Construction of Actinobacillus pleuropneumoniae-Escherichia coli shuttle vectors: expression of antibiotic-resistance genes

We constructed several cloning vectors, designated pGZRS-18/19 and pGZRS-38/39, which were based on an endogenous Actinobacillus pleuropneumoniae (Apl) 4.3-kb plasmid. They carry the lacZα-complementation fragment and MCS from pUC18/19, and either the bla gene under the control of a putative Apl pro...

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Veröffentlicht in:Gene 1995-07, Vol.160 (1), p.81-86
Hauptverfasser: West, Susan E.H., Romero, Mary Jo M., Regassa, Laura B., Zielinski, Nicolette A., Welch, Rodney A.
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container_end_page 86
container_issue 1
container_start_page 81
container_title Gene
container_volume 160
creator West, Susan E.H.
Romero, Mary Jo M.
Regassa, Laura B.
Zielinski, Nicolette A.
Welch, Rodney A.
description We constructed several cloning vectors, designated pGZRS-18/19 and pGZRS-38/39, which were based on an endogenous Actinobacillus pleuropneumoniae (Apl) 4.3-kb plasmid. They carry the lacZα-complementation fragment and MCS from pUC18/19, and either the bla gene under the control of a putative Apl promoter or the Km R gene from Tn903. These vectors replicate in representative strains of Apl serotypes 1 and 7, Escherichia coli, Pasteurella haemolytica (Ph) and Haemophilus (Actinobacillus) actinomycetemcomitans. We also found that Apl and Ph did not express genes under the control of the lacZ or bla promoters, suggesting that their RNA polymerases may not utilize these promoters.
doi_str_mv 10.1016/0378-1119(95)00236-Y
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We also found that Apl and Ph did not express genes under the control of the lacZ or bla promoters, suggesting that their RNA polymerases may not utilize these promoters.</description><subject>Actinobacillus pleuropneumoniae</subject><subject>Actinobacillus pleuropneumoniae - genetics</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>beta-Galactosidase - biosynthesis</subject><subject>beta-lactamase</subject><subject>bla gene</subject><subject>cloning</subject><subject>Cloning, Molecular - methods</subject><subject>DNA replication</subject><subject>drug resistance</subject><subject>Drug Resistance, Microbial - genetics</subject><subject>electroporation</subject><subject>Escherichia coli</subject><subject>Escherichia coli - genetics</subject><subject>gene expression</subject><subject>Genes, Bacterial</subject><subject>Genetic Complementation Test</subject><subject>genetic transformation</subject><subject>Genetic Vectors</subject><subject>Haemophilus - genetics</subject><subject>kanamycin</subject><subject>lacz gene</subject><subject>Mannheimia haemolytica - genetics</subject><subject>Pasteurella haemolytica</subject><subject>Phenotype</subject><subject>plasmid vectors</subject><subject>Plasmids</subject><subject>promoter regions</subject><subject>Promoter Regions, Genetic</subject><subject>recombinant DNA</subject><subject>reporter genes</subject><subject>Restriction Mapping</subject><subject>Species Specificity</subject><subject>streptomycin</subject><issn>0378-1119</issn><issn>1879-0038</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUFv1DAQhS0EKtvCPwCREyqHFDuOY7sHpGpVoFIlDtBDT5bjTLpGWTt4nIqKP4-XXfVY5uKR55un0XuEvGH0jFHWfaRcqpoxpk-1-EBpw7v69hlZMSV1TSlXz8nqEXlJjhF_0lJCNEfkSHaNkk2zIn_WMWBOi8s-hiqO1UXpQuyt89O0YDVPsKQ4B1i2MXgL9SW6DSTvNt5WLk6-ws2S8wTVPbgcE55X8HtOgHjQsyH73sfsXV1-PWYbHFR3EABfkRejnRBeH94TcvP58sf6a3397cvV-uK6dm2rcj2Mkve6d9QpB2wE0bTaDrrhjPZUW94yOg4gYBDSOgm9gs5azbSiqlV8bPkJeb_XnVP8tQBms_XoYJpsgLigkbLlVDLxX5B1SmvFZQHbPehSREwwmjn5rU0PhlGzC8fsnDc7540W5l845rasvT3oL_0WhselQxpl_m4_H2009i55NDffG8o4ZYJ2SulCfNoTUPy695AMOg_F0cGn4r8Zon_6hL-e8qt0</recordid><startdate>19950704</startdate><enddate>19950704</enddate><creator>West, Susan E.H.</creator><creator>Romero, Mary Jo M.</creator><creator>Regassa, Laura B.</creator><creator>Zielinski, Nicolette A.</creator><creator>Welch, Rodney A.