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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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 |
doi_str_mv | 10.1099/00221287-145-9-2507 |
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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</description><identifier>ISSN: 1350-0872</identifier><identifier>EISSN: 1465-2080</identifier><identifier>DOI: 10.1099/00221287-145-9-2507</identifier><identifier>PMID: 10517603</identifier><language>eng</language><publisher>Reading: Soc General Microbiol</publisher><subject>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</subject><ispartof>Microbiology (Society for General Microbiology), 1999-09, Vol.145 (9), p.2507-2518</ispartof><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c395t-48de1890cf8ab633c0e89dc43efacff093a26d3d012ea20e969d3e35ecc86c233</citedby><cites>FETCH-LOGICAL-c395t-48de1890cf8ab633c0e89dc43efacff093a26d3d012ea20e969d3e35ecc86c233</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1980349$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10517603$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mulder, Michelle A</creatorcontrib><creatorcontrib>Zappe, Harold</creatorcontrib><creatorcontrib>Steyn, Lafras M</creatorcontrib><title>The Mycobacterium tuberculosis katG promoter region contains a novel upstream activator</title><title>Microbiology (Society for General Microbiology)</title><addtitle>Microbiology</addtitle><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</description><subject>Bacterial Proteins</subject><subject>Bacteriology</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>DNA Primers</subject><subject>DNA, Bacterial - analysis</subject><subject>Escherichia coli</subject><subject>Escherichia coli - genetics</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Deletion</subject><subject>Gene Expression Regulation, Bacterial</subject><subject>Genetic Vectors</subject><subject>Genetics</subject><subject>katG promoter</subject><subject>Microbiology</subject><subject>Molecular Sequence Data</subject><subject>Mycobacterium smegmatis</subject><subject>Mycobacterium smegmatis - enzymology</subject><subject>Mycobacterium smegmatis - genetics</subject><subject>Mycobacterium smegmatis - growth & development</subject><subject>Mycobacterium tuberculosis</subject><subject>Mycobacterium tuberculosis - enzymology</subject><subject>Mycobacterium tuberculosis - genetics</subject><subject>Mycobacterium tuberculosis - growth & development</subject><subject>Peroxidases - genetics</subject><subject>Peroxidases - metabolism</subject><subject>Polymerase Chain Reaction - methods</subject><subject>Promoter Regions, Genetic - genetics</subject><subject>RNA, Bacterial - analysis</subject><subject>RNA, Bacterial - isolation & purification</subject><subject>Sequence Analysis, DNA</subject><subject>Transcription, Genetic</subject><subject>Transformation, Bacterial</subject><issn>1350-0872</issn><issn>1465-2080</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMFu1DAQhi0EoqXwBEjIB4TEIXRsx4l9RFUpSK24tOJoOZPJriGJFztp1bfHq11Eb5w80nzz-9fH2FsBnwRYew4gpZCmrUStK1tJDe0zdirqRlcSDDwvs9JQgWnlCXuV80-AsgTxkp0I0KJtQJ2yH7db4jePGDuPC6WwTnxZO0q4jjGHzH_55YrvUpxi2fJEmxBnjnFefJgz93yO9zTydZeXRH7iJSTc-yWm1-zF4MdMb47vGbv7cnl78bW6_n717eLzdYXK6qWqTU_CWMDB-K5RCoGM7bFWNHgcBrDKy6ZXPQhJXgLZxvaKlCZE06BU6ox9OOSWjr9XyoubQkYaRz9TXLNrwSipTf1fULS11cruQXUAMcWcEw1ul8Lk06MT4Pbi3V_xroh31u3Fl6t3x_i1m6h_cnMwXYD3R8Bn9OOQ_Iwh_-OsAVXbgn08YNuw2T6ERG5D8xRKly7EUhmf_PkHIReaeA</recordid><startdate>19990901</startdate><enddate>19990901</enddate><creator>Mulder, Michelle A</creator><creator>Zappe, Harold</creator><creator>Steyn, Lafras M</creator><general>Soc General Microbiol</general><general>Society for General Microbiology</general><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>C1K</scope><scope>7X8</scope></search><sort><creationdate>19990901</creationdate><title>The Mycobacterium tuberculosis katG promoter region contains a novel upstream activator</title><author>Mulder, Michelle A ; Zappe, Harold ; Steyn, Lafras M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c395t-48de1890cf8ab633c0e89dc43efacff093a26d3d012ea20e969d3e35ecc86c233</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Bacterial Proteins</topic><topic>Bacteriology</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>DNA Primers</topic><topic>DNA, Bacterial - analysis</topic><topic>Escherichia coli</topic><topic>Escherichia coli - genetics</topic><topic>Fundamental and applied biological sciences. 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 & development</topic><topic>Mycobacterium tuberculosis</topic><topic>Mycobacterium tuberculosis - enzymology</topic><topic>Mycobacterium tuberculosis - genetics</topic><topic>Mycobacterium tuberculosis - growth & 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 & 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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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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