Proposed pathway for the biosynthesis of serovar-specific glycopeptidolipids in Mycobacterium avium serovar 2
Mycobacteria Research Laboratories, Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, CO 80523-1682, USA Correspondence Julia M. Inamine jinamine{at}colostate.edu Members of the Mycobacterium avium complex are distinguished by the presence of highly antig...
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creator | Eckstein, Torsten M Belisle, John T Inamine, Julia M |
description | Mycobacteria Research Laboratories, Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, CO 80523-1682, USA
Correspondence Julia M. Inamine jinamine{at}colostate.edu
Members of the Mycobacterium avium complex are distinguished by the presence of highly antigenic surface molecules called glycopeptidolipids (GPLs) and the oligosaccharide portion of the serovar-specific GPL defines the 28 serovars. Previously, the genomic region ( ser2 ) encoding the enzymes responsible for the glycosylation of the lipopeptide core to generate the serovar-2-specific GPLs has been described. In this work, the ser2 gene clusters of M. avium serovar 2 strains 2151 and TMC 724 were fully sequenced and compared to the homologous regions of M. avium serovar 1 strain 104, M. avium subsp. paratuberculosis and M. avium subsp. silvaticum . It was also determined that 104Rg, a mutant of strain 104 that produces truncated GPLs, lost several GPL biosynthesis genes by deletion. This comparison, together with analysis of protein similarities, supports a biosynthetic model in which serovar-2-specific GPLs are synthesized from a serovar-1-specific GPL intermediate that is derived from a non-specific GPL precursor. We also identified a gene encoding an enzyme that is necessary for the biosynthesis of serovar-3- and 9-specific GPLs, but not serovar-2-specific GPLs, suggesting that the different serovars may have evolved from the acquisition or loss of genetic information. In addition, a subcluster of genes for the biosynthesis and transfer of fucose, which are needed to make serovar-specific GPLs such as those of serovar 2, is found in the non-GPL-producing M. avium subspecies paratuberculosis and silvaticum .
Abbreviations: 6-dTal, 6-deoxytalose; Fuc, fucose; GPLs, glycopeptidolipids; MAC, Mycobacterium avium complex; Me, methyl; nsGPLs, non-specific glycopeptidolipids; Rha, rhamnose; ssGPLs, serovar-specific glycopeptidolipids
The GenBank/EMBL/DDBJ accession numbers for the sequences reported in this paper are AF125999 and AF143772 . |
doi_str_mv | 10.1099/mic.0.26528-0 |
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Correspondence Julia M. Inamine jinamine{at}colostate.edu
Members of the Mycobacterium avium complex are distinguished by the presence of highly antigenic surface molecules called glycopeptidolipids (GPLs) and the oligosaccharide portion of the serovar-specific GPL defines the 28 serovars. Previously, the genomic region ( ser2 ) encoding the enzymes responsible for the glycosylation of the lipopeptide core to generate the serovar-2-specific GPLs has been described. In this work, the ser2 gene clusters of M. avium serovar 2 strains 2151 and TMC 724 were fully sequenced and compared to the homologous regions of M. avium serovar 1 strain 104, M. avium subsp. paratuberculosis and M. avium subsp. silvaticum . It was also determined that 104Rg, a mutant of strain 104 that produces truncated GPLs, lost several GPL biosynthesis genes by deletion. This comparison, together with analysis of protein similarities, supports a biosynthetic model in which serovar-2-specific GPLs are synthesized from a serovar-1-specific GPL intermediate that is derived from a non-specific GPL precursor. We also identified a gene encoding an enzyme that is necessary for the biosynthesis of serovar-3- and 9-specific GPLs, but not serovar-2-specific GPLs, suggesting that the different serovars may have evolved from the acquisition or loss of genetic information. In addition, a subcluster of genes for the biosynthesis and transfer of fucose, which are needed to make serovar-specific GPLs such as those of serovar 2, is found in the non-GPL-producing M. avium subspecies paratuberculosis and silvaticum .
