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Purification of pyoverdines of pseudomonas fluorescens 2-79 by copper-chelate chromatography
Three pyoverdines, Pf-A, Pf-B, and Pf-C, were purified with copper-chelate Sepharose and Sephadex G-15 columns from Pseudomonas fluorescens 2-79, and the yields (per 100 ml of culture supernatant) were 2.8, 21.6, and 3.2 mg, respectively. The absorption and fluorescence spectra of these pyoverdines...
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Published in: | Applied and Environmental Microbiology 1995-11, Vol.61 (11), p.3769-3774 |
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description | Three pyoverdines, Pf-A, Pf-B, and Pf-C, were purified with copper-chelate Sepharose and Sephadex G-15 columns from Pseudomonas fluorescens 2-79, and the yields (per 100 ml of culture supernatant) were 2.8, 21.6, and 3.2 mg, respectively. The absorption and fluorescence spectra of these pyoverdines were strongly pH dependent. Characteristic changes in the maximal absorbance wavelengths were observed when Fe3+ or Cu2+ was added. The addition of Cu2+ shifted the pyoverdine Pf-B absorbance spectrum so that it exhibited a single peak at 410 nm but did not give rise to a new absorbance maximum at approximately 460 nm, which appeared when Fe3+ was added. Fluorescence quenching experiments revealed that the forward reaction rate constant with pyoverdines was much higher with Cu2+ (10(4) to 10(5) M-1 s-1) than with Fe3+ (10(2) M-1 s-1). However, Cu2+-pyoverdine complexes were completely dissociated by EDTA at a low concentration (0.1 mM), while the level of Fe3+-pyoverdine complex dissociation at the same EDTA concentration was relatively low. The dissociation of Fe3+-pyoverdine complexes was EDTA concentration dependent. Formation of free pyoverdine was observed when the three types of Fe3+-pyoverdine complexes were incubated separately with P.fluorescens 2-79 cells, thus demonstrating that pyoverdines Pf-A, Pf-B, and Pf-C mediate iron transport |
doi_str_mv | 10.1128/aem.61.11.3769-3774.1995 |
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(University of Georgia, Athens, GA.) ; Kisaalita, W.S</creator><creatorcontrib>Xiao, R. (University of Georgia, Athens, GA.) ; Kisaalita, W.S</creatorcontrib><description>Three pyoverdines, Pf-A, Pf-B, and Pf-C, were purified with copper-chelate Sepharose and Sephadex G-15 columns from Pseudomonas fluorescens 2-79, and the yields (per 100 ml of culture supernatant) were 2.8, 21.6, and 3.2 mg, respectively. The absorption and fluorescence spectra of these pyoverdines were strongly pH dependent. Characteristic changes in the maximal absorbance wavelengths were observed when Fe3+ or Cu2+ was added. The addition of Cu2+ shifted the pyoverdine Pf-B absorbance spectrum so that it exhibited a single peak at 410 nm but did not give rise to a new absorbance maximum at approximately 460 nm, which appeared when Fe3+ was added. Fluorescence quenching experiments revealed that the forward reaction rate constant with pyoverdines was much higher with Cu2+ (10(4) to 10(5) M-1 s-1) than with Fe3+ (10(2) M-1 s-1). However, Cu2+-pyoverdine complexes were completely dissociated by EDTA at a low concentration (0.1 mM), while the level of Fe3+-pyoverdine complex dissociation at the same EDTA concentration was relatively low. The dissociation of Fe3+-pyoverdine complexes was EDTA concentration dependent. Formation of free pyoverdine was observed when the three types of Fe3+-pyoverdine complexes were incubated separately with P.fluorescens 2-79 cells, thus demonstrating that pyoverdines Pf-A, Pf-B, and Pf-C mediate iron transport</description><identifier>ISSN: 0099-2240</identifier><identifier>EISSN: 1098-5336</identifier><identifier>DOI: 10.1128/aem.61.11.3769-3774.1995</identifier><identifier>PMID: 16535157</identifier><identifier>CODEN: AEMIDF</identifier><language>eng</language><publisher>Washington, DC: American Society for Microbiology</publisher><subject>Bacteria ; Biochemistry ; Biological and medical sciences ; Biology of microorganisms of confirmed or potential industrial interest ; Biotechnology ; CATION ; CATIONES ; CHELATEUR ; CHROMATOGRAPHIE ; COBRE ; CROMATOGRAFIA ; CUIVRE ; ESPECTROMETRIA ; FER ; Flowers & plants ; Fluorescence ; Fundamental and applied biological sciences. Psychology ; HIERRO ; Iron ; METAL ; METALES ; Miscellaneous ; Mission oriented research ; PSEUDOMONAS