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PimT, an amino acid exporter controls polyene production via secretion of the quorum sensing pimaricin-inducer PI-factor in Streptomyces natalensis
Polyenes represent a major class of antifungal agents characterised by the presence of a series of conjugated double bonds in their planar hydroxylated macrolide ring structure. Despite their general interest, very little is known about the factors that modulate their biosynthesis. Among these facto...
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Published in: | Microbial cell factories 2009-06, Vol.8 (33), p.33-33, Article 33 |
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description | Polyenes represent a major class of antifungal agents characterised by the presence of a series of conjugated double bonds in their planar hydroxylated macrolide ring structure. Despite their general interest, very little is known about the factors that modulate their biosynthesis. Among these factors, we have recently discovered a new inducing compound (PI-factor) in the pimaricin producer Streptomyces natalensis, which elicits polyene production in a manner characteristic of quorum sensing. Here, we describe the involvement of an amino-acid exporter from S. natalensis in modulating the expression of pimaricin biosynthetic genes via secretion of the quorum-sensing pimaricin-inducer PI-factor.
Adjacent to the pimaricin gene cluster lies a member of the RhtB family of amino-acid exporters. Gene deletion and complementation experiments provided evidence for a role for PimT in the export of L-homoserine, L-serine, and L-homoserine lactone. Expression of the gene was shown to be induced by homoserine and by the quorum-sensing pimaricin-inducer PI-factor. Interestingly, the mutant displayed 65% loss of pimaricin production, and also 50% decrease in the production of PI, indicating that PimT is used as PI-factor exporter, and suggesting that the effect in antifungal production might be due to limited secretion of the inducer.
This report describes the involvement of an amino acid exporter (encoded by pimT in the vicinity of the pimaricin cluster) in modulating the expression of antibiotic biosynthetic genes via secretion of the quorum-sensing pimaricin-inducer PI-factor. The discovery of the participation of amino acid exporters in a signal transduction cascade for the production of polyene macrolides is unexpected, and represents an important step forward towards understanding the regulatory network for polyene regulation. Additionally, this finding constitutes the first detailed characterization of an amino-acid exporter in an Actinomycete, and to our knowledge, the first evidence for the implication of this type of exporters in quorum sensing. |
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Adjacent to the pimaricin gene cluster lies a member of the RhtB family of amino-acid exporters. Gene deletion and complementation experiments provided evidence for a role for PimT in the export of L-homoserine, L-serine, and L-homoserine lactone. Expression of the gene was shown to be induced by homoserine and by the quorum-sensing pimaricin-inducer PI-factor. Interestingly, the mutant displayed 65% loss of pimaricin production, and also 50% decrease in the production of PI, indicating that PimT is used as PI-factor exporter, and suggesting that the effect in antifungal production might be due to limited secretion of the inducer.
This report describes the involvement of an amino acid exporter (encoded by pimT in the vicinity of the pimaricin cluster) in modulating the expression of antibiotic biosynthetic genes via secretion of the quorum-sensing pimaricin-inducer PI-factor. The discovery of the participation of amino acid exporters in a signal transduction cascade for the production of polyene macrolides is unexpected, and represents an important step forward towards understanding the regulatory network for polyene regulation. Additionally, this finding constitutes the first detailed characterization of an amino-acid exporter in an Actinomycete, and to our knowledge, the first evidence for the implication of this type of exporters in quorum sensing.</description><identifier>ISSN: 1475-2859</identifier><identifier>EISSN: 1475-2859</identifier><identifier>DOI: 10.1186/1475-2859-8-33</identifier><identifier>PMID: 19505319</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Amino acids ; Biochemistry, Molecular Biology ; Biotechnology ; Control ; Life Sciences ; Molecular biology ; Polyenes ; Streptomyces</subject><ispartof>Microbial cell factories, 2009-06, Vol.8 (33), p.33-33, Article 33</ispartof><rights>COPYRIGHT 2009 BioMed Central Ltd.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>Copyright © 2009 Vicente et al; licensee BioMed Central Ltd. 2009 Vicente et al; licensee BioMed Central Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b714t-48f727ce2e066e8d744df314fbbd8e61a03e6dda34483799ea45ad904549eec13</citedby><cites>FETCH-LOGICAL-b714t-48f727ce2e066e8d744df314fbbd8e61a03e6dda34483799ea45ad904549eec13</cites><orcidid>0000-0001-8205-6486</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2698837/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2698837/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,36990,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19505319$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://insa-toulouse.hal.science/hal-02547645$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Vicente, Cláudia M</creatorcontrib><creatorcontrib>Santos-Aberturas, Javier</creatorcontrib><creatorcontrib>Guerra, Susana M</creatorcontrib><creatorcontrib>Payero, Tamara D</creatorcontrib><creatorcontrib>Martín, Juan F</creatorcontrib><creatorcontrib>Aparicio, Jesús F</creatorcontrib><title>PimT, an amino acid exporter controls polyene production via secretion of the quorum sensing pimaricin-inducer PI-factor in Streptomyces natalensis</title><title>Microbial cell factories</title><addtitle>Microb Cell Fact</addtitle><description>Polyenes represent a major class of antifungal agents characterised by the presence of a series of conjugated double bonds in their planar hydroxylated macrolide ring structure. Despite their general interest, very little is known about the factors that modulate their biosynthesis. Among these factors, we have recently discovered a new inducing compound (PI-factor) in the pimaricin producer Streptomyces natalensis, which elicits polyene production in a manner characteristic of quorum sensing. Here, we describe the involvement of an amino-acid exporter from S. natalensis in modulating the expression of pimaricin biosynthetic genes via secretion of the quorum-sensing pimaricin-inducer PI-factor.
