Author ORCID Identifier

Year of Publication


Degree Name

Doctor of Philosophy (PhD)

Document Type

Doctoral Dissertation




Chemical and Materials Engineering

First Advisor

Dr. Christina M. Payne

Second Advisor

Dr. Stephen Rankin


The world is presently faced with a sustainability crisis; it is becoming increasingly difficult to meet the energy and material needs of a growing global population without depleting and polluting our planet. Greenhouse gases released from the continuous combustion of fossil fuels engender accelerated climate change, and plastic waste accumulates in the environment. There is need for a circular economy, where energy and materials are renewably derived from waste items, rather than by consuming limited resources. Deconstruction of the recalcitrant linkages in natural and synthetic polymers is crucial for a circular economy, as deconstructed monomers can be used to manufacture new products. In Nature, organisms utilize enzymes for the efficient depolymerization and conversion of macromolecules. Consequently, by employing enzymes industrially, biotechnology holds great promise for energy- and cost-efficient conversion of materials for a circular economy. However, there is need for enhanced molecular-level understanding of enzymes to enable economically viable technologies that can be applied on a global scale. This work is a computational study of key enzymes that catalyze important reactions that can be utilized for a bio-based circular economy. Specifically, bioinformatics and data- mining approaches were employed to study family 7 glycoside hydrolases (GH7s), which are the principal enzymes in Nature for deconstructing cellulose to simple sugars; a cytochrome P450 enzyme (GcoA) that catalyzes the demethylation of lignin subunits; and MHETase, a tannase-family enzyme utilized by the bacterium, Ideonella sakaiensis, in the degradation and assimilation of polyethylene terephthalate (PET). Since enzyme function is fundamentally dependent on the primary amino-acid sequence, we hypothesize that machine-learning algorithms can be trained on an ensemble of functionally related enzymes to reveal functional patterns in the enzyme family, and to map the primary sequence to enzyme function such that functional properties can be predicted for a new enzyme sequence with significant accuracy. We find that supervised machine learning identifies important residues for processivity and accurately predicts functional subtypes and domain architectures in GH7s. Bioinformatic analyses revealed conserved active-site residues in GcoA and informed protein engineering that enabled expanded enzyme specificity and improved activity. Similarly, bioinformatic studies and phylogenetic analysis provided evolutionary context and identified crucial residues for MHET-hydrolase activity in a tannase-family enzyme (MHETase). Lastly, we developed machine-learning models to predict enzyme thermostability, allowing for high-throughput screening of enzymes that can catalyze reactions at elevated temperatures. Altogether, this work provides a solid basis for a computational data-driven approach to understanding, identifying, and engineering enzymes for biotechnological applications towards a more sustainable world.

Digital Object Identifier (DOI)

Funding Information

This study was supported by the National Science Foundation Chemical, Bioengineering, Environmental and Transport Systems (CBET) Grant (no.: 1552355) from 2016 to 2021.

Available for download on Sunday, January 30, 2022