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dc.contributor.advisorGregory Stephanopoulos.en_US
dc.contributor.authorUranukul, Boonsom.en_US
dc.contributor.otherMassachusetts Institute of Technology. Department of Chemical Engineering.en_US
dc.date.accessioned2019-10-11T22:00:34Z
dc.date.available2019-10-11T22:00:34Z
dc.date.copyright2019en_US
dc.date.issued2019en_US
dc.identifier.urihttps://hdl.handle.net/1721.1/122531
dc.descriptionThesis: Ph. D., Massachusetts Institute of Technology, Department of Chemical Engineering, 2019en_US
dc.descriptionCataloged from PDF version of thesis.en_US
dc.descriptionIncludes bibliographical references.en_US
dc.description.abstractCurrently, plastics are almost exclusively produced from feedstocks derived from crude oil refining and natural gas processing. Despite the increasing awareness of the negative environmental and climate-related impacts associated with fossil fuel consumption, the relevance of fossil fuels has held steady as a result of the recent proliferation of plastics industry. The recent growing attempts to replace conventional petroleum-based production processes with renewable direct bioconversion processes, however, have not yet been made successful due to low production efficiency. Here, we studied the development of a bioprocess for the renewable production of monoethylene glycol (MEG), a precursor chemical of polyethylene terephthalate (PET) plastics, by using yeast Saccharomyces cerevisiae as biosynthesis platform. During the process, we found evidence for the existence of an endogenous biosynthetic route for MEG production from D-xylose in S. cerevisiae.en_US
dc.description.abstractBased on the discovered biosynthetic pathway, we then demonstrated the implementation of metabolic engineering and fermentation operational strategies that led to an overproduction of MEG, as well as improved strain performance during prolonged bioreactor cultivation. Using the MEG bioconversion process as the starting point, we developed another bioprocess which allowed direct conversion of D-xylose to glycolic acid, a chemical precursor of polylactic-co-glycolic acid (PLGA). Furthermore, we investigated the biosynthesis of 1,4- butanediol, a chemical precursor of thermoplastic engineering polymer polybutylene terephthalate (PBT), in S. cerevisiae. In all of these studies, ethanol fermentation emerged as an important limitation that negatively affected the efficiency of the yeast-based processes. Our attempts to disrupt ethanol fermentation, while successfully reducing ethanol production, led to a compromise in MEG production. An analysis on the energetics of our engineered S.en_US
dc.description.abstractcerevisiae, revealed that ethanol fermentation might, in fact, be a necessary requirement for maintaining the energy balance in certain systems, including the biosynthesis of MEG. These findings provide some insights as well as a better understanding of Saccharonyces cerevisiae as the microbial cell factory for the biosynthesis of small molecules other than ethanol.en_US
dc.description.statementofresponsibilityby Boonsom Uranukul.en_US
dc.format.extent220 pagesen_US
dc.language.isoengen_US
dc.publisherMassachusetts Institute of Technologyen_US
dc.rightsMIT theses are protected by copyright. They may be viewed, downloaded, or printed from this source but further reproduction or distribution in any format is prohibited without written permission.en_US
dc.rights.urihttp://dspace.mit.edu/handle/1721.1/7582en_US
dc.subjectChemical Engineering.en_US
dc.titleEngineering of Saccharomyces cerevisiae for renewable production of plastic precursor chemicals from plant biomassen_US
dc.typeThesisen_US
dc.description.degreePh. D.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineeringen_US
dc.identifier.oclc1121594768en_US
dc.description.collectionPh.D. Massachusetts Institute of Technology, Department of Chemical Engineeringen_US
dspace.imported2019-10-11T22:00:33Zen_US
mit.thesis.degreeDoctoralen_US
mit.thesis.departmentChemEngen_US


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