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Structural features of lipoarabinomannan from Mycobacterium bovis BCG. Determination of molecular mass by laser desorption mass spectrometry
It was recently shown that mycobacterial lipoarabinomannan (LAM) can be classified into two types (Chatterjee, D., Lowell, K., Rivoire B., McNeil M. R., and Brennan, P. J. (1992) J. Biol. Chem. 267, 6234-6239) according to the presence or absence of mannosyl residues (Manp) located at the nonreducin...
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Published in: | The Journal of biological chemistry 1993-06, Vol.268 (17), p.12401-12411 |
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description | It was recently shown that mycobacterial lipoarabinomannan (LAM) can be classified into two types (Chatterjee, D., Lowell,
K., Rivoire B., McNeil M. R., and Brennan, P. J. (1992) J. Biol. Chem. 267, 6234-6239) according to the presence or absence
of mannosyl residues (Manp) located at the nonreducing end of the oligoarabinosyl side chains. These two types of LAM were
found in a pathogenic Mycobacterium tuberculosis strain and in an avirulent M. tuberculosis strain, respectively, suggesting
that LAM with Manp characterizes virulent and "disease-inducing strains." We now report the structure of the LAM from Mycobacterium
bovis Bacille Calmette-Guérin (BCG) strain Pasteur, largely used throughout the world as vaccine against tuberculosis. Using
an up-to-date analytical approach, we found that the LAM of M. bovis BCG belongs to the class of LAMs capped with Manp. By
means of two-dimensional homonuclear and heteronuclear scalar coupling NMR analysis and methylation data, the sugar spin system
assignments were partially established, revealing that the LAM contained two types of terminal Manp and 2-O-linked Manp. From
the following four-step process: (i) partial hydrolysis of deacylated LAM (dLAM), (ii) oligosaccharide derivatization with
aminobenzoic ethyl ester, (iii) HPLC purification, (iv) FAB/MS-MS analysis; it was shown that the dimannosyl unit alpha-D-Manp-(1-->2)-alpha-D-Manp
is the major residue capping the termini of the arabinan of the LAM. In this report, LAM molecular mass determination was
established using matrix-assisted UV-laser desorption/ionization mass spectrometry which reveals that the LAM molecular mass
is around 17.4 kDa. The similarity of the LAM structures between M. bovis BCG and M. tuberculosis H37Rv is discussed in regard
to their function in the immunopathology of mycobacterial infection. |
doi_str_mv | 10.1016/s0021-9258(18)31404-2 |
format | article |
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K., Rivoire B., McNeil M. R., and Brennan, P. J. (1992) J. Biol. Chem. 267, 6234-6239) according to the presence or absence
of mannosyl residues (Manp) located at the nonreducing end of the oligoarabinosyl side chains. These two types of LAM were
found in a pathogenic Mycobacterium tuberculosis strain and in an avirulent M. tuberculosis strain, respectively, suggesting
that LAM with Manp characterizes virulent and "disease-inducing strains." We now report the structure of the LAM from Mycobacterium
bovis Bacille Calmette-Guérin (BCG) strain Pasteur, largely used throughout the world as vaccine against tuberculosis. Using
an up-to-date analytical approach, we found that the LAM of M. bovis BCG belongs to the class of LAMs capped with Manp. By
means of two-dimensional homonuclear and heteronuclear scalar coupling NMR analysis and methylation data, the sugar spin system
assignments were partially established, revealing that the LAM contained two types of terminal Manp and 2-O-linked Manp. From
the following four-step process: (i) partial hydrolysis of deacylated LAM (dLAM), (ii) oligosaccharide derivatization with
aminobenzoic ethyl ester, (iii) HPLC purification, (iv) FAB/MS-MS analysis; it was shown that the dimannosyl unit alpha-D-Manp-(1-->2)-alpha-D-Manp
is the major residue capping the termini of the arabinan of the LAM. In this report, LAM molecular mass determination was
