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Singlet‐Oxygen Generation by Peroxidases and Peroxygenases for Chemoenzymatic Synthesis

Singlet oxygen is a reactive oxygen species undesired in living cells but a rare and valuable reagent in chemical synthesis. We present a fluorescence spectroscopic analysis of the singlet‐oxygen formation activity of commercial peroxidases and novel peroxygenases. Singlet‐oxygen sensor green (SOSG)...

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Autores principales: Ingenbosch, Kim N., Quint, Stephan, Dyllick‐Brenzinger, Melanie, Wunschik, Dennis S., Kiebist, Jan, Süss, Philipp, Liebelt, Ute, Zuhse, Ralf, Menyes, Ulf, Scheibner, Katrin, Mayer, Christian, Opwis, Klaus, Gutmann, Jochen S., Hoffmann‐Jacobsen, Kerstin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7891382/
https://www.ncbi.nlm.nih.gov/pubmed/32798264
http://dx.doi.org/10.1002/cbic.202000326
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author Ingenbosch, Kim N.
Quint, Stephan
Dyllick‐Brenzinger, Melanie
Wunschik, Dennis S.
Kiebist, Jan
Süss, Philipp
Liebelt, Ute
Zuhse, Ralf
Menyes, Ulf
Scheibner, Katrin
Mayer, Christian
Opwis, Klaus
Gutmann, Jochen S.
Hoffmann‐Jacobsen, Kerstin
author_facet Ingenbosch, Kim N.
Quint, Stephan
Dyllick‐Brenzinger, Melanie
Wunschik, Dennis S.
Kiebist, Jan
Süss, Philipp
Liebelt, Ute
Zuhse, Ralf
Menyes, Ulf
Scheibner, Katrin
Mayer, Christian
Opwis, Klaus
Gutmann, Jochen S.
Hoffmann‐Jacobsen, Kerstin
author_sort Ingenbosch, Kim N.
collection PubMed
description Singlet oxygen is a reactive oxygen species undesired in living cells but a rare and valuable reagent in chemical synthesis. We present a fluorescence spectroscopic analysis of the singlet‐oxygen formation activity of commercial peroxidases and novel peroxygenases. Singlet‐oxygen sensor green (SOSG) is used as fluorogenic singlet oxygen trap. Establishing a kinetic model for the reaction cascade to the fluorescent SOSG endoperoxide permits a kinetic analysis of enzymatic singlet‐oxygen formation. All peroxidases and peroxygenases show singlet‐oxygen formation. No singlet oxygen activity could be found for any catalase under investigation. Substrate inhibition is observed for all reactive enzymes. The commercial dye‐decolorizing peroxidase industrially used for dairy bleaching shows the highest singlet‐oxygen activity and the lowest inhibition. This enzyme was immobilized on a textile carrier and successfully applied for a chemical synthesis. Here, ascaridole was synthesized via enzymatically produced singlet oxygen.
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spelling pubmed-78913822021-03-02 Singlet‐Oxygen Generation by Peroxidases and Peroxygenases for Chemoenzymatic Synthesis Ingenbosch, Kim N. Quint, Stephan Dyllick‐Brenzinger, Melanie Wunschik, Dennis S. Kiebist, Jan Süss, Philipp Liebelt, Ute Zuhse, Ralf Menyes, Ulf Scheibner, Katrin Mayer, Christian Opwis, Klaus Gutmann, Jochen S. Hoffmann‐Jacobsen, Kerstin Chembiochem Full Papers Singlet oxygen is a reactive oxygen species undesired in living cells but a rare and valuable reagent in chemical synthesis. We present a fluorescence spectroscopic analysis of the singlet‐oxygen formation activity of commercial peroxidases and novel peroxygenases. Singlet‐oxygen sensor green (SOSG) is used as fluorogenic singlet oxygen trap. Establishing a kinetic model for the reaction cascade to the fluorescent SOSG endoperoxide permits a kinetic analysis of enzymatic singlet‐oxygen formation. All peroxidases and peroxygenases show singlet‐oxygen formation. No singlet oxygen activity could be found for any catalase under investigation. Substrate inhibition is observed for all reactive enzymes. The commercial dye‐decolorizing peroxidase industrially used for dairy bleaching shows the highest singlet‐oxygen activity and the lowest inhibition. This enzyme was immobilized on a textile carrier and successfully applied for a chemical synthesis. Here, ascaridole was synthesized via enzymatically produced singlet oxygen. John Wiley and Sons Inc. 2020-10-05 2021-01-15 /pmc/articles/PMC7891382/ /pubmed/32798264 http://dx.doi.org/10.1002/cbic.202000326 Text en © 2020 The Authors. Published by Wiley-VCH GmbH This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Full Papers
Ingenbosch, Kim N.
Quint, Stephan
Dyllick‐Brenzinger, Melanie
Wunschik, Dennis S.
Kiebist, Jan
Süss, Philipp
Liebelt, Ute
Zuhse, Ralf
Menyes, Ulf
Scheibner, Katrin
Mayer, Christian
Opwis, Klaus
Gutmann, Jochen S.
Hoffmann‐Jacobsen, Kerstin
Singlet‐Oxygen Generation by Peroxidases and Peroxygenases for Chemoenzymatic Synthesis
title Singlet‐Oxygen Generation by Peroxidases and Peroxygenases for Chemoenzymatic Synthesis
title_full Singlet‐Oxygen Generation by Peroxidases and Peroxygenases for Chemoenzymatic Synthesis
title_fullStr Singlet‐Oxygen Generation by Peroxidases and Peroxygenases for Chemoenzymatic Synthesis
title_full_unstemmed Singlet‐Oxygen Generation by Peroxidases and Peroxygenases for Chemoenzymatic Synthesis
title_short Singlet‐Oxygen Generation by Peroxidases and Peroxygenases for Chemoenzymatic Synthesis
title_sort singlet‐oxygen generation by peroxidases and peroxygenases for chemoenzymatic synthesis
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7891382/
https://www.ncbi.nlm.nih.gov/pubmed/32798264
http://dx.doi.org/10.1002/cbic.202000326
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