Bacteriophage-based biosorbents coupled with bioluminescent ATP assay for rapid concentration and detection of Escherichia coli
Wild type T4 bacteriophage and recombinant T4 bacteriophages displaying biotin binding peptide (BCCP) and cellulose binding module (CBM) on their heads were immobilized on nano-aluminum fiber-based filter (Disruptor™), streptavidin magnetic beads and microcrystalline cellulose, respectively. Infecti...
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Veröffentlicht in: | Journal of microbiological methods 2010-08, Vol.82 (2), p.177-183 |
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creator | Minikh, O. Tolba, M. Brovko, L.Y. Griffiths, M.W. |
description | Wild type T4 bacteriophage and recombinant T4 bacteriophages displaying biotin binding peptide (BCCP) and cellulose binding module (CBM) on their heads were immobilized on nano-aluminum fiber-based filter (Disruptor™), streptavidin magnetic beads and microcrystalline cellulose, respectively. Infectivity of the immobilized phages was investigated by monitoring the phage-mediated growth inhibition of bioluminescent
E. coli B and cell lysis using bioluminescent ATP assay. The results showed that phage immobilization resulted in a partial loss of infectivity as compared with the free phage. Nevertheless, the use of a biosorbent based on T4 bacteriophage immobilized on Disruptor™ filter coupled with a bioluminescent ATP assay allowed simultaneous concentration and detection of as low as 6
×
10
3
cfu/mL of
E. coli in the sample within 2
h with high accuracy (CV
=
1–5% in log scale). Excess of interfering microflora at levels 60-fold greater than the target organism did not affect the results when bacteriophage was immobilized on the filter prior to concentration of bacterial cells. |
doi_str_mv | 10.1016/j.mimet.2010.05.013 |
format | Article |
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E. coli B and cell lysis using bioluminescent ATP assay. The results showed that phage immobilization resulted in a partial loss of infectivity as compared with the free phage. Nevertheless, the use of a biosorbent based on T4 bacteriophage immobilized on Disruptor™ filter coupled with a bioluminescent ATP assay allowed simultaneous concentration and detection of as low as 6
×
10
3
cfu/mL of
E. coli in the sample within 2
h with high accuracy (CV
=
1–5% in log scale). Excess of interfering microflora at levels 60-fold greater than the target organism did not affect the results when bacteriophage was immobilized on the filter prior to concentration of bacterial cells.</description><identifier>ISSN: 0167-7012</identifier><identifier>EISSN: 1872-8359</identifier><identifier>DOI: 10.1016/j.mimet.2010.05.013</identifier><identifier>PMID: 20561957</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Adenosine Triphosphate - analysis ; ATP ; ATP bioluminescence assay ; Bacteriological Techniques ; Bacteriolysis ; Bacteriophage T4 - genetics ; Bacteriophage T4 - physiology ; Biotin - metabolism ; Cellulose - metabolism ; Escherichia coli ; Escherichia coli - chemistry ; Escherichia coli - isolation & purification ; Escherichia coli - virology ; Filtration - methods ; Immobilized T4 bacteriophage ; Luminescence ; Protein Binding ; Recombinant Proteins - metabolism ; Viral Proteins - metabolism ; Virus Attachment ; Water Microbiology</subject><ispartof>Journal of microbiological methods, 2010-08, Vol.82 (2), p.177-183</ispartof><rights>2010 Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c390t-f4f5df08bccd66352b695ecd9dd773211a49593cd00e336b46067d54f8534c0a3</citedby><cites>FETCH-LOGICAL-c390t-f4f5df08bccd66352b695ecd9dd773211a49593cd00e336b46067d54f8534c0a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.mimet.2010.05.013$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27929,27930,46000</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20561957$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Minikh, O.