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Development of a gene reporter system in moderately halophilic bacteria by employing the ice nucleation gene of Pseudomonas syringae
The expression of the ice nucleation gene inaZ of Pseudomonas syringae in several moderate halophiles was investigated to establish its utility as a reporter for promoter activity and gene expression studies in these biotechnologically and environmentally important bacteria. A promoterless version o...
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Published in: | Applied and Environmental Microbiology 1995-11, Vol.61 (11), p.3821-3825 |
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container_title | Applied and Environmental Microbiology |
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creator | Arvanitis, N. (University of Ioannina, Ioannina, Greece.) Vargas, C Tegos, G Perysinakis, A Nieto, J.J Ventosa, A Drainas, C |
description | The expression of the ice nucleation gene inaZ of Pseudomonas syringae in several moderate halophiles was investigated to establish its utility as a reporter for promoter activity and gene expression studies in these biotechnologically and environmentally important bacteria. A promoterless version of inaZ was introduced in two different restriction sites and at both orientations in a recombinant plasmid able to replicate in moderate halophiles and, in particular, within the sequence of its pHE1 part, a native plasmid of Halomonas elongata. One orientation of both recombinant constructs expressed high levels of ice nucleation activity in H. elongata and Volcaniella eurihalina cells, indicating that inaZ was probably introduced in the correct orientation downstream of putative native promoters. A recombinant construct carrying a tandem duplication of inaZ at the same orientation gave significantly higher ice nucleation activity, showing that inaZ is appropriate for gene dosage studies. The ice nucleation gene was also expressed in H. elongata and V. eurihalina under the control of Pbla (the promoter of the beta-lactamase gene of Escherichia coli) and Ppdc (the promoter of the pyruvate decarboxylase gene of Zymomonas mobilis). One of the inaZ reporter plasmids expressing high levels of ice nucleation activity under the control of a native putative promoter was also transferred in Halomonas subglaciescola, Halomonas meridiana, Halomonas halodurans, and Deleya halophila. In all cases, Ice+ transconjugants were successfully isolated, demonstrating that inaZ is expressed in a wide spectrum of moderately halophilic species |
doi_str_mv | 10.1128/AEM.61.11.3821-3825.1995 |
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(University of Ioannina, Ioannina, Greece.) ; Vargas, C ; Tegos, G ; Perysinakis, A ; Nieto, J.J ; Ventosa, A ; Drainas, C</creator><creatorcontrib>Arvanitis, N. (University of Ioannina, Ioannina, Greece.) ; Vargas, C ; Tegos, G ; Perysinakis, A ; Nieto, J.J ; Ventosa, A ; Drainas, C</creatorcontrib><description>The expression of the ice nucleation gene inaZ of Pseudomonas syringae in several moderate halophiles was investigated to establish its utility as a reporter for promoter activity and gene expression studies in these biotechnologically and environmentally important bacteria. A promoterless version of inaZ was introduced in two different restriction sites and at both orientations in a recombinant plasmid able to replicate in moderate halophiles and, in particular, within the sequence of its pHE1 part, a native plasmid of Halomonas elongata. One orientation of both recombinant constructs expressed high levels of ice nucleation activity in H. elongata and Volcaniella eurihalina cells, indicating that inaZ was probably introduced in the correct orientation downstream of putative native promoters. A recombinant construct carrying a tandem duplication of inaZ at the same orientation gave significantly higher ice nucleation