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Quantification of known components of the Escherichia coli TonB energy transduction system: TonB, ExbB, ExbD and FepA
Summary The TonB‐dependent energy transduction system couples cytoplasmic membrane proton motive force to active transport of iron–siderophore complexes across the outer membrane in Gram‐negative bacteria. In Escherichia coli, the primary players known in this process to date are: FepA, the TonB‐gat...
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Published in: | Molecular microbiology 2002-04, Vol.44 (1), p.271-281 |
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creator | Higgs, Penelope I. Larsen, Ray A. Postle, Kathleen |
description | Summary
The TonB‐dependent energy transduction system couples cytoplasmic membrane proton motive force to active transport of iron–siderophore complexes across the outer membrane in Gram‐negative bacteria. In Escherichia coli, the primary
players known in this process to date are: FepA, the TonB‐gated transporter for the
siderophore enterochelin; TonB, the energy‐transducing protein; and two cytoplasmic
membrane proteins with less defined roles, ExbB and ExbD. In this study, we report
the per cell numbers of TonB, ExbB, ExbD and FepA for cells grown under iron‐replete
and iron‐limited conditions. Under iron‐replete conditions, TonB and FepA were present
at 335 ± 78 and 504 ± 165 copies per cell respectively.
ExbB and ExbD, despite being encoded from the same operon, were not equimolar, being
present at 2463 ± 522 and 741 ± 105 copies respectively. The ratio of these proteins was calculated at one TonB:two ExbD:seven ExbB under all four growth conditions tested. In contrast, the TonB:FepA ratio varied with iron status and according to the method used for iron limitation. Differences in the method of iron limitation also resulted in significant differences in cell size, skewing the per cell copy numbers for all proteins. |
doi_str_mv | 10.1046/j.1365-2958.2002.02880.x |
format | article |
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The TonB‐dependent energy transduction system couples cytoplasmic membrane proton motive force to active transport of iron–siderophore complexes across the outer membrane in Gram‐negative bacteria. In Escherichia coli, the primary
players known in this process to date are: FepA, the TonB‐gated transporter for the
siderophore enterochelin; TonB, the energy‐transducing protein; and two cytoplasmic
membrane proteins with less defined roles, ExbB and ExbD. In this study, we report
the per cell numbers of TonB, ExbB, ExbD and FepA for cells grown under iron‐replete
and iron‐limited conditions. Under iron‐replete conditions, TonB and FepA were present
at 335 ± 78 and 504 ± 165 copies per cell respectively.
ExbB and ExbD, despite being encoded from the same operon, were not equimolar, being
present at 2463 ± 522 and 741 ± 105 copies respectively. The ratio of these proteins was calculated at one TonB:two ExbD:seven ExbB under all four growth conditions tested. In contrast, the TonB:FepA ratio varied with iron status and according to the method used for iron limitation. Differences in the method of iron limitation also resulted in significant differences in cell size, skewing the per cell copy numbers for all proteins.</description><identifier>ISSN: 0950-382X</identifier><identifier>EISSN: 1365-2958</identifier><identifier>DOI: 10.1046/j.1365-2958.2002.02880.x</identifier><identifier>PMID: 11967085</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Science Ltd</publisher><subject>Bacterial Outer Membrane Proteins ; Bacterial Proteins - genetics ; Bacterial Proteins - metabolism ; Biological Transport ; Carrier Proteins - genetics ; Carrier Proteins - metabolism ; Enterobactin - metabolism ; Escherichia coli - genetics ; Escherichia coli - growth & development ; Escherichia coli - metabolism ; Escherichia coli Proteins - genetics ; Escherichia coli Proteins - metabolism ; Gene Expression Regulation, Bacterial ; Membrane Proteins - genetics ; Membrane Proteins - metabolism ; Protein Biosynthesis ; Receptors, Cell Surface ; Transcription, Genetic</subject><ispartof>Molecular microbiology, 2002-04, Vol.44 (1), p.271-281</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5120-5730d99425eda3e6893f15d3a317ce606486424736dafe794c85b23321a4b0cb3</citedby><cites>FETCH-LOGICAL-c5120-5730d99425eda3e6893f15d3a317ce606486424736dafe794c85b23321a4b0cb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11967085$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Higgs, Penelope I.