A cell array biosensor for environmental toxicity analysis
In this study, a cell-based array technology that uses recombinant bioluminescent bacteria to detect and classify environmental toxicity has been implemented to develop two biosensor arrays, i.e., a chip and a plate array. Twenty recombinant bioluminescent bacteria, having different promoters fused...
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Veröffentlicht in: | Biosensors & bioelectronics 2005-09, Vol.21 (3), p.500-507 |
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creator | Lee, Jin Hyung Mitchell, Robert J. Kim, Byoung Chan Cullen, David C. Gu, Man Bock |
description | In this study, a cell-based array technology that uses recombinant bioluminescent bacteria to detect and classify environmental toxicity has been implemented to develop two biosensor arrays, i.e., a chip and a plate array. Twenty recombinant bioluminescent bacteria, having different promoters fused with the bacterial
lux genes, were immobilized within LB-agar. About 2
μl of the cell-agar mixture was deposited into the wells of either a cell chip or a 384-well plate. The bioluminescence (BL) from the cell arrays was measured with the use of highly sensitive cooled CCD camera that measured the bioluminescent signal from the immobilized cells and then quantified the pixel density using image analysis software. The responses from the cell arrays were characterized using three chemicals that cause either superoxide damage (paraquat), DNA damage (mitomycin C) or protein/membrane damage (salicylic acid). The responses were found to be dependent upon the promoter fused upstream of the
lux operon within each strain. Therefore, a sample's toxicity can be analyzed and classified through the changes in the BL expression from each well. Moreover, a time of only 2
h was needed for analysis, making either of these arrays a fast, portable and economical high-throughput biosensor system for detecting environmental toxicities. |
doi_str_mv | 10.1016/j.bios.2004.12.015 |
format | Article |
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lux genes, were immobilized within LB-agar. About 2
μl of the cell-agar mixture was deposited into the wells of either a cell chip or a 384-well plate. The bioluminescence (BL) from the cell arrays was measured with the use of highly sensitive cooled CCD camera that measured the bioluminescent signal from the immobilized cells and then quantified the pixel density using image analysis software. The responses from the cell arrays were characterized using three chemicals that cause either superoxide damage (paraquat), DNA damage (mitomycin C) or protein/membrane damage (salicylic acid). The responses were found to be dependent upon the promoter fused upstream of the
lux operon within each strain. Therefore, a sample's toxicity can be analyzed and classified through the changes in the BL expression from each well. Moreover, a time of only 2
h was needed for analysis, making either of these arrays a fast, portable and economical high-throughput biosensor system for detecting environmental toxicities.</description><identifier>ISSN: 0956-5663</identifier><identifier>EISSN: 1873-4235</identifier><identifier>DOI: 10.1016/j.bios.2004.12.015</identifier><identifier>PMID: 16076440</identifier><language>eng</language><publisher>Lausanne: Elsevier B.V</publisher><subject>Arabidopsis Proteins - metabolism ; Biological and medical sciences ; Bioluminescent bacteria ; Biosensing Techniques - instrumentation ; Biosensing Techniques - methods ; Biosensors ; Biotechnology ; Cell array chip ; Cell Culture Techniques - instrumentation ; Cell Culture Techniques - methods ; Environmental biosensor ; Environmental Monitoring - instrumentation ; Environmental Monitoring - methods ; Environmental Pollutants - adverse effects ; Equipment Design ; Equipment Failure Analysis ; Escherichia coli - drug effects ; Escherichia coli - metabolism ; Fundamental and applied biological sciences. Psychology ; Luminescent Measurements - instrumentation ; Luminescent Measurements - methods ; Luminescent Proteins - genetics ; Luminescent Proteins - metabolism ; Methods. Procedures. Technologies ; Microarray Analysis - instrumentation ; Microarray Analysis - methods ; Toxicity analysis ; Toxicity Tests - instrumentation ; Toxicity Tests - methods ; Transcription Factors - metabolism ; Various methods and equipments</subject><ispartof>Biosensors & bioelectronics, 2005-09, Vol.21 (3), p.500-507</ispartof><rights>2004 Elsevier B.V.</rights><rights>2006 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c415t-db34ea82c811b445336c32ab2ad92aecf902a376fa64b15c3e39a94d491fb96e3</citedby><cites>FETCH-LOGICAL-c415t-db34ea82c811b445336c32ab2ad92aecf902a376fa64b15c3e39a94d491fb96e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0956566304005871$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17516821$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16076440$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lee, Jin Hyung</creatorcontrib><creatorcontrib>Mitchell, Robert J.