Literature DB >> 16226456

'Sweetening' natural products via glycorandomization.

Byron R Griffith1, Joseph M Langenhan, 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 for the generation of 'glycorandomized' libraries. Each member of these libraries is uniquely differentiated by an attached carbohydrate. Recently, two complementary glycorandomization strategies have emerged: chemoenzymatic glycorandomization, a biocatalytic approach dependent upon the substrate promiscuity of enzymes to activate and attach sugars to natural products, and neoglycorandomization, an efficient one-step chemical sugar ligation reaction that does not require prior sugar protection or activation. These strategies are likely to have a significant impact on fundamental glycoscience and drug discovery.

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Year:  2005        PMID: 16226456     DOI: 10.1016/j.copbio.2005.10.002

Source DB:  PubMed          Journal:  Curr Opin Biotechnol        ISSN: 0958-1669            Impact factor:   9.740


  33 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.  Complete set of glycosyltransferase structures in the calicheamicin biosynthetic pathway reveals the origin of regiospecificity.

Authors:  Aram Chang; Shanteri Singh; Kate E Helmich; Randal D Goff; Craig A Bingman; Jon S Thorson; George N Phillips
Journal:  Proc Natl Acad Sci U S A       Date:  2011-10-10       Impact factor: 11.205

3.  Molecular cloning of cyanobacterial pteridine glycosyltransferases that catalyze the transfer of either glucose or xylose to tetrahydrobiopterin.

Authors:  Yeol Gyun Lee; Ae Hyun Kim; Mi Bi Park; Hye-Lim Kim; Kon Ho Lee; Young Shik Park
Journal:  Appl Environ Microbiol       Date:  2010-09-17       Impact factor: 4.792

4.  Inactivation of gilGT, encoding a C-glycosyltransferase, and gilOIII, encoding a P450 enzyme, allows the details of the late biosynthetic pathway to gilvocarcin V to be delineated.

Authors:  Tao Liu; Madan Kumar Kharel; Carsten Fischer; Andrew McCormick; Jürgen Rohr
Journal:  Chembiochem       Date:  2006-07       Impact factor: 3.164

5.  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

6.  The in vitro characterization of polyene glycosyltransferases AmphDI and NysDI.

Authors:  Changsheng Zhang; Rocco Moretti; Jiqing Jiang; Jon S Thorson
Journal:  Chembiochem       Date:  2008-10-13       Impact factor: 3.164

7.  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

8.  A comparison of sugar indicators enables a universal high-throughput sugar-1-phosphate nucleotidyltransferase assay.

Authors:  Rocco Moretti; Jon S Thorson
Journal:  Anal Biochem       Date:  2008-03-15       Impact factor: 3.365

9.  Efficient production of L-ribose with a recombinant Escherichia coli biocatalyst.

Authors:  Ryan D Woodyer; Nathan J Wymer; F Michael Racine; Shama N Khan; Badal C Saha
Journal:  Appl Environ Microbiol       Date:  2008-03-14       Impact factor: 4.792

Review 10.  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

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