Literature DB >> 17603199

Determination of the absolute configuration of sialic acids in gangliosides from the sea cucumber Cucumaria echinata.

Fumiaki Kisa1, Koji Yamada, Tomofumi Miyamoto, Masanori Inagaki, Ryuichi Higuchi.   

Abstract

Enantiomeric pairs of sialic acid, D- and L-NeuAc (N-acetylneuraminic acid), were converted to D- and L-arabinose, respectively, by chemical degradation. Using this method, the absolute configuration of the sialic acid residues, NeuAc and NeuGc (N-glycolylneuraminic acid), in the gangliosides from the sea cucumber Cucumaria echinata was determined to be the D-form. Although naturally occurring sialic acids have been believed to be the D-form on the basis of biosynthetic evidence, this is the first report of the determination of the absolute configuration of the sialic acid residues in gangliosides using chemical methods.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17603199     DOI: 10.1248/cpb.55.1051

Source DB:  PubMed          Journal:  Chem Pharm Bull (Tokyo)        ISSN: 0009-2363            Impact factor:   1.645


  3 in total

Review 1.  Advanced Technologies in Sialic Acid and Sialoglycoconjugate Analysis.

Authors:  Ken Kitajima; Nissi Varki; Chihiro Sato
Journal:  Top Curr Chem       Date:  2015

Review 2.  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

Review 3.  Sphingolipids of Asteroidea and Holothuroidea: Structures and Biological Activities.

Authors:  Timofey V Malyarenko; Alla A Kicha; Valentin A Stonik; Natalia V Ivanchina
Journal:  Mar Drugs       Date:  2021-06-08       Impact factor: 5.118

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.