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Partial structure and immunological properties of lipopolysaccharide from marine-derived Pseudomonas stutzeri KMM 226
The partial structure and immunology of the lipopolysaccharide (LPS) of Pseudomonas stutzeri KMM 226, a bacterium isolated from a seawater sample collected at a depth of 2000 m, was characterised. The O-polysaccharide was built up of disaccharide repeating units constituted by l -Rha p and d -Glc p...
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Published in: | Antonie van Leeuwenhoek 2017-12, Vol.110 (12), p.1569-1580 |
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container_title | Antonie van Leeuwenhoek |
container_volume | 110 |
creator | Kokoulin, Maxim S. Sokolova, Ekaterina V. Elkin, Yuriy N. Romanenko, Lyudmila A. Mikhailov, Valery V. Komandrova, Nadezhda A. |
description | The partial structure and immunology of the lipopolysaccharide (LPS) of
Pseudomonas stutzeri
KMM 226, a bacterium isolated from a seawater sample collected at a depth of 2000 m, was characterised. The O-polysaccharide was built up of disaccharide repeating units constituted by
l
-Rha
p
and
d
-Glc
p
NAc: →2)-α-
l
-Rha
p
-(1→3)-α-
d
-Glc
p
NAc-(1→. The structural analysis of the lipid A showed a mixture of different species. The major species were hexa-acylated and penta-acylated lipids A, bearing the 12:0(3-OH) in amide linkage and 10:0(3-OH) in ester linkage, while the secondary fatty acids were present only as 12:0. The presence of 12:0(2-OH) was not detected. The immunology experiments demonstrated that
P. stutzeri
KMM 226 LPS displayed a low ability to induce TNF-α, IL-1β, IL-6, IL-8 and IL-10 cytokine production and acted as an antagonist of hexa-acylated
Escherichia coli
LPS in human blood in vitro. |
doi_str_mv | 10.1007/s10482-017-0907-6 |
format | article |
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Pseudomonas stutzeri
KMM 226, a bacterium isolated from a seawater sample collected at a depth of 2000 m, was characterised. The O-polysaccharide was built up of disaccharide repeating units constituted by
l
-Rha
p
and
d
-Glc
p
NAc: →2)-α-
l
-Rha
p
-(1→3)-α-
d
-Glc
p
NAc-(1→. The structural analysis of the lipid A showed a mixture of different species. The major species were hexa-acylated and penta-acylated lipids A, bearing the 12:0(3-OH) in amide linkage and 10:0(3-OH) in ester linkage, while the secondary fatty acids were present only as 12:0. The presence of 12:0(2-OH) was not detected. The immunology experiments demonstrated that
P. stutzeri
KMM 226 LPS displayed a low ability to induce TNF-α, IL-1β, IL-6, IL-8 and IL-10 cytokine production and acted as an antagonist of hexa-acylated
Escherichia coli
LPS in human blood in vitro.</description><identifier>ISSN: 0003-6072</identifier><identifier>EISSN: 1572-9699</identifier><identifier>DOI: 10.1007/s10482-017-0907-6</identifier><identifier>PMID: 28668995</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Biomedical and Life Sciences ; Chemical analysis ; Cytokines - blood ; Cytokines - metabolism ; E coli ; Fatty acids ; Humans ; Immunology ; Interleukin 10 ; Interleukin 6 ; Interleukin 8 ; Life Sciences ; Lipid A ; Lipid A - chemistry ; Lipid A - immunology ; Lipids ; Lipopolysaccharides ; Lipopolysaccharides - chemistry ; Lipopolysaccharides - immunology ; Magnetic Resonance Spectroscopy ; Marine biology ; Medical Microbiology ; Microbiology ; O Antigens - chemistry ; O Antigens - immunology ; Original Paper ; Plant Sciences ; Pseudomonas ; Pseudomonas Infections - blood ; Pseudomonas Infections - immunology ; Pseudomonas Infections - metabolism ; Pseudomonas stutzeri ; Pseudomonas stutzeri - classification ; Pseudomonas stutzeri - immunology ; Pseudomonas stutzeri - isolation & purification ; Samples ; Seawater ; Seawater - microbiology ; Soil Science & Conservation ; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization ; Structural analysis ; Toxins ; Tumor necrosis factor-α ; Water analysis ; Water Microbiology</subject><ispartof>Antonie van Leeuwenhoek, 2017-12, Vol.110 (12), p.1569-1580</ispartof><rights>Springer International Publishing AG 2017</rights><rights>Antonie van Leeuwenhoek is a copyright of Springer, (2017). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c372t-1ecfbd831b84f838ac868a17be4230f22ced2029db1e460470d3007785bb00cc3</citedby><cites>FETCH-LOGICAL-c372t-1ecfbd831b84f838ac868a17be4230f22ced2029db1e460470d3007785bb00cc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28668995$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kokoulin, Maxim S.</creatorcontrib><creatorcontrib>Sokolova, Ekaterina V.</creatorcontrib><creatorcontrib>Elkin, Yuriy N.</creatorcontrib><creatorcontrib>Romanenko, Lyudmila A.</creatorcontrib><creatorcontrib>Mikhailov, Valery V.</creatorcontrib><creatorcontrib>Komandrova, Nadezhda A.</creatorcontrib><title>Partial structure and immunological properties of lipopolysaccharide from marine-derived Pseudomonas stutzeri KMM 226</title><title>Antonie van Leeuwenhoek</title><addtitle>Antonie van Leeuwenhoek</addtitle><addtitle>Antonie Van Leeuwenhoek</addtitle><description>The partial structure and immunology of the lipopolysaccharide (LPS) of