</creatorcontrib><creatorcontrib>Larsen, Ray A.</creatorcontrib><creatorcontrib>Postle, Kathleen</creatorcontrib><title>Quantification of known components of the Escherichia coli TonB energy transduction system: TonB, ExbB, ExbD and FepA</title><title>Molecular microbiology</title><addtitle>Mol Microbiol</addtitle><description>Summary
The TonB‐dependent energy transduction system couples cytoplasmic membrane proton motive force to active transport of iron–siderophore complexes across the outer membrane in Gram‐negative bacteria. In Escherichia coli, the primary
players known in this process to date are: FepA, the TonB‐gated transporter for the
siderophore enterochelin; TonB, the energy‐transducing protein; and two cytoplasmic
membrane proteins with less defined roles, ExbB and ExbD. In this study, we report
the per cell numbers of TonB, ExbB, ExbD and FepA for cells grown under iron‐replete
and iron‐limited conditions. Under iron‐replete conditions, TonB and FepA were present
at 335 ± 78 and 504 ± 165 copies per cell respectively.
ExbB and ExbD, despite being encoded from the same operon, were not equimolar, being
present at 2463 ± 522 and 741 ± 105 copies respectively. The ratio of these proteins was calculated at one TonB:two ExbD:seven ExbB under all four growth conditions tested. In contrast, the TonB:FepA ratio varied with iron status and according to the method used for iron limitation. Differences in the method of iron limitation also resulted in significant differences in cell size, skewing the per cell copy numbers for all proteins.</description><subject>Bacterial Outer Membrane Proteins</subject><subject>Bacterial Proteins - genetics</subject><subject>Bacterial Proteins - metabolism</subject><subject>Biological Transport</subject><subject>Carrier Proteins - genetics</subject><subject>Carrier Proteins - metabolism</subject><subject>Enterobactin - metabolism</subject><subject>Escherichia coli - genetics</subject><subject>Escherichia coli - growth & development</subject><subject>Escherichia coli - metabolism</subject><subject>Escherichia coli Proteins - genetics</subject><subject>Escherichia coli Proteins - metabolism</subject><subject>Gene Expression Regulation, Bacterial</subject><subject>Membrane Proteins - genetics</subject><subject>Membrane Proteins - metabolism</subject><subject>Protein Biosynthesis</subject><subject>Receptors, Cell Surface</subject><subject>Transcription, Genetic</subject><issn>0950-382X</issn><issn>1365-2958</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNqNkU1P3DAQhq2qqCy0fwH51FMT_BE7dqUeKF0oEgghUak3y3EmrLeJvcSJ2P33bHZX5dgePLZmnnl9eBDClOSUFPJ8mVMuRca0UDkjhOWEKUXy9Ts0-zt4j2ZEC5JxxX4fo5OUloRQTiT_gI4p1bIkSszQ-DDaMPjGOzv4GHBs8J8QXwJ2sVvFAGFIU29YAJ4nt4Deu4W322nr8WMM3zEE6J82eOhtSPXodiFpkwbovu6AL3i-rvb1B7ahxlewuviIjhrbJvh0uE_Rr6v54-XP7Pb--uby4jZzgjKSiZKTWuuCCagtB6k0b6ioueW0dCCJLJQsWFFyWdsGSl04JSrGOaO2qIir-Cn6vM9d9fF5hDSYzicHbWsDxDGZkkqquRL_BKniejpbUO1B18eUemjMqved7TeGEjO5MUszKTCTAjO5MTs3Zr1dPTv8MVYd1G-LBxlb4NseePEtbP472Nzd3Uwv_gope5yD</recordid><startdate>200204</startdate><enddate>200204</enddate><creator>Higgs, Penelope I.</creator><creator>Larsen, Ray A.