</creatorcontrib><creatorcontrib>Kim, Byoung Chan</creatorcontrib><creatorcontrib>Cullen, David C.</creatorcontrib><creatorcontrib>Gu, Man Bock</creatorcontrib><title>A cell array biosensor for environmental toxicity analysis</title><title>Biosensors & bioelectronics</title><addtitle>Biosens Bioelectron</addtitle><description>In this study, a cell-based array technology that uses recombinant bioluminescent bacteria to detect and classify environmental toxicity has been implemented to develop two biosensor arrays, i.e., a chip and a plate array. Twenty recombinant bioluminescent bacteria, having different promoters fused with the bacterial
lux genes, were immobilized within LB-agar. About 2
μl of the cell-agar mixture was deposited into the wells of either a cell chip or a 384-well plate. The bioluminescence (BL) from the cell arrays was measured with the use of highly sensitive cooled CCD camera that measured the bioluminescent signal from the immobilized cells and then quantified the pixel density using image analysis software. The responses from the cell arrays were characterized using three chemicals that cause either superoxide damage (paraquat), DNA damage (mitomycin C) or protein/membrane damage (salicylic acid). The responses were found to be dependent upon the promoter fused upstream of the
lux operon within each strain. Therefore, a sample's toxicity can be analyzed and classified through the changes in the BL expression from each well. Moreover, a time of only 2
h was needed for analysis, making either of these arrays a fast, portable and economical high-throughput biosensor system for detecting environmental toxicities.</description><subject>Arabidopsis Proteins - metabolism</subject><subject>Biological and medical sciences</subject><subject>Bioluminescent bacteria</subject><subject>Biosensing Techniques - instrumentation</subject><subject>Biosensing Techniques - methods</subject><subject>Biosensors</subject><subject>Biotechnology</subject><subject>Cell array chip</subject><subject>Cell Culture Techniques - instrumentation</subject><subject>Cell Culture Techniques - methods</subject><subject>Environmental biosensor</subject><subject>Environmental Monitoring - instrumentation</subject><subject>Environmental Monitoring - methods</subject><subject>Environmental Pollutants - adverse effects</subject><subject>Equipment Design</subject><subject>Equipment Failure Analysis</subject><subject>Escherichia coli - drug effects</subject><subject>Escherichia coli - metabolism</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Luminescent Measurements - instrumentation</subject><subject>Luminescent Measurements - methods</subject><subject>Luminescent Proteins - genetics</subject><subject>Luminescent Proteins - metabolism</subject><subject>Methods. Procedures. Technologies</subject><subject>Microarray Analysis - instrumentation</subject><subject>Microarray Analysis - methods</subject><subject>Toxicity analysis</subject><subject>Toxicity Tests - instrumentation</subject><subject>Toxicity Tests - methods</subject><subject>Transcription Factors - metabolism</subject><subject>Various methods and equipments</subject><issn>0956-5663</issn><issn>1873-4235</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kD1rwzAQhkVpadKPP9CheGk3uzpJlqPSJZR-QaBLO4uzfAYFx04lJzT_vjYJZOtw3PK8L3cPYzfAM-CgH5ZZ6buYCc5VBiLjkJ-wKcwKmSoh81M25SbXaa61nLCLGJec8wIMP2cT0LzQSvEpe5wnjpomwRBwl4x91MYuJPUw1G596NoVtT02Sd_9euf7XYItNrvo4xU7q7GJdH3Yl-z79eXr-T1dfL59PM8XqVOQ92lVSkU4E24GUCqVS6mdFFgKrIxAcrXhAmWha9SqhNxJkgaNqpSBujSa5CW73_euQ_ezodjblY_j0dhSt4kWjBKqUHoAxR50oYsxUG3Xwa8w7CxwOxqzSzt-aEdjFoQdjA2h20P7plxRdYwcFA3A3QHA6LCpA7bOxyNX5KBnAgbuac_R4GLrKdjoPLWOKh_I9bbq_H93_AH-cYmT</recordid><startdate>20050915</startdate><enddate>20050915</enddate><creator>Lee, Jin Hyung</creator><creator>Mitchell, Robert J.</creator><creator>Kim, Byoung Chan</creator><creator>Cullen, David C.