activity, showing that inaZ is appropriate for gene dosage studies. The ice nucleation gene was also expressed in H. elongata and V. eurihalina under the control of Pbla (the promoter of the beta-lactamase gene of Escherichia coli) and Ppdc (the promoter of the pyruvate decarboxylase gene of Zymomonas mobilis). One of the inaZ reporter plasmids expressing high levels of ice nucleation activity under the control of a native putative promoter was also transferred in Halomonas subglaciescola, Halomonas meridiana, Halomonas halodurans, and Deleya halophila. In all cases, Ice+ transconjugants were successfully isolated, demonstrating that inaZ is expressed in a wide spectrum of moderately halophilic species</description><identifier>ISSN: 0099-2240</identifier><identifier>EISSN: 1098-5336</identifier><identifier>DOI: 10.1128/AEM.61.11.3821-3825.1995</identifier><identifier>PMID: 8526492</identifier><identifier>CODEN: AEMIDF</identifier><language>eng</language><publisher>Washington, DC: American Society for Microbiology</publisher><subject>ADN RECOMBINADO ; ADN RECOMBINE ; BACTERIA ; Bacterial Outer Membrane Proteins ; Bacterial Proteins - genetics ; Biochemistry ; Biological and medical sciences ; Biotechnology ; Chromosome Mapping ; DANOS POR LA HELADA ; DEGAT DU AU GEL ; EXPRESION GENICA ; EXPRESSION DES GENES ; Fundamental and applied biological sciences. Psychology ; GENE ; Gene Expression ; GENES ; Genes, Bacterial ; Genes, Reporter ; Genetic engineering ; Genetic technics ; Genetic Techniques ; Gram-Negative Aerobic Bacteria - genetics ; Halomonas ; Methods. Procedures. Technologies ; Modification of gene expression level ; Plasmids - genetics ; Promoter Regions, Genetic ; Pseudomonas - genetics ; Pseudomonas aeruginosa ; PSEUDOMONAS SYRINGAE ; Recombination, Genetic ; TRANSFERENCIA DE GENES ; TRANSFERT DE GENE ; TRANSFORMACION GENETICA ; TRANSFORMATION GENETIQUE</subject><ispartof>Applied and Environmental Microbiology, 1995-11, Vol.61 (11), p.3821-3825</ispartof><rights>1996 INIST-CNRS</rights><rights>Copyright American Society for Microbiology Nov 1995</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c602t-fafdae331d8beca260342404e5f41cbfdad449176325fabf693cc47433e168253</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/PMC167685/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC167685/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,3188,3189,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2916466$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8526492$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Arvanitis, N. (University of Ioannina, Ioannina, Greece.)</creatorcontrib><creatorcontrib>Vargas, C</creatorcontrib><creatorcontrib>Tegos, G</creatorcontrib><creatorcontrib>Perysinakis, A</creatorcontrib><creatorcontrib>Nieto, J.J</creatorcontrib><creatorcontrib>Ventosa, A</creatorcontrib><creatorcontrib>Drainas, C</creatorcontrib><title>Development of a gene reporter system in moderately halophilic bacteria by employing the ice nucleation gene of Pseudomonas syringae</title><title>Applied and Environmental Microbiology</title><addtitle>Appl Environ Microbiol</addtitle><description>The expression of the ice nucleation gene inaZ of Pseudomonas syringae in several moderate halophiles was investigated to establish its utility as a reporter for promoter activity and gene expression studies in these biotechnologically and environmentally important bacteria. A promoterless version of inaZ was introduced in two different restriction sites and at both orientations in a recombinant plasmid able to replicate in moderate halophiles and, in particular, within the sequence of its pHE1 part, a native plasmid of Halomonas elongata. One orientation of both recombinant constructs expressed high levels of ice nucleation activity in H. elongata and Volcaniella eurihalina cells, indicating that inaZ was probably introduced in the correct orientation downstream of