Effect of promoter modification on mosquitocidal cryIVB gene expression in Synechococcus sp. strain PCC 7942

The impact of promoter modification on the expression of the mosquitocidal Bacillus thuringiensis subsp. israelensis cryIVB gene when used to transform the cyanobacterium Synechococcus sp. strain PCC 7942 has been examined. Maximal transcript and protein abundances were achieved by the addition of t...

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Veröffentlicht in:Applied and Environmental Microbiology 1993-08, Vol.59 (8), p.2404-2410
Hauptverfasser: SOLTES-RAK, E, KUSHNER, D. J, WILLIAMS, D. D, COLEMAN, J. R
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container_issue 8
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container_title Applied and Environmental Microbiology
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creator SOLTES-RAK, E
KUSHNER, D. J
WILLIAMS, D. D
COLEMAN, J. R
description The impact of promoter modification on the expression of the mosquitocidal Bacillus thuringiensis subsp. israelensis cryIVB gene when used to transform the cyanobacterium Synechococcus sp. strain PCC 7942 has been examined. Maximal transcript and protein abundances were achieved by the addition of the lacZ promoter upstream of the cryIVB sequence. Replacement of the endogenous corresponding Bacillus sequences with the Synechococcus petF1 promoter, ribosome binding site, and initiation codon also resulted in increased expression of the cryIVB gene relative to the expression obtained with the Bacillus promoter alone but decreased expression relative to the expression achieved with the tandem array of the Bacillus and lacZ promoters. Synechococcus cells carrying plasmids in which the expression of the cryIVB gene was regulated by either the lacZ or the petF1 promoter were readily consumed by first-instar Culex restuans larvae and proved to be toxic for these organisms.
doi_str_mv 10.1128/aem.59.8.2404-2410.1993
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Synechococcus cells carrying plasmids in which the expression of the cryIVB gene was regulated by either the lacZ or the petF1 promoter were readily consumed by first-instar Culex restuans larvae and proved to be toxic for these organisms.</description><identifier>ISSN: 0099-2240</identifier><identifier>EISSN: 1098-5336</identifier><identifier>DOI: 10.1128/aem.59.8.2404-2410.1993</identifier><identifier>PMID: 7690220</identifier><identifier>CODEN: AEMIDF</identifier><language>eng</language><publisher>Washington, DC: American Society for Microbiology</publisher><subject>adn recombinado ; adn recombine ; bacillus thuringiensis ; Bacillus thuringiensis - genetics ; Bacillus thuringiensis israelensis ; Bacteria ; Bacterial Proteins - genetics ; Bacterial Toxins ; Biological and medical sciences ; Biotechnology ; Culex restuans ; Cyanobacteria - genetics ; cyanophyta ; endotoxinas ; endotoxine ; endotoxins ; Endotoxins - genetics ; Escherichia coli - genetics ; expresion genica ; expression des genes ; Freshwater ; Fundamental and applied biological sciences. Psychology ; gene ; Gene Expression ; Genes ; Genes, Bacterial ; Genetic engineering ; Genetic technics ; genetic transformation ; Genetic Vectors ; genetica ; genetics ; genetique ; Hemolysin Proteins ; insecticidas ; insecticide ; insecticides ; Insects ; larvae ; larvas ; larve ; Methods. Procedures. 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J</creatorcontrib><creatorcontrib>WILLIAMS, D. D</creatorcontrib><creatorcontrib>COLEMAN, J. R</creatorcontrib><title>Effect of promoter modification on mosquitocidal cryIVB gene expression in Synechococcus sp. strain PCC 7942</title><title>Applied and Environmental Microbiology</title><addtitle>Appl Environ Microbiol</addtitle><description>The impact of promoter modification on the expression of the mosquitocidal Bacillus thuringiensis subsp. israelensis cryIVB gene when used to transform the cyanobacterium Synechococcus sp. strain PCC 7942 has been examined. Maximal transcript and protein abundances were achieved by the addition of the lacZ promoter upstream of the cryIVB sequence. Replacement of the endogenous corresponding Bacillus sequences with the Synechococcus petF1 promoter, ribosome binding site, and initiation codon also resulted in increased expression of the cryIVB gene relative to the expression obtained with the Bacillus promoter alone but decreased expression relative to the expression achieved with the tandem array of the Bacillus and lacZ promoters. Synechococcus cells carrying plasmids in which the expression of the cryIVB gene was regulated by either the lacZ or the petF1 promoter were readily consumed by first-instar Culex restuans larvae and proved to be toxic for these organisms.</description><subject>adn recombinado</subject><subject>adn recombine</subject><subject>bacillus thuringiensis</subject><subject>Bacillus thuringiensis - genetics</subject><subject>Bacillus thuringiensis israelensis</subject><subject>Bacteria</subject><subject>Bacterial Proteins - genetics</subject><subject>Bacterial Toxins</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Culex restuans</subject><subject>Cyanobacteria - genetics</subject><subject>cyanophyta</subject><subject>endotoxinas</subject><subject>endotoxine</subject><subject>endotoxins</subject><subject>Endotoxins - genetics</subject><subject>Escherichia coli - genetics</subject><subject>expresion genica</subject><subject>expression des genes</subject><subject>Freshwater</subject><subject>Fundamental and applied biological sciences. 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Replacement of the endogenous corresponding Bacillus sequences with the Synechococcus petF1 promoter, ribosome binding site, and initiation codon also resulted in increased expression of the cryIVB gene relative to the expression obtained with the Bacillus promoter alone but decreased expression relative to the expression achieved with the tandem array of the Bacillus and lacZ promoters. Synechococcus cells carrying plasmids in which the expression of the cryIVB gene was regulated by either the lacZ or the petF1 promoter were readily consumed by first-instar Culex restuans larvae and proved to be toxic for these organisms.</abstract><cop>Washington, DC</cop><pub>American Society for Microbiology</pub><pmid>7690220</pmid><doi>10.1128/aem.59.8.2404-2410.1993</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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ispartof Applied and Environmental Microbiology, 1993-08, Vol.59 (8), p.2404-2410
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subjects adn recombinado
adn recombine
bacillus thuringiensis
Bacillus thuringiensis - genetics
Bacillus thuringiensis israelensis
Bacteria
Bacterial Proteins - genetics
Bacterial Toxins
Biological and medical sciences
Biotechnology
Culex restuans
Cyanobacteria - genetics
cyanophyta
endotoxinas
endotoxine
endotoxins
Endotoxins - genetics
Escherichia coli - genetics
expresion genica
expression des genes
Freshwater
Fundamental and applied biological sciences. Psychology
gene
Gene Expression
Genes
Genes, Bacterial
Genetic engineering
Genetic technics
genetic transformation
Genetic Vectors
genetica
genetics
genetique
Hemolysin Proteins
insecticidas
insecticide
insecticides
Insects
larvae
larvas
larve
Methods. Procedures. Technologies
Modification of gene expression level
Pest Control, Biological
Plasmids - genetics
Promoter Regions, Genetic
recombinant dna
RNA, Bacterial - genetics
RNA, Messenger - genetics
Synechococcus
toxinas
toxine
toxins
transformacion genetica
transformation genetique
Transformation, Genetic
title Effect of promoter modification on mosquitocidal cryIVB gene expression in Synechococcus sp. strain PCC 7942
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