Pyrroloquinoline Quinone Aza‐Crown Ether Complexes as Biomimetics for Lanthanide and Calcium Dependent Alcohol Dehydrogenases
Understanding the role of metal ions in biology can lead to the development of new catalysts for several industrially important transformations. Lanthanides are the most recent group of metal ions that have been shown to be important in biology, that is, in quinone‐dependent methanol dehydrogenases...
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creator | Vetsova, Violeta A. Fisher, Katherine R. Lumpe, Henning Schäfer, Alexander Schneider, Erik K. Weis, Patrick Daumann, Lena J. |
description | Understanding the role of metal ions in biology can lead to the development of new catalysts for several industrially important transformations. Lanthanides are the most recent group of metal ions that have been shown to be important in biology, that is, in quinone‐dependent methanol dehydrogenases (MDH). Here we evaluate a literature‐known pyrroloquinoline quinone (PQQ) and 1‐aza‐15‐crown‐5 based ligand platform as scaffold for Ca2+, Ba2+, La3+ and Lu3+ biomimetics of MDH and we evaluate the importance of ligand design, charge, size, counterions and base for the alcohol oxidation reaction using NMR spectroscopy. In addition, we report a new straightforward synthetic route (3 steps instead of 11 and 33 % instead of 0.6 % yield) for biomimetic ligands based on PQQ. We show that when studying biomimetics for MDH, larger metal ions and those with lower charge in this case promote the dehydrogenation reaction more effectively and that this is likely an effect of the ligand design which must be considered when studying biomimetics. To gain more information on the structures and impact of counterions of the complexes, we performed collision induced dissociation (CID) experiments and observe that the nitrates are more tightly bound than the triflates. To resolve the structure of the complexes in the gas phase we combined DFT‐calculations and ion mobility measurements (IMS). Furthermore, we characterized the obtained complexes and reaction mixtures using Electron Paramagnetic Resonance (EPR) spectroscopy and show the presence of a small amount of quinone‐based radical.
A pyrroloquinoline quinone (PQQ) based model system was used for the investigation of different factors that may have an impact on the oxidation reaction in the active sites of alcohol dehydrogenase enzymes. Using various metal salts, the influence of ion size and charge, as well as counterions was investigated. The study involves NMR and EPR analysis as well as advanced mass spectrometry techniques. |
doi_str_mv | 10.1002/chem.202100346 |
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A pyrroloquinoline quinone (PQQ) based model system was used for the investigation of different factors that may have an impact on the oxidation reaction in the active sites of alcohol dehydrogenase enzymes. Using various metal salts, the influence of ion size and charge, as well as counterions was investigated. The study involves NMR and EPR analysis as well as advanced mass spectrometry techniques.</description><identifier>ISSN: 0947-6539</identifier><identifier>EISSN: 1521-3765</identifier><identifier>DOI: 10.1002/chem.202100346</identifier><identifier>PMID: 33872420</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>alcohol oxidation ; bioinorganic chemistry ; Biology ; biomimetic synthesis ; Biomimetics ; Calcium ; Calcium ions ; Catalysts ; Chemistry ; Crown ethers ; Dehydrogenases ; Dehydrogenation ; Electron paramagnetic resonance ; Electron spin resonance ; Evaluation ; Ionic mobility ; Lanthanides ; Ligands ; Magnetic resonance spectroscopy ; Metal ions ; NMR ; NMR spectroscopy ; Nuclear magnetic resonance ; Oxidation ; Pyrroloquinoline quinone ; Quinones ; Spectroscopy ; Spectrum analysis ; Vapor phases</subject><ispartof>Chemistry : a European journal, 2021-07, Vol.27 (39), p.10087-10098</ispartof><rights>2021 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH</rights><rights>2021 Wiley-VCH GmbH.