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김용환

Kim, Yong Hwan
Enzyme and Protein Engineering Lab.
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Improving the synthesis of phenolic polymer using Coprinus cinereus peroxidase mutant Phe230Ala

Author(s)
Kim, Su JinJoo, Jeong ChanSong, Bong KeunYoo, Young JeKim, Yong Hwan
Issued Date
2016-06
DOI
10.1016/j.enzmictec.2016.02.014
URI
https://scholarworks.unist.ac.kr/handle/201301/20316
Fulltext
http://www.sciencedirect.com/science/article/pii/S0141022916300369
Citation
ENZYME AND MICROBIAL TECHNOLOGY, v.87-88, pp.37 - 43
Abstract
The F230A mutant of Coprinus cinereus peroxidase (CiP), which has a high stability against radical inactivation, was previously reported. In the present study, the radical-robust F230A mutant was applied to the oxidative polymerization of phenol. The F230A mutant exhibited better polymerization activities than the wild-type CiP in the presence of water-miscible alcohols i.e., methanol, ethanol, and isopropanol despite its lower stability against alcohols. In particular, the F230A mutant showed a higher consumption of phenol (40%) and yielded phenolic polymer of larger molecular weight (8850 Da) in a 50% (v/v) isopropanol-buffer mixture compared with the wild-type CiP (2% and 1519 Da, respectively). In addition, the wild-type CiP and F230A mutant had no significant differences in enzyme inactivation by physical adsorption on the polymeric products or by heat incubation, and showed comparable kinetic parameters. These results indicate that high radical stability of the F230A mutant and improved solubility of phenolic polymers in alcohol-water cosolvent systems may synergistically contribute to the production of the high molecular weight phenolic polymer.
Publisher
ELSEVIER SCIENCE INC
ISSN
0141-0229
Keyword (Author)
Enzymatic polymerizationCoprinus cinereusPeroxidaseRadical-robust mutantPhenol
Keyword
CATALYZED OXIDATIVE POLYMERIZATIONORGANIC-SOLVENTSENZYMATIC-SYNTHESISNONAQUEOUS MEDIASTABILIZATIONBIOCATALYSISINACTIVATIONDEPENDENCESTABILITYPROTEIN

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