Literature DB >> 12706971

Structure and serological characterization of 5,7-diamino-3,5,7,9-tetradeoxy-non-2-ulosonic acid isolated from lipopolysaccharides of Vibrio parahaemolyticus O2 and O-untypable strain KX-V212.

Noritaka Hashii1, Yasunori Isshiki, Takehiro Iguchi, Kazuhito Hisatsune, Seiichi Kondo.   

Abstract

Lipopolysaccharides (LPS) of Vibrio parahaemolyticus O2 and O-untypable (OUT) strain (KX-V212) isolated from an individual patient were shown to contain 5,7-diamino-3,5,7,9-tetradeoxy-non-2-ulosonic acid (NonlA), which was readily released from LPS by mild acid hydrolysis. In the present study, we investigated the chemical and serological properties of NonlA isolated from LPS of V. parahaemolyticus O2 and OUT KX-V212. GC-MS and NMR analysis identified the NonlA from LPS of O2 to be 5,7-diacetamido-3,5,7,9-tetradeoxy-D-glycero-D-galacto-non-2-ulosonic acid (5NAc7NAcNonlA) and that from LPS of KX-V212 to be 5-acetamido-7-(N-acetyl-D-alanyl)amido-3,5,7,9-tetradeoxy-D-glycero-D-galacto-non-2-ulosonic acid (5NAc7NAlaNAcNonlA). In ELISA inhibition analysis, 5NAc7NAcNonlA inhibited the O2 LPS/anti-O2 antiserum system, whereas, 5NAc7NAlaNAcNonlA did not show any inhibitory activity. However, after N-deacylation of 5NAc7NAlaNAcNonlA followed by N-acetylation, the product (5NAc7NAcNonlA) inhibited the O2 LPS/anti-O2 antiserum system to the same extent as that of 5NAc7NAcNonlA obtained from O2 LPS. These results suggest that 5NAc7NAcNonlA might be related to the serological specificity of O2 LPS as one of main epitope(s) involved in O2 LPS.

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Year:  2003        PMID: 12706971     DOI: 10.1016/s0008-6215(03)00077-6

Source DB:  PubMed          Journal:  Carbohydr Res        ISSN: 0008-6215            Impact factor:   2.104


  5 in total

1.  Identification of a novel sugar 5,7-diacetamido-8-amino-3,5,7,8,9-pentadeoxy-D-glycero-D-galacto-non-2-ulosonic acid present in the lipooligosaccharide of Vibrio parahaemolyticus O3:K6.

Authors:  Koushik Mazumder; Biswa P Choudhury; G Balakrish Nair; Asish K Sen
Journal:  Glycoconj J       Date:  2007-11-10       Impact factor: 2.916

2.  A Diazido Mannose Analogue as a Chemoenzymatic Synthon for Synthesizing Di-N-acetyllegionaminic Acid-Containing Glycosides.

Authors:  Abhishek Santra; An Xiao; Hai Yu; Wanqing Li; Yanhong Li; Linh Ngo; John B McArthur; Xi Chen
Journal:  Angew Chem Int Ed Engl       Date:  2018-02-14       Impact factor: 15.336

3.  A new approach to the synthesis of legionaminic acid analogues.

Authors:  James R Carter; Milton J Kiefel
Journal:  RSC Adv       Date:  2018-10-19       Impact factor: 4.036

Review 4.  Exploration of the Sialic Acid World.

Authors:  Roland Schauer; Johannis P Kamerling
Journal:  Adv Carbohydr Chem Biochem       Date:  2018-11-28       Impact factor: 12.200

5.  Structure of the Exopolysaccharide Secreted by a Marine Strain Vibrio alginolyticus.

Authors:  Sophie Drouillard; Isabelle Jeacomine; Laurine Buon; Claire Boisset; Anthony Courtois; Bertrand Thollas; Pierre-Yves Morvan; Romuald Vallée; William Helbert
Journal:  Mar Drugs       Date:  2018-05-15       Impact factor: 5.118

  5 in total

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