Photoenzymatic Hydroxylation of Ethylbenzene Catalyzed by Unspecific Peroxygenase: Origin of Enzyme Inactivation and the Impact of Light Intensity and Temperature

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

  • Bastien O. Burek
  • Sabrina R. de Boer
  • Florian Tieves
  • Wuyuan Zhang
  • Morten van Schie
  • Sebastian Bormann
  • Miguel Alcalde
  • Dirk Holtmann
  • Frank Hollmann
  • Detlef Bahnemann
  • Jonathan Z. Bloh

Organisationseinheiten

Externe Organisationen

  • DECHEMA-Forschungsinstitut (DFI)
  • Delft University of Technology
  • Institute of Catalysis and Petrochemistry, CSIC, Madrid
  • Staatliche Universität Sankt Petersburg
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Details

OriginalspracheEnglisch
Seiten (von - bis)3093-3100
Seitenumfang8
FachzeitschriftCHEMCATCHEM
Jahrgang11
Ausgabenummer13
Frühes Online-Datum6 Juni 2019
PublikationsstatusVeröffentlicht - 4 Juli 2019

Abstract

Photoenzymatic cascades can be used for selective oxygenation of C−H-Bonds under mild conditions circumventing the hydrogen peroxide mediated peroxygenase inactivation via in situ H 2O 2 generation. Here, we report the “on demand” production of hydrogen peroxide via methanol assisted reduction of molecular oxygen using UV-illuminated titanium dioxide (Aeroxide P25) combined with the enantioselective hydroxylation of ethylbenzene to (R)-1-phenylethanole catalyzed by the Unspecific Peroxygenase from Agrocybe Aegerita. For the application of the system it is important to understand the influence of the reaction parameters to be able to optimize the system. Therefore, we systematically investigated product formation and enzyme inactivation as well as ROS formation (H 2O 2, .OH and .O 2 ) applying different light intensities and temperatures. As a result, Turnover Numbers up to 220 000, photonic efficiencies up to 13.6 % and production rates up to 0.9 mM h −1 were achieved.

ASJC Scopus Sachgebiete

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Photoenzymatic Hydroxylation of Ethylbenzene Catalyzed by Unspecific Peroxygenase: Origin of Enzyme Inactivation and the Impact of Light Intensity and Temperature. / Burek, Bastien O.; Boer, Sabrina R. de; Tieves, Florian et al.
in: CHEMCATCHEM, Jahrgang 11, Nr. 13, 04.07.2019, S. 3093-3100.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Burek, BO, Boer, SRD, Tieves, F, Zhang, W, Schie, MV, Bormann, S, Alcalde, M, Holtmann, D, Hollmann, F, Bahnemann, D & Bloh, JZ 2019, 'Photoenzymatic Hydroxylation of Ethylbenzene Catalyzed by Unspecific Peroxygenase: Origin of Enzyme Inactivation and the Impact of Light Intensity and Temperature', CHEMCATCHEM, Jg. 11, Nr. 13, S. 3093-3100. https://doi.org/10.1002/cctc.201900610
Burek, B. O., Boer, S. R. D., Tieves, F., Zhang, W., Schie, M. V., Bormann, S., Alcalde, M., Holtmann, D., Hollmann, F., Bahnemann, D., & Bloh, J. Z. (2019). Photoenzymatic Hydroxylation of Ethylbenzene Catalyzed by Unspecific Peroxygenase: Origin of Enzyme Inactivation and the Impact of Light Intensity and Temperature. CHEMCATCHEM, 11(13), 3093-3100. https://doi.org/10.1002/cctc.201900610
Burek BO, Boer SRD, Tieves F, Zhang W, Schie MV, Bormann S et al. Photoenzymatic Hydroxylation of Ethylbenzene Catalyzed by Unspecific Peroxygenase: Origin of Enzyme Inactivation and the Impact of Light Intensity and Temperature. CHEMCATCHEM. 2019 Jul 4;11(13):3093-3100. Epub 2019 Jun 6. doi: 10.1002/cctc.201900610
Burek, Bastien O. ; Boer, Sabrina R. de ; Tieves, Florian et al. / Photoenzymatic Hydroxylation of Ethylbenzene Catalyzed by Unspecific Peroxygenase : Origin of Enzyme Inactivation and the Impact of Light Intensity and Temperature. in: CHEMCATCHEM. 2019 ; Jahrgang 11, Nr. 13. S. 3093-3100.
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abstract = "Photoenzymatic cascades can be used for selective oxygenation of C−H-Bonds under mild conditions circumventing the hydrogen peroxide mediated peroxygenase inactivation via in situ H 2O 2 generation. Here, we report the “on demand” production of hydrogen peroxide via methanol assisted reduction of molecular oxygen using UV-illuminated titanium dioxide (Aeroxide P25) combined with the enantioselective hydroxylation of ethylbenzene to (R)-1-phenylethanole catalyzed by the Unspecific Peroxygenase from Agrocybe Aegerita. For the application of the system it is important to understand the influence of the reaction parameters to be able to optimize the system. Therefore, we systematically investigated product formation and enzyme inactivation as well as ROS formation (H 2O 2, .OH and .O 2 −) applying different light intensities and temperatures. As a result, Turnover Numbers up to 220 000, photonic efficiencies up to 13.6 % and production rates up to 0.9 mM h −1 were achieved. ",
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T1 - Photoenzymatic Hydroxylation of Ethylbenzene Catalyzed by Unspecific Peroxygenase

T2 - Origin of Enzyme Inactivation and the Impact of Light Intensity and Temperature

AU - Burek, Bastien O.

AU - Boer, Sabrina R. de

AU - Tieves, Florian

AU - Zhang, Wuyuan

AU - Schie, Morten van

AU - Bormann, Sebastian

AU - Alcalde, Miguel

AU - Holtmann, Dirk

AU - Hollmann, Frank

AU - Bahnemann, Detlef

AU - Bloh, Jonathan Z.

N1 - Funding information: SRdB, BOB and JZB gratefully acknowledge financial support by German Research Foundation (DFG, Grant No: BL 1425/1-1). FH thanks the European Research Council (ERC Consolidator Grant No. 648026) for financial support.

PY - 2019/7/4

Y1 - 2019/7/4

N2 - Photoenzymatic cascades can be used for selective oxygenation of C−H-Bonds under mild conditions circumventing the hydrogen peroxide mediated peroxygenase inactivation via in situ H 2O 2 generation. Here, we report the “on demand” production of hydrogen peroxide via methanol assisted reduction of molecular oxygen using UV-illuminated titanium dioxide (Aeroxide P25) combined with the enantioselective hydroxylation of ethylbenzene to (R)-1-phenylethanole catalyzed by the Unspecific Peroxygenase from Agrocybe Aegerita. For the application of the system it is important to understand the influence of the reaction parameters to be able to optimize the system. Therefore, we systematically investigated product formation and enzyme inactivation as well as ROS formation (H 2O 2, .OH and .O 2 −) applying different light intensities and temperatures. As a result, Turnover Numbers up to 220 000, photonic efficiencies up to 13.6 % and production rates up to 0.9 mM h −1 were achieved.

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SN - 1867-3880

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