Adjacent to the pimaricin gene cluster lies a member of the RhtB family of amino-acid exporters. Gene deletion and complementation experiments provided evidence for a role for PimT in the export of L-homoserine, L-serine, and L-homoserine lactone. Expression of the gene was shown to be induced by homoserine and by the quorum-sensing pimaricin-inducer PI-factor. Interestingly, the mutant displayed 65% loss of pimaricin production, and also 50% decrease in the production of PI, indicating that PimT is used as PI-factor exporter, and suggesting that the effect in antifungal production might be due to limited secretion of the inducer.
This report describes the involvement of an amino acid exporter (encoded by pimT in the vicinity of the pimaricin cluster) in modulating the expression of antibiotic biosynthetic genes via secretion of the quorum-sensing pimaricin-inducer PI-factor. The discovery of the participation of amino acid exporters in a signal transduction cascade for the production of polyene macrolides is unexpected, and represents an important step forward towards understanding the regulatory network for polyene regulation. Additionally, this finding constitutes the first detailed characterization of an amino-acid exporter in an Actinomycete, and to our knowledge, the first evidence for the implication of this type of exporters in quorum sensing.</description><subject>Amino acids</subject><subject>Biochemistry, Molecular Biology</subject><subject>Biotechnology</subject><subject>Control</subject><subject>Life Sciences</subject><subject>Molecular biology</subject><subject>Polyenes</subject><subject>Streptomyces</subject><issn>1475-2859</issn><issn>1475-2859</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNp1k1Fv0zAUhSMEYmPwyiOyxAOaRIYd24nzglRNwCpVYmLj2XKdm9ZTYme2U62_gz-Ms1ZjhSE_JDk-9_N1fJxlbwk-I0SUnwireF4IXucip_RZdvwgPH_0fpS9CuEGY1KJir7MjkjNMaekPs5-XZr--iNSFqneWIeUNg2Cu8H5CB5pZ6N3XUCD67ZgAQ3eNaOOxlm0MQoF0B7uv1yL4hrQ7ej82CfdBmNXaDC98kYbmxub6hLxcp63SkfnkbHoKnoYouu3GgKyKqpuqguvsxet6gK82T9Psp9fv1yfX-SL79_m57NFvqwIizkTbVVUGgrAZQmiqRhrWkpYu1w2AkqiMIWyaRRlTNCqrkExrpoaM85qAE3oSTbfcRunbuTgp2a30ikj7wXnV1L5aHQHkgAIjBNLF4zVmipaEKGXZV1qITieWJ93rGFc9tBoSD9OdQfQwxlr1nLlNrIoa5HaS4DTHWD9V9nFbCEnDRecVSXjm2mx2c67NO4_ix3OaNfLKQxyCoMUktLE-LBv2LvbEUKUvQkauk5ZcGOQFaVFwXlVJuf7nXOVzkca27rE1JNbzgqcBhdcJNfZE640GuhNyhG0JukHBacHBVPW4C6u1BiCnF_9eBKuvQvBQ_uwV4LldA_-3d27x8fxx74PPv0NdkYEWw</recordid><startdate>20090608</startdate><enddate>20090608</enddate><creator>Vicente, Cláudia M</creator><creator>Santos-Aberturas, Javier</creator><creator>Guerra, Susana M</creator><creator>Payero, Tamara D</creator><creator>Martín, Juan F</creator><creator>Aparicio, Jesús F</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>ISR</scope><scope>7X8</scope><scope>1XC</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-8205-6486</orcidid></search><sort><creationdate>20090608</creationdate><title>PimT, an amino acid exporter controls polyene production via secretion of the quorum sensing pimaricin-inducer PI-factor in Streptomyces natalensis</title><author>Vicente, Cláudia M ; Santos-Aberturas, Javier ; Guerra, Susana M ; Payero, Tamara D ; Martín, Juan F ; Aparicio, Jesús F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b714t-48f727ce2e066e8d744df314fbbd8e61a03e6dda34483799ea45ad904549eec13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Amino acids</topic><topic>Biochemistry, Molecular Biology</topic><topic>Biotechnology</topic><topic>Control</topic><topic>Life Sciences</topic><topic>Molecular biology</topic><topic>Polyenes</topic><topic>Streptomyces</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vicente, Cláudia