The Type III Flagellar Export Specificity Switch is Dependent on FliK Ruler and a Molecular Clock
Salmonella flagellar hook length is controlled at the level of export substrate specificity of the FlhB component of the type III flagellar export apparatus. FliK is believed to be the hook length sensor and interacts with FlhB to change its export specificity upon hook completion. To find propertie...
Gespeichert in:
Veröffentlicht in: | Journal of molecular biology 2006-06, Vol.359 (2), p.466-477 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 477 |
---|---|
container_issue | 2 |
container_start_page | 466 |
container_title | Journal of molecular biology |
container_volume | 359 |
creator | Moriya, Nao Minamino, Tohru Hughes, Kelly T. Macnab, Robert M. Namba, Keiichi |
description | Salmonella flagellar hook length is controlled at the level of export substrate specificity of the FlhB component of the type III flagellar export apparatus. FliK is believed to be the hook length sensor and interacts with FlhB to change its export specificity upon hook completion. To find properties of FliK expected of such a molecular ruler, we assayed binding of FliK to the hook and found that the N-terminal domain of FliK (FliK
N) bound to the hook-capping protein FlgD with high affinity and to the hook protein FlgE with low affinity. To investigate a possible role of FlgE in hook length control,
flgE mutants with partially impaired motility were isolated and analyzed. Eight
flgE mutants obtained all formed flagellar filaments. The mutants produced significantly shorter hooks while the hook-type substrates such as FlgE, FliK and FlgD were secreted in large amounts, suggesting defective hook assembly with the mutant FlgE proteins. Upon overexpression, mutant FlgEs produced hooks of normal length and wild-type FlgE produced longer hooks. These results suggest that hook length is dependent on the hook polymerization rate and that the start of hook polymerization initiates a “time countdown” for the specificity switch to occur or for significant slow down of rod/hook-type export after hook length reaches around 55
nm for later infrequent FliK
C–FlhB
C interaction. We propose that FliK
N acts as a flexible tape measure, but that hook length is also dependent on the hook elongation rate and a switch timing mechanism. |
doi_str_mv | 10.1016/j.jmb.2006.03.025 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_67954139</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0022283606003469</els_id><sourcerecordid>67954139</sourcerecordid><originalsourceid>FETCH-LOGICAL-c448t-71d5d81cb2b6677a7d82008918585f32ea2cbca007bc0e4bbb77551d5be2a6933</originalsourceid><addsrcrecordid>eNqFkU1v1DAURS0EotPCD-gGecUu6bOd2I5YoenXqEVIdFhbtvOm9ZBJgp20nX9PohmJHaze5twj3XcJOWeQM2DyYptvdy7nADIHkQMv35AFA11lWgr9liwAOM-4FvKEnKa0BYBSFPo9OWFSCpBcL4hdPyFd73ukq9WKXjf2EZvGRnr12ndxoA89-rAJPgx7-vASBv9EQ6KX2GNbYzvQrp0y4Y7-GBuM1LY1tfRb16AfZ8my6fyvD-TdxjYJPx7vGfl5fbVe3mb3329Wy6_3mS8KPWSK1WWtmXfcSamUVbWeiumK6VKXG8HRcu-8BVDOAxbOOaXKcgo55FZWQpyRzwdvH7vfI6bB7ELyc5sWuzEZqaqyYKL6L8gU01DBDLID6GOXUsSN6WPY2bg3DMw8gNmaaQAzD2BAmGmAKfPpKB_dDuu_iePHJ-DLAcDpF88Bo0k-YOuxDhH9YOou_EP_B6i4lLA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>17180909</pqid></control><display><type>article</type><title>The Type III Flagellar Export Specificity Switch is Dependent on FliK Ruler and a Molecular Clock</title><source>MEDLINE</source><source>ScienceDirect Journals (5 years ago - present)</source><creator>Moriya, Nao ; Minamino, Tohru ; Hughes, Kelly T. ; Macnab, Robert M. ; Namba, Keiichi</creator><creatorcontrib>Moriya, Nao ; Minamino, Tohru ; Hughes, Kelly T. ; Macnab, Robert M. ; Namba, Keiichi</creatorcontrib><description>Salmonella flagellar hook length is controlled at the level of export substrate specificity of the FlhB component of the type III flagellar export apparatus. FliK is believed to be the hook length sensor and interacts with FlhB to change its export specificity upon hook completion. To find properties of FliK expected of such a molecular ruler, we assayed binding of FliK to the hook and found that the N-terminal domain of FliK (FliK
N) bound to the hook-capping protein FlgD with high affinity and to the hook protein FlgE with low affinity. To investigate a possible role of FlgE in hook length control,
flgE mutants with partially impaired motility were isolated and analyzed. Eight
flgE mutants obtained all formed flagellar filaments. The mutants produced significantly shorter hooks while the hook-type substrates such as FlgE, FliK and FlgD were secreted in large amounts, suggesting defective hook assembly with the mutant FlgE proteins. Upon overexpression, mutant FlgEs produced hooks of normal length and wild-type FlgE produced longer hooks. These results suggest that hook length is dependent on the hook polymerization rate and that the start of hook polymerization initiates a “time countdown” for the specificity switch to occur or for significant slow down of rod/hook-type export after hook length reaches around 55
