Loading…
Pseudomonas fluorescens CHA0 Produces Enantio-pyochelin, the Optical Antipode of the Pseudomonas aeruginosa Siderophore Pyochelin
The siderophore pyochelin is made by a thiotemplate mechanism from salicylate and two molecules of cysteine. In Pseudomonas aeruginosa, the first cysteine residue is converted to its D-isoform during thiazoline ring formation whereas the second cysteine remains in its L-configuration, thus determini...
Saved in:
Published in: | The Journal of biological chemistry 2007-12, Vol.282 (49), p.35546-35553 |
---|---|
Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c500t-94344566ee7d1f665ad6684e937a6694f05b5ebb2fab1a51f2401eb7af38c5253 |
---|---|
cites | cdi_FETCH-LOGICAL-c500t-94344566ee7d1f665ad6684e937a6694f05b5ebb2fab1a51f2401eb7af38c5253 |
container_end_page | 35553 |
container_issue | 49 |
container_start_page | 35546 |
container_title | The Journal of biological chemistry |
container_volume | 282 |
creator | Youard, Zeb A. Mislin, Gaëtan L.A. Majcherczyk, Paul A. Schalk, Isabelle J. Reimmann, Cornelia |
description | The siderophore pyochelin is made by a thiotemplate mechanism from salicylate and two molecules of cysteine. In Pseudomonas aeruginosa, the first cysteine residue is converted to its D-isoform during thiazoline ring formation whereas the second cysteine remains in its L-configuration, thus determining the stereochemistry of the two interconvertible pyochelin diastereoisomers as 4 ′R, 2 ″R, 4 ″R (pyochelin I) and 4 ′R, 2 ″S, 4 ″R (pyochelin II). Pseudomonas fluorescens CHA0 was found to make a different stereoisomeric mixture, which promoted growth under iron limitation in strain CHA0 and induced the expression of its biosynthetic genes, but was not recognized as a siderophore and signaling molecule by P. aeruginosa. Reciprocally, pyochelin promoted growth and induced pyochelin gene expression in P. aeruginosa, but was not functional in P. fluorescens. The structure of the CHA0 siderophore was determined by mass spectrometry, thin-layer chromatography, NMR, polarimetry, and chiral HPLC as enantio-pyochelin, the optical antipode of the P. aeruginosa siderophore pyochelin. Enantio-pyochelin was chemically synthesized and confirmed to be active in CHA0. Its potential biosynthetic pathway in CHA0 is discussed. |
doi_str_mv | 10.1074/jbc.M707039200 |
format | article |
fullrecord | <record><control><sourceid>proquest_hal_p</sourceid><recordid>TN_cdi_hal_primary_oai_HAL_hal_02987538v1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0021925820620907</els_id><sourcerecordid>69033836</sourcerecordid><originalsourceid>FETCH-LOGICAL-c500t-94344566ee7d1f665ad6684e937a6694f05b5ebb2fab1a51f2401eb7af38c5253</originalsourceid><addsrcrecordid>eNqFksGL1DAYxYso7rh69ag9iCDY8UvSpO1xGFZHGNmBdcFbSNOv0yxt003alT36n5va0fUi5hJIfnl5eS9R9JLAmkCWfrgp9fpLBhmwggI8ilYEcpYwTr49jlYAlCQF5flZ9Mz7GwgjLcjT6IxkBcuJyFbRj4PHqbKd7ZWP63ayDr3G3sfb3Qbig7PVpNHHF73qR2OT4d7qBlvTv4_HBuPLYTRatfEmbA62wtjWv9b_FlXopqPprVfxlanQ2aEJl8SH30rPoye1aj2-OM3n0fXHi6_bXbK__PR5u9knmgOMSZGyNOVCIGYVqYXgqhIiT7FgmRKiSGvgJceypLUqieKkpikQLDNVs1xzytl59G7RbVQrB2c65e6lVUbuNns5rwEt8oyz_I4E9u3CDs7eTuhH2ZkQS9uqHu3kpSiAsZyJ_4IUOCfBfwDXC6id9d5h_ccCATk3KUOT8qHJcODVSXkqO6we8FN1AXhzeo85Nt-NQ1maOdJO0pzKtJCM83R2-HrBamWlOjrj5fUVBcIgfBQm-BxMvhAY0r8z6KTXBnuNVRDVo6ys-ZfJn5qQwfQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>20551500</pqid></control><display><type>article</type><title>Pseudomonas fluorescens CHA0 Produces Enantio-pyochelin, the Optical Antipode of the Pseudomonas aeruginosa Siderophore Pyochelin</title><source>PubMed (Medline)</source><source>ScienceDirect (Online service)</source><creator>Youard, Zeb A. ; Mislin, Gaëtan L.A. ; Majcherczyk, Paul A. ; Schalk, Isabelle J. ; Reimmann, Cornelia</creator><creatorcontrib>Youard, Zeb A. ; Mislin, Gaëtan L.A. ; Majcherczyk, Paul A. ; Schalk, Isabelle J. ; Reimmann, Cornelia</creatorcontrib><description>The siderophore pyochelin is made by a thiotemplate mechanism from salicylate and two molecules of cysteine. In