Hybrid catalysis for enantioselective Baeyer–Villiger oxidation and stereoselective epoxidation: a Cp*Ir complex to fuel FMN and FAD reduction for flavoprotein monooxygenase modules

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

  • Robert Röllig
  • Caroline E. Paul
  • Pierre Rousselot-Pailley
  • Selin Kara
  • Véronique Alphand

Organisationseinheiten

Externe Organisationen

  • Universite d'Aix-Marseille
  • Delft University of Technology
  • Aarhus University
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Details

OriginalspracheEnglisch
Seiten (von - bis)3117-3123
Seitenumfang7
FachzeitschriftReaction Chemistry & Engineering
Jahrgang8
Ausgabenummer12
Frühes Online-Datum4 Aug. 2023
PublikationsstatusVeröffentlicht - 2023

Abstract

Taking advantage of the unique properties of two-component flavo-monooxygenases and the ability of [Cp*Ir(bpy-OMe)H] + to transfer hydrides to reduce flavins, we extended the scope of the pH- and oxygen-robust iridium(iii)-complex to drive the enzymatic reaction of a FMN-dependent Baeyer-Villiger monooxygenase and a FAD-dependent styrene monooxygenase (respectively FPMO Group C and E), using formic acid as H-donor for NADH recycling.

Zitieren

Hybrid catalysis for enantioselective Baeyer–Villiger oxidation and stereoselective epoxidation: a Cp*Ir complex to fuel FMN and FAD reduction for flavoprotein monooxygenase modules. / Röllig, Robert; Paul, Caroline E.; Rousselot-Pailley, Pierre et al.
in: Reaction Chemistry & Engineering, Jahrgang 8, Nr. 12, 2023, S. 3117-3123.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Röllig R, Paul CE, Rousselot-Pailley P, Kara S, Alphand V. Hybrid catalysis for enantioselective Baeyer–Villiger oxidation and stereoselective epoxidation: a Cp*Ir complex to fuel FMN and FAD reduction for flavoprotein monooxygenase modules. Reaction Chemistry & Engineering. 2023;8(12):3117-3123. Epub 2023 Aug 4. doi: 10.1039/d3re00411b
Röllig, Robert ; Paul, Caroline E. ; Rousselot-Pailley, Pierre et al. / Hybrid catalysis for enantioselective Baeyer–Villiger oxidation and stereoselective epoxidation : a Cp*Ir complex to fuel FMN and FAD reduction for flavoprotein monooxygenase modules. in: Reaction Chemistry & Engineering. 2023 ; Jahrgang 8, Nr. 12. S. 3117-3123.
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abstract = "Taking advantage of the unique properties of two-component flavo-monooxygenases and the ability of [Cp*Ir(bpy-OMe)H] + to transfer hydrides to reduce flavins, we extended the scope of the pH- and oxygen-robust iridium(iii)-complex to drive the enzymatic reaction of a FMN-dependent Baeyer-Villiger monooxygenase and a FAD-dependent styrene monooxygenase (respectively FPMO Group C and E), using formic acid as H-donor for NADH recycling.",
author = "Robert R{\"o}llig and Paul, {Caroline E.} and Pierre Rousselot-Pailley and Selin Kara and V{\'e}ronique Alphand",
note = "Funding Information: The authors acknowledge funding from the European Union's Horizon 2020 MSCA ITN-EJD program under grant agreement No. 764920. They thank Prof. Dr D. Tischler for the plasmid bearing the SfStyA gene and Dr K. Duquesne for the plasmid bearing the 2,5-DKCMO gene.",
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TY - JOUR

T1 - Hybrid catalysis for enantioselective Baeyer–Villiger oxidation and stereoselective epoxidation

T2 - a Cp*Ir complex to fuel FMN and FAD reduction for flavoprotein monooxygenase modules

AU - Röllig, Robert

AU - Paul, Caroline E.

AU - Rousselot-Pailley, Pierre

AU - Kara, Selin

AU - Alphand, Véronique

N1 - Funding Information: The authors acknowledge funding from the European Union's Horizon 2020 MSCA ITN-EJD program under grant agreement No. 764920. They thank Prof. Dr D. Tischler for the plasmid bearing the SfStyA gene and Dr K. Duquesne for the plasmid bearing the 2,5-DKCMO gene.

PY - 2023

Y1 - 2023

N2 - Taking advantage of the unique properties of two-component flavo-monooxygenases and the ability of [Cp*Ir(bpy-OMe)H] + to transfer hydrides to reduce flavins, we extended the scope of the pH- and oxygen-robust iridium(iii)-complex to drive the enzymatic reaction of a FMN-dependent Baeyer-Villiger monooxygenase and a FAD-dependent styrene monooxygenase (respectively FPMO Group C and E), using formic acid as H-donor for NADH recycling.

AB - Taking advantage of the unique properties of two-component flavo-monooxygenases and the ability of [Cp*Ir(bpy-OMe)H] + to transfer hydrides to reduce flavins, we extended the scope of the pH- and oxygen-robust iridium(iii)-complex to drive the enzymatic reaction of a FMN-dependent Baeyer-Villiger monooxygenase and a FAD-dependent styrene monooxygenase (respectively FPMO Group C and E), using formic acid as H-donor for NADH recycling.

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U2 - 10.1039/d3re00411b

DO - 10.1039/d3re00411b

M3 - Article

VL - 8

SP - 3117

EP - 3123

JO - Reaction Chemistry & Engineering

JF - Reaction Chemistry & Engineering

IS - 12

ER -