nm for later infrequent FliK
C–FlhB
C interaction. We propose that FliK
N acts as a flexible tape measure, but that hook length is also dependent on the hook elongation rate and a switch timing mechanism.</description><identifier>ISSN: 0022-2836</identifier><identifier>EISSN: 1089-8638</identifier><identifier>DOI: 10.1016/j.jmb.2006.03.025</identifier><identifier>PMID: 16630628</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Bacterial Proteins - genetics ; Bacterial Proteins - metabolism ; Biological Transport ; Flagella - metabolism ; Flagella - ultrastructure ; flagellar assembly ; hook length control ; Membrane Proteins - genetics ; Membrane Proteins - metabolism ; Models, Biological ; Salmonella ; Salmonella - metabolism ; substrate specificity switching ; type III protein export</subject><ispartof>Journal of molecular biology, 2006-06, Vol.359 (2), p.466-477</ispartof><rights>2006 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c448t-71d5d81cb2b6677a7d82008918585f32ea2cbca007bc0e4bbb77551d5be2a6933</citedby><cites>FETCH-LOGICAL-c448t-71d5d81cb2b6677a7d82008918585f32ea2cbca007bc0e4bbb77551d5be2a6933</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0022283606003469$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16630628$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Moriya, Nao</creatorcontrib><creatorcontrib>Minamino, Tohru</creatorcontrib><creatorcontrib>Hughes, Kelly T.</creatorcontrib><creatorcontrib>Macnab, Robert M.</creatorcontrib><creatorcontrib>Namba, Keiichi</creatorcontrib><title>The Type III Flagellar Export Specificity Switch is Dependent on FliK Ruler and a Molecular Clock</title><title>Journal of molecular biology</title><addtitle>J Mol Biol</addtitle><description>Salmonella flagellar hook length is controlled at the level of export substrate specificity of the FlhB component of the type III flagellar export apparatus. FliK is believed to be the hook length sensor and interacts with FlhB to change its export specificity upon hook completion. To find properties of FliK expected of such a molecular ruler, we assayed binding of FliK to the hook and found that the N-terminal domain of FliK (FliK
N) bound to the hook-capping protein FlgD with high affinity and to the hook protein FlgE with low affinity. To investigate a possible role of FlgE in hook length control,
flgE mutants with partially impaired motility were isolated and analyzed. Eight
flgE mutants obtained all formed flagellar filaments. The mutants produced significantly shorter hooks while the hook-type substrates such as FlgE, FliK and FlgD were secreted in large amounts, suggesting defective hook assembly with the mutant FlgE proteins. Upon overexpression, mutant FlgEs produced hooks of normal length and wild-type FlgE produced longer hooks. These results suggest that hook length is dependent on the hook polymerization rate and that the start of hook polymerization initiates a “time countdown” for the specificity switch to occur or for significant slow down of rod/hook-type export after hook length reaches around 55
nm for later infrequent FliK
C–FlhB
C interaction. We propose that FliK
N acts as a flexible tape measure, but that hook length is also dependent on the hook elongation rate and a switch timing mechanism.</description><subject>Bacterial Proteins - genetics</subject><subject>Bacterial Proteins - metabolism</subject><subject>Biological Transport</subject><subject>Flagella - metabolism</subject><subject>Flagella - ultrastructure</subject><subject>flagellar assembly</subject><subject>hook length control</subject><subject>Membrane Proteins - genetics</subject><subject>Membrane Proteins - metabolism</subject><subject>Models, Biological</subject><subject>Salmonella</subject><subject>Salmonella - metabolism</subject><subject>substrate specificity switching</subject><subject>type III protein export</subject><issn>0022-2836</issn><issn>1089-8638</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1v1DAURS0EotPCD-gGecUu6bOd2I5YoenXqEVIdFhbtvOm9ZBJgp20nX9PohmJHaze5twj3XcJOWeQM2DyYptvdy7nADIHkQMv35AFA11lWgr9liwAOM-4FvKEnKa0BYBSFPo9OWFSCpBcL4hdPyFd73ukq9WKXjf2EZvGRnr12ndxoA89-rAJPgx7-vASBv9EQ6KX2GNbYzvQrp0y4Y7-GBuM1LY1tfRb16AfZ8my6fyvD-TdxjYJPx7vGfl5fbVe3mb3329Wy6_3mS8KPWSK1WWtmXfcSamUVbWeiumK6VKXG8HRcu-8BVDOAxbOOaXKcgo55FZWQpyRzwdvH7vfI6bB7ELyc5sWuzEZqaqyYKL6L8gU01DBDLID6GOXUsSN6WPY2bg3DMw8gNmaaQAzD2BAmGmAKfPpKB_dDuu_iePHJ-DLAcDpF88Bo0k-YOuxDhH9YOou_EP_B6i4lLA</recordid><startdate>20060602</startdate><enddate>20060602</enddate><creator>Moriya, Nao</creator><creator>Minamino, Tohru</creator><creator>Hughes, Kelly T.</creator><creator>Macnab, Robert M.