Literature DB >> 1840432

A simple synthesis of octyl 3,6-di-O-(alpha-D-mannopyranosyl)-beta-D-mannopyranoside and its use as an acceptor for the assay of N-acetylglucosaminyltransferase-I activity.

K J Kaur1, O Hindsgaul.   

Abstract

A simple synthesis of octyl 3,6-di-O-(alpha-D-mannopyranosyl)-beta-D-mannopyranoside is described. The key features of the synthetic scheme are the formation of the beta-mannosidic linkage by 1-O-alkylation of 2,3,4,6-tetra-O-acetyl-alpha,beta-D-mannopyranose with octyl iodide and glycosylation of unprotected octyl beta-D-mannopyranoside using limiting acetobromomannose. The trisaccharide is shown to be an acceptor for N-acetylglucosaminyltransferase-I with KM of 585 microM.

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Year:  1991        PMID: 1840432     DOI: 10.1007/bf00731017

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


  8 in total

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3.  Purification of mammalian glycosyltransferases.

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4.  The properties of a "synthetic" antigen related to the human blood-group Lewis a.

Authors:  R U Lemieux; D R Bundle; D A Baker
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5.  Enzymatic basis for the structural changes of asparagine-linked sugar chains of membrane glycoproteins of baby hamster kidney cells induced by polyoma transformation.

Authors:  K Yamashita; Y Tachibana; T Ohkura; A Kobata
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Review 6.  Biosynthetic controls that determine the branching and microheterogeneity of protein-bound oligosaccharides.

Authors:  H Schachter
Journal:  Biochem Cell Biol       Date:  1986-03       Impact factor: 3.626

7.  Control of glycoprotein synthesis. IX. A terminal Man alpha l-3Man beta 1- sequence in the substrate is the minimum requirement for UDP-N-acetyl-D-glucosamine: alpha-D-mannoside (GlcNAc to Man alpha 1-3) beta 2-N-acetylglucosaminyltransferase I.

Authors:  G J Vella; H Paulsen; H Schachter
Journal:  Can J Biochem Cell Biol       Date:  1984-06

8.  Control of glycoprotein synthesis. The use of oligosaccharide substrates and HPLC to study the sequential pathway for N-acetylglucosaminyltransferases I, II, III, IV, V, and VI in the biosynthesis of highly branched N-glycans by hen oviduct membranes.

Authors:  I Brockhausen; J P Carver; H Schachter
Journal:  Biochem Cell Biol       Date:  1988-10       Impact factor: 3.626

  8 in total
  5 in total

1.  Synthetic substrate analogues for UDP-GlcNAc: Man alpha 1-3R beta 1-2-N-acetylglucosaminyltransferase I. Substrate specificity and inhibitors for the enzyme.

Authors:  F Reck; M Springer; E Meinjohanns; H Paulsen; I Brockhausen; H Schachter
Journal:  Glycoconj J       Date:  1995-12       Impact factor: 2.916

2.  Mapmodulin: a possible modulator of the interaction of microtubule-associated proteins with microtubules.

Authors:  N Ulitzur; M Humbert; S R Pfeffer
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3.  Effect of shape, size, and valency of multivalent mannosides on their binding properties to phytohemagglutinins.

Authors:  R Roy; D Pagé; S F Perez; V V Bencomo
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4.  Control of glycoprotein synthesis: substrate specificity of rat liver UDP-GlcNAc:Man alpha 3R beta 2-N-acetylglucosaminyltransferase I using synthetic substrate analogues.

Authors:  G Möller; F Reck; H Paulsen; K J Kaur; M Sarkar; H Schachter; I Brockhausen
Journal:  Glycoconj J       Date:  1992-08       Impact factor: 2.916

5.  Synthetic substrate analogues for UDP-GlcNAc: Man alpha 1-6R beta(1-2)-N-acetylglucosaminyltransferase II. Substrate specificity and inhibitors for the enzyme.

Authors:  F Reck; E Meinjohanns; M Springer; R Wilkens; J A Van Dorst; H Paulsen; G Möller; I Brockhausen; H Schachter
Journal:  Glycoconj J       Date:  1994-06       Impact factor: 2.916

  5 in total

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