Abbreviations: 6-dTal, 6-deoxytalose; Fuc, fucose; GPLs, glycopeptidolipids; MAC, Mycobacterium avium complex; Me, methyl; nsGPLs, non-specific glycopeptidolipids; Rha, rhamnose; ssGPLs, serovar-specific glycopeptidolipids
The GenBank/EMBL/DDBJ accession numbers for the sequences reported in this paper are AF125999 and AF143772 .</description><identifier>ISSN: 1350-0872</identifier><identifier>EISSN: 1465-2080</identifier><identifier>DOI: 10.1099/mic.0.26528-0</identifier><identifier>PMID: 14523113</identifier><language>eng</language><publisher>Reading: Soc General Microbiol</publisher><subject>Amino Acid Motifs ; Amino Acid Sequence ; Bacteriology ; Biological and medical sciences ; fucose ; Fucose - metabolism ; Fundamental and applied biological sciences. Psychology ; Glucosyltransferases - genetics ; Glycolipids - biosynthesis ; Glycopeptides - biosynthesis ; glycopeptidolipids ; Metabolism. Enzymes ; Microbiology ; Molecular Sequence Data ; Multigene Family ; Mycobacterium avium ; Mycobacterium avium - genetics ; Mycobacterium avium - metabolism</subject><ispartof>Microbiology (Society for General Microbiology), 2003-10, Vol.149 (10), p.2797-2807</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c422t-baded922b5baf590e5d41ec7311e3a81fb9b1a58d8c86fd921b9b8058c88758c3</citedby><cites>FETCH-LOGICAL-c422t-baded922b5baf590e5d41ec7311e3a81fb9b1a58d8c86fd921b9b8058c88758c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15734472$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14523113$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Eckstein, Torsten M</creatorcontrib><creatorcontrib>Belisle, John T</creatorcontrib><creatorcontrib>Inamine, Julia M</creatorcontrib><title>Proposed pathway for the biosynthesis of serovar-specific glycopeptidolipids in Mycobacterium avium serovar 2</title><title>Microbiology (Society for General Microbiology)</title><addtitle>Microbiology</addtitle><description>Mycobacteria Research Laboratories, Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, CO 80523-1682, USA
Correspondence Julia M. Inamine jinamine{at}colostate.edu
Members of the Mycobacterium avium complex are distinguished by the presence of highly antigenic surface molecules called glycopeptidolipids (GPLs) and the oligosaccharide portion of the serovar-specific GPL defines the 28 serovars. Previously, the genomic region ( ser2 ) encoding the enzymes responsible for the glycosylation of the lipopeptide core to generate the serovar-2-specific GPLs has been described. In this work, the ser2 gene clusters of M. avium serovar 2 strains 2151 and TMC 724 were fully sequenced and compared to the homologous regions of M. avium serovar 1 strain 104, M. avium subsp. paratuberculosis and M. avium subsp. silvaticum . It was also determined that 104Rg, a mutant of strain 104 that produces truncated GPLs, lost several GPL biosynthesis genes by deletion. This comparison, together with analysis of protein similarities, supports a biosynthetic model in which serovar-2-specific GPLs are synthesized from a serovar-1-specific GPL intermediate that is derived from a non-specific GPL precursor. We also identified a gene encoding an enzyme that is necessary for the biosynthesis of serovar-3- and 9-specific GPLs, but not serovar-2-specific GPLs, suggesting that the different serovars may have evolved from the acquisition or loss of genetic information. In addition, a subcluster of genes for the biosynthesis and transfer of fucose, which are needed to make serovar-specific GPLs such as those of serovar 2, is found in the non-GPL-producing M. avium subspecies paratuberculosis and silvaticum .
Abbreviations: 6-dTal, 6-deoxytalose; Fuc, fucose; GPLs, glycopeptidolipids; MAC, Mycobacterium avium complex; Me, methyl; nsGPLs, non-specific glycopeptidolipids; Rha, rhamnose; ssGPLs, serovar-specific glycopeptidolipids
The GenBank/EMBL/DDBJ accession numbers for the sequences reported in this paper are AF125999 and AF143772 .</description><subject>Amino Acid Motifs</subject><subject>Amino Acid Sequence</subject><subject>Bacteriology</subject><subject>Biological and medical sciences</subject><subject>fucose</subject><subject>Fucose - metabolism</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Glucosyltransferases - genetics</subject><subject>Glycolipids - biosynthesis</subject><subject>Glycopeptides - biosynthesis</subject><subject>glycopeptidolipids</subject><subject>Metabolism. Enzymes</subject><subject>Microbiology</subject><subject>Molecular Sequence Data</subject><subject>Multigene Family</subject><subject>Mycobacterium avium</subject><subject>Mycobacterium avium - genetics</subject><subject>Mycobacterium avium - metabolism</subject><issn>1350-0872</issn><issn>1465-2080</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU2P1DAMhiMEYj_gyBXlAgekDknatOkRrRYWaREc4BylqTMT1DYl7uxq_j0uU2mPXBzHefzaysvYGyl2UrTtxzH6ndipWitTiGfsUla1LpQw4jnlpRaFMI26YFeIv4WgRyFfsgtZaVVKWV6y8UdOc0Lo-eyWw6M78ZAyXw7Au5jwNFGGEXkKHCGnB5cLnMHHED3fDyefZpiX2KchzrFHHif-jYqd8wvkeBy5e1jj1srVK_YiuAHh9XZes1-fb3_e3BX33798vfl0X_hKqaXoXA99q1SnOxd0K0D3lQTf0MpQOiND13bSadMbb-pApKSCEZqupqFYXrP3Z905pz9HwMWOET0Mg5sgHdE2mrTqqv4vKFvZaCkFgcUZ9DkhZgh2znF0-WSlsKsR1OitsP-MsCv_dhM-diP0T_T28wS82wCH3g0hu8lHfOJow6pqFHEfztwh7g-PMYPdw0SzciKD1qGyatcdVNM25V__06Ha</recordid><startdate>20031001</startdate><enddate>20031001</enddate><creator>Eckstein, Torsten