The Mycobacterium tuberculosis katG promoter region contains a novel upstream activator

Department of Medical Microbiology, University of Cape Town and Groote Schuur Hospital, Medical School, Observatory, 7925 Cape Town, South Africa 1 Author for correspondence: Lafras M. Steyn. Tel: +27 21 406 6363. Fax: +27 21 448 8153. e-mail: lsteyn{at}medmicro.uct.ac.za An Escherichia coli –mycoba...

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Veröffentlicht in:Microbiology (Society for General Microbiology) 1999-09, Vol.145 (9), p.2507-2518
Hauptverfasser: Mulder, Michelle A, Zappe, Harold, Steyn, Lafras M
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creator Mulder, Michelle A
Zappe, Harold
Steyn, Lafras M
description Department of Medical Microbiology, University of Cape Town and Groote Schuur Hospital, Medical School, Observatory, 7925 Cape Town, South Africa 1 Author for correspondence: Lafras M. Steyn. Tel: +27 21 406 6363. Fax: +27 21 448 8153. e-mail: lsteyn{at}medmicro.uct.ac.za An Escherichia coli –mycobacterial shuttle vector, pJCluc, containing a luciferase reporter gene, was constructed and used to analyse the Mycobacterium tuberculosis katG promoter. A 1·9 kb region immediately upstream of katG promoted expression of the luciferase gene in E. coli and Mycobacterium smegmatis . A smaller promoter fragment (559 bp) promoted expression with equal efficiency, and was used in all further studies. Two transcription start sites were mapped by primer extension analysis to 47 and 56 bp upstream of the GTG initiation codon. Putative promoters associated with these show similarity to previously identified mycobacterial promoters. Deletions in the promoter fragment, introduced with BAL-31 nuclease and restriction endonucleases, revealed that a region between 559 and 448 bp upstream of the translation initiation codon, designated the upstream activator region (UAR), is essential for promoter activity in E. coli , and is required for optimal activity in M. smegmatis . The katG UAR was also able to increase expression from the Mycobacterium paratuberculosis P AN promoter 15-fold in E. coli and 12-fold in M. smegmatis . An alternative promoter is active in deletion constructs in which either the UAR or the katG promoters identified here are absent. Expression from the katG promoter peaks during late exponential phase, and declines during stationary phase. The promoter is induced by ascorbic acid, and is repressed by oxygen limitation and growth at elevated temperatures. The promoter constructs exhibited similar activities in Mycobacterium bovis BCG as they did in M. smegmatis . Keywords: Mycobacterium tuberculosis , katG , promoter, regulation Abbreviations: ADC, albumin dextrose catalase; RLU, relative light units; tss, transcription start site; UAR, upstream activator region
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Steyn. Tel: +27 21 406 6363. Fax: +27 21 448 8153. e-mail: lsteyn{at}medmicro.uct.ac.za An Escherichia coli –mycobacterial shuttle vector, pJCluc, containing a luciferase reporter gene, was constructed and used to analyse the Mycobacterium tuberculosis katG promoter. A 1·9 kb region immediately upstream of katG promoted expression of the luciferase gene in E. coli and Mycobacterium smegmatis . A smaller promoter fragment (559 bp) promoted expression with equal efficiency, and was used in all further studies. Two transcription start sites were mapped by primer extension analysis to 47 and 56 bp upstream of the GTG initiation codon. Putative promoters associated with these show similarity to previously identified mycobacterial promoters. Deletions in the promoter fragment, introduced with BAL-31 nuclease and restriction endonucleases, revealed that a region between 559 and 448 bp upstream of the translation initiation codon, designated the upstream activator region (UAR), is essential for promoter activity in E. coli , and is required for optimal activity in M. smegmatis . The katG UAR was also able to increase expression from the Mycobacterium paratuberculosis P AN promoter 15-fold in E. coli and 12-fold in M. smegmatis . An alternative promoter is active in deletion constructs in which either the UAR or the katG promoters identified here are absent. Expression from the katG promoter peaks during late exponential phase, and declines during stationary phase. The promoter is induced by ascorbic acid, and is repressed by oxygen limitation and growth at elevated temperatures. The promoter constructs exhibited similar activities in Mycobacterium bovis BCG as they did in M. smegmatis . 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Steyn. Tel: +27 21 406 6363. Fax: +27 21 448 8153. e-mail: lsteyn{at}medmicro.uct.ac.za An Escherichia coli –mycobacterial shuttle vector, pJCluc, containing a luciferase reporter gene, was constructed and used to analyse the Mycobacterium tuberculosis katG promoter. A 1·9 kb region immediately upstream of katG promoted expression of the luciferase gene in E. coli and Mycobacterium smegmatis . A smaller promoter fragment (559 bp) promoted expression with equal efficiency, and was used in all further studies. Two transcription start sites were mapped by primer extension analysis to 47 and 56 bp upstream of the GTG initiation codon. Putative promoters associated with these show similarity to previously identified mycobacterial promoters. Deletions in the promoter fragment, introduced with BAL-31 nuclease and restriction endonucleases, revealed that a region between 559 and 448 bp upstream of the translation initiation codon, designated the upstream activator region (UAR), is essential for promoter activity in E. coli , and is required for optimal activity in M. smegmatis . The katG UAR was also able to increase expression from the Mycobacterium paratuberculosis P AN promoter 15-fold in E. coli and 12-fold in M. smegmatis . An alternative promoter is active in deletion constructs in which either the UAR or the katG promoters identified here are absent. Expression from the katG promoter peaks during late exponential phase, and declines during stationary phase. The promoter is induced by ascorbic acid, and is repressed by oxygen limitation and growth at elevated temperatures. The promoter constructs exhibited similar activities in Mycobacterium bovis BCG as they did in M. smegmatis . 