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Thermal Stabilization of Erwinia chrysanthemi pectin methylesterase a for application in a sugar beet pulp biorefinery.
- Source :
-
Applied and environmental microbiology [Appl Environ Microbiol] 2009 Dec; Vol. 75 (23), pp. 7343-9. Date of Electronic Publication: 2009 Oct 09. - Publication Year :
- 2009
-
Abstract
- 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 T(m) value that is approximately 11 degrees 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 degrees C and 50 degrees 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 degrees 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%.
- Subjects :
- Amino Acid Substitution genetics
Bacterial Proteins genetics
Biomass
Carboxylic Ester Hydrolases genetics
Directed Molecular Evolution methods
Enzyme Stability
Protein Stability
Bacterial Proteins chemistry
Bacterial Proteins metabolism
Beta vulgaris metabolism
Carboxylic Ester Hydrolases chemistry
Carboxylic Ester Hydrolases metabolism
Dickeya chrysanthemi enzymology
Subjects
Details
- Language :
- English
- ISSN :
- 1098-5336
- Volume :
- 75
- Issue :
- 23
- Database :
- MEDLINE
- Journal :
- Applied and environmental microbiology
- Publication Type :
- Academic Journal
- Accession number :
- 19820151
- Full Text :
- https://doi.org/10.1128/AEM.01010-09