Pseudomonas aeruginosa, the first cysteine residue is converted to its D-isoform during thiazoline ring formation whereas the second cysteine remains in its L-configuration, thus determining the stereochemistry of the two interconvertible pyochelin diastereoisomers as 4 ′R, 2 ″R, 4 ″R (pyochelin I) and 4 ′R, 2 ″S, 4 ″R (pyochelin II). Pseudomonas fluorescens CHA0 was found to make a different stereoisomeric mixture, which promoted growth under iron limitation in strain CHA0 and induced the expression of its biosynthetic genes, but was not recognized as a siderophore and signaling molecule by P. aeruginosa. Reciprocally, pyochelin promoted growth and induced pyochelin gene expression in P. aeruginosa, but was not functional in P. fluorescens. The structure of the CHA0 siderophore was determined by mass spectrometry, thin-layer chromatography, NMR, polarimetry, and chiral HPLC as enantio-pyochelin, the optical antipode of the P. aeruginosa siderophore pyochelin. Enantio-pyochelin was chemically synthesized and confirmed to be active in CHA0. Its potential biosynthetic pathway in CHA0 is discussed.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1074/jbc.M707039200</identifier><identifier>PMID: 17938167</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Cysteine - metabolism ; Gene Expression Regulation, Bacterial - physiology ; Isomerism ; Life Sciences ; Microbiology and Parasitology ; Molecular Structure ; Phenols - chemical synthesis ; Phenols - chemistry ; Phenols - metabolism ; Pseudomonas aeruginosa ; Pseudomonas aeruginosa - metabolism ; Pseudomonas fluorescens ; Pseudomonas fluorescens - metabolism ; Salicylic Acid - metabolism ; Siderophores - biosynthesis ; Siderophores - chemical synthesis ; Siderophores - chemistry ; Thiazoles - chemical synthesis ; Thiazoles - chemistry ; Thiazoles - metabolism</subject><ispartof>The Journal of biological chemistry, 2007-12, Vol.282 (49), p.35546-35553</ispartof><rights>2007 © 2007 ASBMB. Currently published by Elsevier Inc; originally published by American Society for Biochemistry and Molecular Biology.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c500t-94344566ee7d1f665ad6684e937a6694f05b5ebb2fab1a51f2401eb7af38c5253</citedby><cites>FETCH-LOGICAL-c500t-94344566ee7d1f665ad6684e937a6694f05b5ebb2fab1a51f2401eb7af38c5253</cites><orcidid>0000-0002-8351-1679</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0021925820620907$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,3536,27901,27902,45756</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17938167$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-02987538$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Youard, Zeb A.</creatorcontrib><creatorcontrib>Mislin, Gaëtan L.A.</creatorcontrib><creatorcontrib>Majcherczyk, Paul A.</creatorcontrib><creatorcontrib>Schalk, Isabelle J.</creatorcontrib><creatorcontrib>Reimmann, Cornelia</creatorcontrib><title>Pseudomonas fluorescens CHA0 Produces Enantio-pyochelin, the Optical Antipode of the Pseudomonas aeruginosa Siderophore Pyochelin</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><description>The siderophore pyochelin is made by a thiotemplate mechanism from salicylate and two molecules of cysteine. In Pseudomonas aeruginosa, the first cysteine residue is converted to its D-isoform during thiazoline ring formation whereas the second cysteine remains in its L-configuration, thus determining the stereochemistry of the two interconvertible pyochelin diastereoisomers as 4 ′R, 2 ″R, 4 ″R (pyochelin I) and 4 ′R, 2 ″S, 4 ″R (pyochelin II). Pseudomonas fluorescens CHA0 was found to make a different stereoisomeric mixture, which promoted growth under iron limitation in strain CHA0 and induced the expression of its biosynthetic genes, but was not recognized as a siderophore and signaling molecule by P. aeruginosa. Reciprocally, pyochelin promoted growth and induced pyochelin gene expression in P. aeruginosa, but was not functional in P. fluorescens. The structure of the CHA0 siderophore was determined by mass spectrometry, thin-layer chromatography, NMR, polarimetry, and chiral HPLC as enantio-pyochelin, the optical antipode of the P. aeruginosa siderophore pyochelin. Enantio-pyochelin was chemically synthesized and confirmed to be active in CHA0. Its potential biosynthetic pathway in CHA0 is discussed.