putative native promoters. A recombinant construct carrying a tandem duplication of inaZ at the same orientation gave significantly higher ice nucleation activity, showing that inaZ is appropriate for gene dosage studies. The ice nucleation gene was also expressed in H. elongata and V. eurihalina under the control of Pbla (the promoter of the beta-lactamase gene of Escherichia coli) and Ppdc (the promoter of the pyruvate decarboxylase gene of Zymomonas mobilis). One of the inaZ reporter plasmids expressing high levels of ice nucleation activity under the control of a native putative promoter was also transferred in Halomonas subglaciescola, Halomonas meridiana, Halomonas halodurans, and Deleya halophila. In all cases, Ice+ transconjugants were successfully isolated, demonstrating that inaZ is expressed in a wide spectrum of moderately halophilic species</description><subject>ADN RECOMBINADO</subject><subject>ADN RECOMBINE</subject><subject>BACTERIA</subject><subject>Bacterial Outer Membrane Proteins</subject><subject>Bacterial Proteins - genetics</subject><subject>Biochemistry</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Chromosome Mapping</subject><subject>DANOS POR LA HELADA</subject><subject>DEGAT DU AU GEL</subject><subject>EXPRESION GENICA</subject><subject>EXPRESSION DES GENES</subject><subject>Fundamental and applied biological sciences. 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Technologies</subject><subject>Modification of gene expression level</subject><subject>Plasmids - genetics</subject><subject>Promoter Regions, Genetic</subject><subject>Pseudomonas - genetics</subject><subject>Pseudomonas aeruginosa</subject><subject>PSEUDOMONAS SYRINGAE</subject><subject>Recombination, Genetic</subject><subject>TRANSFERENCIA DE GENES</subject><subject>TRANSFERT DE GENE</subject><subject>TRANSFORMACION GENETICA</subject><subject>TRANSFORMATION GENETIQUE</subject><issn>0099-2240</issn><issn>1098-5336</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><recordid>eNqFkt-L1DAQx4so53r6DwhCEPGta9KkafPgw3GeP-BEQe85TNPpNkfbrEl7su_-4c6yy6r3IoFkYD7f-ZXJMib4WoiifnNx9XmtBdlrWRcip6tcC2PKB9lKcFPnpZT6Ybbi3Ji8KBR_nD1J6ZZzrriuz7Kzuiy0MsUq-_UO73AI2xGnmYWOAdvghCziNsQZI0u7NOPI_MTG0GKEGYcd64EUvR-8Yw04wjywZsdw3A5h56cNm3tk3iGbFjcgzD5Mh7CU4GvCpQ1jmCBR8Eg04NPsUQdDwmfH9zy7eX_1_fJjfv3lw6fLi-vcaV7MeQddCyilaOsGHRSaS0W9KSw7JVxDzlYpIyoti7KDptNGOqcqJSUKTROS59nbQ9zt0ozYOuo5wmC30Y8QdzaAt_96Jt_bTbizQle63utfH_Ux_FgwzXb0yeEwwIRhSbaqaKhS1P8FhTZG0yHw5T3wNixxoiHYgpemoG4UQfUBcjGkFLE7VSy43a-DBRytFmTb_Trsr9Lu14GkL_7u-CQ8_j_5Xx39kBwMXYTJ-XTCKL9WWv8ps_eb_qePaCGN97IS9PwAdRAsbCLFuflmSl3Vspa_AXPw1UE</recordid><startdate>19951101</startdate><enddate>19951101</enddate><creator>Arvanitis, N. (University of Ioannina, Ioannina, Greece.)</creator><creator>Vargas, C</creator><creator>Tegos, G</creator><creator>Perysinakis, A</creator><creator>Nieto, J.J</creator><creator>Ventosa, A</creator><creator>Drainas, C</creator><general>American Society for Microbiology</general><scope>FBQ</scope><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>7QL</scope><scope>7QO</scope><scope>7SN</scope><scope>7SS</scope><scope>7ST</scope><scope>7T7</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>SOI</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19951101</creationdate><title>Development of a gene reporter system in moderately halophilic bacteria by employing the ice nucleation gene of Pseudomonas syringae</title><author>Arvanitis, N. 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Psychology</topic><topic>GENE</topic><topic>Gene Expression</topic><topic>GENES</topic><topic>Genes, Bacterial</topic><topic>Genes, Reporter</topic><topic>Genetic engineering</topic><topic>Genetic technics</topic><topic>Genetic Techniques</topic><topic>Gram-Negative Aerobic Bacteria - genetics</topic><topic>Halomonas</topic><topic>Methods. Procedures. Technologies</topic><topic>Modification of gene expression level</topic><topic>Plasmids - genetics</topic><topic>Promoter Regions, Genetic</topic><topic>Pseudomonas - genetics</topic><topic>Pseudomonas aeruginosa</topic><topic>PSEUDOMONAS SYRINGAE</topic><topic>Recombination, Genetic</topic><topic>TRANSFERENCIA DE GENES</topic><topic>TRANSFERT DE GENE</topic><topic>TRANSFORMACION GENETICA</topic><topic>TRANSFORMATION GENETIQUE</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Arvanitis, N. 