Pseudomonas stutzeri
KMM 226, a bacterium isolated from a seawater sample collected at a depth of 2000 m, was characterised. The O-polysaccharide was built up of disaccharide repeating units constituted by
l
-Rha
p
and
d
-Glc
p
NAc: →2)-α-
l
-Rha
p
-(1→3)-α-
d
-Glc
p
NAc-(1→. The structural analysis of the lipid A showed a mixture of different species. The major species were hexa-acylated and penta-acylated lipids A, bearing the 12:0(3-OH) in amide linkage and 10:0(3-OH) in ester linkage, while the secondary fatty acids were present only as 12:0. The presence of 12:0(2-OH) was not detected. The immunology experiments demonstrated that
P. stutzeri
KMM 226 LPS displayed a low ability to induce TNF-α, IL-1β, IL-6, IL-8 and IL-10 cytokine production and acted as an antagonist of hexa-acylated
Escherichia coli
LPS in human blood in vitro.</description><subject>Biomedical and Life Sciences</subject><subject>Chemical analysis</subject><subject>Cytokines - blood</subject><subject>Cytokines - metabolism</subject><subject>E coli</subject><subject>Fatty acids</subject><subject>Humans</subject><subject>Immunology</subject><subject>Interleukin 10</subject><subject>Interleukin 6</subject><subject>Interleukin 8</subject><subject>Life Sciences</subject><subject>Lipid A</subject><subject>Lipid A - chemistry</subject><subject>Lipid A - immunology</subject><subject>Lipids</subject><subject>Lipopolysaccharides</subject><subject>Lipopolysaccharides - chemistry</subject><subject>Lipopolysaccharides - immunology</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>Marine biology</subject><subject>Medical Microbiology</subject><subject>Microbiology</subject><subject>O Antigens - chemistry</subject><subject>O Antigens - immunology</subject><subject>Original Paper</subject><subject>Plant Sciences</subject><subject>Pseudomonas</subject><subject>Pseudomonas Infections - blood</subject><subject>Pseudomonas Infections - immunology</subject><subject>Pseudomonas Infections - metabolism</subject><subject>Pseudomonas stutzeri</subject><subject>Pseudomonas stutzeri - classification</subject><subject>Pseudomonas stutzeri - immunology</subject><subject>Pseudomonas stutzeri - isolation & purification</subject><subject>Samples</subject><subject>Seawater</subject><subject>Seawater - microbiology</subject><subject>Soil Science & Conservation</subject><subject>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</subject><subject>Structural analysis</subject><subject>Toxins</subject><subject>Tumor necrosis factor-α</subject><subject>Water analysis</subject><subject>Water Microbiology</subject><issn>0003-6072</issn><issn>1572-9699</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp1kc1u1TAQhS1ERW8LD8AGWWLDxjB2Ev8sUVWgolW7gLXl2JOSKomDHSO1T4-vbkEIqSuPPd-c8cwh5DWH9xxAfcgcWi0YcMXAgGLyGdnxTglmpDHPyQ4AGiZBiWNykvNdvRqp1QtyLLSU2phuR8qNS9voJpq3VPxWElK3BDrOc1niFG9HX3NriitWDDONA53GNa5xus_O-x8ujQHpkOJM5xovyAKm8RcGepOxhDjHxeUqXraH-k6_Xl1RIeRLcjS4KeOrx_OUfP90_u3sC7u8_nxx9vGS-UaJjXH0Qx90w3vdDrrRzmupHVc9tqKBQQiPQYAwoefYSmgVhKbuRemu7wG8b07Ju4NuneBnwbzZecwep8ktGEu23PCu6yQHXtG3_6F3saSl_q5Sknewb1kpfqB8ijknHOyaxjr4veVg957Ygye2emL3nlhZa948Kpd-xvC34o8JFRAHINfUcovpn9ZPqv4G3iaYIQ</recordid><startdate>20171201</startdate><enddate>20171201</enddate><creator>Kokoulin, Maxim S.</creator><creator>Sokolova, Ekaterina V.</creator><creator>Elkin, Yuriy N.</creator><creator>Romanenko, Lyudmila A.</creator><creator>Mikhailov, Valery V.</creator><creator>Komandrova, Nadezhda A.</creator><general>Springer International Publishing</general><general>Springer Nature B.V</general><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>3V.