established using matrix-assisted UV-laser desorption/ionization mass spectrometry which reveals that the LAM molecular mass
is around 17.4 kDa. The similarity of the LAM structures between M. bovis BCG and M. tuberculosis H37Rv is discussed in regard
to their function in the immunopathology of mycobacterial infection.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1016/s0021-9258(18)31404-2</identifier><identifier>PMID: 8509380</identifier><identifier>CODEN: JBCHA3</identifier><language>eng</language><publisher>Bethesda, MD: American Society for Biochemistry and Molecular Biology</publisher><subject>Analytical, structural and metabolic biochemistry ; Antigens, Bacterial - chemistry ; Bacteriology ; Biochemistry ; Biochemistry, Molecular Biology ; Biological and medical sciences ; Carbohydrate Conformation ; Carbohydrate Sequence ; Carbohydrates ; Fundamental and applied biological sciences. Psychology ; Life Sciences ; Lipopolysaccharides - chemistry ; Lipopolysaccharides - isolation & purification ; Magnetic Resonance Spectroscopy ; Methylation ; Microbiology and Parasitology ; Miscellaneous ; Molecular Sequence Data ; Molecular Weight ; Mycobacterium bovis ; Mycobacterium bovis - chemistry ; Mycobacterium tuberculosis ; Mycobacterium tuberculosis - chemistry ; Oligosaccharides - chemistry ; Oligosaccharides - isolation & purification ; Other biological molecules ; Spectrometry, Mass, Fast Atom Bombardment</subject><ispartof>The Journal of biological chemistry, 1993-06, Vol.268 (17), p.12401-12411</ispartof><rights>1993 INIST-CNRS</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c540t-2fd6cd6609f80f1954be3411609d8eb80809c3630fb45819a7f35ea4aec1ef993</citedby><orcidid>0000-0001-9013-8430 ; 0000-0002-2581-3302</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,777,781,882,27905,27906</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4820553$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8509380$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-03177445$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>VENISSE, A</creatorcontrib><creatorcontrib>BERJEAUD, J.-M</creatorcontrib><creatorcontrib>CHAURAND, P</creatorcontrib><creatorcontrib>GILLERON, M</creatorcontrib><creatorcontrib>PUZO, G</creatorcontrib><title>Structural features of lipoarabinomannan from Mycobacterium bovis BCG. Determination of molecular mass by laser desorption mass spectrometry</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><description>It was recently shown that mycobacterial lipoarabinomannan (LAM) can be classified into two types (Chatterjee, D., Lowell,
K., Rivoire B., McNeil M. R., and Brennan, P. J. (1992) J. Biol. Chem. 267, 6234-6239) according to the presence or absence
of mannosyl residues (Manp) located at the nonreducing end of the oligoarabinosyl side chains. These two types of LAM were
found in a pathogenic Mycobacterium tuberculosis strain and in an avirulent M. tuberculosis strain, respectively, suggesting
that LAM with Manp characterizes virulent and "disease-inducing strains." We now report the structure of the LAM from Mycobacterium
bovis Bacille Calmette-Guérin (BCG) strain Pasteur, largely used throughout the world as vaccine against tuberculosis. Using
an up-to-date analytical approach, we found that the LAM of M. bovis BCG belongs to the class of LAMs capped with Manp. By
means of two-dimensional homonuclear and heteronuclear scalar coupling NMR analysis and methylation data, the sugar spin system
assignments were partially established, revealing that the LAM contained two types of terminal Manp and 2-O-linked Manp. From
the following four-step process: (i) partial hydrolysis of deacylated LAM (dLAM), (ii) oligosaccharide derivatization with
aminobenzoic ethyl ester, (iii) HPLC purification, (iv) FAB/MS-MS analysis; it was shown that the dimannosyl unit alpha-D-Manp-(1-->2)-alpha-D-Manp
is the major residue capping the termini of the arabinan of the LAM. In this report, LAM molecular mass determination was
established using matrix-assisted UV-laser desorption/ionization mass spectrometry which reveals that the LAM molecular mass
