ark:/88435/dsp01hh63sw108 | - |
dc.description.abstract | Cellular metabolism is a complex network of thousands of biochemical reactions, mostly enzyme catalyzed. Enzyme usage depends on the concentration of the small molecule intermediates: metabolites, acting not only as substrates and products but also as regulators. Current technological limitations, however, hinder the direct measurement of certain core metabolites, including centrally located glyceraldehyde-3-phosphate and erythrose-4-phosphate. Here, I introduce an alternative approach, Flux Ratio-based Energy Estimation (FREE), which takes advantage of a previously underappreciated thermodynamic relationship to remedy such shortcomings. In contrast to the canonical way of calculating in vivo Gibbs free energy of reaction ( \(\Delta\) \(_{r}\)G’) from metabolite concentrations and standard Gibbs free energy of reaction ( \(\Delta\) \(_{r}\)G’\(^{o}\) ), FREE directly determines ( \(\Delta\) \(_{r}\)G’) from the ratio of forward to reverse reaction rates (fluxes). With ( \(\Delta\) \(_{r}\)G’) in hand, unknown metabolite concentrations can be computed from ( \(\Delta\) \(_{r}\)G’\(^{o}\) ) and measureable metabolite concentrations. To demonstrate the utility of this approach, FREE was applied in a comparative metabolic study of three organisms: E. coli, S. cerevisiae (baker’s yeast), and immortalized baby mouse kidney cells. Through a joint experimental and computational approach, involving liquid chromatography-mass spectrometry and metabolic flux analysis, in vivo ( \(\Delta\) \(_{r}\)G’) values were classified into three categories: precisely determinable, highly reversible, and close to irreversible. Combining these results with extensive metabolite quantitation, I was able to populate genome-scale metabolic networks with global in vivo metabolite concentrations and ( \(\Delta\) \(_{r}\)G’) values. FREE is broadly applicable and paves the way for future integrative analyses which could lead to breakthroughs in biochemical engineering as well as the study of metabolic diseases. | en_US |
dc.format.extent | 182 pages | en_US |
dc.language.iso | en_US | en_US |
dc.title | FLUX RATIO-BASED ENERGY ESTIMATION: AN INTEGRATIVE INVESTIGATION INTO CELLULAR METABOLISM | en_US |
dc.type | Princeton University Senior Theses | - |
pu.embargo.terms | 2015-07-01 | - |
pu.date.classyear | 2014 | en_US |
pu.department | Chemistry | en_US |
pu.pdf.coverpage | SeniorThesisCoverPage | - |
Appears in Collections: | Chemistry, 1926-2020 |
Files in This Item:
File | Size | Format | |
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Rubin_Sara.pdf | 4.11 MB | Adobe PDF | Request a copy |
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