Sequence analysis of three Bacillus cereus loci carrying PlcR-regulated genes encoding degradative enzymes and enterotoxin

Biotechnology Centre of Oslo and School of Pharmacy, University of Oslo, PO Box 1123, N-0349 Oslo, Norway 1 Unité de Biochimie Microbienne, Centre National de la Recherche Scientifique URA 1300, Institut Pasteur, Paris, France 2 Unité de Biochimie Physiologique, Université Catholique de Louvain, Lou...

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Veröffentlicht in:Microbiology (Society for General Microbiology) 1999-11, Vol.145 (11), p.3129-3138
Hauptverfasser: Okstad, Ole A, Gominet, Myriam, Purnelle, Benedicte, Rose, Matthias, Lereclus, Didier, Kolsto, Anne-Brit
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container_end_page 3138
container_issue 11
container_start_page 3129
container_title Microbiology (Society for General Microbiology)
container_volume 145
creator Okstad, Ole A
Gominet, Myriam
Purnelle, Benedicte
Rose, Matthias
Lereclus, Didier
Kolsto, Anne-Brit
description Biotechnology Centre of Oslo and School of Pharmacy, University of Oslo, PO Box 1123, N-0349 Oslo, Norway 1 Unité de Biochimie Microbienne, Centre National de la Recherche Scientifique URA 1300, Institut Pasteur, Paris, France 2 Unité de Biochimie Physiologique, Université Catholique de Louvain, Louvain-la-Neuve, Belgium 3 Institut für Mikrobiologie, J. W. Göethe Universität, Frankfurt, Germany 4 Unité de Lutte Biologique, Institut National de la Recherche Agronomique, France 5 Author for correspondence: Anne-Brit Kolstø. Tel: +47 22 95 84 60. Fax: +47 22 69 41 30. e-mail: annebko{at}biotek.uio.no PlcR is a pleiotropic regulator of extracellular virulence factors in the opportunistic human pathogen Bacillus cereus and the entomopathogenic Bacillus thuringiensis , and is induced in cells entering stationary phase. Among the genes regulated by PlcR are: plcA , encoding phosphatidylinositol-specific phospholipase C (PI-PLC); plc , encoding phosphatidylcholine-preferring phospholipase C (PC-PLC); nhe , encoding the non-haemolytic enterotoxin; hbl , encoding haemolytic enterotoxin BL (HBL); and genes specifying a putativeS-layer like surface protein and a putative extracellular RNase. By analysing 37·1 kb of DNA sequence surrounding hbl , plcA and plcR , 28 ORFs were predicted. Three novel genes putatively regulated by PlcR and encoding a neutral protease (NprB), a subtilase family serine protease (Sfp) and a putative cell-wall hydrolase (Cwh) were identified. The corresponding sfp and cwh genes were located in the immediate upstream region of plcA and could both be regulated by a putative PlcR-binding site positioned between the inversely transcribed genes. Similarly, nprB was positioned directly upstream and transcribed in the opposite orientation to plcR . Genes surrounding plcA , plcR and hblCDAB that were lacking an upstream PlcR regulatory sequence did not appear to serve functions apparently related to PlcR and did not exhibit a conserved organization in Bacillus subtilis . View this table: [in this window] [in a new window]   Table 1. Genes surrounding the hbl , plcR and plcA loci   Keywords: PlcR regulator, HBL enterotoxin, virulence, Bacillus cereus Abbreviations: PC-PLC, phosphatidylcholine-preferring phospholipase C; PI-PLC, phosphatidylinositol-specific phospholipase C The EMBL accession numbers for the sequences reported in this paper are given in Table 1.
