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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
Main Authors: Arvanitis, N. (University of Ioannina, Ioannina, Greece.), Vargas, C, Tegos, G, Perysinakis, A, Nieto, J.J, Ventosa, A, Drainas, C
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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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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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ispartof Applied and Environmental Microbiology, 1995-11, Vol.61 (11), p.3821-3825
issn 0099-2240
1098-5336
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_167685
source American Society for Microbiology; PubMed Central
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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