Estimation of the bacteriocin ColE7 conjugation‐based “kill” – “anti‐kill” antimicrobial system by real‐time PCR, fluorescence staining and bioluminescence assays
The efficiency of the bacteriocin, colicin ColE7, bacterial conjugation‐based “kill” – “anti‐kill” antimicrobial system, was assessed using real‐time PCR, flow cytometry and bioluminescence. The ColE7 antimicrobial system consists of the genetically modified Escherichia coli strain Nissle 1917 harbo...
Gespeichert in:
Veröffentlicht in: | Letters in applied microbiology 2018-07, Vol.67 (1), p.47-53 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 53 |
---|---|
container_issue | 1 |
container_start_page | 47 |
container_title | Letters in applied microbiology |
container_volume | 67 |
creator | Maslennikova, I.L. Kuznetsova, M.V. Toplak, N. Nekrasova, I.V. Žgur Bertok, D. Starčič Erjavec, M. |
description | The efficiency of the bacteriocin, colicin ColE7, bacterial conjugation‐based “kill” – “anti‐kill” antimicrobial system, was assessed using real‐time PCR, flow cytometry and bioluminescence. The ColE7 antimicrobial system consists of the genetically modified Escherichia coli strain Nissle 1917 harbouring a conjugative plasmid (derivative of the F‐plasmid) encoding the “kill” gene (ColE7 activity gene) and a chromosomally encoded “anti‐kill” gene (ColE7 immunity gene). On the basis of traJ gene expression in the killer donor cells, our results showed that the efficiency of the here studied antimicrobial system against target E. coli was higher at 4 than at 24 h. Flow cytometry was used to indirectly estimate DNase activity of the antimicrobial system, as lysis of target E. coli cells in the conjugative mixture with the killer donor strain led to reduction in cell cytosol fluorescence. According to a lux assay, E. coli TG1 (pXen lux+ Apr) with constitutive luminescence were killed already after 2 h of treatment. Target sensor E. coli C600 with DNA damage SOS‐inducible luminescence showed significantly lower SOS induction 6 and 24 h following treatment with the killer donor strain. Our results thus showed that bioluminescent techniques are quick and suitable for estimation of the ColE7 bacterial conjugation‐based antimicrobial system antibacterial activity.
Significance and Impact of the Study
Bacterial antimicrobial resistance is worldwide rising and causing deaths of thousands of patients infected with multi‐drug resistant bacterial strains. In addition, there is a lack of efficient alternative antimicrobial agents. The significance of our research is the use of a number of methods (real‐time PCR, flow cytometry and bioluminescence‐based technique) to assess the antibacterial activity of the bacteriocin, colicin ColE7, bacterial conjugation‐based “kill” – “anti‐kill” antimicrobial system. Bioluminescent techniques proved to be rapid and suitable for estimation of antibacterial activity of ColE7 bacterial conjugation‐based antimicrobial system and possibly other related systems.
Significance and Impact of the Study: Bacterial antimicrobial resistance is worldwide rising and causing deaths of thousands of patients infected with multi‐drug resistant bacterial strains. In addition, there is a lack of efficient alternative antimicrobial agents. The significance of our research is the use of a number of methods (real‐time PCR, flow cytometry and bioluminescence‐b |
doi_str_mv | 10.1111/lam.12884 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2036205598</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2036205598</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3534-da86b41ad2826d84189f7e42e0a2de08cbdecdd1c3786722edfc6fcb7b62a6013</originalsourceid><addsrcrecordid>eNp1kc2KFDEUhYMoTju68AUk4EbBmklSVanUcmjaH2hRRMFdkZ9bY9pUMiZVSO36EQbc6kv4SP0kpqenXQhmk9yc7x4u9yD0mJIzms-5k8MZZUJUd9CCVg0rGl5_vosWhHFeCFZXJ-hBShtCiKCsvY9OWNuUvBXVAv1epdEOcrTB49Dj8QtgJfUI0QZtPV4Gt2qwDn4zXd5Au-21kgkM3m1_frXO7ba_8vPHvpR-tFk-_u7LweoYlJUOpzmNMGA14wgy69dZBPx--eEF7t0UIiQNXgNOo7Te-svcbrCywU2D9UdRpiTn9BDd66VL8Oj2PkWfXq4-Ll8X63ev3iwv1oUu67IqjBRcVVQaJhg3oqKi7RuoGBDJDBChlQFtDNVlI3jDGJhe816rRnEmOaHlKXp28L2K4dsEaewGmwdxTnoIU-oYKTkjdd2KjD79B92EKfo8XabqsiRUlDxTzw9UXkpKEfruKubdx7mjpNsH2eUgu5sgM_vk1nFSA5i_5DG5DJwfgO_Wwfx_p2598fZg-QeqR7Kp</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2053301836</pqid></control><display><type>article</type><title>Estimation