doi_str_mv 10.1099/00221287-145-11-3129
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W. Göethe Universität, Frankfurt, Germany 4 Unité de Lutte Biologique, Institut National de la Recherche Agronomique, France 5 Author for correspondence: Anne-Brit Kolstø. Tel: +47 22 95 84 60. Fax: +47 22 69 41 30. e-mail: annebko{at}biotek.uio.no PlcR is a pleiotropic regulator of extracellular virulence factors in the opportunistic human pathogen Bacillus cereus and the entomopathogenic Bacillus thuringiensis , and is induced in cells entering stationary phase. Among the genes regulated by PlcR are: plcA , encoding phosphatidylinositol-specific phospholipase C (PI-PLC); plc , encoding phosphatidylcholine-preferring phospholipase C (PC-PLC); nhe , encoding the non-haemolytic enterotoxin; hbl , encoding haemolytic enterotoxin BL (HBL); and genes specifying a putativeS-layer like surface protein and a putative extracellular RNase. By analysing 37·1 kb of DNA sequence surrounding hbl , plcA and plcR , 28 ORFs were predicted. Three novel genes putatively regulated by PlcR and encoding a neutral protease (NprB), a subtilase family serine protease (Sfp) and a putative cell-wall hydrolase (Cwh) were identified. The corresponding sfp and cwh genes were located in the immediate upstream region of plcA and could both be regulated by a putative PlcR-binding site positioned between the inversely transcribed genes. Similarly, nprB was positioned directly upstream and transcribed in the opposite orientation to plcR . Genes surrounding plcA , plcR and hblCDAB that were lacking an upstream PlcR regulatory sequence did not appear to serve functions apparently related to PlcR and did not exhibit a conserved organization in Bacillus subtilis . View this table: [in this window] [in a new window]   Table 1. Genes surrounding the hbl , plcR and plcA loci   Keywords: PlcR regulator, HBL enterotoxin, virulence, Bacillus cereus Abbreviations: PC-PLC, phosphatidylcholine-preferring phospholipase C; PI-PLC, phosphatidylinositol-specific phospholipase C The EMBL accession numbers for the sequences reported in this paper are given in Table 1.</description><identifier>ISSN: 1350-0872</identifier><identifier>EISSN: 1465-2080</identifier><identifier>DOI: 10.1099/00221287-145-11-3129</identifier><identifier>PMID: 10589720</identifier><language>eng</language><publisher>Reading: Soc General Microbiol</publisher><subject>Bacillus cereus ; Bacteriology ; Biological and medical sciences ; Fundamental and applied biological sciences. Psychology ; Genetics ; Life Sciences ; Microbiology ; Microbiology and Parasitology ; PlcR protein</subject><ispartof>Microbiology (Society for General Microbiology), 1999-11, Vol.145 (11), p.3129-3138</ispartof><rights>2000 INIST-CNRS</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0001-9047-9104</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=1209961$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.inrae.fr/hal-02693567$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Okstad, Ole A</creatorcontrib><creatorcontrib>Gominet, Myriam</creatorcontrib><creatorcontrib>Purnelle, Benedicte</creatorcontrib><creatorcontrib>Rose, Matthias</creatorcontrib><creatorcontrib>Lereclus, Didier</creatorcontrib><creatorcontrib>Kolsto, Anne-Brit</creatorcontrib><title>Sequence analysis of three Bacillus cereus loci carrying PlcR-regulated genes encoding degradative enzymes and enterotoxin</title><title>Microbiology (Society for General Microbiology)</title><description>Biotechnology Centre of Oslo and School of Pharmacy, University of Oslo, PO Box 1123, N-0349 Oslo, Norway 1 Unité de Biochimie Microbienne, Centre National de la Recherche Scientifique URA 1300, Institut Pasteur, Paris, France 2 Unité de Biochimie Physiologique, Université Catholique de Louvain, Louvain-la-Neuve, Belgium 3 Institut für Mikrobiologie, J. W. Göethe Universität, Frankfurt, Germany 4 Unité de Lutte Biologique, Institut National de la Recherche Agronomique, France 5 Author for correspondence: Anne-Brit Kolstø. Tel: +47 22 95 84 60. Fax: +47 22 69 41 30. e-mail: annebko{at}biotek.uio.no PlcR is a pleiotropic regulator of extracellular virulence factors in the opportunistic human pathogen Bacillus cereus and the entomopathogenic Bacillus thuringiensis , and is induced in cells entering stationary phase. Among the genes regulated by PlcR are: plcA , encoding phosphatidylinositol-specific phospholipase C (PI-PLC); plc , encoding phosphatidylcholine-preferring phospholipase C (PC-PLC); nhe , encoding the non-haemolytic enterotoxin; hbl , encoding haemolytic enterotoxin BL (HBL); and genes specifying a putativeS-layer like surface protein and a putative extracellular RNase. By analysing 37·1 kb of DNA sequence surrounding hbl , plcA and plcR , 28 ORFs were predicted. Three novel genes putatively regulated by PlcR and encoding a neutral protease (NprB), a subtilase family serine protease (Sfp) and a putative cell-wall hydrolase (Cwh) were identified. The corresponding sfp and cwh genes were located in the immediate upstream region of plcA and could both be regulated by a putative PlcR-binding site positioned between the inversely transcribed genes. Similarly, nprB was positioned directly upstream and transcribed in the opposite orientation to plcR . Genes surrounding plcA , plcR and hblCDAB that were lacking an upstream PlcR regulatory sequence did not appear to serve functions apparently related to PlcR and did not exhibit a conserved organization in Bacillus subtilis . View this table: [in this window] [in a new window]   Table 1. Genes surrounding the hbl , plcR and plcA loci   Keywords: PlcR regulator, HBL enterotoxin, virulence, Bacillus cereus Abbreviations: PC-PLC, phosphatidylcholine-preferring phospholipase C; PI-PLC, phosphatidylinositol-specific phospholipase C The EMBL accession numbers for the sequences reported in this paper are given in Table 1.