</description><subject>Cysteine - metabolism</subject><subject>Gene Expression Regulation, Bacterial - physiology</subject><subject>Isomerism</subject><subject>Life Sciences</subject><subject>Microbiology and Parasitology</subject><subject>Molecular Structure</subject><subject>Phenols - chemical synthesis</subject><subject>Phenols - chemistry</subject><subject>Phenols - metabolism</subject><subject>Pseudomonas aeruginosa</subject><subject>Pseudomonas aeruginosa - metabolism</subject><subject>Pseudomonas fluorescens</subject><subject>Pseudomonas fluorescens - metabolism</subject><subject>Salicylic Acid - metabolism</subject><subject>Siderophores - biosynthesis</subject><subject>Siderophores - chemical synthesis</subject><subject>Siderophores - chemistry</subject><subject>Thiazoles - chemical synthesis</subject><subject>Thiazoles - chemistry</subject><subject>Thiazoles - metabolism</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNqFksGL1DAYxYso7rh69ag9iCDY8UvSpO1xGFZHGNmBdcFbSNOv0yxt003alT36n5va0fUi5hJIfnl5eS9R9JLAmkCWfrgp9fpLBhmwggI8ilYEcpYwTr49jlYAlCQF5flZ9Mz7GwgjLcjT6IxkBcuJyFbRj4PHqbKd7ZWP63ayDr3G3sfb3Qbig7PVpNHHF73qR2OT4d7qBlvTv4_HBuPLYTRatfEmbA62wtjWv9b_FlXopqPprVfxlanQ2aEJl8SH30rPoye1aj2-OM3n0fXHi6_bXbK__PR5u9knmgOMSZGyNOVCIGYVqYXgqhIiT7FgmRKiSGvgJceypLUqieKkpikQLDNVs1xzytl59G7RbVQrB2c65e6lVUbuNns5rwEt8oyz_I4E9u3CDs7eTuhH2ZkQS9uqHu3kpSiAsZyJ_4IUOCfBfwDXC6id9d5h_ccCATk3KUOT8qHJcODVSXkqO6we8FN1AXhzeo85Nt-NQ1maOdJO0pzKtJCM83R2-HrBamWlOjrj5fUVBcIgfBQm-BxMvhAY0r8z6KTXBnuNVRDVo6ys-ZfJn5qQwfQ</recordid><startdate>20071207</startdate><enddate>20071207</enddate><creator>Youard, Zeb A.</creator><creator>Mislin, Gaëtan L.A.</creator><creator>Majcherczyk, Paul A.</creator><creator>Schalk, Isabelle J.</creator><creator>Reimmann, Cornelia</creator><general>Elsevier Inc</general><general>American Society for Biochemistry and Molecular Biology</general><scope>6I.</scope><scope>AAFTH</scope><scope>FBQ</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>7QL</scope><scope>C1K</scope><scope>7X8</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0002-8351-1679</orcidid></search><sort><creationdate>20071207</creationdate><title>Pseudomonas fluorescens CHA0 Produces Enantio-pyochelin, the Optical Antipode of the Pseudomonas aeruginosa Siderophore Pyochelin</title><author>Youard, Zeb A. ; Mislin, Gaëtan L.A. ; Majcherczyk, Paul A. ; Schalk, Isabelle J. ; Reimmann, Cornelia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c500t-94344566ee7d1f665ad6684e937a6694f05b5ebb2fab1a51f2401eb7af38c5253</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Cysteine - metabolism</topic><topic>Gene Expression Regulation, Bacterial - physiology</topic><topic>Isomerism</topic><topic>Life Sciences</topic><topic>Microbiology and Parasitology</topic><topic>Molecular Structure</topic><topic>Phenols - chemical synthesis</topic><topic>Phenols - chemistry</topic><topic>Phenols - metabolism</topic><topic>Pseudomonas aeruginosa</topic><topic>Pseudomonas aeruginosa - metabolism</topic><topic>Pseudomonas fluorescens</topic><topic>Pseudomonas fluorescens - metabolism</topic><topic>Salicylic Acid - metabolism</topic><topic>Siderophores - biosynthesis</topic><topic>Siderophores - chemical synthesis</topic><topic>Siderophores - chemistry</topic><topic>Thiazoles - chemical synthesis</topic><topic>Thiazoles - chemistry</topic><topic>Thiazoles - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Youard, Zeb A.</creatorcontrib><creatorcontrib>Mislin, Gaëtan L.A.</creatorcontrib><creatorcontrib>Majcherczyk, Paul A.</creatorcontrib><creatorcontrib>Schalk, Isabelle J.