A soil-based microbial biofilm exposed to 2,4-D: bacterial community development and establishment of conjugative plasmid pJP4
A soil suspension was used as a source to initiate the development of microbial communities in flow cells irrigated with 2,4-dichlorophenoxyacetic acid (2,4-D) (25 μg ml −1). Culturable bacterial members of the community were identified by 16S rRNA gene sequencing and found to be members of the gene...
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container_title | FEMS microbiology ecology |
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creator | Aspray, Thomas J. Hansen, Susse K. Burns, Richard G. |
description | A soil suspension was used as a source to initiate the development of microbial communities in flow cells irrigated with 2,4-dichlorophenoxyacetic acid (2,4-D) (25
μg
ml
−1). Culturable bacterial members of the community were identified by 16S rRNA gene sequencing and found to be members of the genera
Pseudomonas,
Burkholderia,
Collimonas and
Rhodococcus. A 2,4-D degrading donor strain,
Pseudomonas putida SM1443 (pJP4::
gfp), was inoculated into flow cell chambers containing 2-day old biofilm communities. Transfer of pJP4::
gfp from the donor to the bacterial community was detectable as GFP fluorescing cells and images were captured using confocal scanning laser microscopy (GFP fluorescence was repressed in the donor due to the presence of a chromosomally located
lacI
q repressor gene). Approximately 5–10 transconjugant microcolonies, 20–40
μm in diameter, could be seen to develop in each chamber. A 2,4-D degrading transconjugant strain was isolated from the flow cell system belonging to the genus
Burkholderia. |
doi_str_mv | 10.1016/j.femsec.2005.04.007 |
format | Article |
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μg
ml
−1). Culturable bacterial members of the community were identified by 16S rRNA gene sequencing and found to be members of the genera
Pseudomonas,
Burkholderia,
Collimonas and
Rhodococcus. A 2,4-D degrading donor strain,
Pseudomonas putida SM1443 (pJP4::
gfp), was inoculated into flow cell chambers containing 2-day old biofilm communities. Transfer of pJP4::
gfp from the donor to the bacterial community was detectable as GFP fluorescing cells and images were captured using confocal scanning laser microscopy (GFP fluorescence was repressed in the donor due to the presence of a chromosomally located
lacI
q repressor gene). Approximately 5–10 transconjugant microcolonies, 20–40
μm in diameter, could be seen to develop in each chamber. A 2,4-D degrading transconjugant strain was isolated from the flow cell system belonging to the genus
Burkholderia.</description><identifier>ISSN: 0168-6496</identifier><identifier>EISSN: 1574-6941</identifier><identifier>DOI: 10.1016/j.femsec.2005.04.007</identifier><identifier>PMID: 16332330</identifier><language>eng</language><publisher>Oxford, UK: Elsevier B.V</publisher><subject>2,4-D ; 2,4-D, horizontal plasmid transfer ; 2,4-Dichlorophenoxyacetic Acid - metabolism ; Bacteria ; Bacteria - genetics ; Bacteriology ; Biofilms ; Biological and medical sciences ; Burkholderia ; Collimonas ; Community development ; Conjugation, Genetic ; Dichlorophenoxyacetic acid ; Ecology ; Fluorescence ; Fundamental and applied biological sciences. Psychology ; Gene sequencing ; Green fluorescent protein ; Laser microscopy ; Microbial activity ; Microbiology ; Microorganisms ; Miscellaneous ; pJP4 ; Plasmids ; Polymerase Chain Reaction ; Polymorphism, Single-Stranded Conformational ; Pseudomonas ; Pseudomonas putida ; Rhodococcus ; rRNA 16S ; Soil Microbiology ; Soils</subject><ispartof>FEMS microbiology ecology, 2005-10, Vol.54 (2), p.317-327</ispartof><rights>2005 Federation of European Microbiological Societies</rights><rights>2005 Federation of European Microbiological Societies. Published by Elsevier B.V. All rights reserved. 2005</rights><rights>2005 INIST-CNRS</rights><rights>2005 Federation of European Microbiological Societies. Published by Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c6507-cf8bd6b048ce7597bcf62009ff2f04d677833a8935b23a9fd83714838845d0fc3</citedby><cites>FETCH-LOGICAL-c6507-cf8bd6b048ce7597bcf62009ff2f04d677833a8935b23a9fd83714838845d0fc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1016%2Fj.femsec.2005.04.007$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1016%2Fj.femsec.2005.04.007$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17129276$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16332330$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Aspray, Thomas J.