</rights><rights>2021. This article is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4686-7978dd6d48713860d5a389c7087be5568e97b4daf902d8ac07919dcc7bee5ce3</citedby><cites>FETCH-LOGICAL-c4686-7978dd6d48713860d5a389c7087be5568e97b4daf902d8ac07919dcc7bee5ce3</cites><orcidid>0000-0002-4631-377X ; 0000-0001-7006-6759 ; 0000-0003-2197-136X ; 0000-0003-0260-349X ; 0000-0002-2716-561X ; 0000-0002-2392-3217</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fchem.202100346$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fchem.202100346$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33872420$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Vetsova, Violeta A.</creatorcontrib><creatorcontrib>Fisher, Katherine R.</creatorcontrib><creatorcontrib>Lumpe, Henning</creatorcontrib><creatorcontrib>Schäfer, Alexander</creatorcontrib><creatorcontrib>Schneider, Erik K.</creatorcontrib><creatorcontrib>Weis, Patrick</creatorcontrib><creatorcontrib>Daumann, Lena J.</creatorcontrib><title>Pyrroloquinoline Quinone Aza‐Crown Ether Complexes as Biomimetics for Lanthanide and Calcium Dependent Alcohol Dehydrogenases</title><title>Chemistry : a European journal</title><addtitle>Chemistry</addtitle><description>Understanding the role of metal ions in biology can lead to the development of new catalysts for several industrially important transformations. Lanthanides are the most recent group of metal ions that have been shown to be important in biology, that is, in quinone‐dependent methanol dehydrogenases (MDH). Here we evaluate a literature‐known pyrroloquinoline quinone (PQQ) and 1‐aza‐15‐crown‐5 based ligand platform as scaffold for Ca2+, Ba2+, La3+ and Lu3+ biomimetics of MDH and we evaluate the importance of ligand design, charge, size, counterions and base for the alcohol oxidation reaction using NMR spectroscopy. In addition, we report a new straightforward synthetic route (3 steps instead of 11 and 33 % instead of 0.6 % yield) for biomimetic ligands based on PQQ. We show that when studying biomimetics for MDH, larger metal ions and those with lower charge in this case promote the dehydrogenation reaction more effectively and that this is likely an effect of the ligand design which must be considered when studying biomimetics. To gain more information on the structures and impact of counterions of the complexes, we performed collision induced dissociation (CID) experiments and observe that the nitrates are more tightly bound than the triflates. To resolve the structure of the complexes in the gas phase we combined DFT‐calculations and ion mobility measurements (IMS). Furthermore, we characterized the obtained complexes and reaction mixtures using Electron Paramagnetic Resonance (EPR) spectroscopy and show the presence of a small amount of quinone‐based radical.
A pyrroloquinoline quinone (PQQ) based model system was used for the investigation of different factors that may have an impact on the oxidation reaction in the active sites of alcohol dehydrogenase enzymes. Using various metal salts, the influence of ion size and charge, as well as counterions was investigated. The study involves NMR and EPR analysis as well as advanced mass spectrometry techniques.