English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT
  Automated glycan assembly of arabinomannan oligosaccharides from Mycobacterium tuberculosis

Pardo-Vargas, A., Bharate, P., Delbianco, M., & Seeberger, P. H. (2019). Automated glycan assembly of arabinomannan oligosaccharides from Mycobacterium tuberculosis. Beilstein Journal of Organic Chemistry, 15, 2936-2940. doi:10.3762/bjoc.15.288.

Item is

Files

show Files
hide Files
:
Article.pdf (Publisher version), 2MB
Name:
Article.pdf
Description:
-
OA-Status:
Visibility:
Public
MIME-Type / Checksum:
application/pdf / [MD5]
Technical Metadata:
Copyright Date:
-
Copyright Info:
-

Locators

show

Creators

show
hide
 Creators:
Pardo-Vargas, Alonso1, Author           
Bharate, Priya2, Author           
Delbianco, Martina3, Author           
Seeberger, Peter H.1, Author           
Affiliations:
1Peter H. Seeberger - Automated Systems, Biomolekulare Systeme, Max Planck Institute of Colloids and Interfaces, Max Planck Society, ou_1863306              
2Peter H. Seeberger - Nanoparticles and Colloidal Polymers, Biomolekulare Systeme, Max Planck Institute of Colloids and Interfaces, Max Planck Society, ou_1863307              
3Martina Delbianco, Biomolekulare Systeme, Max Planck Institute of Colloids and Interfaces, Max Planck Society, ou_2559692              

Content

show
hide
Free keywords: arabinomannan; automated glycan assembly; capping
 Abstract: Arabinomannan (AM) polysaccharides are clinical biomarkers for Mycobacterium tuberculosis (MTB) infections due to their roles in the interaction with host cells and interference with macrophage activation. Collections of defined AM oligosaccharides can help to improve the understanding of these polysaccharides and the development of novel therapeutical and diagnostic agents. Automated glycan assembly (AGA) was employed to prepare the core structure of AM from MTB, containing α-(1,6)-Man, α-(1,5)-Ara, and α-(1,2)-Man linkages. The introduction of a capping step after each glycosylation and further optimized reaction conditions allowed for the synthesis of a series of oligosaccharides, ranging from hexa- to branched dodecasaccharides.

Details

show
hide
Language(s): eng - English
 Dates: 2019-12-062019
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Identifiers: DOI: 10.3762/bjoc.15.288
 Degree: -

Event

show

Legal Case

show

Project information

show

Source 1

show
hide
Title: Beilstein Journal of Organic Chemistry
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: Frankfurt, Germany : Beilstein-Institut
Pages: - Volume / Issue: 15 Sequence Number: - Start / End Page: 2936 - 2940 Identifier: ISSN: 1860-5397