of the bacteriocin ColE7 conjugation‐based “kill” – “anti‐kill” antimicrobial system by real‐time PCR, fluorescence staining and bioluminescence assays</title><source>Wiley Journals</source><source>Oxford University Press Journals All Titles (1996-Current)</source><source>EZB-FREE-00999 freely available EZB journals</source><source>Alma/SFX Local Collection</source><creator>Maslennikova, I.L. ; Kuznetsova, M.V. ; Toplak, N. ; Nekrasova, I.V. ; Žgur Bertok, D. ; Starčič Erjavec, M.</creator><creatorcontrib>Maslennikova, I.L. ; Kuznetsova, M.V. ; Toplak, N. ; Nekrasova, I.V. ; Žgur Bertok, D. ; Starčič Erjavec, M.</creatorcontrib><description>The efficiency of the bacteriocin, colicin ColE7, bacterial conjugation‐based “kill” – “anti‐kill” antimicrobial system, was assessed using real‐time PCR, flow cytometry and bioluminescence. The ColE7 antimicrobial system consists of the genetically modified Escherichia coli strain Nissle 1917 harbouring a conjugative plasmid (derivative of the F‐plasmid) encoding the “kill” gene (ColE7 activity gene) and a chromosomally encoded “anti‐kill” gene (ColE7 immunity gene). On the basis of traJ gene expression in the killer donor cells, our results showed that the efficiency of the here studied antimicrobial system against target E. coli was higher at 4 than at 24 h. Flow cytometry was used to indirectly estimate DNase activity of the antimicrobial system, as lysis of target E. coli cells in the conjugative mixture with the killer donor strain led to reduction in cell cytosol fluorescence. According to a lux assay, E. coli TG1 (pXen lux+ Apr) with constitutive luminescence were killed already after 2 h of treatment. Target sensor E. coli C600 with DNA damage SOS‐inducible luminescence showed significantly lower SOS induction 6 and 24 h following treatment with the killer donor strain. Our results thus showed that bioluminescent techniques are quick and suitable for estimation of the ColE7 bacterial conjugation‐based antimicrobial system antibacterial activity.
Significance and Impact of the Study
Bacterial antimicrobial resistance is worldwide rising and causing deaths of thousands of patients infected with multi‐drug resistant bacterial strains. In addition, there is a lack of efficient alternative antimicrobial agents. The significance of our research is the use of a number of methods (real‐time PCR, flow cytometry and bioluminescence‐based technique) to assess the antibacterial activity of the bacteriocin, colicin ColE7, bacterial conjugation‐based “kill” – “anti‐kill” antimicrobial system. Bioluminescent techniques proved to be rapid and suitable for estimation of antibacterial activity of ColE7 bacterial conjugation‐based antimicrobial system and possibly other related systems.
Significance and Impact of the Study: Bacterial antimicrobial resistance is worldwide rising and causing deaths of thousands of patients infected with multi‐drug resistant bacterial strains. In addition, there is a lack of efficient alternative antimicrobial agents. The significance of our research is the use of a number of methods (real‐time PCR, flow cytometry and bioluminescence‐based technique) to assess the antibacterial activity of the bacteriocin, colicin ColE7, bacterial conjugation‐based “kill” – “anti‐kill” antimicrobial system. Bioluminescent techniques proved to be rapid and suitable for estimation of antibacterial activity of ColE7 bacterial conjugation‐based antimicrobial system and possibly other related systems.