Involvement of Ech hydrogenase in energy conservation of Methanosarcina mazei
Methanosarcina mazei belongs to the group of aceticlastic methanogens and converts acetate into the potent greenhouse gases CO₂ and CH₄. The aceticlastic respiratory chain involved in methane formation comprises the three transmembrane proteins Ech hydrogenase, F₄₂₀ nonreducing hydrogenase and heter...
Gespeichert in:
Veröffentlicht in: | The FEBS journal 2010-08, Vol.277 (16), p.3396-3403 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 3403 |
---|---|
container_issue | 16 |
container_start_page | 3396 |
container_title | The FEBS journal |
container_volume | 277 |
creator | Welte, Cornelia Krätzer, Christian Deppenmeier, Uwe |
description | Methanosarcina mazei belongs to the group of aceticlastic methanogens and converts acetate into the potent greenhouse gases CO₂ and CH₄. The aceticlastic respiratory chain involved in methane formation comprises the three transmembrane proteins Ech hydrogenase, F₄₂₀ nonreducing hydrogenase and heterodisulfide reductase. It has been shown that the latter two contribute to the proton motive force. The data presented here clearly demonstrate that Ech hydrogenase is also involved in energy conservation. ATP synthesis was observed in a cytoplasm-free vesicular system of Ms. mazei that was dependent on the oxidation of reduced ferredoxin and the formation of molecular hydrogen (as catalysed by Ech hydrogenase). Such an ATP formation was not observed in a Δech mutant strain. The protonophore 3,5-di-tert-butyl-4-hydroxybenzylidene-malononitrile (SF6847) led to complete inhibition of ATP formation in the Ms. mazei wild-type without inhibiting hydrogen production by Ech hydrogenase, whereas the sodium ion ionophore ETH157 did not affect ATP formation in this system. Thus, we conclude that Ech hydrogenase acts as primary proton pump in a ferredoxin-dependent electron transport system. |
doi_str_mv | 10.1111/j.1742-4658.2010.07744.x |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_748946892</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>748946892</sourcerecordid><originalsourceid>FETCH-LOGICAL-c5364-cdf306f2ed6416a56eb3b90029aed4cc1f2a437562674d2bc96a8c8acb5953663</originalsourceid><addsrcrecordid>eNqNkD1PwzAQhi0E4qPwFyBiYWpxHMeOFySoWqhExQBIbJbjXNpUiV3strT8ehwKHZjw4pP93KO7F6Eoxr04nOtZL-aUdClLsx7B4RVzTmlvvYeOdx_7u5q-HaET72cYJykV4hAdEcyI4DQ7RuORWdl6BQ2YRWTLaKCn0XRTODsBozxElYnAgJtsIm2NB7dSi8qalhzDYqqM9crpyqioUZ9QnaKDUtUezn7uDnodDl76D93Hp_tR__axq9OE0a4uygSzkkDBaMxUyiBPcoExEQoKqnVcEkUTnjLCOC1IrgVTmc6UzlMRBCzpoKutd-7s-xL8QjaV11DXyoBdehlWE5RlggTy8g85s0tnwnCSp5iSGPNWl20h7az3Dko5d1Wj3EbGWLaBy5lss5RtrrINXH4HLteh9fzHv8wbKHaNvwkH4GYLfFQ1bP4tlsPB3XNbBsHFVlAqK9XEVV6-Pgc0wXEWVuAi-QKvZpgX</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>750421076</pqid></control><display><type>article</type><title>Involvement of Ech hydrogenase in energy conservation of Methanosarcina mazei</title><source>MEDLINE</source><source>Wiley Free Content</source><source>IngentaConnect Free/Open Access Journals</source><source>Wiley Online Library All Journals</source><source>Free Full-Text Journals in Chemistry</source><creator>Welte, Cornelia ; Krätzer, Christian ; Deppenmeier, Uwe</creator><creatorcontrib>Welte, Cornelia ; Krätzer, Christian ; Deppenmeier, Uwe</creatorcontrib><description>Methanosarcina mazei belongs to the group of aceticlastic methanogens and converts acetate into the potent greenhouse gases CO₂ and CH₄. The aceticlastic respiratory chain involved in methane formation comprises the three transmembrane proteins Ech hydrogenase, F₄₂₀ nonreducing hydrogenase and heterodisulfide reductase. It has been shown that the latter two contribute to the proton motive force. The data presented here clearly demonstrate that Ech hydrogenase is also involved in energy conservation. ATP synthesis was observed in a cytoplasm-free vesicular system of Ms. mazei that was dependent on the oxidation of reduced ferredoxin and the formation of molecular hydrogen (as catalysed by Ech hydrogenase). Such an ATP formation was not observed in a Δech mutant strain. The protonophore 3,5-di-tert-butyl-4-hydroxybenzylidene-malononitrile (SF6847) led to complete inhibition of ATP formation in the Ms. mazei wild-type without inhibiting hydrogen production by Ech hydrogenase, whereas the sodium ion ionophore ETH157 did not affect ATP formation in this system. Thus, we conclude that Ech hydrogenase acts as primary proton pump in a ferredoxin-dependent electron transport system.