</scope><scope>7QL</scope><scope>7T7</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20171201</creationdate><title>Partial structure and immunological properties of lipopolysaccharide from marine-derived Pseudomonas stutzeri KMM 226</title><author>Kokoulin, Maxim S. ; Sokolova, Ekaterina V. ; Elkin, Yuriy N. ; Romanenko, Lyudmila A. ; Mikhailov, Valery V. ; Komandrova, Nadezhda A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c372t-1ecfbd831b84f838ac868a17be4230f22ced2029db1e460470d3007785bb00cc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Biomedical and Life Sciences</topic><topic>Chemical analysis</topic><topic>Cytokines - 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classification</topic><topic>Pseudomonas stutzeri - immunology</topic><topic>Pseudomonas stutzeri - isolation & purification</topic><topic>Samples</topic><topic>Seawater</topic><topic>Seawater - microbiology</topic><topic>Soil Science & Conservation</topic><topic>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</topic><topic>Structural analysis</topic><topic>Toxins</topic><topic>Tumor necrosis factor-α</topic><topic>Water analysis</topic><topic>Water Microbiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kokoulin, Maxim S.</creatorcontrib><creatorcontrib>Sokolova, Ekaterina V.</creatorcontrib><creatorcontrib>Elkin, Yuriy N.</creatorcontrib><creatorcontrib>Romanenko, Lyudmila A.</creatorcontrib><creatorcontrib>Mikhailov, Valery V.</creatorcontrib><creatorcontrib>Komandrova, Nadezhda A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Virology and AIDS Abstracts</collection><collection>Health Medical collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Science Journals</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>ProQuest Biological Science Journals</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Antonie van Leeuwenhoek</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kokoulin, Maxim S.</au><au>Sokolova, Ekaterina V.</au><au>Elkin, Yuriy N.</au><au>Romanenko, Lyudmila A.</au><au>Mikhailov, Valery V.</au><au>Komandrova, Nadezhda A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Partial structure and immunological properties of lipopolysaccharide from marine-derived Pseudomonas stutzeri KMM 226</atitle><jtitle>Antonie van Leeuwenhoek</jtitle><stitle>Antonie van Leeuwenhoek</stitle><addtitle>Antonie Van Leeuwenhoek</addtitle><date>2017-12-01</date><risdate>2017</risdate><volume>110</volume><issue>12</issue><spage>1569</spage><epage>1580</epage><pages>1569-1580</pages><issn>0003-6072</issn><eissn>1572-9699</eissn><abstract>The partial structure and immunology of the lipopolysaccharide (LPS) of
Pseudomonas stutzeri
KMM 226, a bacterium isolated from a seawater sample collected at a depth of 2000 m, was characterised. The O-polysaccharide was built up of disaccharide repeating units constituted by
l
-Rha
p
and
d
-Glc
p
NAc: →2)-α-
l
-Rha
p
-(1→3)-α-
d
-Glc
p
NAc-(1→. The structural analysis of the lipid A showed a mixture of different species. The major species were hexa-acylated and penta-acylated lipids A, bearing the 12:0(3-OH) in amide linkage and 10:0(3-OH) in ester linkage, while the secondary fatty acids were present only as 12:0. The presence of 12:0(2-OH) was not detected. The immunology experiments demonstrated that
P. stutzeri
KMM 226 LPS displayed a low ability to induce TNF-α, IL-1β, IL-6, IL-8 and IL-10 cytokine production and acted as an antagonist of hexa-acylated
Escherichia coli
LPS in human blood in vitro.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>28668995</pmid><doi>10.1007/s10482-017-0907-6</doi><tpages>12</tpages></addata></record> |
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source | Springer Nature |
subjects | Biomedical and Life Sciences Chemical analysis Cytokines - blood Cytokines - metabolism E coli Fatty acids Humans Immunology Interleukin 10 Interleukin 6 Interleukin 8 Life Sciences Lipid A Lipid A - chemistry Lipid A - immunology Lipids Lipopolysaccharides Lipopolysaccharides - chemistry Lipopolysaccharides - immunology Magnetic Resonance Spectroscopy Marine biology Medical Microbiology Microbiology O Antigens - chemistry O Antigens - immunology Original Paper Plant Sciences Pseudomonas Pseudomonas Infections - blood Pseudomonas Infections - immunology Pseudomonas Infections - metabolism Pseudomonas stutzeri Pseudomonas stutzeri - classification Pseudomonas stutzeri - immunology Pseudomonas stutzeri - isolation & purification Samples Seawater Seawater - microbiology Soil Science & Conservation Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization Structural analysis Toxins Tumor necrosis factor-α Water analysis Water Microbiology |
title | Partial structure and immunological properties of lipopolysaccharide from marine-derived Pseudomonas stutzeri KMM 226 |
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