The mechanism of ferrocytochrome C oxidation by a horseradish isoperoxidase

The oxidation of ferrocytochrome c catalysed by highly purified horseradish isoperoxidase P 2 was studied kinetically. To take into account the low turnover number of the enzyme and the tendency to autocatalytic oxidation of ferrocytochrome c, experimental conditions were used which prevented us fro...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Biochimie 1975-01, Vol.57 (1), p.91-96
1. Verfasser: Santimone, Marius
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 96
container_issue 1
container_start_page 91
container_title Biochimie
container_volume 57
creator Santimone, Marius
description The oxidation of ferrocytochrome c catalysed by highly purified horseradish isoperoxidase P 2 was studied kinetically. To take into account the low turnover number of the enzyme and the tendency to autocatalytic oxidation of ferrocytochrome c, experimental conditions were used which prevented us from using the steady-state treatment. According to kinetic results reported by several authors, a kinetic scheme involving a ternary complex between the enzyme and the substrates was postulated and simulated on a hybrid computer. By assuming that the interaction of peroxidase with hydrogen peroxide is much faster than the interaction with ferrocytochrome c, one can verify that this scheme explains the fact that initial velocity does not vary in relation to the hydrogen peroxide concentration and that a sudden change of slope occurs in the kinetic curve for an initial hydrogen peroxide/ferrocytochrome c ratio lower than 0.5. L'oxydation du ferrocytochrome c catalysée par l'isoperoxydase P 2 de raifort hautement purifiée a été étudiée cinétiquement. Afin de tenir compte du faible turnover de l'enzyme et de la tendance du ferrocytochrome c à s'autoxyder, nous avons été amené à utiliser des conditions expérimentales qui ne nous permettaient pas d'employer le traitement à l'état stationnaire. En accord avec les résultats cinétiques rapportés par plusieurs auteurs, un schéma cinétique mettant en jeu un complexe ternaire entre l'enzyme et les substrats a été postulé et simulé sur un calculateur hybride. Si l'on suppose que l'interaction de la peroxydase avec l'eau oxygénée est beaucoup plus rapide que l'interaction avec le ferrocytochrome c, il est possible de vérifier que ce schéma explique le fait que la vitesse initiale ne varie pas en fonction de la concentration en eau oxygénée et qu'une cassure brutale se produit sur la courbe cinétique enregistrée lorsque le rapport des concentrations initiales [eau oxygénée]/[ferrocytochrome c] est inférieur à 0.5.
doi_str_mv 10.1016/S0300-9084(75)80114-3
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_82923097</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0300908475801143</els_id><sourcerecordid>82923097</sourcerecordid><originalsourceid>FETCH-LOGICAL-c359t-36d72d09c006a1f2a33bb9b2bf8cef918791dd2dc87d2183278b06fc139e7c0b3</originalsourceid><addsrcrecordid>eNqFkEtPwzAQhC3Eqzz-AUg-ITgE1jaJ7RNCFS-BxAE4W469UYyautgpov-etEVw5LSHmdnRfIQcMzhnwKqLFxAAhQZ1eSrLMwWMXRZig4xYJVRRMSU2yejXskv2cn4HgBK43iHbrJJK8hF5fG2RduhaOw25o7GhDaYU3aKPrk2xQzqm8St424c4pfWCWtrGlDFZH3JLQ44zTCtDxgOy1dhJxsOfu0_ebm9ex_fF0_Pdw_j6qXCi1H0hKi-5B-0AKssaboWoa13zulEOG82U1Mx77p2Sng8zuFQ1VI1jQqN0UIt9crL-O0vxY465N13IDicTO8U4z0ZxzQVoORjLtdGlmHPCxsxS6GxaGAZmydCsGJolICNLs2JoxJA7-imY1x36v9QK2iBfrWUcRn4GTCa7gFOHPiR0vfEx_FPwDXzbgUg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>82923097</pqid></control><display><type>article</type><title>The mechanism of ferrocytochrome C oxidation by a horseradish isoperoxidase</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Santimone, Marius</creator><creatorcontrib>Santimone, Marius</creatorcontrib><description>The oxidation of ferrocytochrome c catalysed by highly purified horseradish isoperoxidase P 2 was studied kinetically. To take into account the low turnover number of the enzyme and the tendency to autocatalytic oxidation of ferrocytochrome c, experimental conditions were used which prevented us from using the steady-state treatment. According to kinetic results reported by several authors, a kinetic scheme involving a ternary complex between the enzyme and the substrates was postulated and simulated on a hybrid computer. By assuming that the interaction of peroxidase with hydrogen peroxide is much faster than the interaction with ferrocytochrome c, one can verify that this scheme explains the fact that initial velocity does not vary in relation to the hydrogen peroxide concentration and that a sudden change of slope occurs in the kinetic curve for an initial hydrogen peroxide/ferrocytochrome c ratio lower than 0.5. L'oxydation