</description><identifier>ISSN: 0266-8254</identifier><identifier>EISSN: 1472-765X</identifier><identifier>DOI: 10.1111/lam.12884</identifier><identifier>PMID: 29736984</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Antibacterial activity ; Antimicrobial agents ; Antimicrobial resistance ; Bacteria ; bacteriocin ; Bioluminescence ; colicin ; Conjugation ; conjugation‐based antimicrobial system ; Cytosol ; Deoxyribonuclease ; Deoxyribonucleic acid ; DNA ; DNA damage ; Drug resistance ; E coli ; E. coli ; Flow cytometry ; Fluorescence ; Gene expression ; Genetic modification ; Immunity ; Luminescence ; Lysis ; plasmid ; Polymerase chain reaction ; Reagents ; TraJ gene</subject><ispartof>Letters in applied microbiology, 2018-07, Vol.67 (1), p.47-53</ispartof><rights>2018 The Society for Applied Microbiology</rights><rights>2018 The Society for Applied Microbiology.</rights><rights>Copyright © 2018 The Society for Applied Microbiology</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3534-da86b41ad2826d84189f7e42e0a2de08cbdecdd1c3786722edfc6fcb7b62a6013</citedby><cites>FETCH-LOGICAL-c3534-da86b41ad2826d84189f7e42e0a2de08cbdecdd1c3786722edfc6fcb7b62a6013</cites><orcidid>0000-0003-0200-573X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Flam.12884$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Flam.12884$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29736984$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Maslennikova, I.L.</creatorcontrib><creatorcontrib>Kuznetsova, M.V.</creatorcontrib><creatorcontrib>Toplak, N.</creatorcontrib><creatorcontrib>Nekrasova, I.V.</creatorcontrib><creatorcontrib>Žgur Bertok, D.</creatorcontrib><creatorcontrib>Starčič Erjavec, M.</creatorcontrib><title>Estimation of the bacteriocin ColE7 conjugation‐based “kill” – “anti‐kill” antimicrobial system by real‐time PCR, fluorescence staining and bioluminescence assays</title><title>Letters in applied microbiology</title><addtitle>Lett Appl Microbiol</addtitle><description>The efficiency of the bacteriocin, colicin ColE7, bacterial conjugation‐based “kill” – “anti‐kill” antimicrobial system, was assessed using real‐time PCR, flow cytometry and bioluminescence. The ColE7 antimicrobial system consists of the genetically modified Escherichia coli strain Nissle 1917 harbouring a conjugative plasmid (derivative of the F‐plasmid) encoding the “kill” gene (ColE7 activity gene) and a chromosomally encoded “anti‐kill” gene (ColE7 immunity gene). On the basis of traJ gene expression in the killer donor cells, our results showed that the efficiency of the here studied antimicrobial system against target E. coli was higher at 4 than at 24 h. Flow cytometry was used to indirectly estimate DNase activity of the antimicrobial system, as lysis of target E. coli cells in the conjugative mixture with the killer donor strain led to reduction in cell cytosol fluorescence. According to a lux assay, E. coli TG1 (pXen lux+ Apr) with constitutive luminescence were killed already after 2 h of treatment. Target sensor E. coli C600 with DNA damage SOS‐inducible luminescence showed significantly lower SOS induction 6 and 24 h following treatment with the killer donor strain. Our results thus showed that bioluminescent techniques are quick and suitable for estimation of the ColE7 bacterial conjugation‐based antimicrobial system antibacterial activity.
Significance and Impact of the Study
Bacterial antimicrobial resistance is worldwide rising and causing deaths of thousands of patients infected with multi‐drug resistant bacterial strains. In addition, there is a lack of efficient alternative antimicrobial agents. The significance of our research is the use of a number of methods (real‐time PCR, flow cytometry and bioluminescence‐based technique) to assess the antibacterial activity of the bacteriocin, colicin ColE7, bacterial conjugation‐based “kill” – “anti‐kill” antimicrobial system. Bioluminescent techniques proved to be rapid and suitable for estimation of antibacterial activity of ColE7 bacterial conjugation‐based antimicrobial system and possibly other related systems.
