Teichuronic and teichulosonic acids of actinomycetes
The subject of the present review is the structural diversity and abundance of cell wall teichuronic and teichulosonic acids of representatives of the order Actinomycetales. Recently found teichulosonic acids are a new class of natural glycopolymers with ald-2-ulosonic acid residues: Kdn (3-deoxy-D-...
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| Veröffentlicht in: | Biochemistry (Moscow) 2011-07, Vol.76 (7), p.736-744 |
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| creator | Tul’skaya, E. M. Shashkov, A. S. Streshinskaya, G. M. Senchenkova, S. N. Potekhina, N. V. Kozlova, Yu. I. Evtushenko, L. I. |
| description | The subject of the present review is the structural diversity and abundance of cell wall teichuronic and teichulosonic acids of representatives of the order Actinomycetales. Recently found teichulosonic acids are a new class of natural glycopolymers with ald-2-ulosonic acid residues: Kdn (3-deoxy-D-
glycero
-D-
galacto
-non-2-ulosonic acid) or di-N-acyl derivatives of Pse (5,7-diamino-3,5,7,9-tetradeoxy-L-
glycero
-L-
manno
-non-2-ulosonic or pseudaminic acid) as the obligatory component. The structures of teichuronic and teichulosonic acids are presented. Data are summarized on the occurrence of the glycopolymers of different nature in the cell wall of the studied actinomycetes. The biological role of the glycopolymers and their possible taxonomic implication are discussed. The comprehensive tables given in the Supplement show
13
C NMR spectroscopic data of teichuronic and teichulosonic acids obtained by the authors. |
| doi_str_mv | 10.1134/S0006297911070030 |
| format | Article |
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glycero
-D-
galacto
-non-2-ulosonic acid) or di-N-acyl derivatives of Pse (5,7-diamino-3,5,7,9-tetradeoxy-L-
glycero
-L-
manno
-non-2-ulosonic or pseudaminic acid) as the obligatory component. The structures of teichuronic and teichulosonic acids are presented. Data are summarized on the occurrence of the glycopolymers of different nature in the cell wall of the studied actinomycetes. The biological role of the glycopolymers and their possible taxonomic implication are discussed. The comprehensive tables given in the Supplement show
13
C NMR spectroscopic data of teichuronic and teichulosonic acids obtained by the authors.</description><identifier>ISSN: 0006-2979</identifier><identifier>EISSN: 1608-3040</identifier><identifier>DOI: 10.1134/S0006297911070030</identifier><identifier>PMID: 21999534</identifier><language>eng</language><publisher>Dordrecht: SP MAIK Nauka/Interperiodica</publisher><subject>Acids ; Actinomycetales ; Actinomycetales - chemistry ; Biochemistry ; Biomedical and Life Sciences ; Biomedicine ; Bioorganic Chemistry ; Carbohydrate Sequence ; Cell Wall - chemistry ; Cells ; Life Sciences ; Microbiology ; Nuclear magnetic resonance spectroscopy ; Nuclear Magnetic Resonance, Biomolecular ; Review ; Sialic Acids - chemistry ; Sugar Acids - analysis ; Sugar Acids - chemistry ; Teichoic Acids - analysis ; Teichoic Acids - chemistry ; Uronic Acids - analysis ; Uronic Acids - chemistry</subject><ispartof>Biochemistry (Moscow), 2011-07, Vol.76 (7), p.736-744</ispartof><rights>Pleiades Publishing, Ltd. 2011</rights><rights>COPYRIGHT 2011 Springer</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c469t-ebe3170c7c8efd59fc2bb04b349c8603895aed5f9ab293a35fb7454f6dbfc01b3</citedby><cites>FETCH-LOGICAL-c469t-ebe3170c7c8efd59fc2bb04b349c8603895aed5f9ab293a35fb7454f6dbfc01b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1134/S0006297911070030$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1134/S0006297911070030$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27903,27904,41467,42536,51297</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21999534$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tul’skaya, E. M.</creatorcontrib><creatorcontrib>Shashkov, A. S.</creatorcontrib><creatorcontrib>Streshinskaya, G. M.</creatorcontrib><creatorcontrib>Senchenkova, S. N.</creatorcontrib><creatorcontrib>Potekhina, N. V.</creatorcontrib><creatorcontrib>Kozlova, Yu. I.</creatorcontrib><creatorcontrib>Evtushenko, L. I.</creatorcontrib><title>Teichuronic and teichulosonic acids of actinomycetes</title><title>Biochemistry (Moscow)</title><addtitle>Biochemistry Moscow</addtitle><addtitle>Biochemistry (Mosc)</addtitle><description>The subject of the present review is the structural diversity and abundance of cell wall teichuronic and teichulosonic acids of representatives of the order Actinomycetales. Recently found teichulosonic acids are a new class of natural glycopolymers with ald-2-ulosonic acid residues: Kdn (3-deoxy-D-