du ferrocytochrome c catalysée par l'isoperoxydase P 2 de raifort hautement purifiée a été étudiée cinétiquement. Afin de tenir compte du faible turnover de l'enzyme et de la tendance du ferrocytochrome c à s'autoxyder, nous avons été amené à utiliser des conditions expérimentales qui ne nous permettaient pas d'employer le traitement à l'état stationnaire. En accord avec les résultats cinétiques rapportés par plusieurs auteurs, un schéma cinétique mettant en jeu un complexe ternaire entre l'enzyme et les substrats a été postulé et simulé sur un calculateur hybride. Si l'on suppose que l'interaction de la peroxydase avec l'eau oxygénée est beaucoup plus rapide que l'interaction avec le ferrocytochrome c, il est possible de vérifier que ce schéma explique le fait que la vitesse initiale ne varie pas en fonction de la concentration en eau oxygénée et qu'une cassure brutale se produit sur la courbe cinétique enregistrée lorsque le rapport des concentrations initiales [eau oxygénée]/[ferrocytochrome c] est inférieur à 0.5.</description><identifier>ISSN: 0300-9084</identifier><identifier>EISSN: 1638-6183</identifier><identifier>DOI: 10.1016/S0300-9084(75)80114-3</identifier><identifier>PMID: 167872</identifier><language>eng</language><publisher>France: Elsevier Masson SAS</publisher><subject>Computers ; Cytochrome c Group - metabolism ; Hydrogen Peroxide - metabolism ; Kinetics ; Peroxidases - metabolism ; Plants - enzymology</subject><ispartof>Biochimie, 1975-01, Vol.57 (1), p.91-96</ispartof><rights>1975</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c359t-36d72d09c006a1f2a33bb9b2bf8cef918791dd2dc87d2183278b06fc139e7c0b3</citedby><cites>FETCH-LOGICAL-c359t-36d72d09c006a1f2a33bb9b2bf8cef918791dd2dc87d2183278b06fc139e7c0b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0300908475801143$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/167872$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Santimone, Marius</creatorcontrib><title>The mechanism of ferrocytochrome C oxidation by a horseradish isoperoxidase</title><title>Biochimie</title><addtitle>Biochimie</addtitle><description>The oxidation of ferrocytochrome c catalysed by highly purified horseradish isoperoxidase P 2 was studied kinetically. To take into account the low turnover number of the enzyme and the tendency to autocatalytic oxidation of ferrocytochrome c, experimental conditions were used which prevented us from using the steady-state treatment. According to kinetic results reported by several authors, a kinetic scheme involving a ternary complex between the enzyme and the substrates was postulated and simulated on a hybrid computer. By assuming that the interaction of peroxidase with hydrogen peroxide is much faster than the interaction with ferrocytochrome c, one can verify that this scheme explains the fact that initial velocity does not vary in relation to the hydrogen peroxide concentration and that a sudden change of slope occurs in the kinetic curve for an initial hydrogen peroxide/ferrocytochrome c ratio lower than 0.5. L'oxydation du ferrocytochrome c catalysée par l'isoperoxydase P 2 de raifort hautement purifiée a été étudiée cinétiquement. Afin de tenir compte du faible turnover de l'enzyme et de la tendance du ferrocytochrome c à s'autoxyder, nous avons été amené à utiliser des conditions expérimentales qui ne nous permettaient pas d'employer le traitement à l'état stationnaire. En accord avec les résultats cinétiques rapportés par plusieurs auteurs, un schéma cinétique mettant en jeu un complexe ternaire entre l'enzyme et les substrats a été postulé et simulé sur un calculateur hybride. Si l'on suppose que l'interaction de la peroxydase avec l'eau oxygénée est beaucoup plus rapide que l'interaction avec le ferrocytochrome c, il est possible de vérifier que ce schéma explique le fait que la vitesse initiale ne varie pas en fonction de la concentration en eau oxygénée et qu'une cassure brutale se produit sur la courbe cinétique enregistrée lorsque le rapport des concentrations initiales [eau oxygénée]/[ferrocytochrome c] est inférieur à 0.5.