Analysis of the control of respiration rate, phosphorylation rate, proton leak rate and protonmotive force in isolated mitochondria using the ‘top‐down’ approach of metabolic control theory
The rate of respiration of isolated mitochondria was set at different values by addition of either oligomycin or an ADP‐regenerating system (glucose and different amounts of hexokinase). We measured the relationship between respiration rate and membrane potential as respiration was titrated by the a...
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Veröffentlicht in: | European journal of biochemistry 1990-03, Vol.188 (2), p.313-319 |
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description | The rate of respiration of isolated mitochondria was set at different values by addition of either oligomycin or an ADP‐regenerating system (glucose and different amounts of hexokinase). We measured the relationship between respiration rate and membrane potential as respiration was titrated by the addition of malonate under each condition. We used the flux control summation and connectivity theorems and the branching theorem of metabolic control theory to calculate the control over respiration rate exerted by the respiratory chain (and associated reactions), phosphorylating system (and associated reactions) and proton leak at each respiration rate. The analysis also yielded the flux control coefficients of these three reactions over phosphorylation rate and proton leak rate and their concentration control coefficients over protonmotive force. We found that respiration rate was controlled largely by the proton leak under non‐phosphorylating conditions, by the phosphorylating system at intermediate rates and by both the phosphorylating system and the respiratory chain in state 3. The rate of phosphorylation was controlled largely by the phosphorylating system itself in state 4 and at intermediate rates, while state 3 control was shared between the phosphorylating system and the respiratory chain; the proton leak had insignificant control. In all states the phosphorylating system had large negative control over the proton leak; the chain and the proton leak both had large positive control coefficients. The protonmotive force was controlled by the chain and by the phosphorylating system; the proton leak had little control. |
doi_str_mv | 10.1111/j.1432-1033.1990.tb15405.x |
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We measured the relationship between respiration rate and membrane potential as respiration was titrated by the addition of malonate under each condition. We used the flux control summation and connectivity theorems and the branching theorem of metabolic control theory to calculate the control over respiration rate exerted by the respiratory chain (and associated reactions), phosphorylating system (and associated reactions) and proton leak at each respiration rate. The analysis also yielded the flux control coefficients of these three reactions over phosphorylation rate and proton leak rate and their concentration control coefficients over protonmotive force. We found that respiration rate was controlled largely by the proton leak under non‐phosphorylating conditions, by the phosphorylating system at intermediate rates and by both the phosphorylating system and the respiratory chain in state 3. The rate of phosphorylation was controlled largely by the phosphorylating system itself in state 4 and at intermediate rates, while state 3 control was shared between the phosphorylating system and the respiratory chain; the proton leak had insignificant control. In all states the phosphorylating system had large negative control over the proton leak; the chain and the proton leak both had large positive control coefficients. The protonmotive force was controlled by the chain and by the phosphorylating system; the proton leak had little control.</description><identifier>ISSN: 0014-2956</identifier><identifier>EISSN: 1432-1033</identifier><identifier>DOI: 10.1111/j.1432-1033.1990.tb15405.x</identifier><identifier>PMID: 2156698</identifier><identifier>CODEN: EJBCAI</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adenosine Diphosphate - biosynthesis ; Animals ; Biological and medical sciences ; Biological Transport - drug effects ; Cell structures and functions ; Down-Regulation - drug effects ; Energy Metabolism - drug effects ; Fundamental and applied biological sciences. Psychology ; Glucose - pharmacology ; Hexokinase - metabolism ; Male ; Mathematics ; membrane potential ; Membrane Potentials - drug effects ; Mitochondria - drug effects ; Mitochondria - metabolism ; Mitochondria and cell respiration ; Molecular and cellular biology ; Oligomycins - pharmacology ; Oxygen Consumption - drug effects ; Phosphorylation ; protonmotive force ; Protons ; Rats ; Rats, Inbred Strains ; respiration</subject><ispartof>European journal of biochemistry, 1990-03, Vol.188 (2), p.313-319</ispartof><rights>1991 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5493-ede7052f1b7b885b2491f2dacb48bb7bdcbf78e45458ccbbe885c61c146662ae3</citedby><cites>FETCH-LOGICAL-c5493-ede7052f1b7b885b2491f2dacb48bb7bdcbf78e45458ccbbe885c61c146662ae3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27928,27929</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=19471892$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2156698$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>HAFNER, Roderick P.