</description><identifier>ISSN: 1742-464X</identifier><identifier>EISSN: 1742-4658</identifier><identifier>DOI: 10.1111/j.1742-4658.2010.07744.x</identifier><identifier>PMID: 20629748</identifier><language>eng</language><publisher>Oxford, UK: Oxford, UK : Blackwell Publishing Ltd</publisher><subject>Adenosine triphosphatase ; Adenosine Triphosphate - biosynthesis ; Archaea ; Biochemistry ; Carbon dioxide ; electron transfer ; electron transport ; Electron Transport Chain Complex Proteins - metabolism ; electron transport phosphorylation ; Energy Metabolism ; Ferredoxins - metabolism ; Methane ; methane production ; methanogenesis ; Methanosarcina - enzymology ; Models, Biological ; Oxidoreductases - metabolism ; Proteins ; proton motive force ; proton pump ; Protons</subject><ispartof>The FEBS journal, 2010-08, Vol.277 (16), p.3396-3403</ispartof><rights>2010 The Authors Journal compilation © 2010 FEBS</rights><rights>Journal compilation © 2010 Federation of European Biochemical Societies</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5364-cdf306f2ed6416a56eb3b90029aed4cc1f2a437562674d2bc96a8c8acb5953663</citedby><cites>FETCH-LOGICAL-c5364-cdf306f2ed6416a56eb3b90029aed4cc1f2a437562674d2bc96a8c8acb5953663</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1742-4658.2010.07744.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1742-4658.2010.07744.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,1433,27923,27924,45573,45574,46408,46832</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20629748$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Welte, Cornelia</creatorcontrib><creatorcontrib>Krätzer, Christian</creatorcontrib><creatorcontrib>Deppenmeier, Uwe</creatorcontrib><title>Involvement of Ech hydrogenase in energy conservation of Methanosarcina mazei</title><title>The FEBS journal</title><addtitle>FEBS J</addtitle><description>Methanosarcina mazei belongs to the group of aceticlastic methanogens and converts acetate into the potent greenhouse gases CO₂ and CH₄. The aceticlastic respiratory chain involved in methane formation comprises the three transmembrane proteins Ech hydrogenase, F₄₂₀ nonreducing hydrogenase and heterodisulfide reductase. It has been shown that the latter two contribute to the proton motive force. The data presented here clearly demonstrate that Ech hydrogenase is also involved in energy conservation. ATP synthesis was observed in a cytoplasm-free vesicular system of Ms. mazei that was dependent on the oxidation of reduced ferredoxin and the formation of molecular hydrogen (as catalysed by Ech hydrogenase). Such an ATP formation was not observed in a Δech mutant strain. The protonophore 3,5-di-tert-butyl-4-hydroxybenzylidene-malononitrile (SF6847) led to complete inhibition of ATP formation in the Ms. mazei wild-type without inhibiting hydrogen production by Ech hydrogenase, whereas the sodium ion ionophore ETH157 did not affect ATP formation in this system. Thus, we conclude that Ech hydrogenase acts as primary proton pump in a ferredoxin-dependent electron transport system.</description><subject>Adenosine triphosphatase</subject><subject>Adenosine Triphosphate - biosynthesis</subject><subject>Archaea</subject><subject>Biochemistry</subject><subject>Carbon dioxide</subject><subject>electron transfer</subject><subject>electron transport</subject><subject>Electron Transport Chain Complex Proteins - metabolism</subject><subject>electron transport phosphorylation</subject><subject>Energy Metabolism</subject><subject>Ferredoxins - metabolism</subject><subject>Methane</subject><subject>methane production</subject><subject>methanogenesis</subject><subject>Methanosarcina - enzymology</subject><subject>Models, Biological</subject><subject>Oxidoreductases - metabolism</subject><subject>Proteins</subject><subject>proton motive force</subject><subject>proton pump</subject><subject>Protons</subject><issn>1742-464X</issn><issn>1742-4658</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkD1PwzAQhi0E4qPwFyBiYWpxHMeOFySoWqhExQBIbJbjXNpUiV3strT8ehwKHZjw4pP93KO7F6Eoxr04nOtZL-aUdClLsx7B4RVzTmlvvYeOdx_7u5q-HaET72cYJykV4hAdEcyI4DQ7RuORWdl6BQ2YRWTLaKCn0XRTODsBozxElYnAgJtsIm2NB7dSi8qalhzDYqqM9crpyqioUZ9QnaKDUtUezn7uDnodDl76D93Hp_tR__axq9OE0a4uygSzkkDBaMxUyiBPcoExEQoKqnVcEkUTnjLCOC1IrgVTmc6UzlMRBCzpoKutd-7s-xL8QjaV11DXyoBdehlWE5RlggTy8g85s0tnwnCSp5iSGPNWl20h7az3Dko5d1Wj3EbGWLaBy5lss5RtrrINXH4HLteh9fzHv8wbKHaNvwkH4GYLfFQ1bP4tlsPB3XNbBsHFVlAqK9XEVV6-Pgc0wXEWVuAi-QKvZpgX</recordid><startdate>201008</startdate><enddate>201008</enddate><creator>Welte, Cornelia</creator><creator>Krätzer, Christian</creator><creator>Deppenmeier, Uwe</creator><general>Oxford, UK : Blackwell Publishing Ltd</general><general>Blackwell Publishing Ltd</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>201008</creationdate><title>Involvement