is around 17.4 kDa. The similarity of the LAM structures between M. bovis BCG and M. tuberculosis H37Rv is discussed in regard
to their function in the immunopathology of mycobacterial infection.</description><subject>Analytical, structural and metabolic biochemistry</subject><subject>Antigens, Bacterial - chemistry</subject><subject>Bacteriology</subject><subject>Biochemistry</subject><subject>Biochemistry, Molecular Biology</subject><subject>Biological and medical sciences</subject><subject>Carbohydrate Conformation</subject><subject>Carbohydrate Sequence</subject><subject>Carbohydrates</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Life Sciences</subject><subject>Lipopolysaccharides - chemistry</subject><subject>Lipopolysaccharides - isolation & purification</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>Methylation</subject><subject>Microbiology and Parasitology</subject><subject>Miscellaneous</subject><subject>Molecular Sequence Data</subject><subject>Molecular Weight</subject><subject>Mycobacterium bovis</subject><subject>Mycobacterium bovis - chemistry</subject><subject>Mycobacterium tuberculosis</subject><subject>Mycobacterium tuberculosis - chemistry</subject><subject>Oligosaccharides - chemistry</subject><subject>Oligosaccharides - isolation & purification</subject><subject>Other biological molecules</subject><subject>Spectrometry, Mass, Fast Atom Bombardment</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><recordid>eNqFkUFv1DAQhSMEKtvCT6jkA0L0kOKJ7cQ5tktpkRZxKEjcrIl3zBol8WInRfsf-NEku6vliC-23vtmnqWXZZfAr4FD-T5xXkBeF0q_A30lQHKZF8-yBXAtcqHg-_NscUJeZucp_eTTkTWcZWda8Vpovsj-PA5xtMMYsWWOcHpQYsGx1m8DRmx8Hzrse-yZi6Fjn3c2NGgHin7sWBOefGK3y_tr9oEmrfM9Dj7084IutGTHFiPrMCXW7FiLiSJbUwpxu6f2RtqSHabVNMTdq-yFwzbR6-N9kX37ePd1-ZCvvtx_Wt6scqskH_LCrUu7LkteO80d1Eo2JCTAJKw1NZprXltRCu4aqTTUWDmhCCWSBXJ1LS6yq8PeDbZmG32HcWcCevNwszKzxgVUlZTqCSb27YHdxvBrpDSYzidLbYs9hTGZSlW6EpX8LwilKrXap6sDaGNIKZI7fQG4mas1j3NvZu7NgDb7ak0xzV0eA8amo_Vp6tjl5L85-pgsti5ib306YVIXXCnxD9v4H5vfPpJpfLAb6kxRTnmVgUJyEH8BNV-5uA</recordid><startdate>19930615</startdate><enddate>19930615</enddate><creator>VENISSE, A</creator><creator>BERJEAUD, J.-M</creator><creator>CHAURAND, P</creator><creator>GILLERON, M</creator><creator>PUZO, G</creator><general>American Society for Biochemistry and Molecular Biology</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><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0001-9013-8430</orcidid><orcidid>https://orcid.org/0000-0002-2581-3302</orcidid></search><sort><creationdate>19930615</creationdate><title>Structural features of lipoarabinomannan from Mycobacterium bovis BCG. Determination of molecular mass by laser desorption mass spectrometry</title><author>VENISSE, A ; BERJEAUD, J.-M ; CHAURAND, P ; GILLERON, M ; PUZO, G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c540t-2fd6cd6609f80f1954be3411609d8eb80809c3630fb45819a7f35ea4aec1ef993</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>Analytical, structural and metabolic biochemistry</topic><topic>Antigens, Bacterial - chemistry</topic><topic>Bacteriology</topic><topic>Biochemistry</topic><topic>Biochemistry, Molecular Biology</topic><topic>Biological and medical sciences</topic><topic>Carbohydrate Conformation</topic><topic>Carbohydrate Sequence</topic><topic>Carbohydrates</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Life Sciences</topic><topic>Lipopolysaccharides - chemistry</topic><topic>Lipopolysaccharides - isolation & purification</topic><topic>Magnetic Resonance Spectroscopy</topic><topic>Methylation</topic><topic>Microbiology and Parasitology</topic><topic>Miscellaneous</topic><topic>Molecular Sequence Data</topic><topic>Molecular Weight</topic><topic>Mycobacterium bovis</topic><topic>Mycobacterium bovis - chemistry</topic><topic>Mycobacterium tuberculosis</topic><topic>Mycobacterium tuberculosis - chemistry</topic><topic>Oligosaccharides - chemistry</topic><topic>Oligosaccharides - isolation & purification</topic><topic>Other biological molecules</topic><topic>Spectrometry, Mass, Fast Atom Bombardment</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>VENISSE, A</creatorcontrib><creatorcontrib>BERJEAUD, J.