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Enzymatic Production of Cellulosic Hydrogen by Cell-free Synthetic Pathway Biotransformation(SyPaB)

dc.contributor.authorYe, Xinhaoen
dc.contributor.committeechairZhang, Yi Heng Percivalen
dc.contributor.committeecochairZhang, Chenming Mikeen
dc.contributor.committeememberBarone, Justin R.en
dc.contributor.committeememberLarson, Timothy J.en
dc.contributor.departmentBiological Systems Engineeringen
dc.date.accessioned2017-04-06T15:43:06Zen
dc.date.adate2011-09-30en
dc.date.available2017-04-06T15:43:06Zen
dc.date.issued2011-07-06en
dc.date.rdate2016-10-24en
dc.date.sdate2011-07-20en
dc.description.abstractThe goals of this research were 1) to produce hydrogen in high yields from cellulosic materials and water by synthetic pathway biotranformation (SyPaB), and 2) to increase the hydrogen production rate to a level comparable to microbe-based methods (~ 5 mmol H2/L/h). Cell-free SyPaB is a new biocatalysis technology that integrates a number of enzymatic reactions from four different metabolic pathways, e.g. glucan phosphorylation, pentose phosphate pathway, gluconeogenesis, and hydrogenase-catalyzed hydrogen production, so as to release 12 mol hydrogen per mol glucose equivalent. To ensure the artificial enzymatic pathway would work for hydrogen production, thermodynamic analysis was firstly conducted, suggesting that the artificial enzymatic pathway would spontaneously release hydrogen from cellulosic materials. A kinetic model was constructed to assess the rate-limited step(s) through metabolic control analysis. Three phosphorylases, i.e. α-glucan phosphorylase, cellobiose phosphorylase, and cellodextrin phosphorylase, were cloned from a thermophile Clostridium thermocellum, and heterologously expressed in Escherichia coli, purified and characterized in detail. Finally, up to 93% of hydrogen was produced from cellulosic materials (11.2 mol H2/mol glucose equivalent). A nearly 20-fold enhancement in hydrogen production rates has been achieved by increasing the rate-limiting hydrogenase concentration, increasing the substrate loading, and elevating the reaction temperature slightly from 30 to 32°C. The hydrogen production rates were higher than those of photobiological systems and comparable to the rates reported in dark fermentations. Now the hydrogen production is limited by the low stabilities and low activities of various phosphorylases. Therefore, non-biologically based methods have been applied to prolong the stability of α-glucan phosphorylases. The catalytic potential of cellodextrin phosphorylase has been improved to degrade insoluble cellulose by fusion of a carbohydrate-binding module (CBM) family 9 from Thermotoga maritima Xyn10A. The inactivation halftime of C. thermocellum cellobiose phosphorylase has been enhanced by three-fold at 70°C via a combination of rational design and directed evolution. The phosphorylases with improved properties would work as building blocks for SyPaB and enabled large-scale enzymatic production of cellulosic hydrogen.en
dc.description.degreePh. D.en
dc.identifier.otheretd-07202011-111024en
dc.identifier.sourceurlhttp://scholar.lib.vt.edu/theses/available/etd-07202011-111024/en
dc.identifier.urihttp://hdl.handle.net/10919/77141en
dc.language.isoen_USen
dc.publisherVirginia Techen
dc.rightsIn Copyrighten
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/en
dc.subjectsynthetic pathway biotranformation (SyPaB)en
dc.subjectrational designen
dc.subjectprotein engineeringen
dc.subjectphosphorylaseen
dc.subjectbiofuelen
dc.subjectdirected evolutionen
dc.subjecthydrogenen
dc.titleEnzymatic Production of Cellulosic Hydrogen by Cell-free Synthetic Pathway Biotransformation(SyPaB)en
dc.typeDissertationen
dc.type.dcmitypeTexten
thesis.degree.disciplineBiological Systems Engineeringen
thesis.degree.grantorVirginia Polytechnic Institute and State Universityen
thesis.degree.leveldoctoralen
thesis.degree.namePh. D.en

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