</creatorcontrib><creatorcontrib>Reimmann, Cornelia</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>AGRIS</collection><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><collection>Hyper Article en Ligne (HAL)</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Youard, Zeb A.</au><au>Mislin, Gaëtan L.A.</au><au>Majcherczyk, Paul A.</au><au>Schalk, Isabelle J.</au><au>Reimmann, Cornelia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pseudomonas fluorescens CHA0 Produces Enantio-pyochelin, the Optical Antipode of the Pseudomonas aeruginosa Siderophore Pyochelin</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>2007-12-07</date><risdate>2007</risdate><volume>282</volume><issue>49</issue><spage>35546</spage><epage>35553</epage><pages>35546-35553</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><abstract>The siderophore pyochelin is made by a thiotemplate mechanism from salicylate and two molecules of cysteine. In Pseudomonas aeruginosa, the first cysteine residue is converted to its D-isoform during thiazoline ring formation whereas the second cysteine remains in its L-configuration, thus determining the stereochemistry of the two interconvertible pyochelin diastereoisomers as 4 ′R, 2 ″R, 4 ″R (pyochelin I) and 4 ′R, 2 ″S, 4 ″R (pyochelin II). Pseudomonas fluorescens CHA0 was found to make a different stereoisomeric mixture, which promoted growth under iron limitation in strain CHA0 and induced the expression of its biosynthetic genes, but was not recognized as a siderophore and signaling molecule by P. aeruginosa. Reciprocally, pyochelin promoted growth and induced pyochelin gene expression in P. aeruginosa, but was not functional in P. fluorescens. The structure of the CHA0 siderophore was determined by mass spectrometry, thin-layer chromatography, NMR, polarimetry, and chiral HPLC as enantio-pyochelin, the optical antipode of the P. aeruginosa siderophore pyochelin. Enantio-pyochelin was chemically synthesized and confirmed to be active in CHA0. Its potential biosynthetic pathway in CHA0 is discussed.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>17938167</pmid><doi>10.1074/jbc.M707039200</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-8351-1679</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0021-9258 |
ispartof | The Journal of biological chemistry, 2007-12, Vol.282 (49), p.35546-35553 |
issn | 0021-9258 1083-351X |
language | eng |
recordid | cdi_hal_primary_oai_HAL_hal_02987538v1 |
source | PubMed (Medline); ScienceDirect (Online service) |
subjects | Cysteine - metabolism Gene Expression Regulation, Bacterial - physiology Isomerism Life Sciences Microbiology and Parasitology Molecular Structure Phenols - chemical synthesis Phenols - chemistry Phenols - metabolism Pseudomonas aeruginosa Pseudomonas aeruginosa - metabolism Pseudomonas fluorescens Pseudomonas fluorescens - metabolism Salicylic Acid - metabolism Siderophores - biosynthesis Siderophores - chemical synthesis Siderophores - chemistry Thiazoles - chemical synthesis Thiazoles - chemistry Thiazoles - metabolism |
title | Pseudomonas fluorescens CHA0 Produces Enantio-pyochelin, the Optical Antipode of the Pseudomonas aeruginosa Siderophore Pyochelin |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-07T16%3A11%3A17IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_hal_p&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Pseudomonas%20fluorescens%20CHA0%20Produces%20Enantio-pyochelin,%20the%20Optical%20Antipode%20of%20the%20Pseudomonas%20aeruginosa%20Siderophore%20Pyochelin&rft.jtitle=The%20Journal%20of%20biological%20chemistry&rft.au=Youard,%20Zeb%20A.&rft.date=2007-12-07&rft.volume=282&rft.issue=49&rft.spage=35546&rft.epage=35553&rft.pages=35546-35553&rft.issn=0021-9258&rft.eissn=1083-351X&rft_id=info:doi/10.1074/jbc.M707039200&rft_dat=%3Cproquest_hal_p%3E69033836%3C/proquest_hal_p%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c500t-94344566ee7d1f665ad6684e937a6694f05b5ebb2fab1a51f2401eb7af38c5253%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=20551500&rft_id=info:pmid/17938167&rfr_iscdi=true |