</description><subject>Computers</subject><subject>Cytochrome c Group - metabolism</subject><subject>Hydrogen Peroxide - metabolism</subject><subject>Kinetics</subject><subject>Peroxidases - metabolism</subject><subject>Plants - enzymology</subject><issn>0300-9084</issn><issn>1638-6183</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1975</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtPwzAQhC3Eqzz-AUg-ITgE1jaJ7RNCFS-BxAE4W469UYyautgpov-etEVw5LSHmdnRfIQcMzhnwKqLFxAAhQZ1eSrLMwWMXRZig4xYJVRRMSU2yejXskv2cn4HgBK43iHbrJJK8hF5fG2RduhaOw25o7GhDaYU3aKPrk2xQzqm8St424c4pfWCWtrGlDFZH3JLQ44zTCtDxgOy1dhJxsOfu0_ebm9ex_fF0_Pdw_j6qXCi1H0hKi-5B-0AKssaboWoa13zulEOG82U1Mx77p2Sng8zuFQ1VI1jQqN0UIt9crL-O0vxY465N13IDicTO8U4z0ZxzQVoORjLtdGlmHPCxsxS6GxaGAZmydCsGJolICNLs2JoxJA7-imY1x36v9QK2iBfrWUcRn4GTCa7gFOHPiR0vfEx_FPwDXzbgUg</recordid><startdate>19750101</startdate><enddate>19750101</enddate><creator>Santimone, Marius</creator><general>Elsevier Masson SAS</general><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>7X8</scope></search><sort><creationdate>19750101</creationdate><title>The mechanism of ferrocytochrome C oxidation by a horseradish isoperoxidase</title><author>Santimone, Marius</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c359t-36d72d09c006a1f2a33bb9b2bf8cef918791dd2dc87d2183278b06fc139e7c0b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1975</creationdate><topic>Computers</topic><topic>Cytochrome c Group - metabolism</topic><topic>Hydrogen Peroxide - metabolism</topic><topic>Kinetics</topic><topic>Peroxidases - metabolism</topic><topic>Plants - enzymology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Santimone, Marius</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Biochimie</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Santimone, Marius</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The mechanism of ferrocytochrome C oxidation by a horseradish isoperoxidase</atitle><jtitle>Biochimie</jtitle><addtitle>Biochimie</addtitle><date>1975-01-01</date><risdate>1975</risdate><volume>57</volume><issue>1</issue><spage>91</spage><epage>96</epage><pages>91-96</pages><issn>0300-9084</issn><eissn>1638-6183</eissn><abstract>The oxidation of ferrocytochrome c catalysed by highly purified horseradish isoperoxidase P 2 was studied kinetically. To take into account the low turnover number of the enzyme and the tendency to autocatalytic oxidation of ferrocytochrome c, experimental conditions were used which prevented us from using the steady-state treatment. According to kinetic results reported by several authors, a kinetic scheme involving a ternary complex between the enzyme and the substrates was postulated and simulated on a hybrid computer. By assuming that the interaction of peroxidase with hydrogen peroxide is much faster than the interaction with ferrocytochrome c, one can verify that this scheme explains the fact that initial velocity does not vary in relation to the hydrogen peroxide concentration and that a sudden change of slope occurs in the kinetic curve for an initial hydrogen peroxide/ferrocytochrome c ratio lower than 0.5. L'oxydation du ferrocytochrome c catalysée par l'isoperoxydase P 2 de raifort hautement purifiée a été étudiée cinétiquement. Afin de tenir compte du faible turnover de l'enzyme et de la tendance du ferrocytochrome c à s'autoxyder, nous avons été amené à utiliser des conditions expérimentales qui ne nous permettaient pas d'employer le traitement à l'état stationnaire. En accord avec les résultats cinétiques rapportés par plusieurs auteurs, un schéma cinétique mettant en jeu un complexe ternaire entre l'enzyme et les substrats a été postulé et simulé sur un calculateur hybride. Si l'on suppose que l'interaction de la peroxydase avec l'eau oxygénée est beaucoup plus rapide que l'interaction avec le ferrocytochrome c, il est possible de vérifier que ce schéma explique le fait que la vitesse initiale ne varie pas en fonction de la concentration en eau oxygénée et qu'une cassure brutale se produit sur la courbe cinétique enregistrée lorsque le rapport des concentrations initiales [eau oxygénée]/[ferrocytochrome c] est inférieur à 0.5.</abstract><cop>France</cop><pub>Elsevier Masson SAS</pub><pmid>167872</pmid><doi>10.1016/S0300-9084(75)80114-3</doi><tpages>6</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0300-9084
ispartof Biochimie, 1975-01, Vol.57 (1), p.91-96
issn 0300-9084
1638-6183
language eng
recordid cdi_proquest_miscellaneous_82923097
source MEDLINE; Elsevier ScienceDirect Journals
subjects Computers
Cytochrome c Group - metabolism
Hydrogen Peroxide - metabolism
Kinetics
Peroxidases - metabolism
Plants - enzymology
title The mechanism of ferrocytochrome C oxidation by a horseradish isoperoxidase
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-10T11%3A03%3A12IST&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=The%20mechanism%20of%20ferrocytochrome%20C%20oxidation%20by%20a%20horseradish%20isoperoxidase&rft.jtitle=Biochimie&rft.au=Santimone,%20Marius&rft.date=1975-01-01&rft.volume=57&rft.issue=1&rft.spage=91&rft.epage=96&rft.pages=91-96&rft.issn=0300-9084&rft.eissn=1638-6183&rft_id=info:doi/10.1016/S0300-9084(75)80114-3&rft_dat=%3Cproquest_cross%3E82923097%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=82923097&rft_id=info:pmid/167872&rft_els_id=S0300908475801143&rfr_iscdi=true