Significance and Impact of the Study: Bacterial antimicrobial resistance is worldwide rising and causing deaths of thousands of patients infected with multi‐drug resistant bacterial strains. In addition, there is a lack of efficient alternative antimicrobial agents. The significance of our research is the use of a number of methods (real‐time PCR, flow cytometry and bioluminescence‐based technique) to assess the antibacterial activity of the bacteriocin, colicin ColE7, bacterial conjugation‐based “kill” – “anti‐kill” antimicrobial system. Bioluminescent techniques proved to be rapid and suitable for estimation of antibacterial activity of ColE7 bacterial conjugation‐based antimicrobial system and possibly other related systems.</description><subject>Antibacterial activity</subject><subject>Antimicrobial agents</subject><subject>Antimicrobial resistance</subject><subject>Bacteria</subject><subject>bacteriocin</subject><subject>Bioluminescence</subject><subject>colicin</subject><subject>Conjugation</subject><subject>conjugation‐based antimicrobial system</subject><subject>Cytosol</subject><subject>Deoxyribonuclease</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA damage</subject><subject>Drug resistance</subject><subject>E coli</subject><subject>E. coli</subject><subject>Flow cytometry</subject><subject>Fluorescence</subject><subject>Gene expression</subject><subject>Genetic modification</subject><subject>Immunity</subject><subject>Luminescence</subject><subject>Lysis</subject><subject>plasmid</subject><subject>Polymerase chain reaction</subject><subject>Reagents</subject><subject>TraJ gene</subject><issn>0266-8254</issn><issn>1472-765X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kc2KFDEUhYMoTju68AUk4EbBmklSVanUcmjaH2hRRMFdkZ9bY9pUMiZVSO36EQbc6kv4SP0kpqenXQhmk9yc7x4u9yD0mJIzms-5k8MZZUJUd9CCVg0rGl5_vosWhHFeCFZXJ-hBShtCiKCsvY9OWNuUvBXVAv1epdEOcrTB49Dj8QtgJfUI0QZtPV4Gt2qwDn4zXd5Au-21kgkM3m1_frXO7ba_8vPHvpR-tFk-_u7LweoYlJUOpzmNMGA14wgy69dZBPx--eEF7t0UIiQNXgNOo7Te-svcbrCywU2D9UdRpiTn9BDd66VL8Oj2PkWfXq4-Ll8X63ev3iwv1oUu67IqjBRcVVQaJhg3oqKi7RuoGBDJDBChlQFtDNVlI3jDGJhe816rRnEmOaHlKXp28L2K4dsEaewGmwdxTnoIU-oYKTkjdd2KjD79B92EKfo8XabqsiRUlDxTzw9UXkpKEfruKubdx7mjpNsH2eUgu5sgM_vk1nFSA5i_5DG5DJwfgO_Wwfx_p2598fZg-QeqR7Kp</recordid><startdate>201807</startdate><enddate>201807</enddate><creator>Maslennikova, I.L.</creator><creator>Kuznetsova, M.V.</creator><creator>Toplak, N.</creator><creator>Nekrasova, I.V.</creator><creator>Žgur Bertok, D.</creator><creator>Starčič Erjavec, M.</creator><general>Oxford University Press</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QO</scope><scope>7ST</scope><scope>7T7</scope><scope>7TM</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>SOI</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-0200-573X</orcidid></search><sort><creationdate>201807</creationdate><title>Estimation of the bacteriocin ColE7 conjugation‐based “kill” – “anti‐kill” antimicrobial system by real‐time PCR, fluorescence staining and bioluminescence assays</title><author>Maslennikova, I.L. ; Kuznetsova, M.V. ; Toplak, N. ; Nekrasova, I.V. ; Žgur Bertok, D. ; Starčič Erjavec, M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3534-da86b41ad2826d84189f7e42e0a2de08cbdecdd1c3786722edfc6fcb7b62a6013</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Antibacterial activity</topic><topic>Antimicrobial agents</topic><topic>Antimicrobial resistance</topic><topic>Bacteria</topic><topic>bacteriocin</topic><topic>Bioluminescence</topic><topic>colicin</topic><topic>Conjugation</topic><topic>conjugation‐based antimicrobial system</topic><topic>Cytosol</topic><topic>Deoxyribonuclease</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA damage</topic><topic>Drug resistance</topic><topic>E coli</topic><topic>E. coli</topic><topic>Flow cytometry</topic><topic>Fluorescence</topic><topic>Gene expression</topic><topic>Genetic modification</topic><topic>Immunity</topic><topic>Luminescence</topic><topic>Lysis</topic><topic>plasmid</topic><topic>Polymerase chain reaction</topic><topic>Reagents</topic><topic>TraJ gene</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Maslennikova, I.L.</creatorcontrib><creatorcontrib>Kuznetsova, M.V.</creatorcontrib><creatorcontrib>Toplak, N.</creatorcontrib><creatorcontrib>Nekrasova, I.V.</creatorcontrib><creatorcontrib>Žgur Bertok, D.</creatorcontrib><creatorcontrib>Starčič Erjavec, M.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Letters in applied microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Maslennikova, I.L.</au><au>Kuznetsova, M.V.</au><au>Toplak, N.</au><au>Nekrasova, I.V.</au><au>Žgur Bertok, D.</au><au>Starčič Erjavec, M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Estimation of the bacteriocin ColE7 conjugation‐based “kill” – “anti‐kill” antimicrobial system by real‐time PCR, fluorescence staining and bioluminescence assays</atitle><jtitle>Letters in applied microbiology</jtitle><addtitle>Lett Appl Microbiol</addtitle><date>2018-07</date><risdate>2018</risdate><volume>67</volume><issue>1</issue><spage>47</spage><epage>53</epage><pages>47-53</pages><issn>0266-8254</issn><eissn>1472-765X</eissn><abstract>The efficiency of the bacteriocin, colicin ColE7, bacterial conjugation‐based “kill” – “anti‐kill” antimicrobial system, was assessed using real‐time PCR, flow cytometry and bioluminescence. The ColE7 antimicrobial system consists of the genetically modified Escherichia coli strain Nissle 1917 harbouring a conjugative plasmid (derivative of the F‐plasmid) encoding the “kill” gene (ColE7 activity gene) and a chromosomally encoded “anti‐kill” gene (ColE7 immunity gene). On the basis of traJ gene expression in the killer donor cells, our results showed that the efficiency of the here studied antimicrobial system against target E. coli was higher at 4 than at 24 h. Flow cytometry was used to indirectly estimate DNase activity of the antimicrobial system, as lysis of target E. coli cells in the conjugative mixture with the killer donor strain led to reduction in cell cytosol fluorescence. According to a lux assay, E. coli TG1 (pXen lux+ Apr) with constitutive luminescence were killed already after 2 h of treatment. Target sensor E. coli C600 with DNA damage SOS‐inducible luminescence showed significantly lower SOS induction 6 and 24 h following treatment with the killer donor strain. Our results thus showed that bioluminescent techniques are quick and suitable for estimation of the ColE7 bacterial conjugation‐based antimicrobial system antibacterial activity.