</creatorcontrib><creatorcontrib>Hansen, Susse K.</creatorcontrib><creatorcontrib>Burns, Richard G.</creatorcontrib><title>A soil-based microbial biofilm exposed to 2,4-D: bacterial community development and establishment of conjugative plasmid pJP4</title><title>FEMS microbiology ecology</title><addtitle>FEMS Microbiol Ecol</addtitle><description>A soil suspension was used as a source to initiate the development of microbial communities in flow cells irrigated with 2,4-dichlorophenoxyacetic acid (2,4-D) (25
μg
ml
−1). Culturable bacterial members of the community were identified by 16S rRNA gene sequencing and found to be members of the genera
Pseudomonas,
Burkholderia,
Collimonas and
Rhodococcus. A 2,4-D degrading donor strain,
Pseudomonas putida SM1443 (pJP4::
gfp), was inoculated into flow cell chambers containing 2-day old biofilm communities. Transfer of pJP4::
gfp from the donor to the bacterial community was detectable as GFP fluorescing cells and images were captured using confocal scanning laser microscopy (GFP fluorescence was repressed in the donor due to the presence of a chromosomally located
lacI
q repressor gene). Approximately 5–10 transconjugant microcolonies, 20–40
μm in diameter, could be seen to develop in each chamber. A 2,4-D degrading transconjugant strain was isolated from the flow cell system belonging to the genus
Burkholderia.</description><subject>2,4-D</subject><subject>2,4-D, horizontal plasmid transfer</subject><subject>2,4-Dichlorophenoxyacetic Acid - metabolism</subject><subject>Bacteria</subject><subject>Bacteria - genetics</subject><subject>Bacteriology</subject><subject>Biofilms</subject><subject>Biological and medical sciences</subject><subject>Burkholderia</subject><subject>Collimonas</subject><subject>Community development</subject><subject>Conjugation, Genetic</subject><subject>Dichlorophenoxyacetic acid</subject><subject>Ecology</subject><subject>Fluorescence</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene sequencing</subject><subject>Green fluorescent protein</subject><subject>Laser microscopy</subject><subject>Microbial activity</subject><subject>Microbiology</subject><subject>Microorganisms</subject><subject>Miscellaneous</subject><subject>pJP4</subject><subject>Plasmids</subject><subject>Polymerase Chain Reaction</subject><subject>Polymorphism, Single-Stranded Conformational</subject><subject>Pseudomonas</subject><subject>Pseudomonas putida</subject><subject>Rhodococcus</subject><subject>rRNA 16S</subject><subject>Soil Microbiology</subject><subject>Soils</subject><issn>0168-6496</issn><issn>1574-6941</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqNkU-P1SAUxRujcZ6j38AYEqMr-wYKBerCZDLO-CdjdKFrQuGivNBSS_v0bfzsUvuSSVzorEjgdw7n3lMUjwneEkz42W7roEtgthXG9RazLcbiTrEhtWAlbxi5W2wyJkvOGn5SPEhphzGpKcP3ixPCKa0oxZvi1zlK0Yey1Qks6rwZY-t1QK2PzocOwc8hLi9TRNULVr5-iVptJhgXxsSum3s_HZCFPYQ4dNBPSPcWQZp0G3z69ucmuoz2u_mrnvwe0BB06rxFw_tP7GFxz-mQ4NHxPC2-XF1-vnhbXn988-7i_Lo0vMaiNE62lreYSQOibkRrHM9jN85VDjPLhZCUatnQuq2obpyVVBAmqZSsttgZelo8X32HMX6fczzV-WQgBN1DnJPiUkq87OR_IGkajitZZ_DpX-AuzmOfh1AVxYJILoXIFFupvNeURnBqGH2nx4MiWC01qp1aa1RLjQozlWvMsidH87ntwN6Ijr1l4NkR0Mno4EbdG59uOEGqphI8c3LlfvgAh1t9rq4uP1CyZDhbpXEebpv61aqA3OTew6iS8dAbsH4EMykb_b8NfgPDdt0c</recordid><startdate>200510</startdate><enddate>200510</enddate><creator>Aspray, Thomas J.</creator><creator>Hansen, Susse K.</creator><creator>Burns, Richard G.</creator><general>Elsevier B.V</general><general>Blackwell Publishing Ltd</general><general>Blackwell</general><general>Oxford University Press</general><scope>IQODW</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>3V.