</creator><creator>Postle, Kathleen</creator><general>Blackwell Science Ltd</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>7QL</scope><scope>C1K</scope><scope>7X8</scope></search><sort><creationdate>200204</creationdate><title>Quantification of known components of the Escherichia coli TonB energy transduction system: TonB, ExbB, ExbD and FepA</title><author>Higgs, Penelope I. ; Larsen, Ray A. ; Postle, Kathleen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5120-5730d99425eda3e6893f15d3a317ce606486424736dafe794c85b23321a4b0cb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Bacterial Outer Membrane Proteins</topic><topic>Bacterial Proteins - genetics</topic><topic>Bacterial Proteins - metabolism</topic><topic>Biological Transport</topic><topic>Carrier Proteins - genetics</topic><topic>Carrier Proteins - metabolism</topic><topic>Enterobactin - metabolism</topic><topic>Escherichia coli - genetics</topic><topic>Escherichia coli - growth & development</topic><topic>Escherichia coli - metabolism</topic><topic>Escherichia coli Proteins - genetics</topic><topic>Escherichia coli Proteins - metabolism</topic><topic>Gene Expression Regulation, Bacterial</topic><topic>Membrane Proteins - genetics</topic><topic>Membrane Proteins - metabolism</topic><topic>Protein Biosynthesis</topic><topic>Receptors, Cell Surface</topic><topic>Transcription, Genetic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Higgs, Penelope I.</creatorcontrib><creatorcontrib>Larsen, Ray A.</creatorcontrib><creatorcontrib>Postle, Kathleen</creatorcontrib><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>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Higgs, Penelope I.</au><au>Larsen, Ray A.</au><au>Postle, Kathleen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Quantification of known components of the Escherichia coli TonB energy transduction system: TonB, ExbB, ExbD and FepA</atitle><jtitle>Molecular microbiology</jtitle><addtitle>Mol Microbiol</addtitle><date>2002-04</date><risdate>2002</risdate><volume>44</volume><issue>1</issue><spage>271</spage><epage>281</epage><pages>271-281</pages><issn>0950-382X</issn><eissn>1365-2958</eissn><abstract>Summary
The TonB‐dependent energy transduction system couples cytoplasmic membrane proton motive force to active transport of iron–siderophore complexes across the outer membrane in Gram‐negative bacteria. In Escherichia coli, the primary
players known in this process to date are: FepA, the TonB‐gated transporter for the
siderophore enterochelin; TonB, the energy‐transducing protein; and two cytoplasmic
membrane proteins with less defined roles, ExbB and ExbD. In this study, we report
the per cell numbers of TonB, ExbB, ExbD and FepA for cells grown under iron‐replete
and iron‐limited conditions. Under iron‐replete conditions, TonB and FepA were present
at 335 ± 78 and 504 ± 165 copies per cell respectively.
ExbB and ExbD, despite being encoded from the same operon, were not equimolar, being
present at 2463 ± 522 and 741 ± 105 copies respectively. The ratio of these proteins was calculated at one TonB:two ExbD:seven ExbB under all four growth conditions tested. In contrast, the TonB:FepA ratio varied with iron status and according to the method used for iron limitation. Differences in the method of iron limitation also resulted in significant differences in cell size, skewing the per cell copy numbers for all proteins.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science Ltd</pub><pmid>11967085</pmid><doi>10.1046/j.1365-2958.2002.02880.x</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Bacterial Outer Membrane Proteins Bacterial Proteins - genetics Bacterial Proteins - metabolism Biological Transport Carrier Proteins - genetics Carrier Proteins - metabolism Enterobactin - metabolism Escherichia coli - genetics Escherichia coli - growth & development Escherichia coli - metabolism Escherichia coli Proteins - genetics Escherichia coli Proteins - metabolism Gene Expression Regulation, Bacterial Membrane Proteins - genetics Membrane Proteins - metabolism Protein Biosynthesis Receptors, Cell Surface Transcription, Genetic |
title | Quantification of known components of the Escherichia coli TonB energy transduction system: TonB, ExbB, ExbD and FepA |
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