Significance and Impact of the Study
Bacterial antimicrobial resistance is worldwide rising and causing deaths of thousands of patients infected with multi‐drug resistant bacterial strains. In addition, there is a lack of efficient alternative antimicrobial agents. The significance of our research is the use of a number of methods (real‐time PCR, flow cytometry and bioluminescence‐based technique) to assess the antibacterial activity of the bacteriocin, colicin ColE7, bacterial conjugation‐based “kill” – “anti‐kill” antimicrobial system. Bioluminescent techniques proved to be rapid and suitable for estimation of antibacterial activity of ColE7 bacterial conjugation‐based antimicrobial system and possibly other related systems.
Significance and Impact of the Study: Bacterial antimicrobial resistance is worldwide rising and causing deaths of thousands of patients infected with multi‐drug resistant bacterial strains. In addition, there is a lack of efficient alternative antimicrobial agents. The significance of our research is the use of a number of methods (real‐time PCR, flow cytometry and bioluminescence‐based technique) to assess the antibacterial activity of the bacteriocin, colicin ColE7, bacterial conjugation‐based “kill” – “anti‐kill” antimicrobial system. Bioluminescent techniques proved to be rapid and suitable for estimation of antibacterial activity of ColE7 bacterial conjugation‐based antimicrobial system and possibly other related systems.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>29736984</pmid><doi>10.1111/lam.12884</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0003-0200-573X</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0266-8254 |
ispartof | Letters in applied microbiology, 2018-07, Vol.67 (1), p.47-53 |
issn | 0266-8254 1472-765X |
language | eng |
recordid | cdi_proquest_miscellaneous_2036205598 |
source | Wiley Journals; Oxford University Press Journals All Titles (1996-Current); EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Antibacterial activity Antimicrobial agents Antimicrobial resistance Bacteria bacteriocin Bioluminescence colicin Conjugation conjugation‐based antimicrobial system Cytosol Deoxyribonuclease Deoxyribonucleic acid DNA DNA damage Drug resistance E coli E. coli Flow cytometry Fluorescence Gene expression Genetic modification Immunity Luminescence Lysis plasmid Polymerase chain reaction Reagents TraJ gene |
title | Estimation of the bacteriocin ColE7 conjugation‐based “kill” – “anti‐kill” antimicrobial system by real‐time PCR, fluorescence staining and bioluminescence assays |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-26T06%3A54%3A39IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Estimation%20of%20the%20bacteriocin%20ColE7%20conjugation%E2%80%90based%20%E2%80%9Ckill%E2%80%9D%20%E2%80%93%20%E2%80%9Canti%E2%80%90kill%E2%80%9D%20antimicrobial%20system%20by%20real%E2%80%90time%20PCR,%20fluorescence%20staining%20and%20bioluminescence%20assays&rft.jtitle=Letters%20in%20applied%20microbiology&rft.au=Maslennikova,%20I.L.&rft.date=2018-07&rft.volume=67&rft.issue=1&rft.spage=47&rft.epage=53&rft.pages=47-53&rft.issn=0266-8254&rft.eissn=1472-765X&rft_id=info:doi/10.1111/lam.12884&rft_dat=%3Cproquest_cross%3E2036205598%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2053301836&rft_id=info:pmid/29736984&rfr_iscdi=true |