glycero
-D-
galacto
-non-2-ulosonic acid) or di-N-acyl derivatives of Pse (5,7-diamino-3,5,7,9-tetradeoxy-L-
glycero
-L-
manno
-non-2-ulosonic or pseudaminic acid) as the obligatory component. The structures of teichuronic and teichulosonic acids are presented. Data are summarized on the occurrence of the glycopolymers of different nature in the cell wall of the studied actinomycetes. The biological role of the glycopolymers and their possible taxonomic implication are discussed. The comprehensive tables given in the Supplement show
13
C NMR spectroscopic data of teichuronic and teichulosonic acids obtained by the authors.</description><subject>Acids</subject><subject>Actinomycetales</subject><subject>Actinomycetales - chemistry</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Bioorganic Chemistry</subject><subject>Carbohydrate Sequence</subject><subject>Cell Wall - chemistry</subject><subject>Cells</subject><subject>Life Sciences</subject><subject>Microbiology</subject><subject>Nuclear magnetic resonance spectroscopy</subject><subject>Nuclear Magnetic Resonance, Biomolecular</subject><subject>Review</subject><subject>Sialic Acids - chemistry</subject><subject>Sugar Acids - analysis</subject><subject>Sugar Acids - chemistry</subject><subject>Teichoic Acids - analysis</subject><subject>Teichoic Acids - chemistry</subject><subject>Uronic Acids - analysis</subject><subject>Uronic Acids - chemistry</subject><issn>0006-2979</issn><issn>1608-3040</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqNkctu1TAQhi0EoocDD8AGHcGCVco4dhzPsqq4SZVYUNaW7YyLqyQudrLo2-NDCoibhLywZ-b7f3s8jD3lcMq5kK8-AoBqsUfOoQcQcI_tuALdCJBwn-2O5eZYP2GPSrmuYQsoHrKTliNiJ-SOyUuK_vOa0xz9wc7DYfkWj6lsGR-HckihHpY4p-nW00LlMXsQ7Fjoyd2-Z5_evL48f9dcfHj7_vzsovFS4dKQI8F78L3XFIYOg2-dA-mERK8VCI2dpaELaF2LwoouuF52MqjBBQ_ciT17ufne5PRlpbKYKRZP42hnSmsxGpFLVLL9D1JrgVCv2bPnv5HXac1zbcPoXvX1f5Ss0IsNurIjmTiHtGTrj5bmTMhOodSir9TpX6i6BpqiTzOFWPO_CPgm8DmVkimYmxwnm28NB3OcqPljolXz7O69q5to-KH4PsIKtBtQamm-ovyzoX-7fgUQsKfC</recordid><startdate>20110701</startdate><enddate>20110701</enddate><creator>Tul’skaya, E. 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M.</au><au>Shashkov, A. S.</au><au>Streshinskaya, G. M.</au><au>Senchenkova, S. N.</au><au>Potekhina, N. V.</au><au>Kozlova, Yu. I.</au><au>Evtushenko, L. I.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Teichuronic and teichulosonic acids of actinomycetes</atitle><jtitle>Biochemistry (Moscow)</jtitle><stitle>Biochemistry Moscow</stitle><addtitle>Biochemistry (Mosc)</addtitle><date>2011-07-01</date><risdate>2011</risdate><volume>76</volume><issue>7</issue><spage>736</spage><epage>744</epage><pages>736-744</pages><issn>0006-2979</issn><eissn>1608-3040</eissn><abstract>The subject of the present review is the structural diversity and abundance of cell wall teichuronic and teichulosonic acids of representatives of the order Actinomycetales. Recently found teichulosonic acids are a new class of natural glycopolymers with ald-2-ulosonic acid residues: Kdn (3-deoxy-D-
glycero
-D-
galacto
-non-2-ulosonic acid) or di-N-acyl derivatives of Pse (5,7-diamino-3,5,7,9-tetradeoxy-L-
glycero
-L-
manno
-non-2-ulosonic or pseudaminic acid) as the obligatory component. The structures of teichuronic and teichulosonic acids are presented. Data are summarized on the occurrence of the glycopolymers of different nature in the cell wall of the studied actinomycetes. The biological role of the glycopolymers and their possible taxonomic implication are discussed. The comprehensive tables given in the Supplement show
13
C NMR spectroscopic data of teichuronic and teichulosonic acids obtained by the authors.</abstract><cop>Dordrecht</cop><pub>SP MAIK Nauka/Interperiodica</pub><pmid>21999534</pmid><doi>10.1134/S0006297911070030</doi><tpages>9</tpages></addata></record> |
| fulltext | fulltext |
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| ispartof | Biochemistry (Moscow), 2011-07, Vol.76 (7), p.736-744 |
| issn | 0006-2979 1608-3040 |
| language | eng |
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| source | MEDLINE; SpringerLink Journals - AutoHoldings |
| subjects | Acids Actinomycetales Actinomycetales - chemistry Biochemistry Biomedical and Life Sciences Biomedicine Bioorganic Chemistry Carbohydrate Sequence Cell Wall - chemistry Cells Life Sciences Microbiology Nuclear magnetic resonance spectroscopy Nuclear Magnetic Resonance, Biomolecular Review Sialic Acids - chemistry Sugar Acids - analysis Sugar Acids - chemistry Teichoic Acids - analysis Teichoic Acids - chemistry Uronic Acids - analysis Uronic Acids - chemistry |
| title | Teichuronic and teichulosonic acids of actinomycetes |
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