</creatorcontrib><creatorcontrib>BROWN, Guy C.</creatorcontrib><creatorcontrib>BRAND, Martin D.</creatorcontrib><title>Analysis of the control of respiration rate, phosphorylation rate, proton leak rate and protonmotive force in isolated mitochondria using the ‘top‐down’ approach of metabolic control theory</title><title>European journal of biochemistry</title><addtitle>Eur J Biochem</addtitle><description>The rate of respiration of isolated mitochondria was set at different values by addition of either oligomycin or an ADP‐regenerating system (glucose and different amounts of hexokinase). We measured the relationship between respiration rate and membrane potential as respiration was titrated by the addition of malonate under each condition. We used the flux control summation and connectivity theorems and the branching theorem of metabolic control theory to calculate the control over respiration rate exerted by the respiratory chain (and associated reactions), phosphorylating system (and associated reactions) and proton leak at each respiration rate. The analysis also yielded the flux control coefficients of these three reactions over phosphorylation rate and proton leak rate and their concentration control coefficients over protonmotive force. We found that respiration rate was controlled largely by the proton leak under non‐phosphorylating conditions, by the phosphorylating system at intermediate rates and by both the phosphorylating system and the respiratory chain in state 3. The rate of phosphorylation was controlled largely by the phosphorylating system itself in state 4 and at intermediate rates, while state 3 control was shared between the phosphorylating system and the respiratory chain; the proton leak had insignificant control. In all states the phosphorylating system had large negative control over the proton leak; the chain and the proton leak both had large positive control coefficients. The protonmotive force was controlled by the chain and by the phosphorylating system; the proton leak had little control.</description><subject>Adenosine Diphosphate - biosynthesis</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Biological Transport - drug effects</subject><subject>Cell structures and functions</subject><subject>Down-Regulation - drug effects</subject><subject>Energy Metabolism - drug effects</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Glucose - pharmacology</subject><subject>Hexokinase - metabolism</subject><subject>Male</subject><subject>Mathematics</subject><subject>membrane potential</subject><subject>Membrane Potentials - drug effects</subject><subject>Mitochondria - drug effects</subject><subject>Mitochondria - metabolism</subject><subject>Mitochondria and cell respiration</subject><subject>Molecular and cellular biology</subject><subject>Oligomycins - pharmacology</subject><subject>Oxygen Consumption - drug effects</subject><subject>Phosphorylation</subject><subject>protonmotive force</subject><subject>Protons</subject><subject>Rats</subject><subject>Rats, Inbred Strains</subject><subject>respiration</subject><issn>0014-2956</issn><issn>1432-1033</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVUUGOFCEUJUYztqNHMCEmurJKqKIocGPGyYyaTOJCXROgKJuWKlqgneldH8Glnseb9EmkpittXBlJCPnvv_f_Cw-AJxiVOJ8XqxKTuiowqusSc47KpHBDUFPe3AGLY-suWCCESVHxht4HD2JcIYQop-0JOKlwQylnC_DrbJRuG22EvodpaaD2YwreTWUwcW2DTNaPMD_mOVwvfcw3bN1faPApF87IL7cIlGM3g4NP9puBvQ_aQDtCG32Wmg4ONnm99GMXrISbaMfPt9v3ux_Jr_e7752_Hve7n1Cu8yCpl5OfwSSpvLP6aDJLspmH4F4vXTSP5vcUfLq8-Hj-trh6_-bd-dlVoRvC68J0pkVN1WPVKsYaVRGO-6qTWhGmMtZp1bfMkIY0TGulTCZpijUmlNJKmvoUPDvMzZa-bkxMYrBRG-fkaPwmipZTjllF_0nMn88YpjwTXx6IOvgYg-nFOthBhq3ASExRi5WY8hRTnmKKWsxRi5ssfjxv2ajBdEfpnG3uP537Mmrp-iBHbeOfDZy0mPEq814deNfWme1_OBCXF68_1LiufwMCi89p</recordid><startdate>19900310</startdate><enddate>19900310</enddate><creator>HAFNER, Roderick P.</creator><creator>BROWN, Guy C.</creator><creator>BRAND, Martin D.