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Peroxide stimulated transition between the ferryl intermediates of bovine cytochrome c oxidase
During catalysis of cytochrome c oxidases (CcO) several ferryl intermediates of the catalytic heme a3-CuB center are observed. In the PM ferryl state, produced by the reaction of two-electron reduced CcO with O2, the ferryl iron of heme a3 and a free radical are present at the catalytic center. The...
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Published in: | Biochimica et biophysica acta. Bioenergetics 2021-08, Vol.1862 (8), p.148447-148447, Article 148447 |
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container_title | Biochimica et biophysica acta. Bioenergetics |
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creator | Sztachova, T. Pechova, I. Mikulova, L. Stupak, M. Jancura, D. Fabian, M. |
description | During catalysis of cytochrome c oxidases (CcO) several ferryl intermediates of the catalytic heme a3-CuB center are observed. In the PM ferryl state, produced by the reaction of two-electron reduced CcO with O2, the ferryl iron of heme a3 and a free radical are present at the catalytic center. The radical reduction stimulates the transition of the PM into another ferryl F state. Similar ferryl states can be also generated from the oxidized CcO (O) in the reaction with H2O2. The PM, the product of the reaction of the O with one molecule of peroxide, is transformed into the F state by the second molecule of H2O2. However, the chemical nature of this transition has not been unambiguously elucidated yet. Here, we examined the redox state of the peroxide-produced PM and F states by the one-electron reduction. The F form and interestingly also the major fraction of the PM sample, likely another P-type ferryl form (PR), were found to be the one oxidizing equivalent above the O state. However, the both P-type forms are transformed into the F state by additional molecule of H2O2. It is suggested that the PR-to-F transition is due to the binding of H2O2 to CuB triggering a structural change together with the uptake of H+ at the catalytic center. In the PM-to-F conversion, these two events are complemented with the annihilation of radical by the intrinsic oxidation of the enzyme.
•Two ferryl intermediates of cytochrome c oxidase prepared by peroxide•The redox state of the catalytic center of the ferryl intermediates•The peroxide stimulated the transition between the ferryl intermediates•The catalytic activity of ferryl intermediate |
doi_str_mv | 10.1016/j.bbabio.2021.148447 |
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•Two ferryl intermediates of cytochrome c oxidase prepared by peroxide•The redox state of the catalytic center of the ferryl intermediates•The peroxide stimulated the transition between the ferryl intermediates•The catalytic activity of ferryl intermediate</description><subject>Cytochrome c oxidase</subject><subject>Ferryl intermediates</subject><subject>Hydrogen peroxide</subject><subject>Redox state</subject><issn>0005-2728</issn><issn>1879-2650</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kE1P3DAQhq0K1N3S_oOq8pFLtrZjO86lUoWAIiHBAa61_DHRepXE1PZS9t_jVWiPnGYOz_uO5kHoKyUbSqj8vttYa2yIG0YY3VCuOO8-oDVVXd8wKcgJWhNCRMM6plboU847UmOctR_Rqm37jlIh1-j3PaT4EjzgXMK0H00Bj0sycw4lxBlbKH8BZly2gAdI6TDiMBdIE_hQ2YzjgG18DjNgdyjRbVOc6oqPnSbDZ3Q6mDHDl7d5hh6vLh8ufjW3d9c3Fz9vG8eJKk1rGSjVsZ4IyxVTPXMtePCEGybAWt9T7joh3WAlM4PsnB-ohH7wvfQWVHuGzpfepxT_7CEXPYXsYBzNDHGfNRNMSNkKIivKF9SlmHOCQT-lMJl00JToo1m904tZfTSrF7M19u3twt7W5_-H_qmswI8FgPrnc4CkswswuyoqgSvax_D-hVfqVI3C</recordid><startdate>20210801</startdate><enddate>20210801</enddate><creator>Sztachova, T.</creator><creator>Pechova, I.</creator><creator>Mikulova, L.</creator><creator>Stupak, M.</creator><creator>Jancura, D.</creator><creator>Fabian, M.</creator><general>Elsevier B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20210801</creationdate><title>Peroxide stimulated transition between the ferryl intermediates of bovine cytochrome c oxidase</title><author>Sztachova, T. ; Pechova, I. ; Mikulova, L. ; Stupak, M. ; Jancura, D. ; Fabian, M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c408t-3b2e8872905b482892c3eded04a25ebbd914c756cfb62af67cdf16e9fd96dbe83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Cytochrome c oxidase</topic><topic>Ferryl intermediates</topic><topic>Hydrogen peroxide</topic><topic>Redox state</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sztachova, T.</creatorcontrib><creatorcontrib>Pechova, I.</creatorcontrib><creatorcontrib>Mikulova, L.</creatorcontrib><creatorcontrib>Stupak, M.</creatorcontrib><creatorcontrib>Jancura, D.</creatorcontrib><creatorcontrib>Fabian, M.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Biochimica et biophysica acta. Bioenergetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sztachova, T.</au><au>Pechova, I.</au><au>Mikulova, L.</au><au>Stupak, M.</au><au>Jancura, D.</au><au>Fabian, M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Peroxide stimulated transition between the ferryl intermediates of bovine cytochrome c oxidase</atitle><jtitle>Biochimica et biophysica acta. Bioenergetics</jtitle><addtitle>Biochim Biophys Acta Bioenerg</addtitle><date>2021-08-01</date><risdate>2021</risdate><volume>1862</volume><issue>8</issue><spage>148447</spage><epage>148447</epage><pages>148447-148447</pages><artnum>148447</artnum><issn>0005-2728</issn><eissn>1879-2650</eissn><abstract>During catalysis of cytochrome c oxidases (CcO) several ferryl intermediates of the catalytic heme a3-CuB center are observed. In the PM ferryl state, produced by the reaction of two-electron reduced CcO with O2, the ferryl iron of heme a3 and a free radical are present at the catalytic center. The radical reduction stimulates the transition of the PM into another ferryl F state. Similar ferryl states can be also generated from the oxidized CcO (O) in the reaction with H2O2. The PM, the product of the reaction of the O with one molecule of peroxide, is transformed into the F state by the second molecule of H2O2. However, the chemical nature of this transition has not been unambiguously elucidated yet. Here, we examined the redox state of the peroxide-produced PM and F states by the one-electron reduction. The F form and interestingly also the major fraction of the PM sample, likely another P-type ferryl form (PR), were found to be the one oxidizing equivalent above the O state. However, the both P-type forms are transformed into the F state by additional molecule of H2O2. It is suggested that the PR-to-F transition is due to the binding of H2O2 to CuB triggering a structural change together with the uptake of H+ at the catalytic center. In the PM-to-F conversion, these two events are complemented with the annihilation of radical by the intrinsic oxidation of the enzyme.
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subjects | Cytochrome c oxidase Ferryl intermediates Hydrogen peroxide Redox state |
title | Peroxide stimulated transition between the ferryl intermediates of bovine cytochrome c oxidase |
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