Directed evolution approaches were used to construct a thermally stabilized variant of Erwinia chrysanthemi pectin methylesterase A. The final evolved enzyme has four amino acid substitutions that together confer a Tm value that is approximately 11°C greater than that of the wild-type enzyme, while maintaining near-wild-type kinetic properties. The specific activity, with saturating substrate, of the thermally stabilized enzyme is greater than that of the wild-type enzyme when both are operating at their respective optimal temperatures, 60°C and 50°C. The engineered enzyme may be useful for saccharification of biomass, such as sugar beet pulp, with relatively high pectin content. In particular, the engineered enzyme is able to function in biomass up to temperatures of 65°C without significant loss of activity. Specifically, the thermally stabilized enzyme facilitates the saccharification of sugar beet pulp by the commercial pectinase preparation Pectinex Ultra SPL. Added pectin methylesterase increases the initial rate of sugar production by approximately 50%. © 2009, American Society for Microbiology. All Rights Reserved.
CITATION STYLE
Chakiath, C., Lyons, M. J., Kozak, R. E., & Laufer, C. S. (2009). Thermal stabilization of Erwinia chrysanthemi pectin methylesterase A for application in a sugar beet pulp biorefinery. Applied and Environmental Microbiology, 75(23), 7343–7349. https://doi.org/10.1128/AEM.01010-09
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