Literature DB >> 17006647

A chemical synthesis of UDP-LacNAc and its regioisomer for finding 'oligosaccharide transferases'.

Hironao Takaku1, Junhei Sato, Hide-Ki Ishida, Toshiyuki Inazu, Hideharu Ishida, Makoto Kiso.   

Abstract

A chemical synthesis of uridine 5'-diphospho-N-acetyllactosamine (Galbeta(1-->4)GlcNAc-UDP; UDP-LacNAc) and Galbeta(1-->3)GlcNAc-UDP is described. Coupling of the disaccharide imidate derivatives with dibenzylphosphate gave the corresponding 1-phosphates, which were condensed with UMP-imidazolate to give the target UDP-oligosaccharides after purification by anion exchange HPLC and gel filtration column chromatography. Using this methodology a variety of oligosaccharide nucleotide analogues can be synthesized. These UDP-oligosaccharides may be useful for finding so-called ;oligosaccharide transferases', the glycosyltransferases which transfer the oligosaccharide moiety onto glycosyl acceptors.

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Year:  2006        PMID: 17006647     DOI: 10.1007/s10719-006-7836-3

Source DB:  PubMed          Journal:  Glycoconj J        ISSN: 0282-0080            Impact factor:   2.916


  3 in total

1.  The acid-soluble nucleotides of milk. II. Isolation and identification of two novel uridine nucleotide oligosaccharide conjugates from human milk and colostrum.

Authors:  A KOBATA
Journal:  J Biochem       Date:  1963-03       Impact factor: 3.387

2.  Synthesis of nucleotide-activated oligosaccharides by beta-galactosidase from Bacillus circulans.

Authors:  A Zervosen; V Nieder; R G Gallego; J P Kamerling; J F Vliegenthart; L Elling
Journal:  Biol Chem       Date:  2001-02       Impact factor: 3.915

3.  UDP-N-Acetyl-alpha-D-glucosamine as acceptor substrate of beta-1,4-galactosyltransferase. Enzymatic synthesis of UDP-N-acetyllactosamine.

Authors:  L Elling; A Zervosen; R G Gallego; V Nieder; M Malissard; E G Berger; J F Vliegenthart; J P Kamerling
Journal:  Glycoconj J       Date:  1999-07       Impact factor: 2.916

  3 in total

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