</creator><general>Elsevier B.V</general><scope>FBQ</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>7QL</scope><scope>7TM</scope><scope>C1K</scope><scope>7X8</scope></search><sort><creationdate>19950704</creationdate><title>Construction of Actinobacillus pleuropneumoniae-Escherichia coli shuttle vectors: expression of antibiotic-resistance genes</title><author>West, Susan E.H. ; Romero, Mary Jo M. ; Regassa, Laura B. ; Zielinski, Nicolette A. ; Welch, Rodney A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c448t-df73b9bc0c8ce1fe5249ad92310b09a3410fde5ed57ac7eb8e6aa919808483f43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Actinobacillus pleuropneumoniae</topic><topic>Actinobacillus pleuropneumoniae - genetics</topic><topic>Anti-Bacterial Agents - pharmacology</topic><topic>beta-Galactosidase - biosynthesis</topic><topic>beta-lactamase</topic><topic>bla gene</topic><topic>cloning</topic><topic>Cloning, Molecular - methods</topic><topic>DNA replication</topic><topic>drug resistance</topic><topic>Drug Resistance, Microbial - genetics</topic><topic>electroporation</topic><topic>Escherichia coli</topic><topic>Escherichia coli - genetics</topic><topic>gene expression</topic><topic>Genes, Bacterial</topic><topic>Genetic Complementation Test</topic><topic>genetic transformation</topic><topic>Genetic Vectors</topic><topic>Haemophilus - genetics</topic><topic>kanamycin</topic><topic>lacz gene</topic><topic>Mannheimia haemolytica - genetics</topic><topic>Pasteurella haemolytica</topic><topic>Phenotype</topic><topic>plasmid vectors</topic><topic>Plasmids</topic><topic>promoter regions</topic><topic>Promoter Regions, Genetic</topic><topic>recombinant DNA</topic><topic>reporter genes</topic><topic>Restriction Mapping</topic><topic>Species Specificity</topic><topic>streptomycin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>West, Susan E.H.</creatorcontrib><creatorcontrib>Romero, Mary Jo M.</creatorcontrib><creatorcontrib>Regassa, Laura B.</creatorcontrib><creatorcontrib>Zielinski, Nicolette A.</creatorcontrib><creatorcontrib>Welch, Rodney A.</creatorcontrib><collection>AGRIS</collection><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>Nucleic Acids Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><jtitle>Gene</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>West, Susan E.H.</au><au>Romero, Mary Jo M.</au><au>Regassa, Laura B.</au><au>Zielinski, Nicolette A.</au><au>Welch, Rodney A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Construction of Actinobacillus pleuropneumoniae-Escherichia coli shuttle vectors: expression of antibiotic-resistance genes</atitle><jtitle>Gene</jtitle><addtitle>Gene</addtitle><date>1995-07-04</date><risdate>1995</risdate><volume>160</volume><issue>1</issue><spage>81</spage><epage>86</epage><pages>81-86</pages><issn>0378-1119</issn><eissn>1879-0038</eissn><abstract>We constructed several cloning vectors, designated pGZRS-18/19 and pGZRS-38/39, which were based on an endogenous Actinobacillus pleuropneumoniae (Apl) 4.3-kb plasmid. They carry the lacZα-complementation fragment and MCS from pUC18/19, and either the bla gene under the control of a putative Apl promoter or the Km R gene from Tn903. These vectors replicate in representative strains of Apl serotypes 1 and 7, Escherichia coli, Pasteurella haemolytica (Ph) and Haemophilus (Actinobacillus) actinomycetemcomitans. We also found that Apl and Ph did not express genes under the control of the lacZ or bla promoters, suggesting that their RNA polymerases may not utilize these promoters.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>7628722</pmid><doi>10.1016/0378-1119(95)00236-Y</doi><tpages>6</tpages></addata></record>
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subjects Actinobacillus pleuropneumoniae
Actinobacillus pleuropneumoniae - genetics
Anti-Bacterial Agents - pharmacology
beta-Galactosidase - biosynthesis
beta-lactamase
bla gene
cloning
Cloning, Molecular - methods
DNA replication
drug resistance
Drug Resistance, Microbial - genetics
electroporation
Escherichia coli
Escherichia coli - genetics
gene expression
Genes, Bacterial
Genetic Complementation Test
genetic transformation
Genetic Vectors
Haemophilus - genetics
kanamycin
lacz gene
Mannheimia haemolytica - genetics
Pasteurella haemolytica
Phenotype
plasmid vectors
Plasmids
promoter regions
Promoter Regions, Genetic
recombinant DNA
reporter genes
Restriction Mapping
Species Specificity
streptomycin
title Construction of Actinobacillus pleuropneumoniae-Escherichia coli shuttle vectors: expression of antibiotic-resistance genes
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