</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7T7</scope><scope>7TK</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PATMY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>200510</creationdate><title>A soil-based microbial biofilm exposed to 2,4-D: bacterial community development and establishment of conjugative plasmid pJP4</title><author>Aspray, Thomas J. ; Hansen, Susse K. ; Burns, Richard G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c6507-cf8bd6b048ce7597bcf62009ff2f04d677833a8935b23a9fd83714838845d0fc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>2,4-D</topic><topic>2,4-D, horizontal plasmid transfer</topic><topic>2,4-Dichlorophenoxyacetic Acid - metabolism</topic><topic>Bacteria</topic><topic>Bacteria - genetics</topic><topic>Bacteriology</topic><topic>Biofilms</topic><topic>Biological and medical sciences</topic><topic>Burkholderia</topic><topic>Collimonas</topic><topic>Community development</topic><topic>Conjugation, Genetic</topic><topic>Dichlorophenoxyacetic acid</topic><topic>Ecology</topic><topic>Fluorescence</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene sequencing</topic><topic>Green fluorescent protein</topic><topic>Laser microscopy</topic><topic>Microbial activity</topic><topic>Microbiology</topic><topic>Microorganisms</topic><topic>Miscellaneous</topic><topic>pJP4</topic><topic>Plasmids</topic><topic>Polymerase Chain Reaction</topic><topic>Polymorphism, Single-Stranded Conformational</topic><topic>Pseudomonas</topic><topic>Pseudomonas putida</topic><topic>Rhodococcus</topic><topic>rRNA 16S</topic><topic>Soil Microbiology</topic><topic>Soils</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Aspray, Thomas J.</creatorcontrib><creatorcontrib>Hansen, Susse K.</creatorcontrib><creatorcontrib>Burns, Richard G.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Ecology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>FEMS microbiology ecology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Aspray, Thomas J.</au><au>Hansen, Susse K.</au><au>Burns, Richard G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A soil-based microbial biofilm exposed to 2,4-D: bacterial community development and establishment of conjugative plasmid pJP4</atitle><jtitle>FEMS microbiology ecology</jtitle><addtitle>FEMS Microbiol Ecol</addtitle><date>2005-10</date><risdate>2005</risdate><volume>54</volume><issue>2</issue><spage>317</spage><epage>327</epage><pages>317-327</pages><issn>0168-6496</issn><eissn>1574-6941</eissn><abstract>A soil suspension was used as a source to initiate the development of microbial communities in flow cells irrigated with 2,4-dichlorophenoxyacetic acid (2,4-D) (25
μg
ml
−1). Culturable bacterial members of the community were identified by 16S rRNA gene sequencing and found to be members of the genera
Pseudomonas,
Burkholderia,
Collimonas and
Rhodococcus. A 2,4-D degrading donor strain,
Pseudomonas putida SM1443 (pJP4::
gfp), was inoculated into flow cell chambers containing 2-day old biofilm communities. Transfer of pJP4::
gfp from the donor to the bacterial community was detectable as GFP fluorescing cells and images were captured using confocal scanning laser microscopy (GFP fluorescence was repressed in the donor due to the presence of a chromosomally located
lacI
q repressor gene). Approximately 5–10 transconjugant microcolonies, 20–40
μm in diameter, could be seen to develop in each chamber. A 2,4-D degrading transconjugant strain was isolated from the flow cell system belonging to the genus
Burkholderia.</abstract><cop>Oxford, UK</cop><pub>Elsevier B.V</pub><pmid>16332330</pmid><doi>10.1016/j.femsec.2005.04.007</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
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issn | 0168-6496 1574-6941 |
language | eng |
recordid | cdi_proquest_miscellaneous_68880332 |
source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Oxford Journals Open Access Collection; Wiley Online Library All Journals; Alma/SFX Local Collection |
subjects | 2,4-D 2,4-D, horizontal plasmid transfer 2,4-Dichlorophenoxyacetic Acid - metabolism Bacteria Bacteria - genetics Bacteriology Biofilms Biological and medical sciences Burkholderia Collimonas Community development Conjugation, Genetic Dichlorophenoxyacetic acid Ecology Fluorescence Fundamental and applied biological sciences. Psychology Gene sequencing Green fluorescent protein Laser microscopy Microbial activity Microbiology Microorganisms Miscellaneous pJP4 Plasmids Polymerase Chain Reaction Polymorphism, Single-Stranded Conformational Pseudomonas Pseudomonas putida Rhodococcus rRNA 16S Soil Microbiology Soils |
title | A soil-based microbial biofilm exposed to 2,4-D: bacterial community development and establishment of conjugative plasmid pJP4 |
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