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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)...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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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. |
format | Online Article Text |
id | pubmed-7891382 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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