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Improving the Thermo-Activity and -Stability of Pectate Lyase from Dickeya dadantii DCE-01 for Ramie Degumming
- Source :
- Processes; Volume 9; Issue 12; Pages: 2106, Processes, Vol 9, Iss 2106, p 2106 (2021)
- Publication Year :
- 2021
- Publisher :
- Multidisciplinary Digital Publishing Institute, 2021.
-
Abstract
- To improve the thermal stability of pectate lyase for ramie degumming, we modified the novel pectate lyase gene (pelG403) derived from the Dickeya dadantii DCE-01 high-efficiency ramie degumming strain by site-directed mutagenesis. Twelve mutants were acquired, wherein a prospective mutant (A129V) showed better enzyme activity and thermal stability. Compared with the wild type (PelG403), the specific enzyme activity and the optimal reaction temperature of A129V in the fermentation broth increased by 20.1%, and 5 °C, respectively. Under the conditions of 55 °C and pH 9.0, the weightlessness rate of ramie raw materials of A129V increased by 6.26%. Therefore, this study successfully improved the enzyme activity and heat resistance of PelG403 in an alkaline environment, which may contribute to the development of enzyme preparations and the elucidation of the mechanism for ramie bio-degumming.
- Subjects :
- Mutant
Bioengineering
TP1-1185
degumming
thermal stability
Ramie
pectate lyase
Chemical Engineering (miscellaneous)
Food science
Site-directed mutagenesis
QD1-999
chemistry.chemical_classification
Dickeya dadantii DCE-01
site-directed mutagenesis
biology
Chemistry
Chemical technology
Process Chemistry and Technology
Wild type
biology.organism_classification
Dickeya dadantii
Enzyme assay
Enzyme
Pectate lyase
biology.protein
Subjects
Details
- Language :
- English
- ISSN :
- 22279717
- Database :
- OpenAIRE
- Journal :
- Processes; Volume 9; Issue 12; Pages: 2106
- Accession number :
- edsair.doi.dedup.....0174570b9d246d0548bfbe9143db3338
- Full Text :
- https://doi.org/10.3390/pr9122106