Literature DB >> 24632507

Effect of acyl chain length on selective biocatalytic deacylation on O-aryl glycosides and separation of anomers.

Neha Aggarwal1, Anu Arya1, Divya Mathur1, Sukhdev Singh1, Abhilash Tyagi1, Rajesh Kumar1, Neha Rana1, Rajendra Singh2, Ashok K Prasad3.   

Abstract

It has been demonstrated that Lipozyme® TL IM (Thermomyces lanuginosus lipase immobilised on silica) can selectively deacylate the ester function involving the C-5' hydroxyl group of α-anomers over the other acyl functions of anomeric mixture of peracylated O-aryl α,β-D-ribofuranoside. The analysis of results of biocatalytic deacylation reaction revealed that the reaction time decreases with the increase in the acyl chain length from C1 to C4. The unique selectivity of Lipozyme® TL IM has been harnessed for the separation of anomeric mixture of peracylated O-aryl α,β-D-ribofuranosides, The lipase mediated selective deacylation methodology has been used for the synthesis of O-aryl α-D-ribofuranosides and O-aryl β-D-ribofuranosides in pure forms, which can be used as chromogenic substrate for the detection of pathogenic microbial parasites containing glycosidases.
Copyright © 2014. Published by Elsevier Inc.

Entities:  

Keywords:  Anomeric mixture; Diastereoselective deacylation; Lipozyme® TL IM; O-aryl α-D-ribofuranosides; O-aryl β-D-ribofuranosides; Peracylated O-aryl α,β-D-ribofuranosides

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Year:  2014        PMID: 24632507     DOI: 10.1016/j.bioorg.2014.02.004

Source DB:  PubMed          Journal:  Bioorg Chem        ISSN: 0045-2068            Impact factor:   5.275


  1 in total

1.  Enlarging the substrate portfolio of the thermophilic esterase EST2 from Alicyclobacillus acidocaldarius.

Authors:  Angela Pennacchio; Luigi Mandrich; Giuseppe Manco; Antonio Trincone
Journal:  Extremophiles       Date:  2015-07-28       Impact factor: 2.395

  1 in total

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