</description><subject>Bacillus cereus</subject><subject>Bacteriology</subject><subject>Biological and medical sciences</subject><subject>Fundamental and applied biological sciences. 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Psychology</topic><topic>Genetics</topic><topic>Life Sciences</topic><topic>Microbiology</topic><topic>Microbiology and Parasitology</topic><topic>PlcR protein</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Okstad, Ole A</creatorcontrib><creatorcontrib>Gominet, Myriam</creatorcontrib><creatorcontrib>Purnelle, Benedicte</creatorcontrib><creatorcontrib>Rose, Matthias</creatorcontrib><creatorcontrib>Lereclus, Didier</creatorcontrib><creatorcontrib>Kolsto, Anne-Brit</creatorcontrib><collection>Pascal-Francis</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Microbiology (Society for General Microbiology)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Okstad, Ole A</au><au>Gominet, Myriam</au><au>Purnelle, Benedicte</au><au>Rose, Matthias</au><au>Lereclus, Didier</au><au>Kolsto, Anne-Brit</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sequence analysis of three Bacillus cereus loci carrying PlcR-regulated genes encoding degradative enzymes and enterotoxin</atitle><jtitle>Microbiology (Society for General Microbiology)</jtitle><date>1999-11-01</date><risdate>1999</risdate><volume>145</volume><issue>11</issue><spage>3129</spage><epage>3138</epage><pages>3129-3138</pages><issn>1350-0872</issn><eissn>1465-2080</eissn><abstract>Biotechnology Centre of Oslo and School of Pharmacy, University of Oslo, PO Box 1123, N-0349 Oslo, Norway 1 Unité de Biochimie Microbienne, Centre National de la Recherche Scientifique URA 1300, Institut Pasteur, Paris, France 2 Unité de Biochimie Physiologique, Université Catholique de Louvain, Louvain-la-Neuve, Belgium 3 Institut für Mikrobiologie, J. W. Göethe Universität, Frankfurt, Germany 4 Unité de Lutte Biologique, Institut National de la Recherche Agronomique, France 5 Author for correspondence: Anne-Brit Kolstø. Tel: +47 22 95 84 60. Fax: +47 22 69 41 30. e-mail: annebko{at}biotek.uio.no PlcR is a pleiotropic regulator of extracellular virulence factors in the opportunistic human pathogen Bacillus cereus and the entomopathogenic Bacillus thuringiensis , and is induced in cells entering stationary phase. Among the genes regulated by PlcR are: plcA , encoding phosphatidylinositol-specific phospholipase C (PI-PLC); plc , encoding phosphatidylcholine-preferring phospholipase C (PC-PLC); nhe , encoding the non-haemolytic enterotoxin; hbl , encoding haemolytic enterotoxin BL (HBL); and genes specifying a putativeS-layer like surface protein and a putative extracellular RNase. By analysing 37·1 kb of DNA sequence surrounding hbl , plcA and plcR , 28 ORFs were predicted. Three novel genes putatively regulated by PlcR and encoding a neutral protease (NprB), a subtilase family serine protease (Sfp) and a putative cell-wall hydrolase (Cwh) were identified. The corresponding sfp and cwh genes were located in the immediate upstream region of plcA and could both be regulated by a putative PlcR-binding site positioned between the inversely transcribed genes. Similarly, nprB was positioned directly upstream and transcribed in the opposite orientation to plcR . Genes surrounding plcA , plcR and hblCDAB that were lacking an upstream PlcR regulatory sequence did not appear to serve functions apparently related to PlcR and did not exhibit a conserved organization in Bacillus subtilis . View this table: [in this window] [in a new window]   Table 1. Genes surrounding the hbl , plcR and plcA loci   Keywords: PlcR regulator, HBL enterotoxin, virulence, Bacillus cereus Abbreviations: PC-PLC, phosphatidylcholine-preferring phospholipase C; PI-PLC, phosphatidylinositol-specific phospholipase C The EMBL accession numbers for the sequences reported in this paper are given in Table 1.</abstract><cop>Reading</cop><pub>Soc General Microbiol</pub><pmid>10589720</pmid><doi>10.1099/00221287-145-11-3129</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0001-9047-9104</orcidid></addata></record>
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subjects Bacillus cereus
Bacteriology
Biological and medical sciences
Fundamental and applied biological sciences. Psychology
Genetics
Life Sciences
Microbiology
Microbiology and Parasitology
PlcR protein
title Sequence analysis of three Bacillus cereus loci carrying PlcR-regulated genes encoding degradative enzymes and enterotoxin
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