Solvent-Free Photobiocatalytic Hydroxylation of Cyclohexane

被引:35
作者
Hobisch, Markus [1 ]
van Schie, Morten Martinus Cornelis Harald [2 ]
Kim, Jinhyun [3 ]
Andersen, Kasper Rojkjaer [4 ]
Alcalde, Miguel [5 ]
Kourist, Robert [6 ]
Park, Chan Beum [3 ]
Hollmann, Frank [2 ]
Kara, Selin [1 ]
机构
[1] Aarhus Univ, Dept Engn, Biocatalysis & Bioproc Grp, Gustav Wieds Vej 10, DK-8000 Aarhus C, Denmark
[2] Delft Univ Technol, Biocatalysis Grp, Dept Biotechnol, Van der Maasweg 9, NL-2629 HZ Delft, Netherlands
[3] Korea Adv Inst Sci & Technol MST, Dept Mat Sci & Engn, 335 Sci Rd, Daejeon 305701, South Korea
[4] Aarhus Univ, Dept Mol Biol & Genet, Gustav Wieds Vej 10, DK-8000 Aarhus C, Denmark
[5] CSIC, Inst Catalysis, Dept Biocatalysis, Madrid 28049, Spain
[6] Graz Univ Technol, Inst Mol Biotechnol, Petergasse 14, A-8010 Graz, Austria
关键词
Photobiocatalysis; non-conventional media; carbon nanodots; organic media; hydroxylation; CATALYZED OXYFUNCTIONALIZATION; OXIDATION; PEROXIDASE;
D O I
10.1002/cctc.202000512
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
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.
引用
收藏
页码:4009 / 4013
页数:5
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