Escherichia coli strains that allow antibiotic-free plasmid selection and maintenance by repressor titration
We report the construction of two novel Escherichia coli strains (DH1lacdapD and DH1lacP2dapD) that facilitate the antibiotic-free selection and stable maintenance of recombinant plasmids in complex media. They contain the essential chromosomal gene, dapD, under the control of the lac operator/promo...
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Veröffentlicht in: | Nucleic acids research 2001-03, Vol.29 (5), p.E26-26 |
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description | We report the construction of two novel Escherichia coli strains (DH1lacdapD and DH1lacP2dapD) that facilitate the antibiotic-free selection and stable maintenance of recombinant plasmids in complex media. They contain the essential chromosomal gene, dapD, under the control of the lac operator/promoter. Unless supplemented with IPTG (which induces expression of dapD) or DAP, these cells lyse. However, when the strains are transformed with a multicopy plasmid containing the lac operator, the operator competitively titrates the LacI repressor and allows expression of dapD from the lac promoter. Thus transformants can be isolated and propagated simply by their ability to grow on any medium by repressor titration selection. No antibiotic resistance genes or other protein expressing sequences are required on the plasmid, and antibiotics are not necessary for plasmid selection, making these strains a valuable tool for therapeutic DNA and recombinant protein production. We describe the construction of these strains and demonstrate plasmid selection and maintenance by repressor titration, using the new pORT plasmid vectors designed to facilitate recombinant DNA exploitation. |
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They contain the essential chromosomal gene, dapD, under the control of the lac operator/promoter. Unless supplemented with IPTG (which induces expression of dapD) or DAP, these cells lyse. However, when the strains are transformed with a multicopy plasmid containing the lac operator, the operator competitively titrates the LacI repressor and allows expression of dapD from the lac promoter. Thus transformants can be isolated and propagated simply by their ability to grow on any medium by repressor titration selection. No antibiotic resistance genes or other protein expressing sequences are required on the plasmid, and antibiotics are not necessary for plasmid selection, making these strains a valuable tool for therapeutic DNA and recombinant protein production. We describe the construction of these strains and demonstrate plasmid selection and maintenance by repressor titration, using the new pORT plasmid vectors designed to facilitate recombinant DNA exploitation.</description><identifier>ISSN: 1362-4962</identifier><identifier>ISSN: 0305-1048</identifier><identifier>EISSN: 1362-4962</identifier><identifier>DOI: 10.1093/nar/29.5.e26</identifier><identifier>PMID: 11222777</identifier><identifier>CODEN: NARHAD</identifier><language>eng</language><publisher>England: Oxford Publishing Limited (England)</publisher><subject>Amino Acid Sequence ; Base Sequence ; Chromosomes, Bacterial - genetics ; Cloning, Molecular ; dapD gene ; Drug Resistance, Microbial - genetics ; Escherichia coli ; Escherichia coli - drug effects ; Escherichia coli - genetics ; Gene Expression Regulation, Bacterial ; Genetic Markers ; Kanamycin - pharmacology ; Lac Operon - genetics ; LacI protein ; Molecular Sequence Data ; NAR Methods Online ; Plasmids - genetics ; Transformation, Genetic</subject><ispartof>Nucleic acids research, 2001-03, Vol.29 (5), p.E26-26</ispartof><rights>Copyright Oxford University Press(England) Mar 1, 2001</rights><rights>Copyright © 2001 Oxford University Press 2001</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c436t-dd73e6f3692c565ea9cdbfa78b31a7dafc5ed621c0be44edac573b49180188293</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/PMC29739/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC29739/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11222777$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cranenburgh, R M</creatorcontrib><creatorcontrib>Hanak, J A</creatorcontrib><creatorcontrib>Williams, S G</creatorcontrib><creatorcontrib>Sherratt, D J</creatorcontrib><title>Escherichia coli strains that allow antibiotic-free plasmid selection and maintenance by repressor titration</title><title>Nucleic acids research</title><addtitle>Nucleic Acids Res</addtitle><description>We report the construction of two novel Escherichia coli strains (DH1lacdapD and DH1lacP2dapD) that facilitate the antibiotic-free selection and stable maintenance of recombinant plasmids in complex media. They contain the essential chromosomal gene, dapD, under the control of the lac operator/promoter. Unless supplemented with IPTG (which induces expression of dapD) or DAP, these cells lyse. However, when the strains are transformed with a multicopy plasmid containing the lac operator, the operator competitively titrates the LacI repressor and allows expression of dapD from the lac promoter. Thus transformants can be isolated and propagated simply by their ability to grow on any medium by repressor titration selection. No antibiotic resistance genes or other protein expressing sequences are required on the plasmid, and antibiotics are not necessary for plasmid selection, making these strains a valuable tool for therapeutic DNA and recombinant protein production. We describe the construction of these strains and demonstrate plasmid selection and maintenance by repressor titration, using the new pORT plasmid vectors designed to facilitate recombinant DNA exploitation.