M</creator><creator>Belisle, John T</creator><creator>Inamine, Julia 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>20031001</creationdate><title>Proposed pathway for the biosynthesis of serovar-specific glycopeptidolipids in Mycobacterium avium serovar 2</title><author>Eckstein, Torsten M ; Belisle, John T ; Inamine, Julia M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c422t-baded922b5baf590e5d41ec7311e3a81fb9b1a58d8c86fd921b9b8058c88758c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Amino Acid Motifs</topic><topic>Amino Acid Sequence</topic><topic>Bacteriology</topic><topic>Biological and medical sciences</topic><topic>fucose</topic><topic>Fucose - metabolism</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Glucosyltransferases - genetics</topic><topic>Glycolipids - biosynthesis</topic><topic>Glycopeptides - biosynthesis</topic><topic>glycopeptidolipids</topic><topic>Metabolism. Enzymes</topic><topic>Microbiology</topic><topic>Molecular Sequence Data</topic><topic>Multigene Family</topic><topic>Mycobacterium avium</topic><topic>Mycobacterium avium - genetics</topic><topic>Mycobacterium avium - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Eckstein, Torsten M</creatorcontrib><creatorcontrib>Belisle, John T</creatorcontrib><creatorcontrib>Inamine, Julia 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>Eckstein, Torsten M</au><au>Belisle, John T</au><au>Inamine, Julia M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Proposed pathway for the biosynthesis of serovar-specific glycopeptidolipids in Mycobacterium avium serovar 2</atitle><jtitle>Microbiology (Society for General Microbiology)</jtitle><addtitle>Microbiology</addtitle><date>2003-10-01</date><risdate>2003</risdate><volume>149</volume><issue>10</issue><spage>2797</spage><epage>2807</epage><pages>2797-2807</pages><issn>1350-0872</issn><eissn>1465-2080</eissn><abstract>Mycobacteria Research Laboratories, Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, CO 80523-1682, USA
Correspondence Julia M. Inamine jinamine{at}colostate.edu
Members of the Mycobacterium avium complex are distinguished by the presence of highly antigenic surface molecules called glycopeptidolipids (GPLs) and the oligosaccharide portion of the serovar-specific GPL defines the 28 serovars. Previously, the genomic region ( ser2 ) encoding the enzymes responsible for the glycosylation of the lipopeptide core to generate the serovar-2-specific GPLs has been described. In this work, the ser2 gene clusters of M. avium serovar 2 strains 2151 and TMC 724 were fully sequenced and compared to the homologous regions of M. avium serovar 1 strain 104, M. avium subsp. paratuberculosis and M. avium subsp. silvaticum . It was also determined that 104Rg, a mutant of strain 104 that produces truncated GPLs, lost several GPL biosynthesis genes by deletion. This comparison, together with analysis of protein similarities, supports a biosynthetic model in which serovar-2-specific GPLs are synthesized from a serovar-1-specific GPL intermediate that is derived from a non-specific GPL precursor. We also identified a gene encoding an enzyme that is necessary for the biosynthesis of serovar-3- and 9-specific GPLs, but not serovar-2-specific GPLs, suggesting that the different serovars may have evolved from the acquisition or loss of genetic information. In addition, a subcluster of genes for the biosynthesis and transfer of fucose, which are needed to make serovar-specific GPLs such as those of serovar 2, is found in the non-GPL-producing M. avium subspecies paratuberculosis and silvaticum .
Abbreviations: 6-dTal, 6-deoxytalose; Fuc, fucose; GPLs, glycopeptidolipids; MAC, Mycobacterium avium complex; Me, methyl; nsGPLs, non-specific glycopeptidolipids; Rha, rhamnose; ssGPLs, serovar-specific glycopeptidolipids
The GenBank/EMBL/DDBJ accession numbers for the sequences reported in this paper are AF125999 and AF143772 .</abstract><cop>Reading</cop><pub>Soc General Microbiol</pub><pmid>14523113</pmid><doi>10.1099/mic.0.26528-0</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Amino Acid Motifs Amino Acid Sequence Bacteriology Biological and medical sciences fucose Fucose - metabolism Fundamental and applied biological sciences. Psychology Glucosyltransferases - genetics Glycolipids - biosynthesis Glycopeptides - biosynthesis glycopeptidolipids Metabolism. Enzymes Microbiology Molecular Sequence Data Multigene Family Mycobacterium avium Mycobacterium avium - genetics Mycobacterium avium - metabolism |
title | Proposed pathway for the biosynthesis of serovar-specific glycopeptidolipids in Mycobacterium avium serovar 2 |
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