</description><subject>alcohol oxidation</subject><subject>bioinorganic chemistry</subject><subject>Biology</subject><subject>biomimetic synthesis</subject><subject>Biomimetics</subject><subject>Calcium</subject><subject>Calcium ions</subject><subject>Catalysts</subject><subject>Chemistry</subject><subject>Crown ethers</subject><subject>Dehydrogenases</subject><subject>Dehydrogenation</subject><subject>Electron paramagnetic resonance</subject><subject>Electron spin resonance</subject><subject>Evaluation</subject><subject>Ionic mobility</subject><subject>Lanthanides</subject><subject>Ligands</subject><subject>Magnetic resonance spectroscopy</subject><subject>Metal ions</subject><subject>NMR</subject><subject>NMR spectroscopy</subject><subject>Nuclear magnetic resonance</subject><subject>Oxidation</subject><subject>Pyrroloquinoline quinone</subject><subject>Quinones</subject><subject>Spectroscopy</subject><subject>Spectrum analysis</subject><subject>Vapor phases</subject><issn>0947-6539</issn><issn>1521-3765</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><recordid>eNqFkc2OFCEUhStG4_SMbl0aEjduqoWiqoCNSU_ZOiZt1GT2hIbbU0woaKHKsWejj-Az-iTS6bH92bggF7gfJ-dyiuIJwXOCcfVC9zDMK1zlA63be8WMNBUpKWub-8UMi5qVbUPFSXGa0jXGWLSUPixOKOWsqis8K75-2MUYXPg0WR-c9YA-7ne5Lm7Vj2_fuxhuPFqOPUTUhWHr4AskpBI6t2GwA4xWJ7QJEa2UH3vlrQGkvEGdctpOA3oFW_AG_IgWToc-uHzT70wMV-BVgvSoeLBRLsHju3pWXL5eXnYX5er9m7fdYlXquuVtyQTjxrSm5oxQ3mLTKMqFZpizNTRNy0GwdW3URuDKcKUxE0QYrXMXGg30rHh5kN1O6wGMzoaicnIb7aDiTgZl5d8db3t5FT5LTlvCapYFnt8JxPxXkEY52KTBOeUhTElWDckumprSjD77B70OU_R5ukw1OC8icKbmB0rHkFKEzdEMwXIfrdxHK4_R5gdP_xzhiP_KMgPiANxYB7v_yMnuYvnut_hPXLG0Cw</recordid><startdate>20210712</startdate><enddate>20210712</enddate><creator>Vetsova, Violeta A.</creator><creator>Fisher, Katherine R.</creator><creator>Lumpe, Henning</creator><creator>Schäfer, Alexander</creator><creator>Schneider, Erik K.</creator><creator>Weis, Patrick</creator><creator>Daumann, Lena J.</creator><general>Wiley Subscription Services, Inc</general><general>John Wiley and Sons Inc</general><scope>24P</scope><scope>WIN</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>K9.</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-4631-377X</orcidid><orcidid>https://orcid.org/0000-0001-7006-6759</orcidid><orcidid>https://orcid.org/0000-0003-2197-136X</orcidid><orcidid>https://orcid.org/0000-0003-0260-349X</orcidid><orcidid>https://orcid.org/0000-0002-2716-561X</orcidid><orcidid>https://orcid.org/0000-0002-2392-3217</orcidid></search><sort><creationdate>20210712</creationdate><title>Pyrroloquinoline Quinone Aza‐Crown Ether Complexes as Biomimetics for Lanthanide and Calcium Dependent Alcohol Dehydrogenases</title><author>Vetsova, Violeta A. ; Fisher, Katherine R. ; Lumpe, Henning ; Schäfer, Alexander ; Schneider, Erik K. ; Weis, Patrick ; Daumann, Lena J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4686-7978dd6d48713860d5a389c7087be5568e97b4daf902d8ac07919dcc7bee5ce3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>alcohol oxidation</topic><topic>bioinorganic chemistry</topic><topic>Biology</topic><topic>biomimetic synthesis</topic><topic>Biomimetics</topic><topic>Calcium</topic><topic>Calcium ions</topic><topic>Catalysts</topic><topic>Chemistry</topic><topic>Crown ethers</topic><topic>Dehydrogenases</topic><topic>Dehydrogenation</topic><topic>Electron paramagnetic resonance</topic><topic>Electron spin resonance</topic><topic>Evaluation</topic><topic>Ionic mobility</topic><topic>Lanthanides</topic><topic>Ligands</topic><topic>Magnetic resonance spectroscopy</topic><topic>Metal ions</topic><topic>NMR</topic><topic>NMR spectroscopy</topic><topic>Nuclear magnetic resonance</topic><topic>Oxidation</topic><topic>Pyrroloquinoline quinone</topic><topic>Quinones</topic><topic>Spectroscopy</topic><topic>Spectrum analysis</topic><topic>Vapor phases</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vetsova, Violeta A.</creatorcontrib><creatorcontrib>Fisher, Katherine R.</creatorcontrib><creatorcontrib>Lumpe, Henning</creatorcontrib><creatorcontrib>Schäfer, Alexander</creatorcontrib><creatorcontrib>Schneider, Erik K.</creatorcontrib><creatorcontrib>Weis, Patrick</creatorcontrib><creatorcontrib>Daumann, Lena J.