</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><scope>IQODW</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>8FD</scope><scope>FR3</scope><scope>M7Z</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>19900310</creationdate><title>Analysis of the control of respiration rate, phosphorylation rate, proton leak rate and protonmotive force in isolated mitochondria using the ‘top‐down’ approach of metabolic control theory</title><author>HAFNER, Roderick P. ; BROWN, Guy C. ; BRAND, Martin D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5493-ede7052f1b7b885b2491f2dacb48bb7bdcbf78e45458ccbbe885c61c146662ae3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>Adenosine Diphosphate - biosynthesis</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Biological Transport - drug effects</topic><topic>Cell structures and functions</topic><topic>Down-Regulation - drug effects</topic><topic>Energy Metabolism - drug effects</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Glucose - pharmacology</topic><topic>Hexokinase - metabolism</topic><topic>Male</topic><topic>Mathematics</topic><topic>membrane potential</topic><topic>Membrane Potentials - drug effects</topic><topic>Mitochondria - drug effects</topic><topic>Mitochondria - metabolism</topic><topic>Mitochondria and cell respiration</topic><topic>Molecular and cellular biology</topic><topic>Oligomycins - pharmacology</topic><topic>Oxygen Consumption - drug effects</topic><topic>Phosphorylation</topic><topic>protonmotive force</topic><topic>Protons</topic><topic>Rats</topic><topic>Rats, Inbred Strains</topic><topic>respiration</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>HAFNER, Roderick P.</creatorcontrib><creatorcontrib>BROWN, Guy C.</creatorcontrib><creatorcontrib>BRAND, Martin D.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biochemistry Abstracts 1</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>HAFNER, Roderick P.</au><au>BROWN, Guy C.</au><au>BRAND, Martin D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Analysis of the control of respiration rate, phosphorylation rate, proton leak rate and protonmotive force in isolated mitochondria using the ‘top‐down’ approach of metabolic control theory</atitle><jtitle>European journal of biochemistry</jtitle><addtitle>Eur J Biochem</addtitle><date>1990-03-10</date><risdate>1990</risdate><volume>188</volume><issue>2</issue><spage>313</spage><epage>319</epage><pages>313-319</pages><issn>0014-2956</issn><eissn>1432-1033</eissn><coden>EJBCAI</coden><abstract>The rate of respiration of isolated mitochondria was set at different values by addition of either oligomycin or an ADP‐regenerating system (glucose and different amounts of hexokinase). We measured the relationship between respiration rate and membrane potential as respiration was titrated by the addition of malonate under each condition. We used the flux control summation and connectivity theorems and the branching theorem of metabolic control theory to calculate the control over respiration rate exerted by the respiratory chain (and associated reactions), phosphorylating system (and associated reactions) and proton leak at each respiration rate. The analysis also yielded the flux control coefficients of these three reactions over phosphorylation rate and proton leak rate and their concentration control coefficients over protonmotive force. We found that respiration rate was controlled largely by the proton leak under non‐phosphorylating conditions, by the phosphorylating system at intermediate rates and by both the phosphorylating system and the respiratory chain in state 3. The rate of phosphorylation was controlled largely by the phosphorylating system itself in state 4 and at intermediate rates, while state 3 control was shared between the phosphorylating system and the respiratory chain; the proton leak had insignificant control. In all states the phosphorylating system had large negative control over the proton leak; the chain and the proton leak both had large positive control coefficients. The protonmotive force was controlled by the chain and by the phosphorylating system; the proton leak had little control.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>2156698</pmid><doi>10.1111/j.1432-1033.1990.tb15405.x</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adenosine Diphosphate - biosynthesis Animals Biological and medical sciences Biological Transport - drug effects Cell structures and functions Down-Regulation - drug effects Energy Metabolism - drug effects Fundamental and applied biological sciences. Psychology Glucose - pharmacology Hexokinase - metabolism Male Mathematics membrane potential Membrane Potentials - drug effects Mitochondria - drug effects Mitochondria - metabolism Mitochondria and cell respiration Molecular and cellular biology Oligomycins - pharmacology Oxygen Consumption - drug effects Phosphorylation protonmotive force Protons Rats Rats, Inbred Strains respiration |
title | Analysis of the control of respiration rate, phosphorylation rate, proton leak rate and protonmotive force in isolated mitochondria using the ‘top‐down’ approach of metabolic control theory |
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