Metabolic flux analysis of Escherichia coli MG1655 under octanoic acid (C8) stress

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dc.contributor.advisor Jacqueline V. Shanks
dc.contributor.author Fu, Yanfen
dc.contributor.department Chemical and Biological Engineering
dc.date 2018-08-11T17:59:27.000
dc.date.accessioned 2020-06-30T02:26:52Z
dc.date.available 2020-06-30T02:26:52Z
dc.date.copyright Sat Jan 01 00:00:00 UTC 2011
dc.date.embargo 2013-06-05
dc.date.issued 2011-01-01
dc.description.abstract <p>Metabolic engineering has evolved to the point of fulfilling the dream of having industrial chemicals produced renewably. Carboxylic acids [e.g., short chain fatty acids (SCFAs) such as octanoic acid (C8)] are such chemical intermediates that can be produced by Escherichia coli engineered with thioesterases specific for short chain fatty acids. However, C8 is toxic to E. coli at concentration greater than 10 mM. To design a better host strain for the production of large amount of SCFAs, 13C metabolic flux analysis of E. coli was performed for both C8 stress and control condition (without C8). To investigate central carbon metabolism for the culture environmental change, a mixture of labeled and unlabeled glucose was used as the sole carbon source for bacterial growth and proteinogenic amino acid isotopomers were measured using two-dimensional (13C, 1H) HSQC NMR spectroscopy. Notable differences of several amino acids isotopomer abundance were observed between the control condition and C8 stress condition, suggesting that the precursor nodes of these amino acids in metabolic pathways were responding to the stress. More specifically, the difference suggested that the distribution of fluxes among the tricarboxylic acid (TCA) cycle, pentose phosphate pathway, pyruvate node, alpha-ketoglutarate node and oxaloacetate node changed. By comparing the metabolic flux maps of E. coli MG1655 grown at different conditions, pathways that have flux change under stress were identified. Inhibition effect for several pathways, resulting in a reduction in carbon flux, was found under stress: the TCA cycle flux by ~ 44%; the malic enzyme pathway by ~ 80%; the phosphoenolpyruvate carboxylase pathway ~ 60%; the CO2 production rate by 18%; and pyruvate dehydrogenase pathway by ~50%. Meanwhile, a few pathways were activated under C8 stress: the pyruvate dehydrogenase flux (`PoxB') became active; the malate dehydrogenase pathway (`mdh') in TCA cycle increased by ~55%; and the extracellular acetate production increased by ~ 80%. Based on these results, a hypothesis was proposed that low activity of NADH dehydrogenase may lead to low ratio of NAD+/NADH which in turn causes the low activity of two major pathways (TCA cycle, and pyruvate dehydrogenase). The inefficiency of regeneration of NAD+ from NADH may occur when the cell membrane is disrupted, which has been proven by membrane fluidity study (L. Royce, L. Jarboe, unpublished data) as well as transcriptome (L. Royce, L. Jarboe, unpublished data) and proteomic (M Rodriquez, R. Gonzalez, unpublished data) data. Besides, the other reason for low ratio of NAD+/NADH is that the electron transport chain may be disrupted under stress. It is also possible that the PdhR (pyruvate dehydrogenase complex regulator) is activated by low concentration of intracellular pyruvate, which in turn represses ndh and cyoABCDE that encode two major enzymes in the electron transport chain. This hypothesis is supported by the observation that supplementation of additional pyruvate in the media helps the cell partially recover from the stress.</p>
dc.format.mimetype application/pdf
dc.identifier archive/lib.dr.iastate.edu/etd/10208/
dc.identifier.articleid 1081
dc.identifier.contextkey 2736178
dc.identifier.doi https://doi.org/10.31274/etd-180810-2244
dc.identifier.s3bucket isulib-bepress-aws-west
dc.identifier.submissionpath etd/10208
dc.identifier.uri https://dr.lib.iastate.edu/handle/20.500.12876/24432
dc.language.iso en
dc.source.bitstream archive/lib.dr.iastate.edu/etd/10208/Fu_iastate_0097M_12186.pdf|||Fri Jan 14 18:16:18 UTC 2022
dc.subject.disciplines Biological Engineering
dc.subject.disciplines Chemical Engineering
dc.title Metabolic flux analysis of Escherichia coli MG1655 under octanoic acid (C8) stress
dc.type article
dc.type.genre thesis
dspace.entity.type Publication
relation.isOrgUnitOfPublication 86545861-382c-4c15-8c52-eb8e9afe6b75
thesis.degree.level thesis
thesis.degree.name Master of Science
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