</description><subject>Amino Acid Sequence</subject><subject>Base Sequence</subject><subject>Chromosomes, Bacterial - genetics</subject><subject>Cloning, Molecular</subject><subject>dapD gene</subject><subject>Drug Resistance, Microbial - genetics</subject><subject>Escherichia coli</subject><subject>Escherichia coli - drug effects</subject><subject>Escherichia coli - genetics</subject><subject>Gene Expression Regulation, Bacterial</subject><subject>Genetic Markers</subject><subject>Kanamycin - pharmacology</subject><subject>Lac Operon - genetics</subject><subject>LacI protein</subject><subject>Molecular Sequence Data</subject><subject>NAR Methods Online</subject><subject>Plasmids - genetics</subject><subject>Transformation, Genetic</subject><issn>1362-4962</issn><issn>0305-1048</issn><issn>1362-4962</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkb1vFDEQxS0EIiHQUSOLgip78cfaXks0KEoAKRIN1JbXnuUcee3D9gXlv8ennCDQUM1I83ujN_MQek3JhhLNL5ItF0xvxAaYfIJOKZdsGLVkTx_1J-hFrbeE0JGK8Tk6oZQxppQ6RfGqui2U4LbBYpdjwLUVG1LFbWsbtjHmn9imFuaQW3DDUgDwLtq6Bo8rRHAt5NQJj9cua5BscoDne1xgV6DWXHALfeUBe4meLTZWeHWsZ-jb9dXXy0_DzZePny8_3Axu5LIN3isOcuFSMyekAKudnxerpplTq7xdnAAvGXVkhnEEb51QfB41nQidJqb5GXr_sHe3n1fwDlI3EM2uhNWWe5NtMH9PUtia7_nOMK34Qf7uKC_5xx5qM2uoDmK0CfK-GkWkVJKr_4J0YlToiXfw7T_gbd6X1H9gGCFSaK5Zh84fIFdyrQWW34YpMYeoTY-6WzTC9Kg7_ubxkX_gY7b8FxPEqPo</recordid><startdate>20010301</startdate><enddate>20010301</enddate><creator>Cranenburgh, R M</creator><creator>Hanak, J A</creator><creator>Williams, S G</creator><creator>Sherratt, D J</creator><general>Oxford Publishing Limited (England)</general><general>Oxford University Press</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>7QL</scope><scope>7QO</scope><scope>7QP</scope><scope>7QR</scope><scope>7SS</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20010301</creationdate><title>Escherichia coli strains that allow antibiotic-free plasmid selection and maintenance by repressor titration</title><author>Cranenburgh, R M ; Hanak, J A ; Williams, S G ; Sherratt, D J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c436t-dd73e6f3692c565ea9cdbfa78b31a7dafc5ed621c0be44edac573b49180188293</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Amino Acid Sequence</topic><topic>Base Sequence</topic><topic>Chromosomes, Bacterial - genetics</topic><topic>Cloning, Molecular</topic><topic>dapD gene</topic><topic>Drug Resistance, Microbial - genetics</topic><topic>Escherichia coli</topic><topic>Escherichia coli - drug effects</topic><topic>Escherichia coli - genetics</topic><topic>Gene Expression Regulation, Bacterial</topic><topic>Genetic Markers</topic><topic>Kanamycin - pharmacology</topic><topic>Lac Operon - genetics</topic><topic>LacI protein</topic><topic>Molecular Sequence Data</topic><topic>NAR Methods Online</topic><topic>Plasmids - genetics</topic><topic>Transformation, Genetic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cranenburgh, R M</creatorcontrib><creatorcontrib>Hanak, J A</creatorcontrib><creatorcontrib>Williams, S G</creatorcontrib><creatorcontrib>Sherratt, D J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</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>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Nucleic acids research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cranenburgh, R M</au><au>Hanak, J A</au><au>Williams, S G</au><au>Sherratt, D J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Escherichia coli strains that allow antibiotic-free plasmid selection and maintenance by repressor titration</atitle><jtitle>Nucleic acids research</jtitle><addtitle>Nucleic Acids Res</addtitle><date>2001-03-01</date><risdate>2001</risdate><volume>29</volume><issue>5</issue><spage>E26</spage><epage>26</epage><pages>E26-26</pages><issn>1362-4962</issn><issn>0305-1048</issn><eissn>1362-4962</eissn><coden>NARHAD</coden><abstract>We report the construction of two novel Escherichia coli strains (DH1lacdapD and DH1lacP2dapD) that facilitate the antibiotic-free selection and stable maintenance of recombinant plasmids in complex media. They contain the essential chromosomal gene, dapD, under the control of the lac operator/promoter. Unless supplemented with IPTG (which induces expression of dapD) or DAP, these cells lyse. However, when the strains are transformed with a multicopy plasmid containing the lac operator, the operator competitively titrates the LacI repressor and allows expression of dapD from the lac promoter. Thus transformants can be isolated and propagated simply by their ability to grow on any medium by repressor titration selection. No antibiotic resistance genes or other protein expressing sequences are required on the plasmid, and antibiotics are not necessary for plasmid selection, making these strains a valuable tool for therapeutic DNA and recombinant protein production. We describe the construction of these strains and demonstrate plasmid selection and maintenance by repressor titration, using the new pORT plasmid vectors designed to facilitate recombinant DNA exploitation.</abstract><cop>England</cop><pub>Oxford Publishing Limited (England)</pub><pmid>11222777</pmid><doi>10.1093/nar/29.5.e26</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Amino Acid Sequence Base Sequence Chromosomes, Bacterial - genetics Cloning, Molecular dapD gene Drug Resistance, Microbial - genetics Escherichia coli Escherichia coli - drug effects Escherichia coli - genetics Gene Expression Regulation, Bacterial Genetic Markers Kanamycin - pharmacology Lac Operon - genetics LacI protein Molecular Sequence Data NAR Methods Online Plasmids - genetics Transformation, Genetic |
title | Escherichia coli strains that allow antibiotic-free plasmid selection and maintenance by repressor titration |
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