</creator><creator>Gu, Man Bock</creator><general>Elsevier B.V</general><general>Elsevier Science</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>7QO</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>20050915</creationdate><title>A cell array biosensor for environmental toxicity analysis</title><author>Lee, Jin Hyung ; Mitchell, Robert J. ; Kim, Byoung Chan ; Cullen, David C. ; Gu, Man Bock</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c415t-db34ea82c811b445336c32ab2ad92aecf902a376fa64b15c3e39a94d491fb96e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Arabidopsis Proteins - metabolism</topic><topic>Biological and medical sciences</topic><topic>Bioluminescent bacteria</topic><topic>Biosensing Techniques - instrumentation</topic><topic>Biosensing Techniques - methods</topic><topic>Biosensors</topic><topic>Biotechnology</topic><topic>Cell array chip</topic><topic>Cell Culture Techniques - instrumentation</topic><topic>Cell Culture Techniques - methods</topic><topic>Environmental biosensor</topic><topic>Environmental Monitoring - instrumentation</topic><topic>Environmental Monitoring - methods</topic><topic>Environmental Pollutants - adverse effects</topic><topic>Equipment Design</topic><topic>Equipment Failure Analysis</topic><topic>Escherichia coli - drug effects</topic><topic>Escherichia coli - metabolism</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Luminescent Measurements - instrumentation</topic><topic>Luminescent Measurements - methods</topic><topic>Luminescent Proteins - genetics</topic><topic>Luminescent Proteins - metabolism</topic><topic>Methods. Procedures. Technologies</topic><topic>Microarray Analysis - instrumentation</topic><topic>Microarray Analysis - methods</topic><topic>Toxicity analysis</topic><topic>Toxicity Tests - instrumentation</topic><topic>Toxicity Tests - methods</topic><topic>Transcription Factors - metabolism</topic><topic>Various methods and equipments</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, Jin Hyung</creatorcontrib><creatorcontrib>Mitchell, Robert J.</creatorcontrib><creatorcontrib>Kim, Byoung Chan</creatorcontrib><creatorcontrib>Cullen, David C.</creatorcontrib><creatorcontrib>Gu, Man Bock</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>Biotechnology Research Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Biosensors & bioelectronics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, Jin Hyung</au><au>Mitchell, Robert J.</au><au>Kim, Byoung Chan</au><au>Cullen, David C.</au><au>Gu, Man Bock</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A cell array biosensor for environmental toxicity analysis</atitle><jtitle>Biosensors & bioelectronics</jtitle><addtitle>Biosens Bioelectron</addtitle><date>2005-09-15</date><risdate>2005</risdate><volume>21</volume><issue>3</issue><spage>500</spage><epage>507</epage><pages>500-507</pages><issn>0956-5663</issn><eissn>1873-4235</eissn><abstract>In this study, a cell-based array technology that uses recombinant bioluminescent bacteria to detect and classify environmental toxicity has been implemented to develop two biosensor arrays, i.e., a chip and a plate array. Twenty recombinant bioluminescent bacteria, having different promoters fused with the bacterial
lux genes, were immobilized within LB-agar. About 2
μl of the cell-agar mixture was deposited into the wells of either a cell chip or a 384-well plate. The bioluminescence (BL) from the cell arrays was measured with the use of highly sensitive cooled CCD camera that measured the bioluminescent signal from the immobilized cells and then quantified the pixel density using image analysis software. The responses from the cell arrays were characterized using three chemicals that cause either superoxide damage (paraquat), DNA damage (mitomycin C) or protein/membrane damage (salicylic acid). The responses were found to be dependent upon the promoter fused upstream of the
lux operon within each strain. Therefore, a sample's toxicity can be analyzed and classified through the changes in the BL expression from each well. Moreover, a time of only 2
h was needed for analysis, making either of these arrays a fast, portable and economical high-throughput biosensor system for detecting environmental toxicities.</abstract><cop>Lausanne</cop><pub>Elsevier B.V</pub><pmid>16076440</pmid><doi>10.1016/j.bios.2004.12.015</doi><tpages>8</tpages></addata></record> |
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subjects | Arabidopsis Proteins - metabolism Biological and medical sciences Bioluminescent bacteria Biosensing Techniques - instrumentation Biosensing Techniques - methods Biosensors Biotechnology Cell array chip Cell Culture Techniques - instrumentation Cell Culture Techniques - methods Environmental biosensor Environmental Monitoring - instrumentation Environmental Monitoring - methods Environmental Pollutants - adverse effects Equipment Design Equipment Failure Analysis Escherichia coli - drug effects Escherichia coli - metabolism Fundamental and applied biological sciences. Psychology Luminescent Measurements - instrumentation Luminescent Measurements - methods Luminescent Proteins - genetics Luminescent Proteins - metabolism Methods. Procedures. Technologies Microarray Analysis - instrumentation Microarray Analysis - methods Toxicity analysis Toxicity Tests - instrumentation Toxicity Tests - methods Transcription Factors - metabolism Various methods and equipments |
title | A cell array biosensor for environmental toxicity analysis |
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