</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Wiley Free Content</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Chemistry : a European journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vetsova, Violeta A.</au><au>Fisher, Katherine R.</au><au>Lumpe, Henning</au><au>Schäfer, Alexander</au><au>Schneider, Erik K.</au><au>Weis, Patrick</au><au>Daumann, Lena J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pyrroloquinoline Quinone Aza‐Crown Ether Complexes as Biomimetics for Lanthanide and Calcium Dependent Alcohol Dehydrogenases</atitle><jtitle>Chemistry : a European journal</jtitle><addtitle>Chemistry</addtitle><date>2021-07-12</date><risdate>2021</risdate><volume>27</volume><issue>39</issue><spage>10087</spage><epage>10098</epage><pages>10087-10098</pages><issn>0947-6539</issn><eissn>1521-3765</eissn><abstract>Understanding the role of metal ions in biology can lead to the development of new catalysts for several industrially important transformations. Lanthanides are the most recent group of metal ions that have been shown to be important in biology, that is, in quinone‐dependent methanol dehydrogenases (MDH). Here we evaluate a literature‐known pyrroloquinoline quinone (PQQ) and 1‐aza‐15‐crown‐5 based ligand platform as scaffold for Ca2+, Ba2+, La3+ and Lu3+ biomimetics of MDH and we evaluate the importance of ligand design, charge, size, counterions and base for the alcohol oxidation reaction using NMR spectroscopy. In addition, we report a new straightforward synthetic route (3 steps instead of 11 and 33 % instead of 0.6 % yield) for biomimetic ligands based on PQQ. We show that when studying biomimetics for MDH, larger metal ions and those with lower charge in this case promote the dehydrogenation reaction more effectively and that this is likely an effect of the ligand design which must be considered when studying biomimetics. To gain more information on the structures and impact of counterions of the complexes, we performed collision induced dissociation (CID) experiments and observe that the nitrates are more tightly bound than the triflates. To resolve the structure of the complexes in the gas phase we combined DFT‐calculations and ion mobility measurements (IMS). Furthermore, we characterized the obtained complexes and reaction mixtures using Electron Paramagnetic Resonance (EPR) spectroscopy and show the presence of a small amount of quinone‐based radical.
A pyrroloquinoline quinone (PQQ) based model system was used for the investigation of different factors that may have an impact on the oxidation reaction in the active sites of alcohol dehydrogenase enzymes. Using various metal salts, the influence of ion size and charge, as well as counterions was investigated. The study involves NMR and EPR analysis as well as advanced mass spectrometry techniques.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>33872420</pmid><doi>10.1002/chem.202100346</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-4631-377X</orcidid><orcidid>https://orcid.org/0000-0001-7006-6759</orcidid><orcidid>https://orcid.org/0000-0003-2197-136X</orcidid><orcidid>https://orcid.org/0000-0003-0260-349X</orcidid><orcidid>https://orcid.org/0000-0002-2716-561X</orcidid><orcidid>https://orcid.org/0000-0002-2392-3217</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | alcohol oxidation bioinorganic chemistry Biology biomimetic synthesis Biomimetics Calcium Calcium ions Catalysts Chemistry Crown ethers Dehydrogenases Dehydrogenation Electron paramagnetic resonance Electron spin resonance Evaluation Ionic mobility Lanthanides Ligands Magnetic resonance spectroscopy Metal ions NMR NMR spectroscopy Nuclear magnetic resonance Oxidation Pyrroloquinoline quinone Quinones Spectroscopy Spectrum analysis Vapor phases |
title | Pyrroloquinoline Quinone Aza‐Crown Ether Complexes as Biomimetics for Lanthanide and Calcium Dependent Alcohol Dehydrogenases |
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