Literature DB >> 12633109

Substrate specificity of NovM: implications for novobiocin biosynthesis and glycorandomization.

Christoph Albermann1, Aileen Soriano, Jiqing Jiang, Heidi Vollmer, John B Biggins, William A Barton, Jacob Lesniak, Dimitar B Nikolov, Jon S Thorson.   

Abstract

[reaction: see text] In an effort to expand the scope of natural product in vitro glycorandomization (IVG), the substrate specificity of NovM was investigated. A test of four aglycon analogues and over 40 nucleotide sugars revealed NovM has a surprisingly stringent substrate specificity and provided only three new "unnatural" natural products. On the basis of the determined substrate specificity, an alternative to the sugar nucleotide biosynthetic dogma and a cautionary note for the general applicability of IVG are introduced.

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Year:  2003        PMID: 12633109     DOI: 10.1021/ol0341086

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  11 in total

1.  Tracking down biotransformation to the genetic level: identification of a highly flexible glycosyltransferase from Saccharothrix espanaensis.

Authors:  Tina Strobel; Yvonne Schmidt; Anton Linnenbrink; Andriy Luzhetskyy; Marta Luzhetska; Takaaki Taguchi; Elke Brötz; Thomas Paululat; Maryna Stasevych; Oleg Stanko; Volodymyr Novikov; Andreas Bechthold
Journal:  Appl Environ Microbiol       Date:  2013-06-21       Impact factor: 4.792

2.  Probing 3-hydroxyflavone for in vitro glycorandomization of flavonols by YjiC.

Authors:  Ramesh Prasad Pandey; Prakash Parajuli; Niranjan Koirala; Je Won Park; Jae Kyung Sohng
Journal:  Appl Environ Microbiol       Date:  2013-08-23       Impact factor: 4.792

3.  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

4.  Enzymatic Biosynthesis of Novel Resveratrol Glucoside and Glycoside Derivatives.

Authors:  Ramesh Prasad Pandey; Prakash Parajuli; Ju Yong Shin; Jisun Lee; Seul Lee; Young-Soo Hong; Yong Il Park; Joong Su Kim; Jae Kyung Sohng
Journal:  Appl Environ Microbiol       Date:  2014-09-19       Impact factor: 4.792

5.  An efficient and cost-effective preparation of di-O-acetyl-D-rhamnal.

Authors:  Justin N Miller; Rongson Pongdee
Journal:  Tetrahedron Lett       Date:  2013-06-12       Impact factor: 2.415

6.  Deciphering the late steps in the biosynthesis of the anti-tumour indolocarbazole staurosporine: sugar donor substrate flexibility of the StaG glycosyltransferase.

Authors:  Aaroa P Salas; Lili Zhu; César Sánchez; Alfredo F Braña; Jürgen Rohr; Carmen Méndez; José A Salas
Journal:  Mol Microbiol       Date:  2005-10       Impact factor: 3.501

7.  Recombinant E. coli prototype strains for in vivo glycorandomization.

Authors:  Gavin J Williams; Jie Yang; Changsheng Zhang; Jon S Thorson
Journal:  ACS Chem Biol       Date:  2010-10-22       Impact factor: 5.100

Review 8.  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 9.  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

10.  Creation of the first anomeric D/L-sugar kinase by means of directed evolution.

Authors:  Dirk Hoffmeister; Jie Yang; Lesley Liu; Jon S Thorson
Journal:  Proc Natl Acad Sci U S A       Date:  2003-11-11       Impact factor: 11.205

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