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Enhanced stability and reusability of marine epoxide hydrolase using ship-in-a-bottle approach with magnetically-separable mesoporous silica

Authors
Kim, Young HyunLee, InseonChoi, Sung HeeLee, Ok KyungShim, JongminLee, JinwooKim, JungbaeLee, Eun Yeol
Issue Date
5월-2013
Publisher
ELSEVIER
Keywords
Epoxide hydrolase; Mugil cephalus; Nanoscale enzyme reactor; Mesoporous silica; Enzyme immobilization
Citation
JOURNAL OF MOLECULAR CATALYSIS B-ENZYMATIC, v.89, pp.48 - 51
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF MOLECULAR CATALYSIS B-ENZYMATIC
Volume
89
Start Page
48
End Page
51
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/103280
DOI
10.1016/j.molcatb.2012.12.012
ISSN
1381-1177
Abstract
We developed magnetically-separable and highly-stable biocatalyst system of Mugil cephalus epoxide hydrolase (McEH) for enantioselective hydrolysis of racemic epoxides. McEH protein was adsorbed and cross-linked into mesoporous silica with bottle-neck mesopores, which effectively prevented the leaching of cross-linked McEH in a larger mesocellular pores. This ship-in-a-bottle approach allows for highly loaded and stable McEH system. For example, free McEH showed only 7.5% of initial activity under shaking condition at 80 h while ship-in-a-bottled McEH retained 79.5% of initial activity in the same condition. Stable McEH in magnetically-separable mesoporous silica could achieve the yield of 45% for the preparation of enantiopure (S)-styrene oxide with 98%ee. The magnetic nanoparticles pre-incorporated in mesoporous silica enabled an easy recovery of immobilized McEH for repetitive batch resolutions of racemic styrene oxide, allowing for more than 50% of the initial activity was retained after seven recycled uses. (C) 2012 Elsevier B.V. All rights reserved.
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Kim, Jung bae
공과대학 (화공생명공학과)
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