| Literature DB >> 32798264 |
Kim N Ingenbosch1,2,3, Stephan Quint4, Melanie Dyllick-Brenzinger4, Dennis S Wunschik1,2,3, Jan Kiebist5, Philipp Süss6, Ute Liebelt6,7, Ralf Zuhse4, Ulf Menyes6, Katrin Scheibner5, Christian Mayer3, Klaus Opwis2, Jochen S Gutmann2,3, Kerstin Hoffmann-Jacobsen1.
Abstract
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.Entities:
Keywords: chemo-enzymatic synthesis; fluorescence; peroxidase; peroxygenase; singlet oxygen; singlet oxygen sensor green
Year: 2020 PMID: 32798264 DOI: 10.1002/cbic.202000326
Source DB: PubMed Journal: Chembiochem ISSN: 1439-4227 Impact factor: 3.164