</creatorcontrib><creatorcontrib>Tolba, M.</creatorcontrib><creatorcontrib>Brovko, L.Y.</creatorcontrib><creatorcontrib>Griffiths, M.W.</creatorcontrib><title>Bacteriophage-based biosorbents coupled with bioluminescent ATP assay for rapid concentration and detection of Escherichia coli</title><title>Journal of microbiological methods</title><addtitle>J Microbiol Methods</addtitle><description>Wild type T4 bacteriophage and recombinant T4 bacteriophages displaying biotin binding peptide (BCCP) and cellulose binding module (CBM) on their heads were immobilized on nano-aluminum fiber-based filter (Disruptor™), streptavidin magnetic beads and microcrystalline cellulose, respectively. Infectivity of the immobilized phages was investigated by monitoring the phage-mediated growth inhibition of bioluminescent
E. coli B and cell lysis using bioluminescent ATP assay. The results showed that phage immobilization resulted in a partial loss of infectivity as compared with the free phage. Nevertheless, the use of a biosorbent based on T4 bacteriophage immobilized on Disruptor™ filter coupled with a bioluminescent ATP assay allowed simultaneous concentration and detection of as low as 6
×
10
3
cfu/mL of
E. coli in the sample within 2
h with high accuracy (CV
=
1–5% in log scale). Excess of interfering microflora at levels 60-fold greater than the target organism did not affect the results when bacteriophage was immobilized on the filter prior to concentration of bacterial cells.</description><subject>Adenosine Triphosphate - analysis</subject><subject>ATP</subject><subject>ATP bioluminescence assay</subject><subject>Bacteriological Techniques</subject><subject>Bacteriolysis</subject><subject>Bacteriophage T4 - genetics</subject><subject>Bacteriophage T4 - physiology</subject><subject>Biotin - metabolism</subject><subject>Cellulose - metabolism</subject><subject>Escherichia coli</subject><subject>Escherichia coli - chemistry</subject><subject>Escherichia coli - isolation & purification</subject><subject>Escherichia coli - virology</subject><subject>Filtration - methods</subject><subject>Immobilized T4 bacteriophage</subject><subject>Luminescence</subject><subject>Protein Binding</subject><subject>Recombinant Proteins - metabolism</subject><subject>Viral Proteins - metabolism</subject><subject>Virus Attachment</subject><subject>Water Microbiology</subject><issn>0167-7012</issn><issn>1872-8359</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUFv1DAQhS1ERbeFX4CEfOOUZRzHSXzgUKq2IFUqh3K2HHvCepXEwU5APfWvM9stHOFked43M5r3GHsrYCtA1B_22zGMuGxLoAqoLQj5gm1E25RFK5V-yTZENUUDojxlZznvAYSSVfuKnZagaqFVs2GPn6xbMIU47-x3LDqb0fMuxBxTh9OSuYvrPFDtV1h2B2FYxzBhdiTyi_uv3OZsH3gfE092Dp746aAlu4Q4cTt57nFB9_SLPb_Kbkfr3C5YQofwmp30dsj45vk9Z9-ur-4vPxe3dzdfLi9uCyc1LEVf9cr30HbO-bqWquxqrdB57X3TyFIIW2mlpfMAKGXdVTXUjVdV39LFDqw8Z--Pc-cUf6yYFzMGOmIY7IRxzaahbtBVVf6flFK3SglBpDySLsWcE_ZmTmG06cEIMIeIzN48RWQOERlQhiKirnfP89duRP-3508mBHw8Akh-_AyYTHYByVUfEhlpfAz_XPAbXzalRg</recordid><startdate>20100801</startdate><enddate>20100801</enddate><creator>Minikh, O.</creator><creator>Tolba, M.</creator><creator>Brovko, L.Y.</creator><creator>Griffiths, M.W.