</creator><creator>Namba, Keiichi</creator><general>Elsevier 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>20060602</creationdate><title>The Type III Flagellar Export Specificity Switch is Dependent on FliK Ruler and a Molecular Clock</title><author>Moriya, Nao ; Minamino, Tohru ; Hughes, Kelly T. ; Macnab, Robert M. ; Namba, Keiichi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c448t-71d5d81cb2b6677a7d82008918585f32ea2cbca007bc0e4bbb77551d5be2a6933</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Bacterial Proteins - genetics</topic><topic>Bacterial Proteins - metabolism</topic><topic>Biological Transport</topic><topic>Flagella - metabolism</topic><topic>Flagella - ultrastructure</topic><topic>flagellar assembly</topic><topic>hook length control</topic><topic>Membrane Proteins - genetics</topic><topic>Membrane Proteins - metabolism</topic><topic>Models, Biological</topic><topic>Salmonella</topic><topic>Salmonella - metabolism</topic><topic>substrate specificity switching</topic><topic>type III protein export</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Moriya, Nao</creatorcontrib><creatorcontrib>Minamino, Tohru</creatorcontrib><creatorcontrib>Hughes, Kelly T.</creatorcontrib><creatorcontrib>Macnab, Robert M.</creatorcontrib><creatorcontrib>Namba, Keiichi</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>Journal of molecular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Moriya, Nao</au><au>Minamino, Tohru</au><au>Hughes, Kelly T.</au><au>Macnab, Robert M.</au><au>Namba, Keiichi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Type III Flagellar Export Specificity Switch is Dependent on FliK Ruler and a Molecular Clock</atitle><jtitle>Journal of molecular biology</jtitle><addtitle>J Mol Biol</addtitle><date>2006-06-02</date><risdate>2006</risdate><volume>359</volume><issue>2</issue><spage>466</spage><epage>477</epage><pages>466-477</pages><issn>0022-2836</issn><eissn>1089-8638</eissn><abstract>Salmonella flagellar hook length is controlled at the level of export substrate specificity of the FlhB component of the type III flagellar export apparatus. FliK is believed to be the hook length sensor and interacts with FlhB to change its export specificity upon hook completion. To find properties of FliK expected of such a molecular ruler, we assayed binding of FliK to the hook and found that the N-terminal domain of FliK (FliK
N) bound to the hook-capping protein FlgD with high affinity and to the hook protein FlgE with low affinity. To investigate a possible role of FlgE in hook length control,
flgE mutants with partially impaired motility were isolated and analyzed. Eight
flgE mutants obtained all formed flagellar filaments. The mutants produced significantly shorter hooks while the hook-type substrates such as FlgE, FliK and FlgD were secreted in large amounts, suggesting defective hook assembly with the mutant FlgE proteins. Upon overexpression, mutant FlgEs produced hooks of normal length and wild-type FlgE produced longer hooks. These results suggest that hook length is dependent on the hook polymerization rate and that the start of hook polymerization initiates a “time countdown” for the specificity switch to occur or for significant slow down of rod/hook-type export after hook length reaches around 55
nm for later infrequent FliK
C–FlhB
C interaction. We propose that FliK
N acts as a flexible tape measure, but that hook length is also dependent on the hook elongation rate and a switch timing mechanism.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>16630628</pmid><doi>10.1016/j.jmb.2006.03.025</doi><tpages>12</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0022-2836 |
ispartof | Journal of molecular biology, 2006-06, Vol.359 (2), p.466-477 |
issn | 0022-2836 1089-8638 |
language | eng |
recordid | cdi_proquest_miscellaneous_67954139 |
source | MEDLINE; ScienceDirect Journals (5 years ago - present) |
subjects | Bacterial Proteins - genetics Bacterial Proteins - metabolism Biological Transport Flagella - metabolism Flagella - ultrastructure flagellar assembly hook length control Membrane Proteins - genetics Membrane Proteins - metabolism Models, Biological Salmonella Salmonella - metabolism substrate specificity switching type III protein export |
title | The Type III Flagellar Export Specificity Switch is Dependent on FliK Ruler and a Molecular Clock |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-02T17%3A42%3A23IST&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%20Type%20III%20Flagellar%20Export%20Specificity%20Switch%20is%20Dependent%20on%20FliK%20Ruler%20and%20a%20Molecular%20Clock&rft.jtitle=Journal%20of%20molecular%20biology&rft.au=Moriya,%20Nao&rft.date=2006-06-02&rft.volume=359&rft.issue=2&rft.spage=466&rft.epage=477&rft.pages=466-477&rft.issn=0022-2836&rft.eissn=1089-8638&rft_id=info:doi/10.1016/j.jmb.2006.03.025&rft_dat=%3Cproquest_cross%3E67954139%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=17180909&rft_id=info:pmid/16630628&rft_els_id=S0022283606003469&rfr_iscdi=true |