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Understanding the chemistry of the artificial electron acceptors PES, PMS, DCPIP and Wurster’s Blue in methanol dehydrogenase assays
ABSTRACT: Methanol dehydrogenases (MDH) have recently taken the spotlight with the discovery that a large portion of these enzymes in nature utilize lanthanides in their active sites. The kinetic parameters of these enzymes are determined with a spectrophotometric assay first described by Anthony an...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7082304/ https://www.ncbi.nlm.nih.gov/pubmed/32060650 http://dx.doi.org/10.1007/s00775-020-01752-9 |
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author | Jahn, Bérénice Jonasson, Niko S. W. Hu, Hurina Singer, Helena Pol, Arjan Good, Nathan M. den Camp, Huub J. M. Op Martinez-Gomez, N. Cecilia Daumann, Lena J. |
author_facet | Jahn, Bérénice Jonasson, Niko S. W. Hu, Hurina Singer, Helena Pol, Arjan Good, Nathan M. den Camp, Huub J. M. Op Martinez-Gomez, N. Cecilia Daumann, Lena J. |
author_sort | Jahn, Bérénice |
collection | PubMed |
description | ABSTRACT: Methanol dehydrogenases (MDH) have recently taken the spotlight with the discovery that a large portion of these enzymes in nature utilize lanthanides in their active sites. The kinetic parameters of these enzymes are determined with a spectrophotometric assay first described by Anthony and Zatman 55 years ago. This artificial assay uses alkylated phenazines, such as phenazine ethosulfate (PES) or phenazine methosulfate (PMS), as primary electron acceptors (EAs) and the electron transfer is further coupled to a dye. However, many groups have reported problems concerning the bleaching of the assay mixture in the absence of MDH and the reproducibility of those assays. Hence, the comparison of kinetic data among MDH enzymes of different species is often cumbersome. Using mass spectrometry, UV–Vis and electron paramagnetic resonance (EPR) spectroscopy, we show that the side reactions of the assay mixture are mainly due to the degradation of assay components. Light-induced demethylation (yielding formaldehyde and phenazine in the case of PMS) or oxidation of PES or PMS as well as a reaction with assay components (ammonia, cyanide) can occur. We suggest here a protocol to avoid these side reactions. Further, we describe a modified synthesis protocol for obtaining the alternative electron acceptor, Wurster’s blue (WB), which serves both as EA and dye. The investigation of two lanthanide-dependent methanol dehydrogenases from Methylorubrum extorquens AM1 and Methylacidiphilum fumariolicum SolV with WB, along with handling recommendations, is presented. GRAPHIC ABSTRACT: [Image: see text] Lanthanide-dependent methanol dehydrogenases. Understanding the chemistry of artificial electron acceptors and redox dyes can yield more reproducible results. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00775-020-01752-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7082304 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-70823042020-03-23 Understanding the chemistry of the artificial electron acceptors PES, PMS, DCPIP and Wurster’s Blue in methanol dehydrogenase assays Jahn, Bérénice Jonasson, Niko S. W. Hu, Hurina Singer, Helena Pol, Arjan Good, Nathan M. den Camp, Huub J. M. Op Martinez-Gomez, N. Cecilia Daumann, Lena J. J Biol Inorg Chem Original Paper ABSTRACT: Methanol dehydrogenases (MDH) have recently taken the spotlight with the discovery that a large portion of these enzymes in nature utilize lanthanides in their active sites. The kinetic parameters of these enzymes are determined with a spectrophotometric assay first described by Anthony and Zatman 55 years ago. This artificial assay uses alkylated phenazines, such as phenazine ethosulfate (PES) or phenazine methosulfate (PMS), as primary electron acceptors (EAs) and the electron transfer is further coupled to a dye. However, many groups have reported problems concerning the bleaching of the assay mixture in the absence of MDH and the reproducibility of those assays. Hence, the comparison of kinetic data among MDH enzymes of different species is often cumbersome. Using mass spectrometry, UV–Vis and electron paramagnetic resonance (EPR) spectroscopy, we show that the side reactions of the assay mixture are mainly due to the degradation of assay components. Light-induced demethylation (yielding formaldehyde and phenazine in the case of PMS) or oxidation of PES or PMS as well as a reaction with assay components (ammonia, cyanide) can occur. We suggest here a protocol to avoid these side reactions. Further, we describe a modified synthesis protocol for obtaining the alternative electron acceptor, Wurster’s blue (WB), which serves both as EA and dye. The investigation of two lanthanide-dependent methanol dehydrogenases from Methylorubrum extorquens AM1 and Methylacidiphilum fumariolicum SolV with WB, along with handling recommendations, is presented. GRAPHIC ABSTRACT: [Image: see text] Lanthanide-dependent methanol dehydrogenases. Understanding the chemistry of artificial electron acceptors and redox dyes can yield more reproducible results. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00775-020-01752-9) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2020-02-14 2020 /pmc/articles/PMC7082304/ /pubmed/32060650 http://dx.doi.org/10.1007/s00775-020-01752-9 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Original Paper Jahn, Bérénice Jonasson, Niko S. W. Hu, Hurina Singer, Helena Pol, Arjan Good, Nathan M. den Camp, Huub J. M. Op Martinez-Gomez, N. Cecilia Daumann, Lena J. Understanding the chemistry of the artificial electron acceptors PES, PMS, DCPIP and Wurster’s Blue in methanol dehydrogenase assays |
title | Understanding the chemistry of the artificial electron acceptors PES, PMS, DCPIP and Wurster’s Blue in methanol dehydrogenase assays |
title_full | Understanding the chemistry of the artificial electron acceptors PES, PMS, DCPIP and Wurster’s Blue in methanol dehydrogenase assays |
title_fullStr | Understanding the chemistry of the artificial electron acceptors PES, PMS, DCPIP and Wurster’s Blue in methanol dehydrogenase assays |
title_full_unstemmed | Understanding the chemistry of the artificial electron acceptors PES, PMS, DCPIP and Wurster’s Blue in methanol dehydrogenase assays |
title_short | Understanding the chemistry of the artificial electron acceptors PES, PMS, DCPIP and Wurster’s Blue in methanol dehydrogenase assays |
title_sort | understanding the chemistry of the artificial electron acceptors pes, pms, dcpip and wurster’s blue in methanol dehydrogenase assays |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7082304/ https://www.ncbi.nlm.nih.gov/pubmed/32060650 http://dx.doi.org/10.1007/s00775-020-01752-9 |
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