of Ech hydrogenase in energy conservation of Methanosarcina mazei</title><author>Welte, Cornelia ; Krätzer, Christian ; Deppenmeier, Uwe</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5364-cdf306f2ed6416a56eb3b90029aed4cc1f2a437562674d2bc96a8c8acb5953663</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Adenosine triphosphatase</topic><topic>Adenosine Triphosphate - biosynthesis</topic><topic>Archaea</topic><topic>Biochemistry</topic><topic>Carbon dioxide</topic><topic>electron transfer</topic><topic>electron transport</topic><topic>Electron Transport Chain Complex Proteins - metabolism</topic><topic>electron transport phosphorylation</topic><topic>Energy Metabolism</topic><topic>Ferredoxins - metabolism</topic><topic>Methane</topic><topic>methane production</topic><topic>methanogenesis</topic><topic>Methanosarcina - enzymology</topic><topic>Models, Biological</topic><topic>Oxidoreductases - metabolism</topic><topic>Proteins</topic><topic>proton motive force</topic><topic>proton pump</topic><topic>Protons</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Welte, Cornelia</creatorcontrib><creatorcontrib>Krätzer, Christian</creatorcontrib><creatorcontrib>Deppenmeier, Uwe</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The FEBS journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Welte, Cornelia</au><au>Krätzer, Christian</au><au>Deppenmeier, Uwe</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Involvement of Ech hydrogenase in energy conservation of Methanosarcina mazei</atitle><jtitle>The FEBS journal</jtitle><addtitle>FEBS J</addtitle><date>2010-08</date><risdate>2010</risdate><volume>277</volume><issue>16</issue><spage>3396</spage><epage>3403</epage><pages>3396-3403</pages><issn>1742-464X</issn><eissn>1742-4658</eissn><abstract>Methanosarcina mazei belongs to the group of aceticlastic methanogens and converts acetate into the potent greenhouse gases CO₂ and CH₄. The aceticlastic respiratory chain involved in methane formation comprises the three transmembrane proteins Ech hydrogenase, F₄₂₀ nonreducing hydrogenase and heterodisulfide reductase. It has been shown that the latter two contribute to the proton motive force. The data presented here clearly demonstrate that Ech hydrogenase is also involved in energy conservation. ATP synthesis was observed in a cytoplasm-free vesicular system of Ms. mazei that was dependent on the oxidation of reduced ferredoxin and the formation of molecular hydrogen (as catalysed by Ech hydrogenase). Such an ATP formation was not observed in a Δech mutant strain. The protonophore 3,5-di-tert-butyl-4-hydroxybenzylidene-malononitrile (SF6847) led to complete inhibition of ATP formation in the Ms. mazei wild-type without inhibiting hydrogen production by Ech hydrogenase, whereas the sodium ion ionophore ETH157 did not affect ATP formation in this system. Thus, we conclude that Ech hydrogenase acts as primary proton pump in a ferredoxin-dependent electron transport system.</abstract><cop>Oxford, UK</cop><pub>Oxford, UK : Blackwell Publishing Ltd</pub><pmid>20629748</pmid><doi>10.1111/j.1742-4658.2010.07744.x</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1742-464X |
ispartof | The FEBS journal, 2010-08, Vol.277 (16), p.3396-3403 |
issn | 1742-464X 1742-4658 |
language | eng |
recordid | cdi_proquest_miscellaneous_748946892 |
source | MEDLINE; Wiley Free Content; IngentaConnect Free/Open Access Journals; Wiley Online Library All Journals; Free Full-Text Journals in Chemistry |
subjects | Adenosine triphosphatase Adenosine Triphosphate - biosynthesis Archaea Biochemistry Carbon dioxide electron transfer electron transport Electron Transport Chain Complex Proteins - metabolism electron transport phosphorylation Energy Metabolism Ferredoxins - metabolism Methane methane production methanogenesis Methanosarcina - enzymology Models, Biological Oxidoreductases - metabolism Proteins proton motive force proton pump Protons |
title | Involvement of Ech hydrogenase in energy conservation of Methanosarcina mazei |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T12%3A17%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Involvement%20of%20Ech%20hydrogenase%20in%20energy%20conservation%20of%20Methanosarcina%20mazei&rft.jtitle=The%20FEBS%20journal&rft.au=Welte,%20Cornelia&rft.date=2010-08&rft.volume=277&rft.issue=16&rft.spage=3396&rft.epage=3403&rft.pages=3396-3403&rft.issn=1742-464X&rft.eissn=1742-4658&rft_id=info:doi/10.1111/j.1742-4658.2010.07744.x&rft_dat=%3Cproquest_cross%3E748946892%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=750421076&rft_id=info:pmid/20629748&rfr_iscdi=true |