FLUORESCENS ; PURIFICACION ; PURIFICATION ; QUELATOS ; SIDEROFOROS ; SIDEROPHORE ; SPECTROMETRIE</subject><ispartof>Applied and Environmental Microbiology, 1995-11, Vol.61 (11), p.3769-3774</ispartof><rights>1996 INIST-CNRS</rights><rights>Copyright American Society for Microbiology Nov 1995</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c671t-65463fbd46c930c953b1852bcd035b51e94767ea9f16726d42e84ee85e1a27893</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1388593/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1388593/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,3175,3176,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2916104$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16535157$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Xiao, R. (University of Georgia, Athens, GA.)</creatorcontrib><creatorcontrib>Kisaalita, W.S</creatorcontrib><title>Purification of pyoverdines of pseudomonas fluorescens 2-79 by copper-chelate chromatography</title><title>Applied and Environmental Microbiology</title><addtitle>Appl Environ Microbiol</addtitle><description>Three pyoverdines, Pf-A, Pf-B, and Pf-C, were purified with copper-chelate Sepharose and Sephadex G-15 columns from Pseudomonas fluorescens 2-79, and the yields (per 100 ml of culture supernatant) were 2.8, 21.6, and 3.2 mg, respectively. The absorption and fluorescence spectra of these pyoverdines were strongly pH dependent. Characteristic changes in the maximal absorbance wavelengths were observed when Fe3+ or Cu2+ was added. The addition of Cu2+ shifted the pyoverdine Pf-B absorbance spectrum so that it exhibited a single peak at 410 nm but did not give rise to a new absorbance maximum at approximately 460 nm, which appeared when Fe3+ was added. Fluorescence quenching experiments revealed that the forward reaction rate constant with pyoverdines was much higher with Cu2+ (10(4) to 10(5) M-1 s-1) than with Fe3+ (10(2) M-1 s-1). However, Cu2+-pyoverdine complexes were completely dissociated by EDTA at a low concentration (0.1 mM), while the level of Fe3+-pyoverdine complex dissociation at the same EDTA concentration was relatively low. The dissociation of Fe3+-pyoverdine complexes was EDTA concentration dependent. Formation of free pyoverdine was observed when the three types of Fe3+-pyoverdine complexes were incubated separately with P.fluorescens 2-79 cells, thus demonstrating that pyoverdines Pf-A, Pf-B, and Pf-C mediate iron transport</description><subject>Bacteria</subject><subject>Biochemistry</subject><subject>Biological and medical sciences</subject><subject>Biology of microorganisms of confirmed or potential industrial interest</subject><subject>Biotechnology</subject><subject>CATION</subject><subject>CATIONES</subject><subject>CHELATEUR</subject><subject>CHROMATOGRAPHIE</subject><subject>COBRE</subject><subject>CROMATOGRAFIA</subject><subject>CUIVRE</subject><subject>ESPECTROMETRIA</subject><subject>FER</subject><subject>Flowers & plants</subject><subject>Fluorescence</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>HIERRO</subject><subject>Iron</subject><subject>METAL</subject><subject>METALES</subject><subject>Miscellaneous</subject><subject>Mission oriented research</subject><subject>PSEUDOMONAS FLUORESCENS</subject><subject>PURIFICACION</subject><subject>PURIFICATION</subject><subject>QUELATOS</subject><subject>SIDEROFOROS</subject><subject>SIDEROPHORE</subject><subject>SPECTROMETRIE</subject><issn>0099-2240</issn><issn>1098-5336</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><recordid>eNp9kUtv1DAUhSMEotPCH2CBIoTKKoPfj00lVPGSKoEE3SFZjnMzcZXEwU6K5t_jMKMWumDla_m7557rUxQlRluMiXprYdgKnOstlUJXVEq2xVrzR8UGI60qTql4XGwQ0roihKGT4jSlG4QQQ0I9LU6w4JRjLjfFj69L9K13dvZhLENbTvtwC7HxI6Q_1wRLE4Yw2lS2_RIiJAdjKkkldVnvSxemCWLlOujtDKXrYhjsHHbRTt3-WfGktX2C58fzrLj-8P775afq6svHz5fvrionJJ4rwZmgbd0w4TRFTnNaY8VJ7RpEec0xaCaFBKtbLCQRDSOgGIDigC2RStOz4uKgOy31AE02OEfbmyn6wca9Cdabf19G35lduDWYKsU1zQJvjgIx_FwgzWbwec--tyOEJRlJKWPZF87k-X9JLLRWgq6eXj0Ab8ISx_wNhiCuiZZMZUgdIBdDShHaO88YmTVpk5M2AufarEmbNWmzJp1bX_69833jMdoMvD4CNjnbt9GOzqc7jmgsMGL3Pju_6375CMam4cHYDL04QK0Nxu5i1rn-prmQinD6GwV4xnc</recordid><startdate>19951101</startdate><enddate>19951101</enddate><creator>Xiao, R. (University of Georgia, Athens, GA.)