</creator><general>Elsevier B.V</general><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>7X8</scope><scope>7QL</scope><scope>7T7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope></search><sort><creationdate>20100801</creationdate><title>Bacteriophage-based biosorbents coupled with bioluminescent ATP assay for rapid concentration and detection of Escherichia coli</title><author>Minikh, O. ; Tolba, M. ; Brovko, L.Y. ; Griffiths, M.W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c390t-f4f5df08bccd66352b695ecd9dd773211a49593cd00e336b46067d54f8534c0a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Adenosine Triphosphate - analysis</topic><topic>ATP</topic><topic>ATP bioluminescence assay</topic><topic>Bacteriological Techniques</topic><topic>Bacteriolysis</topic><topic>Bacteriophage T4 - genetics</topic><topic>Bacteriophage T4 - physiology</topic><topic>Biotin - metabolism</topic><topic>Cellulose - metabolism</topic><topic>Escherichia coli</topic><topic>Escherichia coli - chemistry</topic><topic>Escherichia coli - isolation & purification</topic><topic>Escherichia coli - virology</topic><topic>Filtration - methods</topic><topic>Immobilized T4 bacteriophage</topic><topic>Luminescence</topic><topic>Protein Binding</topic><topic>Recombinant Proteins - metabolism</topic><topic>Viral Proteins - metabolism</topic><topic>Virus Attachment</topic><topic>Water Microbiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Minikh, O.</creatorcontrib><creatorcontrib>Tolba, M.</creatorcontrib><creatorcontrib>Brovko, L.Y.</creatorcontrib><creatorcontrib>Griffiths, M.W.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</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>Biotechnology and BioEngineering Abstracts</collection><jtitle>Journal of microbiological methods</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Minikh, O.</au><au>Tolba, M.</au><au>Brovko, L.Y.</au><au>Griffiths, M.W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bacteriophage-based biosorbents coupled with bioluminescent ATP assay for rapid concentration and detection of Escherichia coli</atitle><jtitle>Journal of microbiological methods</jtitle><addtitle>J Microbiol Methods</addtitle><date>2010-08-01</date><risdate>2010</risdate><volume>82</volume><issue>2</issue><spage>177</spage><epage>183</epage><pages>177-183</pages><issn>0167-7012</issn><eissn>1872-8359</eissn><abstract>Wild type T4 bacteriophage and recombinant T4 bacteriophages displaying biotin binding peptide (BCCP) and cellulose binding module (CBM) on their heads were immobilized on nano-aluminum fiber-based filter (Disruptor™), streptavidin magnetic beads and microcrystalline cellulose, respectively. Infectivity of the immobilized phages was investigated by monitoring the phage-mediated growth inhibition of bioluminescent
E. coli B and cell lysis using bioluminescent ATP assay. The results showed that phage immobilization resulted in a partial loss of infectivity as compared with the free phage. Nevertheless, the use of a biosorbent based on T4 bacteriophage immobilized on Disruptor™ filter coupled with a bioluminescent ATP assay allowed simultaneous concentration and detection of as low as 6
×
10
3
cfu/mL of
E. coli in the sample within 2
h with high accuracy (CV
=
1–5% in log scale). Excess of interfering microflora at levels 60-fold greater than the target organism did not affect the results when bacteriophage was immobilized on the filter prior to concentration of bacterial cells.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>20561957</pmid><doi>10.1016/j.mimet.2010.05.013</doi><tpages>7</tpages></addata></record> |
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subjects | Adenosine Triphosphate - analysis ATP ATP bioluminescence assay Bacteriological Techniques Bacteriolysis Bacteriophage T4 - genetics Bacteriophage T4 - physiology Biotin - metabolism Cellulose - metabolism Escherichia coli Escherichia coli - chemistry Escherichia coli - isolation & purification Escherichia coli - virology Filtration - methods Immobilized T4 bacteriophage Luminescence Protein Binding Recombinant Proteins - metabolism Viral Proteins - metabolism Virus Attachment Water Microbiology |
title | Bacteriophage-based biosorbents coupled with bioluminescent ATP assay for rapid concentration and detection of Escherichia coli |
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