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김진현

Kim, Jinhyun
Sustainable Energy Materials Laboratory
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Solvent-Free Photobiocatalytic Hydroxylation of Cyclohexane

Author(s)
Hobisch, Markusvan Schie, Morten Martinus Cornelis HaraldKim, JinhyunAndersen, Kasper RojkjaerAlcalde, MiguelKourist, RobertPark, Chan BeumHollmann, FrankKara, Selin
Issued Date
2020-08
DOI
10.1002/cctc.202000512
URI
https://scholarworks.unist.ac.kr/handle/201301/84438
Citation
CHEMCATCHEM, v.12, no.16, pp.4009 - 4013
Abstract
The use of neat reaction media, that is the avoidance of additional solvents, is the simplest and the most efficient approach to follow in biocatalysis. Here, we show that unspecific peroxygenase fromAgrocybe aegerita(AaeUPO) can hydroxylate the neat model substrate cyclohexane. H(2)O(2)was photocatalytically generated in situ by nitrogen-doped carbon nanodots (N-CNDs) and UV LED illumination.AaeUPO entrapment in alginate beads increased enzyme stability and facilitated the reaction in neat cyclohexane. N-CNDs absorption in beads containingAaeUPO created a 2-in-1 heterogeneous photobiocatalyst that was active for up to seven days under reaction conditions and produced cyclohexanol, 2.5 mM. To increase productivity, the bead size and the photocatalyst-to-enzyme ratio have been identified as promising targets for optimisation.
Publisher
WILEY-V C H VERLAG GMBH
ISSN
1867-3880
Keyword (Author)
organic mediahydroxylationPhotobiocatalysisnon-conventional mediacarbon nanodots
Keyword
CATALYZED OXYFUNCTIONALIZATIONPEROXIDASEOXIDATION

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