</creator><creator>Kisaalita, W.S</creator><general>American Society for Microbiology</general><scope>FBQ</scope><scope>IQODW</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QO</scope><scope>7SN</scope><scope>7SS</scope><scope>7ST</scope><scope>7T7</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>SOI</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19951101</creationdate><title>Purification of pyoverdines of pseudomonas fluorescens 2-79 by copper-chelate chromatography</title><author>Xiao, R. (University of Georgia, Athens, GA.) ; Kisaalita, W.S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c671t-65463fbd46c930c953b1852bcd035b51e94767ea9f16726d42e84ee85e1a27893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Bacteria</topic><topic>Biochemistry</topic><topic>Biological and medical sciences</topic><topic>Biology of microorganisms of confirmed or potential industrial interest</topic><topic>Biotechnology</topic><topic>CATION</topic><topic>CATIONES</topic><topic>CHELATEUR</topic><topic>CHROMATOGRAPHIE</topic><topic>COBRE</topic><topic>CROMATOGRAFIA</topic><topic>CUIVRE</topic><topic>ESPECTROMETRIA</topic><topic>FER</topic><topic>Flowers & plants</topic><topic>Fluorescence</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>HIERRO</topic><topic>Iron</topic><topic>METAL</topic><topic>METALES</topic><topic>Miscellaneous</topic><topic>Mission oriented research</topic><topic>PSEUDOMONAS FLUORESCENS</topic><topic>PURIFICACION</topic><topic>PURIFICATION</topic><topic>QUELATOS</topic><topic>SIDEROFOROS</topic><topic>SIDEROPHORE</topic><topic>SPECTROMETRIE</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xiao, R. (University of Georgia, Athens, GA.)</creatorcontrib><creatorcontrib>Kisaalita, W.S</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Applied and Environmental Microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xiao, R. (University of Georgia, Athens, GA.)</au><au>Kisaalita, W.S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Purification of pyoverdines of pseudomonas fluorescens 2-79 by copper-chelate chromatography</atitle><jtitle>Applied and Environmental Microbiology</jtitle><addtitle>Appl Environ Microbiol</addtitle><date>1995-11-01</date><risdate>1995</risdate><volume>61</volume><issue>11</issue><spage>3769</spage><epage>3774</epage><pages>3769-3774</pages><issn>0099-2240</issn><eissn>1098-5336</eissn><coden>AEMIDF</coden><abstract>Three pyoverdines, Pf-A, Pf-B, and Pf-C, were purified with copper-chelate Sepharose and Sephadex G-15 columns from Pseudomonas fluorescens 2-79, and the yields (per 100 ml of culture supernatant) were 2.8, 21.6, and 3.2 mg, respectively. The absorption and fluorescence spectra of these pyoverdines were strongly pH dependent. Characteristic changes in the maximal absorbance wavelengths were observed when Fe3+ or Cu2+ was added. The addition of Cu2+ shifted the pyoverdine Pf-B absorbance spectrum so that it exhibited a single peak at 410 nm but did not give rise to a new absorbance maximum at approximately 460 nm, which appeared when Fe3+ was added. Fluorescence quenching experiments revealed that the forward reaction rate constant with pyoverdines was much higher with Cu2+ (10(4) to 10(5) M-1 s-1) than with Fe3+ (10(2) M-1 s-1). However, Cu2+-pyoverdine complexes were completely dissociated by EDTA at a low concentration (0.1 mM), while the level of Fe3+-pyoverdine complex dissociation at the same EDTA concentration was relatively low. The dissociation of Fe3+-pyoverdine complexes was EDTA concentration dependent. Formation of free pyoverdine was observed when the three types of Fe3+-pyoverdine complexes were incubated separately with P.fluorescens 2-79 cells, thus demonstrating that pyoverdines Pf-A, Pf-B, and Pf-C mediate iron transport</abstract><cop>Washington, DC</cop><pub>American Society for Microbiology</pub><pmid>16535157</pmid><doi>10.1128/aem.61.11.3769-3774.1995</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Bacteria Biochemistry Biological and medical sciences Biology of microorganisms of confirmed or potential industrial interest Biotechnology CATION CATIONES CHELATEUR CHROMATOGRAPHIE COBRE CROMATOGRAFIA CUIVRE ESPECTROMETRIA FER Flowers & plants Fluorescence Fundamental and applied biological sciences. Psychology HIERRO Iron METAL METALES Miscellaneous Mission oriented research PSEUDOMONAS FLUORESCENS PURIFICACION PURIFICATION QUELATOS SIDEROFOROS SIDEROPHORE SPECTROMETRIE |
title | Purification of pyoverdines of pseudomonas fluorescens 2-79 by copper-chelate chromatography |
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