-M</creatorcontrib><creatorcontrib>CHAURAND, P</creatorcontrib><creatorcontrib>GILLERON, M</creatorcontrib><creatorcontrib>PUZO, G</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><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>VENISSE, A</au><au>BERJEAUD, J.-M</au><au>CHAURAND, P</au><au>GILLERON, M</au><au>PUZO, G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Structural features of lipoarabinomannan from Mycobacterium bovis BCG. Determination of molecular mass by laser desorption mass spectrometry</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>1993-06-15</date><risdate>1993</risdate><volume>268</volume><issue>17</issue><spage>12401</spage><epage>12411</epage><pages>12401-12411</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><coden>JBCHA3</coden><abstract>It was recently shown that mycobacterial lipoarabinomannan (LAM) can be classified into two types (Chatterjee, D., Lowell,
K., Rivoire B., McNeil M. R., and Brennan, P. J. (1992) J. Biol. Chem. 267, 6234-6239) according to the presence or absence
of mannosyl residues (Manp) located at the nonreducing end of the oligoarabinosyl side chains. These two types of LAM were
found in a pathogenic Mycobacterium tuberculosis strain and in an avirulent M. tuberculosis strain, respectively, suggesting
that LAM with Manp characterizes virulent and "disease-inducing strains." We now report the structure of the LAM from Mycobacterium
bovis Bacille Calmette-Guérin (BCG) strain Pasteur, largely used throughout the world as vaccine against tuberculosis. Using
an up-to-date analytical approach, we found that the LAM of M. bovis BCG belongs to the class of LAMs capped with Manp. By
means of two-dimensional homonuclear and heteronuclear scalar coupling NMR analysis and methylation data, the sugar spin system
assignments were partially established, revealing that the LAM contained two types of terminal Manp and 2-O-linked Manp. From
the following four-step process: (i) partial hydrolysis of deacylated LAM (dLAM), (ii) oligosaccharide derivatization with
aminobenzoic ethyl ester, (iii) HPLC purification, (iv) FAB/MS-MS analysis; it was shown that the dimannosyl unit alpha-D-Manp-(1-->2)-alpha-D-Manp
is the major residue capping the termini of the arabinan of the LAM. In this report, LAM molecular mass determination was
established using matrix-assisted UV-laser desorption/ionization mass spectrometry which reveals that the LAM molecular mass
is around 17.4 kDa. The similarity of the LAM structures between M. bovis BCG and M. tuberculosis H37Rv is discussed in regard
to their function in the immunopathology of mycobacterial infection.</abstract><cop>Bethesda, MD</cop><pub>American Society for Biochemistry and Molecular Biology</pub><pmid>8509380</pmid><doi>10.1016/s0021-9258(18)31404-2</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0001-9013-8430</orcidid><orcidid>https://orcid.org/0000-0002-2581-3302</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Analytical, structural and metabolic biochemistry Antigens, Bacterial - chemistry Bacteriology Biochemistry Biochemistry, Molecular Biology Biological and medical sciences Carbohydrate Conformation Carbohydrate Sequence Carbohydrates Fundamental and applied biological sciences. Psychology Life Sciences Lipopolysaccharides - chemistry Lipopolysaccharides - isolation & purification Magnetic Resonance Spectroscopy Methylation Microbiology and Parasitology Miscellaneous Molecular Sequence Data Molecular Weight Mycobacterium bovis Mycobacterium bovis - chemistry Mycobacterium tuberculosis Mycobacterium tuberculosis - chemistry Oligosaccharides - chemistry Oligosaccharides - isolation & purification Other biological molecules Spectrometry, Mass, Fast Atom Bombardment |
title | Structural features of lipoarabinomannan from Mycobacterium bovis BCG. Determination of molecular mass by laser desorption mass spectrometry |
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