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(University of Ioannina, Ioannina, Greece.)</au><au>Vargas, C</au><au>Tegos, G</au><au>Perysinakis, A</au><au>Nieto, J.J</au><au>Ventosa, A</au><au>Drainas, C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of a gene reporter system in moderately halophilic bacteria by employing the ice nucleation gene of Pseudomonas syringae</atitle><jtitle>Applied and Environmental Microbiology</jtitle><addtitle>Appl Environ Microbiol</addtitle><date>1995-11-01</date><risdate>1995</risdate><volume>61</volume><issue>11</issue><spage>3821</spage><epage>3825</epage><pages>3821-3825</pages><issn>0099-2240</issn><eissn>1098-5336</eissn><coden>AEMIDF</coden><abstract>The expression of the ice nucleation gene inaZ of Pseudomonas syringae in several moderate halophiles was investigated to establish its utility as a reporter for promoter activity and gene expression studies in these biotechnologically and environmentally important bacteria. A promoterless version of inaZ was introduced in two different restriction sites and at both orientations in a recombinant plasmid able to replicate in moderate halophiles and, in particular, within the sequence of its pHE1 part, a native plasmid of Halomonas elongata. One orientation of both recombinant constructs expressed high levels of ice nucleation activity in H. elongata and Volcaniella eurihalina cells, indicating that inaZ was probably introduced in the correct orientation downstream of putative native promoters. A recombinant construct carrying a tandem duplication of inaZ at the same orientation gave significantly higher ice nucleation activity, showing that inaZ is appropriate for gene dosage studies. The ice nucleation gene was also expressed in H. elongata and V. eurihalina under the control of Pbla (the promoter of the beta-lactamase gene of Escherichia coli) and Ppdc (the promoter of the pyruvate decarboxylase gene of Zymomonas mobilis). One of the inaZ reporter plasmids expressing high levels of ice nucleation activity under the control of a native putative promoter was also transferred in Halomonas subglaciescola, Halomonas meridiana, Halomonas halodurans, and Deleya halophila. In all cases, Ice+ transconjugants were successfully isolated, demonstrating that inaZ is expressed in a wide spectrum of moderately halophilic species</abstract><cop>Washington, DC</cop><pub>American Society for Microbiology</pub><pmid>8526492</pmid><doi>10.1128/AEM.61.11.3821-3825.1995</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | ADN RECOMBINADO ADN RECOMBINE BACTERIA Bacterial Outer Membrane Proteins Bacterial Proteins - genetics Biochemistry Biological and medical sciences Biotechnology Chromosome Mapping DANOS POR LA HELADA DEGAT DU AU GEL EXPRESION GENICA EXPRESSION DES GENES Fundamental and applied biological sciences. Psychology GENE Gene Expression GENES Genes, Bacterial Genes, Reporter Genetic engineering Genetic technics Genetic Techniques Gram-Negative Aerobic Bacteria - genetics Halomonas Methods. Procedures. Technologies Modification of gene expression level Plasmids - genetics Promoter Regions, Genetic Pseudomonas - genetics Pseudomonas aeruginosa PSEUDOMONAS SYRINGAE Recombination, Genetic TRANSFERENCIA DE GENES TRANSFERT DE GENE TRANSFORMACION GENETICA TRANSFORMATION GENETIQUE |
title | Development of a gene reporter system in moderately halophilic bacteria by employing the ice nucleation gene of Pseudomonas syringae |
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