M</creatorcontrib><creatorcontrib>Santos-Aberturas, Javier</creatorcontrib><creatorcontrib>Guerra, Susana M</creatorcontrib><creatorcontrib>Payero, Tamara D</creatorcontrib><creatorcontrib>Martín, Juan F</creatorcontrib><creatorcontrib>Aparicio, Jesús F</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Microbial cell factories</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vicente, Cláudia M</au><au>Santos-Aberturas, Javier</au><au>Guerra, Susana M</au><au>Payero, Tamara D</au><au>Martín, Juan F</au><au>Aparicio, Jesús F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>PimT, an amino acid exporter controls polyene production via secretion of the quorum sensing pimaricin-inducer PI-factor in Streptomyces natalensis</atitle><jtitle>Microbial cell factories</jtitle><addtitle>Microb Cell Fact</addtitle><date>2009-06-08</date><risdate>2009</risdate><volume>8</volume><issue>33</issue><spage>33</spage><epage>33</epage><pages>33-33</pages><artnum>33</artnum><issn>1475-2859</issn><eissn>1475-2859</eissn><abstract>Polyenes represent a major class of antifungal agents characterised by the presence of a series of conjugated double bonds in their planar hydroxylated macrolide ring structure. Despite their general interest, very little is known about the factors that modulate their biosynthesis. Among these factors, we have recently discovered a new inducing compound (PI-factor) in the pimaricin producer Streptomyces natalensis, which elicits polyene production in a manner characteristic of quorum sensing. Here, we describe the involvement of an amino-acid exporter from S. natalensis in modulating the expression of pimaricin biosynthetic genes via secretion of the quorum-sensing pimaricin-inducer PI-factor.
Adjacent to the pimaricin gene cluster lies a member of the RhtB family of amino-acid exporters. Gene deletion and complementation experiments provided evidence for a role for PimT in the export of L-homoserine, L-serine, and L-homoserine lactone. Expression of the gene was shown to be induced by homoserine and by the quorum-sensing pimaricin-inducer PI-factor. Interestingly, the mutant displayed 65% loss of pimaricin production, and also 50% decrease in the production of PI, indicating that PimT is used as PI-factor exporter, and suggesting that the effect in antifungal production might be due to limited secretion of the inducer.
This report describes the involvement of an amino acid exporter (encoded by pimT in the vicinity of the pimaricin cluster) in modulating the expression of antibiotic biosynthetic genes via secretion of the quorum-sensing pimaricin-inducer PI-factor. The discovery of the participation of amino acid exporters in a signal transduction cascade for the production of polyene macrolides is unexpected, and represents an important step forward towards understanding the regulatory network for polyene regulation. Additionally, this finding constitutes the first detailed characterization of an amino-acid exporter in an Actinomycete, and to our knowledge, the first evidence for the implication of this type of exporters in quorum sensing.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>19505319</pmid><doi>10.1186/1475-2859-8-33</doi><orcidid>https://orcid.org/0000-0001-8205-6486</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Amino acids Biochemistry, Molecular Biology Biotechnology Control Life Sciences Molecular biology Polyenes Streptomyces |
title | PimT, an amino acid exporter controls polyene production via secretion of the quorum sensing pimaricin-inducer PI-factor in Streptomyces natalensis |
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