Literature DB >> 16309329

Neoglycorandomization and chemoenzymatic glycorandomization: two complementary tools for natural product diversification.

Joseph M Langenhan1, Byron R Griffith, Jon S Thorson.   

Abstract

In an effort to explore the contribution of the sugar constituents of pharmaceutically relevant glycosylated natural products, chemists have developed glycosylation methods that are amenable to the generation of libraries of analogues with a broad array of glycosidic attachments. Recently, two complementary glycorandomization strategies have been described, namely, neoglycorandomization, a chemical approach based on a one-step sugar ligation reaction that does not require any prior sugar protection or activation, and chemoenzymatic glycorandomization, a biocatalytic approach that relies on the substrate promiscuity of enzymes to activate and attach sugars to natural products. Since both methods require reducing sugars, this review first highlights recent advances in monosaccharide generation and then follows with an overview of recent progress in the development of neoglycorandomization and chemoenzymatic glycorandomization.

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Year:  2005        PMID: 16309329     DOI: 10.1021/np0502084

Source DB:  PubMed          Journal:  J Nat Prod        ISSN: 0163-3864            Impact factor:   4.050


  30 in total

1.  Assessment of chemoselective neoglycosylation methods using chlorambucil as a model.

Authors:  Randal D Goff; Jon S Thorson
Journal:  J Med Chem       Date:  2010-10-25       Impact factor: 7.446

2.  An approach to the site-selective deoxygenation of hydroxy groups based on catalytic phosphoramidite transfer.

Authors:  Peter A Jordan; Scott J Miller
Journal:  Angew Chem Int Ed Engl       Date:  2012-02-08       Impact factor: 15.336

3.  The evolution of gene collectives: How natural selection drives chemical innovation.

Authors:  Michael A Fischbach; Christopher T Walsh; Jon Clardy
Journal:  Proc Natl Acad Sci U S A       Date:  2008-01-23       Impact factor: 11.205

4.  Probing the aglycon promiscuity of an engineered glycosyltransferase.

Authors:  Richard W Gantt; Randal D Goff; Gavin J Williams; Jon S Thorson
Journal:  Angew Chem Int Ed Engl       Date:  2008       Impact factor: 15.336

5.  Optimizing glycosyltransferase specificity via "hot spot" saturation mutagenesis presents a catalyst for novobiocin glycorandomization.

Authors:  Gavin J Williams; Randal D Goff; Changsheng Zhang; Jon S Thorson
Journal:  Chem Biol       Date:  2008-04

6.  Enzymatic glycosylation of the topical antibiotic mupirocin.

Authors:  Prakash Parajuli; Ramesh Prasad Pandey; Anaya Raj Pokhrel; Gopal Prasad Ghimire; Jae Kyung Sohng
Journal:  Glycoconj J       Date:  2014-07-30       Impact factor: 2.916

7.  A processive carbohydrate polymerase that mediates bifunctional catalysis using a single active site.

Authors:  John F May; Matthew R Levengood; Rebecca A Splain; Christopher D Brown; Laura L Kiessling
Journal:  Biochemistry       Date:  2012-02-03       Impact factor: 3.162

Review 8.  Solid-phase glycan isolation for glycomics analysis.

Authors:  Shuang Yang; Hui Zhang
Journal:  Proteomics Clin Appl       Date:  2012-12       Impact factor: 3.494

Review 9.  Natural-product sugar biosynthesis and enzymatic glycodiversification.

Authors:  Christopher J Thibodeaux; Charles E Melançon; Hung-wen Liu
Journal:  Angew Chem Int Ed Engl       Date:  2008       Impact factor: 15.336

Review 10.  The impact of enzyme engineering upon natural product glycodiversification.

Authors:  Gavin J Williams; Richard W Gantt; Jon S Thorson
Journal:  Curr Opin Chem Biol       Date:  2008-10       Impact factor: 8.822

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