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Psychology</topic><topic>Gene Deletion</topic><topic>Gene Expression Regulation, Bacterial</topic><topic>Genetic Vectors</topic><topic>Genetics</topic><topic>katG promoter</topic><topic>Microbiology</topic><topic>Molecular Sequence Data</topic><topic>Mycobacterium smegmatis</topic><topic>Mycobacterium smegmatis - enzymology</topic><topic>Mycobacterium smegmatis - genetics</topic><topic>Mycobacterium smegmatis - growth &amp; development</topic><topic>Mycobacterium tuberculosis</topic><topic>Mycobacterium tuberculosis - enzymology</topic><topic>Mycobacterium tuberculosis - genetics</topic><topic>Mycobacterium tuberculosis - growth &amp; development</topic><topic>Peroxidases - genetics</topic><topic>Peroxidases - metabolism</topic><topic>Polymerase Chain Reaction - methods</topic><topic>Promoter Regions, Genetic - genetics</topic><topic>RNA, Bacterial - analysis</topic><topic>RNA, Bacterial - isolation &amp; purification</topic><topic>Sequence Analysis, DNA</topic><topic>Transcription, Genetic</topic><topic>Transformation, Bacterial</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mulder, Michelle A</creatorcontrib><creatorcontrib>Zappe, Harold</creatorcontrib><creatorcontrib>Steyn, Lafras M</creatorcontrib><collection>Pascal-Francis</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>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><jtitle>Microbiology (Society for General Microbiology)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mulder, Michelle A</au><au>Zappe, Harold</au><au>Steyn, Lafras M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Mycobacterium tuberculosis katG promoter region contains a novel upstream activator</atitle><jtitle>Microbiology (Society for General Microbiology)</jtitle><addtitle>Microbiology</addtitle><date>1999-09-01</date><risdate>1999</risdate><volume>145</volume><issue>9</issue><spage>2507</spage><epage>2518</epage><pages>2507-2518</pages><issn>1350-0872</issn><eissn>1465-2080</eissn><abstract>Department of Medical Microbiology, University of Cape Town and Groote Schuur Hospital, Medical School, Observatory, 7925 Cape Town, South Africa 1 Author for correspondence: Lafras M. Steyn. Tel: +27 21 406 6363. Fax: +27 21 448 8153. e-mail: lsteyn{at}medmicro.uct.ac.za An Escherichia coli –mycobacterial shuttle vector, pJCluc, containing a luciferase reporter gene, was constructed and used to analyse the Mycobacterium tuberculosis katG promoter. A 1·9 kb region immediately upstream of katG promoted expression of the luciferase gene in E. coli and Mycobacterium smegmatis . A smaller promoter fragment (559 bp) promoted expression with equal efficiency, and was used in all further studies. Two transcription start sites were mapped by primer extension analysis to 47 and 56 bp upstream of the GTG initiation codon. Putative promoters associated with these show similarity to previously identified mycobacterial promoters. Deletions in the promoter fragment, introduced with BAL-31 nuclease and restriction endonucleases, revealed that a region between 559 and 448 bp upstream of the translation initiation codon, designated the upstream activator region (UAR), is essential for promoter activity in E. coli , and is required for optimal activity in M. smegmatis . The katG UAR was also able to increase expression from the Mycobacterium paratuberculosis P AN promoter 15-fold in E. coli and 12-fold in M. smegmatis . An alternative promoter is active in deletion constructs in which either the UAR or the katG promoters identified here are absent. Expression from the katG promoter peaks during late exponential phase, and declines during stationary phase. The promoter is induced by ascorbic acid, and is repressed by oxygen limitation and growth at elevated temperatures. The promoter constructs exhibited similar activities in Mycobacterium bovis BCG as they did in M. smegmatis . Keywords: Mycobacterium tuberculosis , katG , promoter, regulation Abbreviations: ADC, albumin dextrose catalase; RLU, relative light units; tss, transcription start site; UAR, upstream activator region</abstract><cop>Reading</cop><pub>Soc General Microbiol</pub><pmid>10517603</pmid><doi>10.1099/00221287-145-9-2507</doi><tpages>12</tpages></addata></record>
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source MEDLINE; PubMed Central
subjects Bacterial Proteins
Bacteriology
Base Sequence
Biological and medical sciences
DNA Primers
DNA, Bacterial - analysis
Escherichia coli
Escherichia coli - genetics
Fundamental and applied biological sciences. Psychology
Gene Deletion
Gene Expression Regulation, Bacterial
Genetic Vectors
Genetics
katG promoter
Microbiology
Molecular Sequence Data
Mycobacterium smegmatis
Mycobacterium smegmatis - enzymology
Mycobacterium smegmatis - genetics
Mycobacterium smegmatis - growth & development
Mycobacterium tuberculosis
Mycobacterium tuberculosis - enzymology
Mycobacterium tuberculosis - genetics
Mycobacterium tuberculosis - growth & development
Peroxidases - genetics
Peroxidases - metabolism
Polymerase Chain Reaction - methods
Promoter Regions, Genetic - genetics
RNA, Bacterial - analysis
RNA, Bacterial - isolation & purification
Sequence Analysis, DNA
Transcription, Genetic
Transformation, Bacterial
title The Mycobacterium tuberculosis katG promoter region contains a novel upstream activator
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